Author

Annette Zygmunt

Columbia University Irving Medical Center

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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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aliva DeiD· 1 shared Amy J. Wagner· 1 shared Badri Narayan VardarajaniD· 1 shared Brad W. WarneriD· 1 shared Christiana Farkouh‐Karoleski· 1 shared Dai H. ChungiD· 1 shared David J. McCulleyiD· 1 shared David T. Schindel· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aliva DeORCID

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1 paper

Recent·Most cited

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 and ALYREF as new candidate risk genes

Lu Qiao, Le Xu, Lan Yu, Julia Wynn, Rebecca Hernan, Xueya Zhou, Christiana Farkouh‐Karoleski, Usha Krishnan, Julie Khlevner, Aliva De, Annette Zygmunt, Timothy M. Crombleholme, Foong‐Yen Y. Lim, Howard W. Needelman, Robert A. Cusick, , Wendy K. Chung

The paper identifies LONP1 and ALYREF as new candidate risk genes for congenital diaphragmatic hernia through de novo and ultra-rare variant analyses in proband-parent trios and population controls.

The American Journal of Human Genetics · Sep 20, 2021Peer-reviewedGenetic & Genomic Medicine