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Items: 1 to 20 of 79

1.

Author response.

Tan EK, Wu YR.

Neurology. 2014 Feb 4;82(5):461. No abstract available.

PMID:
24649492
2.

Identification of a novel risk variant in the FUS gene in essential tremor.

Kuhlenbaeumer G, Tan EK, Wu YR.

Neurology. 2014 Feb 4;82(5):461. doi: 10.1212/WNL.0000000000000073. No abstract available.

PMID:
24491973
3.

Genetic biomarkers of essential tremor: time to think outside of the box.

Agúndez JA, Jiménez-Jiménez FJ, Alonso-Navarro H, García-Martín E.

Pharmacogenomics. 2013 Nov;14(14):1681-2. No abstract available.

PMID:
24350349
4.

Movement disorders: novel FUS gene variants linked to essential tremor.

Wood H.

Nat Rev Neurol. 2013 Aug;9(8):418. doi: 10.1038/nrneurol.2013.143. Epub 2013 Jul 23. No abstract available.

PMID:
23877643
5.

Identification of a novel risk variant in the FUS gene in essential tremor.

Wu YR, Foo JN, Tan LC, Chen CM, Prakash KM, Chen YC, Bei JX, Au WL, Chang CW, Wong TY, Liu JJ, Zhao Y, Tan EK.

Neurology. 2013 Aug 6;81(6):541-4. doi: 10.1212/WNL.0b013e31829e700c. Epub 2013 Jul 3.

PMID:
23825177
6.

FUS: a putative biomarker for essential tremor raised by whole-exome sequencing analyses.

Agúndez JA, Jiménez-Jiménez FJ, Alonso-Navarro H, García-Martín E.

Pharmacogenomics. 2013 Nov;14(14):1680-1. No abstract available.

PMID:
24350348
7.

FUS in familial essential tremor - the search for common causes is still on.

Hedera P, Davis TL, Phibbs FT, Charles PD, LeDoux MS.

Parkinsonism Relat Disord. 2013 Sep;19(9):818-20. doi: 10.1016/j.parkreldis.2013.04.009. Epub 2013 May 6.

PMID:
23660545
8.

Exome sequencing identifies FUS mutations as a cause of essential tremor.

Merner ND, Girard SL, Catoire H, Bourassa CV, Belzil VV, Rivière JB, Hince P, Levert A, Dionne-Laporte A, Spiegelman D, Noreau A, Diab S, Szuto A, Fournier H, Raelson J, Belouchi M, Panisset M, Cossette P, Dupré N, Bernard G, Chouinard S, Dion PA, Rouleau GA.

Am J Hum Genet. 2012 Aug 10;91(2):313-9. doi: 10.1016/j.ajhg.2012.07.002. Epub 2012 Aug 2.

9.

Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor.

Zheng W, Deng X, Liang H, Song Z, Gao K, Yang Y, Deng H.

Neurobiol Aging. 2013 Aug;34(8):2078.e3-4. doi: 10.1016/j.neurobiolaging.2013.03.001. Epub 2013 Apr 9.

PMID:
23582660
10.

Investigating the role of FUS exonic variants in essential tremor.

Labbé C, Soto-Ortolaza AI, Rayaprolu S, Harriott AM, Strongosky AJ, Uitti RJ, Van Gerpen JA, Wszolek ZK, Ross OA.

Parkinsonism Relat Disord. 2013 Aug;19(8):755-7. doi: 10.1016/j.parkreldis.2013.03.005. Epub 2013 Apr 16.

11.

Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease.

Deng H, Le WD, Guo Y, Huang MS, Xie WJ, Jankovic J.

Neurology. 2005 Aug 23;65(4):651-2. No abstract available.

PMID:
16116142
12.

Genetics of essential tremor.

Tio M, Tan EK.

Parkinsonism Relat Disord. 2016 Jan;22 Suppl 1:S176-8. doi: 10.1016/j.parkreldis.2015.09.022. Epub 2015 Sep 14. Review.

PMID:
26411503
13.

Identification of FUS p.R377W in essential tremor.

Rajput A, Rajput AH, Rajput ML, Encarnacion M, Bernales CQ, Ross JP, Farrer MJ, Vilariño-Güell C.

Eur J Neurol. 2014 Feb;21(2):361-3. doi: 10.1111/ene.12231. Epub 2013 Jul 3.

14.

Fused in Sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in Europeans.

Ortega-Cubero S, Lorenzo-Betancor O, Lorenzo E, Alonso E, Coria F, Pastor MA, Fernández-Santiago R, Martí MJ, Ezquerra M, Valldeoriola F, Compta Y, Tolosa E, Agundez JA, Jiménez-Jiménez FJ, Gironell A, Clarimon J, de Castro P, García-Martín E, Alonso-Navarro H, Pastor P.

Neurobiol Aging. 2013 Oct;34(10):2441.e9-2441.e11. doi: 10.1016/j.neurobiolaging.2013.04.024. Epub 2013 May 31.

PMID:
23731953
15.

The impact of rare variants in FUS in essential tremor.

Hopfner F, Stevanin G, Müller SH, Mundwiller E, Bungeroth M, Durr A, Pendziwiat M, Anheim M, Schneider SA, Tittmann L, Klebe S, Lorenz D, Deuschl G, Brice A, Kuhlenbäumer G.

Mov Disord. 2015 Apr 15;30(5):721-4. doi: 10.1002/mds.26145. Epub 2015 Jan 28.

PMID:
25631824
16.

Human genetics: Individual genomes diversify.

Levy S, Strausberg RL.

Nature. 2008 Nov 6;456(7218):49-51. doi: 10.1038/456049a. No abstract available.

PMID:
18987731
17.

Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease.

Chao YX, Ng EY, Foo JN, Liu J, Zhao Y, Tan EK.

Neurogenetics. 2015 Jul;16(3):241-2. doi: 10.1007/s10048-015-0443-3. Epub 2015 Mar 20. No abstract available.

PMID:
25791756
18.

LINGO1 variant increases risk of familial essential tremor.

Tan EK, Teo YY, Prakash KM, Li R, Lim HQ, Angeles D, Tan LC, Au WL, Yih Y, Zhao Y.

Neurology. 2009 Oct 6;73(14):1161-2. doi: 10.1212/WNL.0b013e3181bacfc9. No abstract available.

19.

Interacting effect of genetic variants of angiotensin II type 1 receptor on susceptibility to essential hypertension in Northern Han Chinese.

Niu WQ, Zhao HY, Zhou L, Dai XX, Wang DY, Cao J, Wang B.

J Hum Hypertens. 2009 Jan;23(1):68-71. doi: 10.1038/jhh.2008.77. Epub 2008 Jul 17. No abstract available.

PMID:
18633425
20.

[Association of the polymorphism in alpha-2 macroglobulin gene with essential tremor and Parkinson's disease].

Xiao Y, Zhang BS.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Feb;23(1):84-5. Chinese.

PMID:
16456795

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