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Author

Charitha Vadlamudi

Observed name: C. Vadlamudi
ORCID: 0000-0001-9662-8326
Observed ORCID: 0000-0001-9662-8326
OpenAlex ID: A5055945197
SARS-CoV-2 Infection–Associated Hemophagocytic Lymphohistiocytosis
2020 · Andrey Prilutskiy, Michael Kritselis, et al. · American Journal of Clinical Pathology · 129
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Psychosocial and Financial Burden of Therapy in USA Patients with Pulmonary Arterial Hypertension
2020 · Scott A. Helgeson, Divya Menon, et al. · Diseases · 36
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An institutional experience with DICER1 mutated thyroid nodules—evaluating the cytomorphology and molecular phenotype
2022 · Soo Hyun Lee, Charitha Vadlamudi, et al. · Journal of the American Society of Cytopathology · 9
Genomic Observations of a Rare/Pathogenic SMAD3 Variant in Loeys–Dietz Syndrome 3 Confirmed by Protein Informatics and Structural Investigations
2019 · John E. Richter, Ayesha Samreen, et al. · Medicina · 7
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Distinctive pseudopalisaded histiocytic hyperplasia characterizes the transition of exudative to proliferative phase of diffuse alveolar damage in patients dying of COVID-19
2021 · Michael Kritselis, Ilyas Yambayev, et al. · Human Pathology · 4
Characterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular Modeling
2020 · John E. Richter Jr., Charitha Vadlamudi, et al. · Case Reports in Genetics · 3
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Implementation of an HIV RNA Qualitative PCR Assay in an HIV Diagnostic Algorithm: A Single-Institution Experience
2023 · Isabela Medeiros, Charitha Vadlamudi, et al. · American Journal of Clinical Pathology · 2
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Examination of Molecular Effects ofMYLKDeletion in a Patient with Extensive Aortic, Carotid, and Abdominal Dissections That Underlie the Genetic Dysfunction
2020 · Sarah K. Macklin, Katelyn A. Bruno, et al. · Case Reports in Medicine · 2
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Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy
2020 · Abhimanyu S. Ahuja, Pavalan Selvam, et al. · Ophthalmic Genetics · 1
Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy
2020 · Abhimanyu S. Ahuja, Pavalan Selvam, et al. · Figshare
A Rare Case of Tuberous Sclerosis Associated Lymphangioleimyomatosis
2019 · Y.T. Debella, V. Arunthari, et al.
Works count: 11
Citation count: 193
H-index: 4
I10-index: 2
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