Dr. Pinku Halder

, , ,.

About

Postdoctoral researcher specializing in neurobiology and omics-driven disease modeling, with expertise in iPSC-derived neuronal differentiation, transcriptomics, metabolomics, and mitochondrial bioenergetics (Seahorse). Proficient in advanced omics data analysis including GSEA, WGCNA, and multivariate statistical methods. Experienced in modeling obesity-related mechanisms in Down syndrome using integrative cellular and molecular approaches. A fast learner and effective collaborator committed to driving impactful biomedical research within multidisciplinary teams.

Work

Institut du Cerveau / Paris Brain Institute - ICM

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Postdoctoral Researcher

, , France

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Summary

University of Calcutta

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Senior Research Fellow

, , India

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Summary

Education

University of Calcutta

, , India
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Ph.D. in Human Genetics

Publications

Genetic aetiology of Down syndrome birth: novel variants of maternal DNMT3B and RFC1 genes increase risk of meiosis II nondisjunction in the oocyte

Molecular Genetics and Genomics

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Risk of Atrioventricular Septal Defects in Down syndrome: Association of MTHFR C677T and RFC1 A80G polymorphisms in Indian Bengali cohort

Journal of Genetics and Genomics

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Differences in clinical presentation, severity, and treatment of COVID-19 among individuals with Down syndrome from India and high-income countries: Data from the Trisomy 21 Research Society survey.

Journal of global health

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Understanding etiology of chromosome 21 nondisjunction from gene × environment models

Scientific Reports

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Understanding etiology of chromosome 21 nondisjunction from gene × environment models

Scientific Reports

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Evaluation of potency of the selected bioactive molecules from Indian medicinal plants with MPro of SARS-CoV-2 through in silico analysis.

Journal of Ayurveda and integrative medicine

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The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.

PLoS genetics

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Polymorphisms of folate metabolism regulators increase risk of meiosis II nondisjunction of chromosome 21 in oocyte

Meta Gene

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Risk of Down syndrome birth: Consanguineous marriage is associated with maternal meiosis-II nondisjunction at younger age and without any detectable recombination error

American Journal of Medical Genetics Part A

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