Author

Radha Rama Devi Akella

Observed names: Akella Radha Rama Devi, Radha Rama Devi A., RadhaRamadevi Akella, Radharamadevi Akella

Institution: Rainbow Children's Hospital

Observed institutions: Rainbow Children's Hospital, Centre for DNA Fingerprinting and Diagnostics

ORCID: 0000-0002-4108-6213

Observed ORCID: 0000-0002-4108-6213

OpenAlex ID: A5043677360

Aberrations in folate metabolic pathway and altered susceptibility to autism

2009 · Naushad Shaik Mohammad, Jamal Md Nurul Jain, et al. · Psychiatric Genetics · 98

Autistic children exhibit distinct plasma amino acid profile.

2013 · Shaik Mohammad Naushad, Jamal Md Nurul Jain, et al. · PubMed · 64

Genetic and environmental influences on total plasma homocysteine and coronary artery disease (CAD) risk among South Indians

2009 · Govindaiah Vinukonda, Naushad Shaik Mohammad, et al. · Clinica Chimica Acta · 56

Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry: Experience of the Pilot Study in Andhra Pradesh, India

2011 · Inderneel Sahai, Thomas Zytkowicz, et al. · The Indian Journal of Pediatrics · 24

Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency

2016 · Elsayed Abdelkreem, Radha Rama Devi Akella, et al. · JIMD Reports · 23

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

2020 · Yedukondalu Kollati, Radha Rama Devi Akella, et al. · Molecular Biology Reports · 18

The rs1991517 polymorphism is a genetic risk factor for congenital hypothyroidism

2020 · Yedukondalu Kollati, Radha Rama Devi Akella, et al. · 3 Biotech · 15

Amniotic fluid glycosaminoglycans in the prenatal diagnosis of mucopolysaccharidoses - A useful biomarker

2016 · Radha Rama Devi Akella, Srilatha Kadali · Clinica Chimica Acta · 15

Metabolic encephalopathy in beta-ketothiolase deficiency: The first report from India

2013 · Radha Rama Devi Akella, Yuka Aoyama, et al. · Brain and Development · 14

Mitochondrial carbonic anhydrase VA deficiency in three Indian infants manifesting early metabolic crisis

2020 · Ramesh Konanki, Radha Rama Devi Akella, et al. · Brain and Development · 13

Functional characterization of novel variants in SMPD1 in Indian patients with acid sphingomyelinase deficiency

2021 · Dipti Deshpande, Shailesh Kumar Gupta, et al. · Human Mutation · 11

SLC25A13 c.1610_1612delinsAT mutation in an Indian patient and literature review of 79 cases of citrin deficiency for genotype-phenotype associations

2018 · Akella Radha Rama Devi, Shaik Mohammad Naushad · Gene · 11

Mutational analysis of androgen receptor gene in two families with androgen insensitivity

2017 · RadhaRamadevi Akella · Indian Journal of Endocrinology and Metabolism · 9

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

2021 · Akella Radha Rama Devi, Shaik Mohammad Naushad, et al. · Clinical Genetics · 7

Molecular insights into the role of genetic determinants of congenital hypothyroidism

2021 · Yedukondalu Kollati, Radha Rama Devi Akella, et al. · Genomics & Informatics · 5

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Molecular genetic analysis of a highly conserved tandemly repeated gene cluster of malarial parasites

1987 · Kathleen Suplick, Radha Rama Devi Akella, et al. · Federation Proceedings · 2

Organic Acidemias in India: Clinical and Molecular Spectrum

2026 · Sunita Bijarnia-Mahay, Deepti Gupta, et al. · The Indian Journal of Pediatrics · 1

Medium-chain acyl-CoA dehydrogenase deficiency: A ten-year single-center case series from India

2026 · Radha Rama Devi Akella, Srilatha Kadali, et al. · Clinica Chimica Acta

Succinyl-CoA:3-ketoacid CoA Transferase (SCOT) Deficiency: Case Series of Eight Patients with Novel OXCT1 Mutations from a Consanguineous Population in India

2026 · Radharamadevi Akella · Journal of Pediatric Genetics

2022 · Radharamadevi Akella · Journal of Pediatric Genetics

3-M syndrome – a primordial short stature disorder with novel CUL7 mutation in two Indian patients

2021 · Radha Rama Devi Akella · Journal of Pediatric Endocrinology and Metabolism

Works count: 21

Citation count: 386

H-index: 11

I10-index: 12