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Lista de obras de Georgia Chenevix-Trench

"I am not a statistic" ovarian cancer survivors' views of factors that influenced their long-term survival

scientific article published on 06 November 2019

11q13 is a susceptibility locus for hormone receptor positive breast cancer

artículo científico publicado en 2012

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

artículo científico publicado en 2012

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

artículo científico publicado en 2014

7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium

artículo científico publicado en 2011

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium

artículo científico publicado en 2012

A BRCA1 promoter variant (rs11655505) and breast cancer risk

artículo científico publicado en 2010

A Common Cancer Risk-Associated Allele in the hTERT Locus Encodes a Dominant Negative Inhibitor of Telomerase

artículo científico publicado en 2015

A Comprehensive Gene-Environment Interaction Analysis in Ovarian Cancer using Genome-wide Significant Common Variants

article

A Mendelian randomization analysis of circulating lipid traits and breast cancer risk

artículo científico publicado en 2019

A Systematic Approach to Analysing Gene-Gene Interactions: Polymorphisms at the Microsomal Epoxide Hydrolase EPHX and Glutathione S-transferase GSTM1, GSTT1, and GSTP1 Loci and Breast Cancer Risk

article

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

article

A common coding variant in CASP8 is associated with breast cancer risk

article

A fine-scale dissection of the DNA double-strand break repair machinery and its implications for breast cancer therapy

artículo científico publicado en 2014

A genome wide linkage search for breast cancer susceptibility genes

artículo científico publicado en 2006

A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk

scientific article published on 29 July 2013

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 caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor

artículo científico publicado en 2012

A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.

artículo científico publicado en 1993

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

artículo científico publicado en 2013

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 network analysis to identify mediators of germline-driven differences in breast cancer prognosis

artículo científico publicado en 2020

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 novel corepressor, BCoR-L1, represses transcription through an interaction with CtBP.

artículo científico publicado en 2007

A protein-truncating mutation inCYP17A1 in three sisters with early-onset breast cancer

A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia

artículo científico publicado en 2013

A role for common genomic variants in the assessment of familial breast cancer

scientific article published on 29 October 2012

A short ERK5 isoform modulates nucleocytoplasmic shuttling of active ERK5 and associates with poor survival in breast cancer

A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers

artículo científico publicado en 2001

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 (MDR 1) polymorphisms and progression-free survival among women with ovarian cancer following paclitaxel/carboplatin chemotherapy.

artículo científico publicado en 2008

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

ATM and genome maintenance: defining its role in breast cancer susceptibility

artículo científico publicado en 2004

AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study

artículo científico publicado en 2007

Abstract 5493: Genome-wide study of carboplatin and paclitaxel disposition in ovarian cancer patients

Abstract P6-10-06: Rational combination therapy against triple-negative breast cancer

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- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

artículo científico publicado en 2016

Allelic loss on chromosome 7q in ovarian adenocarcinomas: two critical regions and a rearrangement of the PLANH1 locus

artículo científico publicado en 1996

Allelic variation of the c-raf-1 oncogene in non-Hodgkin's lymphoma

artículo científico publicado en 1987

Allelic variation of the c-raf-1 proto-oncogene in human lymphoma and leukemia.

artículo científico publicado en 1989

Altered regulation of c-myc in an HL-60 differentiation resistant subclone, HL-60-1E3.

artículo científico publicado en 1987

An Alu VpA marker on chromosome I demonstrates that replication errors manifest at the adenoma-carcinoma transition in sporadic colorectal tumors

artículo científico publicado en 1995

An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA)

artículo científico publicado en 2007

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

artículo científico publicado en 2015

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 RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients

artículo científico publicado en 2012

Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients

artículo científico publicado en 2011

Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource

artículo científico publicado en 2006

Analysis of gene amplification in head-and-neck squamous-cell carcinoma

artículo científico publicado en 1991

Analysis of loss of heterozygosity and KRAS2 mutations in ovarian neoplasms: clinicopathological correlations

artículo científico publicado en 1997

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 the TGF beta functional pathway in epithelial ovarian carcinoma

artículo científico publicado en 2001

Analysis of the candidate 8p21 tumour suppressor, BNIP3L, in breast and ovarian cancer

artículo científico publicado en 2003

Analysis of the transcription regulator, CNOT7, as a candidate chromosome 8 tumor suppressor gene in colorectal cancer

artículo científico publicado en 2003

Androgen receptor exon 1 cag repeat length and risk of ovarian cancer

article

Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis

artículo científico publicado en 2015

Apparent protection from instability of repeat sequences in cancer-related genes in replication error positive gastrointestinal cancers

artículo científico publicado en 1997

Application of molecular findings to the diagnosis and management of breast disease: recent advances and challenges

scientific article published on 24 November 2010

Are estrogen receptor-positive breast cancers in BRCA1 mutation carriers sporadic?

artículo científico publicado en 2010

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 interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study

artículo científico publicado en 2010

Assessing the genetic architecture of epithelial ovarian cancer histological subtypes

artículo científico publicado en 2016

Assessment of hepatocyte growth factor in ovarian cancer mortality

artículo científico publicado en 2011

Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study.

artículo científico publicado en 2017

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Assignment of the human slit homologue SLIT2 to human chromosome band 4p15.2

artículo científico publicado en 1999

Association analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

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

artículo científico publicado en 2012

Association between KRAS rs61764370 and triple-negative breast cancer--a false positive?

artículo científico publicado en 2011

Association between a germline OCA2 polymorphism at chromosome 15q13.1 and estrogen receptor-negative breast cancer survival

artículo científico publicado en 2010

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 ESR1 gene tagging SNPs with breast cancer risk

artículo científico publicado en 2009

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

artículo científico publicado en 2019

Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

artículo científico publicado en 2012

Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis

artículo científico publicado en 2008

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

artículo científico publicado en 2016

Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.

scientific article published on 21 October 2016

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

artículo científico publicado en 2016

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

artículo científico publicado en 2021

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 the SS genotype of the L-myc gene and loss of 18q sequences with a worse clinical prognosis in colorectal cancers

artículo científico publicado en 1994

Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2010

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies

artículo científico publicado en 2010

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 common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2011

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

Atopy in Australia

article

BCoR-L1 variation and breast cancer

artículo científico publicado en 2007

BRAF polymorphisms and the risk of ovarian cancer of low malignant potential

BRCA1 and BRCA2 Pathogenic Sequence Variants in Women of African Origin or Ancestry

artículo científico publicado en 2019

BRCA1 and BRCA2 missense variants of high and low clinical significance influence lymphoblastoid cell line post-irradiation gene expression

artículo científico publicado en 2008

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

artículo científico publicado en 2015

BRCA2 arg372hispolymorphism and epithelial ovarian cancer risk

article

BamHI RFLP of the inhibin beta B (INHBB) chain gene on chromosome 2.

artículo científico publicado en 1990

Basal cell carcinoma in chronic arsenicism occurring in Queensland, Australia, after ingestion of an asthma medication

artículo científico publicado en 2000

Basal cell carcinomas, coarse sparse hair, and milia

artículo científico publicado en 1992

Basal cell naevus syndrome

artículo científico publicado en 1992

BcII RFLP of the plasminogen activator inhibitor type 2 gene (PLANH) on chromosome 18q21-q23.

artículo científico publicado en 1990

Body mass index and breast cancer survival: a Mendelian randomization analysis

artículo científico publicado en 2017

Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

artículo científico publicado en 2020

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

artículo científico publicado en 2022

Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

artículo científico publicado en 2012

Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab

artículo científico publicado en 2016

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

artículo científico publicado en 2016

Breast cancer stem cells: treatment resistance and therapeutic opportunities

scientific article published on 10 February 2011

CDX2, a human homologue of Drosophila caudal, is mutated in both alleles in a replication error positive colorectal cancer

artículo científico publicado en 1998

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

artículo científico publicado en 2013

CYP17 genetic polymorphism, breast cancer, and breast cancer risk factors: Australian Breast Cancer Family Study

artículo científico publicado en 2005

CYP17 promoter polymorphism and breast cancer in Australian women under age forty years

scientific article published on 01 October 2000

CYP17 promotor polymorphism and ovarian cancer risk

scientific article published on 01 May 2000

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

artículo científico publicado en 2019

Cancer Risks Associated With and Pathogenic Variants

artículo científico publicado en 2022

Candidate Causal Variants at the 8p12 Breast Cancer Risk Locus Regulate DUSP4

artículo científico publicado en 2020

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

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

artículo científico publicado en 2015

Cep55 regulates embryonic growth and development by promoting Akt stability in zebrafish

artículo científico publicado en 2015

Characterization of a novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient

artículo científico publicado en 2018

Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

artículo científico publicado en 2020

Characterization of the breast cancer associated ATM 7271T>G (V2424G) mutation by gene expression profiling

artículo científico

Chromatin interactome mapping at 139 independent breast cancer risk signals

artículo científico publicado en 2020

Chromosome 8 genetic analysis and phenotypic characterization of 21 ovarian cancer cell lines

artículo científico

Chromosome analysis of 30 cases of non-Hodgkin's lymphoma

artículo científico publicado en 1988

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

artículo científico publicado en 2015

Classification of BRCA1 missense variants of unknown clinical significance

artículo científico publicado en 2005

Cleft lip with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor loci

artículo científico publicado en 1992

Clinical Classification ofBRCA1andBRCA2DNA Sequence Variants: The Value of Cytokeratin Profiles and Evolutionary Analysis—A Report From the kConFab Investigators

article

Colorectal carcinomas show frequent allelic loss on the long arm of chromosome 17 with evidence for a specific target region

artículo científico publicado en 1995

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

artículo científico publicado en 2013

Combined associations of a polygenic risk score and classical risk factors with breast cancer risk

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Common Polymorphisms in ERCC2 (Xeroderma pigmentosum D) are not Associated with Breast Cancer Risk

scientific article published on 01 July 2005

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2011

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-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2008

Common chromosomal fragile site FRA16D mutation in cancer cells

artículo científico publicado en 2005

Common genetic variants and cancer risk in Mendelian cancer syndromes

artículo científico publicado en 2010

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

artículo científico publicado en 2010

Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers

artículo científico publicado en 2011

Common genomic variants associated with breast cancer predict the risk of second primary breast cancer diagnosis.

artículo científico publicado en 2012

Common germline polymorphisms associated with breast cancer-specific survival

artículo científico publicado en 2015

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2014

Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2010

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

artículo científico publicado en 2012

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 LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

scientific article published on 05 August 2009

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

artículo científico publicado en 2011

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

artículo científico publicado en 2012

Comparison of expression profiles in ovarian epithelium in vivo and ovarian cancer identifies novel candidate genes involved in disease pathogenesis

artículo científico publicado en 2011

Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer

artículo científico publicado en 2011

Consortium analysis of 7 candidate SNPs for ovarian cancer

scientific article published on July 2008

Copy Number Variation and Ovarian Cancer Risk-Letter

artículo científico publicado en 2020

Correction: BCoR-L1 variation and breast cancer.

artículo científico publicado en 2008

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

Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

artículo científico publicado en 2012

Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers

artículo científico publicado en 2019

Current research and treatment for epithelial ovarian cancer. A Position Paper from the Helene Harris Memorial Trust

artículo científico publicado en 2003

Cytogenetic and molecular genetic studies of a patient with atypical lymphoid hyperplasia

artículo científico publicado en 1987

DHPLC analysis of patients with Nevoid Basal Cell Carcinoma Syndrome reveals novel PTCH missense mutations in the sterol-sensing domain

artículo científico publicado en 2005

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status

artículo científico publicado en 2010

DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status

DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

scientific article published on 19 December 2013

De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype

artículo científico publicado en 1997

Decreased expression of the Id3 gene at 1p36.1 in ovarian adenocarcinomas

artículo científico publicado en 2001

Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the Co-operative Family Registry for Breast Cancer Studies (CFRBCS).

artículo científico publicado en 1999

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

scientific article published on 17 June 2020

Distinct phenotype in maternal uniparental disomy of chromosome 14.

artículo científico publicado en 1994

Dominant Negative ATM Mutations in Breast Cancer Families

artículo científico publicado en 2002

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

artículo científico publicado en 2017

Double-Strand Break Repair Gene Polymorphisms and Risk of Breast or Ovarian Cancer

article

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

artículo científico publicado en 2010

Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers

artículo científico publicado en 2012

Elevation of follicular phase inhibin and luteinizing hormone levels in mothers of dizygotic twins suggests nonovarian control of human multiple ovulation

scientific article published on 01 September 1991

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

artículo científico publicado en 2013

Epigenome erosion and SOX10 drive neural crest phenotypic mimicry in triple-negative breast cancer

scientific article published on 02 May 2022

Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk

scholarly article published in Nature Genetics

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

Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer

artículo científico publicado en 2013

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

Evaluating the repair of DNA derived from formalin-fixed paraffin-embedded tissues prior to genomic profiling by SNP-CGH analysis

artículo científico publicado en 2013

Evaluating the role of alcohol consumption in breast and ovarian cancer susceptibility using population-based cohort studies and two-sample Mendelian randomization analyses

scientific article published on 25 September 2020

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 a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA).

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 chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers

artículo científico publicado en 2012

Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers

scientific article published on February 2017

Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2.

artículo científico publicado en 2011

Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

artículo científico publicado en 2011

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

artículo científico publicado en 2010

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

Evidence for an association between nonsyndromic cleft lip with or without cleft palate and a gene located on the long arm of chromosome 4.

artículo científico publicado en 1995

Evidence for microsatellite instability in bilateral breast carcinomas

article

Evidence of a genetic link between endometriosis and ovarian cancer

scientific article published on 15 October 2015

Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

artículo científico publicado en 2014

Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

scientific article published on 03 September 2016

Evolutionary conservation analysis increases the colocalization of predicted exonic splicing enhancers in the BRCA1 gene with missense sequence changes and in-frame deletions, but not polymorphisms

artículo científico publicado en 2005

Exclusion of APC and MCC as the gene defect in one family with familial juvenile polyposis.

artículo científico publicado en 1993

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

artículo científico publicado en 2016

Exploring the link between MORF4L1 and risk of breast cancer

artículo científico publicado en 2011

Expression of beta-catenin, a key mediator of the WNT signaling pathway, in basal cell carcinoma

artículo científico publicado en 2000

Expression of p53 in arsenic-related and sporadic basal cell carcinoma

artículo científico publicado en 2000

FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium

artículo científico publicado en 2014

Fertility and incidence of KRAS2 mutations in borderline ovarian adenocarcinomas

artículo científico publicado en 1997

Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas

artículo científico publicado en 1995

Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome

artículo científico publicado en 1994

Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

artículo científico publicado en 2016

Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus

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 identifies two additional breast cancer susceptibility loci at 9q31.2.

artículo científico publicado en 2015

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

Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

artículo científico publicado en 2016

Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk

artículo científico publicado en 2015

Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.

artículo científico publicado en 2014

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

artículo científico publicado en 2013

Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium

artículo científico publicado en 2009

Folate and related micronutrients, folate-metabolising genes and risk of ovarian cancer

artículo científico publicado en 2011

Frequent PTEN/MMAC mutations in endometrioid but not serous or mucinous epithelial ovarian tumors.

artículo científico publicado en 1998

Frequent loss of heterozygosity and three critical regions on the short arm of chromosome 8 in ovarian adenocarcinomas ⬇️

artículo científico publicado el 3 de septiembre de 1998

Frequent loss of heterozygosity on chromosome 14 occurs in advanced colorectal carcinomas

artículo científico publicado en 1993

Frequent loss of heterozygosity on chromosome 18 in ovarian adenocarcinoma which does not always include the DCC locus

article

Frequent somatic mutations of GATA3 in non-BRCA1/BRCA2 familial breast tumors, but not in BRCA1-, BRCA2- or sporadic breast tumors

artículo científico publicado en 2009

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

artículo científico publicado en 2018

Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

artículo científico publicado en 2021

Functional dissection of breast cancer risk-associated TERT promoter variants

artículo científico publicado en 2017

Functional evidence for a colorectal cancer tumor suppressor gene at chromosome 8p22-23 by monochromosome transfer

scientific article published on 01 November 1996

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

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

artículo científico publicado en 2013

Further evidence for an association between genetic variation in transforming growth factor alpha and cleft lip and palate

artículo científico publicado en 1991

Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity.

artículo científico publicado en 1993

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

artículo científico publicado en 2013

Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome

artículo científico publicado en 2011

Gene expression in melanoma cell lines and cultured melanocytes: correlation between levels of c-src-1, c-myc and p53.

artículo científico publicado en 1990

Gene expression profiling of formalin-fixed, paraffin-embedded familial breast tumours using the whole genome-DASL assay

artículo científico publicado en 2010

Gene expression profiling of tumour epithelial and stromal compartments during breast cancer progression

article

Gene-panel sequencing and the prediction of breast-cancer risk

artículo científico publicado en 2015

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 and Histopathologic Evaluation ofBRCA1andBRCA2DNA Sequence Variants of Unknown Clinical Significance

article

Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study

artículo científico publicado en 2015

Genetic insights into biological mechanisms governing human ovarian ageing

artículo científico publicado en 2021

Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study

artículo científico publicado en 2013

Genetic predisposition to ductal carcinoma in situ of the breast

artículo científico publicado en 2016

Genetic predisposition to in situ and invasive lobular carcinoma of the breast

artículo científico publicado en 2014

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

artículo científico publicado en 2010

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

artículo científico publicado en 2014

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 variation in mitotic regulatory pathway genes is associated with breast tumor grade

artículo científico publicado en 2014

Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants

artículo científico publicado en 2005

Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

artículo científico publicado en 2016

Genetically Predicted Levels of DNA Methylation Biomarkers and Breast Cancer Risk: Data From 228 951 Women of European Descent

scientific article published on 01 March 2020

Genome-Wide Association Meta-Analysis of Single-Nucleotide Polymorphisms and Symptomatic Venous Thromboembolism during Therapy for Acute Lymphoblastic Leukemia and Lymphoma in Caucasian Children

scientific article published on 19 May 2020

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 analysis identifies three new breast cancer susceptibility loci

artículo científico publicado en 2012

Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

artículo científico publicado en 2011

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

artículo científico publicado en 2015

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

article

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

artículo científico publicado en 2013

Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women

artículo científico publicado en 2019

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 identifies novel breast cancer susceptibility loci

artículo científico publicado en 2007

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 germline variants and breast cancer-specific mortality

artículo científico publicado en 2019

Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancer

artículo científico publicado en 2018

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

artículo científico publicado en 2013

Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

artículo científico publicado en 2016

Genomic instability occurs in colorectal carcinomas but not in adenomas

scientific article published on 01 January 1993

Germ-line mutations in BRCA1 or BRCA2 in the normal breast are associated with altered expression of estrogen-responsive proteins and the predominance of progesterone receptor A.

artículo científico publicado en 2004

Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development

artículo científico publicado en 2009

Germline deletion of in familial acute lymphoblastic leukemia

scientific article published on 01 April 2019

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 variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

artículo científico publicado en 2021

Glutathione S-transferase GSTM1 null genotype is not overrepresented in Australian patients with nevoid basal cell carcinoma syndrome or sporadic melanoma

artículo científico publicado en 1995

Glutathione S-transferase M1 and T1 polymorphisms: susceptibility to colon cancer and age of onset

artículo científico publicado en 1995

Growing recognition of the role for rare missense substitutions in breast cancer susceptibility

artículo científico publicado en 2014

Guidelines for whole genome bisulphite sequencing of intact and FFPET DNA on the Illumina HiSeq X Ten.

artículo científico publicado en 2018

HER3 and downstream pathways are involved in colonization of brain metastases from breast cancer

artículo científico publicado en 2010

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2011

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

Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

artículo científico publicado en 2015

Heregulin-HER3-HER2 signaling promotes matrix metalloproteinase-dependent blood-brain-barrier transendothelial migration of human breast cancer cell lines.

artículo científico publicado en 2015

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics

artículo científico publicado en 2008

High content screening application for cell-type specific behaviour in heterogeneous primary breast epithelial subpopulations

artículo científico publicado en 2016

High-throughput allelic expression imbalance analyses identify candidate breast cancer risk genes

scholarly article

Homozygous deletions on the short arm of chromosome 9 in ovarian adenocarcinoma cell lines and loss of heterozygosity in sporadic tumors

artículo científico publicado en 1994

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

artículo científico publicado en 2013

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?

artículo científico publicado en 2007

Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk

artículo científico publicado en 2013

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 genetic variant associated with treatment outcome in ovarian cancer: the potential role of cholesterol metabolism as a determinant of response to chemotherapy

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

artículo científico publicado en 2016

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 new breast cancer predisposition genes via whole exome sequencing

artículo científico publicado en 2012

Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions

artículo científico publicado en 2013

Identification of novel genetic markers of breast cancer survival

artículo científico publicado en 2015

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

Immune Cell Associations with Cancer Risk

artículo científico publicado en 2020

Incessant ovulation, inflammation and epithelial ovarian carcinogenesis: revisiting old hypotheses

artículo científico publicado en 2005

Increased expression of the NME1 gene is associated with metastasis in epithelial ovarian cancer

scientific article published on 01 June 1995

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 the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

artículo científico publicado en 2015

Integrated genomic and transcriptomic analysis of human brain metastases identifies alterations of potential clinical significance

artículo científico

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

Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

artículo científico publicado en 2011

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer

artículo científico publicado en 2016

Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors

artículo científico publicado en 2014

Is Schizophrenia a Risk Factor for Breast Cancer?—Evidence From Genetic Data

artículo científico publicado en 2019

Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.

artículo científico publicado en 1999

Kinome profiling reveals breast cancer heterogeneity and identifies targeted therapeutic opportunities for triple negative breast cancer

artículo científico publicado en 2014

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

artículo científico publicado en 2013

LobSig is a multigene predictor of outcome in invasive lobular carcinoma

scientific article published on 27 June 2019

Localization of the gene for human proliferating nuclear antigen/cyclin by in situ hybridization

artículo científico publicado en 1990

Loss of heterozygosity at chromosome segment Xq25-26.1 in advanced human ovarian carcinomas

artículo científico publicado en 1997

Loss of heterozygosity on the long arm of chromosome 11 in colorectal tumours

artículo científico publicado en 1994

Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals

artículo científico publicado en 2005

Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2011

Lung cancer: intragenic ERBB2 kinase mutations in tumours

artículo científico publicado en 2004

Lymphoblastoid cell lines from frozen whole blood: a quick and economical safeguard for linkage analysis

artículo científico publicado en 1990

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

Mapping of a candidate colorectal cancer tumor-suppressor gene to a 900-kilobase region on the short arm of chromosome 8.

artículo científico publicado en 2004

Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched.

artículo científico publicado en 1997

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

scientific article published on 19 June 2019

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

artículo científico publicado en 2021

Menopausal hormone therapy prior to the diagnosis of ovarian cancer is associated with improved survival

artículo científico publicado en 2020

Meta-analysis of the global gene expression profile of triple-negative breast cancer identifies genes for the prognostication and treatment of aggressive breast cancer

artículo científico publicado en 2014

Meta-analysis of the global gene expression profile of triple-negative breast cancer identifies genes for the prognostication and treatment of aggressive breast cancer.

artículo científico publicado en 2014

MicroRNA related polymorphisms and breast cancer risk

artículo científico publicado en 2014

Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls

artículo científico publicado en 2010

Mixed ductal-lobular carcinomas: evidence for progression from ductal to lobular morphology

artículo científico publicado en 2018

Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriers

artículo científico publicado en 2009

Molecular Characterization and Cancer Risk Associated with BRCA1 and BRCA2 Splice Site Variants Identified in Multiple-Case Breast Cancer Families

Molecular characterization and cancer risk associated withBRCA1 andBRCA2 splice site variants identified in multiple-case breast cancer families

Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers

artículo científico publicado en 2018

Most common 'sporadic' cancers have a significant germline genetic component

artículo científico publicado en 2014

Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident

artículo científico publicado en 1997

MspI RFLP of FSHB on chromosome 11p

artículo científico publicado en 1991

Multidimensional phenotyping of breast cancer cell lines to guide preclinical research

artículo científico publicado en 2017

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

artículo científico publicado en 2013

Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer

artículo científico publicado en 2005

Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families

artículo científico publicado en 2011

Mutation analysis of five candidate genes in familial breast cancer

artículo científico publicado en 2006

Mutation and expression analysis of LZTS1 in ovarian cancer

artículo científico publicado en 2006

Mutation of ERBB2 provides a novel alternative mechanism for the ubiquitous activation of RAS-MAPK in ovarian serous low malignant potential tumors.

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 in EGFR, BRAF and RAS are rare in triple-negative and basal-like breast cancers from Caucasian women

artículo científico publicado en 2013

Mutations of the BRAF gene in human cancer

artículo científico publicado en 2002

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

artículo científico publicado en 1996

MyD88 and TLR4 Expression in Epithelial Ovarian Cancer

artículo científico publicado en 2018

NcoI RFLP of the human LHRH gene on chromosome 8p

artículo científico publicado en 1991

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

artículo científico publicado en 2015

Nevoid basal cell carcinoma syndrome: review of 118 affected individuals

artículo científico publicado en 1994

Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

artículo científico publicado en 2009

Nicholas Gordon Martin

scientific article published on 01 April 2020

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

artículo científico publicado en 2016

No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study

artículo científico publicado en 2008

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

artículo científico publicado en 2015

No evidence for an association between the earwax-associated polymorphism in ABCC11 and breast cancer risk in Caucasian women

artículo científico publicado en 2010

No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer

artículo científico publicado en 2002

No evidence for microsatellite instability from allelotype analysis of benign and low malignant potential ovarian neoplasms

scientific article published on 01 June 1998

No evidence for the H133Y mutation in SONIC HEDGEHOG in a collection of common tumour types

artículo científico publicado en 1998

No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2008

No evidence that GATA3 rs570613 SNP modifies breast cancer risk

scientific article published on 11 December 2008

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

scientific article published on 26 February 2016

No germline mutations in the histone acetyltransferase gene EP300 in BRCA1 and BRCA2 negative families with breast cancer and gastric, pancreatic, or colorectal cancer

artículo científico publicado en 2004

No significant association between progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of ovarian cancer

artículo científico publicado en 2001

Non-coding RNAs underlie genetic predisposition to breast cancer

artículo científico publicado en 2020

Ovarian and breast cancer risks associated with pathogenic variants in RAD51C and RAD51D

artículo científico publicado en 2020

Ovarian cancer risk, ALDH2 polymorphism and alcohol drinking: Asian data from the Ovarian Cancer Association Consortium

artículo científico publicado en 2017

Ovarian cancer survival and polymorphisms in hormone and DNA repair pathway genes

artículo científico

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

artículo científico publicado en 2012

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

artículo científico publicado en 2016

Paclitaxel sensitivity in relation to ABCB1 expression, efflux and single nucleotide polymorphisms in ovarian cancer

artículo científico publicado en 2014

Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families.

artículo científico publicado en 2017

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

artículo científico publicado en 2022

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

Patterns of somatic mutation in human cancer genomes

artículo científico publicado en 2007

Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients

artículo científico publicado en 2011

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

artículo científico publicado en 2016

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

artículo científico publicado en 2019

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

artículo científico publicado en 2020

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 at the glutathione S-transferase GSTM1, GSTT1 and GSTP1 loci: risk of ovarian cancer by histological subtype

artículo científico publicado en 2001

Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

artículo científico publicado en 2015

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 FGF2 gene and risk of serous ovarian cancer: results from the ovarian cancer association consortium

artículo científico publicado en 2009

Pooled analysis indicates that the GSTT1 deletion, GSTM1 deletion, and GSTP1 Ile105Val polymorphisms do not modify breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2009

Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the Breast Cancer Family Registry

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

Prediction of BRCA1 and BRCA2 mutation status using post-irradiation assays of lymphoblastoid cell lines is compromised by inter-cell-line phenotypic variability

artículo científico publicado en 2006

Prediction of breast cancer risk based on profiling with common genetic variants

artículo científico publicado en 2015

Primary treatment patterns in women recruited to the Australian Ovarian Cancer Study.

artículo científico publicado en 2012

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

artículo científico publicado en 2010

Progesterone receptor polymorphisms and risk of breast cancer: results from two Australian breast cancer studies

article

Progesterone receptor promoter +331A polymorphism is associated with a reduced risk of endometrioid and clear cell ovarian cancers.

artículo científico publicado en 2004

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

Prognostic gene expression signature for high-grade serous ovarian cancer

artículo científico publicado en 2020

Prohibitin 3′ untranslated region polymorphism and breast cancer risk in Australian women

artículo científico publicado en 2002

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

artículo científico publicado en 2011

PstI RFLP of the CGB gene

artículo científico publicado en 1990

Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

artículo científico publicado en 2018

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

scientific article published on 23 September 2019

RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies

artículo científico publicado en 2007

RAD51B in Familial Breast Cancer

artículo científico publicado en 2016

RAD52 Y415X truncation polymorphism and epithelial ovarian cancer risk in Australian women

article

Rad51 supports triple negative breast cancer metastasis

artículo científico publicado en 2014

Rare germline copy number variants (CNVs) and breast cancer risk

artículo científico publicado en 2022

Rare mutations and no hypermethylation at the CDKN2A locus in epithelial ovarian tumours

scientific article published on 01 March 1997

Rare variants in the ATM gene and risk of breast cancer

artículo científico publicado en 2011

Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer

artículo científico publicado en 2009

Reduced expression of chemokine (C-C motif) ligand-2 (CCL2) in ovarian adenocarcinoma

artículo científico publicado en 2005

Reduced expression of intercellular adhesion molecule-1 in ovarian adenocarcinomas

artículo científico publicado en 2001

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

artículo científico publicado en 2014

Regressive logistic and proportional hazards disease models for within-family analyses of measured genotypes, with application to a CYP17 polymorphism and breast cancer

artículo científico publicado en 2003

Reproductive hormone genes in mothers of spontaneous dizygotic twins: an association study

article

Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study.

artículo científico publicado en 2017

Restriction fragment length polymorphisms of L-myc and myb in human leukaemia and lymphoma in relation to age-selected controls

artículo científico publicado en 1989

Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042.

artículo científico publicado en 2009

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

artículo científico publicado en 2013

Role of genetic polymorphisms and ovarian cancer susceptibility

scientific article published on 04 February 2009

Role of genetic polymorphisms in ovarian cancer susceptibility: development of an international ovarian cancer association consortium

artículo científico publicado en 2008

SNPs in lncRNA Regions and Breast Cancer Risk

artículo científico publicado en 2020

Searching for BRCA3 by exome sequencing

Sequence variants ofDLC1 in colorectal and ovarian tumours

artículo científico publicado en 2000

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

Simple repeat polymorphism at the D9S151 locus.

artículo científico publicado en 1994

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

artículo científico publicado en 2009

Sodium butyrate differentially modulates plasminogen activator inhibitor type-1, urokinase plasminogen activator, and its receptor in a human colon carcinoma cell

artículo científico publicado en 1993

Somatic and germline mutations of the BRCA2 gene in sporadic ovarian cancer

scientific article published on 01 August 1996

Somatic rearrangement of the c-myc oncogene in primary human diffuse large-cell lymphoma

scientific article published on 01 October 1986

Spastic paresis, glaucoma and mental retardation--a probable autosomal recessive syndrome?

artículo científico publicado en 1986

Subtypes of familial breast tumours revealed by expression and copy number profiling

artículo científico publicado en 2009

Systematic review with meta-analysis: fundic gland polyps and proton pump inhibitors

artículo científico publicado en 2016

TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer

artículo científico publicado en 2017

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

artículo científico publicado en 2007

Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families

artículo científico publicado en 2015

The AIB1 Polyglutamine Repeat Does Not Modify Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

article

The BARD1 Cys557Ser polymorphism and breast cancer risk: an Australian case-control and family analysis

artículo científico publicado en 2008

The BRCA1-Δ11q Alternative Splice Isoform Bypasses Germline Mutations and Promotes Therapeutic Resistance to PARP Inhibition and Cisplatin

artículo científico publicado en 2016

The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years.

artículo científico publicado en 2002

The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

artículo científico publicado en 2018

The CYP17A1 -34T > C polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2010

The CYP3A4*1B polymorphism has no functional significance and is not associated with risk of breast or ovarian cancer

article

The EcoRI RFLP of c-mos in patients with non-Hodgkin's lymphoma and acute lymphoblastic leukemia, compared to geriatric and non-geriatric controls

artículo científico publicado en 1989

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

scientific article published on 01 November 2019

The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

The Landscape of Somatic Genetic Alterations in Breast Cancers From ATM Germline Mutation Carriers

artículo científico publicado en 2018

The MnSOD Val9Ala polymorphism, dietary antioxidant intake, risk and survival in ovarian cancer (Australia).

artículo científico publicado en 2007

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

artículo científico publicado en 2016

The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients

artículo científico publicado en 2015

The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2009

The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2005

The application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genes

artículo científico publicado en 2012

The challenges of finding the gene responsible for a rare, autosomal dominant gastric cancer susceptibility syndrome

article

The diagnostic implication of falcine calcification on plain skull radiographs of patients with basal cell naevus syndrome and the incidence of falcine calcification in their relatives and two control groups

artículo científico publicado en 1995

The effects of splice site mutations in patients with naevoid basal cell carcinoma syndrome

artículo científico publicado en 1998

The human growth-arrest-specific gene GAS1 maps outside the candidate region of the gene for nevoid basal cell carcinoma syndrome

artículo científico publicado en 1995

The importance of using public data to validate reported associations.

artículo científico publicado en 2018

The intronic G13964C variant in p53 is not a high-risk mutation in familial breast cancer in Australia

artículo científico publicado en 2001

The microsomal epoxide hydrolase Tyr113His polymorphism: association with risk of ovarian cancer.

artículo científico publicado en 2001

The molecular genetics of human non-Hodgkin's lymphoma

artículo científico publicado en 1987

The molecular origin and taxonomy of mucinous ovarian carcinoma

scientific article published on 02 September 2019

The prevalence of cervical and thoracic congenital skeletal abnormalities in basal cell naevus syndrome; a review of cervical and chest radiographs in 80 patients with BCNS.

artículo científico publicado en 1995

The progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of breast cancer in Australian women.

artículo científico publicado en 2002

The prohibitin 3′ untranslated region polymorphism is not associated with risk of ovarian cancer

artículo científico publicado en 2003

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

artículo científico publicado en 2011

The role of genetic breast cancer susceptibility variants as prognostic factors

artículo científico publicado en 2012

The role of glutathione-S-transferase polymorphisms in ovarian cancer survival

artículo científico publicado en 2006

The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries

scientific article published on 26 July 2019

The spectrum of patched mutations in a collection of Australian basal cell carcinomas

artículo científico publicado en 2000

The steroid 5alpha-reductase type II TA repeat polymorphism is not associated with risk of breast or ovarian cancer in Australian women.

artículo científico publicado en 2001

The use of the Illumina FFPE Restoration Protocol to obtain suitable quality DNA for SNP-based CGH– a pilot study.

artículo científico publicado en 2012

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

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

artículo científico publicado en 2020

Transfer of chromosome 8 into two breast cancer cell lines: total exclusion of three regions indicates location of putative in vitro growth suppressor genes

artículo científico

Translating Germline Cancer Risk into Precision Prevention

artículo científico publicado en 2017

Treatment of triple-negative breast cancer using anti-EGFR-directed radioimmunotherapy combined with radiosensitizing chemotherapy and PARP inhibitor

artículo científico publicado en 2013

Tumour-specific distribution of BRCA1 promoter region methylation supports a pathogenetic role in breast and ovarian cancer

artículo científico publicado en 2000

Two ATM variants and breast cancer risk

artículo científico publicado en 2005

UV induction of transforming growth factor alpha in melanoma cell lines is a posttranslational event

artículo científico publicado en 1992

Urokinase receptor genotypes in colorectal cancer.

artículo científico publicado en 1998

Using the MCF10A/MCF10CA1a Breast Cancer Progression Cell Line Model to Investigate the Effect of Active, Mutant Forms of EGFR in Breast Cancer Development and Treatment Using Gefitinib

artículo científico publicado en 2015

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

Variation in the RAD51 gene and familial breast cancer

artículo científico publicado en 2006

WGS and targetted sequencing in acute lymphoblastic leukemia identifies putative enhancer mutation associated with over-expression of a growth factor

artículo científico publicado en 2015

What makes a good PhD student?

artículo científico publicado en 2006

What's in a cancer syndrome? Genes, phenotype and pathology

artículo científico publicado en 2008

Xenobiotic-Metabolizing gene polymorphisms and ovarian cancer risk

artículo científico publicado en 2010

eQTL Colocalization Analyses Identify NTN4 as a Candidate Breast Cancer Risk Gene

artículo científico publicado en 2020

kConFab: a research resource of Australasian breast cancer families. Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer

artículo científico publicado en 2000

rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

artículo científico publicado en 2016

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

artículo científico publicado en 2018

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