BL
Binglan Li
Cedars-Sinai Medical Center, Stanford University, University of Pennsylvania, Fudan University
Research areas: Biochemistry, Genetics and Molecular Biology · Genetics · Genetic Associations and Epidemiology · Bioinformatics and Genomic Networks · Genetic Mapping and Diversity in Plants and Animals
0000-0002-0103-6107
Employment
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Cedars-Sinai Medical Center Research Data Scientist2024 - Present
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Stanford University Data Scientist2023 - 2024
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Stanford University Postdoctoral Scholar2020 - 2023
Education
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University of Pennsylvania Doctor of Philosophy2018 - 2020
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Fudan University Bachelor of Science2011 - 2015
Projects & Funding
Projects & funding information is unavailable.
Publications (25)
- Agentic AI and the rise of in silico team science in biomedical research Save
- Drug repurposing for Alzheimer’s disease using a graph-of-thoughts based large language model to infer drug-disease relationships in a comprehensive knowledge graph Save
- Red teaming ChatGPT in medicine to yield real-world insights on model behavior Save
- PGxQA: A Resource for Evaluating LLM Performance for Pharmacogenomic QA Tasks. Save
- From sample to star alleles: a long-read pharmacogenomics pipeline powered by Twist target enrichment and PacBio HiFi sequencing Save
- Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank. Save
- How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT) Save
- Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort. Save
- Genetics of varicose veins reveals polygenic architecture and genetic overlap with arterial and venous disease Save
- Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population Save
- A first update on mapping the human genetic architecture of COVID-19 Save
- Polygenic risk vectors (PRV) improve genetic risk stratification for cardio-metabolic diseases Save
- Whole genome sequencing reveals host factors underlying critical Covid-19 Save
- An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease Genetics. Save
- Multi-ancestry gene-trait connection landscape using electronic health record (EHR) linked biobank data Save
- A Genome-First Approach to Rare Variants in Dominant Postlingual Hearing Loss Genes in a Large Adult Population. Save
- Mapping the human genetic architecture of COVID-19 Save
- Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms Save
- How Does the “Cookie-Bite” Audiogram Shape Perform in Discriminating Genetic Hearing Loss in Adults? Save
- Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults Save