2022
Desai DA, Rao VJ, Jegga AG, Dhandapany PS, Sadayappan S.
2022. Heterogeneous Distribution of Genetic Mutations in Myosin Binding Protein-C Paralogs.. Front Genet. 13:896117. DOI:10.3389/fgene.2022.896117.
Lesurf R, Said A, Akinrinade O, Breckpot J, Delfosse K, Liu T, Yao R, Persad G, McKenna F, Noche RR, Oliveros W, Mattioli K, Shah S, Miron A, Yang Q, Meng G, Yue MChan Seng, Sung WWL, Thiruvahindrapuram B, Lougheed J et al..
2022. Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy.. NPJ Genom Med. 7(1):18. DOI:10.1038/s41525-022-00288-y.
2021
Jain PKumar, Jayappa S, Sairam T, Mittal A, Paul S, Rao VJ, Chittora H, Kashyap DK, Palakodeti D, Thangaraj K, Shenthar J, Koranchery R, Rajendran R, Alireza H, Mohanan KSreedharan, Rathinavel A, Dhandapany PS.
2021. Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathy.. J Med Genet. DOI:10.1136/jmedgenet-2021-107866.