Author

Farah A. Ladha

Baylor College of MedicineORCID 0009-0002-5653-0249Unclaimed 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 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

Jill Anne RosenfeldiD· 2 shared Agnar HelgasoniD· 1 shared Ana S.A. CoheniD· 1 shared Andreina Minicucci· 1 shared Antonio VitobelloiD· 1 shared Benjamin CognéiD· 1 shared Brenda J. BarryiD· 1 shared Carey Ronspies· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jill Anne RosenfeldORCID

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2 papers

Recent·Most cited

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome

Kimberley Jade Anderson, Eirny Tholl Thorolfsdottir, Ilana M. Nodelman, Sara Tholl Halldorsdottir, Stefania Benónísdóttir, Malak Ali Alghamdi, Naif A. M. Almontashiri, Brenda J. Barry, Matthias Begemann, Jacquelyn F. Britton, Sarah Burke, Benjamin Cogné, Ana S.A. Cohen, Carles De Diego Boguñá, Evan E. Eichler, , Hans Tomas Bjornsson

The paper investigates sex-specific penetrance in PILBOS, showing male overrepresentation and androgen-mediated sexual dimorphism through genetic and mouse model studies.

The American Journal of Human Genetics · Sep 1, 2026Peer-reviewedGenetic & Genomic Medicine

Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders

Sara M. Fielder, Marisa W. Friederich, Daniella Helena Hock, Jessie R. Zhang, Liana Valin, Jill Anne Rosenfeld, Kevin T. A. Booth, Natasha J. Brown, Rocío Rius, Tanavi Sharma, Liana N. Semcesen, Kim C. Worley, Lindsay Catherine Burrage, Kayla M. Treat, Tara E. Samson, , Stephen C. Pak

This study identifies de novo ATP5F1A variants causing neurological disorders through dominant negative mechanisms, expanding the known phenotypic and genotypic spectrum of complex V deficiency.

EMBO Molecular Medicine · Aug 26, 2025Peer-reviewedGenetic & Genomic Medicine