125 related articles for article (PubMed ID: 11086979)
1. Identifying autism susceptibility genes.
Maestrini E; Paul A; Monaco AP; Bailey A
Neuron; 2000 Oct; 28(1):19-24. PubMed ID: 11086979
[No Abstract] [Full Text] [Related]
2. Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
; 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. PubMed ID: 17322880
[TBL] [Abstract][Full Text] [Related]
3. Genomic screen and follow-up analysis for autistic disorder.
Shao Y; Wolpert CM; Raiford KL; Menold MM; Donnelly SL; Ravan SA; Bass MP; McClain C; von Wendt L; Vance JM; Abramson RH; Wright HH; Ashley-Koch A; Gilbert JR; DeLong RG; Cuccaro ML; Pericak-Vance MA
Am J Med Genet; 2002 Jan; 114(1):99-105. PubMed ID: 11840513
[TBL] [Abstract][Full Text] [Related]
4. An autosomal genomic screen for autism.
Collaborative Linkage Study of Autism
Am J Med Genet; 2001 Dec; 105(8):609-15. PubMed ID: 11811142
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
Wassink TH; Piven J; Vieland VJ; Jenkins L; Frantz R; Bartlett CW; Goedken R; Childress D; Spence MA; Smith M; Sheffield VC
Am J Med Genet B Neuropsychiatr Genet; 2005 Jul; 136B(1):36-44. PubMed ID: 15892143
[TBL] [Abstract][Full Text] [Related]
6. Ordered-subset analysis of savant skills in autism for 15q11-q13.
Ma DQ; Jaworski J; Menold MM; Donnelly S; Abramson RK; Wright HH; Delong GR; Gilbert JR; Pericak-Vance MA; Cuccaro ML
Am J Med Genet B Neuropsychiatr Genet; 2005 May; 135B(1):38-41. PubMed ID: 15756693
[TBL] [Abstract][Full Text] [Related]
7. Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.
Ramoz N; Reichert JG; Smith CJ; Silverman JM; Bespalova IN; Davis KL; Buxbaum JD
Am J Psychiatry; 2004 Apr; 161(4):662-9. PubMed ID: 15056512
[TBL] [Abstract][Full Text] [Related]
8. A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.
DeLisi LE; Shaw SH; Crow TJ; Shields G; Smith AB; Larach VW; Wellman N; Loftus J; Nanthakumar B; Razi K; Stewart J; Comazzi M; Vita A; Heffner T; Sherrington R
Am J Psychiatry; 2002 May; 159(5):803-12. PubMed ID: 11986135
[TBL] [Abstract][Full Text] [Related]
9. Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
Shao Y; Cuccaro ML; Hauser ER; Raiford KL; Menold MM; Wolpert CM; Ravan SA; Elston L; Decena K; Donnelly SL; Abramson RK; Wright HH; DeLong GR; Gilbert JR; Pericak-Vance MA
Am J Hum Genet; 2003 Mar; 72(3):539-48. PubMed ID: 12567325
[TBL] [Abstract][Full Text] [Related]
10. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.
Hum Mol Genet; 1998 Mar; 7(3):571-8. PubMed ID: 9546821
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD).
Kantojärvi K; Kotala I; Rehnström K; Ylisaukko-Oja T; Vanhala R; von Wendt TN; von Wendt L; Järvelä I
Autism Res; 2011 Jun; 4(3):228-33. PubMed ID: 21384559
[TBL] [Abstract][Full Text] [Related]
13. Autism: recent molecular genetic advances.
Lamb JA; Moore J; Bailey A; Monaco AP
Hum Mol Genet; 2000 Apr; 9(6):861-8. PubMed ID: 10767308
[TBL] [Abstract][Full Text] [Related]
14. Incorporating language phenotypes strengthens evidence of linkage to autism.
Bradford Y; Haines J; Hutcheson H; Gardiner M; Braun T; Sheffield V; Cassavant T; Huang W; Wang K; Vieland V; Folstein S; Santangelo S; Piven J
Am J Med Genet; 2001 Aug; 105(6):539-47. PubMed ID: 11496372
[TBL] [Abstract][Full Text] [Related]
15. Genetic studies in autistic disorder and chromosome 15.
Bass MP; Menold MM; Wolpert CM; Donnelly SL; Ravan SA; Hauser ER; Maddox LO; Vance JM; Abramson RK; Wright HH; Gilbert JR; Cuccaro ML; DeLong GR; Pericak-Vance MA
Neurogenetics; 2000 Mar; 2(4):219-26. PubMed ID: 10983717
[TBL] [Abstract][Full Text] [Related]
16. Autism: an overview of genetic aetiology.
Bayou N; M'rad R; Ahlem B; Béchir Helayem M; Chaabouni H
Tunis Med; 2008 Jun; 86(6):573-8. PubMed ID: 19216451
[TBL] [Abstract][Full Text] [Related]
17. Incorporating language phenotypes strengthens evidence of linkage to autism.
Collaborative Linkage Study of Autism
Am J Med Genet; 2001 Dec; 105(8):539-47. PubMed ID: 11811141
[TBL] [Abstract][Full Text] [Related]
18. Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.
Wassink TH; Vieland VJ; Sheffield VC; Bartlett CW; Goedken R; Childress D; Piven J
Psychiatr Genet; 2008 Apr; 18(2):85-91. PubMed ID: 18349700
[TBL] [Abstract][Full Text] [Related]
19. The genetics of autism spectrum disorders.
Grice DE; Buxbaum JD
Neuromolecular Med; 2006; 8(4):451-60. PubMed ID: 17028369
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]