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Tissue-specific DNase I footprint analysis confirms the association of GATAD2B Q470 variant with intellectual disability

Journal of genetics, 2021-10, Vol.100 (2), Article 61

2021

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Novel two‐lead cardiac resynchronization therapy system provides equivalent CRT responses with less complications than a conventional three‐lead system: Results from the QP ExCELs lead registry

Journal of cardiovascular electrophysiology, 2020-07, Vol.31 (7), p.1784-1792

2020

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Identification and in Silico characterization of a novel CASK c.2546T>C (p.V849A) mutation in a male infant with pontocerebellar hypoplasia

Annals of the Indian Academy of Neurology, 2019-10, Vol.22 (4), p.523-524

2019

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Association of vitamin D receptor TaqI and ApaI genetic polymorphisms with nephrolithiasis and end stage renal disease: a meta-analysis

BMC medical genetics, 2019-12, Vol.20 (1), p.193-193, Article 193

2019

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Application of machine learning algorithms for the differential diagnosis of peroxisomal disorders

Journal of biochemistry (Tokyo), 2019-01, Vol.165 (1), p.67-73

2019

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Probing the epigenetic signatures in subjects with coronary artery disease

Molecular biology reports, 2020-09, Vol.47 (9), p.6693-6703

2020

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Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders

Psychiatric genetics, 2016-12, Vol.26 (6), p.281-286

2016

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Pharmacogenetic profiling of dihydropyrimidine dehydrogenase (DPYD) variants in the Indian population

The journal of gene medicine, 2021-01, Vol.23 (1), p.e3289-n/a

2021

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Predictive value of the PRAETORIAN score for defibrillation test success in patients with subcutaneous ICD: A subanalysis of the PRAETORIAN-DFT trial

Heart rhythm, 2024-06, Vol.21 (6), p.836-844

2024

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Incense smoke exposure augments systemic oxidative stress, inflammation and endothelial dysfunction in male albino rats

Toxicology mechanisms and methods, 2019-03, Vol.29 (3), p.211-218

2019

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Artificial neural network model for predicting the bioavailability of tacrolimus in patients with renal transplantation

PloS one, 2018-04, Vol.13 (4), p.e0191921-e0191921

2018

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A rare case of fatty acyl‐CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype

Clinical genetics, 2021-05, Vol.99 (5), p.744-745

2021

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Interactions of 5'-UTR Thymidylate Synthase Polymorphism with 677C→ T Methylene Tetrahydrofolate Reductase and 66A→ G Methyltetrahydrofolate Homocysteine Methyl-transferase Reductase Polymorphisms Determine Susceptibility to Coronary Artery Disease

Journal of Atherosclerosis and Thrombosis, 2011, Vol.18(1), pp.56-64

2011

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

Scientific reports, 2023-08, Vol.13 (1), p.13078-13078, Article 13078

2023

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Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism

Molecular biology reports, 2020-10, Vol.47 (10), p.7467-7475

2020

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Biochemical, machine learning and molecular approaches for the differential diagnosis of Mucopolysaccharidoses

Molecular and cellular biochemistry, 2019-08, Vol.458 (1-2), p.27-37

2019

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Classification and regression tree-based prediction of 6-mercaptopurine-induced leucopenia grades in children with acute lymphoblastic leukemia

Cancer chemotherapy and pharmacology, 2019-05, Vol.83 (5), p.875-880

2019

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Methodological issues in the development of a pharmacogenomic algorithm for warfarin dosing: comparison of two regression approaches

Pharmacogenomics, 2014-06, Vol.15 (8), p.1125-1132

2014

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A pilot study on machine learning approach to delineate metabolic signatures in intellectual disability

International journal of developmental disabilities, 2021-03, Vol.67 (2), p.94-100

2021

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Performance of first pacemaker to use smart device app for remote monitoring

Heart rhythm O2, 2021-10, Vol.2 (5), p.463-471

2021

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Aberrations in one-carbon metabolism induce oxidative DNA damage in sporadic breast cancer

Molecular and cellular biochemistry, 2011-03, Vol.349 (1-2), p.159-167

2011

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Machine learning algorithm-based risk prediction model of coronary artery disease

Molecular biology reports, 2018-10, Vol.45 (5), p.901-910

2018

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Adaptive Neuro-Fuzzy Inference System-Based Exploration of the Interrelationships of 25-Hydroxyvitamin D, Calcium, Phosphorus with Parathyroid Hormone Production

Indian journal of clinical biochemistry, 2020-01, Vol.35 (1), p.121-126

2020

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Association of Parkinson's disease with altered serum levels of lead and transition metals among South Indian subjects

Indian journal of biochemistry & biophysics, 2014-04, Vol.51 (2), p.121-126

2014

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Identification of Two Novel Mutations in Aminomethyltransferase Gene in Cases of Glycine Encephalopathy

Journal of pediatric genetics (Birmingham, Ala.), 2018-09, Vol.7 (3), p.097-102

2018

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Tissue-specific DNase I footprint analysis confirms the association of GATAD2B Q470 variant with intellectual disability

Novel two‐lead cardiac resynchronization therapy system provides equivalent CRT responses with less complications than a conventional three‐lead system: Results from the QP ExCELs lead registry

Identification and in Silico characterization of a novel CASK c.2546T>C (p.V849A) mutation in a male infant with pontocerebellar hypoplasia

Association of vitamin D receptor TaqI and ApaI genetic polymorphisms with nephrolithiasis and end stage renal disease: a meta-analysis

Application of machine learning algorithms for the differential diagnosis of peroxisomal disorders

Probing the epigenetic signatures in subjects with coronary artery disease

Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders

Pharmacogenetic profiling of dihydropyrimidine dehydrogenase (DPYD) variants in the Indian population

Predictive value of the PRAETORIAN score for defibrillation test success in patients with subcutaneous ICD: A subanalysis of the PRAETORIAN-DFT trial

Incense smoke exposure augments systemic oxidative stress, inflammation and endothelial dysfunction in male albino rats

Artificial neural network model for predicting the bioavailability of tacrolimus in patients with renal transplantation

A rare case of fatty acyl‐CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype

Interactions of 5'-UTR Thymidylate Synthase Polymorphism with 677C→ T Methylene Tetrahydrofolate Reductase and 66A→ G Methyltetrahydrofolate Homocysteine Methyl-transferase Reductase Polymorphisms Determine Susceptibility to Coronary Artery Disease

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

Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism

Biochemical, machine learning and molecular approaches for the differential diagnosis of Mucopolysaccharidoses

Classification and regression tree-based prediction of 6-mercaptopurine-induced leucopenia grades in children with acute lymphoblastic leukemia

Methodological issues in the development of a pharmacogenomic algorithm for warfarin dosing: comparison of two regression approaches

A pilot study on machine learning approach to delineate metabolic signatures in intellectual disability

Performance of first pacemaker to use smart device app for remote monitoring

Aberrations in one-carbon metabolism induce oxidative DNA damage in sporadic breast cancer

Machine learning algorithm-based risk prediction model of coronary artery disease

Adaptive Neuro-Fuzzy Inference System-Based Exploration of the Interrelationships of 25-Hydroxyvitamin D, Calcium, Phosphorus with Parathyroid Hormone Production

Association of Parkinson's disease with altered serum levels of lead and transition metals among South Indian subjects

Identification of Two Novel Mutations in Aminomethyltransferase Gene in Cases of Glycine Encephalopathy

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