WHOLE EXOME SEQUENCING META-ANALYSIS OF DEPRESSION SUGGESTS SUBTLE ROLE FOR FUNCTIONAL VARIANTS IN KNOWN GENETIC ASSOCIATION LOCI

被引：0
|
作者：
Moscati, Arden [1 ]
Rajagopal, Veera M. [1 ]
Di Gioia, Silvio Alessandro [1 ]
Dobbyn, Lee [1 ]
Coppola, Giovanni [1 ]
Stahl, Eli [1 ]
机构：
[1] Regeneron Genet Ctr, Tarrytown, NY USA
来源：
EUROPEAN NEUROPSYCHOPHARMACOLOGY | 2021年 / 51卷
关键词：
D O I：
10.1016/j.euroneuro.2021.07.116
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
24
引用
收藏
页码：E53 / E53
页数：1
相关论文
共 50 条
  • [1] Whole‐exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci
    Abdulrahman H. Al Anazi
    Ahmed S. Ammar
    Mahmoud Al-Hajj
    Cyril Cyrus
    Danah Aljaafari
    Iname Khoda
    Ahmed K. Abdelfatah
    Abdullah A. Alsulaiman
    Firas Alanazi
    Rawan Alanazi
    Divya Gandla
    Hetal Lad
    Samar Barayan
    Brendan J. Keating
    Amein K. Al-Ali
    Human Genomics, 16
  • [2] Association of Genetic Variants in GNβ3 with Functional Dyspepsia: A Meta-Analysis
    Dai, Fei
    Liu, Yaping
    Shi, Haitao
    Ge, Shuqiong
    Song, Jun
    Dong, Lei
    Yang, Jingyun
    DIGESTIVE DISEASES AND SCIENCES, 2014, 59 (08) : 1823 - 1830
  • [3] Association of Genetic Variants in GNβ3 with Functional Dyspepsia: A Meta-Analysis
    Fei Dai
    Yaping Liu
    Haitao Shi
    Shuqiong Ge
    Jun Song
    Lei Dong
    Jingyun Yang
    Digestive Diseases and Sciences, 2014, 59 : 1823 - 1830
  • [4] Genetic Association Analysis of Epilepsy Prognosis Using Whole Exome Sequencing
    Shankar, Ravi G.
    Morris, Andrew P.
    Sills, Graeme
    Marson, Tony
    Jorgensen, Andrea
    GENETIC EPIDEMIOLOGY, 2022, 46 (07) : 530 - 531
  • [5] Whole-exome sequencing reveals genetic variants that may play a role in neurocytomas
    Sapna Khowal
    Dongyun Zhang
    William H Yong
    Anthony P. Heaney
    Journal of Neuro-Oncology, 2024, 166 : 471 - 483
  • [6] Whole-exome sequencing reveals genetic variants that may play a role in neurocytomas
    Khowal, Sapna
    Zhang, Dongyun
    Yong, William H.
    Heaney, Anthony P.
    JOURNAL OF NEURO-ONCOLOGY, 2024, 166 (03) : 471 - 483
  • [7] Whole-exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci
    Al Anazi, Abdulrahman H. H.
    Ammar, Ahmed S. S.
    Al-Hajj, Mahmoud
    Cyrus, Cyril
    Aljaafari, Danah
    Khoda, Iname
    Abdelfatah, Ahmed K. K.
    Alsulaiman, Abdullah A. A.
    Alanazi, Firas
    Alanazi, Rawan
    Gandla, Divya
    Lad, Hetal
    Barayan, Samar
    Keating, Brendan J. J.
    Al-Ali, Amein K. K.
    HUMAN GENOMICS, 2022, 16 (01)
  • [8] Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing
    Floyd, James S.
    Bloch, Katarzyna M.
    Brody, Jennifer A.
    Maroteau, Cyrielle
    Siddiqui, Moneeza K.
    Gregory, Richard
    Carr, Daniel F.
    Molokhia, Mariam
    Liu, Xiaoming
    Bis, Joshua C.
    Ahmed, Ammar
    Liu, Xuan
    Hallberg, Par
    Yue, Qun-Ying
    Magnusson, Patrik K. E.
    Brisson, Diane
    Wiggins, Kerri L.
    Morrison, Alanna C.
    Khoury, Etienne
    McKeigue, Paul
    Stricker, Bruno H.
    Lapeyre-Mestre, Maryse
    Heckbert, Susan R.
    Gallagher, Arlene M.
    Chinoy, Hector
    Gibbs, Richard A.
    Bondon-Guitton, Emmanuelle
    Tracy, Russell
    Boerwinkle, Eric
    Gaudet, Daniel
    Conforti, Anita
    van Staa, Tjeerd
    Sitlani, Colleen M.
    Rice, Kenneth M.
    Maitland-van der Zee, Anke-Hilse
    Wadelius, Mia
    Morris, Andrew P.
    Pirmohamed, Munir
    Palmer, Colin A. N.
    Psaty, Bruce M.
    Alfirevic, Ana
    Palmer, Colin A. N.
    Baranova, Ekaterina V.
    Eriksson, Niclas
    Aaspollu, Anu
    McCarthy, Alun
    Delrieu, Olivier
    PLOS ONE, 2019, 14 (06):
  • [9] Association of genetic variants to multiple sclerosis by performing whole exome sequencing in a high prevalence family
    Mattei, G.
    Mechelli, R.
    Ricigliano, V. A. G.
    Buscarinu, M. C.
    Frontali, M.
    Ristori, G.
    Salvetti, M.
    MULTIPLE SCLEROSIS JOURNAL, 2015, 21 : 441 - 441
  • [10] Application of Whole Exome Sequencing and Functional Annotations to Identify Genetic Variants Associated with Marfan Syndrome
    Lin, Min-Rou
    Chang, Che-Mai
    Ting, Jafit
    Chang, Jan-Gowth
    Chou, Wan-Hsuan
    Huang, Kuei-Jung
    Cheng, Gloria
    Chang, Hsiao-Huang
    Chang, Wei-Chiao
    JOURNAL OF PERSONALIZED MEDICINE, 2022, 12 (02):
12345