Genetic Risk Variants in Hyperuricemia and Gout: Common Disease, Multiple Common and Rare Variant Hypothesis

被引：0
|
作者：
Stiburkova, Blanka [1 ]
Pavelcova, Katerina [1 ]
Masinova, Jana [1 ]
Pavlikova, Marketa [2 ]
Pavelka, Karel [3 ,4 ]
机构：
[1] Inst Rheumatol, Prague 2, Czech Republic
[2] Charles Univ Prague, Dept Probabil & Math Stat, Fac Math & Phys, Prague, Czech Republic
[3] Charles Univ Prague, Inst Rheumatol, Fac Med 1, Prague, Czech Republic
[4] Charles Univ Prague, Dept Rheumatol, Fac Med 1, Prague, Czech Republic
来源：
ARTHRITIS & RHEUMATOLOGY | 2023年 / 75卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
1109
引用
收藏
页码：2181 / 2182
页数：2
相关论文
共 50 条
  • [31] Psoriasis Rupioides: A Rare Variant of a Common Disease
    Salamon, Malgorzata
    Omulecki, Anastazy
    Sysa-Jedrzejowska, Anna
    McCauliffe, Daniel P.
    Wozniacka, Anna
    CUTIS, 2011, 88 (03): : 135 - 137
  • [32] How important are rare variants in common disease?
    Saint Pierre, Aude
    Genin, Emmanuelle
    BRIEFINGS IN FUNCTIONAL GENOMICS, 2014, 13 (05) : 353 - 361
  • [33] The common genetic hypothesis of autoimmune/inflammatory disease
    Becker, Kevin G.
    CURRENT OPINION IN ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 1 (05) : 399 - 405
  • [34] Common Genetic Variants in Rare Disorders: Hematology and Beyond
    Evangelidis, Paschalis
    Gavriilaki, Maria
    Kotsiou, Nikolaos
    Gavriilaki, Eleni
    CURRENT ISSUES IN MOLECULAR BIOLOGY, 2025, 47 (01)
  • [35] The impact of common and rare genetic variants on bradyarrhythmia development
    Weng, Lu-Chen
    Raemoe, Joel T.
    Jurgens, Sean J.
    Khurshid, Shaan
    Chaffin, Mark
    Hall, Amelia Weber
    Morrill, Valerie N.
    Wang, Xin
    Nauffal, Victor
    Sun, Yan V.
    Beer, Dominik
    Lee, Simon
    Nadkarni, Girish N.
    Duong, ThuyVy
    Wang, Biqi
    Czuba, Tomasz
    Austin, Thomas R.
    Yoneda, Zachary T.
    Friedman, Daniel J.
    Clayton, Anne
    Hyman, Matthew C.
    Judy, Renae L.
    Skanes, Allan C.
    Orland, Kate M.
    Treu, Timothy M.
    Oetjens, Matthew T.
    Alonso, Alvaro
    Soliman, Elsayed Z.
    Lin, Honghuang
    Lunetta, Kathryn L.
    van der Pals, Jesper
    Issa, Tariq Z.
    Nafissi, Navid A.
    May, Heidi T.
    Leong-Sit, Peter
    Roselli, Carolina
    Choi, Seung Hoan
    Khan, Habib R.
    Knight, Stacey
    Linner, Richard Karlsson
    Bezzina, Connie R.
    Ripatti, Samuli
    Heckbert, Susan R.
    Gaziano, J. Michael
    Loos, Ruth J. F.
    Psaty, Bruce M.
    Smith, J. Gustav
    Benjamin, Emelia J.
    Arking, Dan E.
    Rader, Daniel J.
    NATURE GENETICS, 2025, 57 (01) : 53 - 64
  • [36] Atrial fibrillation: the role of common and rare genetic variants
    Morten S Olesen
    Morten W Nielsen
    Stig Haunsø
    Jesper H Svendsen
    European Journal of Human Genetics, 2014, 22 : 297 - 306
  • [37] 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
  • [38] 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
  • [39] Detecting Association with Rare Genetic Variants in Common Diseases
    Li, Yali
    Feng, Tao
    Elston, Robert C.
    Zhu, Xiaofeng
    GENETIC EPIDEMIOLOGY, 2009, 33 (08) : 754 - 754
  • [40] 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
12345