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Lista de obras de Meredith Yeager

3D domain swapping modulates the stability of members of an icosahedral virus group

artículo científico publicado en 2000

A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

artículo científico publicado en 2015

A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma

artículo científico publicado en 2011

A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry

artículo científico publicado en 2020

A Large Study of Androgen Receptor Germline Variants and Their Relation to Sex Hormone Levels and Prostate Cancer Risk. Results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium.

artículo científico publicado en 2010

A Two‐Platform Design for Next Generation Genome‐Wide Association Studies ⬇️

artículo científico publicado el 16 de abril de 2012

A comprehensive analysis of common genetic variation in MUC1, MUC5AC, MUC6 genes and risk of stomach cancer

artículo científico publicado en 2010

A comprehensive analysis of the androgen receptor gene and risk of breast cancer: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2006

A comprehensive resequence analysis of the KLK15-KLK3-KLK2 locus on chromosome 19q13.33.

artículo científico publicado en 2009

A comprehensive resequence-analysis of 250 kb region of 8q24.21 in men of African ancestry

artículo científico publicado en 2014

A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiency

artículo científico publicado en 2010

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23

artículo científico publicado en 2011

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

artículo científico publicado en 2007

A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3

scientific journal article

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

artículo científico publicado en 2009

A genome-wide association study of marginal zone lymphoma shows association to the HLA region

artículo científico publicado en 2015

A genome-wide association study of prostate cancer in West African men

artículo científico publicado en 2013

A genome-wide pleiotropy scan for prostate cancer risk

artículo científico publicado en 2014

A large study of androgen receptor germline variants and their relation to sex hormone levels and prostate cancer risk. Results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium

artículo científico publicado en 2010

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

artículo científico publicado en 2012

A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

scientific journal article

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

artículo científico publicado en 2009

A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies

artículo científico publicado en 2009

A pooled analysis of three studies evaluating genetic variation in innate immunity genes and non-Hodgkin lymphoma risk

artículo científico publicado en 2011

A pooled investigation of Toll-like receptor gene variants and risk of non-Hodgkin lymphoma

artículo científico publicado en 2008

A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome

artículo científico publicado en 2013

A resequence analysis of genomic loci on chromosomes 1q32.1, 5p15.33, and 13q22.1 associated with pancreatic cancer risk

artículo científico publicado en 2013

A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma

artículo científico publicado en 2010

A single nucleotide polymorphism tags variation in the arylamine N-acetyltransferase 2 phenotype in populations of European background

artículo científico publicado en 2011

A subset-based approach improves power and interpretation for the combined analysis of genetic association studies of heterogeneous traits

artículo científico publicado en 2012

Abstract 4593: Genome-wide association study identifies novel loci associated with osteosarcoma

Abstract 5574: High prevalence of germline TP53 mutations in young osteosarcoma cases

Abstract LB-272: Genome-wide association study identifies multiple susceptibility loci for diffuse large B-cell lymphoma

Abstract LB-448: Genome-wide association study identifies new prostate cancer susceptibility loci

artículo científico publicado en 2011

Addressing health disparities in Hispanic breast cancer: accurate and inexpensive sequencing of BRCA1 and BRCA2.

artículo científico publicado en 2015

Alcohol, genetics and risk of breast cancer in the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial

artículo científico publicado en 2012

An analysis of growth, differentiation and apoptosis genes with risk of renal cancer

artículo científico publicado en 2009

Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk

artículo científico publicado en 2009

Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types

artículo científico publicado en 2015

Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk

artículo científico publicado en 2009

Application of a novel score test for genetic association incorporating gene-gene interaction suggests functionality for prostate cancer susceptibility regions

artículo científico publicado en 2011

Association between adult height, genetic susceptibility and risk of glioma

artículo científico publicado en 2012

Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity

artículo científico publicado en 2009

Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families

artículo científico publicado en 2013

Association of genetic variants in the calcium-sensing receptor with risk of colorectal adenoma

article

Association of multiple DRD2 polymorphisms with anorexia nervosa

artículo científico publicado en 2005

Association of variants in two vitamin e transport genes with circulating vitamin e concentrations and prostate cancer risk

artículo científico publicado en 2009

Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations

artículo científico publicado en 2010

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

artículo científico publicado en 2016

CYBB, an NADPH-oxidase gene: restricted diversity in humans and evidence for differential long-term purifying selection on transmembrane and cytosolic domains

artículo científico publicado en 2008

CYP17 genetic variation and risk of breast and prostate cancer from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2007

CYP1A1 Val462 and NQO1 Ser187 polymorphisms, cigarette use, and risk for colorectal adenoma

artículo científico publicado en 2005

Candidate gene analysis of the Price Foundation anorexia nervosa affected relative pair dataset.

artículo científico publicado en 2003

Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa.

artículo científico publicado en 2003

Caspase polymorphisms and genetic susceptibility to multiple myeloma

artículo científico publicado en 2008

Characterization of breakpoint regions of large structural autosomal mosaic events

artículo científico publicado en 2017

Characterization of large structural genetic mosaicism in human autosome

artículo científico publicado en 2015

Characterization of population-based variation and putative functional elements for the multiple-cancer susceptibility loci at 5p15.33

artículo científico publicado en 2014

Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.

artículo científico publicado en 2011

Cigarette smoking, N-acetyltransferase genes and the risk of advanced colorectal adenoma

artículo científico publicado en 2006

Cis sequence effects on gene expression

artículo científico publicado en 2007

Colorectal cancer susceptibility loci as predictive markers of rectal cancer prognosis after surgery

artículo científico publicado en 2017

Combined somatic mutation and copy number analysis in the survival of familial CLL

Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk

artículo científico publicado en 2009

Common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer

artículo científico publicado en 2013

Common genetic variants in candidate genes and risk of familial lymphoid malignancies

artículo científico publicado en 2009

Common genetic variants in proinflammatory and other immunoregulatory genes and risk for non-Hodgkin lymphoma

artículo científico publicado en 2006

Common genetic variants in prostate cancer risk prediction--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3)

artículo científico publicado en 2012

Common genetic variants in the 9p21 region and their associations with multiple tumours

artículo científico publicado en 2013

Common genetic variants related to genomic integrity and risk of papillary thyroid cancer ⬇️

artículo científico publicado el 3 de junio de 2011

Common genetic variation in GATA-binding protein 3 and differential susceptibility to breast cancer by estrogen receptor alpha tumor status

artículo científico publicado en 2007

Common genetic variation in TP53 and its flanking genes, WDR79 and ATP1B2, and susceptibility to breast cancer

artículo científico publicado en 2007

Common genetic variation in TP53 and risk of human papillomavirus persistence and progression to CIN3/cancer revisited ⬇️

artículo científico publicado en 2009

Common single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer

artículo científico publicado en 2013

Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut

artículo científico publicado en 2010

Common variation in genes related to innate immunity and risk of adult glioma

artículo científico publicado en 2009

Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2.

artículo científico publicado en 2004

Comprehensive analysis of 5-aminolevulinic acid dehydrogenase (ALAD) variants and renal cell carcinoma risk among individuals exposed to lead

artículo científico publicado en 2011

Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium

artículo científico publicado en 2010

Comprehensive analysis of hormone and genetic variation in 36 genes related to steroid hormone metabolism in pre- and postmenopausal women from the breast and prostate cancer cohort consortium (BPC3).

artículo científico publicado en 2010

Comprehensive assessment of genetic variation of catechol-O-methyltransferase and breast cancer risk

artículo científico publicado en 2006

Comprehensive evaluation of one-carbon metabolism pathway gene variants and renal cell cancer risk

artículo científico publicado en 2011

Comprehensive resequence analysis of a 123-kb region of chromosome 11q13 associated with prostate cancer ⬇️

artículo científico publicado en 2012

Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers

artículo científico publicado en 2008

Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer

artículo científico publicado en 2009

Corrigendum re “Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma” [Eur Urol 2017;72:747–54]

scholarly article published in European Urology

Cytokine polymorphisms in the Th1/Th2 pathway and susceptibility to non-Hodgkin lymphoma

artículo científico publicado en 2006

DNA methylation levels at chromosome 8q24 in peripheral blood are associated with 8q24 cancer susceptibility loci

artículo científico publicado en 2014

DNA repair gene polymorphisms and tobacco smoking in the risk for colorectal adenomas

artículo científico publicado en 2011

DRD2 genetic variation in relation to smoking and obesity in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial

artículo científico publicado en 2006

Deep sequencing of HPV16 genomes: A new high-throughput tool for exploring the carcinogenicity and natural history of HPV16 infection

artículo científico publicado en 2015

Delta-aminolevulinic acid dehydratase polymorphism and risk of brain tumors in adults

artículo científico publicado en 2005

Detectable clonal mosaicism and its relationship to aging and cancer

artículo científico publicado en 2012

Diversity in the glucose transporter-4 gene (SLC2A4) in humans reflects the action of natural selection along the old-world primates evolution

artículo científico publicado en 2010

Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders

artículo científico publicado en 2014

Effect of pre-analytic variables on the reproducibility of qPCR relative telomere length measurement

artículo científico publicado en 2017

Effects of natural selection on interpopulation divergence at polymorphic sites in human protein-coding Loci

artículo científico publicado en 2005

Efficient study design for next generation sequencing ⬇️

artículo científico publicado el 1 de mayo de 2011

Eighteen insulin-like growth factor pathway genes, circulating levels of IGF-I and its binding protein, and risk of prostate and breast cancer

artículo científico publicado en 2010

Evaluating the Causal Link Between Malaria Infection and Endemic Burkitt Lymphoma in Northern Uganda: A Mendelian Randomization Study

artículo científico publicado en 2017

Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk

artículo científico publicado en 2007

Evolutionary Dynamics of the Human NADPH Oxidase Genes CYBB, CYBA, NCF2, and NCF4: Functional Implications ⬇️

artículo científico publicado el 2 de julio de 2013

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

artículo científico publicado en 2016

Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility

scholarly article

Fine mapping of 14q24.1 breast cancer susceptibility locus

artículo científico publicado en 2011

Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer

artículo científico publicado en 2011

Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels

artículo científico publicado en 2011

Folate metabolism genes, vegetable intake and renal cancer risk in central Europe

artículo científico publicado en 2008

Further confirmation of germline glioma risk variant rs78378222 in TP53 and its implication in tumor tissues via integrative analysis of TCGA data

artículo científico publicado en 2015

GSTM1, GSTT1, and GSTP1 polymorphisms and risk of advanced colorectal adenoma

artículo científico publicado en 2005

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies

artículo científico publicado en 2015

GWASdb: a database for human genetic variants identified by genome-wide association studies

artículo científico publicado en 2011

Genetic Polymorphisms of Interleukin-1B (IL-1B), IL-6, IL-8, and IL-10 and Risk of Prostate Cancer

scholarly article by Dominique S. Michaud et al published 15 April 2006 in Cancer Research

Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma ⬇️

artículo científico publicado en 2017

Genetic Variation in the Nucleotide Excision Repair Pathway and Bladder Cancer Risk

artículo científico publicado en 2006

Genetic polymorphisms in alcohol metabolism, alcohol intake and the risk of stomach cancer in Warsaw, Poland

article

Genetic polymorphisms in folate metabolism and the risk of stomach cancer

artículo científico publicado en 2007

Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers

artículo científico publicado en 2014

Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong

artículo científico publicado en 2010

Genetic susceptibility loci, pesticide exposure and prostate cancer risk

artículo científico publicado en 2013

Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations

artículo científico publicado en 2015

Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia

artículo científico publicado en 2012

Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: a report from the female lung cancer consortium in Asia

artículo científico publicado en 2014

Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma‐prone families with/without CDKN2A mutations ⬇️

artículo científico publicado el 9 de agosto de 2011

Genetic variants in T helper cell type 1, 2 and 3 pathways and gastric cancer risk in a Polish population

artículo científico publicado en 2008

Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphoma

artículo científico publicado en 2006

Genetic variants in frizzled-related protein (FRZB) and the risk of colorectal neoplasia

artículo científico publicado en 2008

Genetic variants in the 8q24 locus and risk of testicular germ cell tumors

artículo científico publicado en 2008

Genetic variants reflecting higher vitamin e status in men are associated with reduced risk of prostate cancer

scientific article published on 12 March 2014

Genetic variation at chromosome 8q24 in osteosarcoma cases and controls

artículo científico publicado en 2010

Genetic variation in CLDN1 and susceptibility to hepatitis C virus infection

artículo científico publicado en 2009

Genetic variation in N-acetyltransferases 1 and 2, cigarette smoking, and risk of non-Hodgkin lymphoma

artículo científico publicado en 2009

Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium

artículo científico publicado en 2006

Genetic variation in Th1/Th2 pathway genes and risk of non-Hodgkin lymphoma: a pooled analysis of three population-based case-control studies

artículo científico publicado en 2011

Genetic variation in a4GnT in relation to Helicobacter pylori serology and gastric cancer risk

artículo científico publicado en 2009

Genetic variation in base excision repair pathway genes, pesticide exposure, and prostate cancer risk ⬇️

artículo científico publicado en 2011

Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies

artículo científico publicado en 2009

Genetic variation in cell cycle and apoptosis related genes and multiple myeloma risk

artículo científico publicado en 2009

Genetic variation in metabolic genes, occupational solvent exposure, and risk of non-hodgkin lymphoma

artículo científico publicado en 2011

Genetic variation in nucleotide excision repair pathway genes, pesticide exposure and prostate cancer risk

artículo científico publicado en 2011

Genetic variation in sodium-dependent ascorbic acid transporters and risk of gastric cancer in Poland

artículo científico publicado en 2009

Genetic variation in sodium-dependent vitamin C transporters SLC23A1 and SLC23A2 and risk of advanced colorectal adenoma

artículo científico publicado en 2008

Genetic variation in the sodium-dependent vitamin C transporters, SLC23A1, and SLC23A2 and risk for preterm delivery

artículo científico publicado en 2006

Genetic variation in the vitamin d pathway in relation to risk of prostate cancer--results from the breast and prostate cancer cohort consortium

artículo científico publicado en 2013

Genetic variation in tumor necrosis factor and lymphotoxin-alpha (TNF–LTA) and breast cancer risk

article

Genetic variation of Cytochrome P450 1B1 (CYP1B1) and risk of breast cancer among Polish women

artículo científico publicado en 2006

Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes

artículo científico publicado en 2016

Genome Analysis of Latin American Cervical Cancer: Frequent Activation of the PIK3CA Pathway

artículo científico publicado en 2015

Genome-Wide Association Study Identifies Three Common Variants Associated with Serologic Response to Vitamin E Supplementation in Men ⬇️

artículo científico publicado el 21 de marzo de 2012

Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer

artículo científico publicado en 2017

Genome-wide SNP typing reveals signatures of population history

artículo científico publicado en 2008

Genome-wide and candidate gene association study of cigarette smoking behaviors

artículo científico publicado en 2009

Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia

scientific journal article

Genome-wide association study identifies common variants associated with circulating vitamin E levels

artículo científico publicado en 2011

Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region

artículo científico publicado en 2014

Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

artículo científico publicado en 2013

Genome-wide association study identifies multiple risk loci for renal cell carcinoma ⬇️

artículo científico publicado en 2017

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

artículo científico publicado en 2014

Genome-wide association study identifies new prostate cancer susceptibility loci

scientific journal article

Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients

artículo científico publicado en 2017

Genome-wide association study identifies two susceptibility loci for osteosarcoma

artículo científico publicado en 2013

Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours

artículo científico publicado en 2015

Genome-wide association study of glioma and meta-analysis

artículo científico publicado en 2012

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

artículo científico publicado en 2017

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

artículo científico publicado en 2007

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3

scientific journal article

Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption

artículo científico publicado en 2011

Genomic diversity and phylogenetic relationships of human papillomavirus 16 (HPV16) in Nepal

artículo científico publicado en 2016

Genotype frequency and F ST analysis of polymorphisms in immunoregulatory genes in Chinese and Caucasian populations

artículo científico publicado en 2007

Genotypes and haplotypes in the insulin-like growth factors, their receptors and binding proteins in relation to plasma metabolic levels and mammographic density

artículo científico publicado en 2010

Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies

artículo científico publicado en 2012

Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita

artículo científico publicado en 2013

Germline variation in NCF4, an innate immunity gene, is associated with an increased risk of colorectal cancer

artículo científico publicado en 2013

Green tea consumption, genetic susceptibility, PAH-rich smoky coal, and the risk of lung cancer

artículo científico publicado en 2005

HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis

artículo científico publicado en 2017

Hair dye use is not associated with risk for bladder cancer: evidence from a case-control study in Spain

artículo científico publicado en 2006

Haplotypes of IL6 and IL10 and susceptibility to human T lymphotropic virus type I infection among children

artículo científico publicado en 2006

Haplotypes of the estrogen receptor beta gene and breast cancer risk

artículo científico publicado en 2008

High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays

artículo científico publicado en 2009

Human papillomavirus 16 sub-lineage dispersal and cervical cancer risk worldwide: Whole viral genome sequences from 7116 HPV16-positive women

IGF-1, IGFBP-1, and IGFBP-3 polymorphisms predict circulating IGF levels but not breast cancer risk: findings from the Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2008

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

artículo científico publicado en 2013

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.

artículo científico publicado en 2009

Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations

scientific article published on December 2009

Improved imputation of common and uncommon SNPs with a new reference set.

artículo científico publicado en 2011

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33

artículo científico publicado en 2014

Innate immunity gene polymorphisms and the risk of colorectal neoplasia

artículo científico publicado en 2013

Insulin Resistance-Related Genes and Advanced Left-Sided Colorectal Adenoma

article

Insulin-like Growth Factor Pathway Genetic Polymorphisms, Circulating IGF1 and IGFBP3, and Prostate Cancer Survival.

artículo científico publicado en 2014

Insulin-like growth factor pathway genetic polymorphisms, circulating IGF1 and IGFBP3, and prostate cancer survival

artículo científico publicado en 2014

Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA).

artículo científico publicado en 2015

Invited commentary: more surprises from a gene desert

artículo científico publicado en 2012

Iron homeostasis and distal colorectal adenoma risk in the prostate, lung, colorectal, and ovarian cancer screening trial

artículo científico publicado en 2011

Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations

artículo científico publicado en 2014

Joint associations between genetic variants and reproductive factors in glioma risk among women

artículo científico publicado en 2011

Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk

artículo científico publicado en 2013

Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family.

artículo científico publicado en 2015

KRLMM: an adaptive genotype calling method for common and low frequency variants

artículo científico publicado en 2014

Known glioma risk loci are associated with glioma with a family history of brain tumours--a case-control gene association study

artículo científico publicado en 2013

Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer

artículo científico publicado en 2011

Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity

artículo científico publicado en 2008

Large-scale evaluation of candidate genes identifies associations between VEGF polymorphisms and bladder cancer risk

artículo científico publicado en 2007

Large-scale exploration of gene-gene interactions in prostate cancer using a multistage genome-wide association study

artículo científico publicado en 2011

Large-scale fine mapping of the HNF1B locus and prostate cancer risk

artículo científico publicado en 2011

Lead exposure and glioma among rural residents: the Upper Midwest Health Study

abstract published in 2006

Lead, genetic susceptibility, and risk of adult brain tumors

artículo científico publicado en 2006

MBL2and Hepatitis C Virus Infection among Injection Drug Users

artículo científico publicado en 2008

Mass spectrometry and viral analysis

artículo científico publicado en 1996

Meta-analysis identifies four new loci associated with testicular germ cell tumor

artículo científico publicado en 2013

Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women

artículo científico publicado en 2016

Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls

artículo científico publicado en 2016

Mosaic loss of chromosome Y is associated with common variation near TCL1A

artículo científico publicado en 2016

Movement of rice yellow mottle virus between xylem cells through pit membranes ⬇️

artículo científico publicado el 17 de marzo de 1998

Multiple loci identified in a genome-wide association study of prostate cancer

scientific journal article

NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses

artículo científico publicado en 2005

Novel breast cancer risk alleles and interaction with ionizing radiation among U.S. radiologic technologists

artículo científico publicado en 2010

Nucleotide excision repair gene polymorphisms and risk of advanced colorectal adenoma: XPC polymorphisms modify smoking-related risk

artículo científico publicado en 2006

Origin and dynamics of admixture in Brazilians and its effect on the pattern of deleterious mutations

artículo científico publicado en 2015

Ovarian cancer risk and common variation in the sex hormone-binding globulin gene: a population-based case-control study

artículo científico publicado en 2007

Oxidative damage-related genes AKR1C3 and OGG1 modulate risks for lung cancer due to exposure to PAH-rich coal combustion emissions

artículo científico publicado en 2004

PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2009

Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway

artículo científico publicado en 2008

Personal history of diabetes, genetic susceptibility to diabetes, and risk of brain glioma: a pooled analysis of observational studies

artículo científico publicado en 2014

Pesticide exposure and inherited variants in vitamin d pathway genes in relation to prostate cancer

artículo científico publicado en 2013

Pesticide use modifies the association between genetic variants on chromosome 8q24 and prostate cancer

artículo científico publicado en 2010

Plasma carotenoid- and retinol-weighted multi-SNP scores and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium

artículo científico publicado en 2013

Polymorphic variants in PTGS2 and prostate cancer risk: results from two large nested case-control studies

artículo científico publicado en 2007

Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut

article

Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma in a pooled analysis of three studies

artículo científico publicado en 2010

Polymorphisms in DNA repair genes and susceptibility to primary intracranial brain gliomas

conference abstract published in 2005

Polymorphisms in GSTT1, GSTZ1, and CYP2E1, disinfection by-products, and risk of bladder cancer in Spain

artículo científico publicado en 2010

Polymorphisms in Th1-type cell-mediated response genes and risk of gastric cancer

artículo científico publicado en 2006

Polymorphisms in complement system genes and risk of non-Hodgkin lymphoma

artículo científico publicado en 2011

Polymorphisms in cytokine and cellular adhesion molecule genes and susceptibility to hematotoxicity among workers exposed to benzene

artículo científico publicado en 2005

Polymorphisms in cytokine genes and risk of Helicobacter pylori infection among Jamaican children.

artículo científico publicado en 2006

Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer

artículo científico publicado en 2008

Polymorphisms in folate metabolic genes and lung cancer risk in Xuan Wei, China

artículo científico publicado en 2005

Polymorphisms in immunoregulatory genes, smoky coal exposure and lung cancer risk in Xuan Wei, China

artículo científico publicado en 2007

Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China

artículo científico publicado en 2009

Polymorphisms in integrin genes and lymphoma risk

artículo científico publicado en 2011

Polymorphisms in the estrogen metabolism genes CYP17, CYP1B1, CYP1A2, COMT and ER alpha and susceptibility to primary intracranial brain gliomas in women ⬇️

abstract published in 2004

Polymorphisms of an innate immune gene, toll-like receptor 4, and aggressive prostate cancer risk: a systematic review and meta-analysis.

artículo científico publicado en 2014

Polymorphisms of estrogen receptors and risk of biliary tract cancers and gallstones: a population-based study in Shanghai, China

artículo científico publicado en 2010

Polymorphisms of genes in the lipid metabolism pathway and risk of biliary tract cancers and stones: a population-based case-control study in Shanghai, China

artículo científico publicado en 2008

Pooled analysis of genetic variation at chromosome 8q24 and colorectal neoplasia risk

artículo científico publicado en 2008

Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer

artículo científico publicado en 2010

Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank

artículo científico publicado en 2018

Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts

scientific article published on 04 June 2012

Prostate cancer (PCa) risk variants and risk of fatal PCa in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium

artículo científico publicado en 2014

Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3)

artículo científico publicado en 2009

RNASEL Arg462Gln polymorphism and prostate cancer in PLCO

article

Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma

artículo científico publicado en 2016

Rare germline variants in known melanoma susceptibility genes in familial melanoma

artículo científico publicado en 2017

Rare inactivating PDE11A variants associated with testicular germ cell tumors

artículo científico publicado en 2015

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

artículo científico publicado en 2014

Recombinant tobacco mosaic virus movement protein is an RNA-binding, alpha-helical membrane protein

artículo científico publicado en 2000

Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.

artículo científico publicado en 2010

Replication of five prostate cancer loci identified in an Asian population--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2011

Reply to 'Mosaic loss of chromosome Y in leukocytes matters'

artículo científico publicado en 2019

Risk alleles for chronic hepatitis B are associated with decreased mRNA expression of HLA-DPA1 and HLA-DPB1 in normal human liver ⬇️

artículo científico publicado el 24 de febrero de 2011

Risk of meningioma and common variation in genes related to innate immunity

artículo científico publicado en 2010

Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes

artículo científico publicado en 2006

Risk of non-Hodgkin lymphoma associated with germline variation in genes that regulate the cell cycle, apoptosis, and lymphocyte development

artículo científico publicado en 2009

SLC6A3 and body mass index in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial

artículo científico publicado en 2009

SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes

artículo científico publicado en 2004

SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes

artículo científico publicado en 2006

Selected DNA repair polymorphisms and gastric cancer in Poland

article

Selected single-nucleotide polymorphisms in FOXE1, SERPINA5, FTO, EVPL, TICAM1 and SCARB1 are associated with papillary and follicular thyroid cancer risk: replication study in a German population

artículo científico publicado en 2016

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

artículo científico publicado en 2011

Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study

artículo científico publicado en 2016

Sex specific associations in genome wide association analysis of renal cell carcinoma

scientific article published on 23 June 2019

Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21.

artículo científico publicado en 2018

Smoky coal exposure, NBS1 polymorphisms, p53 protein accumulation, and lung cancer risk in Xuan Wei, China

artículo científico publicado en 2005

Somatic Alterations Contributing to Metastasis of a Castration-Resistant Prostate Cancer ⬇️

artículo científico publicado el 3 de junio de 2013

Somatic sequence alterations in twenty-one genes selected by expression profile analysis of breast carcinomas

artículo científico publicado en 2007

Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays.

artículo científico publicado en 2018

TNF polymorphisms and prostate cancer risk

scholarly article by Kim N. Danforth et al published 2008 in The Prostate

Telomere length and the risk of cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations

artículo científico publicado en 2013

Testicular germ cell tumor susceptibility associated with the UCK2 locus on chromosome 1q23.

artículo científico publicado en 2013

The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia

artículo científico publicado en 2010

The Interaction between Pesticide Use and Genetic Variants Involved in Lipid Metabolism on Prostate Cancer Risk

artículo científico publicado en 2012

The Intersection of HPV Epidemiology, Genomics and Mechanistic Studies of HPV-Mediated Carcinogenesis

artículo científico publicado en 2018

The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma

artículo científico publicado en 2011

The future of pediatric cancer and complex diseases: aren't they all?

artículo científico publicado en 2007

The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study ⬇️

scientific article published on 03 January 2019

The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing ⬇️

artículo científico publicado el 12 de junio de 2013

The population genetics of Quechuas, the largest native South American group: autosomal sequences, SNPs, and microsatellites evidence high level of diversity

artículo científico publicado en 2012

The structure of pariacoto virus reveals a dodecahedral cage of duplex RNA

artículo científico publicado en 2001

Transforming growth factor beta 1 (TGFB1) gene polymorphisms and risk of advanced colorectal adenoma

artículo científico publicado en 2007

Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women

artículo científico publicado en 2019

Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia

artículo científico publicado en 2018

Two susceptibility loci identified for prostate cancer aggressiveness

artículo científico publicado en 2015

Utilizing Fluidigm's Access Array Long-Range Capability and Roche 454 s Titanium Chemistry to Capture and Sequence the Epstein-Barr Virus (EBV) for Variant Detection

artículo científico publicado en 2010

Validation of the performance of a comprehensive genotyping assay panel of single nucleotide polymorphisms in drug metabolism enzyme genes

artículo científico publicado en 2008

Variants in blood pressure genes and the risk of renal cell carcinoma

artículo científico publicado en 2010

Variants in hormone-related genes and the risk of biliary tract cancers and stones: a population-based study in China

artículo científico publicado en 2009

Variants in inflammation genes and the risk of biliary tract cancers and stones: a population-based study in China

artículo científico publicado en 2008

Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour ⬇️

artículo científico publicado el 26 de mayo de 2011

Variation in KLK genes, prostate-specific antigen and risk of prostate cancer

artículo científico publicado en 2008

Variation in innate immunity genes and risk of multiple myeloma

artículo científico publicado en 2011

Viral coinfection analysis using a MinHash toolkit

article published in 2019

Vitamin d pathway genes, diet, and risk of renal cell carcinoma

artículo científico publicado en 2009

Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes

artículo científico publicado en 2016

Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

artículo científico publicado en 2016

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

artículo científico publicado en 2016

Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family

artículo científico publicado en 2015

Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families

artículo científico publicado en 2014

Widespread purifying selection at polymorphic sites in human protein-coding loci

artículo científico publicado en 2003

Worldwide genetic structure in 37 genes important in telomere biology

artículo científico publicado en 2011

Xenobiotic metabolizing genes, meat-related exposures, and risk of advanced colorectal adenoma

artículo científico publicado en 2010

Xenobiotic metabolizing genes, meat-related exposures, and risk of advanced colorectal adenoma

article

Xenobiotic-metabolizing gene variants, pesticide use, and the risk of prostate cancer

artículo científico publicado en 2011

Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry

artículo científico publicado en 2012

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