1412 related articles for article (PubMed ID: 18252227)
1. 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]
2. 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]
3. Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
Roberts JL; Hovanes K; Dasouki M; Manzardo AM; Butler MG
Gene; 2014 Feb; 535(1):70-8. PubMed ID: 24188901
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.
Mahjani B; De Rubeis S; Gustavsson Mahjani C; Mulhern M; Xu X; Klei L; Satterstrom FK; Fu J; Talkowski ME; Reichenberg A; Sandin S; Hultman CM; Grice DE; Roeder K; Devlin B; Buxbaum JD
Mol Autism; 2021 Oct; 12(1):65. PubMed ID: 34615535
[TBL] [Abstract][Full Text] [Related]
11. The genetics of autism.
Muhle R; Trentacoste SV; Rapin I
Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Diagnostic efficacy and new variants in isolated and complex autism spectrum disorder using molecular karyotyping.
Lovrečić L; Rajar P; Volk M; Bertok S; Gnidovec Stražišar B; Osredkar D; Jekovec Vrhovšek M; Peterlin B
J Appl Genet; 2018 May; 59(2):179-185. PubMed ID: 29564645
[TBL] [Abstract][Full Text] [Related]
14. Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database.
Menashe I; Larsen EC; Banerjee-Basu S
PLoS One; 2013; 8(6):e66707. PubMed ID: 23825557
[TBL] [Abstract][Full Text] [Related]
15. Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder.
Chen CH; Chen HI; Liao HM; Chen YJ; Fang JS; Lee KF; Gau SS
Psychiatr Genet; 2017 Feb; 27(1):23-33. PubMed ID: 27846046
[TBL] [Abstract][Full Text] [Related]
16. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
[TBL] [Abstract][Full Text] [Related]
17. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
Woodbury-Smith M; Zarrei M; Wei J; Thiruvahindrapuram B; O'Connor I; Paterson AD; Yuen RKC; Dastan J; Stavropoulos DJ; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Anagnostou E; Scherer SW; Vieland VJ; Szatmari P
Am J Med Genet B Neuropsychiatr Genet; 2020 Jul; 183(5):268-276. PubMed ID: 32372567
[TBL] [Abstract][Full Text] [Related]
18. De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.
Sagar A; Pinto D; Najjar F; Guter SJ; Macmillan C; Cook EH
Am J Med Genet A; 2017 Jun; 173(6):1656-1662. PubMed ID: 28407363
[TBL] [Abstract][Full Text] [Related]
19. Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes.
Gijsbers AC; Bosch CA; Dauwerse JG; Giromus O; Hansson K; Hilhorst-Hofstee Y; Kriek M; van Haeringen A; Bijlsma EK; Bakker E; Breuning MH; Ruivenkamp CA
Eur J Med Genet; 2010; 53(5):227-33. PubMed ID: 20542150
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
