Foo JN - Search Results

1

Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia.

Ng ASL, Tan AH, Tan YJ, Lim JL, Lian MM, Dy Closas AM, Ahmad-Annuar A, Viswanathan S, Chia YK, Foo JN, Lim WK, Tan EK, Lim SY. Ng ASL, et al. Among authors: foo jn. Mov Disord. 2024 Oct;39(10):1829-1842. doi: 10.1002/mds.29932. Epub 2024 Aug 16. Mov Disord. 2024. PMID: 39149795

2

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

Foo JN, Liu JJ, Tan EK. Foo JN, et al. 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.

3

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: foo jn. 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

4

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

Foo JN, Liu J, Tan EK. Foo JN, et al. 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.

5

Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations.

Tan LC, Methawasin K, Teng EW, Ng AR, Seah SH, Au WL, Liu JJ, Foo JN, Zhao Y, Tan EK. Tan LC, et al. Among authors: foo jn. Eur J Neurol. 2014 Apr;21(4):674-8. doi: 10.1111/ene.12142. Epub 2013 Mar 29. Eur J Neurol. 2014. PMID: 23551744

6

SLC1A2 variant associated with essential tremor but not Parkinson disease in Chinese subjects.

Tan EK, Foo JN, Tan L, Au WL, Prakash KM, Ng E, Ikram MK, Wong TY, Liu JJ, Zhao Y. Tan EK, et al. Among authors: foo jn. Neurology. 2013 Apr 23;80(17):1618-9. doi: 10.1212/WNL.0b013e31828f1903. Epub 2013 Apr 17. Neurology. 2013. PMID: 23596072

7

Absence of A673T amyloid-β precursor protein variant in Alzheimer's disease and other neurological diseases.

Ting SK, Chong MS, Kandiah N, Hameed S, Tan L, Au WL, Prakash KM, Pavanni R, Lee TS, Foo JN, Bei JX, Yu XQ, Liu JJ, Zhao Y, Lee WL, Tan EK. Ting SK, et al. Among authors: foo jn. Neurobiol Aging. 2013 Oct;34(10):2441.e7-8. doi: 10.1016/j.neurobiolaging.2013.04.012. Epub 2013 May 4. Neurobiol Aging. 2013. PMID: 23652020

8

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. Wu YR, et al. Among authors: foo jn. Neurology. 2013 Aug 6;81(6):541-4. doi: 10.1212/WNL.0b013e31829e700c. Epub 2013 Jul 3. Neurology. 2013. PMID: 23825177

9

Rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease.

Foo JN, Liany H, Bei JX, Yu XQ, Liu J, Au WL, Prakash KM, Tan LC, Tan EK. Foo JN, et al. Neurobiol Aging. 2013 Dec;34(12):2890.e13-5. doi: 10.1016/j.neurobiolaging.2013.06.010. Epub 2013 Jul 18. Neurobiol Aging. 2013. PMID: 23871123

10

DNAJ mutations are rare in Chinese Parkinson's disease patients and controls.

Foo JN, Liany H, Tan LC, Au WL, Prakash KM, Liu J, Tan EK. Foo JN, et al. Neurobiol Aging. 2014 Apr;35(4):935.e1-2. doi: 10.1016/j.neurobiolaging.2013.09.018. Epub 2013 Oct 12. Neurobiol Aging. 2014. PMID: 24126164

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