S. Mehdi
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Formerly Arkansas Affiliated with UAMS through 2022; recent publications list Henry Ford Health.
Research Areas
Biography and Research Information
OverviewAI-generated summary
S. Mehdi's research has focused on investigating genetic factors contributing to diseases, specifically in the context of rare and complex conditions. Their work includes exome analysis to identify candidate variants associated with familial hidradenitis suppurativa in an African American family. Additionally, Mehdi has studied epigenomic and gene expression defects in Sezary syndrome, a form of cutaneous T-cell lymphoma. These investigations aim to elucidate the molecular underpinnings of these conditions.
Metrics
- Publications: 1
Selected Publications
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867 Epigenomic and gene expression defects in sezary syndrome (2022)
Collaboration Network
Top Collaborators
- 867 Epigenomic and gene expression defects in sezary syndrome
- 867 Epigenomic and gene expression defects in sezary syndrome
- 867 Epigenomic and gene expression defects in sezary syndrome
- 867 Epigenomic and gene expression defects in sezary syndrome
- 867 Epigenomic and gene expression defects in sezary syndrome
- 867 Epigenomic and gene expression defects in sezary syndrome
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