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Atanu Kumar Dutta

Showing results (21-30 of 32) with videos related to

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Biological Trace Element Research|October 23, 2020
Zinc and COVID-19: Basis of Current Clinical TrialsAmit Pal, Rosanna Squitti, Mario Picozza, et al.
Molecular Genetics and Metabolism Reports|March 4, 2016
Cerebrotendinous xanthomatosis: Possibility of founder mutation in CYP27A1 gene (c.526delG) in Eastern Indian and Surinamese populationAtanu Kumar Dutta, Sumita Danda, Karthik Muthusamy, et al.
Journal of Biosciences|June 12, 2025
Whole exome sequencing reveals novel and rare variants in nonsyndromic hearing loss-related genes: A focus on <i>GPSM2</i> compound heterozygositySudipta Chakraborty, Sukanya Mitra, Arnab Ghosh, et al.
Case Reports in Neurology|December 1, 2025
Unraveling Alternating Hemiplegia of Childhood: A Case Report with Genetic and Clinical InsightsSamanwita Mahapatra, Abhishek Singh, Aditi Das, et al.
European Journal of Medical Genetics|April 19, 2023
Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinentSweta Das, Maya Thomas, Sangeetha Yoganathan, et al.
Acta Neurologica Belgica|October 13, 2021
Correlation of ATP7B gene mutations with clinical phenotype and radiological features in Indian Wilson disease patientsJasodhara Chaudhuri, Samar Biswas, Goutam Gangopadhyay, et al.
BMC Psychiatry|October 8, 2024
Pharmacogenomics-assisted treatment versus standard of care in schizophrenia: a systematic review and meta-analysisSaibal Das, Manoj Kalita, Manabendra Makhal, et al.
Plos One|April 10, 2024
Pharmacogenomics-assisted schizophrenia management: A hybrid type 2 effectiveness-implementation study protocol to compare the clinical utility, cost-effectiveness, and barriersAniruddha Basu, Atanu Kumar Dutta, Bhavani Shankara Bagepally, et al.
Experimental Eye Research|March 21, 2016
Genetic analysis of consanguineous families presenting with congenital ocular defectsEhsan Ullah, Muhammad Arif Nadeem Saqib, Sundus Sajid, et al.
American Journal of Medical Genetics. Part A|December 4, 2021
Ectodysplasin pathogenic variants affecting the furin-cleavage site and unusual clinical features define X-linked hypohidrotic ectodermal dysplasia in IndiaAjay Kumar Chaudhary, Aishwarya Gholse, Hampapathalu Adimurthy Nagarajaram, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Biological Trace Element Research|October 23, 2020
Zinc and COVID-19: Basis of Current Clinical TrialsAmit Pal, Rosanna Squitti, Mario Picozza, et al.
Molecular Genetics and Metabolism Reports|March 4, 2016
Cerebrotendinous xanthomatosis: Possibility of founder mutation in CYP27A1 gene (c.526delG) in Eastern Indian and Surinamese populationAtanu Kumar Dutta, Sumita Danda, Karthik Muthusamy, et al.
Journal of Biosciences|June 12, 2025
Whole exome sequencing reveals novel and rare variants in nonsyndromic hearing loss-related genes: A focus on <i>GPSM2</i> compound heterozygositySudipta Chakraborty, Sukanya Mitra, Arnab Ghosh, et al.
Case Reports in Neurology|December 1, 2025
Unraveling Alternating Hemiplegia of Childhood: A Case Report with Genetic and Clinical InsightsSamanwita Mahapatra, Abhishek Singh, Aditi Das, et al.
European Journal of Medical Genetics|April 19, 2023
Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinentSweta Das, Maya Thomas, Sangeetha Yoganathan, et al.
Acta Neurologica Belgica|October 13, 2021
Correlation of ATP7B gene mutations with clinical phenotype and radiological features in Indian Wilson disease patientsJasodhara Chaudhuri, Samar Biswas, Goutam Gangopadhyay, et al.
BMC Psychiatry|October 8, 2024
Pharmacogenomics-assisted treatment versus standard of care in schizophrenia: a systematic review and meta-analysisSaibal Das, Manoj Kalita, Manabendra Makhal, et al.
Plos One|April 10, 2024
Pharmacogenomics-assisted schizophrenia management: A hybrid type 2 effectiveness-implementation study protocol to compare the clinical utility, cost-effectiveness, and barriersAniruddha Basu, Atanu Kumar Dutta, Bhavani Shankara Bagepally, et al.
Experimental Eye Research|March 21, 2016
Genetic analysis of consanguineous families presenting with congenital ocular defectsEhsan Ullah, Muhammad Arif Nadeem Saqib, Sundus Sajid, et al.
American Journal of Medical Genetics. Part A|December 4, 2021
Ectodysplasin pathogenic variants affecting the furin-cleavage site and unusual clinical features define X-linked hypohidrotic ectodermal dysplasia in IndiaAjay Kumar Chaudhary, Aishwarya Gholse, Hampapathalu Adimurthy Nagarajaram, et al.
Pageof 4