Author

Amir S. Zare

23andMe (United States)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 3 Organism:human· 3 Approach:statistical model· 3 Assay:electronic health records· 2 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Aaron Kleinman· 3 shared Adam AutoniD· 3 shared Anjali J. Shastri· 3 shared Barry Hicks· 3 shared Carrie A. M. Northover· 3 shared Chao Tian· 3 shared David A. HindsiD· 3 shared Elizabeth S. Noblin· 3 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Aaron Kleinman

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Author profile →

3 papers

Recent·Most cited

Genetic determinants of daytime napping and effects on cardiometabolic health

Hassan S. Dashti, Iyas Daghlas, Jacqueline M. Lane, Yunru Huang, Miriam S. Udler, Heming Wang, Hanna Maria Ollila, Samuel E. Jones, Jaegil Kim, Andrew R. Wood, Michelle Agee, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah K. Clark, , Richa Saxena

This study identifies genetic loci associated with daytime napping and finds potential causal links between napping and cardiometabolic traits.

Nature Communications · Feb 10, 2021Peer-reviewedGenetic & Genomic Medicine

Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy

Kristi Krebs, Jonas Bovijn, Neil S. Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson, Dage Särg, Erik Abner, Triin Laisk, Yang Luo, Line Skotte, Frank Geller, Bjarke Feenstra, Wei Wang, Adam Auton, , João Fadista

The paper identifies HLA-B*55:01 as a genetic risk factor for penicillin allergy through genome-wide analysis of electronic health records and imputed HLA data.

The American Journal of Human Genetics · Sep 3, 2020Peer-reviewedGenetics

Genome-wide association and multi-omic analyses reveal new mechanisms for Heart Failure

Marios Arvanitis, Emmanouil Tampakakis, Yanxiao Zhang, Wei Wang, Adam Auton, Michelle Agee, Stella W. Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, , Alexis J. Battle

This study identifies one known and two novel genetic variants associated with heart failure through GWAS and multi-omic analyses, revealing potential causal mechanisms and shared heritability with musculoskeletal traits.

Nature Communications · Feb 28, 2020Peer-reviewedGenetic & Genomic Medicine