Author

Kurt N. Hetrick

ORCID 0000-0002-9368-5656Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ada HamoshiD· 1 shared Adam L. Felsenfeld· 1 shared Adam W. HanseniD· 1 shared Alicia B. ByrneiD· 1 shared Arif O. HarmanciiD· 1 shared Arthur L. BeaudetiD· 1 shared Beryl B. CummingsiD· 1 shared Christian D. FrazariD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Ada HamoshORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Centers for Mendelian Genomics: A decade of facilitating gene discovery

Samantha M. Baxter, Jennifer Ellen Posey, Nicole J. Lake, Nara Lygia de Macena Sobreira, Jessica X. Chong, Steven G. Buyske, Elizabeth Blue, Lisa Helbling Chadwick, Zeynep Coban‐Akdemir, Kimberly Floy Doheny, Colleen P. Davis, Monkol Lek, Christopher Wellington, Shalini N. Jhangiani, Mark Gerstein, , Kurt N. Hetrick

The paper describes the role of the Centers for Mendelian Genomics in advancing gene discovery through data sharing, collaboration, and resource development over the past decade.

Genetics in Medicine · Feb 8, 2022Peer-reviewedGenetic & Genomic Medicine