| Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome AM Veerappa, P Padakannaya, NB Ramachandra Functional & integrative genomics 13, 285-293, 2013 | 64 | 2013 |
| Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity AM Veerappa, M Saldanha, P Padakannaya, NB Ramachandra Journal of human genetics 58 (8), 539-547, 2013 | 59 | 2013 |
| Genome‐wide copy number scan identifies disruption of PCDH11X in developmental dyslexia AM Veerappa, M Saldanha, P Padakannaya, NB Ramachandra American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 …, 2013 | 55 | 2013 |
| Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD) U Radhakrishna, S Albayrak, R Zafra, A Baraa, S Vishweswaraiah, ... PloS one 14 (3), e0200229, 2019 | 46 | 2019 |
| Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature SG Kodaganur, S Kapoor, AM Veerappa, SJ Tontanahal, A Sarda, ... Molecular vision 19, 1694, 2013 | 43 | 2013 |
| Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF) U Radhakrishna, S Vishweswaraiah, AM Veerappa, R Zafra, S Albayrak, ... PLoS One 13 (9), e0203893, 2018 | 21 | 2018 |
| Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics AM Veerappa, M Saldanha, P Padakannaya, NB Ramachandra American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2014 | 21 | 2014 |
| Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays AM Veerappa, S Vishweswaraiah, K Lingaiah, M Murthy, DS Manjegowda, ... PLoS One 8 (7), e66843, 2013 | 20 | 2013 |
| Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosis Y Kattimani, AM Veerappa Autoimmunity 51 (4), 147-151, 2018 | 19 | 2018 |
| Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis Y Kattimani, AM Veerappa Multiple Sclerosis and Related Disorders 22, 153-156, 2018 | 17 | 2018 |
| Copy Number Variations Burden on miRNA Genes Reveals Layers of Complexities Involved in the Regulation of Pathways and Phenotypic Expression A Veerappa, M Murthy, V Sangeetha, L Kusuma, S Raviraj, N Somanna, ... PLoS ONE 9 (2), 1-15, 2014 | 16 | 2014 |
| Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma S Vishweswaraiah, AM Veerappa, PA Mahesh, BS Jayaraju, ... Annals of Allergy, Asthma & Immunology 113 (4), 418-424. e1, 2014 | 15 | 2014 |
| Copy Number Variation burden on Asthma sub-genome in normal cohorts identifies susceptibility markers S Vishweswaraiah, AM Veerappa, PA Mahesh, NB Ramachandra Allergy, Asthma & Immunology Research, 2014 | 11 | 2014 |
| Complex interaction between HNRNPD mutations and risk polymorphisms is associated with discordant Crohn’s disease in monozygotic twins T Prakash, A Veerappa, N B. Ramachandra Autoimmunity 50 (5), 275-276, 2017 | 9 | 2017 |
| Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes AM Veerappa, S Vishweswaraiah, K Lingaiah, M Murthy, RV Suresh, ... Plos one 10 (4), e0121846, 2015 | 9 | 2015 |
| Catch Them Before They Fall: A Simple Test of Sight-Word and Pseudo-Word Reading in Kannada for a Quick and Early Assessment PP Marita Saldanha, Anand Siddaiah, Avinash M. Veerappa, Nallur B. Ramachandra SAGE Open, 1-8, 2014 | 7* | 2014 |
| High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts MN Murthy, AM Veerappa, KB Seshachalam, NB Ramachandra Neurological Research 38 (9), 775-785, 2016 | 6 | 2016 |
| A systems omics-based approach to decode substance use disorders and neuroadaptations A Veerappa, G Pendyala, C Guda Neuroscience & Biobehavioral Reviews 130, 61-80, 2021 | 4 | 2021 |
| Impact of Copy Number Variations Burden on Coding Genome in Humans Using Integrated High Resolution Arrays RN Avinash Veerappa, Lingaiah Kusuma, Vishweswaraiah Sangeetha, Megha Murthy ... Genetics Research, 2014 | 4 | 2014 |
| Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization AM Veerappa, RV Suresh, S Vishweswaraiah, K Lingaiah, M Murthy, ... Genetics Research 97, e18, 2015 | 3 | 2015 |
Nallur B. RamachandraDAE- Raja Ramanna Chair, Professor (Retd) & Former Chairman, DOS in Genetics & GenomicsVerified email at genetics.uni-mysore.ac.in
