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Literature DB >> 20351724

Additional support for the association of SLITRK1 var321 and Tourette syndrome.

B J O'Roak, T M Morgan, D O Fishman, E Saus, P Alonso, M Gratacòs, X Estivill, O Teltsh, Y Kohn, K K Kidd, J Cho, R P Lifton, M W State.

Abstract

Entities: Chemical Disease Gene Mutation Species

Mesh：

Substances：

Year: 2010 PMID： 20351724 PMCID： PMC3292207 DOI： 10.1038/mp.2009.105

Source DB: PubMed Journal: Mol Psychiatry ISSN： 1359-4184 Impact factor: 15.992

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11 in total

1. Sequence variants in SLITRK1 are associated with Tourette's syndrome.

Authors: Jesse F Abelson; Kenneth Y Kwan; Brian J O'Roak; Danielle Y Baek; Althea A Stillman; Thomas M Morgan; Carol A Mathews; David L Pauls; Mladen-Roko Rasin; Murat Gunel; Nicole R Davis; A Gulhan Ercan-Sencicek; Danielle H Guez; John A Spertus; James F Leckman; Leon S Dure; Roger Kurlan; Harvey S Singer; Donald L Gilbert; Anita Farhi; Angeliki Louvi; Richard P Lifton; Nenad Sestan; Matthew W State
Journal: Science Date: 2005-10-14 Impact factor: 47.728

2. Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder.

Authors: J R Wendland; M R Kruse; D L Murphy
Journal: Mol Psychiatry Date: 2006-09 Impact factor: 15.992

3. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

Authors: Richard H Duerr; Kent D Taylor; Steven R Brant; John D Rioux; Mark S Silverberg; Mark J Daly; A Hillary Steinhart; Clara Abraham; Miguel Regueiro; Anne Griffiths; Themistocles Dassopoulos; Alain Bitton; Huiying Yang; Stephan Targan; Lisa Wu Datta; Emily O Kistner; L Philip Schumm; Annette T Lee; Peter K Gregersen; M Michael Barmada; Jerome I Rotter; Dan L Nicolae; Judy H Cho
Journal: Science Date: 2006-10-26 Impact factor: 47.728

4. PLINK: a tool set for whole-genome association and population-based linkage analyses.

Authors: Shaun Purcell; Benjamin Neale; Kathe Todd-Brown; Lori Thomas; Manuel A R Ferreira; David Bender; Julian Maller; Pamela Sklar; Paul I W de Bakker; Mark J Daly; Pak C Sham
Journal: Am J Hum Genet Date: 2007-07-25 Impact factor: 11.025

Review 5. MicroRNA target site polymorphisms and human disease.

Authors: Praveen Sethupathy; Francis S Collins
Journal: Trends Genet Date: 2008-09-06 Impact factor: 11.639

6. Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.

Authors: J M Scharf; P Moorjani; J Fagerness; J V Platko; C Illmann; B Galloway; E Jenike; S E Stewart; D L Pauls
Journal: Neurology Date: 2008-04-15 Impact factor: 9.910

Review 7. A genetic profile of contemporary Jewish populations.

Authors: H Ostrer
Journal: Nat Rev Genet Date: 2001-11 Impact factor: 53.242

8. Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.

Authors: E M Valente; S Povey; T T Warner; N W Wood; M B Davis
Journal: Ann Hum Genet Date: 1999-01 Impact factor: 1.670

9. LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

Authors: Cyrus P Zabetian; Carolyn M Hutter; Dora Yearout; Alexis N Lopez; Stewart A Factor; Alida Griffith; Berta C Leis; Thomas D Bird; John G Nutt; Donald S Higgins; John W Roberts; Denise M Kay; Karen L Edwards; Ali Samii; Haydeh Payami
Journal: Am J Hum Genet Date: 2006-08-17 Impact factor: 11.025

Review 10. The behavioral spectrum of Gilles de la Tourette syndrome.

Authors: Andrea Eugenio Cavanna; Serena Servo; Francesco Monaco; Mary May Robertson
Journal: J Neuropsychiatry Clin Neurosci Date: 2009 Impact factor: 2.198

26 in total

Review 1. The genetics of Tourette disorder.

Authors: Matthew W State
Journal: Curr Opin Genet Dev Date: 2011-01-27 Impact factor: 5.578

Review 2. The genetics of Tourette syndrome.

Authors: Hao Deng; Kai Gao; Joseph Jankovic
Journal: Nat Rev Neurol Date: 2012-03-13 Impact factor: 42.937

Additional support for the association of SLITRK1 var321 and Tourette syndrome.

1. Sequence variants in SLITRK1 are associated with Tourette's syndrome.

2. Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder.

3. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

4. PLINK: a tool set for whole-genome association and population-based linkage analyses.

Review 5. MicroRNA target site polymorphisms and human disease.

6. Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.

Review 7. A genetic profile of contemporary Jewish populations.

8. Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.

9. LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

Review 10. The behavioral spectrum of Gilles de la Tourette syndrome.

Review 1. The genetics of Tourette disorder.

Review 2. The genetics of Tourette syndrome.

Review 3. Protein tyrosine phosphatases PTPδ, PTPσ, and LAR: presynaptic hubs for synapse organization.

Review 4. Slitrks as emerging candidate genes involved in neuropsychiatric disorders.

Review 5. Rodent models of obsessive compulsive disorder: Evaluating validity to interpret emerging neurobiology.

6. Differential binding of antibodies in PANDAS patients to cholinergic interneurons in the striatum.

Review 7. Glutamate abnormalities in obsessive compulsive disorder: neurobiology, pathophysiology, and treatment.

Review 8. Animal models of tic disorders: a translational perspective.

9. Tourette Syndrome: Bridging the Gap between Genetics and Biology.

Review 10. Tourette syndrome and comorbid ADHD: causes and consequences.