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Items: 1 to 20 of 88

1.

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
2.

Replication of restless legs syndrome loci in three European populations.

Kemlink D, Polo O, Frauscher B, Gschliesser V, Högl B, Poewe W, Vodicka P, Vavrova J, Sonka K, Nevsimalova S, Schormair B, Lichtner P, Silander K, Peltonen L, Gieger C, Wichmann HE, Zimprich A, Roeske D, Müller-Myhsok B, Meitinger T, Winkelmann J.

J Med Genet. 2009 May;46(5):315-8. doi: 10.1136/jmg.2008.062992. Epub 2009 Mar 10.

3.

Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population.

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

Sleep Med. 2011 Sep;12(8):800-4. doi: 10.1016/j.sleep.2011.06.006.

4.

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.

5.

Genetics of restless legs syndrome.

Winkelmann J.

Curr Neurol Neurosci Rep. 2008 May;8(3):211-6. Review.

PMID:
18541116
6.

Genetic associations of periodic limb movements of sleep in the elderly for the MrOS sleep study.

Winkelman JW, Blackwell T, Stone K, Ancoli-Israel S, Tranah GJ, Redline S; Osteoporotic Fractures in Men (MrOS) Study Research Group.

Sleep Med. 2015 Nov;16(11):1360-1365. doi: 10.1016/j.sleep.2015.07.017. Epub 2015 Aug 11.

7.

MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease.

Schormair B, Plag J, Kaffe M, Gross N, Czamara D, Samtleben W, Lichtner P, Ströhle A, Stefanidis I, Vainas A, Dardiotis E, Sakkas GK, Gieger C, Müller-Myhsok B, Meitinger T, Heemann U, Hadjigeorgiou GM, Oexle K, Winkelmann J.

J Med Genet. 2011 Jul;48(7):462-6. doi: 10.1136/jmg.2010.087858. Epub 2011 May 14.

8.

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.

9.

Recent advances in the diagnosis, genetics and treatment of restless legs syndrome.

Trenkwalder C, Högl B, Winkelmann J.

J Neurol. 2009 Apr;256(4):539-53. doi: 10.1007/s00415-009-0134-9. Epub 2009 Apr 27.

PMID:
19444530
10.

Exploring the genetic link between RLS and ADHD.

Schimmelmann BG, Friedel S, Nguyen TT, Sauer S, Ganz Vogel CI, Konrad K, Wilhelm C, Sinzig J, Renner TJ, Romanos M, Palmason H, Dempfle A, Walitza S, Freitag C, Meyer J, Linder M, Schäfer H, Warnke A, Lesch KP, Herpertz-Dahlman B, Hinney A, Hebebrand J.

J Psychiatr Res. 2009 Jul;43(10):941-5. doi: 10.1016/j.jpsychires.2009.01.003. Epub 2009 Feb 14.

PMID:
19223043
11.

Genetic markers of Restless Legs Syndrome in Parkinson disease.

Gan-Or Z, Alcalay RN, Bar-Shira A, Leblond CS, Postuma RB, Ben-Shachar S, Waters C, Johnson A, Levy O, Mirelman A, Gana-Weisz M, Dupré N, Montplaisir J, Giladi N, Fahn S, Xiong L, Dion PA, Orr-Urtreger A, Rouleau GA.

Parkinsonism Relat Disord. 2015 Jun;21(6):582-5. doi: 10.1016/j.parkreldis.2015.03.010. Epub 2015 Mar 17.

12.

Association of intronic variants of the BTBD9 gene with Tourette syndrome.

Rivière JB, Xiong L, Levchenko A, St-Onge J, Gaspar C, Dion Y, Lespérance P, Tellier G, Richer F, Chouinard S, Rouleau GA; Montreal Tourette Study Group.

Arch Neurol. 2009 Oct;66(10):1267-72. doi: 10.1001/archneurol.2009.213.

PMID:
19822783
13.

Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome.

Gan-Or Z, Zhou S, Ambalavanan A, Leblond CS, Xie P, Johnson A, Spiegelman D, Allen RP, Earley CJ, Desautels A, Montplaisir JY, Dion PA, Xiong L, Rouleau GA.

Sleep Med. 2015 Sep;16(9):1151-5. doi: 10.1016/j.sleep.2015.06.002. Epub 2015 Jun 17.

PMID:
26298793
14.

[Pathophysiology of restless legs syndrome].

Miyamoto M, Miyamoto T, Iwanami M, Suzuki K, Hirata K.

Brain Nerve. 2009 May;61(5):523-32. Review. Japanese.

PMID:
19514512
15.

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.

16.

Restless abdomen: a phenotypic variant of restless legs syndrome.

Pérez-Díaz H, Iranzo A, Rye DB, Santamaría J.

Neurology. 2011 Sep 27;77(13):1283-6. doi: 10.1212/WNL.0b013e318230207a. Epub 2011 Sep 14.

PMID:
21917771
17.

Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.

Schulte EC, Kousi M, Tan PL, Tilch E, Knauf F, Lichtner P, Trenkwalder C, Högl B, Frauscher B, Berger K, Fietze I, Hornyak M, Oertel WH, Bachmann CG, Zimprich A, Peters A, Gieger C, Meitinger T, Müller-Myhsok B, Katsanis N, Winkelmann J.

Am J Hum Genet. 2014 Jul 3;95(1):85-95. doi: 10.1016/j.ajhg.2014.06.005.

18.

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
19.

Restless legs syndrome in Czech patients with multiple sclerosis: an epidemiological and genetic study.

Vávrová J, Kemlink D, Sonka K, Havrdová E, Horáková D, Pardini B, Müller-Myhsok B, Winkelmann J.

Sleep Med. 2012 Aug;13(7):848-51. doi: 10.1016/j.sleep.2012.03.012. Epub 2012 May 19.

PMID:
22609020
20.

Update of the pathophysiology of the restless-legs-syndrome.

Paulus W, Dowling P, Rijsman R, Stiasny-Kolster K, Trenkwalder C.

Mov Disord. 2007;22 Suppl 18:S431-9. Review. Erratum in: Mov Disord. 2008 Jun;23(8):1200-2.

PMID:
18081164

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