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Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype

Clinical cancer research, 2005-07, Vol.11 (14), p.5175-5180

2005

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Colorectal cancer and genetic polymorphisms of CYP1A1, GSTM1 and GSTT1: A case‐control study in the Grampian region of Scotland

International journal of cancer, 2006-11, Vol.119 (9), p.2155-2164

2006

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Human fetal testis Leydig cell disruption by exposure to the pesticide dieldrin at low concentrations

Human reproduction (Oxford), 2007-11, Vol.22 (11), p.2919-2927

2007

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A case-control study of Parkinson's disease and tobacco use: Gene-tobacco interactions

Movement disorders, 2010-05, Vol.25 (7), p.912-919

2010

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Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene, intakes of folate and related B vitamins and colorectal cancer: a case–control study in a population with relatively low folate intake

British journal of nutrition, 2008-02, Vol.99 (2), p.379-389

2008

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Oral Contraceptive Use and BRCA Penetrance: A Case-Only Study

Cancer epidemiology, biomarkers & prevention, 2009-07, Vol.18 (7), p.2107-2113

2009

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Probability estimation models for prediction of BRCA1 and BRCA2 mutation carriers: COS compares favourably with other models

Familial cancer, 2008-09, Vol.7 (3), p.199-212

2008

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CYP3A4 promoter variant is associated with prostate cancer risk in men with benign prostate hyperplasia

Oncology reports, 2002-05, Vol.9 (3), p.653

2002

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Genomic changes identified by comparative genomic hybridisation in docetaxel-resistant breast cancer cell lines

European journal of cancer (1990), 2005-05, Vol.41 (7), p.1086-1094

2005

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Information recovery in cancer families: value for risk estimations

Familial cancer, 2007-12, Vol.6 (4), p.415-443

2007

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p53 mutation is a common genetic event in ovarian carcinoma

Cancer research (Chicago, Ill.), 1993-05, Vol.53 (9), p.2128-2132

1993

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A randomized placebo-controlled prevention trial of aspirin and/or resistant starch in young people with familial adenomatous polyposis

Cancer prevention research (Philadelphia, Pa.), 2011-05, Vol.4 (5), p.655-665

2011

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British Society of Human Genetics

Genetics in medicine, 2002-01, Vol.4 (1), p.37-38

Haites, Neva

2002

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Comparative genomic hybridization analysis of chromosomal alterations induced by the development of resistance to thymidylate synthase inhibitors

Cancer research (Chicago, Ill.), 1998-11, Vol.58 (22), p.5042-5045

1998

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RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies

American journal of human genetics, 2007-12, Vol.81 (6), p.1186-1200

2007

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Vitamin D receptor, HER-2 polymorphisms and risk of prostate cancer in men with benign prostate hyperplasia

Saudi medical journal, 2004-04, Vol.25 (4), p.447

2004

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Does breast cancer genetic counselling meet women's expectations? A qualitative study

Critical public health, 2006-12, Vol.16 (4), p.281-293

2006

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The 8q24 rs6983267G variant is associated with increased thyroid cancer risk

Endocrine-related cancer, 2015-10, Vol.22 (5), p.841-849

2015

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Adhesion molecule interactions in human glomerulonephritis: Importance of the tubulointerstitium

Kidney international, 1996-01, Vol.49 (1), p.127-134

1996

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Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

JNCI : Journal of the National Cancer Institute, 1998-08, Vol.90 (15), p.1138-1145

1998

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Inactivation of the p16INK4A gene by methylation is not a frequent event in sporadic ovarian carcinoma

Oncology reports, 2001-11, Vol.8 (6), p.1359

2001

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Length and somatic mosaicism of CAG and GGN repeats in the androgen receptor gene and the risk of prostate cancer in men with benign prostatic hyperplasia

Annals of Saudi medicine, 2004-01, Vol.24 (1), p.21-26

2004

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Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype

Colorectal cancer and genetic polymorphisms of CYP1A1, GSTM1 and GSTT1: A case‐control study in the Grampian region of Scotland

Human fetal testis Leydig cell disruption by exposure to the pesticide dieldrin at low concentrations

A case-control study of Parkinson's disease and tobacco use: Gene-tobacco interactions

Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene, intakes of folate and related B vitamins and colorectal cancer: a case–control study in a population with relatively low folate intake

The Pathology of Familial Breast Cancer: Histological Features of Cancers in Families Not Attributable to Mutations in BRCA1 or BRCA2

Oral Contraceptive Use and BRCA Penetrance: A Case-Only Study

Probability estimation models for prediction of BRCA1 and BRCA2 mutation carriers: COS compares favourably with other models

Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas

CYP3A4 promoter variant is associated with prostate cancer risk in men with benign prostate hyperplasia

Genomic changes identified by comparative genomic hybridisation in docetaxel-resistant breast cancer cell lines

Information recovery in cancer families: value for risk estimations

Common genetic variants at the CRAC1 ( HMPS ) locus on chromosome 15q13.3 influence colorectal cancer risk

p53 mutation is a common genetic event in ovarian carcinoma

A randomized placebo-controlled prevention trial of aspirin and/or resistant starch in young people with familial adenomatous polyposis

British Society of Human Genetics

Comparative genomic hybridization analysis of chromosomal alterations induced by the development of resistance to thymidylate synthase inhibitors

RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies

Vitamin D receptor, HER-2 polymorphisms and risk of prostate cancer in men with benign prostate hyperplasia

Does breast cancer genetic counselling meet women's expectations? A qualitative study

The 8q24 rs6983267G variant is associated with increased thyroid cancer risk

Adhesion molecule interactions in human glomerulonephritis: Importance of the tubulointerstitium

Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

Inactivation of the p16INK4A gene by methylation is not a frequent event in sporadic ovarian carcinoma

Length and somatic mosaicism of CAG and GGN repeats in the androgen receptor gene and the risk of prostate cancer in men with benign prostatic hyperplasia

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