853 related articles for article (PubMed ID: 22424231)
1. CNVs: harbingers of a rare variant revolution in psychiatric genetics.
Malhotra D; Sebat J
Cell; 2012 Mar; 148(6):1223-41. PubMed ID: 22424231
[TBL] [Abstract][Full Text] [Related]
2. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.
Rudan I
Psychiatr Danub; 2010 Jun; 22(2):190-2. PubMed ID: 20562745
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.
Grozeva D; Kirov G; Ivanov D; Jones IR; Jones L; Green EK; St Clair DM; Young AH; Ferrier N; Farmer AE; McGuffin P; Holmans PA; Owen MJ; O'Donovan MC; Craddock N;
Arch Gen Psychiatry; 2010 Apr; 67(4):318-27. PubMed ID: 20368508
[TBL] [Abstract][Full Text] [Related]
5. High frequencies of de novo CNVs in bipolar disorder and schizophrenia.
Malhotra D; McCarthy S; Michaelson JJ; Vacic V; Burdick KE; Yoon S; Cichon S; Corvin A; Gary S; Gershon ES; Gill M; Karayiorgou M; Kelsoe JR; Krastoshevsky O; Krause V; Leibenluft E; Levy DL; Makarov V; Bhandari A; Malhotra AK; McMahon FJ; Nöthen MM; Potash JB; Rietschel M; Schulze TG; Sebat J
Neuron; 2011 Dec; 72(6):951-63. PubMed ID: 22196331
[TBL] [Abstract][Full Text] [Related]
6. Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
Van Den Bossche MJ; Johnstone M; Strazisar M; Pickard BS; Goossens D; Lenaerts AS; De Zutter S; Nordin A; Norrback KF; Mendlewicz J; Souery D; De Rijk P; Sabbe BG; Adolfsson R; Blackwood D; Del-Favero J
Am J Med Genet B Neuropsychiatr Genet; 2012 Oct; 159B(7):812-22. PubMed ID: 22911887
[TBL] [Abstract][Full Text] [Related]
7. Copy number variation and psychiatric disease risk.
Levy RJ; Xu B; Gogos JA; Karayiorgou M
Methods Mol Biol; 2012; 838():97-113. PubMed ID: 22228008
[TBL] [Abstract][Full Text] [Related]
8. Reduced burden of very large and rare CNVs in bipolar affective disorder.
Grozeva D; Kirov G; Conrad DF; Barnes CP; Hurles M; Owen MJ; O'Donovan MC; Craddock N
Bipolar Disord; 2013 Dec; 15(8):893-8. PubMed ID: 24127788
[TBL] [Abstract][Full Text] [Related]
9. Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases.
Charney AW; Stahl EA; Green EK; Chen CY; Moran JL; Chambert K; Belliveau RA; Forty L; Gordon-Smith K; Lee PH; Bromet EJ; Buckley PF; Escamilla MA; Fanous AH; Fochtmann LJ; Lehrer DS; Malaspina D; Marder SR; Morley CP; Nicolini H; Perkins DO; Rakofsky JJ; Rapaport MH; Medeiros H; Sobell JL; Backlund L; Bergen SE; Juréus A; Schalling M; Lichtenstein P; Knowles JA; Burdick KE; Jones I; Jones LA; Hultman CM; Perlis R; Purcell SM; McCarroll SA; Pato CN; Pato MT; Di Florio A; Craddock N; Landén M; Smoller JW; Ruderfer DM; Sklar P
Biol Psychiatry; 2019 Jul; 86(2):110-119. PubMed ID: 30686506
[TBL] [Abstract][Full Text] [Related]
10. De novo CNVs in bipolar disorder: recurrent themes or new directions?
Girirajan S; Eichler EE
Neuron; 2011 Dec; 72(6):885-7. PubMed ID: 22196322
[TBL] [Abstract][Full Text] [Related]
11. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
Weiss LA
Expert Rev Mol Diagn; 2009 Nov; 9(8):795-803. PubMed ID: 19895225
[TBL] [Abstract][Full Text] [Related]
12. The role of DNA copy number variation in schizophrenia.
Tam GW; Redon R; Carter NP; Grant SG
Biol Psychiatry; 2009 Dec; 66(11):1005-12. PubMed ID: 19748074
[TBL] [Abstract][Full Text] [Related]
13. Genomic copy number variation in disorders of cognitive development.
Morrow EM
J Am Acad Child Adolesc Psychiatry; 2010 Nov; 49(11):1091-104. PubMed ID: 20970697
[TBL] [Abstract][Full Text] [Related]
14. [The etiology of schizophrenia].
Gejman PV; Sanders AR
Medicina (B Aires); 2012; 72(3):227-34. PubMed ID: 22763160
[TBL] [Abstract][Full Text] [Related]
15. Copy number variation and neuropsychiatric illness.
Rees E; Kirov G
Curr Opin Genet Dev; 2021 Jun; 68():57-63. PubMed ID: 33752146
[TBL] [Abstract][Full Text] [Related]
16. Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.
Hochstenbach R; Buizer-Voskamp JE; Vorstman JA; Ophoff RA
Cytogenet Genome Res; 2011; 135(3-4):174-202. PubMed ID: 22056632
[TBL] [Abstract][Full Text] [Related]
17. Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
Fernandez TV; Sanders SJ; Yurkiewicz IR; Ercan-Sencicek AG; Kim YS; Fishman DO; Raubeson MJ; Song Y; Yasuno K; Ho WS; Bilguvar K; Glessner J; Chu SH; Leckman JF; King RA; Gilbert DL; Heiman GA; Tischfield JA; Hoekstra PJ; Devlin B; Hakonarson H; Mane SM; Günel M; State MW
Biol Psychiatry; 2012 Mar; 71(5):392-402. PubMed ID: 22169095
[TBL] [Abstract][Full Text] [Related]
18. De novo CNVs in bipolar affective disorder and schizophrenia.
Georgieva L; Rees E; Moran JL; Chambert KD; Milanova V; Craddock N; Purcell S; Sklar P; McCarroll S; Holmans P; O'Donovan MC; Owen MJ; Kirov G
Hum Mol Genet; 2014 Dec; 23(24):6677-83. PubMed ID: 25055870
[TBL] [Abstract][Full Text] [Related]
19. Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.
Hiroi N; Takahashi T; Hishimoto A; Izumi T; Boku S; Hiramoto T
Mol Psychiatry; 2013 Nov; 18(11):1153-65. PubMed ID: 23917946
[TBL] [Abstract][Full Text] [Related]
20. Exome Sequencing of Familial Bipolar Disorder.
Goes FS; Pirooznia M; Parla JS; Kramer M; Ghiban E; Mavruk S; Chen YC; Monson ET; Willour VL; Karchin R; Flickinger M; Locke AE; Levy SE; Scott LJ; Boehnke M; Stahl E; Moran JL; Hultman CM; Landén M; Purcell SM; Sklar P; Zandi PP; McCombie WR; Potash JB
JAMA Psychiatry; 2016 Jun; 73(6):590-7. PubMed ID: 27120077
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
