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Items: 1 to 20 of 104

1.

Unraveling autism.

Stephan DA.

Am J Hum Genet. 2008 Jan;82(1):7-9. doi: 10.1016/j.ajhg.2007.12.003.

2.

Gene associated with seizures, autism, and hepatomegaly in an Amish girl.

Jackman C, Horn ND, Molleston JP, Sokol DK.

Pediatr Neurol. 2009 Apr;40(4):310-3. doi: 10.1016/j.pediatrneurol.2008.10.013.

PMID:
19302947
3.

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.

Yan J, Oliveira G, Coutinho A, Yang C, Feng J, Katz C, Sram J, Bockholt A, Jones IR, Craddock N, Cook EH Jr, Vicente A, Sommer SS.

Mol Psychiatry. 2005 Apr;10(4):329-32. No abstract available.

PMID:
15622415
4.

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.

Vincent JB, Kolozsvari D, Roberts WS, Bolton PF, Gurling HM, Scherer SW.

Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):82-4.

PMID:
15274046
5.

Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.

Toma C, Hervás A, Torrico B, Balmaña N, Salgado M, Maristany M, Vilella E, Martínez-Leal R, Planelles MI, Cuscó I, del Campo M, Pérez-Jurado LA, Caballero-Andaluz R, de Diego-Otero Y, Pérez-Costillas L, Ramos-Quiroga JA, Ribasés M, Bayés M, Cormand B.

Psychiatr Genet. 2013 Apr;23(2):82-5. doi: 10.1097/YPG.0b013e32835d6fc6.

PMID:
23277129
6.

On the twin risk in autism.

Hallmayer J, Glasson EJ, Bower C, Petterson B, Croen L, Grether J, Risch N.

Am J Hum Genet. 2002 Oct;71(4):941-6. Epub 2002 Sep 12.

7.

No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level.

Wermter AK, Kamp-Becker I, Strauch K, Schulte-Körne G, Remschmidt H.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):535-7. doi: 10.1002/ajmg.b.30618.

PMID:
18189281
8.

A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea.

Rossi E, Verri AP, Patricelli MG, Destefani V, Ricca I, Vetro A, Ciccone R, Giorda R, Toniolo D, Maraschio P, Zuffardi O.

Eur J Med Genet. 2008 Nov-Dec;51(6):631-8. doi: 10.1016/j.ejmg.2008.06.010. Epub 2008 Jul 16.

PMID:
18675947
9.

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.

Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW.

Am J Hum Genet. 2008 Jan;82(1):165-73. doi: 10.1016/j.ajhg.2007.09.017.

10.

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A.

Am J Hum Genet. 2008 Jan;82(1):160-4. doi: 10.1016/j.ajhg.2007.09.015.

11.

Pharmacological probing of type 1 autism.

Manev H, Manev R.

J Autism Dev Disord. 2008 Aug;38(7):1400-1. doi: 10.1007/s10803-008-0594-2. Epub 2008 May 30. No abstract available.

PMID:
18512134
12.

[Neurodevelopmental disturbance in the pathogenesis of major mental disorders].

Kamiya A, Kitabatake Y, Sawa A.

Brain Nerve. 2008 Apr;60(4):445-52. Review. Japanese.

PMID:
18421986
13.

Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.

Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R.

Neurosci Lett. 2008 Aug 15;441(1):56-60. doi: 10.1016/j.neulet.2008.06.022. Epub 2008 Jun 13.

PMID:
18597938
14.

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.

Scott-Van Zeeland AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie JD, Ghahremani D, Mumford JA, Poldrack RA, Dapretto M, Geschwind DH, Bookheimer SY.

Sci Transl Med. 2010 Nov 3;2(56):56ra80. doi: 10.1126/scitranslmed.3001344.

15.

Contact in the genetics of autism and schizophrenia.

Burbach JP, van der Zwaag B.

Trends Neurosci. 2009 Feb;32(2):69-72. doi: 10.1016/j.tins.2008.11.002. Epub 2009 Jan 8.

PMID:
19135727
16.

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.

17.

Medicine. Testing hypotheses about autism.

Crawley JN.

Science. 2007 Oct 5;318(5847):56-7. No abstract available.

PMID:
17916718
18.

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.

Zare S, Mashayekhi F, Bidabadi E.

J Clin Neurosci. 2017 May;39:189-192. doi: 10.1016/j.jocn.2017.01.008. Epub 2017 Mar 9.

PMID:
28284582
19.

Molecular genetics of autism.

Cantor RM.

Curr Psychiatry Rep. 2009 Apr;11(2):137-42. Review.

PMID:
19302767
20.

Association study of six candidate genes asymmetrically expressed in the two cerebral hemispheres suggests the involvement of BAIAP2 in autism.

Toma C, Hervás A, Balmaña N, Vilella E, Aguilera F, Cuscó I, del Campo M, Caballero R, De Diego-Otero Y, Ribasés M, Cormand B, Bayés M.

J Psychiatr Res. 2011 Feb;45(2):280-2. doi: 10.1016/j.jpsychires.2010.09.001. No abstract available.

PMID:
20888579

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