No evidence that protein truncating variants inBRIP1are associated with breast cancer risk: implications for gene panel testing-Reference-Cited by-同舟云学术

No evidence that protein truncating variants inBRIP1are associated with breast cancer risk: implications for gene panel testing

Published:2016-02-26 Issue:5 Volume:53 Page:298-309
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Easton Douglas F,Lesueur Fabienne,Decker Brennan,Michailidou Kyriaki,Li Jun,Allen Jamie,Luccarini Craig,Pooley Karen A,Shah Mitul,Bolla Manjeet K,Wang Qin,Dennis Joe,Ahmad Jamil,Thompson Ella R,Damiola Francesca,Pertesi Maroulio,Voegele Catherine,Mebirouk Noura,Robinot Nivonirina,Durand Geoffroy,Forey Nathalie,Luben Robert N^ORCID,Ahmed Shahana,Aittomäki Kristiina,Anton-Culver Hoda,Arndt Volker,Baynes Caroline,Beckman Matthias W,Benitez Javier,Van Den Berg David,Blot William J,Bogdanova Natalia V,Bojesen Stig E,Brenner Hermann,Chang-Claude Jenny,Chia Kee Seng,Choi Ji-Yeob,Conroy Don M,Cox Angela,Cross Simon S,Czene Kamila,Darabi Hatef,Devilee Peter,Eriksson Mikael,Fasching Peter A,Figueroa Jonine,Flyger Henrik,Fostira Florentia,García-Closas Montserrat,Giles Graham G,Glendon Gord,González-Neira Anna,Guénel Pascal,Haiman Christopher A,Hall Per,Hart Steven N,Hartman Mikael,Hooning Maartje J,Hsiung Chia-Ni,Ito Hidemi,Jakubowska Anna,James Paul A,John Esther M,Johnson Nichola,Jones Michael,Kabisch Maria,Kang Daehee,Kosma Veli-Matti,Kristensen Vessela,Lambrechts Diether,Li Na,Lindblom Annika,Long Jirong,Lophatananon Artitaya,Lubinski Jan,Mannermaa Arto,Manoukian Siranoush,Margolin Sara,Matsuo Keitaro,Meindl Alfons,Mitchell Gillian,Muir Kenneth,Nevelsteen Ines,van den Ouweland Ans,Peterlongo Paolo,Phuah Sze Yee,Pylkäs Katri,Rowley Simone M,Sangrajrang Suleeporn,Schmutzler Rita K,Shen Chen-Yang,Shu Xiao-Ou,Southey Melissa C,Surowy Harald,Swerdlow Anthony,Teo Soo H,Tollenaar Rob A E M,Tomlinson Ian,Torres Diana,Truong Thérèse,Vachon Celine,Verhoef Senno,Wong-Brown Michelle,Zheng Wei,Zheng Ying,Nevanlinna Heli,Scott Rodney J,Andrulis Irene L,Wu Anna H,Hopper John L,Couch Fergus J,Winqvist Robert,Burwinkel Barbara,Sawyer Elinor J,Schmidt Marjanka K,Rudolph Anja,Dörk Thilo,Brauch Hiltrud,Hamann Ute,Neuhausen Susan L,Milne Roger L,Fletcher Olivia,Pharoah Paul D P,Campbell Ian G,Dunning Alison M,Le Calvez-Kelm Florence,Goldgar David E,Tavtigian Sean V,Chenevix-Trench Georgia, , , ,

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference43 articles.

1. Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning?;Ghoussaini;AmJPathol,2013

2. Gene-panel sequencing and the prediction of breast-cancer risk;Easton;N Engl J Med,2015

3. BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function;Cantor;Cell,2001

4. BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ;Litman;Cancer cell,2005

5. The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J;Levitus;Nat Genet,2005

Cited by 95 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Basis of Breast and Ovarian Cancer: Approaches and Lessons Learnt from Three Decades of Inherited Predisposition Testing;Genes;2024-02-08

2. Gender-Specific Genetic Predisposition to Breast Cancer: BRCA Genes and Beyond;Cancers;2024-01-30

3. FANCJ DNA helicase is recruited to the replisome by AND-1 to ensure genome stability;EMBO Reports;2024-01-02

4. Classification of Single-Nucleotide Polymorphisms (SNPs): Tips from the Basic Knowledge to the Clinical Outcomes;Interdisciplinary Cancer Research;2024

5. A comprehensive analysis of Fanconi anemia genes in Chinese patients with high-risk hereditary breast cancer;Journal of Cancer Research and Clinical Oncology;2023-08-11