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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2000 | 1 |
2007 | 2 |
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2012 | 1 |
2013 | 1 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
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Page 1
Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia.
Am J Hum Genet. 2007 Jun;80(6):1188-93. doi: 10.1086/518427. Epub 2007 Apr 27.
Am J Hum Genet. 2007.
PMID: 17503336
Free PMC article.
Mutations in GNAL cause primary torsion dystonia.
Fuchs T, Saunders-Pullman R, Masuho I, Luciano MS, Raymond D, Factor S, Lang AE, Liang TW, Trosch RM, White S, Ainehsazan E, Hervé D, Sharma N, Ehrlich ME, Martemyanov KA, Bressman SB, Ozelius LJ.
Fuchs T, et al.
Nat Genet. 2013 Jan;45(1):88-92. doi: 10.1038/ng.2496. Epub 2012 Dec 9.
Nat Genet. 2013.
PMID: 23222958
Free PMC article.
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Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene.
Heiman GA, Ottman R, Saunders-Pullman RJ, Ozelius LJ, Risch NJ, Bressman SB.
Heiman GA, et al.
Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):361-4. doi: 10.1002/ajmg.b.30431.
Am J Med Genet B Neuropsychiatr Genet. 2007.
PMID: 17066475
Free PMC article.
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A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.
Klein C, Schilling K, Saunders-Pullman RJ, Garrels J, Breakefield XO, Brin MF, deLeon D, Doheny D, Fahn S, Fink JS, Forsgren L, Friedman J, Frucht S, Harris J, Holmgren G, Kis B, Kurlan R, Kyllerman M, Lang AE, Leung J, Raymond D, Robishaw JD, Sanner G, Schwinger E, Tabamo RE, Tagliati M.
Klein C, et al.
Am J Hum Genet. 2000 Nov;67(5):1314-9. Epub 2000 Oct 5.
Am J Hum Genet. 2000.
PMID: 11022010
Free PMC article.
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Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study.
Bressman SB, Raymond D, Fuchs T, Heiman GA, Ozelius LJ, Saunders-Pullman R.
Bressman SB, et al.
Lancet Neurol. 2009 May;8(5):441-6. doi: 10.1016/S1474-4422(09)70081-X. Epub 2009 Apr 1.
Lancet Neurol. 2009.
PMID: 19345147
Free PMC article.
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Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.
Saunders-Pullman R, Fuchs T, San Luciano M, Raymond D, Brashear A, Ortega R, Deik A, Ozelius LJ, Bressman SB.
Saunders-Pullman R, et al.
Mov Disord. 2014 May;29(6):812-8. doi: 10.1002/mds.25818. Epub 2014 Feb 5.
Mov Disord. 2014.
PMID: 24500857
Free PMC article.
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Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.
Mirelman A, Alcalay RN, Saunders-Pullman R, Yasinovsky K, Thaler A, Gurevich T, Mejia-Santana H, Raymond D, Gana-Weisz M, Bar-Shira A, Ozelius L, Clark L, Orr-Urtreger A, Bressman S, Marder K, Giladi N; LRRK2 AJ consortium.
Mirelman A, et al.
Mov Disord. 2015 Jun;30(7):981-6. doi: 10.1002/mds.26213. Epub 2015 Mar 21.
Mov Disord. 2015.
PMID: 25809001
Free PMC article.
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