1095 related articles for article (PubMed ID: 19404257)
1. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Glessner JT; Wang K; Cai G; Korvatska O; Kim CE; Wood S; Zhang H; Estes A; Brune CW; Bradfield JP; Imielinski M; Frackelton EC; Reichert J; Crawford EL; Munson J; Sleiman PM; Chiavacci R; Annaiah K; Thomas K; Hou C; Glaberson W; Flory J; Otieno F; Garris M; Soorya L; Klei L; Piven J; Meyer KJ; Anagnostou E; Sakurai T; Game RM; Rudd DS; Zurawiecki D; McDougle CJ; Davis LK; Miller J; Posey DJ; Michaels S; Kolevzon A; Silverman JM; Bernier R; Levy SE; Schultz RT; Dawson G; Owley T; McMahon WM; Wassink TH; Sweeney JA; Nurnberger JI; Coon H; Sutcliffe JS; Minshew NJ; Grant SF; Bucan M; Cook EH; Buxbaum JD; Devlin B; Schellenberg GD; Hakonarson H
Nature; 2009 May; 459(7246):569-73. PubMed ID: 19404257
[TBL] [Abstract][Full Text] [Related]
2. Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.
Matsunami N; Hadley D; Hensel CH; Christensen GB; Kim C; Frackelton E; Thomas K; da Silva RP; Stevens J; Baird L; Otterud B; Ho K; Varvil T; Leppert T; Lambert CG; Leppert M; Hakonarson H
PLoS One; 2013; 8(1):e52239. PubMed ID: 23341896
[TBL] [Abstract][Full Text] [Related]
3. Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Wang K; Zhang H; Ma D; Bucan M; Glessner JT; Abrahams BS; Salyakina D; Imielinski M; Bradfield JP; Sleiman PM; Kim CE; Hou C; Frackelton E; Chiavacci R; Takahashi N; Sakurai T; Rappaport E; Lajonchere CM; Munson J; Estes A; Korvatska O; Piven J; Sonnenblick LI; Alvarez Retuerto AI; Herman EI; Dong H; Hutman T; Sigman M; Ozonoff S; Klin A; Owley T; Sweeney JA; Brune CW; Cantor RM; Bernier R; Gilbert JR; Cuccaro ML; McMahon WM; Miller J; State MW; Wassink TH; Coon H; Levy SE; Schultz RT; Nurnberger JI; Haines JL; Sutcliffe JS; Cook EH; Minshew NJ; Buxbaum JD; Dawson G; Grant SF; Geschwind DH; Pericak-Vance MA; Schellenberg GD; Hakonarson H
Nature; 2009 May; 459(7246):528-33. PubMed ID: 19404256
[TBL] [Abstract][Full Text] [Related]
4. Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.
Glessner JT; Khan ME; Chang X; Liu Y; Otieno FG; Lemma M; Slaby I; Hain H; Mentch F; Li J; Kao C; Sleiman PMA; March ME; Connolly J; Hakonarson H
J Neurodev Disord; 2023 Apr; 15(1):14. PubMed ID: 37120522
[TBL] [Abstract][Full Text] [Related]
5. Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
Yap CX; Alvares GA; Henders AK; Lin T; Wallace L; Farrelly A; McLaren T; Berry J; Vinkhuyzen AAE; Trzaskowski M; Zeng J; Yang Y; Cleary D; Grove R; Hafekost C; Harun A; Holdsworth H; Jellett R; Khan F; Lawson L; Leslie J; Levis Frenk M; Masi A; Mathew NE; Muniandy M; Nothard M; Visscher PM; Dawson PA; Dissanayake C; Eapen V; Heussler HS; Whitehouse AJO; Wray NR; Gratten J
Mol Autism; 2021 Feb; 12(1):12. PubMed ID: 33568206
[TBL] [Abstract][Full Text] [Related]
6. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
Bucan M; Abrahams BS; Wang K; Glessner JT; Herman EI; Sonnenblick LI; Alvarez Retuerto AI; Imielinski M; Hadley D; Bradfield JP; Kim C; Gidaya NB; Lindquist I; Hutman T; Sigman M; Kustanovich V; Lajonchere CM; Singleton A; Kim J; Wassink TH; McMahon WM; Owley T; Sweeney JA; Coon H; Nurnberger JI; Li M; Cantor RM; Minshew NJ; Sutcliffe JS; Cook EH; Dawson G; Buxbaum JD; Grant SF; Schellenberg GD; Geschwind DH; Hakonarson H
PLoS Genet; 2009 Jun; 5(6):e1000536. PubMed ID: 19557195
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.
Yin CL; Chen HI; Li LH; Chien YL; Liao HM; Chou MC; Chou WJ; Tsai WC; Chiu YN; Wu YY; Lo CZ; Wu JY; Chen YT; Gau SS
Mol Autism; 2016; 7():23. PubMed ID: 27042285
[TBL] [Abstract][Full Text] [Related]
8. Detection and characterization of copy number variation in autism spectrum disorder.
Marshall CR; Scherer SW
Methods Mol Biol; 2012; 838():115-35. PubMed ID: 22228009
[TBL] [Abstract][Full Text] [Related]
9. Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Lionel AC; Crosbie J; Barbosa N; Goodale T; Thiruvahindrapuram B; Rickaby J; Gazzellone M; Carson AR; Howe JL; Wang Z; Wei J; Stewart AF; Roberts R; McPherson R; Fiebig A; Franke A; Schreiber S; Zwaigenbaum L; Fernandez BA; Roberts W; Arnold PD; Szatmari P; Marshall CR; Schachar R; Scherer SW
Sci Transl Med; 2011 Aug; 3(95):95ra75. PubMed ID: 21832240
[TBL] [Abstract][Full Text] [Related]
10. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
[TBL] [Abstract][Full Text] [Related]
11. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
Jarick I; Volckmar AL; Pütter C; Pechlivanis S; Nguyen TT; Dauvermann MR; Beck S; Albayrak Ö; Scherag S; Gilsbach S; Cichon S; Hoffmann P; Degenhardt F; Nöthen MM; Schreiber S; Wichmann HE; Jöckel KH; Heinrich J; Tiesler CM; Faraone SV; Walitza S; Sinzig J; Freitag C; Meyer J; Herpertz-Dahlmann B; Lehmkuhl G; Renner TJ; Warnke A; Romanos M; Lesch KP; Reif A; Schimmelmann BG; Hebebrand J; Scherag A; Hinney A
Mol Psychiatry; 2014 Jan; 19(1):115-21. PubMed ID: 23164820
[TBL] [Abstract][Full Text] [Related]
12. Copy-number variations associated with autism spectrum disorder.
Kakinuma H; Sato H
Pharmacogenomics; 2008 Aug; 9(8):1143-54. PubMed ID: 18681787
[TBL] [Abstract][Full Text] [Related]
13. A genome-wide investigation of SNPs and CNVs in schizophrenia.
Need AC; Ge D; Weale ME; Maia J; Feng S; Heinzen EL; Shianna KV; Yoon W; Kasperaviciūte D; Gennarelli M; Strittmatter WJ; Bonvicini C; Rossi G; Jayathilake K; Cola PA; McEvoy JP; Keefe RS; Fisher EM; St Jean PL; Giegling I; Hartmann AM; Möller HJ; Ruppert A; Fraser G; Crombie C; Middleton LT; St Clair D; Roses AD; Muglia P; Francks C; Rujescu D; Meltzer HY; Goldstein DB
PLoS Genet; 2009 Feb; 5(2):e1000373. PubMed ID: 19197363
[TBL] [Abstract][Full Text] [Related]
14. Neurexin gene family variants as risk factors for autism spectrum disorder.
Wang J; Gong J; Li L; Chen Y; Liu L; Gu H; Luo X; Hou F; Zhang J; Song R
Autism Res; 2018 Jan; 11(1):37-43. PubMed ID: 29045040
[TBL] [Abstract][Full Text] [Related]
15. Structural variation of chromosomes in autism spectrum disorder.
Marshall CR; Noor A; Vincent JB; Lionel AC; Feuk L; Skaug J; Shago M; Moessner R; Pinto D; Ren Y; Thiruvahindrapduram B; Fiebig A; Schreiber S; Friedman J; Ketelaars CE; Vos YJ; Ficicioglu C; Kirkpatrick S; Nicolson R; Sloman L; Summers A; Gibbons CA; Teebi A; Chitayat D; Weksberg R; Thompson A; Vardy C; Crosbie V; Luscombe S; Baatjes R; Zwaigenbaum L; Roberts W; Fernandez B; Szatmari P; Scherer SW
Am J Hum Genet; 2008 Feb; 82(2):477-88. PubMed ID: 18252227
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
Christian SL; Brune CW; Sudi J; Kumar RA; Liu S; Karamohamed S; Badner JA; Matsui S; Conroy J; McQuaid D; Gergel J; Hatchwell E; Gilliam TC; Gershon ES; Nowak NJ; Dobyns WB; Cook EH
Biol Psychiatry; 2008 Jun; 63(12):1111-7. PubMed ID: 18374305
[TBL] [Abstract][Full Text] [Related]
18. The landscape of copy number variations in Finnish families with autism spectrum disorders.
Kanduri C; Kantojärvi K; Salo PM; Vanhala R; Buck G; Blancher C; Lähdesmäki H; Järvelä I
Autism Res; 2016 Jan; 9(1):9-16. PubMed ID: 26052927
[TBL] [Abstract][Full Text] [Related]
19. High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families.
AlAyadhi LY; Hashmi JA; Iqbal M; Albalawi AM; Samman MI; Elamin NE; Bashir S; Basit S
Neuroscience; 2016 Dec; 339():561-570. PubMed ID: 27771533
[TBL] [Abstract][Full Text] [Related]
20. Gene-network analysis identifies susceptibility genes related to glycobiology in autism.
van der Zwaag B; Franke L; Poot M; Hochstenbach R; Spierenburg HA; Vorstman JA; van Daalen E; de Jonge MV; Verbeek NE; Brilstra EH; van 't Slot R; Ophoff RA; van Es MA; Blauw HM; Veldink JH; Buizer-Voskamp JE; Beemer FA; van den Berg LH; Wijmenga C; van Amstel HK; van Engeland H; Burbach JP; Staal WG
PLoS One; 2009 May; 4(5):e5324. PubMed ID: 19492091
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
