S. Muthuswamy and S. Agarwal,"Molecular Diagnosis of Genetic Disorders", Handbook on Medical Genetics and Genetics Counseling, ch.19, pp.170-188, Noble 2021       Inbook

S. Kumari and S. Muthuswamy,"Conventional and Advanced Techniques for N6-Methyladenosine Modifications Mapping in Transcripts", Epitranscriptomics, ch.14, vol.12, pp.391-409, Springer, rna technologies 12 2021, 10.1007/978-3-030-71612-7       Inbook

S. Muthuswamy,"m6A mRNA methylation: A pleiotropic regulator of cancer", Gene, vol.736, no.144415, Elsevier, January 2020, 10.1016/j.gene.2020.144415       Article

S. Kumari and S. Muthuswamy,"SETD2 as a regulator of N6-methyladenosine RNA methylation and modifiers in cancer", European Journal of Cancer Prevention, vol.29, no.6, pp.556-564, Wolter Kluwer 2020, 10.1097/CEJ.0000000000000587       Article

D. D. Dean, S. Agarwal, and S. Muthuswamy,"Fragile X molecular investigation and genetic counselling of intellectual disability/developmental delay patients in an Indian scenario", Expert Review of Molecular Diagnostics, vol.19, no.7, pp.641-649, Taylor & Francis, June 2019, 10.1080/14737159.2019.1622416       Article

D. D. Dean, S. Agarwal, and S. Muthuswamy,"Defining the role of FMR1 gene in unexplained recurrent spontaneous abortion", Journal of Assisted Reproduction and Genetics, vol.36, pp.2245-2250, Springer, July 2019, 10.1007/s10815-019-01591-x       Article

A. Asim, S. Agarwal, I. Panigrahi, A. N. Sarangi, S. Muthuswamy, and A. Kapoor,"CRELD1 gene variants and atrioventricular septal defects in Down syndrome", Gene, vol.641, pp.180-185, Elsevier, January 2018, 10.1016/j.gene.2017.10.044       Article

N. Saiyed, S. Bakshi, S. Muthuswamy, and S. Agarwal,"Young mothers and higher incidence of maternal meiosis-I non- disjunction: Interplay of environmental exposure and genetic alterations during halt phase in trisomy 21", Reproductive Toxicology, vol.79, pp.1-7, Elsevier, August 2018, 10.1016/j.reprotox.2018.04.014       Article

I. Panigrahi, P. Jain, S. Didel, S. Agarwal, S. Muthuswamy, A. Saha, and V. Kulkarni,"Identification of microdeletion and microduplication syndromes by chromosomal microarray in patients with intellectual disability with dysmorphism", Neurology India, vol.66, no.5, pp.1370-1376, Medknow 2018, 10.4103/0028-3886.241346       Article