178 related articles for article (PubMed ID: 29923609)
21. Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients.
Mühleisen TW; Basmanav FB; Forstner AJ; Mattheisen M; Priebe L; Herms S; Breuer R; Moebus S; Nenadic I; Sauer H; Mössner R; Maier W; Rujescu D; Ludwig M; Rietschel M; Nöthen MM; Cichon S
Schizophr Res; 2011 Apr; 127(1-3):35-40. PubMed ID: 21288692
[TBL] [Abstract][Full Text] [Related]
22. Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
Todarello G; Feng N; Kolachana BS; Li C; Vakkalanka R; Bertolino A; Weinberger DR; Straub RE
Schizophr Res; 2014 May; 155(1-3):1-7. PubMed ID: 24680031
[TBL] [Abstract][Full Text] [Related]
23. Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders.
Hu Z; Xiao X; Zhang Z; Li M
Mol Psychiatry; 2019 Oct; 24(10):1400-1414. PubMed ID: 31138894
[TBL] [Abstract][Full Text] [Related]
24. Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
Toma C; Pierce KD; Shaw AD; Heath A; Mitchell PB; Schofield PR; Fullerton JM
PLoS Genet; 2018 Dec; 14(12):e1007535. PubMed ID: 30586385
[TBL] [Abstract][Full Text] [Related]
25. Neurexin 1 variants as risk factors for suicide death.
William N; Reissner C; Sargent R; Darlington TM; DiBlasi E; Li QS; Keeshin B; Callor WB; Ferris E; Jerominski L; Smith KR; Christensen ED; Gray DM; Camp NJ; Missler M; Williams ME; Coon H
Mol Psychiatry; 2021 Dec; 26(12):7436-7445. PubMed ID: 34168285
[TBL] [Abstract][Full Text] [Related]
26. A short primer on the functional analysis of copy number variation for biomedical scientists.
Barnes MR; Breen G
Methods Mol Biol; 2010; 628():119-35. PubMed ID: 20238079
[TBL] [Abstract][Full Text] [Related]
27. Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene.
Takata A; Xu B; Ionita-Laza I; Roos JL; Gogos JA; Karayiorgou M
Neuron; 2014 May; 82(4):773-80. PubMed ID: 24853937
[TBL] [Abstract][Full Text] [Related]
28. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
Sokolowski M; Wasserman J; Wasserman D
PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
[TBL] [Abstract][Full Text] [Related]
29. Neurexins and neuropsychiatric disorders.
Kasem E; Kurihara T; Tabuchi K
Neurosci Res; 2018 Feb; 127():53-60. PubMed ID: 29221905
[TBL] [Abstract][Full Text] [Related]
30. Further investigation of the association between rs7341475 and rs17746501 and schizophrenia.
Ben-David E; Shifman S;
Am J Med Genet B Neuropsychiatr Genet; 2010 Sep; 153B(6):1244-7. PubMed ID: 20468075
[TBL] [Abstract][Full Text] [Related]
31. Influence of neurexin 1 (NRXN1) polymorphisms in clozapine response.
Souza RP; Meltzer HY; Lieberman JA; Le Foll B; Kennedy JL
Hum Psychopharmacol; 2010 Nov; 25(7-8):582-5. PubMed ID: 20860064
[TBL] [Abstract][Full Text] [Related]
32. Prospects and Pitfalls of Plasma Complement C4 in Schizophrenia: Building a Better Biomarker.
Severance EG; Prandovszky E; Yang S; Leister F; Lea A; Wu CL; Tamouza R; Leboyer M; Dickerson F; Yolken RH
Dev Neurosci; 2023; 45(6):349-360. PubMed ID: 37734326
[TBL] [Abstract][Full Text] [Related]
33. Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.
Møller RS; Weber YG; Klitten LL; Trucks H; Muhle H; Kunz WS; Mefford HC; Franke A; Kautza M; Wolf P; Dennig D; Schreiber S; Rückert IM; Wichmann HE; Ernst JP; Schurmann C; Grabe HJ; Tommerup N; Stephani U; Lerche H; Hjalgrim H; Helbig I; Sander T;
Epilepsia; 2013 Feb; 54(2):256-64. PubMed ID: 23294455
[TBL] [Abstract][Full Text] [Related]
34. Novel missense SETD1A variants in Japanese patients with schizophrenia: Resequencing and association analysis.
Morikawa R; Watanabe Y; Igeta H; Arta RK; Ikeda M; Okazaki S; Hoya S; Saito T; Otsuka I; Egawa J; Tanifuji T; Iwata N; Someya T
Psychiatry Res; 2022 Apr; 310():114481. PubMed ID: 35235885
[TBL] [Abstract][Full Text] [Related]
35. Synaptic modulators Nrxn1 and Nrxn3 are disregulated in a Disc1 mouse model of schizophrenia.
Brown SM; Clapcote SJ; Millar JK; Torrance HS; Anderson SM; Walker R; Rampino A; Roder JC; Thomson PA; Porteous DJ; Evans KL
Mol Psychiatry; 2011 Jun; 16(6):585-7. PubMed ID: 21321563
[No Abstract] [Full Text] [Related]
36. Transcriptional Changes following Cellular Knockdown of the Schizophrenia Risk Gene
Cameron D; Blake DJ; Bray NJ; Hill MJ
Mol Neuropsychiatry; 2019 Apr; 5(2):109-114. PubMed ID: 31192223
[TBL] [Abstract][Full Text] [Related]
37. Evaluating risk loci for schizophrenia distilled from genome-wide association studies in Han Chinese from Central China.
Ma L; Tang J; Wang D; Zhang W; Liu W; Wang D; Liu XH; Gong W; Yao YG; Chen X
Mol Psychiatry; 2013 Jun; 18(6):638-9. PubMed ID: 22584866
[No Abstract] [Full Text] [Related]
38. Exome arrays capture polygenic rare variant contributions to schizophrenia.
Richards AL; Leonenko G; Walters JT; Kavanagh DH; Rees EG; Evans A; Chambert KD; Moran JL; Goldstein J; Neale BM; McCarroll SA; Pocklington AJ; Holmans PA; Owen MJ; O'Donovan MC
Hum Mol Genet; 2016 Mar; 25(5):1001-7. PubMed ID: 26740555
[TBL] [Abstract][Full Text] [Related]
39. SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new cases.
Colijn MA; Carrion P; Poirier-Morency G; Rogic S; Torres I; Menon M; Lisonek M; Cook C; DeGraaf A; Thammaiah SP; Neelakant H; Willaeys V; Leonova O; White RF; Yip S; Mungall AJ; MacLeod PM; Gibson WT; Sullivan PF; Honer WG; Pavlidis P; Stowe RM
Prog Neuropsychopharmacol Biol Psychiatry; 2024 Feb; 129():110888. PubMed ID: 37918557
[TBL] [Abstract][Full Text] [Related]
40. Genetics of Childhood-onset Schizophrenia 2019 Update.
Forsyth JK; Asarnow RF
Child Adolesc Psychiatr Clin N Am; 2020 Jan; 29(1):157-170. PubMed ID: 31708045
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]