Year |
Citation |
Score |
2023 |
Shin U, Choi Y, Ko HS, Myung K, Lee S, Cheon CK, Lee Y. A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafish. Human Genomics. 17: 44. PMID 37208785 DOI: 10.1186/s40246-023-00491-7 |
0.619 |
|
2022 |
Ju MK, Lee JR, Choi Y, Park SY, Sul HJ, Chung HJ, An S, Lee S, Jung E, Kim B, Choi BY, Kim BJ, Kim HS, Lim H, Kang HS, et al. PWWP2B promotes DNA end resection and homologous recombination. Embo Reports. e53492. PMID 35582821 DOI: 10.15252/embr.202153492 |
0.578 |
|
2020 |
Cheon CK, Lee YJ, Yoo S, Lee JH, Lee JE, Kim HJ, Choi IJ, Choi Y, Lee S, Yoon JY. Delineation of the genetic and clinical spectrum, including candidate genes, of monogenic diabetes: a multicenter study in South Korea. Journal of Pediatric Endocrinology & Metabolism : Jpem. PMID 33031055 DOI: 10.1515/jpem-2020-0336 |
0.562 |
|
2020 |
Jeon S, Bhak Y, Choi Y, Jeon Y, Kim S, Jang J, Jang J, Blazyte A, Kim C, Kim Y, Shim J, Kim N, Kim YJ, Park SG, Kim J, et al. Korean Genome Project: 1094 Korean personal genomes with clinical information. Science Advances. 6: eaaz7835. PMID 32766443 DOI: 10.1126/Sciadv.Aaz7835 |
0.712 |
|
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