Lista de obras - Irene Orlow - Dominio Público Uruguay

A metastasis or a second independent cancer? Evaluating the clonal origin of tumors using array copy number data

artículo científico publicado en 2010

A replication study and genome-wide scan of single-nucleotide polymorphisms associated with pancreatic cancer risk and overall survival

artículo científico publicado en 2012

APOE polymorphisms and cognitive functions in patients with brain tumors

artículo científico publicado en 2014

Accuracy of Self-reported Smoking Exposure Among Bladder Cancer Patients Undergoing Surveillance at a Tertiary Referral Center

artículo científico publicado en 2015

Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer.

artículo científico publicado en 2018

Alcohol and Lung Cancer Risk Among Never Smokers: A Pooled Analysis from the International Lung Cancer Consortium and the SYNERGY Study

artículo científico publicado en 2017

Allergies, variants in IL-4 and IL-4Rα genes, and risk of pancreatic cancer

article

Alterations in the retinoblastoma pathway of cell cycle control in parathyroid tumors

artículo científico publicado en 2000

Alterations of INK4A and INK4B genes in adult soft tissue sarcomas: effect on survival

artículo científico publicado en 1999

Alterations of cell cycle regulators affecting the RB pathway in nonfamilial retinoblastoma

artículo científico publicado en 2001

Altered patterns of MDM2 and TP53 expression in human bladder cancer

scientific article published on 01 September 1994

Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study

artículo científico publicado en 2019

Analysis of genetic variants in never-smokers with lung cancer facilitated by an Internet-based blood collection protocol: a preliminary report

artículo científico publicado en 2010

Analysis of over 10,000 Cases finds no association between previously reported candidate polymorphisms and ovarian cancer outcome

artículo científico publicado en 2013

Analysis of p21WAF1/CIP1 in primary bladder tumors

artículo científico publicado en 1996

Aspirin and NSAID use and lung cancer risk: a pooled analysis in the International Lung Cancer Consortium (ILCCO).

artículo científico publicado en 2011

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

artículo científico publicado en 2016

Association Between Aryl Hydrocarbon Receptor Genotype and Survival in Soft Tissue Sarcoma

scientific article published on 01 October 2004

Association Between NRAS and BRAF Mutational Status and Melanoma-Specific Survival Among Patients With Higher-Risk Primary Melanoma

artículo científico publicado en 2015

Association of Incident Amelanotic Melanoma With Phenotypic Characteristics, MC1R Status, and Prior Amelanotic Melanoma

artículo científico publicado en 2017

Association of Interferon Regulatory Factor-4 Polymorphism rs12203592 With Divergent Melanoma Pathways

scientific article published on 08 February 2016

Association of known melanoma risk factors with primary melanoma of the scalp and neck

artículo científico publicado en 2020

Associations of MC1R genotype and patient phenotypes with BRAF and NRAS mutations in melanoma

artículo científico publicado en 2017

Associations of cumulative sun exposure and phenotypic characteristics with histologic solar elastosis

artículo científico publicado en 2010

Asthma and lung cancer risk: a systematic investigation by the International Lung Cancer Consortium

artículo científico publicado en 2012

CDKN2A Germline Mutations in Individuals with Cutaneous Malignant Melanoma

artículo científico publicado en 2007

CYP2D6 phenotype, tamoxifen, and risk of contralateral breast cancer in the WECARE Study

Cannabis smoking and lung cancer risk: Pooled analysis in the International Lung Cancer Consortium

artículo científico publicado en 2014

Characterization of large structural genetic mosaicism in human autosome

artículo científico publicado en 2015

Chromosome 9 allelic losses and microsatellite alterations in human bladder tumors

scientific article published on 01 June 1994

Cigarette smoking and chromosome 9 alterations in bladder cancer

artículo científico publicado en 1997

Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer

artículo científico publicado en 2015

Clinicopathologic features of incident and subsequent tumors in patients with multiple primary cutaneous melanomas

artículo científico publicado en 2011

Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk

artículo científico publicado en 2015

Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer

artículo científico publicado en 2015

Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer

artículo científico publicado en 2015

Comparison of clinicopathologic features and survival of histopathologically amelanotic and pigmented melanomas: a population-based study.

artículo científico publicado en 2014

Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk

artículo científico publicado en 2014

Contralateral breast cancers: Independent cancers or metastases?

artículo científico publicado en 2017

Correction: vitamin d metabolic pathway genes and pancreatic cancer risk

artículo científico publicado en 2015

DNA damage and repair capacity in patients with lung cancer: prediction of multiple primary tumors

artículo científico publicado en 2008

Deletion of the p16 and p15 Genes in Human Bladder Tumors

article

Deletions of the INK4A gene in superficial bladder tumors. Association with recurrence

artículo científico publicado en 1999

Deletions of the INK4A gene occur in malignant peripheral nerve sheath tumors but not in neurofibromas

artículo científico publicado en 1999

Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer

artículo científico publicado en 2013

Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk

artículo científico publicado en 2015

Erratum to: Clinicopathologic Features of Incident and Subsequent Tumors in Patients with Multiple Primary Cutaneous Melanomas

scholarly article published in Annals of Surgical Oncology

Estimating the relative risk of developing melanoma in INK4A carriers.

artículo científico publicado en 2004

Evaluating the ovarian cancer gonadotropin hypothesis: a candidate gene study

artículo científico publicado en 2014

Evaluation of Alterations in the Tumor Suppressor Genes INK4A and INK4B in Human Bladder Tumors

article

Evaluation of the clonal origin of multiple primary melanomas using molecular profiling

artículo científico publicado en 2009

Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk

artículo científico publicado en 2016

Exome-wide association study of endometrial cancer in a multiethnic population

artículo científico publicado en 2014

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

artículo científico publicado en 2016

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

artículo científico publicado en 2016

Functional melanoma-risk variant IRF4 rs12203592 associated with Breslow thickness: a pooled international study of primary melanomas

artículo científico publicado en 2017

Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers

artículo científico publicado en 2011

Functional polymorphisms in the promoter regions of MMP2 and MMP3 are not associated with melanoma progression

artículo científico publicado en 2007

GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

artículo científico publicado en 2013

GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer

artículo científico

Gastrointestinal stromal tumors, somatic mutations and candidate genetic risk variants

artículo científico publicado en 2013

Genetic evidence in melanoma and bladder cancers that p16 and p53 function in separate pathways of tumor suppression

artículo científico publicado en 1995

Genetic factors associated with naevus count and dermoscopic patterns: preliminary results from the Study of Nevi in Children (SONIC)

artículo científico publicado en 2015

Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium

artículo científico publicado en 2015

Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk

artículo científico publicado en 2014

Genome-wide association study for ovarian cancer susceptibility using pooled DNA.

artículo científico publicado en 2012

Genome-wide association study of endometrial cancer in E2C2

artículo científico publicado en 2014

Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.

artículo científico publicado en 2013

Genome-wide gene-diabetes and gene-obesity interaction scan in 8,255 cases and 11,900 controls from the PanScan and PanC4 Consortia

artículo científico publicado en 2020

Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer

artículo científico publicado en 2018

Genomic and mutational profiling to assess clonal relationships between multiple non-small cell lung cancers

artículo científico publicado en 2009

Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.

artículo científico publicado en 2013

Identification of gene expression levels in primary melanoma associated with clinically meaningful characteristics

article

Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia

artículo científico publicado en 2015

Identification of nine new susceptibility loci for endometrial cancer

artículo científico publicado en 2018

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

artículo científico publicado en 2015

Identifying Etiologically Distinct Sub-Types of Cancer: A Demonstration Project Involving Breast Cancer

artículo científico publicado en 2015

Including additional controls from public databases improves the power of a genome-wide association study

artículo científico

Increased risk of lung cancer in individuals with a family history of the disease: a pooled analysis from the International Lung Cancer Consortium

artículo científico publicado en 2012

Inherited genetic variants associated with occurrence of multiple primary melanoma

artículo científico publicado en 2015

Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration

artículo científico publicado en 2016

Inherited variation at MC1R and ASIP and association with melanoma-specific survival

artículo científico publicado en 2014

Inherited variation at MC1R and histological characteristics of primary melanoma

artículo científico publicado en 2015

Interaction of CDKN2A and sun exposure in the etiology of melanoma in the general population

artículo científico publicado en 2011

Interpretation of melanoma risk feedback in first-degree relatives of melanoma patients

artículo científico publicado en 2012

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer

artículo científico publicado en 2016

Investigation of the Effect of MDM2 SNP309 and TP53 Arg72Pro Polymorphisms on the Age of Onset of Cutaneous Melanoma

artículo científico publicado en 2012

Large-scale evaluation of common variation in regulatory T cell-related genes and ovarian cancer outcome

artículo científico publicado en 2014

Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample

artículo científico publicado en 2005

Matrix Metalloproteinase-9 (MMP-9) polymorphisms in patients with cutaneous malignant melanoma

artículo científico publicado en 2007

Menstrual and reproductive factors and lung cancer risk: A pooled analysis from the international lung cancer consortium

artículo científico publicado en 2017

Microsatellite instability and deletion analysis of chromosome 10 in human prostate cancer.

artículo científico publicado en 1996

Mitochondrial DNA deletions in skin from melanoma patients

artículo científico publicado en 2008

Molecular analyses of the mitotic checkpoint components hsMAD2, hBUB1 and hBUB3 in human cancer

artículo científico publicado en 2001

Molecular analysis of the INK4A and INK4B gene loci in human breast cancer cell lines and primary carcinomas

article

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

artículo científico publicado en 2013

Mutagen sensitivity as an indicator of soft tissue sarcoma risk

artículo científico publicado en 2001

NC-03POLYMORPHISMS IN THE COMT, BDNF AND DTNBP1 GENES AND COGNITIVE FUNCTIONS IN PATIENTS WITH BRAIN TUMORS.

artículo científico publicado en 2014

Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk

artículo científico publicado en 2015

Nevus count associations with pigmentary phenotype, histopathological melanoma characteristics and survival from melanoma

artículo científico publicado en 2016

No association between prediagnosis exercise and survival in patients with high-risk primary melanoma: A population-based study

artículo científico publicado en 2017

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

artículo científico publicado en 2015

No prognostic value added by vitamin D pathway SNPs to current prognostic system for melanoma survival

artículo científico publicado en 2017

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

artículo científico publicado en 2016

Patterns of persistent DNA damage associated with sun exposure and the glutathione S-transferase M1 genotype in melanoma patients

scientific article published on January 2009

Phase II study of extended-dose temozolomide in patients with melanoma

artículo científico publicado en 2008

Presence of human papilloma virus in tumor tissue from children with retinoblastoma: an alternative mechanism for tumor development

artículo científico publicado en 2000

Previous lung diseases and lung cancer risk: a pooled analysis from the International Lung Cancer Consortium

artículo científico publicado en 2012

Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers

artículo científico publicado en 2012

Risk of ovarian cancer and the NF-κB pathway: genetic association with IL1A and TNFSF10

artículo científico publicado en 2013

Sun exposure and melanoma survival: a GEM study

artículo científico publicado en 2014

Sun exposure, vitamin D receptor genetic variants, and risk of breast cancer in the Agricultural Health Study

artículo científico publicado en 2013

Sun exposure, vitamin D receptor polymorphisms FokI and BsmI and risk of multiple primary melanoma.

artículo científico publicado en 2011

Sunburn, sun exposure, and sun sensitivity in the Study of Nevi in Children

artículo científico publicado en 2015

The interaction between vitamin D receptor polymorphisms and sun exposure around time of diagnosis influences melanoma survival

artículo científico publicado en 2017

The obesity-associated polymorphisms FTO rs9939609 and MC4R rs17782313 and endometrial cancer risk in non-Hispanic white women

artículo científico publicado en 2011

The p.Ser64Leu and p,Pro104Leu missense variants of PALB2 identified in familial pancreatic cancer patients compromise the DNA damage response

scientific article published on 10 November 2020

The prevalence of CDKN2A germ-line mutations and relative risk for cutaneous malignant melanoma: an international population-based study

artículo científico publicado en 2006

The use of hierarchical models for estimating relative risks of individual genetic variants: an application to a study of melanoma

artículo científico publicado en 2008

Tumor-infiltrating lymphocyte grade in primary melanomas is independently associated with melanoma-specific survival in the population-based genes, environment and melanoma study

artículo científico publicado en 2013

Validation of denaturing high performance liquid chromatography as a rapid detection method for the identification of human INK4A gene mutations

artículo científico publicado en 2001

Variants in autophagy-related genes and clinical characteristics in melanoma: a population-based study

artículo científico publicado en 2016

Variants in estrogen biosynthesis genes, sex steroid hormone levels, and endometrial cancer: a HuGE review

artículo científico publicado en 2006

Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility

artículo científico publicado en 2018

Variants in hormone biosynthesis genes and risk of endometrial cancer

scientific article published on 25 April 2008

Variation in NF-κB signaling pathways and survival in invasive epithelial ovarian cancer

artículo científico publicado en 2014

Vitamin D metabolic pathway genes and pancreatic cancer risk

artículo científico publicado en 2015

Vitamin D receptor gene haplotypes and polymorphisms and risk of breast cancer: a nested case-control study

artículo científico publicado en 2012

Vitamin D receptor polymorphisms and survival in patients with cutaneous melanoma: a population-based study

artículo científico publicado en 2015

Vitamin D receptor polymorphisms in patients with cutaneous melanoma

artículo científico publicado en 2011

rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology

artículo científico publicado en 2018

Lista de obras de Irene Orlow

A metastasis or a second independent cancer? Evaluating the clonal origin of tumors using array copy number data

A replication study and genome-wide scan of single-nucleotide polymorphisms associated with pancreatic cancer risk and overall survival

APOE polymorphisms and cognitive functions in patients with brain tumors

Accuracy of Self-reported Smoking Exposure Among Bladder Cancer Patients Undergoing Surveillance at a Tertiary Referral Center

Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer.

Alcohol and Lung Cancer Risk Among Never Smokers: A Pooled Analysis from the International Lung Cancer Consortium and the SYNERGY Study

Allergies, variants in IL-4 and IL-4Rα genes, and risk of pancreatic cancer

Alterations in the retinoblastoma pathway of cell cycle control in parathyroid tumors

Alterations of INK4A and INK4B genes in adult soft tissue sarcomas: effect on survival

Alterations of cell cycle regulators affecting the RB pathway in nonfamilial retinoblastoma

Altered patterns of MDM2 and TP53 expression in human bladder cancer

Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study

Analysis of genetic variants in never-smokers with lung cancer facilitated by an Internet-based blood collection protocol: a preliminary report

Analysis of over 10,000 Cases finds no association between previously reported candidate polymorphisms and ovarian cancer outcome

Analysis of p21WAF1/CIP1 in primary bladder tumors

Aspirin and NSAID use and lung cancer risk: a pooled analysis in the International Lung Cancer Consortium (ILCCO).

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

Association Between Aryl Hydrocarbon Receptor Genotype and Survival in Soft Tissue Sarcoma

Association Between NRAS and BRAF Mutational Status and Melanoma-Specific Survival Among Patients With Higher-Risk Primary Melanoma

Association of Incident Amelanotic Melanoma With Phenotypic Characteristics, MC1R Status, and Prior Amelanotic Melanoma

Association of Interferon Regulatory Factor-4 Polymorphism rs12203592 With Divergent Melanoma Pathways

Association of known melanoma risk factors with primary melanoma of the scalp and neck

Associations of MC1R genotype and patient phenotypes with BRAF and NRAS mutations in melanoma

Associations of cumulative sun exposure and phenotypic characteristics with histologic solar elastosis

Asthma and lung cancer risk: a systematic investigation by the International Lung Cancer Consortium

CDKN2A Germline Mutations in Individuals with Cutaneous Malignant Melanoma

CYP2D6 phenotype, tamoxifen, and risk of contralateral breast cancer in the WECARE Study

Cannabis smoking and lung cancer risk: Pooled analysis in the International Lung Cancer Consortium

Characterization of large structural genetic mosaicism in human autosome

Chromosome 9 allelic losses and microsatellite alterations in human bladder tumors

Cigarette smoking and chromosome 9 alterations in bladder cancer

Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer

Clinicopathologic features of incident and subsequent tumors in patients with multiple primary cutaneous melanomas

Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk

Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer

Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer

Comparison of clinicopathologic features and survival of histopathologically amelanotic and pigmented melanomas: a population-based study.

Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk

Contralateral breast cancers: Independent cancers or metastases?

Correction: vitamin d metabolic pathway genes and pancreatic cancer risk

DNA damage and repair capacity in patients with lung cancer: prediction of multiple primary tumors

Deletion of the p16 and p15 Genes in Human Bladder Tumors

Deletions of the INK4A gene in superficial bladder tumors. Association with recurrence

Deletions of the INK4A gene occur in malignant peripheral nerve sheath tumors but not in neurofibromas

Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer

Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk

Erratum to: Clinicopathologic Features of Incident and Subsequent Tumors in Patients with Multiple Primary Cutaneous Melanomas

Estimating the relative risk of developing melanoma in INK4A carriers.

Evaluating the ovarian cancer gonadotropin hypothesis: a candidate gene study

Evaluation of Alterations in the Tumor Suppressor Genes INK4A and INK4B in Human Bladder Tumors

Evaluation of the clonal origin of multiple primary melanomas using molecular profiling

Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk

Exome-wide association study of endometrial cancer in a multiethnic population

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

Functional melanoma-risk variant IRF4 rs12203592 associated with Breslow thickness: a pooled international study of primary melanomas

Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers

Functional polymorphisms in the promoter regions of MMP2 and MMP3 are not associated with melanoma progression

GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer

Gastrointestinal stromal tumors, somatic mutations and candidate genetic risk variants

Genetic evidence in melanoma and bladder cancers that p16 and p53 function in separate pathways of tumor suppression

Genetic factors associated with naevus count and dermoscopic patterns: preliminary results from the Study of Nevi in Children (SONIC)

Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium

Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk

Genome-wide association study for ovarian cancer susceptibility using pooled DNA.

Genome-wide association study of endometrial cancer in E2C2

Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.

Genome-wide gene-diabetes and gene-obesity interaction scan in 8,255 cases and 11,900 controls from the PanScan and PanC4 Consortia

Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer

Genomic and mutational profiling to assess clonal relationships between multiple non-small cell lung cancers

Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.

Identification of gene expression levels in primary melanoma associated with clinically meaningful characteristics

Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia

Identification of nine new susceptibility loci for endometrial cancer

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Identifying Etiologically Distinct Sub-Types of Cancer: A Demonstration Project Involving Breast Cancer

Including additional controls from public databases improves the power of a genome-wide association study

Increased risk of lung cancer in individuals with a family history of the disease: a pooled analysis from the International Lung Cancer Consortium