Parents
Sign in to add mentor| Emilia Entcheva | grad student | George Washington University (BME Tree) | |
| Gholson James Lyon | grad student | 2012- | CSHL |
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Publications
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| Belbachir N, Wu Y, Shen M, et al. (2023) Studying Long QT Syndrome Caused by Genetic Variants Using Patient-Derived Induced Pluripotent Stem Cells. Circulation. 148: 1598-1601 |
| Li L, Bin Mao, Li S, et al. (2019) Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta. Human Mutation |
| Wu Y, Lyon GJ. (2018) NAA10-related syndrome. Experimental & Molecular Medicine. 50: 85 |
| Fang H, Wu Y, Yang H, et al. (2017) Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine. Bmc Medical Genomics. 10: 10 |
| Fang H, Bergmann EA, Arora K, et al. (2016) Indel variant analysis of short-read sequencing data with Scalpel. Nature Protocols. 11: 2529-2548 |
| Klimas A, Wu Y, Ambrosi CM, et al. (2016) Disease Modeling in Human Induced Pluripotent Stem Cell Derived Cardiomyocytes Using High-Throughput All-Optical Dynamic Cardiac Electrophysiology Frontiers in Optics |
| Jiménez-Barrón LT, O'Rawe JA, Wu Y, et al. (2015) Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline. Cold Spring Harbor Molecular Case Studies. 1: a000422 |
| O'Rawe JA, Wu Y, Dörfel MJ, et al. (2015) TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations. American Journal of Human Genetics. 97: 922-32 |
| Myklebust LM, Van Damme P, Støve SI, et al. (2015) Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects. Human Molecular Genetics. 24: 1956-76 |
| Fang H, Wu Y, Narzisi G, et al. (2014) Reducing INDEL calling errors in whole genome and exome sequencing data. Genome Medicine. 6: 89 |