Wong WH - Search Results

1

ACCURATE CONSTRUCTION OF LONG RANGE HAPLOTYPE IN UNRELATED INDIVIDUALS.

Johnson NA, London SJ, Romieu I, Wong WH, Tang H. Johnson NA, et al. Among authors: wong wh. Stat Sin. 2013;23:1441-1461. doi: 10.5705/ss.2012.141s. Stat Sin. 2013. PMID: 37398638 Free PMC article.

2

Genetic effects of sequence-conserved enhancer-like elements on human complex traits.

Zhu X, Ma S, Wong WH. Zhu X, et al. Among authors: wong wh. Genome Biol. 2024 Jan 2;25(1):1. doi: 10.1186/s13059-023-03142-1. Genome Biol. 2024. PMID: 38167462 Free PMC article.

3

Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders.

Zhou B, Arthur JG, Guo H, Kim T, Huang Y, Pattni R, Wang T, Kundu S, Luo JXJ, Lee H, Nachun DC, Purmann C, Monte EM, Weimer AK, Qu PP, Shi M, Jiang L, Yang X, Fullard JF, Bendl J, Girdhar K, Kim M, Chen X; PsychENCODE Consortium; Greenleaf WJ, Duncan L, Ji HP, Zhu X, Song G, Montgomery SB, Palejev D, Zu Dohna H, Roussos P, Kundaje A, Hallmayer JF, Snyder MP, Wong WH, Urban AE. Zhou B, et al. Among authors: wong wh. Cell. 2024 Nov 14;187(23):6687-6706.e25. doi: 10.1016/j.cell.2024.09.014. Epub 2024 Sep 30. Cell. 2024. PMID: 39353437

4

On the identifiability of the isoform deconvolution problem: application to select the proper fragment length in an RNA-seq library.

Ferrer-Bonsoms JA, Morales X, Afshar PT, Wong WH, Rubio A. Ferrer-Bonsoms JA, et al. Among authors: wong wh. Bioinformatics. 2022 Mar 4;38(6):1491-1496. doi: 10.1093/bioinformatics/btab873. Bioinformatics. 2022. PMID: 34978563 Free PMC article.

5

Heritability enrichment in context-specific regulatory networks improves phenotype-relevant tissue identification.

Feng Z, Duren Z, Xin J, Yuan Q, He Y, Su B, Wong WH, Wang Y. Feng Z, et al. Among authors: wong wh. Elife. 2022 Dec 16;11:e82535. doi: 10.7554/eLife.82535. Elife. 2022. PMID: 36525361 Free PMC article.

6

Current and future perspectives of single-cell multi-omics technologies in cardiovascular research.

Tan WLW, Seow WQ, Zhang A, Rhee S, Wong WH, Greenleaf WJ, Wu JC. Tan WLW, et al. Among authors: wong wh. Nat Cardiovasc Res. 2023 Jan;2(1):20-34. doi: 10.1038/s44161-022-00205-7. Epub 2023 Jan 18. Nat Cardiovasc Res. 2023. PMID: 39196210 Review.

7

EpiGePT: a Pretrained Transformer model for epigenomics.

Gao Z, Liu Q, Zeng W, Jiang R, Wong WH. Gao Z, et al. Among authors: wong wh. bioRxiv [Preprint]. 2024 Feb 3:2023.07.15.549134. doi: 10.1101/2023.07.15.549134. bioRxiv. 2024. PMID: 37502861 Free PMC article. Preprint.

8

Xrare: a machine learning method jointly modeling phenotypes and genetic evidence for rare disease diagnosis.

Li Q, Zhao K, Bustamante CD, Ma X, Wong WH. Li Q, et al. Among authors: wong wh. Genet Med. 2019 Sep;21(9):2126-2134. doi: 10.1038/s41436-019-0439-8. Epub 2019 Jan 24. Genet Med. 2019. PMID: 30675030 Free PMC article.

9

Use of blended feeds in children requiring tube feeding.

Sun J, Chuah I, Drobiszewski A, Arrowsmith F, Low R, Wong WHV, Kaur R, Dalby-Payne J. Sun J, et al. Among authors: wong whv. J Paediatr Child Health. 2024 Dec 20. doi: 10.1111/jpc.16750. Online ahead of print. J Paediatr Child Health. 2024. PMID: 39707605

10

EpiGePT: a pretrained transformer-based language model for context-specific human epigenomics.

Gao Z, Liu Q, Zeng W, Jiang R, Wong WH. Gao Z, et al. Among authors: wong wh. Genome Biol. 2024 Dec 18;25(1):310. doi: 10.1186/s13059-024-03449-7. Genome Biol. 2024. PMID: 39696471 Free PMC article.

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