Detalhe da pesquisa
1.
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
Hum Mol Genet
; 23(10): 2752-68, 2014 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24381304
2.
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Am J Hum Genet
; 93(2): 249-63, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23849776
3.
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
Hum Genet
; 134(2): 191-201, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25432440
4.
Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Am J Hum Genet
; 90(1): 133-41, 2012 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22209245
5.
Conjunctive visual search in individuals with and without mental retardation.
Am J Ment Retard
; 112(1): 54-65, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17181391
6.
Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly.
Mol Autism
; 8: 59, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29152164
7.
Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes.
NPJ Genom Med
; 22017 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28649445
8.
Combining information from multiple sources in the diagnosis of autism spectrum disorders.
J Am Acad Child Adolesc Psychiatry
; 45(9): 1094-1103, 2006 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16926617
9.
Whole-genome sequencing of quartet families with autism spectrum disorder.
Nat Med
; 21(2): 185-91, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25621899