EXOME SEQUENCING IDENTIFIES A COMPOUND HETEROZYGOUS MUTATION IN A GENE FROM HISTONE METHYL TRANSFERASE COMPLEX IN FAMILIAL SCHIZOPHRENIA

被引:0
|
作者
John, Jibin [1 ]
Kukshal, Prachi [2 ]
Bhatia, Triptish [3 ]
Deshpande, Smita N. [3 ]
Nimgaonkar, Vishwajit L. [4 ,5 ]
Thelma, B. K. [3 ]
机构
[1] Univ Delhi, New Delhi, India
[2] Univ Delhi, Dept Genet, South Campus, New Delhi, India
[3] Dr RML Hosp, Dept Psychiat, New Delhi, India
[4] Univ Pittsburgh, Western Psychiat Inst & Clin, Dept Psychiat, Pittsburgh, PA 15260 USA
[5] Univ Pittsburgh, Western Psychiat Inst & Clin, Dept Human Genet, Pittsburgh, PA 15260 USA
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Su86
引用
收藏
页码:S250 / S251
页数:2
相关论文
共 50 条
  • [41] Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia
    Palmer, Duncan S.
    Howrigan, Daniel P.
    Chapman, Sinead B.
    Adolfsson, Rolf
    Bass, Nick
    Blackwood, Douglas
    Boks, Marco P. M.
    Chen, Chia-Yen
    Churchhouse, Claire
    Corvin, Aiden P.
    Craddock, Nicholas
    Curtis, David
    Di Florio, Arianna
    Dickerson, Faith
    Freimer, Nelson B.
    Goes, Fernando S.
    Jia, Xiaoming
    Jones, Ian
    Jones, Lisa
    Jonsson, Lina
    Kahn, Rene S.
    Landen, Mikael
    Locke, Adam E.
    McIntosh, Andrew M.
    McQuillin, Andrew
    Morris, Derek W.
    O'Donovan, Michael C.
    Ophoff, Roel A.
    Owen, Michael J.
    Pedersen, Nancy L.
    Posthuma, Danielle
    Reif, Andreas
    Risch, Neil
    Schaefer, Catherine
    Scott, Laura
    Singh, Tarjinder
    Smoller, Jordan W.
    Solomonson, Matthew
    St Clair, David
    Stahl, Eli A.
    Vreeker, Annabel
    Walters, James T. R.
    Wang, Weiqing
    Watts, Nicholas A.
    Yolken, Robert
    Zandi, Peter P.
    Neale, Benjamin M.
    NATURE GENETICS, 2022, 54 (05) : 541 - +
  • [42] Whole exome sequencing combined with integrated variant annotation prediction identifies asymptomatic Tangier disease with compound heterozygous mutations in ABCA1 gene
    Tada, H.
    Kawashiri, M.
    Nohara, A.
    Inazu, A.
    Mabuchi, H.
    Yamagishi, M.
    EUROPEAN HEART JOURNAL, 2015, 36 : 360 - 360
  • [43] Exome sequencing reveled a compound heterozygous mutations in RTTN gene causing developmental delay and primary microcephaly
    Naseer, Muhammad Imran
    Abdulkareem, Angham Abdulrahman
    Muthaffar, Osama Yousef
    Chaudhary, Adeel G.
    SAUDI JOURNAL OF BIOLOGICAL SCIENCES, 2021, 28 (05) : 2824 - 2829
  • [44] Exome Sequencing Identifies Frequent Mutation of the SWI/SNF Complex Gene PBRM1 in Renal Carcinoma Editorial Comment
    Atala, Anthony
    JOURNAL OF UROLOGY, 2011, 186 (03): : 1150 - 1150
  • [45] Correction: Corrigendum: Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma
    Ignacio Varela
    Patrick Tarpey
    Keiran Raine
    Dachuan Huang
    Choon Kiat Ong
    Philip Stephens
    Helen Davies
    David Jones
    Meng-Lay Lin
    Jon Teague
    Graham Bignell
    Adam Butler
    Juok Cho
    Gillian L. Dalgliesh
    Danushka Galappaththige
    Chris Greenman
    Claire Hardy
    Mingming Jia
    Calli Latimer
    KingWai Lau
    John Marshall
    Stuart McLaren
    Andrew Menzies
    Laura Mudie
    Lucy Stebbings
    David A. Largaespada
    L. F. A.Wessels
    Stephane Richard
    Richard J.Kahnoski
    John Anema
    David A.Tuveson
    Pedro A. Perez-Mancera
    Ville Mustonen
    Andrej Fischer
    David J. Adams
    Alistair Rust
    Waraporn Chan-on
    Chutima Subimerb
    Karl Dykema
    Kyle Furge
    Peter J. Campbell
    Bin Tean Teh
    Michael R. Stratton
    P. Andrew Futreal
    Nature, 2012, 484 : 130 - 130
  • [46] Whole-Exome Sequencing Identifies Novel Heterozygous Mutation in RAF1 in Family With Neonatal Testicular Torsion
    Schlussel, Richard
    UROLOGY, 2019, 129 : 67 - 67
  • [47] Whole-Exome Sequencing Identifies Novel Heterozygous Mutation in RAF1 in Family With Neonatal Testicular Torsion
    Kohn, Taylor P.
    Lopategui, Diana M.
    Arora, Himanshu
    Griswold, Anthony J.
    Ramasamy, Ranjith
    UROLOGY, 2019, 129 : 60 - 67
  • [48] Whole Exome Sequencing Identifies a Causal RBM20 Mutation in a Large Pedigree With Familial Dilated Cardiomyopathy
    Wells, Quinn S.
    Becker, Jason R.
    Su, Yan R.
    Mosley, Jonathan D.
    Weeke, Peter
    D'Aoust, Laura
    Ausborn, Natalie L.
    Ramirez, Andrea H.
    Pfotenhauer, Jean P.
    Naftilan, Allen J.
    Markham, Larry
    Exil, Vernat
    Roden, Dan M.
    Hong, Charles C.
    CIRCULATION-CARDIOVASCULAR GENETICS, 2013, 6 (04) : 317 - 326
  • [49] Autosomal Dominant Familial Dyskinesia and Facial Myokymia Single Exome Sequencing Identifies a Mutation in Adenylyl Cyclase 5
    Chen, Ying-Zhang
    Matsushita, Mark M.
    Robertson, Peggy
    Rieder, Mark
    Girirajan, Santhosh
    Antonacci, Francesca
    Lipe, Hillary
    Eichler, Evan E.
    Nickerson, Deborah A.
    Bird, Thomas D.
    Raskind, Wendy H.
    ARCHIVES OF NEUROLOGY, 2012, 69 (05) : 630 - 635
  • [50] Novel Compound Heterozygous Mutation on MYORG Gene in a Chinese Patient with Primary Familial Brain Calcification
    Lin, Jixiang
    Wang, Yanfei
    Gao, Xiang
    Liu, Xiaomin
    NEUROLOGY INDIA, 2025, 73 (02) : 365 - 367