Author

Nallur B. Ramachandra

UGC-BSR Faculty Fellow, Professor (Retd) & Former Chairman, Department of Studies in Genetics and - Cited by 2,266 - Genetics of Drosophila and Human - Genomics of Drosophila and Human - Evolution - Molecular biology - Microbial Genomics

Biography

The contributions of Dr. N. B. Ramachandra, to science, have been recognized by the State Government and he has been awarded Sir C. V. Raman Young Scientist State Award for the Year 2007. After his postdoctoral work at Canada, he joined as a Lecturer, in the Department of Zoology, University of Mysore, Mysore during 1992. Since then he has worked with Prof. H. A. Ranganath as a collaborator as well as independently. He currently serves as the Chairman of Department of studies in Genetics and Genomics, University of Mysore, Mysuru.  
Title
Cited by
Year
Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations
M Prabhanjan, RV Suresh, MN Murthy, NB RamachandraDiabetes research and clinical practice 113, 160-170, 2016201
24
2016
IL-10 and IL-17F Promoter Single Nucleotide Polymorphism and Asthma: A Case-Control Study in South India
S Raeiszadeh Jahromi, PA Mahesh, BS Jayaraj, AD Holla, ...Lung 193, 739-747, 151
20
2015
Development of rapid automatized naming (RAN) in simultaneous Kannada-English biliterate children
A Siddaiah, M Saldanha, SK Venkatesh, NB Ramachandra, ...Journal of psycholinguistic research 45, 177-187, 202
16
2016
A preliminary study on the association of single nucleotide polymorphisms of interleukin 4 (IL4), IL13, IL4 receptor alpha (IL4Rα) & Toll-like receptor 4 (TLR4) genes with …
P Davoodi, PA Mahesh, AD Holla, NB RamachandraThe Indian journal of medical research 142 (6), 675, 202
15
2015
Integrated functional analysis implicates syndromic and rare copy number variation genes as prominent molecular players in pathogenesis of autism spectrum disorders
SNM Ashitha, NB RamachandraNeuroscience 438, 25-40, 2020202
9
2020
Haplotype analysis of ADAM33 polymorphisms in asthma: A pilot study
S Vishweswaraiah, NB Ramachandra, BS Jayaraj, AD Holla, ...The Indian journal of medical research 150 (3), 272, 2019201
8
2019
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse
S Agarwala, NB RamachandraEgyptian Journal of Medical Human Genetics 22, 1-13, 2021202
7
2021
Effect of structural changes in proteins derived from GATA4 nonsynonymous single nucleotide polymorphisms in congenital heart disease
DS Manjegowda, P Karunakar, NB RamachandraIndian Journal of Pharmaceutical Sciences 77 (), 735, 2015201
6
2015
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 RamachandraNeurological Research 38 (9), 775-785, 20120
6
2016
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), 1-10, 2020202
4
2020
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, 2020202
4
2020
Mucosa-associated specific bacterial species disrupt the intestinal epithelial barrier in the autism phenome
S Agarwala, B Naik, NB RamachandraBrain, Behavior, & Immunity-Health 15, 100269, 2021202
4
2021
Detection of first-line drug resistance mutations and drug–protein interaction dynamics from tuberculosis patients in South India
SA Nachappa, SM Neelambike, C Amruthavalli, NB RamachandraMicrobial Drug Resistance 2 (), 377-385, 2018201
4
2018
High-risk genes involved in common septal defects of congenital heart disease
S Chaithra, S Agarwala, NB RamachandraGene 80, 1675, 2022202
4
2022
Association of RFC1 A80G gene polymorphism with advanced maternal age in risk of Down syndrome
RV Suresh, AS Udupa, K Lingaiah, SK Polapalli, NB RamachandraCurrent Medicine Research and Practice 7 (1), 6-10, 2017201
3
2017
Diversity of gut microbiota in autism reveals differential abundance of Prevotella and Akkermansia species
S Agarwala, B Naik, NB RamachandraPreprints, 2018201
3
2018
Comprehensive in silico mutational-sensitivity analysis of PTEN establishes signature regions implicated in pathogenesis of Autism Spectrum Disorders
ASN Murthy, RV SureshGenomics 113 (1), 999-1017, 010
2
2021
The possible role of point mutations and activation of the CDC27 Gene in progression of multiple myeloma
The possible role of point mutations and activation of the CDC7 Gene in progression of multiple myelomaM Abbaspourkharyeki, NJ Anvekar, NB RamachandraMeta Gene 6, 100761, 000
2
2020
Integrated network and gene ontology analysis identifies key genes and pathways for coronary artery diseases
T Prakash, NB RamachandraAvicenna Journal of Medical Biotechnology 13 (1), 15, 010
2
2021
Allopatric sibling species pair Drosophila nasuta nasuta and Drosophila nasuta albomicans exhibit expression divergence in ovarian transcriptomes
K Ponnanna, SM DSouza, C Amruthavalli, NB RamachandraGene 777, 145189, 010
2
2021

Referred From: https://scholar.google.com/citations?user=CBqZv1oAAAAJ

Cited by
Citations 2266
h-index 25
i10-index 65
Recommended Journals
Open Access Journals