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Items: 8

1.

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.

Kumar RA, Sudi J, Babatz TD, Brune CW, Oswald D, Yen M, Nowak NJ, Cook EH, Christian SL, Dobyns WB.

J Med Genet. 2010 Feb;47(2):81-90. doi: 10.1136/jmg.2008.065821. Epub 2009 Jun 21.

2.

Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review.

Quintero-Rivera F, Sharifi-Hannauer P, Martinez-Agosto JA.

Am J Med Genet A. 2010 Oct;152A(10):2459-67. doi: 10.1002/ajmg.a.33573. Review.

PMID:
20830797
3.

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.

Guilmatre A, Dubourg C, Mosca AL, Legallic S, Goldenberg A, Drouin-Garraud V, Layet V, Rosier A, Briault S, Bonnet-Brilhault F, Laumonnier F, Odent S, Le Vacon G, Joly-Helas G, David V, Bendavid C, Pinoit JM, Henry C, Impallomeni C, Germano E, Tortorella G, Di Rosa G, Barthelemy C, Andres C, Faivre L, Frébourg T, Saugier Veber P, Campion D.

Arch Gen Psychiatry. 2009 Sep;66(9):947-56. doi: 10.1001/archgenpsychiatry.2009.80. Review.

4.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
5.

De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: a case report and literature review.

Jolley A, Corbett M, McGregor L, Waters W, Brown S, Nicholl J, Yu S.

Am J Med Genet A. 2013 Jun;161A(6):1508-12. doi: 10.1002/ajmg.a.35922. Epub 2013 May 6. Review. No abstract available.

PMID:
23650183
6.

Autism and chromosome abnormalities-A review.

Bergbaum A, Ogilvie CM.

Clin Anat. 2016 Jul;29(5):620-7. doi: 10.1002/ca.22719. Epub 2016 Apr 19. Review.

PMID:
27012322
7.

Advances in autism genetics: on the threshold of a new neurobiology.

Abrahams BS, Geschwind DH.

Nat Rev Genet. 2008 May;9(5):341-55. doi: 10.1038/nrg2346. Review. Erratum in: Nat Rev Genet. 2008 Jun;9(6):493.

8.

A genomic view on epilepsy and autism candidate genes.

Jabbari K, Nürnberg P.

Genomics. 2016 Jul;108(1):31-6. doi: 10.1016/j.ygeno.2016.01.001. Epub 2016 Jan 7. Review.

PMID:
26772991

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