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Results: 20

1.

Identifying autism loci and genes by tracing recent shared ancestry.

Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA.

Science. 2008 Jul 11;321(5886):218-23. doi: 10.1126/science.1157657. Erratum in: Science. 2010 Dec 24;330(6012):1746.

PMID:
18621663
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Advances in autism genetics: on the threshold of a new neurobiology.

Abrahams BS, Geschwind DH.

Nat Rev Genet. 2008 May;9(5):341-55. doi: 10.1038/nrg2346. Review. Erratum in: Nat Rev Genet. 2008 Jun;9(6):493.

PMID:
18414403
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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. Epub 2008 Jan 17.

PMID:
18252227
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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. Epub 2007 Mar 15.

PMID:
17363630
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Autism Genome Project Consortium, Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Rogé B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bölte S, Feineis-Matthews S, Herbrecht E, Schmötzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Langemeijer M, Hijmans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A, Meyer KJ.

Nat Genet. 2007 Mar;39(3):319-28. Epub 2007 Feb 18. Erratum in: Nat Genet. 2007 Oct;39(10):1285. Meyer, Kacie J [added]; Koop, Frederike [corrected to Koop, Frederieke]; Langemeijer, Marjolijn [corrected to Langemeijer, Marjolein]; Hijimans, Channa [corrected to Hijmans, Channa].

PMID:
17322880
[PubMed - indexed for MEDLINE]
6.

Evaluation of a methodology for a collaborative multiple source surveillance network for autism spectrum disorders--Autism and Developmental Disabilities Monitoring Network, 14 sites, United States, 2002.

Van Naarden Braun K, Pettygrove S, Daniels J, Miller L, Nicholas J, Baio J, Schieve L, Kirby RS, Washington A, Brocksen S, Rahbar H, Rice C; Centers for Disease Control and Prevention.

MMWR Surveill Summ. 2007 Feb 9;56(1):29-40.

PMID:
17287716
[PubMed - indexed for MEDLINE]
7.

A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence.

Yang MS, Gill M.

Int J Dev Neurosci. 2007 Apr;25(2):69-85. Epub 2006 Dec 20. Review.

PMID:
17236739
[PubMed - indexed for MEDLINE]
8.

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.

Durand CM, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F, Nygren G, Rastam M, Gillberg IC, Anckarsäter H, Sponheim E, Goubran-Botros H, Delorme R, Chabane N, Mouren-Simeoni MC, de Mas P, Bieth E, Rogé B, Héron D, Burglen L, Gillberg C, Leboyer M, Bourgeron T.

Nat Genet. 2007 Jan;39(1):25-7. Epub 2006 Dec 17.

PMID:
17173049
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

The genetics of autistic disorders and its clinical relevance: a review of the literature.

Freitag CM.

Mol Psychiatry. 2007 Jan;12(1):2-22. Epub 2006 Oct 10. Review.

PMID:
17033636
[PubMed - indexed for MEDLINE]
10.

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues.

Persico AM, Bourgeron T.

Trends Neurosci. 2006 Jul;29(7):349-58. Epub 2006 Jun 30. Review.

PMID:
16808981
[PubMed - indexed for MEDLINE]
11.

Epidemiology of autistic disorder and other pervasive developmental disorders.

Fombonne E.

J Clin Psychiatry. 2005;66 Suppl 10:3-8.

PMID:
16401144
[PubMed - indexed for MEDLINE]
12.

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.

Vorstman JA, Staal WG, van Daalen E, van Engeland H, Hochstenbach PF, Franke L.

Mol Psychiatry. 2006 Jan;11(1):1, 18-28. Review.

PMID:
16205736
[PubMed - indexed for MEDLINE]
13.

Specific genetic disorders and autism: clinical contribution towards their identification.

Cohen D, Pichard N, Tordjman S, Baumann C, Burglen L, Excoffier E, Lazar G, Mazet P, Pinquier C, Verloes A, Héron D.

J Autism Dev Disord. 2005 Feb;35(1):103-16. Review.

PMID:
15796126
[PubMed - indexed for MEDLINE]
14.

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.

Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T; Paris Autism Research International Sibpair Study.

Nat Genet. 2003 May;34(1):27-9.

PMID:
12669065
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

Rogers SJ, Wehner DE, Hagerman R.

J Dev Behav Pediatr. 2001 Dec;22(6):409-17.

PMID:
11773805
[PubMed - indexed for MEDLINE]
16.

Genetics of autism: complex aetiology for a heterogeneous disorder.

Folstein SE, Rosen-Sheidley B.

Nat Rev Genet. 2001 Dec;2(12):943-55. Review.

PMID:
11733747
[PubMed - indexed for MEDLINE]
17.

Pervasive developmental disorders in preschool children.

Chakrabarti S, Fombonne E.

JAMA. 2001 Jun 27;285(24):3093-9.

PMID:
11427137
[PubMed - indexed for MEDLINE]
18.

Autism spectrum disorders.

Lord C, Cook EH, Leventhal BL, Amaral DG.

Neuron. 2000 Nov;28(2):355-63. Review. No abstract available.

PMID:
11144346
[PubMed - indexed for MEDLINE]
Free Article
19.

A broader phenotype of autism: the clinical spectrum in twins.

Le Couteur A, Bailey A, Goode S, Pickles A, Robertson S, Gottesman I, Rutter M.

J Child Psychol Psychiatry. 1996 Oct;37(7):785-801.

PMID:
8923222
[PubMed - indexed for MEDLINE]
20.

Autism as a strongly genetic disorder: evidence from a British twin study.

Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E, Rutter M.

Psychol Med. 1995 Jan;25(1):63-77.

PMID:
7792363
[PubMed - indexed for MEDLINE]

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