Jeffery P Struewing

Jeffery P Struewing

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Jeffery P Struewing

Jeffery P Struewing

Publications by authors named "Jeffery P Struewing"

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No evidence of excess breast cancer risk among mutation-negative women from BRCA mutation-positive families.

Breast Cancer Res Treat 2011 Jan 11;125(1):169-73. Epub 2010 May 11.

Division of Medical Oncology, University of Washington/Seattle Cancer Care Alliance, 825 Eastlake Ave, E., G3-630, Seattle, WA 98109, USA.

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http://dx.doi.org/10.1007/s10549-010-0923-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3110729PMC
January 2011

Polymorphisms in estrogen biosynthesis and metabolism-related genes, ionizing radiation exposure, and risk of breast cancer among US radiologic technologists.

Breast Cancer Res Treat 2009 Nov 12;118(1):177-84. Epub 2009 Feb 12.

Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, 6120 Executive Boulevard, EPS 7060, MSC 7238, Bethesda, MD, 20892-7238, USA.

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http://dx.doi.org/10.1007/s10549-009-0307-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860373PMC
November 2009

Breast cancer risk polymorphisms and interaction with ionizing radiation among U.S. radiologic technologists.

Cancer Epidemiol Biomarkers Prev 2008 Aug;17(8):2007-11

Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Department of Health and Human Services, Bethesda, MD 20892-7238, USA.

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http://cebp.aacrjournals.org/cgi/doi/10.1158/1055-9965.EPI-0
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http://dx.doi.org/10.1158/1055-9965.EPI-08-0300DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2583248PMC
August 2008

Similar prevalence of founder BRCA1 and BRCA2 mutations among Ashkenazi and non-Ashkenazi men with breast cancer: evidence from 261 cases in Israel, 1976-1999.

Eur J Med Genet 2008 Mar-Apr;51(2):141-7. Epub 2007 Nov 22.

Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Bethesda, MD 20892-7238, USA.

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http://dx.doi.org/10.1016/j.ejmg.2007.11.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386175PMC
June 2008

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

Am J Hum Genet 2007 Dec 16;81(6):1186-200. Epub 2007 Oct 16.

Cancer Research UK, Genetic Epidemiology Unit, Strangeways Research Laboratory, Cambridge, CB1 8RN, UK.

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http://linkinghub.elsevier.com/retrieve/pii/S000292970763768
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http://dx.doi.org/10.1086/522611DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276351PMC
December 2007

Systematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB).

Genome Res 2007 Jul 24;17(7):1111-7. Epub 2007 May 24.

Laboratory of Population Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

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http://www.genome.org/cgi/doi/10.1101/gr.5963407
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http://dx.doi.org/10.1101/gr.5963407DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1899122PMC
July 2007

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

Cancer Epidemiol Biomarkers Prev 2007 Jul;16(7):1416-21

Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, 200 First Street Southwest, Rochester, MN 55905, USA.

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http://cebp.aacrjournals.org/cgi/doi/10.1158/1055-9965.EPI-0
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http://dx.doi.org/10.1158/1055-9965.EPI-07-0129DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775799PMC
July 2007

Genome-wide association study identifies novel breast cancer susceptibility loci.

Authors:
Douglas F Easton Karen A Pooley Alison M Dunning Paul D P Pharoah Deborah Thompson Dennis G Ballinger Jeffery P Struewing Jonathan Morrison Helen Field Robert Luben Nicholas Wareham Shahana Ahmed Catherine S Healey Richard Bowman Kerstin B Meyer Christopher A Haiman Laurence K Kolonel Brian E Henderson Loic Le Marchand Paul Brennan Suleeporn Sangrajrang Valerie Gaborieau Fabrice Odefrey Chen-Yang Shen Pei-Ei Wu Hui-Chun Wang Diana Eccles D Gareth Evans Julian Peto Olivia Fletcher Nichola Johnson Sheila Seal Michael R Stratton Nazneen Rahman Georgia Chenevix-Trench Stig E Bojesen Børge G Nordestgaard Christen K Axelsson Montserrat Garcia-Closas Louise Brinton Stephen Chanock Jolanta Lissowska Beata Peplonska Heli Nevanlinna Rainer Fagerholm Hannaleena Eerola Daehee Kang Keun-Young Yoo Dong-Young Noh Sei-Hyun Ahn David J Hunter Susan E Hankinson David G Cox Per Hall Sara Wedren Jianjun Liu Yen-Ling Low Natalia Bogdanova Peter Schürmann Thilo Dörk Rob A E M Tollenaar Catharina E Jacobi Peter Devilee Jan G M Klijn Alice J Sigurdson Michele M Doody Bruce H Alexander Jinghui Zhang Angela Cox Ian W Brock Gordon MacPherson Malcolm W R Reed Fergus J Couch Ellen L Goode Janet E Olson Hanne Meijers-Heijboer Ans van den Ouweland André Uitterlinden Fernando Rivadeneira Roger L Milne Gloria Ribas Anna Gonzalez-Neira Javier Benitez John L Hopper Margaret McCredie Melissa Southey Graham G Giles Chris Schroen Christina Justenhoven Hiltrud Brauch Ute Hamann Yon-Dschun Ko Amanda B Spurdle Jonathan Beesley Xiaoqing Chen Arto Mannermaa Veli-Matti Kosma Vesa Kataja Jaana Hartikainen Nicholas E Day David R Cox Bruce A J Ponder

Nature 2007 Jun;447(7148):1087-93

CR-UK Genetic Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8RN, UK.

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http://dx.doi.org/10.1038/nature05887DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714974PMC
June 2007

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

Nat Genet 2007 Mar 11;39(3):352-8. Epub 2007 Feb 11.

Sheffield University Medical School, Sheffield S10 2RX, UK.

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http://dx.doi.org/10.1038/ng1981DOI Listing
March 2007

Papillary thyroid cancer and polymorphic variants in TSHR- and RET-related genes: a nested case-control study within a cohort of U.S. radiologic technologists.

Cancer Epidemiol Biomarkers Prev 2007 Jan;16(1):174-7

Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Room 7053, 6120 Executive Boulevard, Bethesda, MD 20892-7238, USA.

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http://cebp.aacrjournals.org/cgi/doi/10.1158/1055-9965.EPI-0
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http://dx.doi.org/10.1158/1055-9965.EPI-06-0665DOI Listing
January 2007

Candidate single nucleotide polymorphism selection using publicly available tools: a guide for epidemiologists.

Am J Epidemiol 2006 Oct 21;164(8):794-804. Epub 2006 Aug 21.

Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892-7238, USA.

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http://dx.doi.org/10.1093/aje/kwj269DOI Listing
October 2006

BRCA1/2 testing in hereditary breast and ovarian cancer families III: risk perception and screening.

Am J Med Genet A 2006 Oct;140(20):2198-206

Genetic Disease Research Branch, NHGRI, Bethesda, Maryland 20892-0249, USA.

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http://dx.doi.org/10.1002/ajmg.a.31432DOI Listing
October 2006

Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses.

Hum Genet 2006 May 17;119(4):376-88. Epub 2006 Feb 17.

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, 6120 Executive Boulevard, Room 7076, Rockville, MD 20952-7234, USA.

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http://dx.doi.org/10.1007/s00439-006-0135-zDOI Listing
May 2006

Prophylactic oophorectomy reduces breast cancer penetrance during prospective, long-term follow-up of BRCA1 mutation carriers.

J Clin Oncol 2005 Dec;23(34):8629-35

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, 6120 Executive Blvd, Room 7016, MSC 7231, Rockville, MD 20852, USA.

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http://ascopubs.org/doi/10.1200/JCO.2005.02.9199
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http://dx.doi.org/10.1200/JCO.2005.02.9199DOI Listing
December 2005

DNA damage among thyroid cancer and multiple cancer cases, controls, and long-lived individuals.

Mutat Res 2005 Oct;586(2):173-88

Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, 6120 Executive Boulevard, EPS 7092, MSC 7238, Bethesda, MD 20892-7238, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S138357180500177
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http://dx.doi.org/10.1016/j.mrgentox.2005.07.001DOI Listing
October 2005

BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships.

Am J Med Genet A 2005 Mar;133A(2):165-9

Medical Genetics Branch, National Human Genome Research Institute/NIH, Bldg. 10, 10 Center Drive, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1002/ajmg.a.30566DOI Listing
March 2005

Genomic approaches to identifying breast cancer susceptibility factors.

Breast Dis 2004 ;19:3-9

Laboratory of Population Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892-5060, USA.

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March 2005

Breast cancer risks for BRCA1/2 carriers.

Science 2004 Dec;306(5705):2187-91; author reply 2187-91

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December 2004

BRCA1 and sex ratio.

Eur J Hum Genet 2004 Aug;12(8):663-7

Laboratory of Population Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-5060, USA.

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http://dx.doi.org/10.1038/sj.ejhg.5201210DOI Listing
August 2004

Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes.

BMC Cancer 2004 Mar 12;4. Epub 2004 Mar 12.

Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, 6120 Executive Boulevard, Bethesda, Maryland, 20892-7238, USA.

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http://dx.doi.org/10.1186/1471-2407-4-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC408462PMC
March 2004

Segregation analysis of 231 Ashkenazi Jewish families for evidence of additional breast cancer susceptibility genes.

Cancer Epidemiol Biomarkers Prev 2003 Oct;12(10):1045-52

Laboratory of Population Genetics, National Cancer Institute, NIH, Bethesda, Maryland 20892, USA.

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October 2003

CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF.

Oncogene 2003 Jul;22(28):4444-8

Laboratory of Population Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD, USA.

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http://dx.doi.org/10.1038/sj.onc.1206564DOI Listing
July 2003

Gynecologic surgeries and risk of ovarian cancer in women with BRCA1 and BRCA2 Ashkenazi founder mutations: an Israeli population-based case-control study.

J Natl Cancer Inst 2003 Jul;95(14):1072-8

Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-7246, USA.

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http://dx.doi.org/10.1093/jnci/95.14.1072DOI Listing
July 2003

HapScope: a software system for automated and visual analysis of functionally annotated haplotypes.

Nucleic Acids Res 2002 Dec;30(23):5213-21

Laboratory of Population Genetics, National Cancer Institute/National Institutes of Health, 8424 Helgerman Court, Room 101, MSC 8302, Bethesda, MD 20892-8302, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC137968PMC
http://dx.doi.org/10.1093/nar/gkf654DOI Listing
December 2002

A natural history of melanomas and dysplastic nevi: an atlas of lesions in melanoma-prone families.

Cancer 2002 Jun;94(12):3192-209

Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland 20892-7236, USA.

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http://dx.doi.org/10.1002/cncr.10605DOI Listing
June 2002

Breast cancer risk in Ashkenazi BRCA1/2 mutation carriers: effects of reproductive history.

Epidemiology 2002 May;13(3):255-61

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892-7246, USA.

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May 2002