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. doi: 10.1007/s12263-015-0474-2. Epub 2015 May 30. PMID: 26024779; PMCID: PMC4449341.

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. doi: 10.1007/s12263-015-0474-2. Epub 2015 May 30. PMID: 26024779; PMCID: PMC4449341. Link

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. doi: 10.1007/s12263-015-0474-2. Epub 2015 May 30. PMID: 26024779; PMCID: PMC4449341. Link

Athiyarath R, George B, Abraham A, Viswabandya A, Srivastava A, Edison ES. Genetic modifiers of secondary iron overload in beta thalassemia major. Blood Cells Mol Dis. 2015 Mar;54(3):242-3. doi: 10.1016/j.bcmd.2014.12.006. Epub 2015 Jan 8. PMID: 25601433. Link

Athiyarath R, George B, Mathews V, Srivastava A, Edison ES. Association of growth differentiation factor 15 (GDF15) polymorphisms with serum GDF15 and ferritin levels in β-thalassemia. Ann Hematol. 2014 Dec;93(12):2093-5. doi: 10.1007/s00277-014-2113-1. Epub 2014 May 28. PMID: 24867648. Link

Athiyarath R, Arora N, Fuster F, Schwarzenbacher R, Ahmed R, George B, Chandy M, Srivastava A, Rojas AM, Sanchez M, Edison ES. Two novel missense mutations in iron transport protein transferrin causing hypochromic microcytic anaemia and haemosiderosis: molecular characterization and structural implications. Br J Haematol. 2013 Nov;163(3):404-7. doi: 10.1111/bjh.12487. Epub 2013 Jul 24. PMID: 23888904. Link

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. doi: 10.1007/s12263-015-0474-2. Epub 2015 May 30. PMID: 26024779; PMCID: PMC4449341.

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. doi: 10.1007/s12263-015-0474-2. Epub 2015 May 30. PMID: 26024779; PMCID: PMC4449341. Link

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. doi: 10.1007/s12263-015-0474-2. Epub 2015 May 30. PMID: 26024779; PMCID: PMC4449341. Link

Athiyarath R, George B, Abraham A, Viswabandya A, Srivastava A, Edison ES. Genetic modifiers of secondary iron overload in beta thalassemia major. Blood Cells Mol Dis. 2015 Mar;54(3):242-3. doi: 10.1016/j.bcmd.2014.12.006. Epub 2015 Jan 8. PMID: 25601433. Link

Athiyarath R, George B, Mathews V, Srivastava A, Edison ES. Association of growth differentiation factor 15 (GDF15) polymorphisms with serum GDF15 and ferritin levels in β-thalassemia. Ann Hematol. 2014 Dec;93(12):2093-5. doi: 10.1007/s00277-014-2113-1. Epub 2014 May 28. PMID: 24867648. Link

Athiyarath R, Arora N, Fuster F, Schwarzenbacher R, Ahmed R, George B, Chandy M, Srivastava A, Rojas AM, Sanchez M, Edison ES. Two novel missense mutations in iron transport protein transferrin causing hypochromic microcytic anaemia and haemosiderosis: molecular characterization and structural implications. Br J Haematol. 2013 Nov;163(3):404-7. doi: 10.1111/bjh.12487. Epub 2013 Jul 24. PMID: 23888904. Link

Jaleel R, Sharma A, Selvaraj V, Aaron R, Muliyil J, Vijayalekshmi B, Dynamic scoring of appetite predicts inpatient survival in patients with acute‑on‑chronic liver failure. Gastroenterol Hepatol Endosc Pract 2021;1:143-7. DOI:10.4103/ghep.ghep_8_21

Chouksey A, Mohan S, Aaron R, Mathew V. The multiple twists in the tale: Brain iron accumulation, facial jerks, and truncal dystonia. Parkinsonism Relat Disord. 2022 Mar 18:S1353-8020(22)00062-1. doi: 10.1016/j.parkreldis.2022.03.004. Epub ahead of print. PMID: 35339370.

Varkki S, Benjamin AT, Athiyarath R, Danda S, Sowmya R, Connett G. Meconium Ileus due to GUCY2C gene mutations in three unrelated South Indian families. J Cyst Fibros. 2021 Sep;20(5):e84-e86. doi: 10.1016/j.jcf.2021.03.023. Epub 2021 Apr 18. PMID: 33883099.

Aaron, R., Beck, M.M., Arunachal, G. et al. NLRP7 Mutation in Recurrent Non-familial Molar Pregnancies: A Case Series. Indian J Gynecol Oncolog 20, 55 (2022). https://doi.org/10.1007/s40944-022-00661-w

Chouksey A, Mohan S, Aaron R, Mathew V. The multiple twists in the tale: Brain iron accumulation, facial jerks, and truncal dystonia. Parkinsonism Relat Disord. 2022 Mar 18:S1353-8020(22)00062-1. doi: 10.1016/j.parkreldis.2022.03.004. Epub ahead of print. PMID: 35339370.

Bharathi NK, Thomas MM, Yoganathan S, Chandran M, Aaron R, Danda S. Phenotypic Pleiotropy in Arginase Deficiency: A Single Center Cohort. Ann Indian Acad Neurol. 2022 Nov-Dec;25(6):1104-1108. doi: 10.4103/aian.aian_612_22. Epub 2022 Dec 3. PMID: 36911443; PMCID: PMC9996474.

Das S, Thomas M, Yoganathan S, Muthusamy K, Barney AM, A SSC, Dutta AK, A R, Mohan S, Danda S. Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinent. Eur J Med Genet. 2023 Jun;66(6):104766. doi: 10.1016/j.ejmg.2023.104766. Epub 2023 Apr 17. PMID: 37075885.

Santhakumar S, Athiyarath R, Cherian AG, Abraham VJ, George B, Lipiński P, Edison ES. Corrigendum to "Impact of maternal iron deficiency anemia on fetal iron status and placental iron transporters in human pregnancy" [Blood Cells Mol. Dis. 99 (2023) 102727]. Blood Cells Mol Dis. 2023 Jul;101:102744. doi: 10.1016/j.bcmd.2023.102744. Epub 2023 Apr 23. Erratum for: Blood Cells Mol Dis. 2023 Mar;99:102727. PMID: 37095038. Link

Athiyarath R, Srivastava A, Edison ES. Molecular basis of primary iron overload in India and the role of serum-derived factors in hepcidin regulation. Ann Hematol. 2013 Jun;92(6):843-4. doi: 10.1007/s00277-012-1621-0. Epub 2012 Nov 15. PMID: 23154866.

A R, Chandran S, Ghatak AR, Thomas N, Danda S. Novel Mutations in CRLF1: Case Reports with Crisponi Syndrome. Indian J Pediatr. 2022 Nov;89(11):1148-1150. doi: 10.1007/s12098-022-04263-4. Epub 2022 Aug 19. PMID: 35984556.

Rajeeb Jaleel, Anand Sharma, Vimala Selvaraj, Rekha Aaron, Jayaprakash Muliyil, Balakrishnan Vijayalekshmi, Kunnisery Ananthsubramanian Balasubramanian, Balavendra Antonisamy, Ashish Goel, Uday George Zachariah, Chundamannil Eapen Eapen. Dynamic scoring of appetite predicts inpatient survival in patients with acute‑on‑chronic liver failure. Gastroenterol Hepatol Endosc Pract 2021;1:143-7. DOI:10.4103/ghep.ghep_8_21

Rekha Aaron, Aaron Chapla, Sumita Danda, Uday Zachariah, Chundamannil E. Eapen, Ashish Goel, Multiplex PCR-based Sequencing of ATP7B Gene in Wilson's Disease – A Preliminary Study, Journal of Clinical and Experimental Hepatology,2021, , ISSN 0973-6883, https://doi.org/10.1016/j.jceh.2021.08.001. (https://www.sciencedirect.com/science/article/pii/S0973688321001845)

Chiramel MJ, Mathew L, Athirayath R, Chapla A, Sathishkumar D, Mani T, Danda S, George R. Genotype of autosomal recessive congenital ichthyosis from a tertiary care center in India. Pediatr Dermatol. 2022 May;39(3):420-424. doi: 10.1111/pde.14944. Epub 2022 Apr 12. PMID: 35412663.

Aaron R, Chapla A, Danda S, Zachariah U, Eapen CE, Goel A. Multiplex PCR-based Sequencing of ATP7B Gene in Wilson's Disease - A Preliminary Study. J Clin Exp Hepatol. 2022 Mar-Apr;12(2):711-713. doi: 10.1016/j.jceh.2021.08.001. Epub 2021 Aug 6. PMID: 35535059; PMCID: PMC9077194.

Sivamani P, Eriyat V, Mathew SK, Singh A, Aaron R, Chacko RT, Joel A, Prabha R, Mathew BS. Identification of DPYD variants and estimation of uracil and dihydrouracil in a healthy Indian population. Per Med. 2023 Jan;20(1):39-53. doi: 10.2217/pme-2022-0042. Epub 2022 Nov 23. PMID: 36416570.

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. Link

Mahadevan N, Thiruvadi V, C P, A R, A M. Cerebrotendinous Xanthomatosis: Report of Two Siblings With the Same Mutation but Variable Presentation. Cureus. 2023 Jan 5;15(1):e33378. doi: 10.7759/cureus.33378. PMID: 36628393; PMCID: PMC9821311. Link

Kumar M, Aaron R, Varkki SD, Danda S, Ranganathan S, Paul GR. A rare variant c.1802T>C (p. Ile601Thr) associated with severe phenotype among people with cystic fibrosis from south India, and potential genetic admixture in Réunion, France. Pediatr Pulmonol. 2024 Mar 19. doi: 10.1002/ppul.26965. Epub ahead of print. PMID: 38501349.

Ilangovan H, Elangovan J, Danda S, Beck MM, Navaneethan P, Athiyarath R. Exploring the clinical utility of exome sequencing/mono, duo, trio in prenatal testing: a retrospective study in a tertiary care centre in south India. J Perinat Med. 2024 May 7. doi: 10.1515/jpm-2023-0485. Epub ahead of print. PMID: 38709224.