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Mitesh Shetty

Observed names: Mitesh S. Shetty, Shetty, M.
Institution: Manipal Hospital
ORCID: 0000-0002-0321-3197
Observed ORCID: 0000-0002-0321-3197
OpenAlex ID: A5087607413
Novel Glioblastoma Markers with Diagnostic and Prognostic Value Identified through Transcriptome Analysis
2008 · Sreekanth P. Reddy, Ramona Britto, et al. · Clinical Cancer Research · 148
Upregulation of ASCL1 and inhibition of Notch signaling pathway characterize progressive astrocytoma
2005 · Kumaravel Somasundaram, Sreekanth P Reddy, et al. · Oncogene · 130
Identification of intronic-splice site mutations in GATA4 gene in Indian patients with congenital heart disease
2017 · Divya Bose, Vaigundan D., et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 15
Freeman-Sheldon syndrome-prenatal and postnatal diagnosis
2009 · Sridevi S. Hegde, Mitesh S. Shetty, et al. · The Indian Journal of Pediatrics · 12
A Homozygous Missense Variant in INPP5E Associated with Joubert Syndrome and Related Disorders
2017 · Mitesh Shetty, Nimmy Ramdas, et al. · Molecular Syndromology · 9
Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay
2015 · Divya Bose, Venkatesh Krishnamurthy, et al. · Cytogenetic and Genome Research · 9
A retrospective study of the yield of next‐generation sequencing in the diagnosis of developmental and epileptic encephalopathies and epileptic encephalopathies in 0–12 years aged children at a single tertiary care hospital in South India
2024 · Manasa C. Murthy, Bidisha Banerjee, et al. · Epileptic Disorders · 8
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A multidisciplinary approach for prenatal diagnosis of FRASER SYNDROME-report of a novel variant in FRAS1
2022 · Jyothsna Madan, Mitesh Shetty, et al. · Taiwanese Journal of Obstetrics and Gynecology · 6
Genetics in Congenital Heart Diseases
2013 · Sridevi Hegde, Mitesh Shetty · Jaypee Brothers Medical Publishers (P) Ltd. eBooks · 6
A Novel Mutation in GATA3 Gene in a Case of Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome
2023 · Pooja Prakash Prabhu, Sudarshan Ballal, et al. · Indian Journal of Nephrology · 4
Association of maternal angiotensinogen gene M235T polymorphism with preeclampsia in South India: A tertiary care hospital based case-control study
2016 · Krishnaveni Chengalvala, Pushpa Kotur, et al. · Meta Gene · 3
Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers
2016 · Mitesh Shetty, Ambika Srikanth, et al. · Cytogenetic and Genome Research · 3
Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum
2015 · Mitesh Shetty, Ambika Srikanth, et al. · Molecular Syndromology · 3
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A Novel PGK1 Gene Variant with Neurological Dysfunction, Haemolytic Anaemia and Myopathy: A Case Report from India
2023 · Sameeta M. Prabhu, Bidisha Banerjee, et al. · Annals of Indian Academy of Neurology · 2
Genomics in Infectious Diseases
2021 · Mitesh Shetty · Pediatric Infectious Disease · 2
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A Retrospective Study of the Profile and Outcome of Children with Dravet Syndrome in a Tertiary Care Hospital of Southern India
2022 · Bidisha Banerjee, Sameeta M. Prabhu, et al. · Journal of Pediatric Epilepsy · 1
Maternal Factor V Leiden Mutation in Pre-eclampsia: A Case-Control South Eastern Indian Tertiary Care Hospital Based Study
2020 · Krishnaveni Changalvala, Pushpa Kotur, et al. · JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH · 1
Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia
2015 · Mitesh Shetty, Jayarama Kadandale, et al. · Molecular Syndromology · 1
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Impact of Etiology and Lead Time to Treatment with First-Line Agents on Outcome of Infantile Epileptic Spasms Syndrome: A Retrospective Cohort from Low- and Middle-Income Country
2026 · Shravani Krishna Goparaju, Bidisha Banerjee, et al. · Neuropediatrics
Genomic testing in the neonatal intensive care unit: a 5-year retrospective single-centre study from a tertiary care hospital in Bengaluru, India
2026 · Ranganatha A. Devaranavadagi, Nikitha K. Nekkileru, et al. · European Journal of Pediatrics
A Phenotypically Normal Homozygous Balanced Reciprocal Translocation Carrier: Report of an Extremely Rare Genetic Occurrence
2025 · Mitila Thirupathy, Mitesh Shetty, et al. · Cureus
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MELAS (Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes)—Usual and Unusual MRI Finding
2022 · Sameeta M. Prabhu, Bidisha Banerjee, et al. · Indian journal of radiology and imaging - new series/Indian journal of radiology and imaging/Indian Journal of Radiology & Imaging
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Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India
2019 · Mitesh Shetty, Sharath Balakrishna, et al. · Indian Journal of Hematology and Blood Transfusion
A novel de novo heterozygous deletion at 13q14.2-q21.1 in two siblings with mild intellectual disability
2018 · Kirti Mittal, Laxmi Kirola, et al. · Gene Reports
Factor V Leiden mutation in preeclampsia – A case-control South Eastern Indian study in a tertiary care hospital
2017 · Krishnaveni Chengalvala, Puspha Kotur, et al. · Journal of Anatomical Society of India
Works count: 30
Citation count: 363
H-index: 7
I10-index: 4
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