Author

Ivette Zelaya

University of California, Los Angeles

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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Genetics· 3

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Organism:non-human primate· 2 Assay:bulk RNA-seq· 1 Research Focus:eQTL / molecular QTL mapping· 1 Research Focus:GWAS / association mapping· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anna J. JasinskaiD· 2 shared Giovanni CoppolaiD· 2 shared Hannes SvardaliD· 2 shared Jay R. KaplaniD· 2 shared Matthew J. JorgenseniD· 2 shared Nelson B. FreimeriD· 2 shared Richard K. WilsoniD· 2 shared Susan K. ServiceiD· 2 shared

Activity by Year

2016-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Anna J. JasinskaORCID

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3 papers

Recent·Most cited

The burden of deleterious variants in a non-human primate biomedical model

Vasily E. Ramensky, Anna J. Jasinska, Sandeep Deverasetty, Hannes Svardal, Ivette Zelaya, Matthew J. Jorgensen, Jay R. Kaplan, J. Mark Cline, Anastasia A. Zharikova, Susan K. Service, Richard K. Wilson, Giovanni Coppola, Nelson B. Freimer, Wesley C. Warren

The paper identifies homozygous protein-truncating variants in vervet monkeys using whole genome sequencing and explores their potential impact on early infant mortality.

bioRxiv · Sep 27, 2019 · PreprintGenetics

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

Anna J. Jasinska, Ivette Zelaya, Susan K. Service, Christine B. Peterson, Rita M. Cantor, Oi‐Wa Choi, Joseph A. DeYoung, Eleazar Eskin, Lynn A. Fairbanks, Scott C. Fears, Allison Furterer, Yu Shu Huang, Vasily E. Ramensky, Christopher A. Schmitt, Hannes Svardal, , Nelson B. Freimer

The paper generates a transcriptome resource and eQTL catalogue in vervet monkeys, revealing sex and age-related expression patterns and key regulatory loci.

Nature Genetics · Oct 30, 2017Peer-reviewedGenetics

Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

Alden Y Huang, Dongmei Yu, Lea K Davis, Jae-Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen, Lauren M McGrath, Cornelia Illmann, Paul Sandor, Cathy L Barr, Marco Grados, , Danielle C Cath

The paper identifies two rare copy number variants, NRXN1 and CNTN6, significantly increasing the risk of Tourette syndrome in a European ancestry sample.

bioRxiv · Jul 8, 2016Genetics