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Items: 1 to 20 of 107

1.

Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.

Winkelmann J, Czamara D, Schormair B, Knauf F, Schulte EC, Trenkwalder C, Dauvilliers Y, Polo O, Högl B, Berger K, Fuhs A, Gross N, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Xiong L, Montplaisir J, Rouleau GA, Fietze I, Vávrová J, Kemlink D, Sonka K, Nevsimalova S, Lin SC, Wszolek Z, Vilariño-Güell C, Farrer MJ, Gschliesser V, Frauscher B, Falkenstetter T, Poewe W, Allen RP, Earley CJ, Ondo WG, Le WD, Spieler D, Kaffe M, Zimprich A, Kettunen J, Perola M, Silander K, Cournu-Rebeix I, Francavilla M, Fontenille C, Fontaine B, Vodicka P, Prokisch H, Lichtner P, Peppard P, Faraco J, Mignot E, Gieger C, Illig T, Wichmann HE, Müller-Myhsok B, Meitinger T.

PLoS Genet. 2011 Jul;7(7):e1002171. doi: 10.1371/journal.pgen.1002171. Epub 2011 Jul 14. Erratum in: PLoS Genet. 2011 Aug;7(8). doi: 10.1371/annotation/393ad2d3-df4f-4770-87bc-00bfabf79362.

2.

A novel locus for restless legs syndrome on chromosome 13q.

Balaban H, Bayrakli F, Kartal U, Pinarbasi E, Topaktas S, Kars HZ.

Eur Neurol. 2012;68(2):111-6. doi: 10.1159/000338779. Epub 2012 Jul 10.

PMID:
22797413
3.

Association of candidate genetic variants with restless legs syndrome in end stage renal disease: a multicenter case-control study in Taiwan.

Lin CH, Chen ML, Wu VC, Li WY, Sy HN, Wu SL, Chang CC, Chiu PF, Liou HH, Lin CY, Chang HW, Lin SY, Wu KD, Chen YM, Wu RM.

Eur J Neurol. 2014 Mar;21(3):492-8. doi: 10.1111/ene.12337. Epub 2014 Jan 16.

PMID:
24433515
4.

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.

Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.

Mov Disord. 2006 Jan;21(1):28-33.

PMID:
16124010
5.

Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndrome.

Yang Q, Li L, Yang R, Shen GQ, Chen Q, Foldvary-Schaefer N, Ondo WG, Wang QK.

Mov Disord. 2011 Feb 15;26(3):516-9. doi: 10.1002/mds.23459. Epub 2011 Jan 24.

6.

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.

Winkelmann J, Schormair B, Lichtner P, Ripke S, Xiong L, Jalilzadeh S, Fulda S, Pütz B, Eckstein G, Hauk S, Trenkwalder C, Zimprich A, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Peglau I, Eisensehr I, Montplaisir J, Turecki G, Rouleau G, Gieger C, Illig T, Wichmann HE, Holsboer F, Müller-Myhsok B, Meitinger T.

Nat Genet. 2007 Aug;39(8):1000-6. Epub 2007 Jul 18.

PMID:
17637780
7.

A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree.

Skehan EB, Abdulrahim MM, Parfrey NA, Hand CK.

Neurogenetics. 2012 May;13(2):125-32. doi: 10.1007/s10048-012-0317-x. Epub 2012 Mar 14.

PMID:
22411506
8.

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;79(4):716-23. Epub 2006 Aug 14.

9.

Association of restless legs syndrome variants in Korean patients with restless legs syndrome.

Kim MK, Cho YW, Shin WC, Cho JW, Shon YM, Kim JH, Yang KI, Earley CJ, Allen RP.

Sleep. 2013 Dec 1;36(12):1787-91. doi: 10.5665/sleep.3200.

10.

Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.

Johnson MP, Brennecke SP, East CE, Göring HH, Kent JW Jr, Dyer TD, Said JM, Roten LT, Iversen AC, Abraham LJ, Heinonen S, Kajantie E, Kere J, Kivinen K, Pouta A, Laivuori H; FINNPEC Study Group, Austgulen R, Blangero J, Moses EK.

PLoS One. 2012;7(3):e33666. doi: 10.1371/journal.pone.0033666. Epub 2012 Mar 14.

11.

Periodic leg movements during sleep are associated with polymorphisms in BTBD9, TOX3/BC034767, MEIS1, MAP2K5/SKOR1, and PTPRD.

Moore H 4th, Winkelmann J, Lin L, Finn L, Peppard P, Mignot E.

Sleep. 2014 Sep 1;37(9):1535-42. doi: 10.5665/sleep.4006.

12.

Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome.

Schulte EC, Schramm K, Schurmann C, Lichtner P, Herder C, Roden M, Gieger C, Peters A, Trenkwalder C, Högl B, Frauscher B, Berger K, Fietze I, Gross N, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Zimprich A, Völzke H, Schminke U, Nauck M, Illig T, Meitinger T, Müller-Myhsok B, Prokisch H, Winkelmann J.

PLoS One. 2014 May 29;9(5):e98092. doi: 10.1371/journal.pone.0098092. eCollection 2014.

13.

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. Epub 2004 Apr 7.

14.

A genetic risk factor for periodic limb movements in sleep.

Stefansson H, Rye DB, Hicks A, Petursson H, Ingason A, Thorgeirsson TE, Palsson S, Sigmundsson T, Sigurdsson AP, Eiriksdottir I, Soebech E, Bliwise D, Beck JM, Rosen A, Waddy S, Trotti LM, Iranzo A, Thambisetty M, Hardarson GA, Kristjansson K, Gudmundsson LJ, Thorsteinsdottir U, Kong A, Gulcher JR, Gudbjartsson D, Stefansson K.

N Engl J Med. 2007 Aug 16;357(7):639-47. Epub 2007 Jul 18.

15.

Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.

Sas AM, Di Fonzo A, Bakker SL, Simons EJ, Oostra BA, Maat-Kievit AJ, Boon AJ, Bonifati V.

Mov Disord. 2010 Aug 15;25(11):1715-22. doi: 10.1002/mds.23248.

PMID:
20645405
16.

Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?

Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.

Neurology. 2008 Feb 26;70(9):686-94. Epub 2007 Nov 21.

PMID:
18032746
17.

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;49(3):600-5. doi: 10.1007/s12031-012-9891-5. Epub 2012 Oct 2.

PMID:
23054586
18.

MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels.

Xiong L, Catoire H, Dion P, Gaspar C, Lafrenière RG, Girard SL, Levchenko A, Rivière JB, Fiori L, St-Onge J, Bachand I, Thibodeau P, Allen R, Earley C, Turecki G, Montplaisir J, Rouleau GA.

Hum Mol Genet. 2009 Mar 15;18(6):1065-74. doi: 10.1093/hmg/ddn443. Epub 2009 Jan 6.

19.

Childhood-onset restless legs syndrome: clinical and genetic features of 22 families.

Muhle H, Neumann A, Lohmann-Hedrich K, Lohnau T, Lu Y, Winkler S, Waltz S, Fischenbeck A, Kramer PL, Klein C, Stephani U.

Mov Disord. 2008 Jun 15;23(8):1113-21; quiz 1203. doi: 10.1002/mds.22016.

PMID:
18381645
20.

Restless legs syndrome: an update on genetics and future perspectives.

Pichler I, Hicks AA, Pramstaller PP.

Clin Genet. 2008 Apr;73(4):297-305. Epub 2007 Dec 6. Review.

PMID:
18070136
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