Author

Drew Bradbury

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 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Francesco ScolariiD· 2 shared Adele MitrottiiD· 1 shared Agnieszka SzmigielskaiD· 1 shared Aleksandra GliwińskaiD· 1 shared Ali G. GharaviiD· 1 shared Andrea Ranghino· 1 shared Andrew BeenkeniD· 1 shared Andrew S. BombackiD· 1 shared

Activity by Year

2017-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Francesco ScolariORCID

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2 papers

Recent·Most cited

Exome-wide analysis of congenital kidney anomalies reveals new genes and shared architecture with developmental disorders

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil, Andrew Beenken, Miguel Verbitsky, Shirlee Shril, Iris Lekkerkerker, Sandy Yu-Rung Yang, Atlas Khan, David A. Fasel, Janewit Wongboonsin, Jeremiah Martino, Juntao Ke, Naama Elefant, , Yaşar Çalışkan

This study identifies new genes and shared genetic architecture between kidney anomalies and other developmental disorders using exome-wide analysis of clinical cohorts.

Nature Communications · Aug 7, 2025Peer-reviewedGenetic & Genomic Medicine

GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway

Krzysztof Kiryluk, Yifu Li, Zina Moldoveanu, Hitoshi Suzuki, Colin Reily, Ping Hou, Jingyuan Xie, Nikol Mladkova, Sindhuri Prakash, Clara Fischman, Samantha Shapiro, Robert A. LeDesma, Drew Bradbury, Iuliana Ionita-Laza, Frank Eitner, , Jan Novak

This paper identifies two genetic loci associated with serum galactose-deficient IgA1 levels and shows their role in O-glycosylation regulation.

PLOS Genetics · Feb 10, 2017Peer-reviewedGenetics