Year |
Citation |
Score |
2023 |
Xu Y, Liu K, Li C, Li M, Liu F, Zhou X, Sun M, Ranganathan M, Zhang L, Wang S, Hu X, Xu Y. The Largest Chinese Cohort Study Indicates Homologous Recombination Pathway Gene Mutations as Another Major Genetic Risk Factor for Colorectal Cancer with Heterogeneous Clinical Phenotypes. Research (Washington, D.C.). 6: 0249. PMID 37854294 DOI: 10.34133/research.0249 |
0.335 |
|
2023 |
Lasser M, Sun N, Xu Y, Wang S, Drake S, Law K, Gonzalez S, Wang B, Drury V, Castillo O, Zaltsman Y, Dea J, Bader E, McCluskey KE, State MW, et al. Pleiotropy of autism-associated chromatin regulators. Development (Cambridge, England). PMID 37366052 DOI: 10.1242/dev.201515 |
0.578 |
|
2023 |
Ma C, Xue T, Peng Q, Zhang J, Guan J, Ding W, Li Y, Xia P, Zhou L, Zhao T, Wang S, Quan L, Li CY, Liu Y. A novel N-Deoxyadenine methyltransferase METL-9 modulates C. elegans immunity via dichotomous mechanisms. Cell Research. PMID 37271765 DOI: 10.1038/s41422-023-00826-y |
0.564 |
|
2023 |
Li Z, Wang L, Wang S. A heterozygous mutation in ITGB4 causing a mild phenotype of junctional epidermolysis bullosa. Pediatric Dermatology. PMID 36813478 DOI: 10.1111/pde.15282 |
0.311 |
|
2023 |
Xu H, Woicik A, Poon H, Altman RB, Wang S. Multilingual translation for zero-shot biomedical classification using BioTranslator. Nature Communications. 14: 738. PMID 36759510 DOI: 10.1038/s41467-023-36476-2 |
0.364 |
|
2022 |
Yang L, Wang S, Altman RB. POPDx: an automated framework for patient phenotyping across 392 246 individuals in the UK Biobank study. Journal of the American Medical Informatics Association : Jamia. PMID 36469791 DOI: 10.1093/jamia/ocac226 |
0.385 |
|
2021 |
Wang S, Pisco AO, McGeever A, Brbic M, Zitnik M, Darmanis S, Leskovec J, Karkanias J, Altman RB. Leveraging the Cell Ontology to classify unseen cell types. Nature Communications. 12: 5556. PMID 34548483 DOI: 10.1038/s41467-021-25725-x |
0.397 |
|
2021 |
Li Z, Wang L, Wang S. Hyperpigmentation in a Chinese family with autosomal dominant Cole disease. Experimental Dermatology. PMID 34297442 DOI: 10.1111/exd.14434 |
0.316 |
|
2021 |
McInnes G, Sharo AG, Koleske ML, Brown JEH, Norstad M, Adhikari AN, Wang S, Brenner SE, Halpern J, Koenig BA, Magnus DC, Gallagher RC, Giacomini KM, Altman RB. Opportunities and challenges for the computational interpretation of rare variation in clinically important genes. American Journal of Human Genetics. 108: 535-548. PMID 33798442 DOI: 10.1016/j.ajhg.2021.03.003 |
0.479 |
|
2021 |
Cao F, Wu Q, Sui Y, Wang S, Dou Y, Hua W, Kong L, Wang L, Zhang J, Jiang T, Yang X. All-Inorganic Quantum Dot Light-Emitting Diodes with Suppressed Luminance Quenching Enabled by Chloride Passivated Tungsten Phosphate Hole Transport Layers. Small (Weinheim An Der Bergstrasse, Germany). e2100030. PMID 33783126 DOI: 10.1002/smll.202100030 |
0.433 |
|
2020 |
Brbić M, Zitnik M, Wang S, Pisco AO, Altman RB, Darmanis S, Leskovec J. MARS: discovering novel cell types across heterogeneous single-cell experiments. Nature Methods. PMID 33077966 DOI: 10.1038/s41592-020-00979-3 |
0.387 |
|
2020 |
Wang S, Flynn ER, Altman RB. Gaussian Embedding for Large-scale Gene Set Analysis. Nature Machine Intelligence. 2: 387-395. PMID 32968711 DOI: 10.1038/s42256-020-0193-2 |
0.376 |
|
2019 |
Zhao X, Wang S, Hao J, Zhu P, Zhang X, Wu M. A Whole-Exome Sequencing Study of Tourette Disorder in a Chinese Population. Dna and Cell Biology. PMID 31855460 DOI: 10.1089/dna.2019.4746 |
0.361 |
|
2019 |
Yang X, Yang X, Chen J, Li S, Zeng Q, Huang AY, Ye AY, Yu Z, Wang S, Jiang Y, Wu X, Wu Q, Wei L, Zhang Y. ATP1A3 mosaicism in families with alternating hemiplegia of childhood. Clinical Genetics. PMID 30891744 DOI: 10.1111/Cge.13539 |
0.781 |
|
2019 |
Zhou WZ, Zhang J, Li Z, Lin X, Li J, Wang S, Yang C, Wu Q, Ye AY, Wang M, Wang D, Pu TZ, Wu YY, Wei L. Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Human Mutation. PMID 30763456 DOI: 10.1002/Humu.23724 |
0.782 |
|
2018 |
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 25: 3544. PMID 30566877 DOI: 10.1016/j.celrep.2018.12.024 |
0.761 |
|
2018 |
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 24: 3441-3454.e12. PMID 30257206 DOI: 10.1016/J.Celrep.2018.08.082 |
0.79 |
|
2018 |
Willsey AJ, Morris MT, Wang S, Willsey HR, Sun N, Teerikorpi N, Baum TB, Cagney G, Bender KJ, Desai TA, Srivastava D, Davis GW, Doudna J, Chang E, Sohal V, et al. The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders. Cell. 174: 505-520. PMID 30053424 DOI: 10.1016/J.Cell.2018.06.016 |
0.561 |
|
2018 |
Ye AY, Dou Y, Yang X, Wang S, Huang AY, Wei L. A model for postzygotic mosaicisms quantifies the allele fraction drift, mutation rate, and contribution to de novo mutations. Genome Research. PMID 29875290 DOI: 10.1101/Gr.230003.117 |
0.755 |
|
2018 |
Huang AY, Yang X, Wang S, Zheng X, Wu Q, Ye AY, Wei L. Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs. Plos Genetics. 14: e1007395. PMID 29763432 DOI: 10.1371/Journal.Pgen.1007395 |
0.768 |
|
2017 |
Yang X, Liu A, Xu X, Yang X, Zeng Q, Ye AY, Yu Z, Wang S, Huang AY, Wu X, Wu Q, Wei L, Zhang Y. Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort. Scientific Reports. 7: 15677. PMID 29142202 DOI: 10.1038/S41598-017-15814-7 |
0.782 |
|
2017 |
Dou Y, Yang X, Li Z, Wang S, Zhang Z, Ye AY, Yan L, Yang C, Wu Q, Li J, Zhao B, Huang AY, Wei L. Post-zygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations. Human Mutation. PMID 28503910 DOI: 10.1002/Humu.23255 |
0.738 |
|
2015 |
Xu X, Yang X, Wu Q, Liu A, Yang X, Ye AY, Huang AY, Li J, Wang M, Yu Z, Wang S, Zhang Z, Wu X, Wei L, Zhang Y. Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome. Human Mutation. PMID 26096185 DOI: 10.1002/Humu.22819 |
0.777 |
|
2014 |
Huang AY, Xu X, Ye AY, Wu Q, Yan L, Zhao B, Yang X, He Y, Wang S, Zhang Z, Gu B, Zhao HQ, Wang M, Gao H, Gao G, et al. Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals. Cell Research. 24: 1311-27. PMID 25312340 DOI: 10.1038/Cr.2014.131 |
0.756 |
|
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