Author

Delphine Yung

ORCID 0000-0002-4571-4977Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Adaani FrostiD· 2 shared Ankit A. DesaiiD· 2 shared Anna W. Coleman· 2 shared Carrie L. WelchiD· 2 shared Claudia G. Gonzaga-JaureguiiD· 2 shared Erika B. RosenzweigiD· 2 shared Ferhaan AhmadiD· 2 shared Fernando TorresiD· 2 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Adaani FrostORCID

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2 papers

Recent·Most cited

Rare variant analysis of 4,241 pulmonary arterial hypertension cases from an international consortium implicate FBLN2, PDGFD and rare de novo variants in PAH

Na Zhu, Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob Hagen, Xueya Zhou, Yicheng Guo, Johannes Karten, Divya Pandya, Tobias Tilly, Katie A. Lutz, Jennifer M. Martin, Carmen M. Treacy, Erika B. Rosenzweig, Usha Krishnan, , National Cohort Study of Idiopathic and Heritable PAH

This study identifies two new PAH risk genes, FBLN2 and PDGFD, through rare variant analysis of 4,241 PAH cases, with de novo variants contributing to ~15% of pediatric IPAH.

Genome Medicine · May 10, 2021Peer-reviewedGenetics

Novel risk genes and mechanisms implicated by exome sequencing of 2,572 individuals with pulmonary arterial hypertension

Na Zhu, Michael W. Pauciulo, Carrie L. Welch, Katie A. Lutz, Anna W. Coleman, Claudia G. Gonzaga-Jauregui, Jiayao Wang, Joseph M. Grimes, Lisa Joy Martin, Hua He, Russel Hirsch, R. James White, Marc Simon, David Badesch, Erika B. Rosenzweig, , William C. Nichols

The paper identifies two new risk genes for idiopathic pulmonary arterial hypertension through exome sequencing of 2,572 individuals.

Genome Medicine · Nov 14, 2019Peer-reviewedGenetics