Kim JY - Search Results

1

Phase analysis identifies compound heterozygous deletions of the PARK2 gene in patients with early-onset Parkinson disease.

Kim SY, Seong MW, Jeon BS, Kim SY, Ko HS, Kim JY, Park SS. Kim SY, et al. Among authors: kim jy. Clin Genet. 2012 Jul;82(1):77-82. doi: 10.1111/j.1399-0004.2011.01693.x. Epub 2011 May 29. Clin Genet. 2012. PMID: 21534944

2

Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation.

Seong MW, Cho S, Noh DY, Han W, Kim SW, Park CM, Park HW, Kim SY, Kim JY, Park SS. Seong MW, et al. Among authors: kim jy, kim sw, kim sy. Clin Genet. 2009 Aug;76(2):152-60. doi: 10.1111/j.1399-0004.2009.01202.x. Epub 2009 Jul 28. Clin Genet. 2009. PMID: 19656164

3

Mitochondrial DNA content is decreased in autosomal dominant optic atrophy.

Kim JY, Hwang JM, Ko HS, Seong MW, Park BJ, Park SS. Kim JY, et al. Neurology. 2005 Mar 22;64(6):966-72. doi: 10.1212/01.WNL.0000157282.76715.B1. Neurology. 2005. PMID: 15781809

4

Investigation of the association between 677C>T and 1298A>C 5,10-methylenetetra- hydrofolate reductase gene polymorphisms and normal-tension glaucoma.

Woo SJ, Kim JY, Kim DM, Park SS, Ko HS, Yoo T. Woo SJ, et al. Among authors: kim jy, kim dm. Eye (Lond). 2009 Jan;23(1):17-24. doi: 10.1038/sj.eye.6702920. Epub 2007 Jul 6. Eye (Lond). 2009. PMID: 17618244

5

alpha-Synuclein gene duplication is present in sporadic Parkinson disease.

Ahn TB, Kim SY, Kim JY, Park SS, Lee DS, Min HJ, Kim YK, Kim SE, Kim JM, Kim HJ, Cho J, Jeon BS. Ahn TB, et al. Among authors: kim jy, kim yk, kim se, kim hj, kim jm, kim sy. Neurology. 2008 Jan 1;70(1):43-9. doi: 10.1212/01.wnl.0000271080.53272.c7. Epub 2007 Jul 11. Neurology. 2008. PMID: 17625105

6

Mutation spectrum of RB1 gene in Korean bilateral retinoblastoma patients using direct sequencing and gene dosage analysis.

Seo SH, Ahn HS, Yu YS, Kang HJ, Park KD, Cho SI, Park JS, Hyun YJ, Kim JY, Seong MW, Park SS. Seo SH, et al. Among authors: kim jy. Clin Genet. 2013 May;83(5):494-6. doi: 10.1111/j.1399-0004.2012.01954.x. Epub 2012 Sep 10. Clin Genet. 2013. PMID: 22963398 No abstract available.

7

Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.

Kim JY, Park SS, Joo SI, Kim JM, Jeon BS. Kim JY, et al. Among authors: kim jm. Mol Cells. 2001 Dec 31;12(3):336-41. Mol Cells. 2001. PMID: 11804332 Free article.

8

Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism.

Kim JY, Kim SY, Kim JM, Kim YK, Yoon KY, Kim JY, Lee BC, Kim JS, Paek SH, Park SS, Kim SE, Jeon BS. Kim JY, et al. Among authors: kim yk, kim se, kim jm, kim sy, kim js. Neurology. 2009 Apr 21;72(16):1385-9. doi: 10.1212/WNL.0b013e3181a18876. Neurology. 2009. PMID: 19380697

9

Extrapyramidal signs are a common feature of spinocerebellar ataxia type 17.

Lee WW, Kim SY, Kim JY, Kim HJ, Park SS, Jeon BS. Lee WW, et al. Among authors: kim jy, kim hj, kim sy. Neurology. 2009 Nov 17;73(20):1708-9. doi: 10.1212/WNL.0b013e3181c1df0c. Neurology. 2009. PMID: 19917997 No abstract available.

10

Lymphoid preponderance and the absence of basophilia and splenomegaly are frequent in m-bcr-positive chronic myelogenous leukemia.

Hur M, Song EY, Kang SH, Shin DH, Kim JY, Park SS, Cho HI. Hur M, et al. Among authors: kim jy. Ann Hematol. 2002 Apr;81(4):219-23. doi: 10.1007/s00277-002-0433-z. Epub 2002 Feb 28. Ann Hematol. 2002. PMID: 11976825 Review.

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