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Items: 1 to 20 of 247

1.

Epigenetics of autism spectrum disorders.

Schanen NC.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R138-50. Review.

2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
3.

Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.

Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C.

Biol Psychiatry. 2009 Aug 15;66(4):349-59. doi: 10.1016/j.biopsych.2009.01.025. Epub 2009 Mar 17.

PMID:
19278672
4.

Autism spectrum disorders and epigenetics.

Grafodatskaya D, Chung B, Szatmari P, Weksberg R.

J Am Acad Child Adolesc Psychiatry. 2010 Aug;49(8):794-809. doi: 10.1016/j.jaac.2010.05.005. Epub 2010 Jul 3. Review.

PMID:
20643313
5.

Genomic imprinting in the development and evolution of psychotic spectrum conditions.

Crespi B.

Biol Rev Camb Philos Soc. 2008 Nov;83(4):441-93. doi: 10.1111/j.1469-185X.2008.00050.x. Epub 2008 Sep 9. Review.

PMID:
18783362
6.

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study.

Weidmer-Mikhail E, Sheldon S, Ghaziuddin M.

J Intellect Disabil Res. 1998 Feb;42 ( Pt 1):8-12.

PMID:
9534109
7.

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders.

Bolton PF, Dennis NR, Browne CE, Thomas NS, Veltman MW, Thompson RJ, Jacobs P.

Am J Med Genet. 2001 Dec 8;105(8):675-85. Review.

PMID:
11803514
8.

Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders.

Lopez-Rangel E, Lewis ME.

Clin Genet. 2006 Jan;69(1):21-2. No abstract available.

PMID:
16451129
9.

[Genetic factors in Asperger syndrome].

Sasaki T.

Nihon Rinsho. 2007 Mar;65(3):443-8. Review. Japanese.

PMID:
17354555
10.

Autism and cytogenetic abnormalities: solving autism one chromosome at a time.

Martin CL, Ledbetter DH.

Curr Psychiatry Rep. 2007 Apr;9(2):141-7. Review.

PMID:
17389126
11.

Copy number and sequence variants implicate APBA2 as an autism candidate gene.

Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL.

Autism Res. 2009 Dec;2(6):359-64. doi: 10.1002/aur.107.

PMID:
20029827
12.

The molecular genetics of autism.

Wassink TH, Piven J.

Curr Psychiatry Rep. 2000 Apr;2(2):170-5. Review.

PMID:
11122951
13.

Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders.

Estécio M, Fett-Conte AC, Varella-Garcia M, Fridman C, Silva AE.

J Autism Dev Disord. 2002 Feb;32(1):35-41.

PMID:
11916331
14.

Syndromic autism: causes and pathogenetic pathways.

Benvenuto A, Moavero R, Alessandrelli R, Manzi B, Curatolo P.

World J Pediatr. 2009 Aug;5(3):169-76. doi: 10.1007/s12519-009-0033-2. Epub 2009 Aug 20. Review.

PMID:
19693459
15.

The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression.

Herzing LB, Kim SJ, Cook EH Jr, Ledbetter DH.

Am J Hum Genet. 2001 Jun;68(6):1501-5. Epub 2001 May 11.

16.

Autism, the big unkown.

García-Primo P, Martín-Arribas MC, Ferrari-Arroyo MJ, Boada L, García-de-Andres E, Posada de la Paz M.

Georgian Med News. 2008 Mar;(156):9-14.

PMID:
18403803
17.

Autism spectrum disorders associated with X chromosome markers in French-Canadian males.

Gauthier J, Joober R, Dubé MP, St-Onge J, Bonnel A, Gariépy D, Laurent S, Najafee R, Lacasse H, St-Charles L, Fombonne E, Mottron L, Rouleau GA.

Mol Psychiatry. 2006 Feb;11(2):206-13.

PMID:
16261168
18.

Molecular genetics of autism spectrum disorder.

Veenstra-VanderWeele J, Cook EH Jr.

Mol Psychiatry. 2004 Sep;9(9):819-32. Review.

PMID:
15197396
19.

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.

Hogart A, Wu D, LaSalle JM, Schanen NC.

Neurobiol Dis. 2010 May;38(2):181-91. doi: 10.1016/j.nbd.2008.08.011. Epub 2008 Sep 18. Review.

20.

Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders.

Keller K, Williams C, Wharton P, Paulk M, Bent-Williams A, Gray B, Ward A, Stalker H, Wallace M, Carter R, Zori R.

Am J Med Genet A. 2003 Mar 1;117A(2):105-11.

PMID:
12567405
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