Whole-exome sequencing reveals ANO8 as a genetic risk factor for intrahepatic cholestasis of pregnancy

被引：0
|
作者：
Xianxian Liu
Hua Lai
Xiaoming Zeng
Siming Xin
Liju Nie
Zhenyi Liang
Meiling Wu
Yu Chen
Jiusheng Zheng
Yang Zou
机构：
[1] Jiangxi Provincial Maternal and Child Health Hospital,Key Laboratory of Women’s Reproductive Health of Jiangxi Province
[2] Jiangxi Provincial Maternal and Child Health Hospital,Central Lab
[3] Jiangxi Provincial Maternal and Child Health Hospital,Department of Obstetrics
来源：
BMC Pregnancy and Childbirth | / 20卷
关键词：
Whole-exome sequencing; Mutations; Intrahepatic cholestasis of pregnancy;
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
  • [41] Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali
    Yalcouye, Abdoulaye
    Schrauwen, Isabelle
    Traore, Oumou
    Bamba, Salia
    Aboagye, Elvis Twumasi
    Acharya, Anushree
    Bharadwaj, Thashi
    Latanich, Rachel
    Esoh, Kevin
    Fortes-Lima, Cesar A.
    de Kock, Carmen
    Jonas, Mario
    Maiga, Alassane dit Baneye
    Cisse, Cheick A. K.
    Sangare, Moussa A.
    Guinto, Cheick O.
    Landoure, Guida
    Leal, Suzanne M.
    Wonkam, Ambroise
    HUMAN GENETICS AND GENOMICS ADVANCES, 2025, 6 (01):
  • [42] Whole-Exome Sequencing Reveals Rare Germline Mutations in Patients With Hemifacial Microsomia
    Chen, Xiaojun
    Liu, Fatao
    Mar Aung, Zin
    Zhang, Yan
    Chai, Gang
    FRONTIERS IN GENETICS, 2021, 12
  • [43] Whole-Exome Sequencing to Identify Potential Genetic Risk in Substance Use Disorders: A Pilot Feasibility Study
    AshaRani, P., V
    Amron, Syidda
    Zainuldin, Noor Azizah Bte
    Tohari, Sumanty
    Ng, Alvin Y. J.
    Song, Guo
    Venkatesh, Byrappa
    Mathuru, Ajay S.
    JOURNAL OF CLINICAL MEDICINE, 2021, 10 (13)
  • [44] Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
    Page, Donna J.
    Miossec, Matthieu J.
    Williams, Simon G.
    Monaghan, Richard M.
    Fotiou, Elisavet
    Cordell, Heather J.
    Sutcliffe, Louise
    Topf, Ana
    Bourgey, Mathieu
    Bourque, Guillaume
    Eveleigh, Robert
    Dunwoodie, Sally L.
    Winlaw, David S.
    Bhattacharya, Shoumo
    Breckpot, Jeroen
    Devriendt, Koenraad
    Gewillig, Marc
    Brook, J. David
    Setchfield, Kerry J.
    Bu'Lock, Frances A.
    O'Sullivan, John
    Stuart, Graham
    Bezzina, Connie R.
    Mulder, Barbara J. M.
    Postma, Alex V.
    Bentham, James R.
    Baron, Martin
    Bhaskar, Sanjeev S.
    Black, Graeme C.
    Newman, William G.
    Hentges, Kathryn E.
    Lathrop, G. Mark
    Santibanez-Koref, Mauro
    Keavney, Bernard D.
    CIRCULATION RESEARCH, 2019, 124 (04) : 553 - 563
  • [45] Identification of risk genes in Chinese nonobstructive azoospermia patients based on whole-exome sequencing
    Liu, Yu-Jun
    Zhuang, Xin-Jie
    An, Jian-Ting
    Jiang, Hui
    Li, Rong
    Qiao, Jie
    Yan, Li-Ying
    Zhi, Xu
    ASIAN JOURNAL OF ANDROLOGY, 2023, 25 (01) : 66 - 72
  • [46] Whole-exome sequencing identified a variant in EFTUD2 gene in establishing a genetic diagnosis
    Venugopalan, S. Rengasamy
    Farrow, E. G.
    Lypka, M.
    ORTHODONTICS & CRANIOFACIAL RESEARCH, 2017, 20 : 50 - 56
  • [47] Specific genetic aberrations of parathyroid in Chinese patients with tertiary hyperparathyroidism using whole-exome sequencing
    Li, Lei
    Sheng, Qixuan
    Zeng, Huajin
    Li, Wei
    Wang, Qiang
    Ma, Guanjun
    Xu, Xinyun
    Qiu, Ming
    Zhang, Wei
    Shan, Chengxiang
    FRONTIERS IN ENDOCRINOLOGY, 2023, 14
  • [48] Whole-Exome Sequencing in Turkish Patients with Inherited Retinal Dystrophies Reveals Novel Variants in Ten Genes
    Basdemirci, Muserref
    Kocak Eker, Hatice
    MOLECULAR SYNDROMOLOGY, 2024, 15 (03) : 202 - 210
  • [49] Identification of potential genetic causal variants for rheumatoid arthritis by whole-exome sequencing
    Li, Ying
    Leung, Elaine Lai-Han
    Pan, Hudan
    Yao, Xiaojun
    Huang, Qingchun
    Wu, Min
    Xu, Ting
    Wang, Yuwei
    Cai, Jun
    Li, Runze
    Liu, Wei
    Liu, Liang
    ONCOTARGET, 2017, 8 (67) : 111119 - 111129
  • [50] Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan
    Lin, Pei-Chin
    Chiou, Shyh-Shin
    Lin, Chien-Yu
    Wang, Shu-Chen
    Huang, Hsi-Yuan
    Chang, Ya-Sian
    Tseng, Yu-Hsin
    Kan, Tzu-Min
    Liao, Yu-Mei
    Tsai, Shih-Pien
    Peng, Ching-Tien
    Chang, Jan-Gowth
    CLINICA CHIMICA ACTA, 2018, 487 : 311 - 317
12345