Meenal Agarwal

Employment

• GenePath Dx, Causeway Healthcare Private Ltd. Head, Clinical Genetics and Laboratory Medical Director
  2015 - 2022
• Sanjay Gandhi Post Graduate Institute of Medical Sciences Assistant Professor
  2013 - 2015
• Happy Genes Genetic Clinic
• KEM Hospital Pune

Education

• Sanjay Gandhi Post Graduate Institute of Medical Sciences DM
  2008 - 2011
• King George's Medical University MD
  2002 - 2005
• King George's Medical University MBBS
  1995 - 2000

Projects & Funding

Projects & funding information is unavailable.

Publications (22)

• Chromosomal Microarray: Still Relevant in NGS Era
  Indian Journal of Pediatrics 2026 DOI: 10.1007/s12098-025-05848-5
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• A Rare Pathogenic Variant in the SERPINF1 Gene in Association with Early-Onset Severe Presentation of Autosomal Recessive Type of Osteogenesis Imperfecta VI: A Case Report
  Case Reports in Orthopedic Research 2023 DOI: 10.1159/000527988
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• SMN1 gene copy number analysis for spinal muscular atrophy (SMA) in a Turkish cohort by CODE-SEQ technology, an integrated solution for detection of SMN1 and SMN2 copy numbers and the “2+0” genotype
  Neurological Sciences 2020 DOI: 10.1007/s10072-020-04365-x
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• A case of familial hypercholesterolemia caused by homozygous deletion in the LDLR gene diagnosed by targeted next-generation sequencing
  Clinical Lipidology and Metabolic Disorders 2019 DOI: 10.1080/26415321.2019.1670555
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• Severe Familial Hypertriglyceridemia: Successful Treatment With Insulin and a Modified Meal Plan
  Journal of the Endocrine Society 2018 DOI: 10.1210/js.2018-00299
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• Apparently balanced complex chromosomal translocation involving five chromosomes – Delineation of imbalances by cytogenetic micro-array.
  Clin Dysmorphol 2016
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• Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy
  Am J Med Genet A. 2016
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• Knowledge of Cord Blood Banking in General Population and Doctors: A Questionnaire Based Survey
  Indian J Pediatr 2016
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• The clinical utility of a custom-developed targeted next-generation sequencing assay for detection of mutations associated with Philadelphia-negative chronic myeloproliferative neoplasms: Two case examples with CALR exon 9 mutations.
  International Journal of Molecular and Immuno Oncology 2016
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• Feasibility Study of an Outreach Program of New Born Screening in Indian Scenario.
  Indian J Pediatr 2015
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