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
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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
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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
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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?
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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
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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
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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
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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
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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
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artículo científico publicado en 2016
Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia.
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artículo científico publicado en 2018
Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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