131 related articles for article (PubMed ID: 16556609)
1. An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.
Vincent JB; Horike SI; Choufani S; Paterson AD; Roberts W; Szatmari P; Weksberg R; Fernandez B; Scherer SW
J Med Genet; 2006 May; 43(5):429-34. PubMed ID: 16556609
[TBL] [Abstract][Full Text] [Related]
2. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
Vincent JB; Choufani S; Horike S; Stachowiak B; Li M; Dill FJ; Marshall C; Hrynchak M; Pewsey E; Ukadike KC; Friedman JM; Srivastava AK; Scherer SW
Psychiatr Genet; 2008 Jun; 18(3):101-9. PubMed ID: 18496206
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genetic studies of autistic disorder and chromosome 7.
Ashley-Koch A; Wolpert CM; Menold MM; Zaeem L; Basu S; Donnelly SL; Ravan SA; Powell CM; Qumsiyeh MB; Aylsworth AS; Vance JM; Gilbert JR; Wright HH; Abramson RK; DeLong GR; Cuccaro ML; Pericak-Vance MA
Genomics; 1999 Nov; 61(3):227-36. PubMed ID: 10552924
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Evaluation of q11-q13 locus of chromosome 15 aberrations and polymorphisms in the B3 subunit of the GABA-A receptor gene (GABRB3) in autistic patients].
Słopień A; Rajewski A; Budny B; Czerski P
Psychiatr Pol; 2002; 36(5):779-91. PubMed ID: 12491987
[TBL] [Abstract][Full Text] [Related]
7. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
Lukusa T; Vermeesch JR; Holvoet M; Fryns JP; Devriendt K
Genet Couns; 2004; 15(3):293-301. PubMed ID: 15517821
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
[TBL] [Abstract][Full Text] [Related]
10. Possible association between the androgen receptor gene and autism spectrum disorder.
Henningsson S; Jonsson L; Ljunggren E; Westberg L; Gillberg C; Råstam M; Anckarsäter H; Nygren G; Landén M; Thuresson K; Betancur C; Leboyer M; Gillberg C; Eriksson E; Melke J
Psychoneuroendocrinology; 2009 Jun; 34(5):752-61. PubMed ID: 19167832
[TBL] [Abstract][Full Text] [Related]
11. No association between the ryanodine receptor 3 gene and autism in a Japanese population.
Tochigi M; Kato C; Ohashi J; Koishi S; Kawakubo Y; Yamamoto K; Matsumoto H; Hashimoto O; Kim SY; Watanabe K; Kano Y; Nanba E; Kato N; Sasaki T
Psychiatry Clin Neurosci; 2008 Jun; 62(3):341-4. PubMed ID: 18588595
[TBL] [Abstract][Full Text] [Related]
12. Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations.
Vorsanova SG; Iourov IY; Demidova IA; Kolotii AD; Soloviev IV; Yurov YB
Tsitol Genet; 2006; 40(3):45-8. PubMed ID: 16933852
[TBL] [Abstract][Full Text] [Related]
13. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
Hirsch B; Baldinger S
Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
[TBL] [Abstract][Full Text] [Related]
14. Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility.
Cukier HN; Skaar DA; Rayner-Evans MY; Konidari I; Whitehead PL; Jaworski JM; Cuccaro ML; Pericak-Vance MA; Gilbert JR
Autism Res; 2009 Oct; 2(5):258-66. PubMed ID: 19877165
[TBL] [Abstract][Full Text] [Related]
15. Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.
Floris C; Rassu S; Boccone L; Gasperini D; Cao A; Crisponi L
Eur J Hum Genet; 2008 Jun; 16(6):696-704. PubMed ID: 18270536
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
Battaglia A; Brothman AR; Carey JC
Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
[TBL] [Abstract][Full Text] [Related]
18. Recurrent 16p11.2 microdeletions in autism.
Kumar RA; KaraMohamed S; Sudi J; Conrad DF; Brune C; Badner JA; Gilliam TC; Nowak NJ; Cook EH; Dobyns WB; Christian SL
Hum Mol Genet; 2008 Feb; 17(4):628-38. PubMed ID: 18156158
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]