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Items: 8


Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.

Villanueva P, Newbury DF, Jara L, De Barbieri Z, Mirza G, Palomino HM, Fernández MA, Cazier JB, Monaco AP, Palomino H.

Eur J Hum Genet. 2011 Jun;19(6):687-95. doi: 10.1038/ejhg.2010.251. Epub 2011 Jan 19.


Consanguinity mapping of congenital heart disease in a South Indian population.

McGregor TL, Misri A, Bartlett J, Orabona G, Friedman RD, Sexton D, Maheshwari S, Morgan TM.

PLoS One. 2010 Apr 21;5(4):e10286. doi: 10.1371/journal.pone.0010286.


Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.

Wassink TH, Vieland VJ, Sheffield VC, Bartlett CW, Goedken R, Childress D, Piven J.

Psychiatr Genet. 2008 Apr;18(2):85-91. doi: 10.1097/YPG.0b013e3282f9b48e.


Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH.

Am J Hum Genet. 2008 Jan;82(1):150-9. doi: 10.1016/j.ajhg.2007.09.005.


Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.

Am J Hum Genet. 2005 Aug;77(2):265-79. Epub 2005 Jul 1.


Executive dysfunction and its relation to language ability in verbal school-age children with autism.

Joseph RM, McGrath LM, Tager-Flusberg H.

Dev Neuropsychol. 2005;27(3):361-78.


Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.

McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS.

BMC Med Genet. 2005 Jan 12;6:1.


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