169 related articles for article (PubMed ID: 16752361)
21. A review of endophenotypes in schizophrenia and autism: The next phase for understanding genetic etiologies.
DiLalla LF; McCrary M; Diaz E
Am J Med Genet C Semin Med Genet; 2017 Sep; 175(3):354-361. PubMed ID: 28661580
[TBL] [Abstract][Full Text] [Related]
22. Strategies for autism candidate gene analysis.
Barnby G; Monaco AP
Novartis Found Symp; 2003; 251():48-63; discussion 63-9, 109-11, 281-97. PubMed ID: 14521187
[TBL] [Abstract][Full Text] [Related]
23. Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.
Liu XQ; Paterson AD; Szatmari P;
Biol Psychiatry; 2008 Oct; 64(7):561-70. PubMed ID: 18632090
[TBL] [Abstract][Full Text] [Related]
24. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
[TBL] [Abstract][Full Text] [Related]
25. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.
Rabionet R; Jaworski JM; Ashley-Koch AE; Martin ER; Sutcliffe JS; Haines JL; Delong GR; Abramson RK; Wright HH; Cuccaro ML; Gilbert JR; Pericak-Vance MA
Neurosci Lett; 2004 Dec; 372(3):209-14. PubMed ID: 15542242
[TBL] [Abstract][Full Text] [Related]
26. Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes.
Pulver AE; Mulle J; Nestadt G; Swartz KL; Blouin JL; Dombroski B; Liang KY; Housman DE; Kazazian HH; Antonarakis SE; Lasseter VK; Wolyniec PS; Thornquist MH; McGrath JA
Mol Psychiatry; 2000 Nov; 5(6):650-3. PubMed ID: 11126395
[TBL] [Abstract][Full Text] [Related]
27. Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.
Ylisaukko-oja T; Alarcón M; Cantor RM; Auranen M; Vanhala R; Kempas E; von Wendt L; Järvelä I; Geschwind DH; Peltonen L
Ann Neurol; 2006 Jan; 59(1):145-55. PubMed ID: 16288458
[TBL] [Abstract][Full Text] [Related]
28. An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene.
Ramoz N; Cai G; Reichert JG; Silverman JM; Buxbaum JD
Am J Med Genet B Neuropsychiatr Genet; 2008 Oct; 147B(7):1152-8. PubMed ID: 18348195
[TBL] [Abstract][Full Text] [Related]
29. Evidence for multiple loci from a genome scan of autism kindreds.
Schellenberg GD; Dawson G; Sung YJ; Estes A; Munson J; Rosenthal E; Rothstein J; Flodman P; Smith M; Coon H; Leong L; Yu CE; Stodgell C; Rodier PM; Spence MA; Minshew N; McMahon WM; Wijsman EM
Mol Psychiatry; 2006 Nov; 11(11):1049-60, 979. PubMed ID: 16880825
[TBL] [Abstract][Full Text] [Related]
30. A high-density SNP genome-wide linkage scan in a large autism extended pedigree.
Allen-Brady K; Miller J; Matsunami N; Stevens J; Block H; Farley M; Krasny L; Pingree C; Lainhart J; Leppert M; McMahon WM; Coon H
Mol Psychiatry; 2009 Jun; 14(6):590-600. PubMed ID: 18283277
[TBL] [Abstract][Full Text] [Related]
31. Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.
SLI Consortium (SLIC)
Am J Hum Genet; 2004 Jun; 74(6):1225-38. PubMed ID: 15133743
[TBL] [Abstract][Full Text] [Related]
32. Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.
McCauley JL; Olson LM; Dowd M; Amin T; Steele A; Blakely RD; Folstein SE; Haines JL; Sutcliffe JS
Am J Med Genet B Neuropsychiatr Genet; 2004 May; 127B(1):104-12. PubMed ID: 15108191
[TBL] [Abstract][Full Text] [Related]
33. 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. PubMed ID: 15877280
[TBL] [Abstract][Full Text] [Related]
34. [Autism and language: some molecular aspects].
Benítez-Burraco A
Rev Neurol; 2008 Jan 1-15; 46(1):40-8. PubMed ID: 18214826
[TBL] [Abstract][Full Text] [Related]
35. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12.
Schmidt S; Scott WK; Postel EA; Agarwal A; Hauser ER; De La Paz MA; Gilbert JR; Weeks DE; Gorin MB; Haines JL; Pericak-Vance MA
BMC Genet; 2004 Jul; 5():18. PubMed ID: 15238159
[TBL] [Abstract][Full Text] [Related]
36. Genome-wide scan of bipolar disorder and investigation of population stratification effects on linkage: support for susceptibility loci at 4q21, 7q36, 9p21, 12q24, 14q24, and 16p13.
Cassidy F; Zhao C; Badger J; Claffey E; Dobrin S; Roche S; McKeon P
Am J Med Genet B Neuropsychiatr Genet; 2007 Sep; 144B(6):791-801. PubMed ID: 17455214
[TBL] [Abstract][Full Text] [Related]
37. 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. PubMed ID: 19360691
[TBL] [Abstract][Full Text] [Related]
38. A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
International Molecular Genetic Study of Autism Consortium (IMGSAC)
Am J Hum Genet; 2001 Sep; 69(3):570-81. PubMed ID: 11481586
[TBL] [Abstract][Full Text] [Related]
39. The WNT2 gene polymorphism associated with speech delay inherent to autism.
Lin PI; Chien YL; Wu YY; Chen CH; Gau SS; Huang YS; Liu SK; Tsai WC; Chiu YN
Res Dev Disabil; 2012; 33(5):1533-40. PubMed ID: 22522212
[TBL] [Abstract][Full Text] [Related]
40. Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.
Sutcliffe JS; Delahanty RJ; Prasad HC; McCauley JL; Han Q; Jiang L; Li C; Folstein SE; Blakely RD
Am J Hum Genet; 2005 Aug; 77(2):265-79. PubMed ID: 15995945
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
