Oommen SP, Santhanam S, John H, Roshan R, Swathi TO, Padankatti C, Grace H, Beulah R, Jana AK, Kumar M, Thomas N, Yadav B. Neurodevelopmental Outcomes of Very Low Birth Weight Infants at 18-24 Months, Corrected Gestational Age in a Tertiary Health Centre: A Prospective Cohort Study. J Trop Pediatr. 2019 Dec 1;65(6):552-560. doi: 10.1093/tropej/fmz006. PMID: 30793756.

Oommen SP, Santhanam S, John H, Roshan R, Swathi TO, Padankatti C, Grace H, Beulah R, Jana AK, Kumar M, Thomas N, Yadav B. Neurodevelopmental Outcomes of Very Low Birth Weight Infants at 18-24 Months, Corrected Gestational Age in a Tertiary Health Centre: A Prospective Cohort Study. J Trop Pediatr. 2019 Dec 1;65(6):552-560. doi: 10.1093/tropej/fmz006. PMID: 30793756.

Varala S, George R, Mathew L, Russell P, Koshy B, Oommen SP, Thomas M, Muthusamy K, Yoganathan S, Jeyaseelan L, Muliyil J. The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study. Indian Dermatol Online J. 2021 Jan 16;12(1):84-89. doi: 10.4103/idoj.IDOJ_275_20. PMID: 33768027; PMCID: PMC7982006

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.

Juneja M, Gupta A, Sairam S, Jain R, Sharma M, Thadani A, Srinivasan R, Lingappa L, Ahmed S, Multani KS, Buch P, Chatterjee N, Dalwai S, Kabra M, Kapoor S, Patel PK, Girisha KM, Kulkarni M, Kunju P, Malhi P, Meenai Z, Mishra D, Mundkur N, Nair MKC, Oommen SP, Prasad C, Singh A, Srivastava L, Suman P, Thakur R. Diagnosis and Management of Global Development Delay: Consensus Guidelines of Growth, Development and Behavioral Pediatrics Chapter, Neurology Chapter and Neurodevelopment Pediatrics Chapter of the Indian Academy of Pediatrics. Indian Pediatr. 2022 Feb 19:S097475591600406. Epub ahead of print. PMID: 35188106.

Yoganathan S, Arunachal G, Kratz L, Varman M, Sudhakar SV, Oommen SP, Jain S, Thomas M, Babuji M. Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder. Ann Indian Acad Neurol. 2020 May-Jun;23(3):419-421. doi: 10.4103/aian.AIAN_172_19. Epub 2020 Jan 3. PMID: 32606564; PMCID: PMC7313585. Link

Oommen SP, Santhanam S, John H, Roshan R, Swathi TO, Padankatti C, Grace H, Beulah R, Jana AK, Kumar M, Thomas N, Yadav B. Neurodevelopmental Outcomes of Very Low Birth Weight Infants at 18-24 Months, Corrected Gestational Age in a Tertiary Health Centre: A Prospective Cohort Study. J Trop Pediatr. 2019 Dec 1;65(6):552-560. doi: 10.1093/tropej/fmz006. PMID: 30793756.

Oommen SP, Santhanam S, John H, Roshan R, Swathi TO, Padankatti C, Grace H, Beulah R, Jana AK, Kumar M, Thomas N, Yadav B. Neurodevelopmental Outcomes of Very Low Birth Weight Infants at 18-24 Months, Corrected Gestational Age in a Tertiary Health Centre: A Prospective Cohort Study. J Trop Pediatr. 2019 Dec 1;65(6):552-560. doi: 10.1093/tropej/fmz006. PMID: 30793756.

Varala S, George R, Mathew L, Russell P, Koshy B, Oommen SP, Thomas M, Muthusamy K, Yoganathan S, Jeyaseelan L, Muliyil J. The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study. Indian Dermatol Online J. 2021 Jan 16;12(1):84-89. doi: 10.4103/idoj.IDOJ_275_20. PMID: 33768027; PMCID: PMC7982006

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.

Juneja M, Gupta A, Sairam S, Jain R, Sharma M, Thadani A, Srinivasan R, Lingappa L, Ahmed S, Multani KS, Buch P, Chatterjee N, Dalwai S, Kabra M, Kapoor S, Patel PK, Girisha KM, Kulkarni M, Kunju P, Malhi P, Meenai Z, Mishra D, Mundkur N, Nair MKC, Oommen SP, Prasad C, Singh A, Srivastava L, Suman P, Thakur R. Diagnosis and Management of Global Development Delay: Consensus Guidelines of Growth, Development and Behavioral Pediatrics Chapter, Neurology Chapter and Neurodevelopment Pediatrics Chapter of the Indian Academy of Pediatrics. Indian Pediatr. 2022 Feb 19:S097475591600406. Epub ahead of print. PMID: 35188106.

Yoganathan S, Arunachal G, Kratz L, Varman M, Sudhakar SV, Oommen SP, Jain S, Thomas M, Babuji M. Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder. Ann Indian Acad Neurol. 2020 May-Jun;23(3):419-421. doi: 10.4103/aian.AIAN_172_19. Epub 2020 Jan 3. PMID: 32606564; PMCID: PMC7313585. Link

Juneja M, Gupta A, Sairam S, Jain R, Sharma M, Thadani A, Srinivasan R, Lingappa L, Ahmed S, Multani KS, Buch P, Chatterjee N, Dalwai S, Kabra M, Kapoor S, Patel PK, Girisha KM, Kulkarni M, Kunju PAM, Malhi P, Meenai Z, Mishra D, Mundkur N, Nair MKC, Oommen SP, Prasad C, Singh A, Srivastava L, Suman P, Thakur R. Diagnosis and Management of Global Development Delay: Consensus Guidelines of Growth, Development and Behavioral Pediatrics Chapter, Neurology Chapter and Neurodevelopment Pediatrics Chapter of the Indian Academy of Pediatrics. Indian Pediatr. 2022 May 15;59(5):401-415. Epub 2022 Feb 19. PMID: 35188106.

Simon B, Oommen SP, Shah K, Mani SE, Gibikote S. Cockayne syndrome: characteristic neuroimaging features. Acta Neurol Belg. 2015 Sep;115(3):427-8. doi: 10.1007/s13760-014-0390-z. Epub 2014 Nov 9. PMID: 25381627.

Danda S, Datar C, Kher A, Deshpande T, Thomas MM, Oommen SP. First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1. Am J Med Genet A. 2022 Aug;188(8):2501-2504. doi: 10.1002/ajmg.a.62844. Epub 2022 May 21. PMID: 35596688.

Zachariah SM, Oommen SP, Padankatti CS, Grace H, Glory L. Dysmorphism in Non-Syndromic Autism: A Cross-Sectional Study. Indian Pediatr. 2017 Jul 15;54(7):560-562. doi: 10.1007/s13312-017-1068-4. Epub 2017 Feb 2. PMID: 28159942.

Adde L, Thomas N, John HB, Oommen S, Vågen RT, Fjørtoft T, Jensenius AR, Støen R. Early motor repertoire in very low birth weight infants in India is associated with motor development at one year. Eur J Paediatr Neurol. 2016 Nov;20(6):918-924. doi: 10.1016/j.ejpn.2016.07.019. Epub 2016 Jul 30. PMID: 27524392.

Srinivasaraghavan R, Oommen SP. Developmental Delay with Intermittent Twisting of Neck. Indian Pediatr. 2020 May 15;57(5):469-470. PMID: 32444522. Link

Danda S, Datar C, Kher A, Deshpande T, Thomas MM, Oommen SP. First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1. Am J Med Genet A. 2022 Aug;188(8):2501-2504. doi: 10.1002/ajmg.a.62844. Epub 2022 May 21. PMID: 35596688.

Yoganathan S, Arunachal G, Kratz L, Varman M, Thomas M, Sudhakar SV, Oommen SP, Danda S. Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):259-261. doi: 10.4103/aian.AIAN_360_20. Epub 2021 Apr 28. PMID: 34220078; PMCID: PMC8232515.

John D, Oommen SP, Gowri SM, Ramani S, Ravi D, Nagarajan K, Dutton GN. Visual outcome in young children presenting with profound cerebral visual impairment: Preliminary evidence for success of vision therapy. Indian J Ophthalmol. 2021 Aug;69(8):2232-2233. doi: 10.4103/ijo.IJO_3307_20. PMID: 34304220; PMCID: PMC8482888.

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.

Yoganathan S, Bhasin H, Garg D, Malik P, Saini AG, Chandran M, Korula S, Arunachal G, Danda S, Thomas M, Oommen SP, Sharma S. Childhood Neurological Disorders With Hyperhomocystinemia: A Case-Based Review. Pediatr Neurol. 2023 Sep;146:26-30. doi: 10.1016/j.pediatrneurol.2023.06.003. Epub 2023 Jun 13. PMID: 37413720.

John HB, Oommen SP, Kumar M. Trajectories of general movements in very preterm infants: An experience from South India, a prospective cohort study. Curr Med Issues 2022;20(1):16-21. DOI: 10.4103/cmi.cmi_58_21

Koshy B, Oommen SP, Jasper S, Danda S, Surendrababu NR. Development and dysmorphism in Joubert syndrome--short case series from India. J Trop Pediatr. 2010 Jun;56(3):209-12. doi: 10.1093/tropej/fmp084. Epub 2009 Sep 15. PMID: 19755534. Link

Yoganathan S, Arunachal G, Kratz L, Varman M, Sudhakar SV, Oommen SP, Jain S, Thomas M, Babuji M. Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder. Ann Indian Acad Neurol. 2020 May-Jun;23(3):419-421. doi: 10.4103/aian.AIAN_172_19. Epub 2020 Jan 3. PMID: 32606564; PMCID: PMC7313585. Link

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.

John D, Oommen SP, Gowri SM, Ramani S, Ravi D, Nagarajan K, Dutton GN. Visual outcome in young children presenting with profound cerebral visual impairment: Preliminary evidence for success of vision therapy. Indian J Ophthalmol. 2021 Aug;69(8):2232-2233. doi: 10.4103/ijo.IJO_3307_20. PMID: 34304220; PMCID: PMC8482888. Link

John HB, Oommen SP, Swathi TO, Kumar M, Stoen R, Adde L. Preterm General Movements in Prediction of Neurodevelopmental Disability and Cerebral Palsy at Two Years: A Prospective Cohort Study. Indian Pediatr. 2022 Oct 15;59(10):769-773. Epub 2022 Aug 10. PMID: 35959757. Link

Yoganathan S, Kumar M, John D, Danda S, Oommen SP, Umakant SB, Thomas M. Oculodigital Sign: A Clinical Clue for Diagnosis. Ann Indian Acad Neurol. 2022 May-Jun;25(3):560-561. doi: 10.4103/aian.aian_755_21. Epub 2022 May 3. PMID: 35936593; PMCID: PMC9350766.

Srinivasaraghavan R, Sharma S, Kratz L, Malik P, Yoganathan S, Danda S, Oommen SP. Child with D-2-Hydroxyglutaric Aciduria Type II: A Rare Neurometabolic Disorder. Ann Indian Acad Neurol. 2021 Nov-Dec;24(6):933-934. doi: 10.4103/aian.AIAN_231_20. Epub 2021 Dec 17. PMID: 35359529; PMCID: PMC8965948.

Raghupathy P, Ramakrishna BS, Oommen SP, Ahmed MS, Priyaa G, Dziura J, Young GP, Binder HJ. Amylase-resistant starch as adjunct to oral rehydration therapy in children with diarrhea. J Pediatr Gastroenterol Nutr. 2006 Apr;42(4):362-8. doi: 10.1097/01.mpg.0000214163.83316.41. PMID: 16641573.

Yoganathan S, Arunachal G, Kratz L, Varman M, Thomas M, Sudhakar SV, Oommen SP, Danda S. Metabolic Stroke: A Novel Presentation in a Child with Succinic Semialdehyde Dehydrogenase Deficiency. Ann Indian Acad Neurol. 2020 Jan-Feb;23(1):113-117. doi: 10.4103/aian.AIAN_213_18. PMID: 32055132; PMCID: PMC7001443.

Yoganathan S, Varman M, Oommen SP, Thomas M. A Tale of Treatable Infantile Neuroregression and Diagnostic Dilemma with Glutaric Aciduria Type I. J Pediatr Neurosci. 2017 Oct-Dec;12(4):356-359. doi: 10.4103/jpn.JPN_35_17. PMID: 29675077; PMCID: PMC5890558.