295 related articles for article (PubMed ID: 25943950)
1. Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.
Suárez-Rama JJ; Arrojo M; Sobrino B; Amigo J; Brenlla J; Agra S; Paz E; Brión M; Carracedo Á; Páramo M; Costas J
J Psychiatr Res; 2015; 66-67():38-44. PubMed ID: 25943950
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Role of DISC1 interacting proteins in schizophrenia risk from genome-wide analysis of missense SNPs.
Costas J; Suárez-Rama JJ; Carrera N; Paz E; Páramo M; Agra S; Brenlla J; Ramos-Ríos R; Arrojo M
Ann Hum Genet; 2013 Nov; 77(6):504-12. PubMed ID: 23909765
[TBL] [Abstract][Full Text] [Related]
4. Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility.
O'Dushlaine C; Kenny E; Heron E; Donohoe G; Gill M; Morris D; ; Corvin A
Mol Psychiatry; 2011 Mar; 16(3):286-92. PubMed ID: 20157312
[TBL] [Abstract][Full Text] [Related]
5. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium.
Milne RL; Burwinkel B; Michailidou K; Arias-Perez JI; Zamora MP; Menéndez-Rodríguez P; Hardisson D; Mendiola M; González-Neira A; Pita G; Alonso MR; Dennis J; Wang Q; Bolla MK; Swerdlow A; Ashworth A; Orr N; Schoemaker M; Ko YD; Brauch H; Hamann U; ; Andrulis IL; Knight JA; Glendon G; Tchatchou S; ; ; Matsuo K; Ito H; Iwata H; Tajima K; Li J; Brand JS; Brenner H; Dieffenbach AK; Arndt V; Stegmaier C; Lambrechts D; Peuteman G; Christiaens MR; Smeets A; Jakubowska A; Lubinski J; Jaworska-Bieniek K; Durda K; Hartman M; Hui M; Yen Lim W; Wan Chan C; Marme F; Yang R; Bugert P; Lindblom A; Margolin S; García-Closas M; Chanock SJ; Lissowska J; Figueroa JD; Bojesen SE; Nordestgaard BG; Flyger H; Hooning MJ; Kriege M; van den Ouweland AM; Koppert LB; Fletcher O; Johnson N; dos-Santos-Silva I; Peto J; Zheng W; Deming-Halverson S; Shrubsole MJ; Long J; Chang-Claude J; Rudolph A; Seibold P; Flesch-Janys D; Winqvist R; Pylkäs K; Jukkola-Vuorinen A; Grip M; Cox A; Cross SS; Reed MW; Schmidt MK; Broeks A; Cornelissen S; Braaf L; Kang D; Choi JY; Park SK; Noh DY; Simard J; Dumont M; Goldberg MS; Labrèche F; Fasching PA; Hein A; Ekici AB; Beckmann MW; Radice P; Peterlongo P; Azzollini J; Barile M; Sawyer E; Tomlinson I; Kerin M; Miller N; Hopper JL; Schmidt DF; Makalic E; Southey MC; Hwang Teo S; Har Yip C; Sivanandan K; Tay WT; Shen CY; Hsiung CN; Yu JC; Hou MF; Guénel P; Truong T; Sanchez M; Mulot C; Blot W; Cai Q; Nevanlinna H; Muranen TA; Aittomäki K; Blomqvist C; Wu AH; Tseng CC; Van Den Berg D; Stram DO; Bogdanova N; Dörk T; Muir K; Lophatananon A; Stewart-Brown S; Siriwanarangsan P; Mannermaa A; Kataja V; Kosma VM; Hartikainen JM; Shu XO; Lu W; Gao YT; Zhang B; Couch FJ; Toland AE; ; Yannoukakos D; Sangrajrang S; McKay J; Wang X; Olson JE; Vachon C; Purrington K; Severi G; Baglietto L; Haiman CA; Henderson BE; Schumacher F; Le Marchand L; Devilee P; Tollenaar RA; Seynaeve C; Czene K; Eriksson M; Humphreys K; Darabi H; Ahmed S; Shah M; Pharoah PD; Hall P; Giles GG; Benítez J; Dunning AM; Chenevix-Trench G; Easton DF
Hum Mol Genet; 2014 Nov; 23(22):6096-111. PubMed ID: 24943594
[TBL] [Abstract][Full Text] [Related]
6. Association study of DISC1 genetic variants with the risk of schizophrenia.
Luo X; Jin C; Zhou Z; Zhang F; Yuan J; Liu X; Cheng Z
Psychiatr Genet; 2016 Jun; 26(3):132-5. PubMed ID: 26945459
[TBL] [Abstract][Full Text] [Related]
7. Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.
González-Peñas J; Amigo J; Santomé L; Sobrino B; Brenlla J; Agra S; Paz E; Páramo M; Carracedo Á; Arrojo M; Costas J
Schizophr Res; 2016 Jul; 174(1-3):10-16. PubMed ID: 27066855
[TBL] [Abstract][Full Text] [Related]
8. Evidence of association of the DISC1 interactome gene set with schizophrenia from GWAS.
Facal F; Costas J
Prog Neuropsychopharmacol Biol Psychiatry; 2019 Dec; 95():109729. PubMed ID: 31398428
[TBL] [Abstract][Full Text] [Related]
9. A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population.
Yue W; Yang Y; Zhang Y; Lu T; Hu X; Wang L; Ruan Y; Lv L; Zhang D
Behav Brain Funct; 2011 Apr; 7():7. PubMed ID: 21477380
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders.
Voineskos AN; Lett TA; Lerch JP; Tiwari AK; Ameis SH; Rajji TK; Müller DJ; Mulsant BH; Kennedy JL
PLoS One; 2011; 6(6):e20982. PubMed ID: 21687627
[TBL] [Abstract][Full Text] [Related]
12. Cumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility.
González-Peñas J; Arrojo M; Paz E; Brenlla J; Páramo M; Costas J
Am J Med Genet B Neuropsychiatr Genet; 2015 Oct; 168(7):528-35. PubMed ID: 25982957
[TBL] [Abstract][Full Text] [Related]
13. Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.
Teng S; Thomson PA; McCarthy S; Kramer M; Muller S; Lihm J; Morris S; Soares DC; Hennah W; Harris S; Camargo LM; Malkov V; McIntosh AM; Millar JK; Blackwood DH; Evans KL; Deary IJ; Porteous DJ; McCombie WR
Mol Psychiatry; 2018 May; 23(5):1270-1277. PubMed ID: 28630456
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
[TBL] [Abstract][Full Text] [Related]
16. Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder.
Song W; Li W; Noltner K; Yan J; Green E; Grozeva D; Jones IR; Craddock N; Longmate J; Feng J; Sommer SS
Neurosci Lett; 2010 Dec; 486(3):136-40. PubMed ID: 20850505
[TBL] [Abstract][Full Text] [Related]
17. Mutation burden of rare variants in schizophrenia candidate genes.
Girard SL; Dion PA; Bourassa CV; Geoffroy S; Lachance-Touchette P; Barhdadi A; Langlois M; Joober R; Krebs MO; Dubé MP; Rouleau GA
PLoS One; 2015; 10(6):e0128988. PubMed ID: 26039597
[TBL] [Abstract][Full Text] [Related]
18. Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia.
Song W; Li W; Feng J; Heston LL; Scaringe WA; Sommer SS
Biochem Biophys Res Commun; 2008 Mar; 367(3):700-6. PubMed ID: 18164685
[TBL] [Abstract][Full Text] [Related]
19. DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.
Alkelai A; Lupoli S; Greenbaum L; Kohn Y; Kanyas-Sarner K; Ben-Asher E; Lancet D; Macciardi F; Lerer B
Int J Neuropsychopharmacol; 2012 May; 15(4):459-69. PubMed ID: 21682944
[TBL] [Abstract][Full Text] [Related]
20. 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.
Thomson PA; Parla JS; McRae AF; Kramer M; Ramakrishnan K; Yao J; Soares DC; McCarthy S; Morris SW; Cardone L; Cass S; Ghiban E; Hennah W; Evans KL; Rebolini D; Millar JK; Harris SE; Starr JM; MacIntyre DJ; ; McIntosh AM; Watson JD; Deary IJ; Visscher PM; Blackwood DH; McCombie WR; Porteous DJ
Mol Psychiatry; 2014 Jun; 19(6):668-75. PubMed ID: 23732877
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
