S S. Naushad-Mohammad

Banjara Hills, Road No.3
Hyderabad, TG, India

Last Updated: 09/26/2026

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Found 86 publications

Elucidation of crucial metabolic pathways in the etiology of autism spectrum disorder through whole exome sequencing and chromosomal microarray.

Elucidation of crucial metabolic pathways in the etiology of autism spectrum disorder through whole exome sequencing and chromosomal microarray.

Journal: Psychiatric genetics

Published: February 09, 2026

Clinical utility of chromosomal microarray and whole exome sequencing in evaluating genetic causes for pregnancy loss using products of conception specimens.

Clinical utility of chromosomal microarray and whole exome sequencing in evaluating genetic causes for pregnancy loss using products of conception specimens.

Journal: Journal of perinatal medicine

Published: May 06, 2025

Unveiling hidden risks: pharmacogenetic insights from a cross-sectional study of statin therapy in the Indian population.

Unveiling hidden risks: pharmacogenetic insights from a cross-sectional study of statin therapy in the Indian population.

Journal: Pharmacological reports : PR

Published: January 28, 2025

High penetrance and phenotypic landscape of methylenetetrahydrofolate reductase c.665 C>T polymorphism in the absence of folate fortification.

High penetrance and phenotypic landscape of methylenetetrahydrofolate reductase c.665 C>T polymorphism in the absence of folate fortification.

Journal: Clinical nutrition ESPEN

Published: June 26, 2024

Phenotypic Evolution in Fabry Disease: Our Experience in Indian Cohort.

Phenotypic Evolution in Fabry Disease: Our Experience in Indian Cohort.

Journal: Indian journal of clinical biochemistry : IJCB

Published: November 24, 2023

Elucidation of genetic determinants of dyslipidaemia using a global screening array for the early detection of coronary artery disease.

Elucidation of genetic determinants of dyslipidaemia using a global screening array for the early detection of coronary artery disease.

Journal: Mammalian genome : official journal of the International Mammalian Genome Society

Published: June 19, 2023

The role of TLR7 agonists in modulating COVID-19 severity in subjects with loss-of-function TLR7 variants.

The role of TLR7 agonists in modulating COVID-19 severity in subjects with loss-of-function TLR7 variants.

Journal: Scientific reports

Published: February 01, 2023

Application of machine learning tools and integrated OMICS for screening and diagnosis of inborn errors of metabolism.

Application of machine learning tools and integrated OMICS for screening and diagnosis of inborn errors of metabolism.

Journal: Metabolomics : Official journal of the Metabolomic Society

Published: October 31, 2022

Development of pharmacogenomic algorithm to optimize nateglinide dose for the treatment of type 2 diabetes mellitus.

Development of pharmacogenomic algorithm to optimize nateglinide dose for the treatment of type 2 diabetes mellitus.

Journal: Pharmacological reports : PR

Published: May 12, 2022

Molecular insights into the role of genetic determinants of congenital hypothyroidism.

Molecular insights into the role of genetic determinants of congenital hypothyroidism.

Journal: Genomics & informatics

Published: June 14, 2021

Pharmacogenetic determinants of warfarin in the Indian population.

Pharmacogenetic determinants of warfarin in the Indian population.

Journal: Pharmacological reports : PR

Published: April 11, 2021

Influence of RFC1 c.80A>G Polymorphism on Methotrexate-Mediated Toxicity and Therapeutic Efficacy in Rheumatoid Arthritis: A Meta-analysis.

Influence of RFC1 c.80A>G Polymorphism on Methotrexate-Mediated Toxicity and Therapeutic Efficacy in Rheumatoid Arthritis: A Meta-analysis.

Journal: The Annals of pharmacotherapy

Published: March 22, 2021

Showing 1-12 of 86

Last Updated: 09/26/2026