Wei-Qi Wei
Genetics · 2010–2021
A researcher in the Science corpus: 8 papers; trusts 8 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 98 citations into it
- Molecular Biology — 62 citations into it
- Public Health, Environmental and Occupational Health — 13 citations into it
- Cancer Research — 9 citations into it
Whom Wei-Qi Wei trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Isaac S. Kohane
- Joshua Charles Denny
- Abel N. Kho
- Michael Kuhn
- Teri Manolio
- Omri Gottesman
- Michael L. Metzker
- Elaine R. Mardis
- George Hripcsak
- Marylyn DeRiggi Ritchie
Who trusts Wei-Qi Wei overall
Papers from Wei-Qi Wei's perspective
Ordered by how strongly the researchers Wei-Qi Wei trusts endorse each paper. Same corpus, a different order for every researcher.
- The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies (BMC Medical Genomics)
- Quality Control Procedures for Genome Wide Association Studies (Current Protocols in Human Genetics)
- PLINK: a tool set for whole-genome association and population-based linkage analyses.
- R: A language and environment for statistical computing.
- Genomics, type 2 diabetes, and obesity. (New England Journal of Medicine)
- Stimulating the adoption of health information technology. (West Virginia Medical Journal)
- Next-generation phenotyping of electronic health records
- Portability of an algorithm to identify rheumatoid arthritis in electronic health records
- Electronic medical records for discovery research in rheumatoid arthritis
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Their papers
- Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies (2017) — 1,245 citations
- Extracting research-quality phenotypes from electronic health records to support precision medicine (2015) — 228 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Precision Medicine, AI, and the Future of Personalized Health Care (2020) — 1,308 citations
- Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals (2017) — 87 citations
- Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record (2017) — 336 citations
- Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study (2012) — 287 citations
- A high throughput semantic concept frequency based approach for patient identification: a case study using type 2 diabetes mellitus clinical notes. (2010) — 33 citations