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PubPharm (32)
1
Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms
enthalten in:
bioRxiv.org
| 2024
von
Pividori, M.
|
Lu, S.
|
Li, B.
| +14
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2
Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population
enthalten in:
bioRxiv.org
| 2024
von
Verma, S.
|
Keat, K.
|
Li, B.
| +9
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3
Red Teaming Large Language Models in Medicine: Real-World Insights on Model Behavior
enthalten in:
bioRxiv.org
| 2024
von
Chang, C.
|
Farah, H.
|
Gui, H.
| +77
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4
Multi-ancestry Genome-wide Association Study of Varicose Veins Reveals Polygenic Architecture, Genetic Overlap with Arterial and Venous Disease, and Novel Therapeutic Opportunities
enthalten in:
bioRxiv.org
| 2023
von
Levin, M.
|
Huffman, J.
|
Verma, A.
| +16
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5
Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank
enthalten in:
American journal of human genetics
| 2023
von
Li, B.
|
Sangkuhl, K.
|
Whaley, R.
| +5
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6
Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms
enthalten in:
Nature communications
| 2023
von
Pividori, M.
|
Lu, S.
|
Li, B.
| +15
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7
Collective feature selection to identify crucial epistatic variants
enthalten in:
bioRxiv.org
| 2023
von
Verma, S.
|
Lucas, A.
|
Zhang, X.
| +8
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8
How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT)
enthalten in:
Clinical pharmacology and therapeutics
| 2023
von
Li, B.
|
Sangkuhl, K.
|
Keat, K.
| +9
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9
Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort
enthalten in:
PLoS genetics
| 2023
von
Hui, D.
|
Mehrabi, S.
|
Quimby, A.
| +12
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10
How to Run the Pharmacogenomics Clinical Annotation Tool ( PharmCAT)
enthalten in:
Clinical Pharmacology & Therapeutics
| 2023
von
Li, B.
|
Sangkuhl, K.
|
Keat, K.
| +9
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570
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