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Results: 1 to 20 of 36

1.

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.

Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, Martin ER, Hussman JP, Gilbert JR, Cuccaro ML, Haines JL, Pericak-Vance MA.

Ann Hum Genet. 2009 May;73(Pt 3):263-73. doi: 10.1111/j.1469-1809.2009.00523.x.

PMID:
19456320
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):528-33. doi: 10.1038/nature07999. Epub 2009 Apr 28.

PMID:
19404256
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Examination of association to autism of common genetic variationin genes related to dopamine.

Anderson BM, Schnetz-Boutaud N, Bartlett J, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL.

Autism Res. 2008 Dec;1(6):364-9. doi: 10.1002/aur.55.

PMID:
19360691
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Examination of association of genes in the serotonin system to autism.

Anderson BM, Schnetz-Boutaud NC, Bartlett J, Wotawa AM, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL.

Neurogenetics. 2009 Jul;10(3):209-16. doi: 10.1007/s10048-009-0171-7. Epub 2009 Jan 28.

PMID:
19184136
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Metabolism of tetrahydrobiopterin: its relevance in monoaminergic neurons and neurological disorders.

Ichinose H, Nomura T, Sumi-Ichinose C.

Chem Rec. 2008;8(6):378-85. doi: 10.1002/tcr.20166.

PMID:
19107867
[PubMed - indexed for MEDLINE]
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.

PMID:
18184952
[PubMed - indexed for MEDLINE]
Free Article
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.

PMID:
18179894
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Genetic heterogeneity is not as threatening as you might think.

Ritchie MD, Edwards TL, Fanelli TJ, Motsinger AA.

Genet Epidemiol. 2007 Nov;31(7):797-800. Review. No abstract available.

PMID:
17654613
[PubMed - indexed for MEDLINE]
9.

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]
10.

Analysis of plasma biopterin levels in psychiatric disorders suggests a common BH4 deficit in schizophrenia and schizoaffective disorder.

Richardson MA, Read LL, Reilly MA, Clelland JD, Clelland CL.

Neurochem Res. 2007 Jan;32(1):107-13. Epub 2006 Dec 9.

PMID:
17160504
[PubMed - indexed for MEDLINE]
11.

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups.

Collins AL, Ma D, Whitehead PL, Martin ER, Wright HH, Abramson RK, Hussman JP, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA.

Neurogenetics. 2006 Jul;7(3):167-74. Epub 2006 Jun 13.

PMID:
16770606
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

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]
13.

Tetrahydrobiopterin in the treatment of children with autistic disorder: a double-blind placebo-controlled crossover study.

Danfors T, von Knorring AL, Hartvig P, Langstrom B, Moulder R, Stromberg B, Torstenson R, Wester U, Watanabe Y, Eeg-Olofsson O.

J Clin Psychopharmacol. 2005 Oct;25(5):485-9.

PMID:
16160627
[PubMed - indexed for MEDLINE]
14.

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.

Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA.

Am J Hum Genet. 2005 Sep;77(3):377-88. Epub 2005 Jul 15.

PMID:
16080114
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Replication of autism linkage: fine-mapping peak at 17q21.

Cantor RM, Kono N, Duvall JA, Alvarez-Retuerto A, Stone JL, Alarcón M, Nelson SF, Geschwind DH.

Am J Hum Genet. 2005 Jun;76(6):1050-6. Epub 2005 Apr 1.

PMID:
15877280
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Haploview: analysis and visualization of LD and haplotype maps.

Barrett JC, Fry B, Maller J, Daly MJ.

Bioinformatics. 2005 Jan 15;21(2):263-5. Epub 2004 Aug 5.

PMID:
15297300
[PubMed - indexed for MEDLINE]
Free Article
17.

Molecular genetics of autism spectrum disorder.

Veenstra-VanderWeele J, Cook EH Jr.

Mol Psychiatry. 2004 Sep;9(9):819-32. Review.

PMID:
15197396
[PubMed - indexed for MEDLINE]
18.

Genotype-based association test for general pedigrees: the genotype-PDT.

Martin ER, Bass MP, Gilbert JR, Pericak-Vance MA, Hauser ER.

Genet Epidemiol. 2003 Nov;25(3):203-13.

PMID:
14557988
[PubMed - indexed for MEDLINE]
19.

Epidemiological surveys of autism and other pervasive developmental disorders: an update.

Fombonne E.

J Autism Dev Disord. 2003 Aug;33(4):365-82. Review.

PMID:
12959416
[PubMed - indexed for MEDLINE]
20.

Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.

Oliveira SA, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons KE, Pahwa R, Stern MB, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Scott BL, Goetz CG, Small GW, Mastaglia FL, Stajich JM, Zhang F, Booze MW, Reaves JA, Middleton LT, Haines JL, Pericak-Vance MA, Vance JM, Martin ER.

Arch Neurol. 2003 Jul;60(7):975-80.

PMID:
12873854
[PubMed - indexed for MEDLINE]

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