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Stem Cell Research|March 13, 2024
Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3Sudipta Mahato, Savitri Maddileti, Milind Naik, et al.
European Journal of Pediatrics|June 27, 2023
Performance of smartphone application to accurately quantify hyperbilirubinemia in neonates: a systematic review with meta-analysisDeeparaj Hegde, Chandra Rath, Sathika Amarasekara, et al.
Chronic Illness|September 15, 2023
Experiences and expectations of physician communication: A focus group discussion with Indian patients with type 2 diabetes mellitusTejal Lathia, Mahati Chittem, Shweta Chawak, et al.
Cardiology in the Young|April 1, 2026
Effect of preoperative oral iron supplementation on postoperative outcomes in children with acyanotic congenital heart disease undergoing cardiac surgery: a pragmatic randomised clinical trialAbishek Murugaiyan, Ajay Kumar Jha, Satyen Parida, et al.
Indian Journal of Psychiatry|January 27, 2025
Depression, anxiety, stress, and coping among men with infertility seeking treatment at a tertiary care hospital in South India: A mixed-method studyMamta Mor, Venkatachalam Jayaseelan, Shivanand Kattimani, et al.
Environmental Research|October 13, 2020
Measurement harmonization and traceability for trace element analyses across the Children's Health Exposure Analysis Resource laboratory networkAubrey L Galusha, Lori Merrill, Christopher D Palmer, et al.
International Journal of Molecular Sciences|July 29, 2023
Potential Roles for the GluN2D NMDA Receptor Subunit in SchizophreniaChitra Vinnakota, Matthew R Hudson, Nigel C Jones, et al.
World Journal of Gastrointestinal Endoscopy|November 28, 2019
Oesophageal carcinoma mimicking a submucosal lesion: A case reportRevathy Marimuthu Shanmugam, Chitra Shanmugam, Manimaran Murugesan, et al.
Marine Genomics|May 11, 2015
Draft genome sequence of Vitellibacter vladivostokensis KMM 3516(T): a protease-producing bacteriumSuganthi Thevarajoo, Chitra Selvaratnam, Kok-Gan Chan, et al.
American Journal of Medical Genetics. Part A|July 2, 2021
Functional analysis of novel genetic variants of NKX2-5 associated with nonsyndromic congenital heart diseaseRitu Dixit, Chitra Narasimhan, Vijayalakshmi I Balekundri, et al.
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