Author

Jessica W. Chen

Stanford MedicineORCID 0000-0003-4425-6369Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Jessica W. Chen2 papers · Broad Institute

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexandra SockelliD· 1 shared Andrés Moreno‐EstradaiD· 1 shared Andrés Ruiz‐LinaresiD· 1 shared Carla GalloiD· 1 shared Carlos D. BustamanteiD· 1 shared Celeste S. EngiD· 1 shared Christian A. KunderiD· 1 shared Christopher R. GignouxiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexandra SockellORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedMay 18, 2022

Clotting factor genes are associated with preeclampsia in high altitude pregnant women in the Peruvian Andes

María A. Nieves-Colón, Keyla M. Badillo Rivera, Karla Sandoval…·Andrés Moreno‐Estrada

This study identifies clotting factor genes PROZ, F7, and F10 on chromosome 13 as associated with preeclampsia in high-altitude Andean families.

30 citationstop 3%

humanbulk RNA-seq

𝕏 PostBluesky

GenomicsbioRxivPreprintSep 18, 2020

STAMPede: A Precision Oncology Catalogue of Solid Tumors

Jessica W. Chen, Haik Kalantarian, Christian A. Kunder…·Helio A. Costa

STAMPede is a web-based portal for visualizing somatic tumor sequencing data from a solid tumor oncology panel, enabling query and display of gene-, variant-, and cancer-level summary statistics.

DOI 10.1101/2020.09.18.290635

humanwhole-exome sequencing

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