Binglan Li
Affiliations: | Pennsylvania State University, State College, PA, United States |
Area:
BioinformaticsGoogle:
"Binglan Li"
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Publications
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| Li B, Sangkuhl K, Whaley R, et al. (2023) Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank. American Journal of Human Genetics. 110: 1628-1647 |
| Pividori M, Lu S, Li B, et al. (2023) Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms. Nature Communications. 14: 5562 |
| Hui D, Mehrabi S, Quimby AE, et al. (2023) Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort. Plos Genetics. 19: e1010584 |
| Verma SS, Keat K, Li B, et al. (2022) Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population. Journal of Translational Medicine. 20: 550 |
| Li B, Sangkuhl K, Keat K, et al. (2022) How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT). Clinical Pharmacology and Therapeutics |
| Li B, Whirl-Carrillo M, Wright MW, et al. (2022) An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease Genetics. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 27: 385-396 |
| Li B, Ritchie MD. (2021) From GWAS to Gene: Transcriptome-Wide Association Studies and Other Methods to Functionally Understand GWAS Discoveries. Frontiers in Genetics. 12: 713230 |
| Ahmadmehrabi S, Li B, Hui D, et al. (2021) A Genome-First Approach to Rare Variants in Dominant Postlingual Hearing Loss Genes in a Large Adult Population. Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery. 1945998211029544 |
| Li B, Veturi Y, Verma A, et al. (2021) Tissue specificity-aware TWAS (TSA-TWAS) framework identifies novel associations with metabolic, immunologic, and virologic traits in HIV-positive adults. Plos Genetics. 17: e1009464 |
| Ahmadmehrabi S, Li B, Park J, et al. (2021) Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults. Human Genetics |