GENOME-WIDE COPY NUMBER VARIATION AND WARFARIN DOSE RESPONSE IN AFRICAN AMERICANS

被引：0
|
作者：
Hernandez, W. [1 ]
Gamazon, E. R. [2 ]
Konkashbaev, A. I. [2 ]
Cavallari, L. H. [3 ]
Stranger, B. [1 ]
Perera, M. A. [4 ]
机构：
[1] Univ Chicago, Dept Med, Med Genet Sect, 5841 S Maryland Ave, Chicago, IL 60637 USA
[2] Vanderbilt Univ, Dept Med, Div Med Genet, Nashville, TN USA
[3] Univ Florida, Coll Pharm, Dept Pharmacotherapy & Translat Res, Ctr Pharmacogen, Gainesville, FL USA
[4] Northwestern Univ, Dept Pharmacol, Chicago, IL 60611 USA
来源：
CLINICAL PHARMACOLOGY & THERAPEUTICS | 2017年 / 101卷 / S1期
关键词：
D O I：
暂无
中图分类号：
R9 [药学];
学科分类号：
1007 ;
摘要：
PWIV-005
引用
收藏
页码：S96 / S96
页数：1
相关论文
共 50 条
  • [21] Genome-wide copy number variations in a large cohort of bantu African children
    Feyza Yilmaz
    Megan Null
    David Astling
    Hung-Chun Yu
    Joanne Cole
    Stephanie A. Santorico
    Benedikt Hallgrimsson
    Mange Manyama
    Richard A. Spritz
    Audrey E. Hendricks
    Tamim H. Shaikh
    BMC Medical Genomics, 14
  • [22] Genome-wide copy number variations in a large cohort of bantu African children
    Yilmaz, Feyza
    Null, Megan
    Astling, David
    Yu, Hung-Chun
    Cole, Joanne
    Santorico, Stephanie A.
    Hallgrimsson, Benedikt
    Manyama, Mange
    Spritz, Richard A.
    Hendricks, Audrey E.
    Shaikh, Tamim H.
    BMC MEDICAL GENOMICS, 2021, 14 (01)
  • [23] Genome-wide Analysis of Common Copy Number Variation and Epithelial Ovarian Cancer Risk-Response
    Reid, Brett M.
    Sellers, Thomas A.
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2020, 29 (06) : 1279 - 1279
  • [24] Genome-Wide Screen for Common and Rare Copy Number Variation in Metabolic Syndrome
    Kristiansson, Kati
    Barnes, Chris
    Perola, Markus
    Jula, Antti
    Salomaa, Veikko
    Ripatti, Samuli
    Hurles, Matthew
    Peltonen, Leena
    CIRCULATION, 2010, 122 (02) : E90 - E91
  • [25] Analysis of genome-wide copy number variation in Irish and Dutch ALS populations
    Cronin, Simon
    Blauw, Hylke M.
    Veldink, Jan H.
    van Es, Michael A.
    Ophoff, Roel A.
    Bradley, Daniel G.
    van den Berg, Leonard H.
    Hardiman, Orla
    HUMAN MOLECULAR GENETICS, 2008, 17 (21) : 3392 - 3398
  • [26] CONAN: copy number variation analysis software for genome-wide association studies
    Lukas Forer
    Sebastian Schönherr
    Hansi Weissensteiner
    Florian Haider
    Thomas Kluckner
    Christian Gieger
    Heinz-Erich Wichmann
    Günther Specht
    Florian Kronenberg
    Anita Kloss-Brandstätter
    BMC Bioinformatics, 11
  • [27] COLLABORATIVE GENOME-WIDE ASSOCIATION AND COPY NUMBER VARIATION ANALYSIS OF TOURETTE SYNDROME
    Scharf, Jeremiah
    Yu, Dongmei
    Huang, Alden
    Tsetsos, Fotis
    Paschou, Peristera
    Coppola, Giovanni
    Mathews, Carol
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : S736 - S737
  • [28] Copy number variation and cytidine analogue cytotoxicity: A genome-wide association approach
    Krishna R Kalari
    Scott J Hebbring
    High Seng Chai
    Liang Li
    Jean-Pierre A Kocher
    Liewei Wang
    Richard M Weinshilboum
    BMC Genomics, 11
  • [29] Genome-wide identification of copy number variation in diverse black pepper accessions
    Das, Parinita
    Sheeja, T. E.
    Saha, Bibek
    Fayad, A.
    Chandra, Tilak
    Angadi, U. B.
    Shivakumar, M. S.
    Azharudheen, T. P. Muhammed
    Jaiswal, Sarika
    Iquebal, Mir Asif
    Kumar, Dinesh
    PLANTA, 2025, 261 (04)
  • [30] Genome-wide association analysis of copy number variation in recurrent depressive disorder
    Rucker, J. J. H.
    Breen, G.
    Pinto, D.
    Pedroso, I.
    Lewis, C. M.
    Cohen-Woods, S.
    Uher, R.
    Schosser, A.
    Rivera, M.
    Aitchison, K. J.
    Craddock, N.
    Owen, M. J.
    Jones, L.
    Jones, I.
    Korszun, A.
    Muglia, P.
    Barnes, M. R.
    Preisig, M.
    Mors, O.
    Gill, M.
    Maier, W.
    Rice, J.
    Rietschel, M.
    Holsboer, F.
    Farmer, A. E.
    Craig, I. W.
    Scherer, S. W.
    McGuffin, P.
    MOLECULAR PSYCHIATRY, 2013, 18 (02) : 183 - 189
12345