Search for rare copy number variants associated with hereditary breast cancer in Finnish case-control cohorts

被引：0
|
作者：
Kumpula, T. A. [1 ]
Vorimo, S. [1 ]
Tervasmaki, A. [1 ]
Koivuluoma, S. [1 ]
Mattila, T. [1 ]
Winqvist, R. [1 ]
Mantere, T. [1 ]
Pylkas, K. [1 ]
机构：
[1] Univ Oulu, Fac Med, FBMM, Oulu, Finland
来源：
ANNALS OF ONCOLOGY | 2024年 / 35卷
基金：
芬兰科学院;
关键词：
D O I：
10.1016/j.annonc.2024.08.048
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
39P
引用
收藏
页码：S227 / S227
页数：1
相关论文
共 50 条
  • [1] Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility
    Kumpula, Timo A. A.
    Vorimo, Sandra
    Mattila, Taneli T. T.
    O'Gorman, Luke
    Astuti, Galuh
    Tervasmaki, Anna
    Koivuluoma, Susanna
    Mattila, Tiina M. M.
    Grip, Mervi
    Winqvist, Robert
    Kuismin, Outi
    Moilanen, Jukka
    Hoischen, Alexander
    Gilissen, Christian
    Mantere, Tuomo
    Pylkas, Katri
    PLOS GENETICS, 2023, 19 (08):
  • [2] Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility
    Mantere, Tuomo
    Kumpula, Timo
    Vorimo, Sandra
    Mattila, Taneli
    O'Gorman, Luke
    Astuti, Galuh
    Tervasmaki, Anna
    Koivuluoma, Susanna
    Mattila, Tiina
    Grip, Mervi
    Winqvist, Robert
    Kuismin, Outi
    Moilanen, Jukka
    Hoischen, Alexander
    Gilissen, Christian
    Pylkas, Katri
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1250 - 1250
  • [3] Rare germline copy number variants (CNVs) and breast cancer risk
    Joe Dennis
    Jonathan P. Tyrer
    Logan C. Walker
    Kyriaki Michailidou
    Leila Dorling
    Manjeet K. Bolla
    Qin Wang
    Thomas U. Ahearn
    Irene L. Andrulis
    Hoda Anton-Culver
    Natalia N. Antonenkova
    Volker Arndt
    Kristan J. Aronson
    Laura E. Beane Freeman
    Matthias W. Beckmann
    Sabine Behrens
    Javier Benitez
    Marina Bermisheva
    Natalia V. Bogdanova
    Stig E. Bojesen
    Hermann Brenner
    Jose E. Castelao
    Jenny Chang-Claude
    Georgia Chenevix-Trench
    Christine L. Clarke
    J. Margriet Collée
    Fergus J. Couch
    Angela Cox
    Simon S. Cross
    Kamila Czene
    Peter Devilee
    Thilo Dörk
    Laure Dossus
    A. Heather Eliassen
    Mikael Eriksson
    D. Gareth Evans
    Peter A. Fasching
    Jonine Figueroa
    Olivia Fletcher
    Henrik Flyger
    Lin Fritschi
    Marike Gabrielson
    Manuela Gago-Dominguez
    Montserrat García-Closas
    Graham G. Giles
    Anna González-Neira
    Pascal Guénel
    Eric Hahnen
    Christopher A. Haiman
    Per Hall
    Communications Biology, 5
  • [4] Rare germline copy number variants (CNVs) and breast cancer risk
    Dennis, Joe
    Tyrer, Jonathan P.
    Walker, Logan C.
    Michailidou, Kyriaki
    Dorling, Leila
    Bolla, Manjeet K.
    Wang, Qin
    Ahearn, Thomas U.
    Andrulis, Irene L.
    Anton-Culver, Hoda
    Antonenkova, Natalia N.
    Arndt, Volker
    Aronson, Kristan J.
    Freeman, Laura E. Beane
    Beckmann, Matthias W.
    Behrens, Sabine
    Benitez, Javier
    Bermisheva, Marina
    Bogdanova, Natalia, V
    Bojesen, Stig E.
    Brenner, Hermann
    Castelao, Jose E.
    Chang-Claude, Jenny
    Chenevix-Trench, Georgia
    Clarke, Christine L.
    Collee, J. Margriet
    Couch, Fergus J.
    Cox, Angela
    Cross, Simon S.
    Czene, Kamila
    Devilee, Peter
    Dork, Thilo
    Dossus, Laure
    Eliassen, A. Heather
    Eriksson, Mikael
    Evans, D. Gareth
    Fasching, Peter A.
    Figueroa, Jonine
    Fletcher, Olivia
    Flyger, Henrik
    Fritschi, Lin
    Gabrielson, Marike
    Gago-Dominguez, Manuela
    Garcia-Closas, Montserrat
    Giles, Graham G.
    Gonzalez-Neira, Anna
    Guenel, Pascal
    Hahnen, Eric
    Haiman, Christopher A.
    Hall, Per
    COMMUNICATIONS BIOLOGY, 2022, 5 (01)
  • [5] Endometriosis Is Associated with Rare Copy Number Variants
    Chettier, Rakesh
    Ward, Kenneth
    Albertsen, Hans M.
    PLOS ONE, 2014, 9 (08):
  • [6] Performance of case-control rare copy number variation annotation in classification of autism
    Worrawat Engchuan
    Kiret Dhindsa
    Anath C Lionel
    Stephen W Scherer
    Jonathan H Chan
    Daniele Merico
    BMC Medical Genomics, 8
  • [7] Performance of case-control rare copy number variation annotation in classification of autism
    Engchuan, Worrawat
    Dhindsa, Kiret
    Lionel, Anath C.
    Scherer, Stephen W.
    Chan, Jonathan H.
    Merico, Daniele
    BMC MEDICAL GENOMICS, 2015, 8
  • [8] Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia
    Hubbard, Leon
    Rees, Elliott
    Morris, Derek W.
    Lynham, Amy J.
    Richards, Alex L.
    Pardinas, Antonio F.
    Legge, Sophie E.
    Harold, Denise
    Zammit, Stanley
    Corvin, Aiden C.
    Gill, Michael G.
    Hall, Jeremy
    Holmans, Peter
    O'Donovan, Michael C.
    Owen, Michael J.
    Donohoe, Gary
    Kirov, George
    Pocklington, Andrew
    Walters, James T. R.
    BIOLOGICAL PSYCHIATRY, 2021, 90 (01) : 28 - 34
  • [9] IDENTIFYING PATTERNS OF COPY NUMBER VARIANTS IN CASE-CONTROL STUDIES OF HUMAN GENETIC DISORDERS
    Alqallaf, Abdullah K.
    Tewfik, Ahmed H.
    Krakowiak, Paula
    Tassone, Flora
    Davis, Ryan
    Hansen, Robin
    Hertz-Picciotto, Irva
    Pessah, Isaac
    Gregg, Jeff
    Selleck, Scott B.
    2009 IEEE INTERNATIONAL WORKSHOP ON GENOMIC SIGNAL PROCESSING AND STATISTICS (GENSIPS 2009), 2009, : 142 - +
  • [10] Copy number variations associated with hereditary breast and colorectal carcinomas
    Abreu, Francine B.
    Monteiro Santos, Erika Maria
    Rossi, Benedito Mauro
    Achatz, Maria Isabel
    Cristina, Ana
    Krepischi, Victorino
    Kowalski, Luiz Paulo
    Brentani, Ricardo Renzo
    Rogatto, Silvia Regina
    CANCER RESEARCH, 2011, 71
12345