Priyamvada Guha Roy on Muck Rack

Priyamvada Guha Roy

As seen in: Wiley Online Library, medRxiv
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Articles

How Rare Is Rare? TNFAIP3 Variants and the High Collective Burden of Haploinsufficiency

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By Danica Lee, Priyamvada Guha Roy, Urekha Karri
| medRxiv
Abstract Background Monogenic diseases are considered rare, yet many remain underdiagnosed when clinical manifestations are heterogeneous. A20 haploinsufficiency (HA20) is an early-onset inborn error of immunity (IEI) caused by heterozygous germline TNFAIP3 variants, resulting in dysregulated inflammatory signaling and diverse immune phenotypes.
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Multimodal Integration of Protein Interactomes With Genomic and Molecular Data Discovers Distinct Rheumatoid Arthritis Endotypes

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By Javad Rahimikollu, Priyamvada Guha Roy, Akash Kishore
| Wiley Online Library Verified
INTRODUCTION Rheumatoid arthritis (RA) is a chronic, progressive autoimmune disease characterized by inflammation of synovial joints and systemic immune dysregulation. According to the Global Burden of Diseases, Injuries, and Risk Factors Study 2021, approximately 17.6 million people worldwide are affected by RA.1 Beyond its clinical manifestations, RA exhibits considerable molecular and cellular heterogeneity, which contributes to variations in disease onset, progression, and treatment response.
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Comprehensive Atomic-Scale 3D Viral-Host Protein Interactomes Enable Dissection of Key Mechanisms and Evolutionary Processes Underlying Viral Pathogenesis

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By Le Li, Yilin Liu, Zizhao Zhang, Priyamvada Guha Roy
| biorxiv.org
Abstract Viral-human protein interactions are critical for viral replication and modulation of the host immune response. Structural modeling of these interactions is vital for developing effective antiviral therapies and vaccines. However, 99% of experimentally determined binary host-viral interactions currently lack structural information. We aimed to address this gap by leveraging computational protein structure prediction methods.
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