Author

Jovia L. Nierenberg

University of California, San FranciscoORCID 0000-0003-2376-6714Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Genomics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 4 Approach:statistical model· 3 Research Focus:variant effect prediction· 2 Assay:whole-exome sequencing· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Elad ZiviD· 3 shared Lawrence H. KushiiD· 2 shared Aaron W. AdamsoniD· 1 shared Alan B. ZondermaniD· 1 shared Alisa Knodle ManningiD· 1 shared Amy R. BentleyiD· 1 shared Ana BaraciD· 1 shared André Gerardus UitterlindeniD· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 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

3 shared papersGenetic & Genomic Medicine

Elad ZivORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

GenomicsMolecular CellPeer-reviewedDec 1, 2023

High throughput PRIME editing screens identify functional DNA variants in the human genome

Xingjie Ren, Han Kwang Yang, Jovia L. Nierenberg…·Yin Shen

This paper introduces PRIME, a high-throughput prime editing screen that identifies functional DNA variants in the human genome with base-pair resolution.

70 citationstop 2%

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJan 25, 2023

Whole exome sequencing and replication for breast cancer among Hispanic/Latino women identifies FANCM as a susceptibility gene for estrogen-receptor-negative breast cancer.

Jovia L. Nierenberg, Aaron W. Adamson, Donglei Hu…·Susan L. Neuhausen

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintFeb 11, 2022

Assessment of Genetic Susceptibility to Multiple Primary Cancers through Whole-Exome Sequencing in Two Large Multi-Ancestry Studies

Taylor B. Cavazos, Linda Kachuri, Rebecca E. Graff…·John S. Witte

This study identifies 22 genetic variant-phenotype associations linked to multiple primary cancers using whole-exome sequencing in two large multi-ancestry cohorts.

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsMolecular PsychiatryPeer-reviewedApr 15, 2021

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

Heming Wang, Raymond Noordam, Brian E. Cade…·Wei Zheng

The paper identifies novel genetic loci associated with blood pressure that interact with sleep duration across multiple ancestries.

23 citations

humanwhole-genome sequencing

𝕏 PostBluesky