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Pranjali Bhagwat

Observed names: Pranjali K. Bhagwat, Pranjali Kishor Bhagwat
ORCID: 0000-0003-1982-5996
Observed ORCID: 0000-0003-1982-5996
OpenAlex ID: A5076352650
Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy
2019 · Nurit Assia Batzir, Pranjali Kishor Bhagwat, et al. · Human Mutation · 46
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De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures
2019 · Nurit Assia Batzir, Pranjali K. Bhagwat, et al. · Molecular Case Studies · 39
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ABCD1 and X‐linked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models
2021 · Joshua Manor, Hyunglok Chung, et al. · Journal of Neuroscience Research · 32
A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins
2023 · Annabel Guichard, Shenzhao Lu, et al. · Cell Reports · 13
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Genetic analysis of the X-linked Adrenoleukodystrophy ABCD1 gene in Drosophila uncovers a role in Peroxisomal dynamics
2024 · Joshua Manor, Sharayu V Jangam, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 2
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ACTG2 Visceral Myopathy
1993 · Pranjali Bhagwat, Michael F. Wangler · 2
Metabolomic Profiling Reveals Brain Lipid Alterations in PEX7-Deficient Models of Rhizomelic Chondrodysplasia Punctata
2025 · Riya Sankhe, Meredith I. Williams, et al. · Biomolecules · 1
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Genetic analysis of the X-linked adrenoleukodystrophy gene ABCD1 in Drosophila uncovers a conserved phenotype
2026 · Joshua Manor, Sharayu V. Jangam, et al. · Communications Biology
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eP024: Metabolomic mapping of rhizomelic chondrodysplasia punctata
2022 · Laura Mackay, Michael Wangler, et al. · Genetics in Medicine
Works count: 9
Citation count: 135
H-index: 4
I10-index: 4
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