A common coding variant in CASP8 is associated with breast cancer risk (Q57250674)

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Language	Label	Description	Also known as
English	A common coding variant in CASP8 is associated with breast cancer risk	article

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scholarly article

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

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corrigendum / erratum

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

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Serena Scollen

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Jaana M Hartikainen

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Jaana Hartikainen

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Gloria Ribas Despuig

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Gloria Ribas

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Jeffery Struewing

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Jeffery P Struewing

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Anna González-Neira

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Anna Gonzalez-Neira

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Angela Risch

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Olivia Fletcher

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Olivia Fletcher

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Georgia Chenevix-Trench

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Paul D P Pharoah

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Per Hall

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Jonathan Beesley

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Ute Hamann

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Shan Wang-Gohrke

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Hiltrud Brauch

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Arto Mannermaa

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Stephen Chanock

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Stephen Chanock

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John L Hopper

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Børge G. Nordestgaard

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Børge G Nordestgaard

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Veli-Matti Kosma

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Stig E Bojesen

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Javier Benitez

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Montserrat Garcia-Closas

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Michael R Stratton

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Annegien Broeks

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Daehee Kang

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Malcolm W. R. Reed

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Malcolm W R Reed

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Suleeporn Sangrajrang

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Nichola Johnson

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Nichola Johnson

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Natalia Bogdanova

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Dong-Young Noh

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Janet E Olson

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Anthony Renwick

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Ellen L Goode

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Peter Schürmann

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Lorna Gibson

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Alice J Sigurdson

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Alice J Sigurdson

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Rainer Fagerholm

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Rainer Fagerholm

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Karen A Pooley

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Frans Hogervorst

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Frans B L Hogervorst

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Laura J. van't Veer

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Laura J Van't Veer

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Christina Justenhoven

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Christina Justenhoven

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Sabapathy P Balasubramanian

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Sabapathy Balasubramanian

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Kirsimari Aaltonen

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Fabrice Odefrey

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Fabrice Odefrey

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Sheila Seal

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Keun-Young Yoo

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Christen K Axelsson

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Christen K Axelsson

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Silke Kropp

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Sara Wedrén

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Sei-Hyun Ahn

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Margaret McCredie

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Margaret R E McCredie

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Denise L Stredrick

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Denise L Stredrick

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author name string

Caroline Baynes

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Bruce A J Ponder

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Diana Torres

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David Hughes

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Paul Brennan

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Yen-Ling Low

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Jianjun Liu

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Bruce H Alexander

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language of work or name

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publication date

11 February 2007

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Nature Genetics

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39

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3

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352-358

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The ATM missense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer

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The biochemistry of apoptosis

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Re: Association of a common variant of the CASP8 gene with reduced risk of breast cancer

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CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies

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ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

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The future of genetic studies of complex human diseases

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TGF-beta signaling in tumor suppression and cancer progression

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Association between the T29-->C polymorphism in the transforming growth factor beta1 gene and breast cancer among elderly white women: The Study of Osteoporotic Fractures.

1 reference

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The L10P polymorphism of the transforming growth factor-beta 1 gene is not associated with breast cancer risk

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Genetic polymorphisms of the transforming growth factor-beta1 gene and breast cancer risk: a possible dual role at different cancer stages

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Transforming growth factor beta receptor type I and transforming growth factor beta1 polymorphisms are not associated with postmenopausal breast cancer.

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Polymorphic variation at the -202 locus in IGFBP3: Influence on serum levels of insulin-like growth factors, interaction with plasma retinol and vitamin D and breast cancer risk

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Polygenic susceptibility to breast cancer and implications for prevention

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Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium

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https://api.crossref.org/works/10.1038%2FNG1981

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Association of a common variant of the CASP8 gene with reduced risk of breast cancer

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https://api.crossref.org/works/10.1038%2FNG1981

7 January 2021

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Association of a T29-->C polymorphism of the transforming growth factor-beta1 gene with genetic susceptibility to myocardial infarction in Japanese

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Combined genetic assessment of transforming growth factor-beta signaling pathway variants may predict breast cancer risk

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IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancer

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Non-hierarchical logistic models and case-only designs for assessing susceptibility in population-based case-control studies

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Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease

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7 January 2021

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inferred from DOI database lookup

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