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Lista de obras de Kari Hemminki

5-Fluorouracil-based chemotherapy for colorectal cancer and MTHFR/MTRR genotypes

artículo científico publicado en 2011

7-Alkylguanine adduct levels in urine, lungs and liver of mice exposed to styrene by inhalation

artículo científico publicado en 2005

A Comprehensive Meta-analysis of Case-Control Association Studies to Evaluate Polymorphisms Associated with the Risk of Differentiated Thyroid Carcinoma.

artículo científico publicado en 2016

A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer

scientific article published on 01 June 2020

A bias in genotyping the ERBB2 (HER2) Ile655Val variant

artículo científico publicado en 2005

A candidate CpG SNP approach identifies a breast cancer associated ESR1‐SNP

artículo científico publicado el 11 de marzo de 2011

A case-control study of childhood acute lymphoblastic leukaemia and polymorphisms in the TGF-beta and receptor genes

artículo científico publicado en 2009

A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.

artículo científico publicado en 2016

A comprehensive investigation on common polymorphisms in the MDR1/ABCB1 transporter gene and susceptibility to colorectal cancer

artículo científico publicado en 2012

A functional promoter polymorphism in the TERT gene does not affect inherited susceptibility to breast cancer

artículo científico publicado en 2009

A gene-wide investigation on polymorphisms in the ABCG2/BRCP transporter and susceptibility to colorectal cancer

article

A gene-wide investigation on polymorphisms in the taste receptor 2R14 (TAS2R14) and susceptibility to colorectal cancer

artículo científico publicado en 2010

A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk

scientific article published on 18 November 2009

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

article

A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)

scientific journal article

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

artículo científico publicado en 2011

A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults

artículo científico publicado en 2008

A pooled analysis of second primary pancreatic cancer.

artículo científico publicado en 2006

A population-based comparison of second primary cancers in Germany and Sweden between 1997 and 2006: clinical implications and etiologic aspects

scientific article published on 27 August 2013

A rapid fluorescence based multiplex polymerase chain reaction — single-strand conformation polymorphism method forp53 mutation detection

artículo científico publicado en 2000

A simple-to-use method incorporating genomic markers into prostate cancer risk prediction tools facilitated future validation

artículo científico publicado en 2015

A single nucleotide polymorphism in the 3?untranslated region of theCDKN2A gene is common in sporadic primary melanomas but mutations in theCDKN2B,CDKN2C,CDK4 andp53 genes are rare

article

A single-nucleotide polymorphism in the XPG gene, and tumour stage, grade, and clinical course in patients with nonmuscle-invasive neoplasms of the urinary bladder.

artículo científico publicado en 2006

A study of occupational exposure to antineoplastic drugs and fetal loss in nurses

artículo científico publicado en 1985

A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women.

artículo científico publicado en 2008

A variant affecting miRNAs binding in the circadian gene Neuronal PAS domain protein 2 (NPAS2) is not associated with breast cancer risk.

artículo científico publicado en 2010

ARLTS1 polymorphisms and basal cell carcinoma of the skin

artículo científico publicado en 2007

ARLTS1 variants and melanoma risk

artículo científico publicado en 2006

ARLTS1 variants and risk of colorectal cancer

Abstract 1832: Associations between ovarian cancer and other malignant neoplasms in an international population-based study

Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9.

artículo científico publicado en 2003

Age at diagnosis and age at death in familial prostate cancer

scientific article published on 25 November 2009

Age specific and attributable risks of familial prostate carcinoma from the family-cancer database

Age- and time-dependent changes in cancer incidence among immigrants to Sweden: colorectal, lung, breast and prostate cancers

scientific article published on 05 December 2011

Age-Dependent Metastatic Spread and Survival: Cancer of Unknown Primary as a Model

artículo científico publicado en 2016

Age-specific familial risks for renal cell carcinoma with evidence on recessive heritable effects

scientific article published on 01 June 2004

Age-specific risk of incident prostate cancer and risk of death from prostate cancer defined by the number of affected family members

artículo científico publicado en 2010

Age-time risk patterns of solid cancers in 60 901 non-Hodgkin lymphoma survivors from Finland, Norway and Sweden

artículo científico publicado en 2013

Ala228 variant of trail receptor 1 affecting the ligand binding site is associated with chronic lymphocytic leukemia, mantle cell lymphoma, prostate cancer, head and neck squamous cell carcinoma and bladder cancer

Allelotyping of pooled DNA with 250 K SNP microarrays

artículo científico publicado en 2007

Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk

artículo científico publicado en 2019

Analysis of G1/S checkpoint regulators in metastatic melanoma

artículo científico publicado en 2000

Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population

artículo científico publicado en 2016

Ancestral susceptibility to colorectal cancer

artículo científico publicado en 2012

Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus

artículo científico publicado en 2010

Are twins at risk of cancer: results from the Swedish family-cancer database.

artículo científico publicado en 2005

Associated cancers in parents and offspring of polycythaemia vera and myelofibrosis patients

artículo científico publicado en 2009

Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin

artículo científico publicado en 2011

Association between number of siblings and nervous system tumors suggests an infectious etiology

artículo científico publicado en 2006

Association between the germline MC1R variants and somatic BRAF/NRAS mutations in melanoma tumors.

artículo científico publicado en 2010

Association between tumor characteristics and second primary cancers with cutaneous melanoma survival: A nationwide cohort study

artículo científico publicado en 2020

Association of () polymorphisms with breast cancer risk

Association of DNA repair polymorphisms with DNA repair functional outcomes in healthy human subjects

artículo científico publicado en 2006

Association of HLA-DRB1, interleukin-6 and cyclin D1 polymorphisms with cervical cancer in the Swedish population--a candidate gene approach

artículo científico publicado en 2009

Association of NCOA3 polymorphisms with breast cancer risk

artículo científico publicado en 2005

Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis

artículo científico publicado en 2008

Association of death receptor 4 haplotype 626C-683C with an increased breast cancer risk.

artículo científico publicado en 2005

Association of first ocular melanoma with subsequent cutaneous melanoma: Results from the Swedish Family-Cancer Database

article published in 2003

Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer.

artículo científico publicado en 2005

Association of inherited variation in Toll-like receptor genes with malignant melanoma susceptibility and survival

artículo científico publicado en 2011

Association of prolactin and its receptor gene regions with familial breast cancer.

artículo científico publicado en 2006

Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk

artículo científico publicado en 2006

Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant.

artículo científico publicado en 2005

Association study identifying polymorphisms in CD47 and other extracellular matrix pathway genes as putative prognostic markers for colorectal cancer.

artículo científico publicado en 2012

Associations between autoimmune conditions and hepatobiliary cancer risk among elderly US adults

artículo científico publicado en 2018

Associations between ocular melanoma and other primary cancers: an international population-based study.

artículo científico publicado en 2007

Associations between small intestine cancer and other primary cancers: an international population-based study

artículo científico

Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer

artículo científico publicado en 2006

Attributable risks for familial breast cancer by proband status and morphology: a nationwide epidemiologic study from Sweden

scholarly article by Kari Hemminki et al published 10 July 2002 in International Journal of Cancer

Attributable risks of familial cancer from the Family-Cancer Database

artículo científico publicado en 2002

Aurora kinases A and B and familial breast cancer risk

artículo científico publicado en 2006

Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

scientific article published in Nature Communications

Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

artículo científico publicado en 2019

Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

artículo científico publicado en 2019

Autoimmune disease and subsequent urological cancer

artículo científico publicado en 2012

Autoimmune disease in individuals and close family members and susceptibility to non-Hodgkin's lymphoma

article

Autoimmune diseases and hematological malignancies: Exploring the underlying mechanisms from epidemiological evidence

scientific article published on 07 June 2019

Autoimmunity and susceptibility to Hodgkin lymphoma: a population-based case-control study in Scandinavia

artículo científico publicado en 2006

B-RAF and N-RAS mutations are preserved during short time in vitro propagation and differentially impact prognosis

artículo científico publicado en 2007

B-RAFmutations in tumors from melanoma-breast cancer families

BRAF and NRAS Mutations Are Frequent in Nodular Melanoma but Are not Associated with Tumor Cell Proliferation or Patient Survival

article

BRAF mutations are common somatic events in melanocytic nevi

artículo científico publicado en 2004

BRAF mutations in metastatic melanoma: a possible association with clinical outcome.

artículo científico publicado en 2003

BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study

artículo científico publicado en 2007

Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism

artículo científico publicado en 2005

Bladder neoplasms--regions at chromosome 9 with putative tumour suppressor genes.

artículo científico publicado en 2003

Bleomycin-induced chromosomal damage and shortening of telomeres in peripheral blood lymphocytes of incident cancer patients.

artículo científico publicado en 2017

Borderline Ovarian Tumors Share Familial Risks with Themselves and Invasive Cancers

scientific article published on 17 July 2018

Bortezomib-induced peripheral neuropathy: A genome-wide association study on multiple myeloma patients

artículo científico publicado en 2017

Brain cancers in siblings of salivary gland cancer patients suggest viral etiology?

artículo científico publicado en 2008

Breast Cancer Genomics Based on Biobanks

artículo científico publicado el 1 de enero de 2011

Breast and prostate cancer: familial associations

artículo científico publicado en 2010

Breast cancer histology in immigrants to Sweden: do ethnic differences exist?

artículo científico publicado en 2012

Breast cancer risk in women who fulfill high-risk criteria: at what age should surveillance start?

artículo científico publicado en 2009

CDH1 mutations are present in both ductal and lobular breast cancer, but promoter allelic variants show no detectable breast cancer risk

artículo científico publicado en 2002

Cancer Characteristics in Swedish Families Fulfilling Criteria for Hereditary Nonpolyposis Colorectal Cancer

Cancer Predisposition Genes in Cancer-Free Families

artículo científico publicado en 2020

Cancer Risk in Relatives of Testicular Cancer Patients by Histology Type and Age at Diagnosis: A Joint Study from Five Nordic Countries.

artículo científico publicado en 2015

Cancer in immigrants as a pointer to the causes of cancer

artículo científico publicado en 2014

Cancer incidence among Iranian immigrants in Sweden and Iranian residents compared to the native Swedish population

artículo científico publicado en 2009

Cancer incidence among Turkish, Chilean, and North African first-generation immigrants in Sweden compared with residents in the countries of origin and native Swedes

artículo científico publicado en 2013

Cancer incidence, trends, and survival among immigrants to Sweden: a population-based study

artículo científico publicado en 2015

Cancer of unknown primary is associated with diabetes

artículo científico publicado en 2015

Cancer risk and mortality in asthma patients: A Swedish national cohort study

artículo científico publicado en 2015

Cancer risk in patients hospitalized with polymyalgia rheumatica and giant cell arteritis: a follow-up study in Sweden

artículo científico publicado en 2010

Cancer risk in patients with type 2 diabetes mellitus and their relatives.

artículo científico publicado en 2015

Cancer risks in childhood and adolescence among the offspring of immigrants to Sweden

artículo científico publicado en 2002

Cancer risks in first-generation immigrants to Sweden

scholarly article by Kari Hemminki et al published 22 April 2002 in International Journal of Cancer

Cancer risks in hairdressers: Assessment of carcinogenicity of hair dyes and gels

Cancer risks in second-generation immigrants to Sweden

artículo científico publicado en 2002

Cancer risks in twins: results from the Swedish family-cancer database.

artículo científico publicado en 2002

Cancer risks in ulcerative colitis patients

artículo científico publicado en 2008

Candidate gene association studies and risk of Hodgkin lymphoma: a systematic review and meta-analysis.

artículo científico publicado en 2015

Carcinogenicity of quinoline, styrene, and styrene-7,8-oxide.

publication published in 2018

Case-control estimation of the impact of oncolytic adenovirus on the survival of patients with refractory solid tumors

artículo científico publicado en 2014

Causes of death in patients with extranodal cancer of unknown primary: searching for the primary site

artículo científico publicado en 2014

Celiac disease confers a 1.6-fold increased risk of asthma: a nationwide population-based cohort study

artículo científico publicado en 2011

Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients

Chromosomal aberrations in tire plant workers and interaction with polymorphisms of biotransformation and DNA repair genes

artículo científico publicado en 2008

Chromosomal damage among medical staff occupationally exposed to volatile anesthetics, antineoplastic drugs, and formaldehyde

artículo científico publicado en 2013

Chromosomal damage and telomere length in peripheral blood lymphocytes of cancer patients

artículo científico publicado en 2020

Chromosomal damage in peripheral blood lymphocytes of newly diagnosed cancer patients and healthy controls.

artículo científico publicado en 2010

Chromosome 7p11.2 (EGFR) variation influences glioma risk

scientific journal article

Clinical Prognostic Markers of Non-seminomatous Germ Cell Tumours: An Insight from Swedish Family-cancer Database

artículo científico publicado el 1 de noviembre de 2010

Clinical course of bladder neoplasms and single nucleotide polymorphisms in theCDKN2Agene

article by Shigeru Sakano et al published 16 December 2002 in International Journal of Cancer

Clinical landscape of cancer metastases

artículo científico publicado en 2018

Cloning of genes involved in chromosomal translocations by high-resolution single nucleotide polymorphism genomic microarray

artículo científico publicado en 2008

Clustering of concordant and discordant cancer types in Swedish couples is rare

artículo científico publicado en 2010

Co-morbidity between early-onset leukemia and type 1 diabetes--suggestive of a shared viral etiology?

artículo científico publicado en 2012

Coding variants in NOD-like receptors: An association study on risk and survival of colorectal cancer.

artículo científico publicado en 2018

Collection and use of family history in oncology clinics

artículo científico publicado en 2014

Colorectal cancer patients: what do they die of?

artículo científico publicado en 2012

Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors

artículo científico publicado en 2014

Common cancers share familial susceptibility: implications for cancer genetics and counselling

artículo científico publicado en 2016

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk

scientific journal article

Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk

scientific journal article

Comparability of cancer identification among Death Registry, Cancer Registry and Hospital Discharge Registry

artículo científico publicado en 2012

Comparison of Familial Clustering of Anogenital and Skin Cancers Between In Situ and Invasive Types

scientific article published on 06 November 2019

Comparison of six statistics of genetic association regarding their ability to discriminate between causal variants and genetically linked markers

artículo científico publicado en 2011

Comparison of survival of patients with metastases from known versus unknown primaries: survival in metastatic cancer

artículo científico publicado en 2013

Concordance of survival in family members with prostate cancer

artículo científico publicado en 2008

Concordant and discordant familial cancer: Familial risks, proportions and population impact

artículo científico publicado en 2016

Consensus pathways implicated in prognosis of colorectal cancer identified through systematic enrichment analysis of gene expression profiling studies

artículo científico publicado en 2011

Consideration of family history of cancer in medical routine: a survey in the primary care setting in Germany

artículo científico publicado en 2014

Constraints for genetic association studies imposed by attributable fraction and familial risk

artículo científico publicado en 2006

Contribution of the Defective BRCA1, BRCA2 and CHEK2 Genes to the Familial Aggregation of Breast Cancer: a Simulation Study Based on the Swedish Family-Cancer Database

artículo científico publicado en 2004

Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk

artículo científico publicado en 2007

Copy number variation in patients with cervical artery dissection

artículo científico publicado en 2012

Copy number variations of GSTT1 and GSTM1, colorectal cancer risk and possible effect modification of cigarette smoking and menopausal hormone therapy

artículo científico publicado en 2012

Correction: Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study.

artículo científico publicado en 2018

Correction: Familial risks of ovarian cancer by age at diagnosis, proband type and histology

artículo científico publicado en 2018

Correction: Inherited variants in genes somatically mutated in thyroid cancer

artículo científico publicado en 2018

Correction: Single nucleotide polymorphisms within MUC4 are associated with colorectal cancer survival

scientific article published on 06 June 2019

Correlation analysis of production and photoisomerization of epidermal urocanic acid versus induction and repair of DNA photoproducts in the human skin in situ

artículo científico publicado en 2002

Correspondence re: Risch, N.: Genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches. Cancer Epidemiol. Biomark. Prev., 10: 733-741, 2001

scientific article published on 01 April 2002

Correspondence re: Zheng et al, Haplotype of two variants in p16 (CDKN2/MTS-1/INK4a) exon 3 and risk of squamous cell carcinoma of the head and neck: a case-control study. 11: 640-645, 2002.

artículo científico publicado en 2003

Correspondence: SEMA4A variation and risk of colorectal cancer

artículo científico publicado en 2016

Could polymorphisms in ATP-binding cassette C3/multidrug resistance associated protein 3 (ABCC3/MRP3) modify colorectal cancer risk?

Cytogenetic aberrations in multiple myeloma are associated with shifts in serum immunoglobulin isotypes distribution and levels

artículo científico publicado en 2018

Cytogenetic markers, DNA single-strand breaks, urinary metabolites, and DNA repair rates in styrene-exposed lamination workers

artículo científico publicado en 2004

DNA damage, DNA repair rates and mRNA expression levels of cell cycle genes (TP53, p21(CDKN1A), BCL2 and BAX) with respect to occupational exposure to styrene.

artículo científico publicado en 2010

DNA repair gene and MTHFR gene polymorphisms as prognostic markers in locally advanced adenocarcinoma of the esophagus or stomach treated with cisplatin and 5-fluorouracil-based neoadjuvant chemotherapy

artículo científico publicado en 2011

Death receptor 4 variants and colorectal cancer risk.

artículo científico publicado en 2006

Deciphering the 8q24.21 association for glioma

artículo científico publicado en 2013

Dectin-1 and DC-SIGN polymorphisms associated with invasive pulmonary Aspergillosis infection

artículo científico publicado en 2012

Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study

artículo científico

Demonstration of UV-dimers in human skin DNA in situ 3 weeks after exposure

artículo científico publicado en 2002

Detecting homozygous deletions in the CDKN2A(p16(INK4a))/ARF(p14(ARF)) gene in urinary bladder cancer using real-time quantitative PCR.

artículo científico publicado en 2003

Determinants of unfavorable presentation of primary cutaneous melanoma

artículo científico publicado en 2011

Determination of allele frequency in pooled DNA: comparison of three PCR-based methods

artículo científico publicado en 2005

Determining the Appropriate Risk-Adapted Screening Age for Familial Breast Cancer

artículo científico publicado en 2020

Differences in global gene expression in melanoma cell lines with and without homozygous deletion of the CDKN2A locus genes.

artículo científico publicado en 2006

Differential gene expression in melanocytic nevi with the V600E BRAF mutation.

artículo científico publicado en 2007

Direct evidence for a polygenic etiology in familial multiple myeloma

scientific article published on 07 April 2017

Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population

scientific article published on 04 October 2019

Distribution and risk of the second discordant primary cancers combined after a specific first primary cancer in German and Swedish cancer registries

artículo científico publicado en 2015

Do GST polymorphisms modulate the frequency of chromosomal aberrations in healthy subjects?

artículo científico publicado en 2009

Do discordant cancers share familial susceptibility?

artículo científico publicado en 2011

Do inflammatory bowel disease and cancer share susceptibility: a family study

artículo científico publicado en 2008

Do reproductive factors influence T, N, and M classes of ductal and lobular breast cancers? A nation-wide follow-up study

artículo científico publicado en 2013

Does immigration play a role in the risk of gastric cancer by site and by histological type? A study of first-generation immigrants in Sweden.

artículo científico publicado en 2011

Does immigration play a role in the risk of pancreatic cancer? A study on immigrants to Sweden

artículo científico publicado en 2010

Does solar exposure, as indicated by the non-melanoma skin cancers, protect from solid cancers: vitamin D as a possible explanation

artículo científico

Does the breast cancer age at diagnosis differ by ethnicity? A study on immigrants to Sweden

artículo científico publicado en 2011

Does the risk of stomach cancer remain among second-generation immigrants in Sweden?

artículo científico publicado en 2011

Does the time interval between first and last birth influence the risk of endometrial and ovarian cancer?

artículo científico publicado el 4 de noviembre de 2010

Editorial

artículo científico publicado en 2009

Effect of a detailed family history of melanoma on risk for other tumors: a cohort study based on the nationwide Swedish Family-Cancer Database

artículo científico publicado en 2013

Effect of autoimmune diseases on incidence and survival in subsequent multiple myeloma

artículo científico publicado en 2012

Effect of autoimmune diseases on risk and survival in female cancers

artículo científico publicado en 2012

Effect of autoimmune diseases on risk and survival in histology-specific lung cancer

artículo científico publicado en 2012

Effect of common B-RAF and N-RAS mutations on global gene expression in melanoma cell lines

artículo científico publicado en 2005

Effect of multiplicity, laterality, and age at onset of breast cancer on familial risk of breast cancer: a nationwide prospective cohort study

artículo científico publicado en 2014

Effect of the spectral range of a UV lamp on the production of cyclobutane pyrimidine dimers in human skin in situ

artículo científico publicado el 1 de diciembre de 2003

Effect of type 2 diabetes predisposing genetic variants on colorectal cancer risk

artículo científico publicado en 2012

Effects of screening for breast cancer on its age-incidence relationships and familial risk

artículo científico publicado en 2005

Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance

artículo científico publicado en 2019

Emigration flows from North Africa to Europe

artículo científico publicado en 2014

Endometrial cancer: population attributable risks from reproductive, familial and socioeconomic factors

artículo científico publicado en 2005

Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.

artículo científico publicado en 2018

Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish Family-Cancer Database.

artículo científico publicado en 2002

Epistatic effect of TLR3 and cGAS-STING-IKKε-TBK1-IFN signaling variants on colorectal cancer risk

artículo científico publicado en 2019

Erratum: Molecular and genetic damage in humans from environmental pollution in Poland

scientific article published in Nature

Esophageal cancer risk among immigrants in Sweden

artículo científico publicado en 2011

Ethnic differences in breast cancer risk and survival: a study on immigrants in Sweden

artículo científico publicado en 2013

Ethnic differences in incidence of type 1 diabetes among second-generation immigrants and adoptees from abroad

scientific article published on 18 December 2009

Etiologic impact of known cancer susceptibility genes

artículo científico publicado en 2007

Evaluation of SNPs in miR-146a, miR196a2 and miR-499 as low-penetrance alleles in German and Italian familial breast cancer cases

artículo científico publicado en 2010

Evidence of Inbreeding in Hodgkin Lymphoma

artículo científico publicado en 2016

Exposure to low environmental levels of benzene: evaluation of micronucleus frequencies and S-phenylmercapturic acid excretion in relation to polymorphisms in genes encoding metabolic enzymes

artículo científico publicado en 2010

Familial Associations Between Prostate Cancer and Other Cancers

artículo científico publicado en 2016

Familial Associations in Testicular Cancer with Other Cancers

scientific article published on 18 July 2018

Familial Associations of Colon and Rectal Cancers With Other Cancers

artículo científico publicado en 2019

Familial Associations of Colorectal Cancer with Other Cancers

artículo científico publicado en 2017

Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family

artículo científico publicado en 2018

Familial Cancer: How to Successfully Recruit Families for Germline Mutations Studies? Multiple Myeloma as an Example

artículo científico publicado en 2019

Familial Clustering, Second Primary Cancers and Causes of Death in Penile, Vulvar and Vaginal Cancers

articulo cientifico

Familial Ovarian Cancer Clusters with Other Cancers

artículo científico publicado en 2018

Familial Risks Between Urolithiasis and Cancer

artículo científico publicado en 2018

Familial Risks and Mortality in Second Primary Cancers in Melanoma

artículo científico publicado en 2018

Familial Risks in Cancer of Unknown Primary: Tracking the Primary Sites

artículo científico publicado el 28 de diciembre de 2010

Familial Urinary Bladder Cancer with Other Cancers

artículo científico publicado en 2018

Familial [corrected] transmission of coronary heart disease: a cohort study of 80,214 Swedish adoptees linked to their biological and adoptive parents

scientific article published on 18 July 2011

Familial aggregation and heterogeneity of non-Hodgkin lymphoma in population-based samples

artículo científico publicado en 2005

Familial aggregation of Hodgkin lymphoma and related tumors

artículo científico publicado en 2004

Familial and attributable risks in cutaneous melanoma: effects of proband and age

article published in 2003

Familial and second esophageal cancers: a nation-wide epidemiologic study from Sweden

scientific article published on 01 March 2002

Familial and second gastric carcinomas: a nationwide epidemiologic study from Sweden

artículo científico publicado en 2002

Familial and second lung cancers: a nation-wide epidemiologic study from Sweden

artículo científico publicado en 2003

Familial and second primary pancreatic cancers: a nationwide epidemiologic study from Sweden

artículo científico publicado en 2003

Familial association of colorectal adenocarcinoma with cancers at other sites

scientific article published on 01 November 2004

Familial association of histology specific breast cancers with cancers at other sites

artículo científico publicado en 2004

Familial association of inflammatory bowel diseases with other autoimmune and related diseases

artículo científico publicado en 2009

Familial association of leukemia with colorectal cancer

artículo científico publicado en 2004

Familial association of prostate cancer with other cancers in the Swedish Family-Cancer Database

artículo científico publicado en 2005

Familial association of specific histologic types of ovarian malignancy with other malignancies

artículo científico publicado en 2004

Familial associations between autoimmune hepatitis and primary biliary cholangitis and other autoimmune diseases

artículo científico publicado en 2020

Familial associations for Addison disease and between Addison disease and other autoimmune diseases

artículo científico publicado en 2020

Familial associations for rheumatoid autoimmune diseases

artículo científico publicado en 2020

Familial associations of female breast cancer with other cancers

artículo científico publicado en 2017

Familial associations of male breast cancer with other cancers

artículo científico publicado en 2017

Familial associations of rheumatoid arthritis with autoimmune diseases and related conditions

artículo científico publicado en 2009

Familial bladder cancer and the related genes

artículo científico publicado en 2011

Familial breast cancer: scope for more susceptibility genes?

artículo científico publicado en 2003

Familial breast carcinoma risks by morphology: a nationwide epidemiologic study from Sweden

scientific article published on 01 June 2002

Familial characteristics of autoimmune and hematologic disorders in 8,406 multiple myeloma patients: a population-based case-control study.

artículo científico publicado en 2006

Familial clustering of cancer at human papillomavirus-associated sites according to the Swedish Family-Cancer Database

artículo científico publicado en 2008

Familial invasive and borderline ovarian tumors by proband status, age and histology

artículo científico publicado el 10 de julio de 2003

Familial lung cancer and aggregation of smoking habits: a simulation of the effect of shared environmental factors on the familial risk of cancer

artículo científico publicado en 2005

Familial melanoma by histology and age: joint data from five Nordic countries

artículo científico publicado en 2014

Familial mortality and familial incidence in cancer

artículo científico publicado en 2011

Familial multiple primary lung cancers: a population-based analysis from Sweden

scientific article published on 01 March 2005

Familial myeloid leukemias from the Swedish Family-Cancer Database

artículo científico publicado en 2002

Familial renal cell carcinoma from the Swedish Family-Cancer Database

artículo científico publicado en 2011

Familial risk and familial survival in prostate cancer

artículo científico publicado en 2011

Familial risk for colon and rectal cancers

artículo científico publicado en 2004

Familial risk for colorectal cancers are mainly due to heritable causes

artículo científico publicado en 2004

Familial risk for esophageal cancer: an updated epidemiologic study from Sweden

scientific article published on 04 May 2006

Familial risk for histology-specific bone cancers: an updated study in Sweden

scientific article published on 21 July 2006

Familial risk for lung cancer by histology and age of onset: evidence for recessive inheritance

artículo científico publicado en 2005

Familial risk for non-Hodgkin lymphoma and other lymphoproliferative malignancies by histopathologic subtype: the Swedish Family-Cancer Database

artículo científico publicado en 2005

Familial risk for soft tissue tumors: a nation-wide epidemiological study from Sweden

scholarly article by Jianguang Ji et al published 11 October 2007 in Journal of Cancer Research and Clinical Oncology

Familial risk of cancer by site and histopathology

artículo científico publicado en 2003

Familial risk of cancer shortly after diagnosis of the first familial tumor

artículo científico publicado en 2005

Familial risk of cancer: data for clinical counseling and cancer genetics

artículo científico publicado en 2004

Familial risk of ischemic and hemorrhagic stroke: a large-scale study of the Swedish population

artículo científico publicado en 2006

Familial risk of lymphoproliferative tumors in families of patients with chronic lymphocytic leukemia: results from the Swedish Family-Cancer Database

artículo científico publicado en 2004

Familial risk of pleural mesothelioma increased drastically in certain occupations: A nationwide prospective cohort study

artículo científico publicado en 2018

Familial risk of small intestinal carcinoid and adenocarcinoma

artículo científico publicado en 2013

Familial risk of urological cancers: data for clinical counseling

artículo científico publicado en 2003

Familial risks and temporal incidence trends of multiple myeloma

artículo científico publicado en 2006

Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden

artículo científico publicado en 2020

Familial risks between giant cell arteritis and Takayasu arteritis and other autoimmune diseases in the population of Sweden

artículo científico publicado en 2020

Familial risks for amyotrophic lateral sclerosis and autoimmune diseases

artículo científico publicado en 2008

Familial risks for cancer as the basis for evidence-based clinical referral and counseling

scientific article published on 01 March 2008

Familial risks for cervical tumors in full and half siblings: etiologic apportioning

artículo científico publicado en 2006

Familial risks for childhood acute lymphocytic leukaemia in Sweden and Finland: far exceeding the effects of known germline variants

artículo científico publicado en 2012

Familial risks for colorectal cancer show evidence on recessive inheritance

artículo científico publicado en 2005

Familial risks for common diseases: etiologic clues and guidance to gene identification

artículo científico publicado en 2008

Familial risks for depression among siblings based on hospitalizations in Sweden

artículo científico publicado en 2008

Familial risks for diseases of myoneural junction and muscle in siblings based on hospitalizations and deaths in sweden.

artículo científico publicado en 2006

Familial risks for epilepsy among siblings based on hospitalizations in Sweden.

artículo científico publicado en 2006

Familial risks for eye melanoma and retinoblastoma: results from the Swedish Family-Cancer Database

artículo científico publicado en 2006

Familial risks for gallstones in the population of Sweden

artículo científico publicado en 2017

Familial risks for hospitalization with endocrine diseases

artículo científico publicado en 2008

Familial risks for hospitalized Graves' disease and goiter

artículo científico publicado en 2009

Familial risks for main neurological diseases in siblings based on hospitalizations in Sweden

artículo científico publicado en 2006

Familial risks for migraine and other headaches among siblings based on hospitalizations in Sweden

artículo científico publicado en 2005

Familial risks for nerve, nerve root and plexus disorders in siblings based on hospitalisations in Sweden

artículo científico publicado en 2007

Familial risks for nonmedullary thyroid cancer

artículo científico publicado en 2005

Familial risks for type 2 diabetes in Sweden

artículo científico publicado en 2009

Familial risks in and between stone diseases: sialolithiasis, urolithiasis and cholelithiasis in the population of Sweden.

artículo científico publicado en 2018

Familial risks in nervous system tumors.

artículo científico publicado en 2003

Familial risks in nervous-system tumours: a histology-specific analysis from Sweden and Norway

artículo científico publicado en 2009

Familial risks in testicular cancer as aetiological clues

artículo científico publicado en 2006

Familial risks in understanding type 1 diabetes genetics

artículo científico publicado en 2011

Familial risks in urolithiasis in the population of sweden

artículo científico publicado en 2017

Familial risks of acute myeloid leukemia, myelodysplastic syndromes, and myeloproliferative neoplasms

artículo científico publicado en 2018

Familial risks of age-related macular degeneration

artículo científico publicado en 2011

Familial risks of aortic aneurysms among siblings in a nationwide Swedish study

artículo científico publicado en 2006

Familial risks of breast and prostate cancers: does the definition of the at risk period matter?

artículo científico publicado en 2010

Familial risks of cancer as a guide to gene identification and mode of inheritance.

artículo científico publicado en 2004

Familial risks of hospitalization for Parkinson's disease in first-degree relatives: a nationwide follow-up study from Sweden

artículo científico publicado en 2006

Familial risks of ovarian cancer by age at diagnosis, proband type and histology

scientific article published in PLoS ONE

Familial risks of psychotic disorders and schizophrenia among siblings based on hospitalizations in Sweden

artículo científico publicado en 2009

Familial risks of second primary cancers and mortality in ovarian cancer patients

Familial sarcoma: challenging pedigrees

artículo científico publicado en 2004

Familial upper aerodigestive tract cancers: incidence trends, familial clustering and subsequent cancers

artículo científico publicado en 2003

Finnish and Swedish genotypes and risk of cancer in Sweden

artículo científico publicado en 2003

Foreword: Euro-Mediterranean partnership and EUNAM.

artículo científico publicado en 2014

Frequent DPH3 promoter mutations in skin cancers

artículo científico publicado en 2015

Functional TLR5 genetic variants affect human colorectal cancer survival

artículo científico publicado en 2013

Functional dissection of inherited non-coding variation influencing multiple myeloma risk

artículo científico publicado en 2022

Functional germline variants in driver genes of breast cancer

artículo científico publicado en 2017

GWAS-identified common variants for obesity are not associated with the risk of developing colorectal cancer

artículo científico publicado en 2014

Gender effects in familial cancer

artículo científico publicado en 2002

Gender-specific effects of genetic variants within Th1 and Th17 cell-mediated immune response genes on the risk of developing rheumatoid arthritis

artículo científico publicado en 2013

Gene-environment interactions in cancer: do they exist?

artículo científico publicado en 2006

Gene-environment studies: any advantage over environmental studies?

artículo científico publicado en 2007

Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism

artículo científico publicado en 2017

Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy: Replication of the Reported Candidate Susceptibility Loci

artículo científico publicado en 2016

Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population

scientific article published on 10 January 2020

Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology

scholarly article by Molly Went et al published 21 December 2018 in Blood Cancer Journal

Genetic epidemiology of cancer: from families to heritable genes

artículo científico publicado en 2004

Genetic epidemiology of colorectal cancer and associated cancers

scientific article published on 19 August 2019

Genetic polymorphisms and possible gene–gene interactions in metabolic and DNA repair genes: Effects on DNA damage

article

Genetic polymorphisms in DNA repair genes and possible links with DNA repair rates, chromosomal aberrations and single-strand breaks in DNA

article

Genetic polymorphisms in host innate immune sensor genes and the risk of nasopharyngeal carcinoma in North Africa

artículo científico publicado en 2013

Genetic predisposition for multiple myeloma

scientific article published on 08 January 2020

Genetic risks caused by occupational chemicals. Use of experimental methods and occupational risk group monitoring in the detection of environmental chemicals causing mutations, cancer and malformations.

artículo científico publicado en 2011

Genetic signature of differentiated thyroid carcinoma susceptibility: a machine learning approach

artículo científico publicado en 2022

Genetic status of cell cycle regulators in squamous cell carcinoma of the oesophagus: the CDKN2A (p16(INK4a) and p14(ARF) ) and p53 genes are major targets for inactivation

artículo científico publicado en 2002

Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome

artículo científico publicado en 2013

Genetic variants in hormone-related genes and risk of breast cancer

artículo científico publicado en 2013

Genetic variants within miR-126 and miR-335 are not associated with breast cancer risk.

artículo científico publicado en 2010

Genetic variation associated with chromosomal aberration frequency: A genome-wide association study

artículo científico publicado en 2018

Genetic variation in ALCAM and other chromosomal instability genes in breast cancer survival.

artículo científico publicado en 2011

Genetic variation in adipokine genes and risk of colorectal cancer.

artículo científico publicado en 2009

Genetic variation in genes encoding for polymerase ζ subunits associates with breast cancer risk, tumour characteristics and survival

artículo científico publicado en 2011

Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans.

artículo científico publicado en 2016

Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer risk

artículo científico publicado en 2007

Genetic variation of acquired structural chromosomal aberrations

artículo científico publicado en 2018

Genetics of gallbladder cancer

artículo científico publicado en 2017

Genetics of inflammatory bowel disease: population aspects

artículo científico publicado en 2008

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

artículo científico publicado en 2013

Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci

artículo científico publicado en 2017

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

artículo científico publicado en 2010

Genome-wide association study identifies multiple susceptibility loci for multiple myeloma

artículo científico publicado en 2016

Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia.

artículo científico publicado en 2018

Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma

artículo científico publicado en 2016

Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma

artículo científico publicado en 2018

Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

artículo científico publicado en 2017

Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.

artículo científico publicado en 2017

Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma

artículo científico publicado en 2019

Genome-wide association study on differentiated thyroid cancer

scientific journal article

Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma

artículo científico publicado en 2019

Genome-wide investigation of gene-environment interactions in colorectal cancer

artículo científico publicado en 2012

Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1

scientific article published on 01 April 2020

Genomewide association study on monoclonal gammopathy of unknown significance (MGUS).

artículo científico publicado en 2017

Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis

artículo científico publicado en 2020

Genotypes, haplotypes and diplotypes of three XPC polymorphisms in urinary-bladder cancer patients

article published in 2010

Germline genetics of cancer of unknown primary (CUP) and its specific subtypes

artículo científico publicado en 2016

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma

scientific journal article

HLA and KIR Associations of Cervical Neoplasia

artículo científico publicado en 2018

Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach

artículo científico publicado en 2014

Heritable and environmental components in cervical tumors

artículo científico publicado en 2006

High constant incidence rates of second primary cancers of the head and neck: a pooled analysis of 13 cancer registries

artículo científico publicado en 2010

High familial risks for cerebral palsy implicate partial heritable aetiology.

artículo científico publicado en 2007

High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk

artículo científico publicado en 2007

Higher risk of primary cancers after polycythaemia vera and vice versa

scientific article published on 31 January 2011

Histology-specific risks in testicular cancer in immigrants to Sweden

artículo científico publicado en 2010

How fast are UV-dimers repaired in human skin DNA in situ?

artículo científico publicado en 2002

Human estrogen receptor beta 548 is not a common variant in three distinct populations

artículo científico publicado en 2003

IARC monographs: 40 years of evaluating carcinogenic hazards to humans

artículo científico publicado en 2015

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing

artículo científico publicado en 2020

Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity

artículo científico publicado en 2010

Identification of frequent chromosome copy-number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays

artículo científico publicado en 2006

Identification of miRSNPs associated with the risk of multiple myeloma.

artículo científico publicado en 2016

Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

scientific article published in Nature Communications

Immigrant health, our health

artículo científico publicado en 2014

Impact of family history of cancer on risk and mortality of second cancers in patients with prostate cancer

artículo científico publicado en 2018

Impact of functional germline variants and a deletion polymorphism in APOBEC3A and APOBEC3B on breast cancer risk and survival in a Swedish study population

artículo científico publicado en 2015

Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans

scientific article published on 15 September 2020

Impact of immigration on HIV-1 molecular epidemiology in West Africa, Maghreb and Southern Europe

artículo científico

Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma

Implications of results of molecular epidemiology on DNA adducts, their repair and mutations for mechanisms of human cancer.

artículo científico publicado en 2004

Importance of tumor location and histology in familial risk of upper gastrointestinal cancers: a nationwide cohort study

In situ repair of cyclobutane pyrimidine dimers in skin and melanocytic nevi of cutaneous melanoma patients

artículo científico publicado en 2002

Inbreeding and homozygosity in breast cancer survival

artículo científico publicado en 2015

Incidence Differences Between First Primary Cancers and Second Primary Cancers Following Skin Squamous Cell Carcinoma as Etiological Clues

artículo científico publicado en 2020

Incidence and familial risks in pituitary adenoma and associated tumors

artículo científico publicado en 2007

Incidence and mortality in epithelial ovarian cancer by family history of any cancer

artículo científico publicado el 1 de septiembre de 2011

Incidence and survival in non-hereditary amyloidosis in Sweden

artículo científico publicado en 2012

Incidence differences for gallbladder cancer between occupational groups suggest an etiological role for alcohol

artículo científico publicado en 2005

Incidence of cancer of unknown primary in Sweden: analysis by location of metastasis.

artículo científico publicado en 2012

Incidence of celiac disease among second-generation immigrants and adoptees from abroad in Sweden: evidence for ethnic differences in susceptibility

artículo científico publicado en 2011

Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases

artículo científico publicado en 2013

Incidence of multiple primary malignancies among patients with bone cancers in Sweden

artículo científico publicado en 2006

Incidence trends and familial risks in invasive and in situ cutaneous melanoma by sun-exposed body sites

artículo científico publicado en 2003

Incidence trends of squamous cell and rare skin cancers in the Swedish national cancer registry point to calendar year and age-dependent increases

artículo científico

Incorporation of detailed family history from the Swedish Family Cancer Database into the PCPT risk calculator

artículo científico publicado en 2014

Increased risk of hepatobiliary cancers after hospitalization for autoimmune disease

artículo científico publicado en 2013

Infectious diseases in North Africa and North African immigrants to Europe

artículo científico publicado en 2014

Influence of GSTM1, GSTT1, GSTP1 and NAT2 genotypes on the p53 mutational spectrum in bladder tumours

artículo científico publicado en 2005

Influence of education level on breast cancer risk and survival in Sweden between 1990 and 2004

scientific article published on 01 January 2008

Influence of family size and birth order on risk of cancer: a population-based study

artículo científico publicado en 2011

Influence of genetic variants in type I interferon genes on melanoma survival and therapy

artículo científico publicado en 2012

Influence of polymorphism in DNA repair and defence genes on p53 mutations in bladder tumours.

artículo científico publicado en 2005

Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example

scientific article published on 31 July 2020

Inherited genetic susceptibility to monoclonal gammopathy of unknown significance

artículo científico publicado en 2014

Inherited predisposition to early onset lung cancer according to histological type

artículo científico publicado en 2004

Inherited susceptibility to bleomycin-induced micronuclei: correlating polymorphisms in GSTT1, GSTM1 and DNA repair genes with mutagen sensitivity

artículo científico publicado en 2007

Inherited variants in genes somatically mutated in thyroid cancer

artículo científico publicado en 2017

Inorganic arsenic and basal cell carcinoma in areas of Hungary, Romania, and Slovakia: a case-control study

artículo científico publicado en 2012

Insulin pathway related genes and risk of colorectal cancer: INSR promoter polymorphism shows a protective effect

scientific article published on 01 September 2007

Integrin genes and susceptibility to human melanoma.

artículo científico publicado en 2011

Interaction between functional polymorphic variants in cytokine genes, established risk factors and susceptibility to basal cell carcinoma of skin

artículo científico publicado en 2011

Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer

artículo científico publicado en 2006

Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects.

artículo científico publicado en 2015

Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer

artículo científico publicado en 2018

Is family history associated with improved survival in patients with gastric cancer?

artículo científico publicado en 2012

Is risk of pleural mesothelioma an environmental risk outside Turkey? A study on immigrants to Sweden

scientific article published on 13 February 2010

Joint occurrence of Merkel cell carcinoma and non-Hodgkin lymphomas in four Nordic countries.

artículo científico publicado en 2015

Kaposi sarcoma and Merkel cell carcinoma after autoimmune disease

scientific article published on 27 January 2012

Kidney cancer in the Swedish Family Cancer Database: familial risks and second primary malignancies

article by Kamila Czene & Kari Hemminki published May 2002 in Kidney International

Level of education and the risk of cancer in Sweden.

artículo científico publicado en 2003

Levels of DNA damage (Micronuclei) in patients suffering from chronic kidney disease. Role of GST polymorphisms

artículo científico publicado en 2018

Life style and cancer: effect of divorce

artículo científico publicado en 2002

Lifestyle and cancer: effect of parental divorce

artículo científico publicado en 2006

Lifestyle and cancer: effect of widowhood and divorce

artículo científico publicado el 1 de septiembre de 2003

Liver and gallbladder cancer in immigrants to Sweden

artículo científico publicado en 2010

Location of metastases in cancer of unknown primary are not random and signal familial clustering

artículo científico publicado en 2016

Loci associated with genomic damage levels in chronic kidney disease patients and controls

scientific article published on 10 March 2020

Low expression of hexokinase-2 is associated with false-negative FDG-positron emission tomography in multiple myeloma

artículo científico publicado en 2017

Low frequency ofBRAFandCDKN2Amutations in endometrial cancer

Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients

artículo científico publicado en 2010

MC1R variants associated susceptibility to basal cell carcinoma of skin: interaction with host factors and XRCC3 polymorphism

artículo científico publicado en 2008

MDM2 SNP309 and cancer risk: a combined analysis.

artículo científico publicado en 2007

MTHFR and MTRR genotype and haplotype analysis and colorectal cancer susceptibility in a case–control study from the Czech Republic

article

MTHFR genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukemia

artículo científico publicado en 2005

Mammographic screening is dramatically changing age-incidence data for breast cancer.

artículo científico publicado en 2004

Mapping of deletion breakpoints at the CDKN2A locus in melanoma: detection of MTAP-ANRIL fusion transcripts

artículo científico publicado en 2016

Markers of individual susceptibility and DNA repair rate in workers exposed to xenobiotics in a tire plant

artículo científico publicado en 2004

Measurement of cyclobutane thymidine dimers in melanocytic nevi and surrounding epidermis in human skin in situ

artículo científico publicado en 2002

Melanocortin receptor 1 variants and melanoma risk: a study of 2 European populations

artículo científico publicado en 2009

Mesothelioma incidence has leveled off in Sweden

scientific article published on 01 March 2008

Mesothelioma incidence seems to have leveled off in Sweden

artículo científico publicado en 2003

Mesothelioma is a killer of urban men in Sweden

scientific article published on 01 May 2003

Metabolic gene variants associated with chromosomal aberrations in healthy humans

artículo científico publicado en 2015

Metastatic spread in patients with gastric cancer

scientific article published on 20 July 2016

Micronuclei in cord blood lymphocytes and associations with biomarkers of exposure to carcinogens and hormonally active factors, gene polymorphisms, and gene expression: the NewGeneris cohort

artículo científico publicado en 2013

Micronuclei in humans induced by exposure to low level of ionizing radiation: influence of polymorphisms in DNA repair genes

article

Micronuclei, DNA single-strand breaks and DNA-repair activity in mice exposed to 1,3-butadiene by inhalation.

artículo científico publicado en 2006

Modification of risk for subsequent cancer after female breast cancer by a family history of breast cancer.

artículo científico publicado en 2007

Modulation of DNA repair capacity and mRNA expression levels of XRCC1, hOGG1 and XPC genes in styrene-exposed workers

artículo científico publicado en 2010

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

artículo científico publicado en 2008

Molecular epidemiology of VHL gene mutations in renal cell carcinoma patients: relation to dietary and other factors

artículo científico publicado en 2002

Molecular genetic analysis of NBS1 in German melanoma patients.

artículo científico publicado en 2007

Morbidity and mortality in gynecological cancers among first- and second-generation immigrants in Sweden

artículo científico publicado en 2011

Morphological types of breast cancer in family members and multiple primary tumours: is morphology genetically determined?

artículo científico publicado en 2002

Mortality causes in cancer patients with type 2 diabetes mellitus

scientific article published on 01 May 2012

Multiple Melanomas After Treatment for Hodgkin Lymphoma in a Non-Dutch p16-Leiden Mutation Carrier With 2 MC1R High-Risk Variants

Multiple myeloma risk variant at 7p15.3 creates an IRF4-binding site and interferes with CDCA7L expression

artículo científico publicado en 2016

Multiple myeloma: family history and mortality in second primary cancers

scholarly article by Subhayan Chattopadhyay et al published 7 August 2018 in Blood Cancer Journal

Multiple primary (even in situ) melanomas in a patient pose significant risk to family members

artículo científico publicado en 2014

Multiple primary cancers as clues to environmental and heritable causes of cancer and mechanisms of carcinogenesis.

artículo científico publicado en 2004

Mutations in TERT promoter and FGFR3 and telomere length in bladder cancer.

artículo científico publicado en 2015

Mutations in the CDKN2A ( p16INK4a ) gene in microdissected sporadic primary melanomas

article

MyelomA Genetics International Consortium

artículo científico

Myeloproliferative disorders in Sweden: Incidence trends and multiple tumors

artículo científico publicado en 2008

NBN and XRCC3 genetic variants in childhood acute lymphoblastic leukaemia.

artículo científico publicado en 2014

Nasopharyngeal and hypopharyngeal carcinoma risk among immigrants in Sweden

artículo científico publicado el 15 de diciembre de 2010

New aspects in the biomonitoring of occupational exposure to styrene

artículo científico publicado en 2002

New cancer susceptibility loci: population and familial risks

artículo científico publicado en 2008

New common variants affecting susceptibility to basal cell carcinoma

artículo científico publicado en 2009

No evidence for anticipation in lymphoproliferative tumors in population-based samples.

artículo científico publicado en 2005

Non-Hodgkin lymphoma in familial amyloid polyneuropathy patients in Sweden

artículo científico publicado en 2013

Nonendocrine cancers associated with benign and malignant parathyroid tumors

artículo científico publicado en 2011

Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk

artículo científico publicado en 2015

Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk

artículo científico publicado en 2014

Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis

artículo científico publicado en 2017

Nuclear receptor coregulator SNP discovery and impact on breast cancer risk

artículo científico publicado en 2009

Number of siblings and the risk of lymphoma, leukemia, and myeloma by histopathology

artículo científico publicado en 2006

Obesity and familial obesity and risk of cancer

artículo científico publicado en 2011

Obligation for cell line authentication: appeal for concerted action

artículo científico publicado en 2010

Obstructive sleep apnea syndrome in siblings: an 8-year Swedish follow-up study

artículo científico publicado en 2008

Occupation and upper aerodigestive tract cancers: a follow-up study in Sweden

artículo científico publicado en 2005

Occupational risk factors for kidney cancer: a cohort study in Sweden

scientific article published on 01 September 2005

Occupational risks for nasal cancer in Sweden

artículo científico publicado en 2004

Occurrences of leukemia subtypes by socioeconomic and occupational groups in Sweden.

artículo científico publicado en 2005

Origin of B-Cell Neoplasms in Autoimmune Disease

artículo científico publicado en 2016

Other cancers in lung cancer families are overwhelmingly smoking-related cancers

artículo científico publicado en 2017

Overview on health research ethics in Egypt and North Africa

artículo científico publicado en 2014

PAI-1 -675 4G/5G polymorphism as a prognostic biomarker in breast cancer

scientific article published on 07 July 2007

POMC and TP53 genetic variability and risk of basal cell carcinoma of skin: Interaction between host and genetic factors

artículo científico publicado en 2011

Parental cancer as a risk factor for bone cancer: a nation-wide study from Sweden

scientific article published on 01 February 2002

Parental lung cancer as predictor of cancer risks in offspring: clues about multiple routes of harmful influence?

artículo científico publicado en 2006

Patterns of autoimmunity and subsequent chronic lymphocytic leukemia in Nordic countries

artículo científico publicado en 2006

Patterns of metastasis in colon and rectal cancer

scientific article published on 15 July 2016

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

artículo científico publicado en 2016

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

scientific article published on 29 October 2019

Polyglutamine repeat length in the NCOA3 does not affect risk in familial breast cancer

scientific article published on 01 January 2005

Polymorphisms and haplotype structures in genes for transforming growth factor beta1 and its receptors in familial and unselected breast cancers

artículo científico publicado en 2004

Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk

artículo científico publicado en 2009

Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications

artículo científico publicado en 2010

Polymorphisms in DNA repair and metabolic genes in bladder cancer

artículo científico publicado en 2003

Polymorphisms in genes involved in GH1 release and their association with breast cancer risk

artículo científico publicado en 2006

Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer: ITGB4 as prognostic marker

artículo científico publicado en 2008

Polymorphisms in telomere-associated genes, breast cancer susceptibility and prognosis

artículo científico publicado en 2009

Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis?

artículo científico publicado en 2010

Polymorphisms in the IGF-1 and IGFBP 3 promoter and the risk of breast cancer.

artículo científico publicado en 2005

Polymorphisms in the Janus kinase 2 (JAK)/signal transducer and activator of transcription (STAT) genes: putative association of the STAT gene region with familial breast cancer

scientific article published on 01 June 2007

Polymorphisms in the KDR and POSTN genes: association with breast cancer susceptibility and prognosis

artículo científico publicado en 2006

Polymorphisms in the estrogen receptor beta gene and risk of breast cancer: no association

artículo científico publicado en 2003

Polymorphisms in the growth hormone receptor: a case-control study in breast cancer

artículo científico publicado en 2006

Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer

artículo científico publicado en 2012

Polymorphisms in the transforming growth factor beta 1 pathway in relation to colorectal cancer progression.

artículo científico publicado en 2010

Polymorphisms inNQO1and the clinical course of urinary bladder neoplasms

Polymorphisms inXPD,XPCand the risk of death in patients with urinary bladder neoplasms

artículo científico publicado en 2007

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

artículo científico publicado en 2010

Polymorphisms within base and nucleotide excision repair pathways and risk of differentiated thyroid carcinoma.

artículo científico publicado en 2016

Polymorphisms within micro-RNA-binding sites and risk of sporadic colorectal cancer

artículo científico

Population attributable risks for breast cancer in Swedish women by morphological type

scientific article published on 08 November 2007

Predictive and Prognostic Clinical Variables in Cancer Patients Treated With Adenoviral Oncolytic Immunotherapy

artículo científico publicado en 2016

Prevalence of overweight and obesity in adults from North Africa

artículo científico publicado en 2014

Preventable breast cancer is postmenopausal

Profound impact of sample processing delay on gene expression of multiple myeloma plasma cells.

artículo científico publicado en 2015

Prognostic impact of polymorphisms in the MYBL2 interacting genes in breast cancer

artículo científico publicado en 2011

Prognostic significance of homozygous deletions and multiple duplications at the CDKN2A (p16INK4a)/ARF (p14ARF) locus in urinary bladder cancer.

artículo científico publicado en 2006

Promoter polymorphisms in matrix metalloproteinases and their inhibitors: few associations with breast cancer susceptibility and progression

artículo científico publicado en 2006

Proper controls for SNP studies?

artículo científico publicado en 2002

Prostate cancer incidence and survival in immigrants to Sweden

artículo científico publicado en 2013

Prostate cancer risk assessment model: a scoring model based on the Swedish Family-Cancer Database

artículo científico publicado en 2012

Prostate cancer screening, changing age-specific incidence trends and implications on familial risk

artículo científico

Prostate cancer survivors: Risk and mortality in second primary cancers

artículo científico publicado en 2018

Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches

artículo científico publicado en 2015

RE: Familial Cancer Clustering of Urothelial Cancer: A Population-Based Case-Control Study.

artículo científico publicado en 2018

Rate differences between first and second primary cancers may outline immune dysfunction as a key risk factor

scientific article published on 22 September 2020

Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia

artículo científico publicado en 2011

Re: "Familial risk of multiple sclerosis: a nationwide cohort study"

artículo científico publicado en 2006

Re: "underlying genetic models of inheritance in established type 2 diabetes associations".

artículo científico publicado en 2010

Re: Association Between Endothelin Receptor B Nonsynonymous Variants and Melanoma Risk

article published in 2006

Re: Association of a common variant of the CASP8 gene with reduced risk of breast cancer

artículo científico publicado en 2005

Re: Integrin beta3 Leu33Pro homozygosity and risk of cancer

artículo científico publicado en 2004

Re: Multifocality in testicular germ cell tumors Y. Ehrlich, M. Konichezky, O. Yossepowitch and J. Baniel J Urol 2009, 181: 1114-1120

artículo científico publicado en 2010

Re: Prostate cancer in fathers with fewer male offspring: the Jerusalem Perinatal Study cohort

artículo científico publicado en 2007

Re: Risk of subsequent cancer following breast cancer in men

artículo científico publicado en 2002

Re: Risks of cancer and families

scientific article published on 01 April 2006

Re: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis

artículo científico publicado en 2014

Re: familial multiple myeloma: a family study and review of the literature

artículo científico publicado en 2002

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer

artículo científico publicado en 2015

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer

article

Relationships between familial risks of cancer and the effects of heritable genes and their SNP variants

artículo científico publicado en 2005

Renal cell carcinoma as first and second primary cancer: etiological clues from the Swedish Family-Cancer Database.

artículo científico publicado en 2011

Repair of UV dimers in skin DNA of patients with basal cell carcinoma

artículo científico publicado en 2008

Repeat polymorphisms in ESR2 and AR and colorectal cancer risk and prognosis: results from a German population-based case-control study

artículo científico publicado en 2014

Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis

artículo científico publicado en 2009

Research recommendations for selected IARC-classified agents

artículo científico publicado en 2010

Response: Methods for second primary cancers evaluation have to be standardized

artículo científico publicado en 2017

Risk factors for cancers of unknown primary site: Results from the prospective EPIC cohort

Risk for contralateral breast cancers in a population covered by mammography: effects of family history, age at diagnosis and histology

artículo científico publicado en 2006

Risk for familial breast cancer increases with age.

artículo científico publicado en 2002

Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions

artículo científico publicado en 2008

Risk of Kaposi sarcoma among immigrants to Sweden

artículo científico publicado en 2014

Risk of Next Melanoma in Patients With Familial and Sporadic Melanoma by Number of Previous Melanomas

artículo científico publicado en 2015

Risk of Second Cancer in Hodgkin Lymphoma Survivors and Influence of Family History

artículo científico publicado en 2017

Risk of Second Primary Cancers in Multiple Myeloma Survivors in German and Swedish Cancer Registries

artículo científico publicado en 2016

Risk of asthma and autoimmune diseases and related conditions in patients hospitalized for obesity

artículo científico publicado en 2011

Risk of breast cancer in families of multiple affected women and men.

artículo científico publicado en 2011

Risk of cancer among the offspring of women who experienced parental death during pregnancy

artículo científico publicado en 2007

Risk of cancer following hospitalization for type 2 diabetes

artículo científico publicado en 2010

Risk of cancer in patients with medically diagnosed hay fever or allergic rhinitis

artículo científico publicado en 2014

Risk of cancer of unknown primary after hospitalization for autoimmune diseases

artículo científico publicado en 2015

Risk of cancer of unknown primary among immigrants to Sweden

scientific article published on 01 January 2012

Risk of familial breast cancer is not increased after pregnancy

artículo científico publicado en 2007

Risk of familial classical Hodgkin lymphoma by relationship, histology, age, and sex: a joint study from five Nordic countries

artículo científico publicado en 2015

Risk of inflammatory bowel disease in first- and second-generation immigrants in Sweden: a nationwide follow-up study

artículo científico publicado en 2010

Risk of lung cancer by histology among immigrants to Sweden

artículo científico publicado en 2011

Risk of other Cancers in Families with Melanoma: Novel Familial Links

artículo científico publicado en 2017

Risk of second cancer among women with breast cancer

article by Lene Mellemkjær et al published 2006 in International Journal of Cancer

Risk of second malignant neoplasms after childhood leukemia and lymphoma: an international study

artículo científico publicado en 2007

Risk of second malignant neoplasms among lymphoma patients with a family history of cancer.

artículo científico publicado en 2007

Risk of second primary cancer among esophageal cancer patients: a pooled analysis of 13 cancer registries

artículo científico

Risk of second primary cancer among patients with head and neck cancers: A pooled analysis of 13 cancer registries

artículo científico publicado en 2008

Risk of second primary cancer following myeloid neoplasia and risk of myeloid neoplasia as second primary cancer: a nationwide, observational follow up study in Sweden

scientific article published on 01 August 2018

Risk of second primary cancers after malignant mesothelioma and vice versa

artículo científico publicado en 2016

Risk of second primary cancers in women diagnosed with endometrial cancer in German and Swedish cancer registries

artículo científico publicado en 2017

Risk of subsequent cancers in renal cell carcinoma survivors with a family history

artículo científico publicado en 2014

Risk of subsequent solid tumors after non-Hodgkin's lymphoma: effect of diagnostic age and time since diagnosis

artículo científico publicado en 2008

Risk of thyroid cancer in first-degree relatives of patients with non-medullary thyroid cancer by histology type and age at diagnosis: a joint study from five Nordic countries

artículo científico publicado en 2013

Risk of thyroid cancer in relatives of patients with medullary thyroid carcinoma by age at diagnosis

artículo científico publicado en 2013

Risk of transitional-cell carcinoma of the bladder in first- and second-generation immigrants to Sweden

artículo científico publicado en 2010

Risks for familial and contralateral breast cancer interact multiplicatively and cause a high risk

scientific article published on 01 February 2007

Risks of breast, endometrial, and ovarian cancers after twin births

scientific article published on 01 September 2007

Risks of papillary and follicular thyroid cancer among immigrants to Sweden

artículo científico publicado el 8 de marzo de 2011

Risks of subarachnoid hemorrhage in siblings: a nationwide epidemiological study from Sweden

artículo científico publicado en 2007

Runs of homozygosity and inbreeding in thyroid cancer

artículo científico publicado en 2016

SNP microarray analysis for genome-wide detection of crossover regions

artículo científico publicado en 2005

SNP_tools: A compact tool package for analysis and conversion of genotype data for MS-Excel

artículo científico publicado en 2009

SNPs in ultraconserved elements and familial breast cancer risk

scientific article published on 03 January 2008

STR markers for kinship analysis

scientific article published on 01 February 2006

Screening detected prostate cancers in type 2 diabetics

artículo científico publicado en 2011

Search for multiple myeloma risk factors using Mendelian randomization

scientific article published on 01 May 2020

Searching for the missing heritability of complex diseases

Seasonal and regional variations of asthma and association with osteoporosis: possible role of vitamin D in asthma

artículo científico publicado el 1 de noviembre de 2010

Second Primary Cancers in Melanoma Patients Critically Shorten Survival

scientific article published on 23 January 2020

Second Primary Cancers in Patients with Invasive and In Situ Squamous Cell Skin Carcinoma, Kaposi Sarcoma, and Merkel Cell Carcinoma: Role for Immune Mechanisms?

scientific article published on 06 July 2019

Second cancer risk following Hodgkin lymphoma

artículo científico publicado en 2017

Second cancers and causes of death in patients with testicular cancer in Sweden

artículo científico publicado en 2019

Second malignancies after childhood noncentral nervous system solid cancer: Results from 13 cancer registries

article by Milena Maule et al published 21 July 2011 in International Journal of Cancer

Second malignancies among survivors of germ-cell testicular cancer: A pooled analysis between 13 cancer registries

article

Second primary cancer after female breast cancer: Familial risks and cause of death.

artículo científico publicado en 2018

Second primary cancers after cancer of unknown primary in Sweden and Germany: efficacy of the modern work-up

artículo científico publicado en 2013

Second primary cancers in non-Hodgkin lymphoma: Bidirectional analyses suggesting role for immune dysfunction

artículo científico publicado en 2018

Second primary cancers in non-Hodgkin lymphoma: Family history and survival

scientific article published on 15 May 2019

Second primary cancers in patients with acute lymphoblastic, chronic lymphocytic and hairy cell leukaemia

artículo científico publicado en 2019

Second primary cancers in patients with nasopharyngeal carcinoma: a pooled analysis of 13 cancer registries

artículo científico publicado en 2007

Second primary cancers in thyroid cancer patients: a multinational record linkage study

artículo científico

Second primary malignancies among patients with soft tissue tumors in Sweden

scientific article published on 01 August 2006

Second primary malignancies among women with uterine sarcoma

artículo científico publicado en 2012

Second primary malignancies in females with primary fallopian tube cancer

artículo científico publicado en 2007

Selected polymorphisms in sex hormone-related genes, circulating sex hormones and risk of endometrial cancer.

artículo científico publicado en 2012

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

artículo científico publicado en 2009

Serum growth factors in asbestosis patients

artículo científico publicado en 2009

Serum oncoproteins and growth factors in asbestosis and silicosis patients

artículo científico publicado el 1 de abril de 1992

Sex hormone-binding globulin polymorphisms in familial and sporadic breast cancer

artículo científico publicado en 2002

Sex-specific familial risks of urinary bladder cancer and associated neoplasms in Sweden

artículo científico publicado en 2009

Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases

artículo científico publicado en 2012

Shared familial aggregation of susceptibility to autoimmune diseases

artículo científico publicado en 2009

Shared susceptibility for celiac disease and inflammatory bowel disease?

artículo científico publicado en 2008

Short article: Influence of regulatory NLRC5 variants on colorectal cancer survival and 5-fluorouracil-based chemotherapy

scientific article published on 01 August 2018

Sibling risk of pediatric obstructive sleep apnea syndrome and adenotonsillar hypertrophy

artículo científico publicado en 2009

Significant impact of promoter hypermethylation and the 540 C>T polymorphism of CDKN2A in cutaneous melanoma of the vertical growth phase

artículo científico publicado en 2002

Simultaneous detection of the exon 10 polymorphism and a novel intronic single base insertion polymorphism in the XPD gene using single strand conformation polymorphism

article

Single nucleotide polymorphism analyses of the human proliferating cell nuclear antigen (pCNA) and flap endonuclease (FEN1) genes

article

Single nucleotide polymorphisms (SNPs) are inherited from parents and they measure heritable events

artículo científico publicado en 2005

Single nucleotide polymorphisms in DNA repair genes XRCC1 and APEX1 in progression and survival of primary cutaneous melanoma patients

artículo científico publicado en 2008

Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin

artículo científico publicado en 2006

Single nucleotide polymorphisms in breast cancer

artículo científico publicado en 2004

Single nucleotide polymorphisms in chromosomal instability genes and risk and clinical outcome of breast cancer: a Swedish prospective case-control study

artículo científico publicado en 2008

Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome

artículo científico publicado en 2011

Single nucleotide polymorphisms in the DMBT1 promoter and the progression of breast cancer

artículo científico publicado en 2007

Single nucleotide polymorphisms in theXPGgene: Determination of role in DNA repair and breast cancer risk

article by Rajiv Kumar et al published 25 November 2002 in International Journal of Cancer

Single nucleotide polymorphisms within MUC4 are associated with colorectal cancer survival

artículo científico publicado en 2019

Single nucleotide polymorphisms within interferon signaling pathway genes are associated with colorectal cancer susceptibility and survival

artículo científico publicado en 2014

Single-nucleotide polymorphisms in DNA-repair genes and cutaneous melanoma

article

Site-specific survival rates for cancer of unknown primary according to location of metastases

artículo científico publicado en 2013

Skilled use of DNA polymorphisms as a tool for polygenic cancers.

artículo científico publicado en 2002

Smoking and body mass index as risk factors for subtypes of cancer of unknown primary

artículo científico publicado en 2014

Socio-economic and occupational risk factors for gastric cancer: a cohort study in Sweden.

artículo científico publicado en 2006

Socio-economic status and overall and cause-specific mortality in Sweden

artículo científico publicado en 2008

Socioeconomic and occupational risk factors for pancreatic cancer: a cohort study in Sweden

scientific article published on 01 March 2006

Socioeconomic factors in cancer in Sweden

artículo científico publicado en 2003

Somatic alterations in the melanoma genome: a high-resolution array-based comparative genomic hybridization study

artículo científico publicado en 2010

Somatic mutations in exocrine pancreatic tumors: association with patient survival

artículo científico publicado en 2013

Special section editorial

artículo científico publicado en 2014

Special section editorial: Cancer incidence in five continents including Africa

artículo científico publicado en 2015

Spectrum of styrene-induced DNA adducts: the relationship to other biomarkers and prospects in human biomonitoring.

artículo científico publicado en 2002

Sporadic colorectal cancer and individual susceptibility: a review of the association studies investigating the role of DNA repair genetic polymorphisms.

artículo científico publicado en 2007

Structural chromosomal aberrations as potential risk markers in incident cancer patients

artículo científico publicado en 2015

Styrene metabolism, genotoxicity, and potential carcinogenicity.

artículo científico publicado en 2006

Subsequent Type 2 Diabetes in Patients with Autoimmune Disease

artículo científico publicado en 2015

Subsequent autoimmune or related disease in asthma patients: clustering of diseases or medical care?

artículo científico publicado en 2009

Subsequent brain tumors in patients with autoimmune disease

artículo científico publicado en 2013

Subsequent leukaemia in autoimmune disease patients

artículo científico publicado en 2013

Subsequent primary malignancies after endometrial carcinoma and ovarian carcinoma

artículo científico publicado en 2003

Subsequent risk of hospitalization for neuropsychiatric disorders in patients with rheumatic diseases: a nationwide study from Sweden

artículo científico publicado en 2008

Surveillance Bias in Cancer Risk After Unrelated Medical Conditions: Example Urolithiasis

artículo científico

Surveying germline genomic landscape of breast cancer

artículo científico publicado en 2008

Surveying the genomic landscape of colorectal cancer

artículo científico publicado en 2009

Survival in bladder and renal cell cancers is familial

artículo científico publicado en 2008

Survival in breast cancer is familial

artículo científico publicado en 2007

Survival in cancer patients hospitalized for inflammatory bowel disease in Sweden

artículo científico publicado en 2011

Survival in familial and non-familial breast cancer by age and stage at diagnosis

artículo científico publicado en 2015

Survival in familial pancreatic cancer

artículo científico publicado en 2008

Survival in non-Hodgkin's lymphoma by histology and family history

artículo científico publicado en 2009

Survival in ovarian cancer patients by histology and family history

artículo científico publicado en 2008

Survival patterns among lymphoma patients with a family history of lymphoma

artículo científico publicado en 2008

Systematic enrichment analysis of gene expression profiling studies identifies consensus pathways implicated in colorectal cancer development

artículo científico publicado en 2011

Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome

artículo científico publicado en 2014

TERT promoter mutations and telomere length in adult malignant gliomas and recurrences.

artículo científico publicado en 2015

TERT promoter mutations in actinic keratosis before and after treatment

scientific article published on 30 January 2020

TERT promoter mutations in bladder cancer affect patient survival and disease recurrence through modification by a common polymorphism

artículo científico publicado en 2013

TERT promoter mutations in cancer development

artículo científico

TERT promoter mutations in clear cell renal cell carcinoma.

artículo científico publicado en 2014

TERT promoter mutations in familial and sporadic melanoma

artículo científico publicado en 2013

TERT promoter mutations in melanoma survival

artículo científico publicado en 2016

TERT promoter mutations: a novel independent prognostic factor in primary glioblastomas

artículo científico publicado en 2015

TP53-binding protein variants and breast cancer risk: a case-control study

artículo científico publicado en 2005

Telomerase reverse transcriptase promoter mutations in primary cutaneous melanoma.

artículo científico publicado en 2014

Telomere length in circulating lymphocytes: Association with chromosomal aberrations

artículo científico publicado en 2014

Telomere length in peripheral blood lymphocytes related to genetic variation in telomerase, prognosis and clinicopathological features in breast cancer patients

artículo científico publicado en 2020

Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families

article

Thalassemia and sickle cell anemia in Swedish immigrants: Genetic diseases have become global

artículo científico publicado en 2015

The 'common disease-common variant' hypothesis and familial risks

artículo científico publicado en 2008

The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells

artículo científico publicado en 2014

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A

artículo científico publicado en 2015

The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study

artículo científico publicado en 2007

The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

artículo científico publicado en 2013

The GH1/IGF-1 axis polymorphisms and their impact on breast cancer development

artículo científico publicado en 2007

The Incidence of Senile Cataract and Glaucoma is Increased in Patients with Plasma Cell Dyscrasias: Etiologic Implications

artículo científico publicado en 2016

The Swedish Family-Cancer Database 2009: prospects for histology-specific and immigrant studies

artículo científico publicado en 2010

The Swedish family-cancer database: update, application to colorectal cancer and clinical relevance

artículo científico publicado en 2005

The XPD 751Gln allele is associated with an increased risk for esophageal adenocarcinoma: a population-based case-control study in Sweden

artículo científico publicado en 2006

The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk

artículo científico publicado en 2002

The balance between heritable and environmental aetiology of human disease

artículo científico publicado en 2006

The challenges of understanding cancer of unknown primary

artículo científico publicado en 2013

The effect of having an affected parent or sibling on invasive and in situ skin cancer risk in Sweden

artículo científico publicado en 2009

The epidemiology of Graves' disease: evidence of a genetic and an environmental contribution

artículo científico publicado en 2009

The epidemiology of metastases in neuroendocrine tumors

artículo científico publicado en 2016

The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer

artículo científico

The impact of type 2 diabetes mellitus on cancer-specific survival: a follow-up study in Sweden

artículo científico publicado en 2011

The in vivo levels of DNA alkylation products in human lymphocytes are not age dependent: an assay of 7-methyl- and 7-(2-hydroxyethyl)-guanine DNA adducts

artículo científico publicado en 2002

The insulin-like growth factor-1 pathway mediator genes: SHC1 Met300Val shows a protective effect in breast cancer.

artículo científico publicado en 2004

The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression.

artículo científico publicado en 2018

The population impact of familial cancer, a major cause of cancer

artículo científico publicado en 2013

The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk

artículo científico publicado en 2004

The single nucleotide polymorphism IVS1+309 in mouse double minute 2 does not affect risk of familial breast cancer.

artículo científico publicado en 2006

The updated Swedish family-cancer database used to assess familial risks of prostate cancer during rapidly increasing incidence

artículo científico publicado en 2006

Time to pregnancy among the wives of Finnish greenhouse workers

artículo científico publicado el 1 de abril de 2003

Time trends and familial risks in squamous cell carcinoma of the skin

artículo científico publicado en 2003

Time trends and occupational risk factors for peritoneal mesothelioma in Sweden

artículo científico publicado en 2003

Time trends and occupational risk factors for pleural mesothelioma in Sweden

artículo científico publicado en 2003

Time trends in incidence, causes of death, and survival of cancer of unknown primary in Sweden

artículo científico publicado en 2012

Time trends in the incidence of cervical and other genital squamous cell carcinomas and adenocarcinomas in Sweden, 1958-1996

artículo científico publicado en 2002

Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study

artículo científico publicado en 2006

Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes

scientific article published on 20 August 2019

Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphoma

scientific article published on 01 August 2006

Tumor location and patient characteristics of colon and rectal adenocarcinomas in relation to survival and TNM classes

artículo científico publicado en 2010

Types of second primary cancers influence survival in chronic lymphocytic and hairy cell leukemia patients

artículo científico publicado en 2019

Ultraviolet photoproduct levels in melanocytic nevi and surrounding epidermis in human skin in situ

artículo científico publicado en 2002

Understanding the agreement of histology of familial testicular tumors

artículo científico publicado en 2010

Update on genetic predisposition to colorectal cancer and polyposis

artículo científico publicado en 2019

Urinary thymidine dimer as a marker of total body burden of UV-inflicted DNA damage in humans

artículo científico publicado en 2005

Use of pyrosequencing to detect clinically relevant polymorphisms of genes in basal cell carcinoma

artículo científico publicado en 2004

VHL down-regulation and differential localization as mechanisms in tumorigenesis.

artículo científico publicado en 2003

Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer

artículo científico publicado en 2006

Variants at chromosome 20 (ASIP locus) and melanoma risk

artículo científico publicado en 2012

Variants at the 9p21 locus and melanoma risk

artículo científico publicado en 2013

Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype

scientific journal article

Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma

scientific journal article

Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk

artículo científico publicado en 2010

Variation in the risk for liver and gallbladder cancers in socioeconomic and occupational groups in Sweden with etiological implications

artículo científico publicado en 2005

Vascular endothelial growth factor polymorphisms in relation to breast cancer development and prognosis

artículo científico publicado en 2005

Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood.

artículo científico publicado en 2009

What do prostate cancer patients die of?

artículo científico publicado en 2011

What is the major prognostic factor in tumor-node-metastasis staging of pancreatic adenocarcinoma?

artículo científico publicado en 2010

Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways

artículo científico publicado en 2019

Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma

article

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

artículo científico publicado en 2017

c-MYC Asn11Ser is associated with increased risk for familial breast cancer

artículo científico publicado en 2005

p53 autoantibodies predict subsequent development of cancer

artículo científico publicado en 2005

Factores de riesgo socioeconómicos/laborales de enfermedades linfoproliferativas en Suecia

artículo científico publicado en 2005