194 related articles for article (PubMed ID: 12682296)
1. Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.
State MW; Greally JM; Cuker A; Bowers PN; Henegariu O; Morgan TM; Gunel M; DiLuna M; King RA; Nelson C; Donovan A; Anderson GM; Leckman JF; Hawkins T; Pauls DL; Lifton RP; Ward DC
Proc Natl Acad Sci U S A; 2003 Apr; 100(8):4684-9. PubMed ID: 12682296
[TBL] [Abstract][Full Text] [Related]
2. Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22.
Cuker A; State MW; King RA; Davis N; Ward DC
Am J Med Genet A; 2004 Sep; 130A(1):37-9. PubMed ID: 15368493
[TBL] [Abstract][Full Text] [Related]
3. Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.
Petek E; Windpassinger C; Vincent JB; Cheung J; Boright AP; Scherer SW; Kroisel PM; Wagner K
Am J Hum Genet; 2001 Apr; 68(4):848-58. PubMed ID: 11254443
[TBL] [Abstract][Full Text] [Related]
4. Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome.
Matsumoto N; David DE; Johnson EW; Konecki D; Burmester JK; Ledbetter DH; Weber JL
Eur J Hum Genet; 2000 Nov; 8(11):875-83. PubMed ID: 11093278
[TBL] [Abstract][Full Text] [Related]
5. Multiple childhood behavioral disorders (Tourette syndrome, multiple tics, ADD and OCD) presenting in a family with a balanced chromosome translocation (t1;8)(q21.1;q22.1).
Devor EJ; Magee HJ
Psychiatr Genet; 1999 Sep; 9(3):149-51. PubMed ID: 10551546
[No Abstract] [Full Text] [Related]
6. [Searching for Tourette's syndrome gene. Part 1. Heterogeneity of clinical phenotypes].
Kowalska A; Midro AT; Janik P; Gogol A; Służewski W; Rajewski A
Postepy Hig Med Dosw (Online); 2012 Feb; 66():85-8. PubMed ID: 22371410
[TBL] [Abstract][Full Text] [Related]
7. Candidate region for Gilles de la Tourette syndrome at 7q31.
Kroisel PM; Petek E; Emberger W; Windpassinger C; Wladika W; Wagner K
Am J Med Genet; 2001 Jul; 101(3):259-61. PubMed ID: 11424142
[TBL] [Abstract][Full Text] [Related]
8. A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD.
Bertelsen B; Melchior L; Jensen LR; Groth C; Nazaryan L; Debes NM; Skov L; Xie G; Sun W; Brøndum-Nielsen K; Kuss AW; Chen W; Tümer Z
Psychiatry Res; 2015 Feb; 225(3):268-75. PubMed ID: 25595337
[TBL] [Abstract][Full Text] [Related]
9. Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.
Boghosian-Sell L; Comings DE; Overhauser J
Am J Hum Genet; 1996 Nov; 59(5):999-1005. PubMed ID: 8900226
[TBL] [Abstract][Full Text] [Related]
10. Gilles de la Tourette's syndrome with and without obsessive-compulsive disorder compared with obsessive-compulsive disorder without tics: which symptoms discriminate?
Cath DC; Spinhoven P; van Woerkom TC; van de Wetering BJ; Hoogduin CA; Landman AD; Roos RA; Rooijmans HG
J Nerv Ment Dis; 2001 Apr; 189(4):219-28. PubMed ID: 11339317
[TBL] [Abstract][Full Text] [Related]
11. The Gilles de la Tourette syndrome: a principal component factor analytic study of a large pedigree.
Robertson MM; Cavanna AE
Psychiatr Genet; 2007 Jun; 17(3):143-52. PubMed ID: 17417057
[TBL] [Abstract][Full Text] [Related]
12. A controlled study of sensory tics in Gilles de 1a Tourette syndrome and obsessive-compulsive disorder using a structured interview.
Chee KY; Sachdev P
J Neurol Neurosurg Psychiatry; 1997 Feb; 62(2):188-92. PubMed ID: 9048721
[TBL] [Abstract][Full Text] [Related]
13. Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder.
Crawford FC; Ait-Ghezala G; Morris M; Sutcliffe MJ; Hauser RA; Silver AA; Mullan MJ
Hum Genet; 2003 Jul; 113(2):154-61. PubMed ID: 12698358
[TBL] [Abstract][Full Text] [Related]
14. Tourette syndrome, obsessive compulsive behavior, and dysmorphic features in a patient with deletions at chromosome 18q22.1 and chromosome 13q12.3-q13.1.
Bhatti D; Balasetti V; Malgireddy K; Rush ET; Torres-Russotto D
Parkinsonism Relat Disord; 2016 Nov; 32():133-134. PubMed ID: 27637283
[No Abstract] [Full Text] [Related]
15. CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.
Verkerk AJ; Mathews CA; Joosse M; Eussen BH; Heutink P; Oostra BA;
Genomics; 2003 Jul; 82(1):1-9. PubMed ID: 12809671
[TBL] [Abstract][Full Text] [Related]
16. Latent class analysis of gilles de la tourette syndrome using comorbidities: clinical and genetic implications.
Grados MA; Mathews CA;
Biol Psychiatry; 2008 Aug; 64(3):219-25. PubMed ID: 18359008
[TBL] [Abstract][Full Text] [Related]
17. [Genetic linkage analysis of Gilles de la Tourette Syndrome in a Colombian family].
García-Cerén JJ; Valencia-Duarte AV; Cornejo JW; Carrizosa J; Cuartas JM; Zuluaga-Espinosa NA; Bedoya G; Ruiz-Linares A
Rev Neurol; 2006 Feb 16-28; 42(4):211-6. PubMed ID: 16521059
[TBL] [Abstract][Full Text] [Related]
18. No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.
Heutink P; van de Wetering BJ; Breedveld GJ; Weber J; Sandkuyl LA; Devor EJ; Heiberg A; Niermeijer MF; Oostra BA
J Med Genet; 1990 Jul; 27(7):433-6. PubMed ID: 2395161
[TBL] [Abstract][Full Text] [Related]
19. Efficacy of a Gluten-Free Diet in the Gilles de la Tourette Syndrome: A Pilot Study.
Rodrigo L; Álvarez N; Fernández-Bustillo E; Salas-Puig J; Huerta M; Hernández-Lahoz C
Nutrients; 2018 May; 10(5):. PubMed ID: 29735930
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder.
Hooper SD; Johansson AC; Tellgren-Roth C; Stattin EL; Dahl N; Cavelier L; Feuk L
BMC Med Genet; 2012 Dec; 13():123. PubMed ID: 23253088
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
