Author

Shaun Dabe

Desert Research InstituteORCID 0000-0002-2494-962XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexandre BolzeiD· 2 shared Gai ElhananiD· 2 shared Harry Reed· 2 shared Joseph J. GrzymskiiD· 2 shared Nicole L. WashingtoniD· 2 shared William J. Metcalf· 2 shared Alexa Anderson· 1 shared Anthony D. SlonimiD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alexandre BolzeORCID

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2 papers

Recent·Most cited

Combining rare and common genetic variants improves population risk stratification for breast cancer

Alexandre Bolze, Daniel Kiser, Kelly M. Schiabor Barrett, Gai Elhanan, Jamie M. Schnell Blitstein, Iva Neveux, Shaun Dabe, Harry Reed, Alexa Anderson, William J. Metcalf, Ekaterina Orlova, Ildiko Thibodeau, Natalie Telis, Ruomu Jiang, Nicole L. Washington, , Joseph J. Grzymski

This study evaluates genetic screening approaches for breast cancer risk, finding that combining rare and common variants improves risk stratification.

Genetics in Medicine Open · Jan 1, 2024Peer-reviewedGenetic & Genomic Medicine

Population Health Genetic Screening for Tier 1 Inherited Diseases in Northern Nevada: 90% of At-Risk Carriers are Missed

Joseph J. Grzymski, Gai Elhanan, E Smith, Chris J. Rowan, Nathan R. Slotnick, Shaun Dabe, Karen A. Schlauch, Robert W. Read, William J. Metcalf, Bruce Lipp, Harry Reed, Elissa Levin, Jau‐Tsuen Kao, Misha D. Rashkin, Johnathan Bowes, , James T. Lu

The paper finds that 90% of carriers of inherited disease variants are missed in current medical practice, highlighting the need for population-based genetic screening.

bioRxiv · May 27, 2019 · PreprintGenetics