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Journal Abstract Search

100 related items for PubMed ID: 17133505

  • 21. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.
    Chen S, Ondo WG, Rao S, Li L, Chen Q, Wang Q.
    Am J Hum Genet; 2004 May; 74(5):876-85. PubMed ID: 15077200
    [Abstract] [Full Text] [Related]

  • 22. A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.
    Levchenko A, Provost S, Montplaisir JY, Xiong L, St-Onge J, Thibodeau P, Rivière JB, Desautels A, Turecki G, Dubé MP, Rouleau GA.
    Neurology; 2006 Sep 12; 67(5):900-1. PubMed ID: 16966564
    [Abstract] [Full Text] [Related]

  • 23. Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families.
    Xiong L, Dion P, Montplaisir J, Levchenko A, Thibodeau P, Karemera L, Rivière JB, St-Onge J, Gaspar C, Dubé MP, Desautels A, Turecki G, Rouleau GA.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Oct 05; 144B(7):911-7. PubMed ID: 17510944
    [Abstract] [Full Text] [Related]

  • 24. Genetics in restless legs syndrome.
    Ferini-Strambi L, Bonati MT, Oldani A, Aridon P, Zucconi M, Casari G.
    Sleep Med; 2004 May 05; 5(3):301-4. PubMed ID: 15165539
    [Abstract] [Full Text] [Related]

  • 25. Restless legs syndrome.
    Ekbom K, Ulfberg J.
    J Intern Med; 2009 Nov 05; 266(5):419-31. PubMed ID: 19817966
    [Abstract] [Full Text] [Related]

  • 26. 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 05; 12(4):376-84. PubMed ID: 17179998
    [Abstract] [Full Text] [Related]

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  • 28. Analysis of linkage and linkage disequilibrium for eight X-STR markers.
    Tillmar AO, Mostad P, Egeland T, Lindblom B, Holmlund G, Montelius K.
    Forensic Sci Int Genet; 2008 Dec 05; 3(1):37-41. PubMed ID: 19083865
    [Abstract] [Full Text] [Related]

  • 29. Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.
    Desautels A, Turecki G, Montplaisir J, Sequeira A, Verner A, Rouleau GA.
    Am J Hum Genet; 2001 Dec 05; 69(6):1266-70. PubMed ID: 11704926
    [Abstract] [Full Text] [Related]

  • 30. CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians.
    Gragnoli C.
    J Cell Physiol; 2008 Nov 05; 217(2):291-5. PubMed ID: 18680108
    [Abstract] [Full Text] [Related]

  • 31. Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q.
    Wintle RF, Nygaard TG, Herbrick JA, Kvaløy K, Cox DW.
    Genomics; 1997 Mar 15; 40(3):409-14. PubMed ID: 9073508
    [Abstract] [Full Text] [Related]

  • 32. Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes.
    Pichler I, Schwienbacher C, Zanon A, Fuchsberger C, Serafin A, Facheris MF, Marroni F, Pattaro C, Shen Y, Tellgren-Roth C, Gyllensten U, Gusella JF, Hicks AA, Pramstaller PP.
    J Mol Neurosci; 2013 Mar 15; 49(3):600-5. PubMed ID: 23054586
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  • 34. Primary genome scan to identify putative quantitative trait loci for feedlot growth rate, feed intake, and feed efficiency of beef cattle.
    Nkrumah JD, Sherman EL, Li C, Marques E, Crews DH, Bartusiak R, Murdoch B, Wang Z, Basarab JA, Moore SS.
    J Anim Sci; 2007 Dec 15; 85(12):3170-81. PubMed ID: 17709790
    [Abstract] [Full Text] [Related]

  • 35. Linked vs unlinked markers: multilocus microsatellite haplotype-sharing as a tool to estimate gene flow and introgression.
    Koopman WJ, Li Y, Coart E, van de Weg WE, Vosman B, Roldán-Ruiz I, Smulders MJ.
    Mol Ecol; 2007 Jan 15; 16(2):243-56. PubMed ID: 17217342
    [Abstract] [Full Text] [Related]

  • 36. Association between restless legs syndrome and CLOCK and NPAS2 gene polymorphisms in schizophrenia.
    Jung JS, Lee HJ, Cho CH, Kang SG, Yoon HK, Park YM, Moon JH, Yang HJ, Song HM, Kim L.
    Chronobiol Int; 2014 Aug 15; 31(7):838-44. PubMed ID: 24824748
    [Abstract] [Full Text] [Related]

  • 37. Linkage analysis identifies a novel locus for restless legs syndrome on chromosome 2q in a South Tyrolean population isolate.
    Pichler I, Marroni F, Volpato CB, Gusella JF, Klein C, Casari G, De Grandi A, Pramstaller PP.
    Am J Hum Genet; 2006 Oct 15; 79(4):716-23. PubMed ID: 16960808
    [Abstract] [Full Text] [Related]

  • 38. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
    Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A, French Research Network on FTD/FTD-MND.
    Neurology; 2009 May 12; 72(19):1669-76. PubMed ID: 19433740
    [Abstract] [Full Text] [Related]

  • 39. Evidence for transmission disequilibrium at the DAOA gene locus in a schizophrenia family sample.
    Ma J, Sun J, Zhang H, Zhang R, Kang WH, Gao CG, Liu HS, Ma XH, Min ZX, Zhao WX, Ning QL, Wang SH, Zhang YC, Guo TW, Lu SM.
    Neurosci Lett; 2009 Sep 22; 462(2):105-8. PubMed ID: 19560517
    [Abstract] [Full Text] [Related]

  • 40. A genome-wide association screen identifies regions on chromosomes 1q25 and 7p21 as risk loci for sporadic prostate cancer.
    Nam RK, Zhang WW, Loblaw DA, Klotz LH, Trachtenberg J, Jewett MA, Stanimirovic A, Davies TO, Toi A, Venkateswaran V, Sugar L, Siminovitch KA, Narod SA.
    Prostate Cancer Prostatic Dis; 2008 Sep 22; 11(3):241-6. PubMed ID: 17876339
    [Abstract] [Full Text] [Related]

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