Publications by authors named "Sm Naushad"

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Clinical utility of chromosomal microarray and whole exome sequencing in evaluating genetic causes for pregnancy loss using products of conception specimens.
Kanaka Durga Devi Yadam Reddy, Suresh Kumaraswamy, Palanichamy Palanikumar, Tajamul Hussain, Shaik Mohammad Naushad

J Perinat Med· December 2025

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Unveiling hidden risks: pharmacogenetic insights from a cross-sectional study of statin therapy in the Indian population.
Shaik Mohammad Naushad, Palani Kumar Palanichamy, Jagadeesh Babu Sreemanthula, Yadam Reddy Kanaka Durga Devi, Palakonda Gopi

Pharmacol Rep· August 2025

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Phenotypic Evolution in Fabry Disease: Our Experience in Indian Cohort.
Usha Dave, Srilatha Kadali, Tajamul Hussain, Ananthaneni Radhika, Sagar Patel, Shaik Mohammad Naushad

Indian J Clin Biochem· April 2025

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High penetrance and phenotypic landscape of methylenetetrahydrofolate reductase c.665 C>T polymorphism in the absence of folate fortification.
Srilatha Kadali, Ananthaneni Radhika, Yadam Reddy Kanaka Durga Devi, Jagadeesh Babu Sreemanthula, Gopi Palakonda, Shaik Mohammad Naushad

Clin Nutr ESPEN· February 2025

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Elucidation of genetic determinants of dyslipidaemia using a global screening array for the early detection of coronary artery disease.
Ananthaneni Radhika, Sandeepta Burgula, Chandan Badapanda, Tajamul Hussain, Shaik Mohammad Naushad

Mamm Genome· December 2023

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The role of TLR7 agonists in modulating COVID-19 severity in subjects with loss-of-function TLR7 variants.
Shaik Mohammad Naushad, Gowtham Mandadapu, Mekala Janaki Ramaiah, Fahad N Almajhdi, Tajamul Hussain

Sci Rep· August 2023

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Application of machine learning tools and integrated OMICS for screening and diagnosis of inborn errors of metabolism.
Ganni Usha Rani, Srilatha Kadali, Banka Kurma Reddy, Dudekula Shaheena, Shaik Mohammad Naushad

Metabolomics· May 2023

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Development of pharmacogenomic algorithm to optimize nateglinide dose for the treatment of type 2 diabetes mellitus.
Shaik Mohammad Naushad, Tajamul Hussain, Salman A Alrokayan, Vijay Kumar Kutala

Pharmacol Rep· October 2022

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Influence of RFC1 c.80A>G Polymorphism on Methotrexate-Mediated Toxicity and Therapeutic Efficacy in Rheumatoid Arthritis: A Meta-analysis.
Shaik Mohammad Naushad, Salman A Alrokayan, Fahad N Almajhdi, Tajamul Hussain

Ann Pharmacother· December 2021

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Pharmacogenetic determinants of warfarin in the Indian population.
Shaik Mohammad Naushad, Vijay Kumar Kutala, Tajamul Hussain, Salman A Alrokayan

Pharmacol Rep· October 2021

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Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1.
Parag M Tamhankar, Lakshmi Vasudevan, Pratima Kondurkar, Sarfaraj Niazi, Rita Christopher, Shaik M Naushad

J Pediatr Genet· September 2021

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Molecular insights into the role of genetic determinants of congenital hypothyroidism.
Yedukondalu Kollati, Radha Rama Devi Akella, Shaik Mohammad Naushad, Rajesh K Patel, G Bhanuprakash Reddy

Genomics Inform· September 2021

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Mechanistic insights into the CYP2C19 genetic variants prevalent in the Indian population.
Shaik Mohammad Naushad, Kiran Kumar Vattam, Yadamreddy Kanaka Durga Devi, Tajamul Hussain, Salman Alrokayan

Gene· June 2021

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A rare case of fatty acyl-CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype.
Akella Radha Rama Devi, Shaik Mohammad Naushad, Romit Jain, Lokesh Lingappa

Clin Genet· May 2021

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Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling.
Shaik Mohammad Naushad, Tajamul Hussain, Salman Alrokayan, Vijay Kumar Kutala

Neurosci Lett· April 2021

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Pharmacogenetic determinants of thiopurines in an Indian cohort.
Shaik Mohammad Naushad, Mekala Janaki Ramaiah, Vijay Kumar Kutala, Tajamul Hussain, Salman A Alrokayan

Pharmacol Rep· February 2021

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Pharmacogenetic profiling of dihydropyrimidine dehydrogenase (DPYD) variants in the Indian population.
Shaik Mohammad Naushad, Tajamul Hussain, Salman A Alrokayan, Vijay Kumar Kutala

J Gene Med· January 2021

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Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism.
Yedukondalu Kollati, Radha Rama Devi Akella, Shaik Mohammad Naushad, Divya Borkar, Maunika Thalla

Mol Biol Rep· October 2020

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Probing the epigenetic signatures in subjects with coronary artery disease.
Bobbala Indumathi, Sai Satish Oruganti, Shaik Mohammad Naushad, Vijay Kumar Kutala

Mol Biol Rep· September 2020

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Artificial neural network and bioavailability of the immunosuppression drug.
Shaik Mohammad Naushad, Vijay Kumar Kutala

Curr Opin Organ Transplant· August 2020

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Evaluation of Galectin-3 as a Novel Diagnostic Biomarker in Patients with Heart Failure with Preserved Ejection Fraction.
Jyothirmayi Kanukurti, Noorjahan Mohammed, N N Sreedevi, Siraj Ahmed Khan, K S S Sai Baba, Shaik Mohammad Naushad

J Lab Physicians· August 2020

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The rs1991517 polymorphism is a genetic risk factor for congenital hypothyroidism.
Yedukondalu Kollati, Radha Rama Devi Akella, Shaik Mohammad Naushad, Maunika Thalla, G Bhanuprakash Reddy

3 Biotech· June 2020

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Clinical and Molecular Diagnosis of Joubert Syndrome and Related Disorders.
Akella Radha Rama Devi, Shaik Mohammad Naushad, Lokesh Lingappa

Pediatr Neurol· May 2020

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Adaptive Neuro-Fuzzy Inference System-Based Exploration of the Interrelationships of 25-Hydroxyvitamin D, Calcium, Phosphorus with Parathyroid Hormone Production.
Iyyapu Krishna Mohan, Siraj Ahmed Khan, D Shiva Krishna, M Vijaya Bhaskar, K S S Sai Baba, Shaik Mohammad Naushad

Indian J Clin Biochem· January 2020

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Association of vitamin D receptor TaqI and ApaI genetic polymorphisms with nephrolithiasis and end stage renal disease: a meta-analysis.
Tajamul Hussain, Shaik M Naushad, Anwar Ahmed, Salman Alamery, Arif A Mohammed

BMC Med Genet· December 2019

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