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Author Correction: Analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
Moynihan D, Monaco S, Ting TW, Narasimhalu K, Hsieh J, Kam S, Lim JY, Lim WK, Davila S, Bylstra Y, Balakrishnan ID, Heng M, Chia E, Yeo KK, Goh BK, Gupta R, Tan T, Baynam G, Jamuar SS. Moynihan D, et al. Among authors: lim wk. Sci Rep. 2024 May 2;14(1):10084. doi: 10.1038/s41598-024-60776-2. Sci Rep. 2024. PMID: 38698204 Free PMC article. No abstract available.
Cluster analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
Moynihan D, Monaco S, Ting TW, Narasimhalu K, Hsieh J, Kam S, Lim JY, Lim WK, Davila S, Bylstra Y, Balakrishnan ID, Heng M, Chia E, Yeo KK, Goh BK, Gupta R, Tan T, Baynam G, Jamuar SS. Moynihan D, et al. Among authors: lim wk. Sci Rep. 2024 Mar 1;14(1):5056. doi: 10.1038/s41598-024-55424-8. Sci Rep. 2024. PMID: 38424111 Free PMC article.
Correction to: Family history assessment significantly enhances delivery of precision medicine in the genomics era.
Bylstra Y, Lim WK, Kam S, Tham KW, Wu RR, Teo JX, Davila S, Kuan JL, Chan SH, Bertin N, Yang CX, Rozen S, Teh BT, Yeo KK, Cook SA, Jamuar SS, Ginsburg GS, Orlando LA, Tan P. Bylstra Y, et al. Among authors: lim wk. Genome Med. 2021 Jul 5;13(1):109. doi: 10.1186/s13073-021-00916-9. Genome Med. 2021. PMID: 34225778 Free PMC article. No abstract available.
Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.
Bylstra Y, Kuan JL, Lim WK, Bhalshankar JD, Teo JX, Davila S, Teh BT, Rozen S, Tan EC, Liew WKM, Yeo KK, Tan P; SinGapore Incidental Finding (SGIF) study group; Saw SM, Cheng CY, Cook S, Foo R, Jamuar SS. Bylstra Y, et al. Among authors: lim wk. Genet Med. 2019 Jan;21(1):207-212. doi: 10.1038/s41436-018-0008-6. Epub 2018 Jul 2. Genet Med. 2019. PMID: 29961769 Free article.
Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.
Bylstra Y, Kuan JL, Lim WK, Bhalshankar JD, Teo JX, Davila S, Teh BT, Rozen S, Tan EC, Liew WKM, Yeo KK, Tan P; SinGapore Incidental Finding (SGIF) study group; Saw SM, Cheng CY, Cook S, Foo R, Jamuar SS. Bylstra Y, et al. Among authors: lim wk. Genet Med. 2018 Dec;20(12):1692. doi: 10.1038/s41436-018-0142-1. Genet Med. 2018. PMID: 30089799 Free article.
DEGS1 -related leukodystrophy: a clinical report and review of literature.
Wong MST, Thomas T, Lim JY, Kam S, Teo JX, Ching J, Goh CYJ, Jamuar SS, Lim WK, Koh AL. Wong MST, et al. Among authors: lim wk, lim jy. Clin Dysmorphol. 2023 Jul 1;32(3):106-111. doi: 10.1097/MCD.0000000000000457. Epub 2023 May 1. Clin Dysmorphol. 2023. PMID: 37195341 Review.
339 results