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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 2 |
2022 | 2 |
2024 | 1 |
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5 results
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Page 1
Quantifying concordant genetic effects of de novo mutations on multiple disorders.
Elife. 2022 Jun 6;11:e75551. doi: 10.7554/eLife.75551.
Elife. 2022.
PMID: 35666111
Free PMC article.
Integrative modeling of transmitted and de novo variants identifies novel risk genes for congenital heart disease.
Li M, Zeng X, Jin C, Jin SC, Dong W, Brueckner M, Lifton R, Lu Q, Zhao H.
Li M, et al.
Quant Biol. 2021 Jun;9(2):216-227. doi: 10.15302/j-qb-021-0248.
Quant Biol. 2021.
PMID: 35414959
Free PMC article.
Item in Clipboard
Statistical methods for assessing the effects of de novo variants on birth defects.
Xie Y, Wu R, Li H, Dong W, Zhou G, Zhao H.
Xie Y, et al.
Hum Genomics. 2024 Mar 14;18(1):25. doi: 10.1186/s40246-024-00590-z.
Hum Genomics. 2024.
PMID: 38486307
Free PMC article.
Review.
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M-DATA: A statistical approach to jointly analyzing de novo mutations for multiple traits.
Xie Y, Li M, Dong W, Jiang W, Zhao H.
Xie Y, et al.
PLoS Genet. 2021 Nov 4;17(11):e1009849. doi: 10.1371/journal.pgen.1009849. eCollection 2021 Nov.
PLoS Genet. 2021.
PMID: 34735430
Free PMC article.
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Network assisted analysis of de novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart disease.
Xie Y, Jiang W, Dong W, Li H, Jin SC, Brueckner M, Zhao H.
Xie Y, et al.
PLoS Genet. 2022 Jun 7;18(6):e1010252. doi: 10.1371/journal.pgen.1010252. eCollection 2022 Jun.
PLoS Genet. 2022.
PMID: 35671298
Free PMC article.
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