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Lista de obras de Susan J. Ramus

A Kallikrein 15 (KLK15) single nucleotide polymorphism located close to a novel exon shows evidence of association with poor ovarian cancer survival

artículo científico publicado en 2011

A SPONTANEOUS MUTATION CAUSING UNSTABLE Hb HAMMERSMITH: DETECTION OF THE β42 TTT→TCT CHANGE BY CCM AND DIRECT SEQUENCING

artículo científico publicado en 1991

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

article

A breast/ovarian cancer patient with germline mutations in both BRCA1 and BRCA2

scientific article published on 01 January 1997

A combination of the immunohistochemical markers CK7 and SATB2 is highly sensitive and specific for distinguishing primary ovarian mucinous tumors from colorectal and appendiceal metastases

scientific article published on 25 June 2019

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 locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

artículo científico publicado en 2010

A multi-center study to evaluate the impact of germline BRCA1 and BRCA2 mutations on ovarian cancer survival.

artículo científico publicado en 2012

A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers

artículo científico publicado en 2012

A polymorphism in the GALNT2 gene and ovarian cancer risk in four population based case-control studies

artículo científico publicado en 2010

A splicing variant of TERT identified by GWAS interacts with menopausal estrogen therapy in risk of ovarian cancer

artículo científico publicado en 2016

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

artículo científico publicado en 2012

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

Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer.

artículo científico publicado en 2010

An Immunohistochemical Algorithm for Ovarian Carcinoma Typing

artículo científico publicado en 2016

An epigenetic signature in peripheral blood predicts active ovarian cancer

artículo científico publicado en 2009

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

artículo científico publicado en 2015

Analysis of BRCA1 and BRCA2 mutations in Hungarian families with breast or breast-ovarian cancer

artículo científico publicado en 1997

Analysis of Sequence Contexts Flanking T·G Mismatches Leads to Predictions about Reactivity of the Mismatched T to Osmium Tetroxide

artículo científico publicado en 1993

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

artículo científico publicado en 2013

Aspirin, nonaspirin nonsteroidal anti-inflammatory drug, and acetaminophen use and risk of invasive epithelial ovarian cancer: a pooled analysis in the Ovarian Cancer Association Consortium

artículo científico publicado en 2014

Assessing the genetic architecture of epithelial ovarian cancer histological subtypes

artículo científico publicado en 2016

Assessing the usefulness of a novel MRI-based breast density estimation algorithm in a cohort of women at high genetic risk of breast cancer: the UK MARIBS study

artículo científico publicado en 2009

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

artículo científico publicado en 2016

Association Between Menopausal Estrogen-Only Therapy and Ovarian Carcinoma Risk

artículo científico publicado en 2016

Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer

artículo científico publicado en 2012

Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer

artículo científico publicado en 2009

Association between endometriosis and risk of histological subtypes of ovarian cancer: a pooled analysis of case-control studies

artículo científico publicado en 2012

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

artículo científico publicado en 2009

Association between single-nucleotide polymorphisms in hormone metabolism and DNA repair genes and epithelial ovarian cancer: results from two Australian studies and an additional validation set.

artículo científico publicado en 2007

Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Association study of prostate cancer susceptibility variants with risks of invasive ovarian, breast, and colorectal cancer

artículo científico publicado en 2008

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

artículo científico publicado en 2014

BRCA1 and BRCA2 mutation prevalence and clinical characteristics of a population-based series of ovarian cancer cases from Denmark.

artículo científico publicado en 2008

BRCA1 promoter deletions in young women with breast cancer and a strong family history: a population-based study

artículo científico publicado en 2007

BRCA1/2 mutation status influences somatic genetic progression in inherited and sporadic epithelial ovarian cancer cases

artículo científico publicado en 2003

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

artículo científico publicado en 2013

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

artículo científico publicado en 2019

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

artículo científico publicado en 2009

Candidate tumor-suppressor genes on chromosome arm 8p in early-onset and high-grade breast cancers

artículo científico publicado en 2004

Cell cycle genes and ovarian cancer susceptibility: a tagSNP analysis

artículo científico publicado en 2009

Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci

artículo científico publicado en 2015

Characterization of phenylalanine hydroxylase alleles in untreated phenylketonuria patients from Victoria, Australia: origin of alleles and haplotypes

artículo científico publicado en 1995

Chromosomes 6 and 18 induce neoplastic suppression in epithelial ovarian cancer cells.

artículo científico publicado en 2009

Cigarette smoking and risk of ovarian cancer: a pooled analysis of 21 case-control studies

artículo científico publicado en 2013

Cigarette smoking is associated with adverse survival among women with ovarian cancer: Results from a pooled analysis of 19 studies

artículo científico publicado en 2017

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

artículo científico publicado en 2015

Clinical and Emergent Biomarkers and Their Relationship to the Prognosis of Ovarian Cancer

artículo científico publicado en 2016

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 and Susceptibility to Ovarian Cancer: Current Insights and Future Directions

artículo científico

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

artículo científico publicado en 2015

Common Variants in RB1 Gene and Risk of Invasive Ovarian Cancer

article

Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer

artículo científico publicado en 2011

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction

artículo científico publicado en 2010

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

artículo científico publicado en 2011

Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk

artículo científico publicado en 2012

Common genetic variants and modification of penetrance of BRCA2-associated breast cancer

artículo científico publicado en 2010

Common origins of MDA-MB-435 cells from various sources with those shown to have melanoma properties.

artículo científico publicado en 2004

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

artículo científico publicado en 2010

Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

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

artículo científico publicado en 2015

Common variants in mismatch repair genes and risk of invasive ovarian cancer.

artículo científico publicado en 2006

Comparative study of roles of the lobus parolfactorius and intermediate medial hyperstriatum ventrale in memory formation in the chick brain

artículo científico publicado el 1 de abril de 1992

Comparison of genotype and intellectual phenotype in untreated PKU patients

artículo científico publicado en 1993

Complete mutation detection using unlabeled chemical cleavage.

artículo científico publicado en 1992

Complex CGH alterations on chromosome arm 8p at candidate tumor suppressor gene loci in breast cancer cell lines

artículo científico publicado en 2005

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

Contribution of large genomic BRCA1 alterations to early-onset breast cancer selected for family history and tumour morphology: a report from The Breast Cancer Family Registry

artículo científico publicado en 2011

Contribution ofBRCA1andBRCA2mutations to inherited ovarian cancer

artículo científico publicado en 2007

Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

scholarly article by Mia M Gaudet published in November 2010

Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer.

artículo científico publicado en 2010

Cost-effectiveness of Population-Based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 Mutation Testing in Unselected General Population Women

artículo científico publicado en 2018

CpG hotspot causes second mutation in codon 408 of the phenylalanine hydroxylase gene

article

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

DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

artículo científico publicado en 2001

Development and validation of the gene-expression Predictor of high-grade-serous Ovarian carcinoma molecular subTYPE (PrOTYPE)

scientific article published on 17 June 2020

Does the primary site really matter? Profiling mucinous ovarian cancers of uncertain primary origin (MO-CUP) to personalise treatment and inform the design of clinical trials

Dose-Response Association of CD8+ Tumor-Infiltrating Lymphocytes and Survival Time in High-Grade Serous Ovarian Cancer.

artículo científico publicado en 2017

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

artículo científico publicado en 2010

Effects of common germ-line genetic variation in cell cycle genes on ovarian cancer survival

artículo científico publicado en 2008

Efficient molecular subtype classification of high-grade serous ovarian cancer

artículo científico publicado en 2015

Eligibility for magnetic resonance imaging screening in the United Kingdom: effect of strict selection criteria and anonymous DNA testing on breast cancer incidence in the MARIBS Study

artículo científico publicado en 2009

Enhanced GAB2 Expression Is Associated with Improved Survival in High-Grade Serous Ovarian Cancer and Sensitivity to PI3K Inhibition

artículo científico publicado en 2015

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

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

scholarly article published in British Journal of Cancer

Estrogen receptor beta rs1271572 polymorphism and invasive ovarian carcinoma risk: pooled analysis within the Ovarian Cancer Association Consortium

artículo científico publicado en 2011

Evaluating the ovarian cancer gonadotropin hypothesis: a candidate gene study

artículo científico publicado en 2014

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

artículo científico publicado en 2017

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 polygenic risk scores for ovarian cancer risk prediction in a prospective cohort study

Evidence for a time-dependent association between FOLR1 expression and survival from ovarian carcinoma: implications for clinical testing. An Ovarian Tumour Tissue Analysis consortium study

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

artículo científico publicado en 2016

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

article

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

artículo científico publicado en 2020

Frequent loss of BRCA1 mRNA and protein expression in sporadic ovarian cancers

artículo científico publicado en 2000

Functional Analysis and Fine Mapping of the 9p22.2 Ovarian Cancer Susceptibility Locus.

artículo científico publicado en 2018

Functional complementation studies identify candidate genes and common genetic variants associated with ovarian cancer survival

artículo científico publicado en 2009

Functional complementation studies identify candidate genes and common genetic variants associated with ovarian cancer survival

article

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

artículo científico publicado en 2016

Functional polymorphisms in the TERT promoter are associated with risk of serious ovarian and breast cancer

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

artículo científico publicado en 2011

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk

artículo científico publicado en 2018

Genetic intra-tumour heterogeneity in epithelial ovarian cancer and its implications for molecular diagnosis of tumours

artículo científico publicado en 2007

Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2010

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 insulin-like growth factor 2 may play a role in ovarian cancer risk

artículo científico publicado en 2011

Genetic variations and subclinical markers of carotid atherosclerosis in patients with type 2 diabetes mellitus.

artículo científico publicado en 2018

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 association study for ovarian cancer susceptibility using pooled DNA.

artículo científico publicado en 2012

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

scientific article published on 18 May 2020

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 subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.

artículo científico publicado en 2013

Genotype and Intellectual Phenotype in Untreated Phenylketonuria Patients

scientific article published on 01 April 1999

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

artículo científico publicado en 2019

High frequency of germ-line BRCA2 mutations among Hungarian male breast cancer patients without family history

artículo científico publicado en 1999

Histopathology of familial ovarian tumors in women from families with and without germline BRCA1 mutations

artículo científico publicado en 2000

Histopathology, FIGO stage, and BRCA mutation status of ovarian cancers from the Gilda Radner Familial Ovarian Cancer Registry

artículo científico publicado en 2004

History of Comorbidities and Survival of Ovarian Cancer Patients, Results from the Ovarian Cancer Association Consortium

artículo científico publicado en 2017

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

artículo científico publicado en 2013

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 germ-line E-cadherin mutations in gastric cancer families of European origin

artículo científico publicado en 1998

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

artículo científico publicado en 2016

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

artículo científico publicado en 2015

Illegitimate transcription of phenylalanine hydroxylase for detection of mutations in patients with phenylketonuria

artículo científico publicado en 1992

In vivo disposal of phenylalanine in phenylketonuria: a study of two siblings

artículo científico publicado en 1996

Increased frequency ofTP53 mutations inBRCA1 andBRCA2 ovarian tumours

scientific article published on 01 June 1999

Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

artículo científico publicado en 2016

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 regulatory T cell genes and outcome of ovarian cancer

artículo científico publicado en 2013

Inhibition of the Nuclear Export Receptor XPO1 as a Therapeutic Target for Platinum-Resistant Ovarian Cancer

artículo científico publicado en 2016

Integration of Population-Level Genotype Data with Functional Annotation Reveals Over-Representation of Long Noncoding RNAs at Ovarian Cancer Susceptibility Loci

artículo científico publicado en 2016

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer

artículo científico publicado en 2016

LCC15-MB cells are MDA-MB-435: a review of misidentified breast and prostate cell lines

artículo científico publicado en 2004

LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer

artículo científico publicado en 2011

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

artículo científico publicado en 2014

Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2.

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Microcell-mediated chromosome transfer identifies EPB41L3 as a functional suppressor of epithelial ovarian cancers.

artículo científico publicado en 2010

Mismatch repair gene polymorphisms and survival in invasive ovarian cancer patients

artículo científico publicado en 2008

Molecular Classification of Epithelial Ovarian Cancer Based on Methylation Profiling: Evidence for Survival Heterogeneity

artículo científico publicado en 2019

Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutation.

artículo científico publicado en 1993

Morphological predictors of BRCA1 germline mutations in young women with breast cancer.

artículo científico publicado en 2011

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 loci with different cancer specificities within the 8q24 gene desert

artículo científico publicado en 2008

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

artículo científico publicado en 2018

Mutations Ivs4nt1, 47delCT, and G148S identified in the phenylalanine hydroxylase gene by RT-PCR of illegitimate transcripts and chemical cleavage of mismatch

article

MyD88 and TLR4 Expression in Epithelial Ovarian Cancer

artículo científico publicado en 2018

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

artículo científico publicado en 2015

No Evidence That Genetic Variation in the Myeloid-Derived Suppressor Cell Pathway Influences Ovarian Cancer Survival

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Obesity and risk of ovarian cancer subtypes: evidence from the Ovarian Cancer Association Consortium

artículo científico publicado en 2013

Offspring sex and risk of epithelial ovarian cancer: a multinational pooled analysis of 12 case-control studies

scientific article published on 21 September 2020

Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations

artículo científico publicado en 2004

Ovarian cancer risk associated with inherited inflammation-related variants

artículo científico publicado en 2012

Ovarian cancer survival in Ashkenazi Jewish patients with BRCA1 and BRCA2 mutations

artículo científico publicado en 2001

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

Ovarian carcinoma in situ with germline BRCA1 mutation and loss of heterozygosity at BRCA1 and TP53.

artículo científico publicado en 2000

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

Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

artículo científico publicado en 2011

Phenotype-directed analysis of genotype in early-onset, familial breast cancers

artículo científico publicado en 2006

Polymorphism in the 3? untranslated region of the phenylalanine hydroxylase gene detected by enzyme mismatch cleavage: evolution of haplotypes

article

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

artículo científico publicado en 2011

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

Predicting clinical outcome in patients diagnosed with synchronous ovarian and endometrial cancer.

artículo científico publicado en 2008

Primary ovarian dysgerminoma in a patient with a germline BRCA1 mutation

artículo científico publicado en 2000

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

artículo científico publicado en 2010

Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the Ovarian Cancer Association Consortium pooled analysis

artículo científico publicado en 2008

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

Recruitment of newly diagnosed ovarian cancer patients proved challenging in a multicentre biobanking study.

artículo científico publicado en 2010

Refined cut-off for TP53 immunohistochemistry improves prediction of TP53 mutation status in ovarian mucinous tumors: implications for outcome analyses

artículo científico publicado en 2020

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

artículo científico publicado en 2013

Risk of ovarian cancer in women with first-degree relatives with cancer

artículo científico publicado en 2009

Robust Tests for Additive Gene-Environment Interaction in Case-Control Studies Using Gene-Environment Independence

artículo científico publicado en 2017

Role of genetic polymorphisms and ovarian cancer susceptibility

scientific article published on 04 February 2009

Screening for theBRCA1-ins6kbEx13mutation: potential for misdiagnosis

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

Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatch

artículo científico publicado en 1991

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

artículo científico publicado en 2009

Single-Patient Molecular Testing with NanoString nCounter Data Using a Reference-Based Strategy for Batch Effect Correction

artículo científico publicado en 2016

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

artículo científico publicado en 2007

Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancer

artículo científico publicado en 2007

Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer

artículo científico publicado en 2009

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

artículo científico publicado en 2016

The Effects of Common Genetic Variants in Oncogenes on Ovarian Cancer Survival

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

scientific article published on 01 November 2019

The association between socioeconomic status and tumour stage at diagnosis of ovarian cancer: A pooled analysis of 18 case-control studies

artículo científico publicado en 2016

The clonal evolution of metastases from primary serous epithelial ovarian cancers

artículo científico publicado en 2009

The contribution of BRCA1 and BRCA2 to ovarian 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 role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing

artículo científico publicado en 2011

The sex hormone system in carriers of BRCA1/2 mutations: a case-control study.

artículo científico publicado en 2013

Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach

artículo científico publicado en 2017

Use of common analgesic medications and ovarian cancer survival: results from a pooled analysis in the Ovarian Cancer Association Consortium

artículo científico publicado en 2017

Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers.

artículo científico publicado en 2012

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

artículo científico publicado en 2009

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

artículo científico publicado en 2018

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

artículo científico publicado en 2014

Vascular endothelial growth factor gene polymorphisms and ovarian cancer survival

artículo científico publicado en 2010

Vitamin D receptor rs2228570 polymorphism and invasive ovarian carcinoma risk: pooled analysis in five studies within the Ovarian Cancer Association Consortium

artículo científico publicado en 2011

p53 and ovarian carcinoma survival: an Ovarian Tumor Tissue Analysis consortium study

artículo científico publicado en 2023

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

artículo científico publicado en 2018

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