Author

Uma M. Reddy

Columbia UniversityORCID 0000-0002-8599-6040Unclaimed 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· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:whole-exome sequencing· 2 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Robert M. SilveriD· 2 shared Aaron R. QuinlaniD· 1 shared Allen E. Bale· 1 shared Amy L MooreiD· 1 shared Anya L. ArthursiD· 1 shared Chen ZhaoiD· 1 shared Claire Trelford RobertsiD· 1 shared David M. HaasiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Robert M. SilverORCID

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3 papers

Recent·Most cited

Genetic Variants Associated with Placental Abnormalities in Stillbirths

Tsegaselassie Workalemahu, Thomas J. Nicholas, Aaron R. Quinlan, Xiaoxu Yang, Laurie Beth Griffin, Susannah Hopkins Leisher, Nathan R. Blue, Anya L. Arthurs, Jessica Pagé, David Ware Branch, Nicola J. Camp, Lynn B. Jorde, Claire Trelford Roberts, Giordano L Jessica, Ronald J. Wapner, , Robert M. Silver

The paper identifies genetic variants associated with placental abnormalities in stillbirths by analyzing exome sequencing data from placental and fetal samples.

medRxiv · Oct 21, 2026 · PreprintGenetic & Genomic Medicine

Maternal and offspring genome-wide association study of C-reactive protein reveals limited polygenic association with gestational diabetes mellitus

Yu Zhang, Amy L Moore, Kelli K. Ryckman, Qi Yan, Rafael F. Guerrero, Ming Li, Robert M. Silver, Lynn M. Yee, Uma M. Reddy, Maisa N. Feghali, Judith M. Chung, David M. Haas, Kok Lim Kua, Nianjun Liu

This study investigates the genetic associations of early pregnancy C-reactive protein (CRP) levels with gestational diabetes mellitus (GDM) using maternal and offspring genome-wide association studies (GWAS).

medRxiv · Sep 30, 2025 · PreprintGenetic & Genomic Medicine

Whole-exome sequencing analysis on products of conception: A cohort study to evaluate clinical utility and genetic etiology for pregnancy loss

Chen Zhao, Hongyan Chai, Qinghua Zhou, Jiadi Wen, Uma M. Reddy, Rama D. Kastury, Yong‐hui Jiang, Winifred Mak, Allen E. Bale, Hui Zhang, Peining Li

This study uses whole-exome sequencing on products of conception to identify genetic causes of pregnancy loss, finding pathogenic variants in 22% of cases and a higher rate with uncertain variants included.

Genetics in Medicine · Oct 25, 2020Peer-reviewedGenetic & Genomic Medicine