| Maturity onset diabetes of the young in India–a distinctive mutation pattern identified through targeted next‐generation sequencing A Chapla, MD Mruthyunjaya, HS Asha, D Varghese, M Varshney, ... Clinical Endocrinology 82 (4), 533-542, 2015 | 138 | 2015 |
| Nuclear factor (NF)‐κB and its associated pathways are major molecular regulators of blood‐induced joint damage in a murine model of hemophilia D Sen, A Chapla, N Walter, V Daniel, A Srivastava, GR Jayandharan Journal of Thrombosis and Haemostasis 11 (2), 293-306, 2013 | 74 | 2013 |
| Comprehensive maturity onset diabetes of the young (MODY) gene screening in pregnant women with diabetes in India M Doddabelavangala Mruthyunjaya, A Chapla, ... PLoS One 12 (1), e0168656, 2017 | 43 | 2017 |
| Molecular diagnosis of maturity onset diabetes of the young in India VV Nair, A Chapla, N Arulappan, N Thomas Indian journal of endocrinology and metabolism 17 (3), 430-441, 2013 | 31 | 2013 |
| Zinc protects against indomethacin-induced damage in the rat small intestine N Sivalingam, S Pichandi, A Chapla, A Dinakaran, M Jacob European journal of pharmacology 654 (1), 106-116, 2011 | 27 | 2011 |
| An atypical form of diabetes among individuals with low BMI E Lontchi-Yimagou, R Dasgupta, S Anoop, S Kehlenbrink, S Koppaka, ... Diabetes Care 45 (6), 1428-1437, 2022 | 23 | 2022 |
| Heterogeneity in the aetiology of diabetes mellitus in young adults: A prospective study from north India SK Sahoo, G Zaidi, VP Vipin, A Chapla, N Thomas, L Yu, P Asthana, ... Indian Journal of Medical Research 149 (4), 479-488, 2019 | 23 | 2019 |
| Genetics of obesity in consanguineous populations–A road map to provide novel insights in the molecular basis and management of obesity N Kapoor, A Chapla, J Furler, TV Paul, S Harrap, B Oldenburg, N Thomas EBioMedicine 40, 33-34, 2019 | 21 | 2019 |
| Congenital myasthenic syndrome: spectrum of mutations in an Indian cohort P Selvam, G Arunachal, S Danda, A Chapla, A Sivadasan, M Alexander, ... Journal of clinical neuromuscular disease 20 (1), 14-27, 2018 | 17 | 2018 |
| Association of genetic variants with response to iron supplements in pregnancy R Athiyarath, K Shaktivel, V Abraham, D Singh, JD Bondu, A Chapla, ... Genes & Nutrition 10, 1-8, 2015 | 14 | 2015 |
| Ichthyosis prematurity syndrome caused by a novel missense mutation in FATP4 gene‐a case report from India R George, S Santhanam, R Samuel, A Chapla, HT Hilmarsen, ... Clinical Case Reports 4 (1), 87, 2016 | 12 | 2016 |
| Genotype and phenotypic spectrum of vitamin D dependent rickets type 1A: our experience and systematic review MH Dodamani, M Sehemby, SS Memon, V Sarathi, AR Lila, A Chapla, ... Journal of Pediatric Endocrinology and Metabolism 34 (12), 1505-1513, 2021 | 10 | 2021 |
| The H syndrome: molecular diagnosis using next-generation sequencing MD Mruthyunjaya, A Chapla, S Shetty, AH Shyamasunder, L Mathew, ... AACE Clinical Case Reports 2 (1), e65-e69, 2016 | 10 | 2016 |
| ADAMTS13 missense variants associated with defective activity and secretion of ADAMTS13 in a patient with non-cirrhotic portal hypertension A Goel, V Raghupathy, GJ Amirtharaj, A Chapla, A Venkatraman, ... Indian Journal of Gastroenterology 36, 380-389, 2017 | 9 | 2017 |
| Sirolimus therapy for congenital hyperinsulinism in an infant with a novel homozygous KCNJ11 mutation S Korula, A Chapla, L Priyambada, S Mathai, A Simon Journal of Pediatric Endocrinology and Metabolism 31 (1), 87-89, 2018 | 8 | 2018 |
| Does TCF7L2 polymorphisms increase the risk of gestational diabetes mellitus in South Indian population? N Thomas, DM Mahesh, A Chapla, J Paul, N Shwetha, F Christina, ... Endocrine Abstracts 34, 2014 | 8 | 2014 |
| Genotype of autosomal recessive congenital ichthyosis from a tertiary care center in India MJ Chiramel, L Mathew, R Athirayath, A Chapla, D Sathishkumar, T Mani, ... Pediatric Dermatology 39 (3), 420-424, 2022 | 6 | 2022 |
| WFS1 Gene–associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India A Chapla, J Johnson, S Korula, N Mohan, A Ahmed, D Varghese, ... The Journal of Clinical Endocrinology & Metabolism 107 (5), 1328-1336, 2022 | 6 | 2022 |
| Low genetic confirmation rate in South Indian subjects with a clinical diagnosis of maturity-onset diabetes of the young (MODY) who underwent targeted next-generation … G Sampathkumar, PP Valiyaparambil, H Kumar, N Bhavani, V Nair, ... Journal of Endocrinological Investigation 45 (3), 607-615, 2022 | 6 | 2022 |
| Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India L Ravichandran, S Korula, HS Asha, D Varghese, R Parthiban, J Johnson, ... European Journal of Medical Genetics 64 (12), 104369, 2021 | 6 | 2021 |
