Identification of potential susceptibility genes in patients with primary Sjögren’s syndrome-associated pulmonary arterial hypertension through whole exome sequencing

被引：0
|
作者：
Mucong Li
Yue Shi
Jiuliang Zhao
Qian Wang
Mengtao Li
Xiuli Zhao
机构：
[1] Peking Union Medical College,Department of Medical Genetics, Institute of Basic Medical Sciences & Chinese Academy of Medical Sciences and School of Basic Medicine
[2] Peking Union Medical College Hospital,Department of Rheumatology, Peking Union Medical College Hospital (PUMCH), Peking Union Medical College and Chinese Academy of Medical Sciences, National Clinical Research Center for Dermatologic and Immunologic Diseas
[3] Chinese Academy of Medical Science and Peking Union Medical College,DID), Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Chinese Rheumatism Data Center (CRDC), Chinese SLE Treatment and Research Group (CSTAR), State Key Lab
来源：
Arthritis Research & Therapy | / 25卷
关键词：
Primary Sjögren’s syndrome; Pulmonary arterial hypertension; Whole-exome sequencing;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [31] A Combined Targeted and Whole Exome Sequencing Approach Identified Novel Candidate Genes Involved in Heritable Pulmonary Arterial Hypertension
    Chiara Barozzi
    Margherita Galletti
    Luciana Tomasi
    Sara De Fanti
    Massimiliano Palazzini
    Alessandra Manes
    Marco Sazzini
    Nazzareno Galiè
    Scientific Reports, 9
  • [32] Identification of putative cancer susceptibility genes through whole exome sequencing of a family presenting hereditary colorectal cancer
    Torrezan, Giovana T.
    Smirnova, Anna
    Silva, Felipe C.
    Santos, Erika M.
    Valieris, Renan
    De Souza, Jorge E.
    Aguiar, Samuel
    Rossi, Benedito M.
    de Souza, Sandro J.
    Carraro, Dirce M.
    CANCER RESEARCH, 2017, 77
  • [33] Identification Of Rare Variants In Asb2 Influencing Susceptibility Of Scleroderma-Associated Pulmonary Arterial Hypertension By Exome Sequencing And Network Analysis
    Liu, Q.
    Rafaels, N.
    Boorgula, M.
    Berger, A.
    Hassoun, P. M.
    Barnes, K.
    Gao, L.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2017, 195
  • [34] Identification of novel candidate genes in heterotaxy syndrome patients with congenital heart diseases by whole exome sequencing
    Liang, Shuzhang
    Shi, Xin
    Yu, Chunxiao
    Shao, Xuelian
    Zhou, Haitao
    Li, Xueyu
    Chang, Cheng
    Lai, Kaa Seng
    Ma, Jinmin
    Zhang, Ruilin
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2020, 1866 (12):
  • [35] Potential susceptibility genes in patients with stage III and IV periodontitis: A whole-exome sequencing pilot study
    Xue, Fan
    Zhao, Jianjiang
    Gao, XiaoCui
    Jiang, Xuehai
    Lan, Zedong
    BIOMOLECULES AND BIOMEDICINE, 2024, 24 (01): : 73 - 81
  • [36] Identification of rare pathogenic variants associated with pulmonary fibrosis susceptibility through whole genome sequencing
    Wang, Dapeng
    Wain, Louise
    Maher, Toby
    Molyneaux, Philip
    Fahy, Billy
    Jenkins, Gisli
    Stewart, Iain
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 395 - 395
  • [37] Parotid elastography: a potential alternative to replace labial biopsy in classification of patients with primary Sjögren’s syndrome?
    Hasan Satış
    E. Cindil
    R. B. Salman
    D. Yapar
    N. B. Demir
    E. Temel
    H. Babaoğlu
    N. Ataş
    H. Karadeniz
    Aslıhan Avanoğlu Güler
    S. Oktar
    A. Tufan
    M. A. Öztürk
    Ş. Haznedaroğlu
    B. Göker
    Clinical Rheumatology, 2020, 39 : 3707 - 3713
  • [38] Whole Exome Sequencing Identifies Potential Defects in Multiple Immunodeficiency-Associated Genes in Individual Patients and Families with Primary Immunodeficiency Diseases
    Chinn, Ivan
    Forbes, Lisa R.
    Nicholas, Sarah K.
    Mace, Emily
    Coban-Akdemir, Zeynep
    Rider, Nicholas L.
    Jhangiani, Shalini N.
    Wiszniewski, Wojciech K.
    Gibbs, Richard A.
    Lupski, James R.
    Orange, Jordan
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2017, 139 (02) : AB172 - AB172
  • [39] Whole-exome sequencing screening for candidate genes and variants associated with primary sporadic keratoconus in Chinese patients
    Song, Chunyuan
    Li, Ling
    Liu, Chang
    Hu, Luping
    Bai, Jie
    Liang, Weiyan
    Zhao, Lin
    Song, Wenxiu
    Li, Shaowei
    EXPERIMENTAL EYE RESEARCH, 2024, 245
  • [40] Respiratory symptoms are poor predictors of concomitant chronic obstructive pulmonary disease in patients with primary Sjögren’s syndrome
    Victor Strevens Bolmgren
    Peter Olsson
    Per Wollmer
    Roger Hesselstrand
    Thomas Mandl
    Rheumatology International, 2017, 37 : 813 - 818
12345