| Mucosa-associated specific bacterial species disrupt the intestinal epithelial barrier in the autism phenome S Agarwala, B Naik, NB Ramachandra Brain, Behavior, & Immunity-Health 15, 100269, 2021 | 11 | 2021 |
| Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse S Agarwala, NB Ramachandra Egyptian Journal of Medical Human Genetics 22, 1-13, 2021 | 9 | 2021 |
| High-risk genes involved in common septal defects of congenital heart disease S Chaithra, S Agarwala, NB Ramachandra Gene 840, 146745, 2022 | 6 | 2022 |
| Nuclear co-repressor 1: a potential candidate gene in the manifestation of congenital heart diseases R Gholipoorfeshkecheh, S Agarwala, S Krishnappa, MR Savitha, ... Int J Hum Genet 20 (2), 55-65, 2020 | 5 | 2020 |
| Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects R Gholipoorfeshkecheh, S Agarwala, S Krishnappa, MR Savitha, ... Egyptian Journal of Medical Human Genetics 21, 1-10, 2020 | 4 | 2020 |
| Diversity of gut microbiota in autism reveals differential abundance of Prevotella and Akkermansia species S Agarwala, B Naik, NB Ramachandra Preprints, 2018 | 3 | 2018 |
| Variants in HEY genes manifest in ventricular septal defects of congenital heart disease R Gholipoorfeshkecheh, S Agarwala, S Krishnappa, MR Savitha, ... Gene Reports 19, 100613, 2020 | 2 | 2020 |
| Integrated whole exome sequencing and homozygosity mapping identifies variants in known and novel autism Genes involved in neuronal migration and adhesion pathways S Agarwala, KC Shyamala, P Padakannaya, N Ramachandra European Neuropsychopharmacology 29, S894-S895, 2019 | 2 | 2019 |
| Risk homozygous haplotype regions for autism identifies population-specific ten genes for numerous pathways S Agarwala, NB Ramachandra The Egyptian Journal of Neurology, Psychiatry and Neurosurgery 57 (1), 69, 2021 | 1 | 2021 |
| Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism S Agarwala, AM Veerappa, NB Ramachandra Egyptian Journal of Medical Human Genetics 21, 1-14, 2020 | | 2020 |
| Damaging stop gain/loss and frameshift mutations in autism subjects outline impairment in neuronal migration and adhesion pathways S Agarwala, KC Shyamala, P Padakannaya, NB Ramachandra Canadian Journal of Biotechnology 1 (Special), 94, 2017 | | 2017 |
| Genomic mutational landscape and gut microbiome profiling in autism subjects with delayed speech language phenotype S Agarwala Mysore, 0 | | |
Nallur B. RamachandraDAE- Raja Ramanna Chair, Professor (Retd) & Former Chairman, DOS in Genetics & Genomics在 genetics.uni-mysore.ac.in 的电子邮件经过验证
