503 related articles for article (PubMed ID: 19216451)
21. Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13.
Nurmi EL; Dowd M; Tadevosyan-Leyfer O; Haines JL; Folstein SE; Sutcliffe JS
J Am Acad Child Adolesc Psychiatry; 2003 Jul; 42(7):856-63. PubMed ID: 12819446
[TBL] [Abstract][Full Text] [Related]
22. [Genetic studies in communication disorders].
Narbona J; Patiño A
Rev Neurol; 2002 Jul 1-15; 35(1):32-6. PubMed ID: 12389190
[TBL] [Abstract][Full Text] [Related]
23. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
Xu S; Han JC; Morales A; Menzie CM; Williams K; Fan YS
Cytogenet Genome Res; 2008; 122(2):181-7. PubMed ID: 19096215
[TBL] [Abstract][Full Text] [Related]
24. Epigenetics of autism spectrum disorders.
Schanen NC
Hum Mol Genet; 2006 Oct; 15 Spec No 2():R138-50. PubMed ID: 16987877
[TBL] [Abstract][Full Text] [Related]
25. Heterogeneity and the genetics of autism.
Szatmari P
J Psychiatry Neurosci; 1999 Mar; 24(2):159-65. PubMed ID: 10212560
[TBL] [Abstract][Full Text] [Related]
26. The search for autism disease genes.
Wassink TH; Brzustowicz LM; Bartlett CW; Szatmari P
Ment Retard Dev Disabil Res Rev; 2004; 10(4):272-83. PubMed ID: 15666342
[TBL] [Abstract][Full Text] [Related]
27. [Genetics of autism].
Sedlácek Z; Havlovicová M; Hrdlicka M
Cas Lek Cesk; 2002 Jun; 141(12):376-80. PubMed ID: 12238023
[TBL] [Abstract][Full Text] [Related]
28. Association between a GABRB3 polymorphism and autism.
Buxbaum JD; Silverman JM; Smith CJ; Greenberg DA; Kilifarski M; Reichert J; Cook EH; Fang Y; Song CY; Vitale R
Mol Psychiatry; 2002; 7(3):311-6. PubMed ID: 11920158
[TBL] [Abstract][Full Text] [Related]
29. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
[TBL] [Abstract][Full Text] [Related]
30. Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues.
Dykens EM; Sutcliffe JS; Levitt P
Ment Retard Dev Disabil Res Rev; 2004; 10(4):284-91. PubMed ID: 15666333
[TBL] [Abstract][Full Text] [Related]
31. Genetics of autism.
Cook EH
Child Adolesc Psychiatr Clin N Am; 2001 Apr; 10(2):333-50. PubMed ID: 11351802
[TBL] [Abstract][Full Text] [Related]
32. Examination of AVPR1a as an autism susceptibility gene.
Wassink TH; Piven J; Vieland VJ; Pietila J; Goedken RJ; Folstein SE; Sheffield VC
Mol Psychiatry; 2004 Oct; 9(10):968-72. PubMed ID: 15098001
[TBL] [Abstract][Full Text] [Related]
33. Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.
Castermans D; Vermeesch JR; Fryns JP; Steyaert JG; Van de Ven WJ; Creemers JW; Devriendt K
Eur J Hum Genet; 2007 Apr; 15(4):422-31. PubMed ID: 17290275
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
Gilling M; Lauritsen MB; Møller M; Henriksen KF; Vicente A; Oliveira G; Cintin C; Eiberg H; Andersen PS; Mors O; Rosenberg T; Brøndum-Nielsen K; Cotterill RM; Lundsteen C; Ropers HH; Ullmann R; Bache I; Tümer Z; Tommerup N
Eur J Hum Genet; 2008 Mar; 16(3):312-9. PubMed ID: 18183041
[TBL] [Abstract][Full Text] [Related]
36. Variable expression of the autism broader phenotype: findings from extended pedigrees.
Pickles A; Starr E; Kazak S; Bolton P; Papanikolaou K; Bailey A; Goodman R; Rutter M
J Child Psychol Psychiatry; 2000 May; 41(4):491-502. PubMed ID: 10836679
[TBL] [Abstract][Full Text] [Related]
37. Autism and Williams syndrome: a case report.
Herguner S; Mukaddes NM
World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145
[TBL] [Abstract][Full Text] [Related]
38. [Genetics and epigenetics in autism].
Nakayama A; Masaki S; Aoki E
Nihon Shinkei Seishin Yakurigaku Zasshi; 2006 Nov; 26(5-6):209-12. PubMed ID: 17240846
[TBL] [Abstract][Full Text] [Related]
39. Advances in behavioral genetics: mouse models of autism.
Moy SS; Nadler JJ
Mol Psychiatry; 2008 Jan; 13(1):4-26. PubMed ID: 17848915
[TBL] [Abstract][Full Text] [Related]
40. Deletion 2p25.2: a cryptic chromosome abnormality in a patient with autism and mental retardation detected using aCGH.
Lo-Castro A; Giana G; Fichera M; Castiglia L; Grillo L; Musumeci SA; Galasso C; Curatolo P
Eur J Med Genet; 2009; 52(1):67-70. PubMed ID: 18992374
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
