Kim JH - Search Results

1

Homozygote CRIM1 variant is associated with thiopurine-induced neutropenia in leukemic patients with both wildtype NUDT15 and TPMT.

Park Y, Kim H, Seo H, Choi JY, Ma Y, Yun S, Min BJ, Seo ME, Yoo KH, Kang HJ, Im HJ, Kim JH. Park Y, et al. Among authors: kim h, kim jh. J Transl Med. 2020 Jul 1;18(1):265. doi: 10.1186/s12967-020-02416-7. J Transl Med. 2020. PMID: 32611418 Free PMC article.

2

Gastrointestinal tuberculosis is not associated with proton pump inhibitors: a retrospective cohort study.

Hong KS, Kang SJ, Choi JK, Kim JH, Seo H, Lee S, Jung JW, Kang HR, Cho SH, Kim JS. Hong KS, et al. Among authors: kim js, kim jh. World J Gastroenterol. 2013 Jan 14;19(2):258-64. doi: 10.3748/wjg.v19.i2.258. World J Gastroenterol. 2013. PMID: 23345949 Free PMC article.

3

Development of korean rare disease knowledge base.

Seo H, Kim D, Chae JH, Kang HG, Lim BC, Cheong HI, Kim JH. Seo H, et al. Among authors: kim d, kim jh. Healthc Inform Res. 2012 Dec;18(4):272-8. doi: 10.4258/hir.2012.18.4.272. Epub 2012 Dec 31. Healthc Inform Res. 2012. PMID: 23346478 Free PMC article.

4

GEE: An Informatics Tool for Gene Expression Data Explore.

Lee SY, Park CH, Yoon JH, Yun S, Kim JH. Lee SY, et al. Among authors: kim jh. Healthc Inform Res. 2016 Apr;22(2):81-8. doi: 10.4258/hir.2016.22.2.81. Epub 2016 Apr 30. Healthc Inform Res. 2016. PMID: 27200217 Free PMC article.

5

Markers of disease and steroid responsiveness in paediatric idiopathic nephrotic syndrome: Whole-transcriptome sequencing of peripheral blood mononuclear cells.

Kang HG, Seo H, Lim JH, Kim JI, Han KH, Park HW, Koo JW, Kim KH, Kim JH, Cheong HI, Ha IS. Kang HG, et al. Among authors: kim ji, kim kh, kim jh. J Int Med Res. 2017 Jun;45(3):948-963. doi: 10.1177/0300060516652762. Epub 2017 Jan 1. J Int Med Res. 2017. PMID: 28639503 Free PMC article.

6

Evaluation of exome variants using the Ion Proton Platform to sequence error-prone regions.

Seo H, Park Y, Min BJ, Seo ME, Kim JH. Seo H, et al. Among authors: kim jh. PLoS One. 2017 Jul 24;12(7):e0181304. doi: 10.1371/journal.pone.0181304. eCollection 2017. PLoS One. 2017. PMID: 28742110 Free PMC article.

7

APEX1 Polymorphism and Mercaptopurine-Related Early Onset Neutropenia in Pediatric Acute Lymphoblastic Leukemia.

Kim H, Seo H, Park Y, Min BJ, Seo ME, Park KD, Shin HY, Kim JH, Kang HJ. Kim H, et al. Among authors: kim jh. Cancer Res Treat. 2018 Jul;50(3):823-834. doi: 10.4143/crt.2017.351. Epub 2017 Sep 4. Cancer Res Treat. 2018. PMID: 28882023 Free PMC article.

8

Deleterious genetic variants in ciliopathy genes increase risk of ritodrine-induced cardiac and pulmonary side effects.

Seo H, Kwon EJ, You YA, Park Y, Min BJ, Yoo K, Hwang HS, Kim JH, Kim YJ. Seo H, et al. Among authors: kim yj, kim jh. BMC Med Genomics. 2018 Jan 24;11(1):4. doi: 10.1186/s12920-018-0323-4. BMC Med Genomics. 2018. PMID: 29368655 Free PMC article.

9

Discovery of donor genotype associated with long-term survival of patients with hematopoietic stem cell transplantation in refractory acute myeloid leukemia.

Ock CY, Seo H, Kim DY, Min BJ, Park Y, Cheong HS, Kim HL, Song EY, Kim I, Yoon SS, Kim JH, Koh Y. Ock CY, et al. Among authors: kim hl, kim dy, kim i, kim jh. Leuk Lymphoma. 2019 Jul;60(7):1775-1781. doi: 10.1080/10428194.2018.1542142. Epub 2018 Dec 3. Leuk Lymphoma. 2019. PMID: 30507323

10

Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.

Choi HS, Choi Q, Kim JA, Im KO, Park SN, Park Y, Shin HY, Kang HJ, Kook H, Kim SY, Kim SJ, Kim I, Kim JY, Kim H, Park KD, Park KB, Park M, Park SK, Park ES, Park JA, Park JE, Park JK, Baek HJ, Seo JH, Shim YJ, Ahn HS, Yoo KH, Yoon HS, Won YW, Lee KS, Lee KC, Lee MJ, Lee SA, Lee JA, Lee JM, Lee JH, Lee JW, Lim YT, Jung HJ, Chueh HW, Choi EJ, Jung HL, Kim JH, Lee DS; Hereditary Hemolytic Anemia Working Party of the Korean Society of Hematology. Choi HS, et al. Among authors: kim jy, kim h, kim sy, kim ja, kim sj, kim i, kim jh. Orphanet J Rare Dis. 2019 May 23;14(1):114. doi: 10.1186/s13023-019-1070-0. Orphanet J Rare Dis. 2019. PMID: 31122244 Free PMC article.

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