WHOLE EXOME SEQUENCING IDENTIFIES RARE PROTEIN-CODING VARIANTS IN DERMATOMYOSITIS

被引：0
|
作者：
Li, Liubing [2 ]
Liu, Chenxi [1 ]
Yan, Songxin [1 ]
Li, Yongzhe [1 ]
机构：
[1] Peking Union Med Coll & Chinese Acad Med Sci, Dept Clin Lab, Peking Union Med Coll Hosp, Beijing, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Lab Med, Guangzhou, Peoples R China
来源：
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY | 2023年 / 41卷 / 02期
基金：
中国国家自然科学基金;
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：
P-10
引用
收藏
页码：439 / 439
页数：1
相关论文
共 50 条
  • [41] Whole Exome Sequencing Analysis of Common Rare Variants in Parkinson and ALS
    Vance, Jeffery
    Nuytemans, Karen
    Dressen, Amy
    Beecham, Gary
    Inchausti, Vanessa
    Martin, Eden
    Mehta, Arpit
    Scott, William
    NEUROLOGY, 2013, 80
  • [42] Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions
    Lelieveld, Stefan H.
    Spielmann, Malte
    Mundlos, Stefan
    Veltman, Joris A.
    Gilissen, Christian
    HUMAN MUTATION, 2015, 36 (08) : 815 - 822
  • [43] Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect
    D'Alessandro, Lisa C. A.
    Al Turki, Saeed
    Manickaraj, Ashok Kumar
    Manase, Dorin
    Mulder, Barbara J. M.
    Bergin, Lynn
    Rosenberg, Herschel C.
    Mondal, Tapas
    Gordon, Elaine
    Lougheed, Jane
    Smythe, John
    Devriendt, Koen
    Bhattacharya, Shoumo
    Watkins, Hugh
    Bentham, Jamie
    Bowdin, Sarah
    Hurles, Matthew E.
    Mital, Seema
    GENETICS IN MEDICINE, 2016, 18 (02) : 189 - 198
  • [44] Whole-exome sequencing identifies rare genetic variants that may contribute to isoniazid (INH)-induced liver injury
    Urban, Thomas J.
    Shianna, Kevin
    Barnhart, Huiman X.
    Chalasani, Naga P.
    Fontana, Robert J.
    Serrano, Jose
    Stolz, Andrew
    Goldstein, David B.
    Watkins, Paul B.
    HEPATOLOGY, 2012, 56 : 593A - 594A
  • [45] WHOLE EXOME SEQUENCING OF TWO RARE FAMILIAL COHORTS IDENTIFIES PUTATIVE GENETIC VARIANTS IN CHILDHOOD SJOGREN'S DISEASE
    Winn, N.
    Kim, S.
    Mun, S.
    Khan, Z.
    Thatayatikom, A.
    Han, K.
    Cha, S.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2022, 40 (12) : 26 - 26
  • [46] Multiethnic Whole Exome Sequencing Identifies Low Frequency and Rare Coding Variants Associated With Glycemic Traits: Results from T2D-GENES
    Im, Hae Kyung
    DIABETES, 2013, 62 : A427 - A427
  • [47] Exome sequencing identifies risk variants for AD
    Kiani, Lisa
    NATURE REVIEWS NEUROLOGY, 2022, 19 (1) : 3 - 3
  • [48] Search For Rare Coding Variants Associated With Obesity: The NHLBI Exome Sequencing Project
    Auer, Paul W.
    Carlson, Chris
    Jackson, Rebecca
    Lange, Leslie A.
    North, Kari
    Heard-Costa, Nancy L.
    Siscovick, David
    Meigs, James
    Wilson, James G.
    Hsu, Li
    Bowden, Donald W.
    Cupples, L. A.
    Lin, Danyu
    Willer, Cristen
    Kooperberg, Charles
    Gross, Myron
    Shendure, Jay
    Peters, Ulrike
    Li, Yun
    Lettre, Guillaume
    Franceschini, Nora
    Monda, Keri L.
    Rotter, Jerome
    OBESITY, 2011, 19 : S64 - S64
  • [49] Exome sequencing identifies risk variants for AD
    Lisa Kiani
    Nature Reviews Neurology, 2023, 19 : 3 - 3
  • [50] Whole Exome Sequencing Identifies Novel, Nonsynonymous Variants in a Large Pedigree with Tourette Syndrome
    Sundaram, S. K.
    Hug, A. H. M.
    Sun, Z.
    Wilson, B. J.
    Yu, W.
    Chugani, H. T.
    ANNALS OF NEUROLOGY, 2010, 68 (04) : S131 - S131
12345