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Results: 17

Cited In for PubMed (Select 1828000)


Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?

Amiet C, Gourfinkel-An I, Laurent C, Bodeau N, Génin B, Leguern E, Tordjman S, Cohen D.

Mol Autism. 2013 Dec 1;4(1):47. doi: 10.1186/2040-2392-4-47.


Prenatal and perinatal analgesic exposure and autism: an ecological link.

Bauer AZ, Kriebel D.

Environ Health. 2013 May 9;12:41. doi: 10.1186/1476-069X-12-41.


Sociodemographic factors in Arab children with Autism Spectrum Disorders.

Amr M, Bu Ali W, Hablas H, Raddad D, El-Mehesh F, El-Gilany AH, Al-Shamy H.

Pan Afr Med J. 2012;13:65. Epub 2012 Nov 26.


Social phenotypes of autism spectrum disorders and williams syndrome: similarities and differences.

Asada K, Itakura S.

Front Psychol. 2012 Jul 30;3:247. doi: 10.3389/fpsyg.2012.00247. eCollection 2012.


Global prevalence of autism and other pervasive developmental disorders.

Elsabbagh M, Divan G, Koh YJ, Kim YS, Kauchali S, Marcín C, Montiel-Nava C, Patel V, Paula CS, Wang C, Yasamy MT, Fombonne E.

Autism Res. 2012 Jun;5(3):160-79. doi: 10.1002/aur.239. Epub 2012 Apr 11. Review.


Autism risk assessment in siblings of affected children using sex-specific genetic scores.

Carayol J, Schellenberg GD, Dombroski B, Genin E, Rousseau F, Dawson G.

Mol Autism. 2011 Oct 21;2(1):17. doi: 10.1186/2040-2392-2-17.


DIA1R is an X-linked gene related to Deleted In Autism-1.

Aziz A, Harrop SP, Bishop NE.

PLoS One. 2011 Jan 17;6(1):e14534. doi: 10.1371/journal.pone.0014534.


Systematic review of prevalence studies of autism spectrum disorders.

Williams JG, Higgins JP, Brayne CE.

Arch Dis Child. 2006 Jan;91(1):8-15. Epub 2005 Apr 29. Review.


A global perspective on vaccine safety and public health: the Global Advisory Committee on Vaccine Safety.

Folb PI, Bernatowska E, Chen R, Clemens J, Dodoo AN, Ellenberg SS, Farrington CP, John TJ, Lambert PH, Macdonald NE, Miller E, Salisbury D, Schmitt HJ, Siegrist CA, Wimalaratne O.

Am J Public Health. 2004 Nov;94(11):1926-31.


Disabilities and trends over time in a French county, 1980-91.

Cans C, Guillem P, Fauconnier J, Rambaud P, Jouk PS.

Arch Dis Child. 2003 Feb;88(2):114-7.


The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions.

Geschwind DH, Sowinski J, Lord C, Iversen P, Shestack J, Jones P, Ducat L, Spence SJ; AGRE Steering Committee.

Am J Hum Genet. 2001 Aug;69(2):463-6. No abstract available.


An infection-based model of neurodevelopmental damage.

Hornig M, Weissenböck H, Horscroft N, Lipkin WI.

Proc Natl Acad Sci U S A. 1999 Oct 12;96(21):12102-7.


The puzzle of autism: an ophthalmologic contribution.

Miller MT, Strömland K, Gillberg C, Johansson M, Nilsson EW.

Trans Am Ophthalmol Soc. 1998;96:369-85; discussion 385-7.


Etiology of infantile autism: a review of recent advances in genetic and neurobiological research.

Trottier G, Srivastava L, Walker CD.

J Psychiatry Neurosci. 1999 Mar;24(2):103-15. Review.

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