Wang K - Search Results

1

Assessing the utility of large language models for phenotype-driven gene prioritization in the diagnosis of rare genetic disease.

Kim J, Wang K, Weng C, Liu C. Kim J, et al. Among authors: wang k. Am J Hum Genet. 2024 Oct 3;111(10):2190-2202. doi: 10.1016/j.ajhg.2024.08.010. Epub 2024 Sep 9. Am J Hum Genet. 2024. PMID: 39255797 Free PMC article.

2

Enhancing Phenotype Recognition in Clinical Notes Using Large Language Models: PhenoBCBERT and PhenoGPT.

Yang J, Liu C, Deng W, Wu D, Weng C, Zhou Y, Wang K. Yang J, et al. Among authors: wang k. ArXiv [Preprint]. 2023 Nov 9:arXiv:2308.06294v2. ArXiv. 2023. Update in: Patterns (N Y). 2023 Dec 05;5(1):100887. doi: 10.1016/j.patter.2023.100887 PMID: 37986722 Free PMC article. Updated. Preprint.

3

Phenotype-Driven Molecular Genetic Test Recommendation for Diagnosing Pediatric Rare Disorders.

Chen F, Ahimaz P, Wang K, Chung WK, Ta C, Weng C, Liu C. Chen F, et al. Among authors: wang k. Res Sq [Preprint]. 2023 Nov 22:rs.3.rs-3593490. doi: 10.21203/rs.3.rs-3593490/v1. Res Sq. 2023. Update in: NPJ Digit Med. 2024 Nov 21;7(1):333. doi: 10.1038/s41746-024-01331-1 PMID: 38045411 Free PMC article. Updated. Preprint.

4

Enhancing phenotype recognition in clinical notes using large language models: PhenoBCBERT and PhenoGPT.

Yang J, Liu C, Deng W, Wu D, Weng C, Zhou Y, Wang K. Yang J, et al. Among authors: wang k. Patterns (N Y). 2023 Dec 5;5(1):100887. doi: 10.1016/j.patter.2023.100887. eCollection 2024 Jan 12. Patterns (N Y). 2023. PMID: 38264716 Free PMC article.

5

Exploring the reversal curse and other deductive logical reasoning in BERT and GPT-based large language models.

Wu D, Yang J, Wang K. Wu D, et al. Among authors: wang k. Patterns (N Y). 2024 Jul 25;5(9):101030. doi: 10.1016/j.patter.2024.101030. eCollection 2024 Sep 13. Patterns (N Y). 2024. PMID: 39568650 Free PMC article.

6

Utility of genome sequencing in exome-negative pediatric patients with neurodevelopmental phenotypes.

Nomakuchi TT, Teferedegn EY, Li D, Muirhead KJ, Dubbs H, Leonard J, Muraresku C, Sergio E, Arnold K, Pizzino A, Skraban CM, Zackai EH, Wang K, Ganetzky RD, Vanderver AL, Ahrens-Nicklas RC, Bhoj EJK. Nomakuchi TT, et al. Among authors: wang k. Am J Med Genet A. 2024 Dec;194(12):e63817. doi: 10.1002/ajmg.a.63817. Epub 2024 Jul 19. Am J Med Genet A. 2024. PMID: 39031459

7

Bioformer: an efficient transformer language model for biomedical text mining.

Fang L, Chen Q, Wei CH, Lu Z, Wang K. Fang L, et al. Among authors: wang k. ArXiv [Preprint]. 2023 Feb 3:arXiv:2302.01588v1. ArXiv. 2023. PMID: 36945685 Free PMC article. Preprint.

8

Genetic variant classification by predicted protein structure: A case study on IRF6.

Murali H, Wang P, Liao EC, Wang K. Murali H, et al. Among authors: wang k, wang p. Comput Struct Biotechnol J. 2024 Feb 3;23:892-904. doi: 10.1016/j.csbj.2024.01.019. eCollection 2024 Dec. Comput Struct Biotechnol J. 2024. PMID: 38370976 Free PMC article.

9

Multi-label topic classification for COVID-19 literature with Bioformer.

Fang L, Wang K. Fang L, et al. Among authors: wang k. ArXiv [Preprint]. 2022 Apr 14:arXiv:2204.06758v1. ArXiv. 2022. PMID: 35441084 Free PMC article. Preprint.

10

KOLF2.1J iPSCs carry CNVs associated with neurodevelopmental disorders.

Gracia-Diaz C, Perdomo JE, Khan ME, Roule T, Disanza BL, Cajka GG, Lei S, Gagne AL, Maguire JA, Shalem O, Bhoj EJ, Ahrens-Nicklas RC, French DL, Goldberg EM, Wang K, Glessner JT, Akizu N. Gracia-Diaz C, et al. Among authors: wang k. Cell Stem Cell. 2024 Mar 7;31(3):288-289. doi: 10.1016/j.stem.2024.02.007. Cell Stem Cell. 2024. PMID: 38458176 No abstract available.

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