Tan EK - Search Results

1

Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore.

Wu D, Dou J, Chai X, Bellis C, Wilm A, Shih CC, Soon WWJ, Bertin N, Lin CB, Khor CC, DeGiorgio M, Cheng S, Bao L, Karnani N, Hwang WYK, Davila S, Tan P, Shabbir A, Moh A, Tan EK, Foo JN, Goh LL, Leong KP, Foo RSY, Lam CSP, Richards AM, Cheng CY, Aung T, Wong TY, Ng HH; SG10K Consortium; Liu J, Wang C. Wu D, et al. Among authors: tan p, tan ek. Cell. 2019 Oct 17;179(3):736-749.e15. doi: 10.1016/j.cell.2019.09.019. Cell. 2019. PMID: 31626772 Free article.

2

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

Skipper L, Li Y, Bonnard C, Pavanni R, Yih Y, Chua E, Sung WK, Tan L, Wong MC, Tan EK, Liu J. Skipper L, et al. Among authors: tan l, tan ek. Hum Mol Genet. 2005 Dec 1;14(23):3549-56. doi: 10.1093/hmg/ddi376. Epub 2005 Nov 3. Hum Mol Genet. 2005. PMID: 16269443

3

DYT1 mutations amongst adult primary dystonia patients in Singapore with review of literature comparing East and West.

Jamora RD, Tan EK, Liu CP, Kathirvel P, Burgunder JM, Tan LC. Jamora RD, et al. Among authors: tan lc, tan ek. J Neurol Sci. 2006 Aug 15;247(1):35-7. doi: 10.1016/j.jns.2006.03.009. Epub 2006 Apr 24. J Neurol Sci. 2006. PMID: 16631205 Free article.

4

Polymorphisms in candidate genes: implications for the current treatment of Parkinson's disease.

Skipper L, Liu JJ, Tan EK. Skipper L, et al. Among authors: tan ek. Expert Opin Pharmacother. 2006 May;7(7):849-55. doi: 10.1517/14656566.7.7.849. Expert Opin Pharmacother. 2006. PMID: 16634708 Review.

5

LRRK2 G2019S founder haplotype in the Chinese population.

Tan EK, Skipper L, Tan L, Liu JJ. Tan EK, et al. Among authors: tan l. Mov Disord. 2007 Jan;22(1):105-7. doi: 10.1002/mds.21206. Mov Disord. 2007. PMID: 17083102

6

Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians.

Tan EK, Zhao Y, Tan L, Lim HQ, Lee J, Yuen Y, Pavanni R, Wong MC, Fook-Chong S, Liu JJ. Tan EK, et al. Among authors: tan l. Mov Disord. 2007 Sep 15;22(12):1816-8. doi: 10.1002/mds.21658. Mov Disord. 2007. PMID: 17659642

7

CALHM1 variant is not associated with Alzheimer's disease among Asians.

Tan EK, Ho P, Cheng SY, Yih Y, Li HH, Fook-Chong S, Lee WL, Zhao Y. Tan EK, et al. Neurobiol Aging. 2011 Mar;32(3):546.e11-2. doi: 10.1016/j.neurobiolaging.2009.05.008. Epub 2009 Jul 9. Neurobiol Aging. 2011. PMID: 19545933

8

Whole-genome and whole-exome sequencing in neurological diseases.

Foo JN, Liu JJ, Tan EK. Foo JN, et al. Among authors: tan ek. Nat Rev Neurol. 2012 Sep;8(9):508-17. doi: 10.1038/nrneurol.2012.148. Epub 2012 Jul 31. Nat Rev Neurol. 2012. PMID: 22847385 Review.

9

Analysis of EIF4G1 in Parkinson's disease among Asians.

Zhao Y, Ho P, Prakash KM, Foo JN, Liu JJ, Au WL, Tan LC, Tan EK. Zhao Y, et al. Among authors: tan lc, tan ek. Neurobiol Aging. 2013 Apr;34(4):1311.e5-6. doi: 10.1016/j.neurobiolaging.2012.09.003. Epub 2012 Oct 23. Neurobiol Aging. 2013. PMID: 23092605

10

Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspective.

Foo JN, Liu J, Tan EK. Foo JN, et al. Among authors: tan ek. Hum Genet. 2013 Jul;132(7):721-34. doi: 10.1007/s00439-013-1287-2. Epub 2013 Mar 23. Hum Genet. 2013. PMID: 23525706 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

898 results

Search Page