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Items: 1 to 20 of 100

1.

A unified genetic theory for sporadic and inherited autism.

Zhao X, Leotta A, Kustanovich V, Lajonchere C, Geschwind DH, Law K, Law P, Qiu S, Lord C, Sebat J, Ye K, Wigler M.

Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12831-6. Epub 2007 Jul 25.

2.

A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families.

Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H.

Autism Res. 2010 Apr;3(2):47-52. doi: 10.1002/aur.119.

PMID:
20437600
3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
4.

Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins.

Werling DM, Geschwind DH.

Mol Autism. 2015 May 13;6:27. doi: 10.1186/s13229-015-0004-5. eCollection 2015.

5.

Changing the landscape of autism research: the autism genetic resource exchange.

Lajonchere CM; AGRE Consortium..

Neuron. 2010 Oct 21;68(2):187-91. doi: 10.1016/j.neuron.2010.10.009.

6.

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. Epub 2008 Jan 9.

7.

[Molecular aspects of autism spectrum disorders].

Lisik MZ.

Psychiatr Pol. 2014 Jul-Aug;48(4):689-700. Review. Polish.

PMID:
25314797
8.

DE NOVO MUTATIONS IN AUTISM IMPLICATE THE SYNAPTIC ELIMINATION NETWORK.

Ram Venkataraman G, O'Connell C, Egawa F, Kashef-Haghighi D, Wall DP.

Pac Symp Biocomput. 2016;22:521-532.

9.

Brief Report: Relationship between non-verbal IQ and gender in autism.

Banach R, Thompson A, Szatmari P, Goldberg J, Tuff L, Zwaigenbaum L, Mahoney W.

J Autism Dev Disord. 2009 Jan;39(1):188-93. doi: 10.1007/s10803-008-0612-4. Epub 2008 Jul 2.

PMID:
18594959
10.

Male-to-male transmission in extended pedigrees with multiple cases of autism.

Hallmayer J, Spiker D, Lotspeich L, McMahon WM, Petersen PB, Nicholas P, Pingree C, Ciaranello RD.

Am J Med Genet. 1996 Feb 16;67(1):13-8.

PMID:
8678108
11.

Sex differences in repetitive stereotyped behaviors in autism: implications for genetic liability.

Szatmari P, Liu XQ, Goldberg J, Zwaigenbaum L, Paterson AD, Woodbury-Smith M, Georgiades S, Duku E, Thompson A.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):5-12. doi: 10.1002/ajmg.b.31238. Epub 2011 Nov 16.

PMID:
22095612
12.

The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling.

Ritvo ER, Jorde LB, Mason-Brothers A, Freeman BJ, Pingree C, Jones MB, McMahon WM, Petersen PB, Jenson WR, Mo A.

Am J Psychiatry. 1989 Aug;146(8):1032-6.

PMID:
2750975
13.

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.

Hettinger JA, Liu X, Schwartz CE, Michaelis RC, Holden JJ.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):628-36. doi: 10.1002/ajmg.b.30655.

PMID:
18205172
14.

Complex segregation analysis of autism.

Jorde LB, Hasstedt SJ, Ritvo ER, Mason-Brothers A, Freeman BJ, Pingree C, McMahon WM, Petersen B, Jenson WR, Mo A.

Am J Hum Genet. 1991 Nov;49(5):932-8.

15.
16.

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.

Molloy CA, Keddache M, Martin LJ.

Mol Psychiatry. 2005 Aug;10(8):741-6.

PMID:
15940295
17.

Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.

Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, Lindenbaum P, Benajjou A, Fontaine K, Vazart C, Gesnouin P, Brooks P, Hager J.

BMC Med Genet. 2007 Dec 6;8:74.

18.

Effects of familial risk factors and place of birth on the risk of autism: a nationwide register-based study.

Lauritsen MB, Pedersen CB, Mortensen PB.

J Child Psychol Psychiatry. 2005 Sep;46(9):963-71.

PMID:
16108999
19.

Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities.

Kolevzon A, Cai G, Soorya L, Takahashi N, Grodberg D, Kajiwara Y, Willner JP, Tryfon A, Buxbaum JD.

Brain Res. 2011 Mar 22;1380:98-105. doi: 10.1016/j.brainres.2010.11.005. Epub 2010 Nov 6. Review.

PMID:
21062623
20.

An autosomal genomic screen for autism.

Collaborative Linkage Study of Autism..

Am J Med Genet. 2001 Dec 8;105(8):609-15.

PMID:
11811142

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