Veeraraghavan B, Anandan S, Rajamani Sekar SK, Gopi R, Devanga Ragupathi NK, Ramesh S, Verghese VP, Korulla S, Mathai S, Sangal L, Joshi S. First Report on the Draft Genome Sequences of Corynebacterium diphtheriae Isolates from India. Genome Announc. 2016 Nov 23;4(6):e01316-16. doi: 10.1128/genomeA.01316-16. PMID: 27881543; PMCID: PMC5122685.

Chapla A, Mruthyunjaya MD, Asha HS, Varghese D, Varshney M, Vasan SK, Venkatesan P, Nair V, Mathai S, Paul TV, Thomas N. Maturity onset diabetes of the young in India - a distinctive mutation pattern identified through targeted next-generation sequencing. Clin Endocrinol (Oxf). 2015 Apr;82(4):533-42. doi: 10.1111/cen.12541. Epub 2014 Aug 7. PMID: 25041077.

Arun S, Kumar M, Paul T, Thomas N, Mathai S, Rebekah G, Thomas N. An Open-label Randomized Controlled Trial to Compare Weight Gain of Very Low Birth Weight Babies with or without Addition of Coconut Oil to Breast Milk. J Trop Pediatr. 2019 Feb 1;65(1):63-70. doi: 10.1093/tropej/fmy012. PMID: 29584924.

Korula S, Danda S, Paul PG, Mathai S, Simon A. Hepatic Glycogenoses Among Children-Clinical and Biochemical Characterization: Single-Center Study. J Clin Exp Hepatol. 2020 May-Jun;10(3):222-227. doi: 10.1016/j.jceh.2019.07.007. Epub 2019 Jul 25. PMID: 32405178; PMCID: PMC7212290.

Barney AM, Danda S, Abraham A, Fouzia NA, Gowdra A, Abraham SSC, Sony M, Das S, Korula S, Mathai S, Simon A, Kumar S. Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study. Public Health Genomics. 2021;24(3-4):139-148. doi: 10.1159/000514507. Epub 2021 Apr 6. PMID: 33823526.

Ravichandran L, Korula S, Asha HS, Varghese D, Parthiban R, Johnson J, Ishwarya J, Shetty S, Cherian KE, Jebasingh F, Kapoor N, Pachat D, Mathai S, Simon A, Rajaratnam S, Paul TV, Thomas N, Chapla A. Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India. Eur J Med Genet. 2021 Dec;64(12):104369. doi: 10.1016/j.ejmg.2021.104369. Epub 2021 Oct 27. PMID: 34718183.

Veeraraghavan B, Anandan S, Rajamani Sekar SK, Gopi R, Devanga Ragupathi NK, Ramesh S, Verghese VP, Korulla S, Mathai S, Sangal L, Joshi S. First Report on the Draft Genome Sequences of Corynebacterium diphtheriae Isolates from India. Genome Announc. 2016 Nov 23;4(6):e01316-16. doi: 10.1128/genomeA.01316-16. PMID: 27881543; PMCID: PMC5122685.

Chapla A, Mruthyunjaya MD, Asha HS, Varghese D, Varshney M, Vasan SK, Venkatesan P, Nair V, Mathai S, Paul TV, Thomas N. Maturity onset diabetes of the young in India - a distinctive mutation pattern identified through targeted next-generation sequencing. Clin Endocrinol (Oxf). 2015 Apr;82(4):533-42. doi: 10.1111/cen.12541. Epub 2014 Aug 7. PMID: 25041077.

Arun S, Kumar M, Paul T, Thomas N, Mathai S, Rebekah G, Thomas N. An Open-label Randomized Controlled Trial to Compare Weight Gain of Very Low Birth Weight Babies with or without Addition of Coconut Oil to Breast Milk. J Trop Pediatr. 2019 Feb 1;65(1):63-70. doi: 10.1093/tropej/fmy012. PMID: 29584924.

Korula S, Danda S, Paul PG, Mathai S, Simon A. Hepatic Glycogenoses Among Children-Clinical and Biochemical Characterization: Single-Center Study. J Clin Exp Hepatol. 2020 May-Jun;10(3):222-227. doi: 10.1016/j.jceh.2019.07.007. Epub 2019 Jul 25. PMID: 32405178; PMCID: PMC7212290.

Barney AM, Danda S, Abraham A, Fouzia NA, Gowdra A, Abraham SSC, Sony M, Das S, Korula S, Mathai S, Simon A, Kumar S. Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study. Public Health Genomics. 2021;24(3-4):139-148. doi: 10.1159/000514507. Epub 2021 Apr 6. PMID: 33823526.

Ravichandran L, Korula S, Asha HS, Varghese D, Parthiban R, Johnson J, Ishwarya J, Shetty S, Cherian KE, Jebasingh F, Kapoor N, Pachat D, Mathai S, Simon A, Rajaratnam S, Paul TV, Thomas N, Chapla A. Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India. Eur J Med Genet. 2021 Dec;64(12):104369. doi: 10.1016/j.ejmg.2021.104369. Epub 2021 Oct 27. PMID: 34718183.

Ghosh U, Mathai S. Leprechaunism (Donohue syndrome). Indian Pediatr. 2015 Aug;52(8):724. PMID: 26388649.

Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. PMID: 34303877.

Paul PG, Rebekah G, Korula S, Kumar M, Bondu JD, Palany R, Simon A, Mathai S. Optimizing Cord Blood Thyroid Stimulating Hormone Cutoff for Screening of Congenital Hypothyroidism-Experience from Screening 164,000 Newborns in a Tertiary Hospital in India. Indian J Endocrinol Metab. 2021 Jul-Aug;25(4):348-353. doi: 10.4103/ijem.ijem_220_21. Epub 2021 Dec 15. PMID: 35136744; PMCID: PMC8793950.

Paul PG, Rebekah G, Korula S, Kumar M, Bondu JD, Palany R, Simon A, Mathai S. Optimizing Cord Blood Thyroid Stimulating Hormone Cutoff for Screening of Congenital Hypothyroidism-Experience from Screening 164,000 Newborns in a Tertiary Hospital in India. Indian J Endocrinol Metab. 2021 Jul-Aug;25(4):348-353. doi: 10.4103/ijem.ijem_220_21. Epub 2021 Dec 15. PMID: 35136744; PMCID: PMC8793950.

Malik P, Bidkar SU, Yoganathan S, Mathai S, Danda S, Koshy B. Imaging findings in TRPM6-Related hypomagnesemia with secondary hypocalcemia. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):247-248. doi: 10.4103/aian.AIAN_243_20. Epub 2021 Apr 28. PMID: 34220071; PMCID: PMC8232497.

Korula S, Ravichandran L, Paul PG, Johnson J, Chapla A, Santhanam S, Simon A, Mathai S. Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South India. Indian J Endocrinol Metab. 2022 Jan-Feb;26(1):79-86. doi: 10.4103/ijem.ijem_429_21. Epub 2022 Apr 27. PMID: 35662751; PMCID: PMC9162257.

Yoganathan S, Thomas MM, Mathai S, Ghosh U. Neuroregression as an initial manifestation in a toddler with acquired pernicious anaemia. BMJ Case Rep. 2015 Dec 17;2015:bcr2015213540. doi: 10.1136/bcr-2015-213540. PMID: 26678841; PMCID: PMC4691932.

Mohan S, Danda S, Mathai S, Simon A. Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India. Natl Med J India. 2019 May-Jun;32(3):141-143. doi: 10.4103/0970-258X.278692. PMID: 32129306.

Basker MM, Mathai S, Korula S, Mammen PM. Eating disorders among adolescents in a tertiary care centre in India. Indian J Pediatr. 2013 Mar;80(3):211-4. doi: 10.1007/s12098-012-0819-4. Epub 2012 Jul 14. PMID: 22798272.

Hokken-Koelega ACS, van der Steen M, Boguszewski MCS, Cianfarani S, Dahlgren J, Horikawa R, Mericq V, Rapaport R, Alherbish A, Braslavsky D, Charmandari E, Chernausek SD, Cutfield WS, Dauber A, Deeb A, Goedegebuure WJ, Hofman PL, Isganatis E, Jorge AA, Kanaka-Gantenbein C, Kashimada K, Khadilkar V, Luo XP, Mathai S, Nakano Y, Yau M. International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early Adulthood. Endocr Rev. 2023 May 8;44(3):539-565. doi: 10.1210/endrev/bnad002. PMID: 36635911; PMCID: PMC10166266.

Sarkar S, Chacko SR, Korula S, Hesarghatta A, Balakrishnan R, Mathai S, Simon A, Chacko G, Prabhu K, Chacko AG. A Comparison of Long-Term Treatment Outcomes Between Giant and Nongiant Craniopharyngiomas. World Neurosurg. 2022 Mar 20:S1878-8750(22)00363-1. doi: 10.1016/j.wneu.2022.03.073. Epub ahead of print. PMID: 35321841.

Korula S, Ravichandran L, Paul PG, Johnson J, Chapla A, Santhanam S, Simon A, Mathai S. Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South India. Indian J Endocrinol Metab. 2022 Jan-Feb;26(1):79-86. doi: 10.4103/ijem.ijem_429_21. Epub 2022 Apr 27. PMID: 35662751; PMCID: PMC9162257.

Srinivasaraghavan R, Jagadeesh A, Yoganathan S, Mathai S, Oommen SP. Unusual Presentation of Adrenal Hypoplasia Congenita. Indian J Pediatr. 2020 Oct;87(10):865-866. doi: 10.1007/s12098-020-03239-6. Epub 2020 Jul 9. PMID: 32643053.

Sarkar S, Chacko SR, Korula S, Simon A, Mathai S, Chacko G, Chacko AG. Long-term outcomes following maximal safe resection in a contemporary series of childhood craniopharyngiomas. Acta Neurochir (Wien). 2021 Feb;163(2):499-509. doi: 10.1007/s00701-020-04591-4. Epub 2020 Oct 19. PMID: 33078364.

Shetty S, Kapoor N, Mathai S, Paul TV. Hyperphosphatemic tumoural calcinosis. BMJ Case Rep. 2016 Jan 25;2016:bcr2015213537. doi: 10.1136/bcr-2015-213537. PMID: 26811414; PMCID: PMC4735367.

Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. PMID: 34303877.

Hokken-Koelega ACS, van der Steen M, Boguszewski MCS, Cianfarani S, Dahlgren J, Horikawa R, Mericq V, Rapaport R, Alherbish A, Braslavsky D, Charmandari E, Chernausek SD, Cutfield WS, Dauber A, Deeb A, Goedegebuure WJ, Hofman PL, Isganatis E, Jorge AA, Kanaka-Gantenbein C, Kashimada K, Khadilkar V, Luo XP, Mathai S, Nakano Y, Yau M. International Consensus Guideline on Small for Gestational Age (SGA): Etiology and Management from Infancy to Early Adulthood. Endocr Rev. 2023 Jan 13:bnad002. doi: 10.1210/endrev/bnad002. Epub ahead of print. PMID: 36635911.

Sarkar S, Korula S, Mathai S, Simon A, Balakrishnan R, Backianathan S, Chacko AG. Upfront adjuvant irradiation versus postoperative surveillance following incomplete surgical resection of craniopharyngiomas in children and young adults. Childs Nerv Syst. 2022 Oct;38(10):1877-1883. doi: 10.1007/s00381-022-05635-z. Epub 2022 Aug 9. PMID: 35945339.

Harriet, Gibeah et al. “Bone Mineral Density and Serum Bone Turnover Markers among Post-Menarchal Girls from Rural South India.” Indian journal of endocrinology and metabolism vol. 27,3 (2023): 242-248. doi:10.4103/ijem.ijem_111_22

Ravichandran L, Paul S, A R, Hs A, Mathai S, Simon A, Danda S, Thomas N, Chapla A. High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia. Endocrine. 2024 Mar 5. doi: 10.1007/s12020-024-03747-x. Epub ahead of print. PMID: 38441846.

Almahmoud R, Hussein A, Khaja FA, Soliman AF, Dewedar H, Shareef ZA, Mathai S. Growth and endocrinopathies among children with β-Thalassemia major treated at Dubai Thalassemia centre. BMC Pediatr. 2024 Apr 5;24(1):244. doi: 10.1186/s12887-024-04670-w. PMID: 38580952; PMCID: PMC10996095.

Chiramel MJ, George A, Sathishkumar D, Simon A, Mathai S. Vitamin D Dependent Rickets 2A With Alopecia: Three Cases With Novel Genetic Variants. Pediatr Dermatol. 2025 May-Jun;42(3):615-619. doi: 10.1111/pde.15853. Epub 2024 Dec 23. PMID: 39716449.

Kompithra RZ, Mathew LG, Verghese VP, Mathai S, John TJ. High public demand and acceptance of newer vaccines in private sector immunisation in Vellore, South India: Implications for India's national immunisation program. Indian J Med Microbiol. 2025 Jul-Aug;56:100913. doi: 10.1016/j.ijmmb.2025.100913. Epub 2025 Jul 4. PMID: 40617355.