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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 3 |
2022 | 3 |
2023 | 1 |
2024 | 0 |
Search Results
7 results
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Page 1
Template-based prediction of protein structure with deep learning.
BMC Genomics. 2020 Dec 29;21(Suppl 11):878. doi: 10.1186/s12864-020-07249-8.
BMC Genomics. 2020.
PMID: 33372607
Free PMC article.
Predicting functional effect of missense variants using graph attention neural networks.
Zhang H, Xu MS, Fan X, Chung WK, Shen Y.
Zhang H, et al.
Nat Mach Intell. 2022 Nov;4(11):1017-1028. doi: 10.1038/s42256-022-00561-w. Epub 2022 Nov 15.
Nat Mach Intell. 2022.
PMID: 37484202
Free PMC article.
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Accurate in silico confirmation of rare copy number variant calls from exome sequencing data using transfer learning.
Tan R, Shen Y.
Tan R, et al.
Nucleic Acids Res. 2022 Nov 28;50(21):e123. doi: 10.1093/nar/gkac788.
Nucleic Acids Res. 2022.
PMID: 36124672
Free PMC article.
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Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas.
Zhong G, Ahimaz P, Edwards NA, Hagen JJ, Faure C, Lu Q, Kingma P, Middlesworth W, Khlevner J, El Fiky M, Schindel D, Fialkowski E, Kashyap A, Forlenza S, Kenny AP, Zorn AM, Shen Y, Chung WK.
Zhong G, et al.
HGG Adv. 2022 Apr 16;3(3):100107. doi: 10.1016/j.xhgg.2022.100107. eCollection 2022 Jul 14.
HGG Adv. 2022.
PMID: 35519826
Free PMC article.
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VBASS enables integration of single cell gene expression data in Bayesian association analysis of rare variants.
Zhong G, Choi YA, Shen Y.
Zhong G, et al.
Commun Biol. 2023 Jul 25;6(1):774. doi: 10.1038/s42003-023-05155-9.
Commun Biol. 2023.
PMID: 37491581
Free PMC article.
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EM-mosaic detects mosaic point mutations that contribute to congenital heart disease.
Hsieh A, Morton SU, Willcox JAL, Gorham JM, Tai AC, Qi H, DePalma S, McKean D, Griffin E, Manheimer KB, Bernstein D, Kim RW, Newburger JW, Porter GA Jr, Srivastava D, Tristani-Firouzi M, Brueckner M, Lifton RP, Goldmuntz E, Gelb BD, Chung WK, Seidman CE, Seidman JG, Shen Y.
Hsieh A, et al.
Genome Med. 2020 Apr 29;12(1):42. doi: 10.1186/s13073-020-00738-1.
Genome Med. 2020.
PMID: 32349777
Free PMC article.
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Genomic analyses implicate noncoding de novo variants in congenital heart disease.
Richter F, Morton SU, Kim SW, Kitaygorodsky A, Wasson LK, Chen KM, Zhou J, Qi H, Patel N, DePalma SR, Parfenov M, Homsy J, Gorham JM, Manheimer KB, Velinder M, Farrell A, Marth G, Schadt EE, Kaltman JR, Newburger JW, Giardini A, Goldmuntz E, Brueckner M, Kim R, Porter GA Jr, Bernstein D, Chung WK, Srivastava D, Tristani-Firouzi M, Troyanskaya OG, Dickel DE, Shen Y, Seidman JG, Seidman CE, Gelb BD.
Richter F, et al.
Nat Genet. 2020 Aug;52(8):769-777. doi: 10.1038/s41588-020-0652-z. Epub 2020 Jun 29.
Nat Genet. 2020.
PMID: 32601476
Free PMC article.
Clinical Trial.
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