Tushar Bhangale, Ph.D.
Affiliations: | 2006 | University of Washington, Seattle, Seattle, WA |
Area:
Biomedical Engineering, Molecular BiologyGoogle:
"Tushar Bhangale"Parents
Sign in to add mentor| Deborah A. Nickerson | grad student | 2006 | University of Washington | |
| (Small insertion -deletion polymorphisms in the human genome: Characterization and automation of detection by resequencing.) | ||||
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Publications
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| Loomis SJ, Sadhu N, Fisher E, et al. (2023) Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials. Scientific Reports. 13: 14313 |
| Wall JD, Sathirapongsasuti JF, Gupta R, et al. (2023) South Asian medical cohorts reveal strong founder effects and high rates of homozygosity. Nature Communications. 14: 3377 |
| Orozco LD, Chen HH, Cox C, et al. (2020) Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration. Cell Reports. 30: 1246-1259.e6 |
| Lim YW, Chen-Harris H, Mayba O, et al. (2018) Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration. Proceedings of the National Academy of Sciences of the United States of America |
| Ye CJ, Chen J, Villani AC, et al. (2018) Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of transcripts under balancing selection. Genome Research |
| Rathore N, Ramani SR, Pantua H, et al. (2018) Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease. Plos Genetics. 14: e1007427 |
| Tom J, Chang D, Wuster A, et al. (2018) Enabling genome-wide association testing with multiple diseases and no healthy controls. Gene |
| Dressen A, Abbas AR, Cabanski C, et al. (2018) Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study. The Lancet. Respiratory Medicine |
| Mohan V, Radha V, Nguyen TT, et al. (2018) Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India. Bmc Medical Genetics. 19: 22 |
| Chang D, Choy D, Bhangale T, et al. (2018) A whole genome sequencing association study of severe, uncontrolled asthma European Respiratory Journal. 52 |