RARE INHERITED DNA VARIANTS IN OCD IDENTIFY CANDIDATE RISK GENES AND BIOLOGICAL PATHWAYS

被引：0
|
作者：
Masroor, Kiran [1 ]
Cappi, Carolina
Lima, Monicke O.
Fernandez, Thomas V. [2 ]
机构：
[1] Yale Coll, New Haven, CT USA
[2] Yale Sch Med, New Haven, CT USA
来源：
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY | 2023年 / 62卷 / 10期
关键词：
D O I：
10.1016/j.jaac.2023.09.362
中图分类号：
B844 [发展心理学（人类心理学）];
学科分类号：
040202 ;
摘要：
5.38
引用
收藏
页码：S271 / S271
页数：1
相关论文
共 50 条
  • [21] Post-transcriptional control of candidate risk genes for type 1 diabetes by rare genetic variants
    V M de Jong
    A Zaldumbide
    A R van der Slik
    S P Persengiev
    B O Roep
    B P C Koeleman
    Genes & Immunity, 2013, 14 : 58 - 61
  • [22] Post-transcriptional control of candidate risk genes for type 1 diabetes by rare genetic variants
    de Jong, V. M.
    Zaldumbide, A.
    van der Slik, A. R.
    Persengiev, S. P.
    Roep, B. O.
    Koeleman, B. P. C.
    GENES AND IMMUNITY, 2013, 14 (01) : 58 - 61
  • [23] Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes
    Astuti, Galuh D. N.
    van den Born, L. Ingeborgh
    Khan, M. Imran
    Hamel, Christian P.
    Bocquet, Beatrice
    Manes, Gael
    Quinodoz, Mathieu
    Ali, Manir
    Toomes, Carmel
    McKibbin, Martin
    El-Asrag, Mohammed E.
    Haer-Wigman, Lonneke
    Inglehearn, Chris F.
    Black, Graeme C. M.
    Hoyng, Carel B.
    Cremers, Frans P. M.
    Roosing, Susanne
    GENES, 2018, 9 (01):
  • [24] A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing
    X Hu
    B Zhang
    W Liu
    S Paciga
    W He
    T A Lanz
    R Kleiman
    B Dougherty
    S K Hall
    A M McIntosh
    S M Lawrie
    A Power
    S L John
    D Blackwood
    D St Clair
    N J Brandon
    Molecular Psychiatry, 2014, 19 : 858 - 859
  • [25] A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing
    Hu, X.
    Zhang, B.
    Liu, W.
    Paciga, S.
    He, W.
    Lanz, T. A.
    Kleiman, R.
    Dougherty, B.
    Hall, S. K.
    McIntosh, A. M.
    Lawrie, S. M.
    Power, A.
    John, S. L.
    Blackwood, D.
    St Clair, D.
    Brandon, N. J.
    MOLECULAR PSYCHIATRY, 2014, 19 (08) : 857 - 858
  • [26] Inherited mutations in DNA repair genes and cancer risk
    Romero-Laorden, Nuria
    Castro, Elena
    CURRENT PROBLEMS IN CANCER, 2017, 41 (04) : 251 - 264
  • [27] Detection of rare single nucleotide variants affecting genes in the DNA repair pathways in hereditary breast cancer
    Shireen Hussein
    Adnan Merdad
    Jaudah Al-Maghrabi
    Mamdooh A. Gari
    Fatma Al-Thubaiti
    Ibtessam R. Hussein
    Adeel G. Chaudhary
    Adel M. Abuzenadah
    Hanaa Tashkandi
    Shadi Al-Khayyat
    Taha Kumosani
    Mohammed H. Al-Qahtani
    Ashraf Dallol
    BMC Genomics, 15 (Suppl 2)
  • [28] Rare, Low-Frequency, and Common Variants in the Protein-Coding Sequence of Biological Candidate Genes from GWASs Contribute to Risk of Rheumatoid Arthritis
    Diogo, Dorothee
    Kurreeman, Fina
    Stahl, Eli A.
    Liao, Katherine P.
    Gupta, Namrata
    Greenberg, Jeffrey D.
    Rivas, Manuel A.
    Hickey, Brendan
    Flannick, Jason
    Thomson, Brian
    Guiducci, Candace
    Ripke, Stephan
    Adzhubey, Ivan
    Barton, Anne
    Kremer, Joel M.
    Alfredsson, Lars
    Sunyaev, Shamil
    Martin, Javier
    Zhernakova, Alexandra
    Bowes, John
    Eyre, Steve
    Siminovitch, Katherine A.
    Gregersen, Peter K.
    Worthington, Jane
    Klareskog, Lars
    Padyukov, Leonid
    Raychaudhuri, Soumya
    Plenge, Robert M.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2013, 92 (01) : 15 - 27
  • [29] Inherited Rare, Deleterious Variants in ATM Increase Lung Adenocarcinoma Risk
    Selvan, Myvizhi Esai
    Zauderer, Marjorie G.
    Rudin, Charles M.
    Jones, Sian
    Mukherjee, Semanti
    Offit, Kenneth
    Onel, Kenan
    Rennert, Gad
    Velculescu, Victor E.
    Lipkin, Steven M.
    Klein, Robert J.
    Gumus, Zeynep H.
    JOURNAL OF THORACIC ONCOLOGY, 2020, 15 (12) : 1871 - 1879
  • [30] A survey of haplotype variants at several disease candidate genes: the importance of rare variants for complex diseases
    Liu, PY
    Zhang, YY
    Lu, Y
    Long, JR
    Shen, H
    Zhao, LJ
    Xu, FH
    Xiao, P
    Xiong, DH
    Liu, YJ
    Recker, RR
    Deng, HW
    JOURNAL OF MEDICAL GENETICS, 2005, 42 (03) : 221 - 227
12345