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Aaron Chapla, Ph.D.

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Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Senthilraja M, Chapla A, Jebasingh FK, Naik D, Paul TV, Thomas N. Parallel Multi-Gene Panel Testing for Diagnosis of Idiopathic Hypogonadotropic Hypogonadism/Kallmann Syndrome. Case Rep Genet. 2019; 2019:4218514. PMID: 31781422.
    Citations:    
  2. Sahoo SK, Zaidi G, Vipin VP, Chapla A, Thomas N, Yu L, Asthana P, Bhatia E. Heterogeneity in the aetiology of diabetes mellitus in young adults: A prospective study from north India. Indian J Med Res. 2019 04; 149(4):479-488. PMID: 31411171.
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  3. Kapoor N, Chapla A, Furler J, Paul TV, Harrap S, Oldenburg B, Thomas N. Genetics of obesity in consanguineous populations - A road map to provide novel insights in the molecular basis and management of obesity. EBioMedicine. 2019 Feb; 40:33-34. PMID: 30638866.
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  4. Selvam P, Arunachal G, Danda S, Chapla A, Sivadasan A, Alexander M, Thomas MM, Thomas NJ. Congenital Myasthenic Syndrome: Spectrum of Mutations in an Indian Cohort. J Clin Neuromuscul Dis. 2018 Sep; 20(1):14-27. PMID: 30124556.
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  5. Korula S, Chapla A, Priyambada L, Mathai S, Simon A. Sirolimus therapy for congenital hyperinsulinism in an infant with a novel homozygous KCNJ11 mutation. J Pediatr Endocrinol Metab. 2018 Jan 26; 31(1):87-89. PMID: 29176012.
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  6. Goel A, Raghupathy V, Amirtharaj GJ, Chapla A, Venkatraman A, Ramakrishna B, Ramachandran A, Thomas N, Balasubramanian KA, Mackie I, Elias E, Eapen CE. ADAMTS13 missense variants associated with defective activity and secretion of ADAMTS13 in a patient with non-cirrhotic portal hypertension. Indian J Gastroenterol. 2017 Sep; 36(5):380-389. PMID: 28980147.
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  7. Doddabelavangala Mruthyunjaya M, Chapla A, Hesarghatta Shyamasunder A, Varghese D, Varshney M, Paul J, Inbakumari M, Christina F, Varghese RT, Kuruvilla KA, V Paul T, Jose R, Regi A, Lionel J, Jeyaseelan L, Mathew J, Thomas N. Comprehensive Maturity Onset Diabetes of the Young (MODY) Gene Screening in Pregnant Women with Diabetes in India. PLoS One. 2017; 12(1):e0168656. PMID: 28095440.
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  8. George R, Santhanam S, Samuel R, Chapla A, Hilmarsen HT, Braathen GJ, Reinholt FP, Jahnsen F, Khnykin D. Ichthyosis prematurity syndrome caused by a novel missense mutation in FATP4 gene-a case report from India. Clin Case Rep. 2016 01; 4(1):87-9. PMID: 26783444.
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  9. Athiyarath R, Shaktivel K, Abraham V, Singh D, Bondu JD, Chapla A, George B, Srivastava A, Edison ES. Association of genetic variants with response to iron supplements in pregnancy. Genes Nutr. 2015 Jul; 10(4):474. PMID: 26024779.
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  10. 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. PMID: 25041077.
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  11. Nair VV, Chapla A, Arulappan N, Thomas N. Molecular diagnosis of maturity onset diabetes of the young in India. Indian J Endocrinol Metab. 2013 May; 17(3):430-41. PMID: 23869298.
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  12. Sivalingam N, Pichandi S, Chapla A, Dinakaran A, Jacob M. Zinc protects against indomethacin-induced damage in the rat small intestine. Eur J Pharmacol. 2011 Mar 01; 654(1):106-16. PMID: 21185825.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.