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Items: 1 to 20 of 31

1.

Genome-wide association study of Tourette's syndrome.

Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, Davis LK, Han B, Crane J, Moorjani P, Crenshaw AT, Parkin MA, Reus VI, Lowe TL, Rangel-Lugo M, Chouinard S, Dion Y, Girard S, Cath DC, Smit JH, King RA, Fernandez TV, Leckman JF, Kidd KK, Kidd JR, Pakstis AJ, State MW, Herrera LD, Romero R, Fournier E, Sandor P, Barr CL, Phan N, Gross-Tsur V, Benarroch F, Pollak Y, Budman CL, Bruun RD, Erenberg G, Naarden AL, Lee PC, Weiss N, Kremeyer B, Berrío GB, Campbell DD, Cardona Silgado JC, Ochoa WC, Mesa Restrepo SC, Muller H, Valencia Duarte AV, Lyon GJ, Leppert M, Morgan J, Weiss R, Grados MA, Anderson K, Davarya S, Singer H, Walkup J, Jankovic J, Tischfield JA, Heiman GA, Gilbert DL, Hoekstra PJ, Robertson MM, Kurlan R, Liu C, Gibbs JR, Singleton A; North American Brain Expression Consortium, Hardy J; UK Human Brain Expression Database, Strengman E, Ophoff RA, Wagner M, Moessner R, Mirel DB, Posthuma D, Sabatti C, Eskin E, Conti DV, Knowles JA, Ruiz-Linares A, Rouleau GA, Purcell S, Heutink P, Oostra BA, McMahon WM, Freimer NB, Cox NJ, Pauls DL.

Mol Psychiatry. 2013 Jun;18(6):721-8. doi: 10.1038/mp.2012.69. Epub 2012 Aug 14.

2.

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.

Fernandez TV, Sanders SJ, Yurkiewicz IR, Ercan-Sencicek AG, Kim YS, Fishman DO, Raubeson MJ, Song Y, Yasuno K, Ho WS, Bilguvar K, Glessner J, Chu SH, Leckman JF, King RA, Gilbert DL, Heiman GA, Tischfield JA, Hoekstra PJ, Devlin B, Hakonarson H, Mane SM, Günel M, State MW.

Biol Psychiatry. 2012 Mar 1;71(5):392-402. doi: 10.1016/j.biopsych.2011.09.034. Epub 2011 Dec 14.

3.

The genetics of Tourette disorder.

State MW.

Curr Opin Genet Dev. 2011 Jun;21(3):302-9. doi: 10.1016/j.gde.2011.01.007. Epub 2011 Jan 27. Review.

4.

The genetics of child psychiatric disorders: focus on autism and Tourette syndrome.

State MW.

Neuron. 2010 Oct 21;68(2):254-69. doi: 10.1016/j.neuron.2010.10.004. Review.

5.

L-histidine decarboxylase and Tourette's syndrome.

Ercan-Sencicek AG, Stillman AA, Ghosh AK, Bilguvar K, O'Roak BJ, Mason CE, Abbott T, Gupta A, King RA, Pauls DL, Tischfield JA, Heiman GA, Singer HS, Gilbert DL, Hoekstra PJ, Morgan TM, Loring E, Yasuno K, Fernandez T, Sanders S, Louvi A, Cho JH, Mane S, Colangelo CM, Biederer T, Lifton RP, Gunel M, State MW.

N Engl J Med. 2010 May 20;362(20):1901-8. doi: 10.1056/NEJMoa0907006. Epub 2010 May 5.

6.

Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate.

Herzberg I, Valencia-Duarte AV, Kay VA, White DJ, Müller H, Rivas IC, Mesa SC, Cuartas M, García J, Bedoya G, Cornejo W, Ruiz-Linares A, Kremeyer B.

Psychiatr Genet. 2010 Aug;20(4):179-83. doi: 10.1097/YPG.0b013e32833a215a.

PMID:
20431429
7.

Tourette syndrome is associated with recurrent exonic copy number variants.

Sundaram SK, Huq AM, Wilson BJ, Chugani HT.

Neurology. 2010 May 18;74(20):1583-90. doi: 10.1212/WNL.0b013e3181e0f147. Epub 2010 Apr 28.

8.

Copy number variation in Tourette syndrome: another case of neurodevelopmental generalist genes?

Scharf JM, Mathews CA.

Neurology. 2010 May 18;74(20):1564-5. doi: 10.1212/WNL.0b013e3181e24161. Epub 2010 Apr 28. No abstract available.

PMID:
20427746
9.

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

Clarke RA, Fang ZM, Diwan AD, Gilbert DL.

Case Rep Med. 2009;2009:361518. doi: 10.1155/2009/361518. Epub 2009 Dec 22.

10.

The genetics of Tourette syndrome: a review.

O'Rourke JA, Scharf JM, Yu D, Pauls DL.

J Psychosom Res. 2009 Dec;67(6):533-45. doi: 10.1016/j.jpsychores.2009.06.006. Epub 2009 Sep 30. Review.

11.

Copy-number variants in neurodevelopmental disorders: promises and challenges.

Merikangas AK, Corvin AP, Gallagher L.

Trends Genet. 2009 Dec;25(12):536-44. doi: 10.1016/j.tig.2009.10.006. Epub 2009 Nov 10. Review.

PMID:
19910074
12.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, Miller J, Posey DJ, Michaels S, Kolevzon A, Silverman JM, Bernier R, Levy SE, Schultz RT, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SF, Bucan M, Cook EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):569-73. doi: 10.1038/nature07953. Epub 2009 Apr 28.

13.

Population analysis of large copy number variants and hotspots of human genetic disease.

Itsara A, Cooper GM, Baker C, Girirajan S, Li J, Absher D, Krauss RM, Myers RM, Ridker PM, Chasman DI, Mefford H, Ying P, Nickerson DA, Eichler EE.

Am J Hum Genet. 2009 Feb;84(2):148-61. doi: 10.1016/j.ajhg.2008.12.014. Epub 2009 Jan 22.

14.

Collagens in the developing and diseased nervous system.

Hubert T, Grimal S, Carroll P, Fichard-Carroll A.

Cell Mol Life Sci. 2009 Apr;66(7):1223-38. doi: 10.1007/s00018-008-8561-9. Review.

PMID:
19031044
15.

Recurrent CNVs disrupt three candidate genes in schizophrenia patients.

Vrijenhoek T, Buizer-Voskamp JE, van der Stelt I, Strengman E; Genetic Risk and Outcome in Psychosis (GROUP) Consortium, Sabatti C, Geurts van Kessel A, Brunner HG, Ophoff RA, Veltman JA.

Am J Hum Genet. 2008 Oct;83(4):504-10. doi: 10.1016/j.ajhg.2008.09.011.

16.

Novel roles for collagens in wiring the vertebrate nervous system.

Fox MA.

Curr Opin Cell Biol. 2008 Oct;20(5):508-13. doi: 10.1016/j.ceb.2008.05.003. Epub 2008 Jun 21. Review.

PMID:
18573651
17.

Strong association of de novo copy number mutations with sporadic schizophrenia.

Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M.

Nat Genet. 2008 Jul;40(7):880-5. doi: 10.1038/ng.162. Epub 2008 May 30.

PMID:
18511947
18.

Geographic patterns of genome admixture in Latin American Mestizos.

Wang S, Ray N, Rojas W, Parra MV, Bedoya G, Gallo C, Poletti G, Mazzotti G, Hill K, Hurtado AM, Camrena B, Nicolini H, Klitz W, Barrantes R, Molina JA, Freimer NB, Bortolini MC, Salzano FM, Petzl-Erler ML, Tsuneto LT, Dipierri JE, Alfaro EL, Bailliet G, Bianchi NO, Llop E, Rothhammer F, Excoffier L, Ruiz-Linares A.

PLoS Genet. 2008 Mar 21;4(3):e1000037. doi: 10.1371/journal.pgen.1000037.

19.

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.

Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, Hakonarson H, Bucan M.

Genome Res. 2007 Nov;17(11):1665-74. Epub 2007 Oct 5.

20.

A controlled family study of attention-deficit/hyperactivity disorder and Tourette's disorder.

Stewart SE, Illmann C, Geller DA, Leckman JF, King R, Pauls DL.

J Am Acad Child Adolesc Psychiatry. 2006 Nov;45(11):1354-62.

PMID:
17075358

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