Author

Shareef M. Dabdoub

University of IowaORCID 0000-0002-1374-8347Unclaimed 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-genome sequencing· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Aline Lourenço PetriniD· 2 shared Jeffrey Clark MurrayiD· 2 shared Ligiane Alves Machado‐PaulaiD· 2 shared Lina M. Moreno‐UribeiD· 2 shared Michael S. ChimentiiD· 2 shared Patrick John BrehenyiD· 2 shared Shankar Rengasamy VenugopalaniD· 2 shared Waheed A. AwotoyeiD· 2 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aline Lourenço PetrinORCID

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2 papers

Recent·Most cited

Genetic and Epigenetic Contributors to Cleft Laterality: Evidence from Monozygotic Mirror Twins and Replication Cohorts

Aline Lourenço Petrin, Waheed A. Awotoye, Christina Spencer, Ligiane Alves Machado‐Paula, Luke Hovey, Henry Keen, Michael S. Chimenti, Patrick John Breheny, Fang Qian, Shareef M. Dabdoub, James C. Thomas, Azeez Butali, Jeffrey C. Murray, Shankar Rengasamy Venugopalan, Lina M. Moreno‐Uribe

This study identifies genetic and epigenetic factors contributing to cleft laterality using monozygotic twins and replication cohorts, finding methylation differences in ARID5B, ZFP57, and HOOK2 associated with cleft side and severity.

Human Molecular Genetics · Jan 1, 2026Peer-reviewedGenetic & Genomic Medicine

Whole genome sequencing of a family with autosomal dominant features within the oculoauriculovertebral spectrum

Aline Lourenço Petrin, Ligiane Alves Machado‐Paula, Ashley Hinkle, L Hovey, Waheed A. Awotoye, Michael S. Chimenti, Benjamin W. Darbro, Lucilene Arilho Ribeiro, Shareef M. Dabdoub, Tabitha K. Peter, Patrick John Breheny, Jeffrey Clark Murray, Eric Van Otterloo, Shankar Rengasamy Venugopalan, Lina M. Moreno Uribe

The paper identifies rare mutations in SIX1, PDGFRA, and KDR/VEGFR2 associated with OAVS phenotypes through whole genome sequencing and statistical analysis of a family.

medRxiv · Feb 7, 2024 · PreprintGenetic & Genomic Medicine