Author

Ben Fowler

Oklahoma Medical Research Foundation

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 2 Neuroscience· 1

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Approach:statistical model· 3 Research Focus:differential expression· 2 Organism:mouse· 2 Organism:zebrafish· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1

Frequent Co-Authors

Abolfazl RadiD· 1 shared Alireza SedaghatiD· 1 shared Aziz El-AmraouiiD· 1 shared Barbara VonaiD· 1 shared Cassidy PetreeiD· 1 shared Chengcheng TaniD· 1 shared Chinthalapally V. RaoiD· 1 shared Chinthapally V. Rao· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperGenetics

Abolfazl RadORCID

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3 papers

Recent·Most cited

The MET growth signaling complex drives Alzheimers Disease-associated brain pathology in aged Shugoshin 1 mouse cohesinopathy model

Chinthalapally V. Rao, Julie Crane, Ben Fowler, Yuting Zhang, Hiroshi Y. Yamada

This study identifies oncogenic MET signaling activation in aged Sgo1-/+ mice brains, linking it to Alzheimer's Disease pathology and suggesting potential drug repurposing.

bioRxiv · Mar 26, 2024 · PreprintNeuroscience

Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans

Barbara Vona, Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez, Kevin T. A. Booth, Sandrine Vitry, Abolfazl Rad, Franz Rüschendorf, Pratishtha Varshney, Ben Fowler, Christian Beetz, Kumar N. Alagramam, David P. Murphy, , Hamid Galehdari

This study identifies biallelic mutations in CLRN2 as a cause of non-syndromic hearing loss through genetic analysis of a consanguineous family and functional validation in zebrafish and mouse models.

Human Genetics · Jan 26, 2021Peer-reviewedGenetics

Targeted sequencing of candidate genes of dyslipidemia in Punjabi Sikhs: Population-specific rare variants in GCKR promote ectopic fat deposition

Dharambir K. Sanghera, Ruth Hopkins, Megan W. Malone-Perez, Cynthia Bejar, Chengcheng Tan, Huda J. Mussa, Paul W. Whitby, Ben Fowler, Chinthapally V. Rao, Kar-Ming A. Fung, Stan A. Lightfoot, John Kimble Frazer

The paper identifies population-specific rare variants in GCKR associated with hypertriglyceridemia and ectopic fat deposition using targeted sequencing and zebrafish models.

PLoS ONE · Aug 1, 2019Peer-reviewedGenetics