653 related articles for article (PubMed ID: 23375656)
21. A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
Derks EM; Ayub M; Chambert K; Del Favero J; Johnstone M; MacGregor S; Maclean A; McKechanie AG; McRae AF; Moran JL; Pickard BS; Purcell S; Sklar P; StClair DM; Wray NR; Visscher PM; Blackwood DH
Am J Med Genet B Neuropsychiatr Genet; 2013 Dec; 162B(8):847-54. PubMed ID: 24115684
[TBL] [Abstract][Full Text] [Related]
22. Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.
Nava C; Keren B; Mignot C; Rastetter A; Chantot-Bastaraud S; Faudet A; Fonteneau E; Amiet C; Laurent C; Jacquette A; Whalen S; Afenjar A; Périsse D; Doummar D; Dorison N; Leboyer M; Siffroi JP; Cohen D; Brice A; Héron D; Depienne C
Eur J Hum Genet; 2014 Jan; 22(1):71-8. PubMed ID: 23632794
[TBL] [Abstract][Full Text] [Related]
23. Dissecting Molecular Genetic Mechanisms of 1q21.1 CNV in Neuropsychiatric Disorders.
Yoon J; Mao Y
Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34071723
[TBL] [Abstract][Full Text] [Related]
24. Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
Wang P; Carrion P; Qiao Y; Tyson C; Hrynchak M; Calli K; Lopez-Rangel E; Andrieux J; Delobel B; Duban-Bedu B; Thuresson AC; Annerén G; Liu X; Rajcan-Separovic E; Suzanne Lewis ME
Eur J Med Genet; 2013 Aug; 56(8):420-5. PubMed ID: 23727450
[TBL] [Abstract][Full Text] [Related]
25. Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.
Tropeano M; Ahn JW; Dobson RJ; Breen G; Rucker J; Dixit A; Pal DK; McGuffin P; Farmer A; White PS; Andrieux J; Vassos E; Ogilvie CM; Curran S; Collier DA
PLoS One; 2013; 8(4):e61365. PubMed ID: 23637818
[TBL] [Abstract][Full Text] [Related]
26. The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
Hippolyte L; Maillard AM; Rodriguez-Herreros B; Pain A; Martin-Brevet S; Ferrari C; Conus P; Macé A; Hadjikhani N; Metspalu A; Reigo A; Kolk A; Männik K; Barker M; Isidor B; Le Caignec C; Mignot C; Schneider L; Mottron L; Keren B; David A; Doco-Fenzy M; Gérard M; Bernier R; Goin-Kochel RP; Hanson E; Green Snyder L; ; Ramus F; Beckmann JS; Draganski B; Reymond A; Jacquemont S
Biol Psychiatry; 2016 Jul; 80(2):129-139. PubMed ID: 26742926
[TBL] [Abstract][Full Text] [Related]
27. Understanding the impact of 1q21.1 copy number variant.
Harvard C; Strong E; Mercier E; Colnaghi R; Alcantara D; Chow E; Martell S; Tyson C; Hrynchak M; McGillivray B; Hamilton S; Marles S; Mhanni A; Dawson AJ; Pavlidis P; Qiao Y; Holden JJ; Lewis SM; O'Driscoll M; Rajcan-Separovic E
Orphanet J Rare Dis; 2011 Aug; 6():54. PubMed ID: 21824431
[TBL] [Abstract][Full Text] [Related]
28. Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders.
Iyer J; Girirajan S
Brief Funct Genomics; 2015 Sep; 14(5):315-28. PubMed ID: 25971441
[TBL] [Abstract][Full Text] [Related]
29. The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications.
Gillentine MA; Berry LN; Goin-Kochel RP; Ali MA; Ge J; Guffey D; Rosenfeld JA; Hannig V; Bader P; Proud M; Shinawi M; Graham BH; Lin A; Lalani SR; Reynolds J; Chen M; Grebe T; Minard CG; Stankiewicz P; Beaudet AL; Schaaf CP
J Autism Dev Disord; 2017 Mar; 47(3):549-562. PubMed ID: 27853923
[TBL] [Abstract][Full Text] [Related]
30. Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.
Nagamani SC; Erez A; Ben-Zeev B; Frydman M; Winter S; Zeller R; El-Khechen D; Escobar L; Stankiewicz P; Patel A; Cheung SW
Eur J Hum Genet; 2013 Mar; 21(3):343-6. PubMed ID: 22872102
[TBL] [Abstract][Full Text] [Related]
31. A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Prasad A; Merico D; Thiruvahindrapuram B; Wei J; Lionel AC; Sato D; Rickaby J; Lu C; Szatmari P; Roberts W; Fernandez BA; Marshall CR; Hatchwell E; Eis PS; Scherer SW
G3 (Bethesda); 2012 Dec; 2(12):1665-85. PubMed ID: 23275889
[TBL] [Abstract][Full Text] [Related]
32. Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.
Riley KN; Catalano LM; Bernat JA; Adams SD; Martin DM; Lalani SR; Patel A; Burnside RD; Innis JW; Rudd MK
Am J Med Genet A; 2015 Nov; 167A(11):2664-73. PubMed ID: 26227573
[TBL] [Abstract][Full Text] [Related]
33. Epilepsy and the new cytogenetics.
Mulley JC; Mefford HC
Epilepsia; 2011 Mar; 52(3):423-32. PubMed ID: 21269290
[TBL] [Abstract][Full Text] [Related]
34. The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.
Giannuzzi G; Schmidt PJ; Porcu E; Willemin G; Munson KM; Nuttle X; Earl R; Chrast J; Hoekzema K; Risso D; Männik K; De Nittis P; Baratz ED; ; Herault Y; Gao X; Philpott CC; Bernier RA; Kutalik Z; Fleming MD; Eichler EE; Reymond A
Am J Hum Genet; 2019 Nov; 105(5):947-958. PubMed ID: 31668704
[TBL] [Abstract][Full Text] [Related]
35. Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies.
Lal D; Ruppert AK; Trucks H; Schulz H; de Kovel CG; Kasteleijn-Nolst Trenité D; Sonsma AC; Koeleman BP; Lindhout D; Weber YG; Lerche H; Kapser C; Schankin CJ; Kunz WS; Surges R; Elger CE; Gaus V; Schmitz B; Helbig I; Muhle H; Stephani U; Klein KM; Rosenow F; Neubauer BA; Reinthaler EM; Zimprich F; Feucht M; Møller RS; Hjalgrim H; De Jonghe P; Suls A; Lieb W; Franke A; Strauch K; Gieger C; Schurmann C; Schminke U; Nürnberg P; ; Sander T
PLoS Genet; 2015 May; 11(5):e1005226. PubMed ID: 25950944
[TBL] [Abstract][Full Text] [Related]
36. Identification of two inherited copy number variants in a male with autism supports two-hit and compound heterozygosity models of autism.
Gau SS; Liao HM; Hong CC; Chien WH; Chen CH
Am J Med Genet B Neuropsychiatr Genet; 2012 Sep; 159B(6):710-7. PubMed ID: 22778016
[TBL] [Abstract][Full Text] [Related]
37. Functional impact of global rare copy number variation in autism spectrum disorders.
Pinto D; Pagnamenta AT; Klei L; Anney R; Merico D; Regan R; Conroy J; Magalhaes TR; Correia C; Abrahams BS; Almeida J; Bacchelli E; Bader GD; Bailey AJ; Baird G; Battaglia A; Berney T; Bolshakova N; Bölte S; Bolton PF; Bourgeron T; Brennan S; Brian J; Bryson SE; Carson AR; Casallo G; Casey J; Chung BH; Cochrane L; Corsello C; Crawford EL; Crossett A; Cytrynbaum C; Dawson G; de Jonge M; Delorme R; Drmic I; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Fombonne E; Freitag CM; Gilbert J; Gillberg C; Glessner JT; Goldberg J; Green A; Green J; Guter SJ; Hakonarson H; Heron EA; Hill M; Holt R; Howe JL; Hughes G; Hus V; Igliozzi R; Kim C; Klauck SM; Kolevzon A; Korvatska O; Kustanovich V; Lajonchere CM; Lamb JA; Laskawiec M; Leboyer M; Le Couteur A; Leventhal BL; Lionel AC; Liu XQ; Lord C; Lotspeich L; Lund SC; Maestrini E; Mahoney W; Mantoulan C; Marshall CR; McConachie H; McDougle CJ; McGrath J; McMahon WM; Merikangas A; Migita O; Minshew NJ; Mirza GK; Munson J; Nelson SF; Noakes C; Noor A; Nygren G; Oliveira G; Papanikolaou K; Parr JR; Parrini B; Paton T; Pickles A; Pilorge M; Piven J; Ponting CP; Posey DJ; Poustka A; Poustka F; Prasad A; Ragoussis J; Renshaw K; Rickaby J; Roberts W; Roeder K; Roge B; Rutter ML; Bierut LJ; Rice JP; Salt J; Sansom K; Sato D; Segurado R; Sequeira AF; Senman L; Shah N; Sheffield VC; Soorya L; Sousa I; Stein O; Sykes N; Stoppioni V; Strawbridge C; Tancredi R; Tansey K; Thiruvahindrapduram B; Thompson AP; Thomson S; Tryfon A; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Wallace S; Wang K; Wang Z; Wassink TH; Webber C; Weksberg R; Wing K; Wittemeyer K; Wood S; Wu J; Yaspan BL; Zurawiecki D; Zwaigenbaum L; Buxbaum JD; Cantor RM; Cook EH; Coon H; Cuccaro ML; Devlin B; Ennis S; Gallagher L; Geschwind DH; Gill M; Haines JL; Hallmayer J; Miller J; Monaco AP; Nurnberger JI; Paterson AD; Pericak-Vance MA; Schellenberg GD; Szatmari P; Vicente AM; Vieland VJ; Wijsman EM; Scherer SW; Sutcliffe JS; Betancur C
Nature; 2010 Jul; 466(7304):368-72. PubMed ID: 20531469
[TBL] [Abstract][Full Text] [Related]
38. Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.
Liu P; Erez A; Nagamani SC; Bi W; Carvalho CM; Simmons AD; Wiszniewska J; Fang P; Eng PA; Cooper ML; Sutton VR; Roeder ER; Bodensteiner JB; Delgado MR; Prakash SK; Belmont JW; Stankiewicz P; Berg JS; Shinawi M; Patel A; Cheung SW; Lupski JR
Hum Mol Genet; 2011 May; 20(10):1975-88. PubMed ID: 21355048
[TBL] [Abstract][Full Text] [Related]
39. Epilepsy with cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.
Nicholl J; Waters W; Suwalski S; Brown S; Hull Y; Harbord MG; Entwistle J; Thompson S; Clark D; Pridmore C; Haan E; Barnett C; McGregor L; Liebelt J; Thompson EM; Friend K; Bain SM; Yu S; Mulley JC
Am J Med Genet B Neuropsychiatr Genet; 2013 Jan; 162B(1):24-35. PubMed ID: 23184456
[TBL] [Abstract][Full Text] [Related]
40. Autism genetics.
Persico AM; Napolioni V
Behav Brain Res; 2013 Aug; 251():95-112. PubMed ID: 23769996
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
