Deciphering the genetic basis of common diseases by integrated functional annotation of common and rare variants

被引：0
|
作者：
Olivier Harismendy
Gaurav Bhatia
Nazli G Rahim
Vikas Bansal
Masakazu Nakano
Michael Scott
Xiaoyun Wang
Colette Dib
Edouard Turlotte
Nathaniel Heintzman
Sarah S Murray
Jean-Francois Deleuze
Jack C Sipe
Bing Ren
Vineet Bafna
Eric J Topol
Kelly A Frazer
机构：
[1] Moores UCSD Cancer Center,Department of Pediatrics
[2] University of California Dan Diego,Department of Computer Sciences
[3] University of California San Diego,Department of Molecular and Experimental Medicine
[4] Scripps Translational Institute,Ludwig Institute
[5] The Scripps Research Institute,undefined
[6] Sanofi-Aventis Evry Genetics Center,undefined
[7] University of California San Diego,undefined
来源：
Genome Biology | / 11卷 / Suppl 1期
关键词：
Coronary Artery Disease; Morbid Obesity; Rare Variant; Anandamide; Marker Test;
D O I：
10.1186/gb-2010-11-s1-i8
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [21] The relative contribution of common and rare genetic variants to ADHD
    J Martin
    M C O'Donovan
    A Thapar
    K Langley
    N Williams
    Translational Psychiatry, 2015, 5 : e506 - e506
  • [22] The relative contribution of common and rare genetic variants to ADHD
    Martin, J.
    O'Donovan, M. C.
    Thapar, A.
    Langley, K.
    Williams, N.
    TRANSLATIONAL PSYCHIATRY, 2015, 5 : e506 - e506
  • [23] Atrial fibrillation: the role of common and rare genetic variants
    Olesen, Morten S.
    Nielsen, Morten W.
    Haunso, Stig
    Svendsen, Jesper H.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2014, 22 (03) : 297 - 306
  • [24] Spectrum of rare and common genetic variants in arrhythmogenic cardiomyopathy
    Lippi, M.
    Chiesa, M.
    Ascione, C.
    Pedrazzini, M.
    Mushtaq, S.
    Rovina, D.
    Riggio, D.
    Di Blasio, A.
    Biondi, M. L.
    Pompilio, G.
    Colombo, G. I.
    Novelli, V.
    Casella, M.
    Sommariva, E.
    EUROPEAN HEART JOURNAL, 2022, 43 : 362 - 362
  • [25] Integrated methods to solve the biological basis of common diseases
    Warden, CH
    Fisler, JS
    METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1997, 13 (04): : 347 - 357
  • [26] A Genome-wide Comparison of the Functional Properties of Rare and Common Genetic Variants in Humans
    Zhu, Qianqian
    Ge, Dongliang
    Maia, Jessica M.
    Zhu, Mingfu
    Petrovski, Slave
    Dickson, Samuel P.
    Heinzen, Erin L.
    Shianna, Kevin V.
    Goldstein, David B.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2011, 88 (04) : 458 - 468
  • [27] Variants in common diseases
    Nelson B. Freimer
    Chiara Sabatti
    Nature, 2007, 445 : 828 - 829
  • [28] Progress and promise in understanding the genetic basis of common diseases
    Price, Alkes L.
    Spencer, Chris C. A.
    Donnelly, Peter
    PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2015, 282 (1821)
  • [29] Detecting associations of rare variants with common diseases: collapsing or haplotyping?
    Wang, Meng
    Lin, Shili
    BRIEFINGS IN BIOINFORMATICS, 2015, 16 (05) : 759 - 768
  • [30] BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN
    Kim, Dokyoon
    Lucas, Anastasia
    Glessner, Joseph
    Verma, Shefali S.
    Bradford, Yuki
    Li, Ruowang
    Frase, Alex T.
    Hakonarson, Hakon
    Peissig, Peggy
    Brilliant, Murray
    Ritchie, Marylyn D.
    PACIFIC SYMPOSIUM ON BIOCOMPUTING 2016, 2016, : 357 - 368
12345