Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 141

1.

Parents of Children with Asperger Syndrome: What is the Cognitive Phenotype?

Baron-Cohen S, Hammer J.

J Cogn Neurosci. 1997 Jul;9(4):548-54. doi: 10.1162/jocn.1997.9.4.548.

PMID:
23968217
2.

Structural variation of chromosomes in autism spectrum disorder.

Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW.

Am J Hum Genet. 2008 Feb;82(2):477-88. doi: 10.1016/j.ajhg.2007.12.009.

3.

Familial deletion within NLGN4 associated with autism and Tourette syndrome.

Lawson-Yuen A, Saldivar JS, Sommer S, Picker J.

Eur J Hum Genet. 2008 May;16(5):614-8. doi: 10.1038/sj.ejhg.5202006.

4.

Association between microdeletion and microduplication at 16p11.2 and autism.

Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, Tanzi RE, Stefansson K, Santangelo SL, Gusella JF, Sklar P, Wu BL, Daly MJ; Autism Consortium..

N Engl J Med. 2008 Feb 14;358(7):667-75. doi: 10.1056/NEJMoa075974.

5.

Disruption of neurexin 1 associated with autism spectrum disorder.

Kim HG, Kishikawa S, Higgins AW, Seong IS, Donovan DJ, Shen Y, Lally E, Weiss LA, Najm J, Kutsche K, Descartes M, Holt L, Braddock S, Troxell R, Kaplan L, Volkmar F, Klin A, Tsatsanis K, Harris DJ, Noens I, Pauls DL, Daly MJ, MacDonald ME, Morton CC, Quade BJ, Gusella JF.

Am J Hum Genet. 2008 Jan;82(1):199-207. doi: 10.1016/j.ajhg.2007.09.011.

6.

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.

7.

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.

8.

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.

9.

Contribution of SHANK3 mutations to autism spectrum disorder.

Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer SW.

Am J Hum Genet. 2007 Dec;81(6):1289-97.

10.

Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families.

Losh M, Childress D, Lam K, Piven J.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):424-33.

11.

Disruption of cerebral cortex MET signaling in autism spectrum disorder.

Campbell DB, D'Oronzio R, Garbett K, Ebert PJ, Mirnics K, Levitt P, Persico AM.

Ann Neurol. 2007 Sep;62(3):243-50.

PMID:
17696172
12.

[Investigation of the behavioural phenotype of parents of autistic children through the new FAQ self-report].

Piana H, Fortin C, Noulhiane M, Golse B, Robel L.

Encephale. 2007 May-Jun;33(3 Pt 1):285-92. French.

PMID:
17675925
13.

Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.

Ashley-Koch AE, Jaworski J, Ma DQ, Mei H, Ritchie MD, Skaar DA, Robert Delong G, Worley G, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA.

Psychiatr Genet. 2007 Aug;17(4):221-6.

PMID:
17621165
14.

Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.

Wassink TH, Hazlett HC, Epping EA, Arndt S, Dager SR, Schellenberg GD, Dawson G, Piven J.

Arch Gen Psychiatry. 2007 Jun;64(6):709-17.

PMID:
17548752
15.

Autism: highly heritable but not inherited.

Beaudet AL.

Nat Med. 2007 May;13(5):534-6. No abstract available.

PMID:
17479094
16.

Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.

Buxbaum JD, Cai G, Chaste P, Nygren G, Goldsmith J, Reichert J, Anckarsäter H, Rastam M, Smith CJ, Silverman JM, Hollander E, Leboyer M, Gillberg C, Verloes A, Betancur C.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):484-91.

17.

Early social-communicative and cognitive development of younger siblings of children with autism spectrum disorders.

Stone WL, McMahon CR, Yoder PJ, Walden TA.

Arch Pediatr Adolesc Med. 2007 Apr;161(4):384-90.

PMID:
17404136
18.

A quantitative trait locus analysis of social responsiveness in multiplex autism families.

Duvall JA, Lu A, Cantor RM, Todd RD, Constantino JN, Geschwind DH.

Am J Psychiatry. 2007 Apr;164(4):656-62. Erratum in: Am J Psychiatry. 2007 Jun;164(6):980.

PMID:
17403980
19.

Strong association of de novo copy number mutations with autism.

Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimäki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M.

Science. 2007 Apr 20;316(5823):445-9.

20.

Mendelian Inheritance in Man and its online version, OMIM.

McKusick VA.

Am J Hum Genet. 2007 Apr;80(4):588-604. No abstract available.

Items per page

Supplemental Content

Support Center