Ki CS - Search Results

1

Pharmacokinetics and Genetic Factors of Atorvastatin in Healthy Korean Subjects.

Kim S, Seo JD, Yun YM, Kim H, Kim TE, Lee T, Lee TR, Lee JH, Cho EH, Ki CS. Kim S, et al. Among authors: ki cs. Front Genet. 2022 May 19;13:836970. doi: 10.3389/fgene.2022.836970. eCollection 2022. Front Genet. 2022. PMID: 35664336 Free PMC article.

2

Identification of a Novel De Novo Variant in the PAX3 Gene in Waardenburg Syndrome by Diagnostic Exome Sequencing: The First Molecular Diagnosis in Korea.

Jang MA, Lee T, Lee J, Cho EH, Ki CS. Jang MA, et al. Among authors: ki cs. Ann Lab Med. 2015 May;35(3):362-5. doi: 10.3343/alm.2015.35.3.362. Epub 2015 Apr 1. Ann Lab Med. 2015. PMID: 25932447 Free PMC article.

3

Genetic and functional analysis of TBK1 variants in Korean patients with sporadic amyotrophic lateral sclerosis.

Kim YE, Oh KW, Noh MY, Nahm M, Park J, Lim SM, Jang JH, Cho EH, Ki CS, Lee S, Kim SH. Kim YE, et al. Among authors: ki cs. Neurobiol Aging. 2017 Feb;50:170.e1-170.e6. doi: 10.1016/j.neurobiolaging.2016.11.003. Epub 2016 Nov 19. Neurobiol Aging. 2017. PMID: 27939697

4

Radiological Findings of Two Sisters with Aceruloplasminemia Presenting with Chorea.

Kim HK, Ki CS, Kim YJ, Lee MS. Kim HK, et al. Among authors: ki cs. Clin Neuroradiol. 2017 Sep;27(3):385-388. doi: 10.1007/s00062-017-0573-0. Epub 2017 Mar 3. Clin Neuroradiol. 2017. PMID: 28258281 No abstract available.

5

Analysis of frontotemporal dementia, amyotrophic lateral sclerosis, and other dementia-related genes in 107 Korean patients with frontotemporal dementia.

Kim EJ, Kim YE, Jang JH, Cho EH, Na DL, Seo SW, Jung NY, Jeong JH, Kwon JC, Park KH, Park KW, Lee JH, Roh JH, Kim HJ, Yoon SJ, Choi SH, Jang JW, Ki CS, Kim SH. Kim EJ, et al. Among authors: ki cs. Neurobiol Aging. 2018 Dec;72:186.e1-186.e7. doi: 10.1016/j.neurobiolaging.2018.06.031. Epub 2018 Jun 30. Neurobiol Aging. 2018. PMID: 30054184

6

Genomic Analysis of Korean Patient With Microcephaly.

Lee J, Park JE, Lee C, Kim AR, Kim BJ, Park WY, Ki CS, Lee J. Lee J, et al. Among authors: ki cs. Front Genet. 2021 Jan 28;11:543528. doi: 10.3389/fgene.2020.543528. eCollection 2020. Front Genet. 2021. PMID: 33584783 Free PMC article.

7

Carrier frequency and incidence estimation of Smith-Lemli-Opitz syndrome in East Asian populations by Genome Aggregation Database (gnomAD) based analysis.

Park JE, Lee T, Ha K, Ki CS. Park JE, et al. Among authors: ki cs. Orphanet J Rare Dis. 2021 Apr 9;16(1):166. doi: 10.1186/s13023-021-01789-2. Orphanet J Rare Dis. 2021. PMID: 33836803 Free PMC article.

8

Case report of juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome: first report in Korea with a novel mutation in the SMAD4 gene.

Kang B, Hwang SK, Choi S, Kim ES, Lee SY, Ki CS, Cho EH, Lee JH, Choe BH. Kang B, et al. Among authors: ki cs. Transl Pediatr. 2021 May;10(5):1369-1376. doi: 10.21037/tp-21-12. Transl Pediatr. 2021. PMID: 34189096 Free PMC article.

9

Genomic Instability of Circulating Tumor DNA as a Prognostic Marker for Pancreatic Cancer Survival: A Prospective Cohort Study.

Woo SM, Kim MK, Park B, Cho EH, Lee TR, Ki CS, Yoon KA, Kim YH, Choi W, Kim DY, Hwang JH, Cho JH, Han SS, Lee WJ, Park SJ, Kong SY. Woo SM, et al. Among authors: ki cs. Cancers (Basel). 2021 Oct 30;13(21):5466. doi: 10.3390/cancers13215466. Cancers (Basel). 2021. PMID: 34771630 Free PMC article.

10

Carrier frequency and incidence estimation of RPE65-associated inherited retinal diseases in East Asian population by population database-based analysis.

Cho EH, Park JE, Lee T, Ha K, Ki CS. Cho EH, et al. Among authors: ki cs. Orphanet J Rare Dis. 2022 Nov 9;17(1):409. doi: 10.1186/s13023-022-02566-5. Orphanet J Rare Dis. 2022. PMID: 36352427 Free PMC article.

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