Filtros de búsqueda

Lista de obras de Cunningham JM

-Synuclein, pesticides, and Parkinson disease: A case-control study

artículo científico publicado en 2008

35th Annual Meeting of the European Association for the Study of Diabetes

artículo científico

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

article

A Two-Stage Evaluation of Genetic Variation in Immune and Inflammation Genes with Risk of Non-Hodgkin Lymphoma Identifies New Susceptibility Locus in 6p21.3 Region ⬇️

artículo científico publicado el 21 de agosto de 2012

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

artículo científico publicado en 2005

A genome wide association study suggests the association of muskelin with early onset bipolar disorder: Implications for a GABAergic epileptogenic neurogenesis model

artículo científico publicado en 2016

A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.

artículo científico publicado en 2009

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.

artículo científico publicado en 2010

A genome‐wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q ⬇️

artículo científico publicado el 1 de agosto de 2012

A prospective trial of midwest breast cancer patients: a p53 gene mutation is the most important predictor of adverse outcome

artículo científico publicado en 2000

A rigorous and comprehensive validation: common genetic variations and lung cancer

artículo científico publicado en 2010

A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair

artículo científico publicado en 2001

A targeted genetic association study of epithelial ovarian cancer susceptibility

artículo científico publicado en 2016

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

artículo científico publicado en 2018

ABCA transporter gene expression and poor outcome in epithelial ovarian cancer

artículo científico publicado en 2014

ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: a comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas

scientific article published on August 2013

ABO blood group and risk of epithelial ovarian cancer within the Ovarian Cancer Association Consortium

artículo científico publicado en 2012

APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma.

artículo científico publicado en 2013

Accumulating evidence for a role of TCF7L2 variants in bipolar disorder with elevated body mass index

artículo científico publicado en 2016

Acetylcholine receptors in small cell carcinomas

artículo científico publicado en 1985

Adult body mass index and risk of ovarian cancer by subtype: a Mendelian randomization study

artículo científico

Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study

artículo científico publicado en 2018

Aggressive medulloblastoma with high-level N-myc amplification.

artículo científico publicado en 1994

Alpha-synuclein, alcohol use disorders, and Parkinson disease: a case-control study

artículo científico publicado en 2009

Alpha1-antitrypsin and neutrophil elastase imbalance and lung cancer risk

artículo científico publicado en 2005

Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes

artículo científico publicado en 1996

Analyses of germline variants associated with ovarian cancer survival identify functional candidates at the 1q22 and 19p12 outcome loci

artículo científico publicado en 2017

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 proliferation markers and p53 expression in gliomas of astrocytic origin: relationships and prognostic value

artículo científico publicado en 1997

Analysis of the RNASEL gene in familial and sporadic prostate cancer

artículo científico publicado en 2002

Analysis of the prostate cancer-susceptibility locus HPC20 in 172 families affected by prostate cancer

artículo científico publicado en 2001

Androgen receptor gene polymorphisms and increased risk of urologic measures of benign prostatic hyperplasia

artículo científico publicado en 2004

Arginase expression and modulation of IL-1beta-induced nitric oxide generation in rat and human islets of Langerhans

artículo científico publicado en 2002

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

artículo científico publicado en 2015

Assessing the genetic architecture of epithelial ovarian cancer histological subtypes

artículo científico publicado en 2016

Assessment of Multifactor Gene-Environment Interactions and Ovarian Cancer Risk: Candidate Genes, Obesity, and Hormone-Related Risk Factors

artículo científico publicado en 2016

Assessment of hepatocyte growth factor in ovarian cancer mortality

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 analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study

artículo científico publicado en 2009

Association of GATA4 sequence variation with alcohol dependence

artículo científico publicado en 2012

Association of TNFSF8 polymorphisms with peripheral neutrophil count

artículo científico publicado en 2011

Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer

scientific article published on 10 September 2020

Association of single nucleotide polymorphisms in glycosylation genes with risk of epithelial ovarian cancer

artículo científico publicado en 2008

Association of the PDYN gene with alcohol dependence and the propensity to drink in negative emotional states

scientific article published on 29 October 2012

Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study

artículo científico publicado en 2016

Associations between measles vaccine immunity and single-nucleotide polymorphisms in cytokine and cytokine receptor genes

artículo científico publicado en 2006

Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

article by Xiang Shu et al published 1 October 2018 in International Journal of Epidemiology

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

artículo científico publicado en 2015

Base resolution methylome profiling: considerations in platform selection, data preprocessing and analysis

artículo científico publicado en 2015

Beta-synuclein gene variants and Parkinson's disease: a preliminary case-control study

artículo científico publicado en 2007

Biomarker-based ovarian carcinoma typing: a histologic investigation in the ovarian tumor tissue analysis consortium

artículo científico publicado en 2013

CXCR5 polymorphisms in non-Hodgkin lymphoma risk and prognosis ⬇️

artículo científico publicado el 28 de junio de 2013

CYP2C19 variation and citalopram response

artículo científico publicado en 2011

Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk

artículo científico publicado en 2009

Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

artículo científico publicado en 2015

Caution on pedigree haplotype inference with software that assumes linkage equilibrium

artículo científico publicado en 2002

Cell cycle genes and ovarian cancer susceptibility: a tagSNP analysis

artículo científico publicado en 2009

Characterization of fusion genes in common and rare epithelial ovarian cancer histologic subtypes

artículo científico publicado en 2017

Childhood exposure to secondhand smoke and functional mannose binding lectin polymorphisms are associated with increased lung cancer risk

artículo científico publicado en 2009

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

artículo científico publicado en 2015

Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status

artículo científico publicado en 2014

Clinical validation of genetic variants associated with in vitro chemotherapy-related lymphoblastoid cell toxicity

artículo científico publicado en 2017

Coffee, caffeine-related genes, and Parkinson's disease: a case-control study

artículo científico publicado en 2008

Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22.

artículo científico publicado en 2012

Combined and interactive effects of environmental and GWAS-identified risk factors in ovarian cancer

artículo científico publicado en 2013

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

artículo científico publicado en 2015

Common Genetic Variation in Circadian Rhythm Genes and Risk of Epithelial Ovarian Cancer (EOC).

artículo científico publicado en 2015

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

scientific journal article

Common variants at 19p13 are associated with susceptibility to ovarian cancer

artículo científico publicado en 2010

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

artículo científico publicado en 2015

Common variants in PARK loci and related genes and Parkinson's disease

artículo científico publicado en 2010

Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non-Hodgkin lymphoma subtypes

artículo científico publicado en 2012

Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia

artículo científico publicado en 2012

Comparison of inhibition of glucose-stimulated insulin secretion in rat islets of Langerhans by streptozotocin and methyl and ethyl nitrosoureas and methanesulphonates. Lack of correlation with nitric oxide-releasing or O6-alkylating ability

artículo científico publicado en 1995

Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci

artículo científico publicado en 2004

Comparison of the DNA methylation profiles of human peripheral blood cells and transformed B-lymphocytes

artículo científico publicado en 2010

Confirmation of linkage of prostate cancer aggressiveness with chromosome 19q.

artículo científico publicado en 2003

Consortium analysis of 7 candidate SNPs for ovarian cancer

scientific article published on July 2008

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

artículo científico publicado en 2014

Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population

artículo científico publicado en 2015

Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22.

artículo científico publicado en 2012

Correction: Evaluation of Clustering and Genotype Distribution for Replication in Genome Wide Association Studies: The Age-Related Eye Disease Study

artículo científico publicado en 2008

Cross-cancer genome-wide association study of endometrial cancer and epithelial ovarian cancer identifies genetic risk regions associated with risk of both cancers

artículo científico publicado en 2020

Current status of adjuvant chemotherapy for colorectal cancer. Can molecular markers play a role in predicting prognosis?

artículo científico publicado el 15 de septiembre de 1992

Cystic fibrosis transmembrane conductance regulator gene mutation and lung cancer risk

artículo científico publicado en 2010

DNA methylation changes in epithelial ovarian cancer histotypes

artículo científico publicado en 2015

DNA methylation profiling: comparison of genome-wide sequencing methods and the Infinium Human Methylation 450 Bead Chip

artículo científico publicado en 2015

Design and validity of a clinic-based case-control study on the molecular epidemiology of lymphoma

artículo científico publicado en 2011

Do interactions between SNCA, MAPT, and LRRK2 genes contribute to Parkinson’s disease susceptibility? ⬇️

artículo científico publicado el 3 de agosto de 2011

Does α-synuclein have a dual and opposing effect in preclinical vs. clinical Parkinson's disease?

artículo científico publicado en 2014

ESR1/SYNE1 polymorphism and invasive epithelial ovarian cancer risk: an Ovarian Cancer Association Consortium study

artículo científico publicado en 2010

Effect of catechol-O-methyltransferase (rs4680) single-nucleotide polymorphism on opioid-induced hyperalgesia in adults with chronic pain

Effects of Age and Estrogen on Skeletal Gene Expression in Humans as Assessed by RNA Sequencing

artículo científico publicado en 2015

Endothelial Nitric Oxide Synthase Gene Variation Associated With Chronic Kidney Disease After Liver Transplant ⬇️

artículo científico publicado el 1 de septiembre de 2010

Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci

artículo científico publicado en 2017

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

artículo científico publicado en 2013

Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel

artículo científico publicado en 2013

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

artículo científico publicado en 2015

Erratum: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer

scholarly article published in Nature Genetics

Erratum: Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

scientific article published in Nature Communications

Erratum: Validating genetic risk associations for ovarian cancer through the International Ovarian Cancer Association Consortium

scholarly article published in British Journal of Cancer

Estrogen bioactivation, genetic polymorphisms, and ovarian cancer

artículo científico publicado en 2005

Evaluating the influence of quality control decisions and software algorithms on SNP calling for the affymetrix 6.0 SNP array platform

artículo científico publicado en 2011

Evaluating the ovarian cancer gonadotropin hypothesis: a candidate gene study

artículo científico publicado en 2014

Evaluation of Genetic Variations in the Androgen and Estrogen Metabolic Pathways as Risk Factors for Sporadic and Familial Prostate Cancer

artículo científico publicado en 2007

Evaluation of a new high-dimensional miRNA profiling platform

artículo científico publicado en 2009

Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"

artículo científico publicado en 2010

Evaluation of clustering and genotype distribution for replication in genome wide association studies: the age-related eye disease study

artículo científico publicado en 2008

Evaluation of glutathione metabolic genes on outcomes in advanced non-small cell lung cancer patients after initial treatment with platinum-based chemotherapy: an NCCTG-97-24-51 based study

artículo científico publicado en 2009

Evidence for a prostate cancer-susceptibility locus on chromosome 20.

artículo científico publicado en 2000

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

artículo científico publicado en 2016

Expression profiling of formalin-fixed paraffin-embedded primary breast tumors using cancer-specific and whole genome gene panels on the DASL® platform

artículo científico publicado en 2010

FCGR2A and FCGR3A polymorphisms in classical Hodgkin lymphoma by Epstein-Barr virus status.

artículo científico publicado en 2013

Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene

artículo científico publicado en 2009

Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

artículo científico publicado en 2014

Five endometrial cancer risk loci identified through genome-wide association analysis

artículo científico publicado en 2016

Functional and clinical significance of variants localized to 8q24 in colon cancer

artículo científico publicado en 2009

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

artículo científico publicado en 2013

Gene networks and microRNAs implicated in aggressive prostate cancer

artículo científico publicado en 2009

Gene set analysis of survival following ovarian cancer implicates macrolide binding and intracellular signaling genes

artículo científico publicado en 2012

Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study

artículo científico publicado en 2017

Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist:Hip Ratio, Is Causal for Endometrial Cancer

artículo científico publicado en 2016

Genetic Variants Associated with the Risk of Chronic Obstructive Pulmonary Disease with and without Lung Cancer ⬇️

artículo científico publicado el 1 de noviembre de 2011

Genetic Variation Predicting Cisplatin Cytotoxicity Associated with Overall Survival in Lung Cancer Patients Receiving Platinum-Based Chemotherapy ⬇️

artículo científico publicado el 20 de julio de 2011

Genetic Variations in Multiple Drug Action Pathways and Survival in Advanced Stage Non–Small Cell Lung Cancer Treated with Chemotherapy ⬇️

artículo científico publicado el 1 de junio de 2011

Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study

artículo científico publicado en 2012

Genetic markers associated with abstinence length in alcohol-dependent subjects treated with acamprosate

artículo científico publicado en 2014

Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses.

artículo científico publicado en 2018

Genetic polymorphisms associated with carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study

artículo científico publicado en 2012

Genetic susceptibility loci, environmental exposures, and Parkinson's disease: A case–control study of gene–environment interactions ⬇️

artículo científico publicado el 16 de marzo de 2013

Genetic susceptibility variants for chronic lymphocytic leukemia

artículo científico publicado en 2010

Genetic variants and risk of lung cancer in never smokers: a genome-wide association study

artículo científico publicado en 2010

Genetic variation in 1253 immune and inflammation genes and risk of non-Hodgkin lymphoma

artículo científico publicado en 2007

Genetic variation in TYMS in the one-carbon transfer pathway is associated with ovarian carcinoma types in the Ovarian Cancer Association Consortium

artículo científico publicado en 2010

Genetic variation in glutathione metabolism and DNA repair genes predicts survival of small-cell lung cancer patients

artículo científico publicado en 2010

Genetic variation in the one-carbon transfer pathway and ovarian cancer risk

artículo científico publicado en 2008

Genetic variation in tumor necrosis factor and the nuclear factor-kappaB canonical pathway and risk of non-Hodgkin's lymphoma

artículo científico publicado en 2008

Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism ⬇️

artículo científico publicado el 1 de junio de 2011

Genome linkage screen for prostate cancer susceptibility loci: results from the Mayo Clinic Familial Prostate Cancer Study

artículo científico publicado en 2003

Genome partitioning of genetic variation for complex traits using common SNPs

artículo científico publicado en 2011

Genome-Wide Association Study of Event-Free Survival in Diffuse Large B-Cell Lymphoma Treated With Immunochemotherapy

artículo científico publicado en 2015

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

artículo científico publicado en 2016

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 Common Copy Number Variation and Epithelial Ovarian Cancer Risk

artículo científico publicado en 2019

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction

artículo científico publicado en 2011

Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL

scientific journal article

Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

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 in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

artículo científico publicado en 2013

Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.

artículo científico publicado en 2010

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

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

artículo científico publicado en 2013

Genome-wide investigation of regional blood-based DNA methylation adjusted for complete blood counts implicates BNC2 in ovarian cancer

artículo científico publicado en 2014

Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

artículo científico publicado en 2009

Genomic Analysis Using Regularized Regression in High-Grade Serous Ovarian Cancer

artículo científico publicado en 2018

Genomic determinants of motor and cognitive outcomes in Parkinson's disease

scientific journal article

Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer

artículo científico publicado en 2015

Germline copy number variation and ovarian cancer survival

artículo científico publicado en 2012

Germline mutation in BRCA1 or BRCA2 and ten-year survival for women diagnosed with epithelial ovarian cancer

artículo científico publicado en 2014

Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer

artículo científico publicado en 2016

Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene

artículo científico publicado en 2017

Global transcriptional profiling using RNA sequencing and DNA methylation patterns in highly enriched mesenchymal cells from young versus elderly women

artículo científico publicado en 2015

Gluthatione-S-transferase P1 polymorphism I105V in familial and sporadic prostate cancer

artículo científico publicado en 2004

Growth factor, cytokine, and vitamin D receptor polymorphisms and risk of benign prostatic hyperplasia in a community-based cohort of men.

artículo científico publicado en 2006

Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease

scientific article published on 01 January 2005

High frequency of p53 gene mutations in primary breast cancers in Japanese women, a low-incidence population

artículo científico publicado en 1996

Higher risk of mismatch repair-deficient colorectal cancer in alpha(1)-antitrypsin deficiency carriers and cigarette smokers

artículo científico publicado en 2000

Hormone-receptor expression and ovarian cancer survival: an Ovarian Tumor Tissue Analysis consortium study

artículo científico publicado en 2013

Human SULT1A1 gene: copy number differences and functional implications

artículo científico publicado en 2006

Human colon cancer profiles show differential microRNA expression depending on mismatch repair status and are characteristic of undifferentiated proliferative states

artículo científico publicado en 2009

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability ⬇️

artículo científico publicado el 1 de agosto de 1998

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

artículo científico publicado en 2013

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

artículo científico publicado en 2017

Identification of a Locus Near <i>ULK1</i> Associated With Progression-Free Survival in Ovarian Cancer

publication published on 23 June 2021

Identification of a novel percent mammographic density locus at 12q24.

artículo científico publicado en 2012

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

artículo científico publicado en 2016

Identification of novel variants in colorectal cancer families by high-throughput exome sequencing

artículo científico publicado en 2013

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

artículo científico publicado en 2015

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

artículo científico publicado en 2002

Inflammation-Related Gene Variants as Risk Factors for Pancreatic Cancer ⬇️

artículo científico publicado el 5 de abril de 2011

Inherited determinants of ovarian cancer survival

artículo científico publicado en 2010

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

artículo científico publicado en 2016

Inherited variants in mitochondrial biogenesis genes may influence epithelial ovarian cancer risk

artículo científico publicado en 2011

Inherited variants in regulatory T cell genes and outcome of ovarian cancer

artículo científico publicado en 2013

Integrative genomic analysis identifies epigenetic marks that mediate genetic risk for epithelial ovarian cancer

artículo científico publicado en 2014

Interaction of SLC6A4 and DRD2 polymorphisms is associated with a history of delirium tremens

artículo científico publicado en 2010

Interleukin-1? effects on cyclic GMP and cyclic AMP in cultured rat islets of Langerhans ? arginine ? dependence and relationship to insulin secretion ⬇️

artículo científico publicado el 1 de enero de 1993

Intra-Gene DNA Methylation Variability Is a Clinically Independent Prognostic Marker in Women's Cancers

artículo científico publicado en 2015

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer

artículo científico publicado en 2016

LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer

artículo científico publicado en 2011

Large Kindred Evaluation of Mitofusin 2 Novel Mutation, Extremes of Neurologic Presentations, and Preserved Nerve Mitochondria ⬇️

artículo científico publicado el 1 de octubre de 2011

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

artículo científico publicado en 2014

Linkage analysis of obesity phenotypes in pre- and post-menopausal women from a United States mid-western population

artículo científico publicado en 2010

Low frequency of p53 gene mutations in breast cancers of Japanese-American women

artículo científico publicado en 2001

Luteinizing hormone beta polymorphism and risk of familial and sporadic prostate cancer.

artículo científico publicado en 2003

Mapping of the IRF8 gene identifies a 3'UTR variant associated with risk of chronic lymphocytic leukemia but not other common non-Hodgkin lymphoma subtypes

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 common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

artículo científico publicado en 2015

Methylation of leukocyte DNA and ovarian cancer: relationships with disease status and outcome

artículo científico publicado en 2014

MicroRNA processing and binding site polymorphisms are not replicated in the Ovarian Cancer Association Consortium

artículo científico publicado en 2011

Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer

artículo científico publicado en 1996

Microsatellite instability in colorectal cancer: different mutator phenotypes and the principal involvement of hMLH1 ⬇️

artículo científico publicado el 15 de abril de 1998

Microsatellite instability in hereditary and sporadic breast cancers ⬇️

artículo científico publicado el 20 de noviembre de 2003

Migration of Lymphocytes Sensitized against Syngeneic and Allogeneic Spinal Cord after Infusion into Susceptible and Resistant Syngeneic and Semi-Allogeneic Hosts ⬇️

artículo científico publicado el 1 de enero de 1981

Mitochondrial genetic polymorphisms and pancreatic cancer risk

scientific article published on 01 July 2007

Mitochondrial genetic polymorphisms do not predict survival in patients with pancreatic cancer

artículo científico publicado en 2008

Molecular biology of squamous cell carcinoma of the anus: a comparison of HIV-positive and HIV-negative patients.

artículo científico publicado en 2004

Molecular signatures of X chromosome inactivation and associations with clinical outcomes in epithelial ovarian cancer

scientific article published on 01 April 2019

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

artículo científico publicado en 2013

Multiple-level validation identifies PARK2 in the development of lung cancer and chronic obstructive pulmonary disease

scientific article published on 13 June 2016

Mutation detection by highly sensitive methods indicates that p53 gene mutations in breast cancer can have important prognostic value

artículo científico publicado en 1996

Mutation detection in colorectal cancers : direct sequencing of DNA mismatch repair genes

artículo científico publicado en 2001

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling

artículo científico publicado en 2000

Mutations in CHEK2 associated with prostate cancer risk

artículo científico publicado en 2003

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

artículo científico publicado en 2011

Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis

artículo científico publicado en 2006

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

artículo científico publicado en 2015

Nitric oxide donors decrease the function and survival of human pancreatic islets

scientific article published on 01 April 1996

No association of germline alteration of MSR1 with prostate cancer risk

artículo científico publicado en 2003

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

artículo científico publicado en 2015

No evidence for association of inherited variation in genes involved in mitosis and percent mammographic density

artículo científico publicado en 2012

Nonparametric tests of association of multiple genes with human disease

artículo científico publicado en 2005

Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures

artículo científico publicado en 2015

Novel pattern of P53 mutation in breast cancers from Austrian women.

artículo científico publicado en 1995

Novel pattern of p53 gene mutations in an American black cohort with high mortality from breast cancer

artículo científico publicado en 1994

Nucleotide excision repair pathway polymorphisms and pancreatic cancer risk: evidence for role of MMS19L.

artículo científico publicado en 2009

Ovarian cancer risk associated with inherited inflammation-related variants

artículo científico publicado en 2012

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

artículo científico publicado en 2016

PPM1D Mosaic Truncating Variants in Ovarian Cancer Cases May Be Treatment-Related Somatic Mutations

artículo científico publicado en 2016

Partial characterization of the Purkinje cell antigens in paraneoplastic cerebellar degeneration

artículo científico publicado en 1986

Pattern of p53 Gene Mutations in Breast Cancers of Women of the Midwestern United States ⬇️

artículo científico publicado el 19 de febrero de 1992

Performance of amplified DNA in an Illumina GoldenGate BeadArray assay

artículo científico publicado en 2008

Pharmacogenomics of antidepressant induced mania: a review and meta-analysis of the serotonin transporter gene (5HTTLPR) association

artículo científico publicado en 2011

Polymorphic variants in hereditary pancreatic cancer genes are not associated with pancreatic cancer risk

scientific article published on 18 August 2009

Polymorphism in the GALNT1 gene and epithelial ovarian cancer in non-Hispanic white women: the Ovarian Cancer Association Consortium

artículo científico publicado en 2010

Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women

artículo científico publicado en 2008

Polymorphisms in ABCB1 and ERCC2 associated with ovarian cancer outcome ⬇️

artículo científico publicado el 2 de mayo de 2011

Polymorphisms in DNA repair genes, smoking, and pancreatic adenocarcinoma risk

scientific article published on 10 June 2008

Polymorphisms in NF-kappaB inhibitors and risk of epithelial ovarian cancer

artículo científico publicado en 2009

Polymorphisms in TCEAL7 and risk of epithelial ovarian cancer

artículo científico publicado en 2009

Polymorphisms in genes involved in sex hormone metabolism may increase risk of benign prostatic hyperplasia

article

Polymorphisms in metabolism/antioxidant genes may mediate the effect of dietary intake on pancreatic cancer risk

artículo científico publicado en 2013

Polymorphisms in mitochondrial genes and prostate cancer risk

artículo científico publicado en 2008

Polymorphisms in stromal genes and susceptibility to serous epithelial ovarian cancer: a report from the Ovarian Cancer Association Consortium

artículo científico publicado en 2011

Polymorphisms in the 5alpha reductase type 2 gene and urologic measures of BPH.

artículo científico publicado en 2005

Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics

artículo científico publicado en 2006

Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer

artículo científico publicado en 2020

Progesterone receptor gene polymorphisms and risk of endometriosis: results from an international collaborative effort

artículo científico publicado en 2010

Prostate cancer susceptibility polymorphism rs2660753 is not associated with invasive ovarian cancer

artículo científico publicado en 2011

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

scientific article published on 23 September 2019

Receptors for polytropic and xenotropic mouse leukaemia viruses encoded by a single gene at Rmc1

artículo científico publicado en 1999

Regular Multivitamin Supplement Use, Single Nucleotide Polymorphisms in ATIC, SHMT2, and SLC46A1, and Risk of Ovarian Carcinoma

artículo científico publicado en 2012

Regulatory T cells, inherited variation, and clinical outcome in epithelial ovarian cancer

artículo científico publicado en 2015

Replication of genome wide association studies of alcohol dependence: support for association with variation in ADH1C.

artículo científico publicado en 2013

Risk Prediction for Epithelial Ovarian Cancer in 11 United States-Based Case-Control Studies: Incorporation of Epidemiologic Risk Factors and 17 Confirmed Genetic Loci

artículo científico publicado en 2016

Risk of ovarian cancer and inherited variants in relapse-associated genes

artículo científico publicado en 2010

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

artículo científico publicado en 2013

Role of HPC2/ELAC2 in hereditary prostate cancer

artículo científico publicado en 2001

SAT-383 Prevalence of Opioid Induced Adrenal Insufficiency in Patients Taking Chronic Opioids.

artículo científico publicado en 2019

SEPT9 mutations and a conserved 17q25 sequence in sporadic and hereditary brachial plexus neuropathy

artículo científico publicado en 2009

SLC6A4 variation and citalopram response

artículo científico publicado en 2009

SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies

artículo científico publicado en 2005

Search for Chromosome Instability in Lymphocytes with Germ-Line Mutations in DNA Mismatch Repair Genes ⬇️

artículo científico publicado el 1 de julio de 1998

Sequencing of Charcot-Marie-Tooth disease genes in a toxic polyneuropathy

artículo científico publicado en 2014

Sex-Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction

artículo científico publicado en 2016

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

artículo científico publicado en 2015

Shared heritability and functional enrichment across six solid cancers

artículo científico publicado en 2019

Shared heritability and functional enrichment across six solid cancers

Single nucleotide polymorphisms associated with abnormal coronary microvascular function

artículo científico publicado en 2014

Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer

artículo científico publicado en 2009

Specific inhibition of anti-self reactivity following exposure of neonatal rats to lymphocytes with anti-neural activity.

artículo científico publicado en 1981

Strong evidence of a genetic determinant for mammographic density, a major risk factor for breast cancer

artículo científico publicado en 2007

Survival Is Associated With Genetic Variation in Inflammatory Pathway Genes Among Patients With Resected and Unresected Pancreatic Cancer ⬇️

artículo científico publicado el 1 de junio de 2013

Susceptibility genes and B-chronic lymphocytic leukaemia

artículo científico publicado en 2007

TP53 mutations, tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer

artículo científico publicado en 2015

TRIM16 acts as a tumour suppressor by inhibitory effects on cytoplasmic vimentin and nuclear E2F1 in neuroblastoma cells

artículo científico publicado en 2010

Tagging single nucleotide polymorphisms in cell cycle control genes and susceptibility to invasive epithelial ovarian cancer

artículo científico publicado en 2007

Telomere length varies by DNA extraction method: implications for epidemiologic research

artículo científico publicado en 2013

Telomere structure and maintenance gene variants and risk of five cancer types

artículo científico publicado en 2016

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

artículo científico publicado en 2008

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.

artículo científico publicado en 2008

The JNK inhibitor SP600129 enhances apoptosis of HCC cells induced by the tumor suppressor WWOX.

artículo científico publicado en 2008

The Minnesota Center for Twin and Family Research genome-wide association study

artículo científico publicado en 2012

The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers

artículo científico publicado en 2016

The androgen receptor CAG and GGN repeat polymorphisms and prostate cancer susceptibility in African-American men: results from the Flint Men's Health Study

artículo científico publicado en 2008

The association of copy number variation and percent mammographic density

artículo científico publicado en 2015

The association of telomere length with colorectal cancer differs by the age of cancer onset

artículo científico publicado en 2014

The cancer anorexia/weight loss syndrome: exploring associations with single nucleotide polymorphisms (SNPs) of inflammatory cytokines in patients with non-small cell lung cancer

artículo científico publicado en 2009

The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population

artículo científico publicado en 2014

The contributions of breast density and common genetic variation to breast cancer risk

artículo científico publicado en 2015

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas

artículo científico publicado en 2001

The gene for HMSN2C maps to 12q23-24: a region of neuromuscular disorders

artículo científico publicado en 2003

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

artículo científico publicado en 2002

The genomic landscape of small intestine neuroendocrine tumors ⬇️

artículo científico publicado el 15 de mayo de 2013

The inducible nitric oxide synthase gene, Nos2, maps to mouse chromosome 11

artículo científico publicado en 1994

The presence of tandem endothelial nitric oxide synthase gene polymorphisms identifying brain aneurysms more prone to rupture

artículo científico publicado en 2005

The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing

artículo científico publicado en 2011

Transcriptomic Characterization of Endometrioid, Clear Cell, and High-Grade Serous Epithelial Ovarian Carcinoma

artículo científico publicado en 2018

Tumor hypomethylation at 6p21.3 associates with longer time to recurrence of high-grade serous epithelial ovarian cancer

artículo científico publicado en 2014

Tumor necrosis factor-alpha and interferon-gamma inhibit insulin secretion and cause DNA damage in unweaned-rat islets. Extent of nitric oxide involvement

artículo científico publicado en 1996

Tumor suppressor gene alterations in malignant gliomas: histopathological associations and prognostic evaluation.

artículo científico publicado en 1999

Two Common Chromosome 8q24 Variants Are Associated with Increased Risk for Prostate Cancer

artículo científico publicado en 2007

UCHL1 is associated with Parkinson's disease: A case-unaffected sibling and case-unrelated control study

scholarly article by Maurizio Facheris et al published June 2005 in Neuroscience Letters

Use of FFPE-Derived DNA in Next Generation Sequencing: DNA extraction methods

Use of FFPE-derived DNA in next generation sequencing: DNA extraction methods

artículo científico publicado en 2019

Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium

artículo científico publicado en 2009

Variants in Inflammation Genes Are Implicated in Risk of Lung Cancer in Never Smokers Exposed to Second-hand Smoke ⬇️

artículo científico publicado el 25 de agosto de 2011

Variants in estrogen‐related genes and risk of Parkinson's disease ⬇️

artículo científico publicado el 5 de abril de 2011

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

artículo científico publicado en 2018

Variation at 8q24 and 9p24 and risk of epithelial ovarian cancer

artículo científico publicado en 2010

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

artículo científico publicado en 2014

Variations in measles vaccine-specific humoral immunity by polymorphisms in SLAM and CD46 measles virus receptors

artículo científico publicado en 2007

Widespread Non-Canonical Epigenetic Modifications in MMTV-NeuT Breast Cancer

artículo científico publicado en 2015

Xenobiotic-Metabolizing gene polymorphisms and ovarian cancer risk

artículo científico publicado en 2010

hSulf1 Sulfatase promotes apoptosis of hepatocellular cancer cells by decreasing heparin-binding growth factor signaling.

artículo científico publicado en 2004

miRNA expression in colon polyps provides evidence for a multihit model of colon cancer

artículo científico publicado en 2011

p53 gene expression in node-positive breast cancer: relationship to DNA ploidy and prognosis

artículo científico publicado en 1994

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

artículo científico publicado en 2018

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda