Author

Catherine Hypes

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

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aleksandar RajkoviciD· 1 shared Amrita NagasuriiD· 1 shared Aryo Garakani· 1 shared Bryan Walters· 1 shared Christina G. TiseiD· 1 shared David K. StevensoniD· 1 shared Gary Michael ShawiD· 1 shared Jonathan Adam BernsteiniD· 1 shared

Activity by Year

2026-2026 · 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

Aleksandar RajkovicORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

The Human Intolerome: a curated database to prioritize genomic variants in stillbirth, pregnancy loss, and neonatal death

Svetlana A. Yatsenko, Amrita Nagasuri, Vishal Soman, Aryo Garakani, Mona Amin‐Beidokhti, Uma Chandran, Mahmoud Aarabi, Tomiko Oskotsky, Syed Hassan Bukhari, Catherine Hypes, Zhiping Gu, Ruth Monteiro, Sammi E. Smith, Bryan Walters, Michael P. Snyder, , Aleksandar Rajkovic

The paper introduces the Intolerome Database, a curated resource of genes essential for human viability, to help prioritize genomic variants in cases of stillbirth, pregnancy loss, and neonatal death.

Genetics in Medicine · Mar 3, 2026Peer-reviewedGenetic & Genomic Medicine