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Items: 1 to 20 of 85

1.

A genetic risk factor for periodic limb movements in sleep.

Vilariño-Güell C, Farrer MJ, Lin SC.

N Engl J Med. 2008 Jan 24;358(4):425-7. doi: 10.1056/NEJMc072518. No abstract available.

2.

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):1360-5. doi: 10.1016/j.sleep.2015.07.017. Epub 2015 Aug 11.

3.

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.

4.

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.

5.

Periodic limb movements in sleep--endophenotype for restless legs syndrome?

Winkelman JW.

N Engl J Med. 2007 Aug 16;357(7):703-5. Epub 2007 Jul 18. No abstract available.

PMID:
17634452
6.

What's next after the exciting discovery and reassuring replications of genome-wide association studies of restless legs syndrome?

Xiong L.

Sleep Med. 2011 Sep;12(8):733-4. doi: 10.1016/j.sleep.2011.08.001. Epub 2011 Aug 31. No abstract available.

PMID:
21885332
7.

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
8.

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
9.

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.

10.

Genetics of restless legs syndrome.

Winkelmann J.

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

PMID:
18541116
11.

Association of low ferritin with PLM in the Wisconsin Sleep Cohort.

Li J, Moore H 4th, Lin L, Young T, Finn L, Peppard PE, Mignot E.

Sleep Med. 2015 Nov;16(11):1413-8. doi: 10.1016/j.sleep.2015.05.015. Epub 2015 Jun 18.

PMID:
26498245
12.

Genetic variants associated with sleep disorders.

Kripke DF, Kline LE, Nievergelt CM, Murray SS, Shadan FF, Dawson A, Poceta JS, Cronin J, Jamil SM, Tranah GJ, Loving RT, Grizas AP, Hahn EK.

Sleep Med. 2015 Feb;16(2):217-24. doi: 10.1016/j.sleep.2014.11.003. Epub 2014 Dec 5.

13.

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.

14.

Polymorphisms in human homeobox HLX1 and DNA repair RAD51 genes increase the risk of therapy-related acute myeloid leukemia.

Jawad M, Seedhouse CH, Russell N, Plumb M.

Blood. 2006 Dec 1;108(12):3916-8. Epub 2006 Aug 10.

15.

Prevalence and determinants of periodic limb movements in the general population.

Haba-Rubio J, Marti-Soler H, Marques-Vidal P, Tobback N, Andries D, Preisig M, Waeber G, Vollenweider P, Kutalik Z, Tafti M, Heinzer R.

Ann Neurol. 2016 Mar;79(3):464-74. doi: 10.1002/ana.24593. Epub 2016 Feb 12.

PMID:
26703954
16.

Preliminary evidence that polymorphisms in dopamine-related transcription factors LMX1A, LMX1B and PITX3 are associated with schizophrenia.

Bergman O, Westberg L, Nilsson LG, Adolfsson R, Eriksson E.

Prog Neuropsychopharmacol Biol Psychiatry. 2010 Aug 16;34(6):1094-7. doi: 10.1016/j.pnpbp.2010.05.032. Epub 2010 Jun 4.

PMID:
20570600
17.

Genetic variants and effects on milk traits of the caprine paired-like homeodomain transcription factor 2 (PITX2) gene in dairy goats.

Zhao H, Wu X, Cai H, Pan C, Lei C, Chen H, Lan X.

Gene. 2013 Dec 15;532(2):203-10. doi: 10.1016/j.gene.2013.09.062. Epub 2013 Sep 25.

PMID:
24076438
18.

Transcription factor PITX3 gene in Parkinson's disease.

Le W, Nguyen D, Lin XW, Rawal P, Huang M, Ding Y, Xie W, Deng H, Jankovic J.

Neurobiol Aging. 2011 Apr;32(4):750-3. doi: 10.1016/j.neurobiolaging.2009.03.015. Epub 2009 Apr 24.

PMID:
19394114
19.

Restless legs syndrome and periodic limb movements.

Trenkwalder C.

Adv Neurol. 2002;89:145-51. Review. No abstract available.

PMID:
11968440
20.

PITX3 variants in Chinese patients with Parkinson's disease.

Sand PG, Welz T.

Swiss Med Wkly. 2014 Feb 4;144:w13702. doi: 10.4414/smw.2014.13702. No abstract available.

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