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Nallur Basappa Ramachandra

Observed names: N B Ramachandra, N. B. Ramachandra, N.B. Ramachandra, NALLUR B. RAMACHANDRA, Nallur Basappa Ramachandra, Nallur B Ramachandra, Nallur B. Ramachandra, Nallur Ramachandra, NallurBasappa Ramachandra, Ramachandra Nallur B., Ramachandra, Nallur B.
Observed institution: University of Mysore
ORCID: 0000-0002-7679-1617
Observed ORCID: 0000-0002-7679-1617
OpenAlex ID: A5101489871
Serum levels of IL-10, IL-17F and IL-33 in patients with asthma: a case–control study
2014 · Sareh Raeiszadeh Jahromi, P. A. Mahesh, et al. · Journal of Asthma · 76
Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome
2013 · Avinash M. Veerappa, Prakash Padakannaya, et al. · Functional & Integrative Genomics · 52
Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity
2013 · Avinash M Veerappa, Marita Saldanha, et al. · Journal of Human Genetics · 47
Genome‐wide copy number scan identifies disruption of PCDH11X in developmental dyslexia
2013 · Avinash M. Veerappa, Marita Saldanha, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 44
Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population
2013 · Shyamala K Venkatesh, Anand Siddaiah, et al. · Journal of Human Genetics · 39
Mucosa-associated specific bacterial species disrupt the intestinal epithelial barrier in the autism phenome
2021 · Swati Agarwala, Bindushree Naik, et al. · Brain Behavior & Immunity - Health · 33
Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population
2013 · Shyamala K. Venkatesh, Anand Siddaiah, et al. · Psychiatric Genetics · 24
De novo isochromosome 18p in a female dysmorphic child
2006 · Smitha Ramegowda, Harshavardhan M. Gawde, et al. · Journal of Applied Genetics · 24
An Examination of Candidate Gene SNPs for Dyslexia in an Indian Sample
2011 · Shyamala K. Venkatesh, Anand Siddaiah, et al. · Behavior Genetics · 23
The evolution of centriole degradation in mouse sperm
2024 · Sushil Khanal, Ankit Jaiswal, et al. · Nature Communications · 22
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Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations
2016 · Manasa Prabhanjan, Raviraj V. Suresh, et al. · Diabetes Research and Clinical Practice · 21
Evolutionary experimentation through hybridization under laboratory condition in Drosophila: Evidence for Recombinational Speciation
2003 · Ballagere P Harini, Nallur B Ramachandra · BMC Evolutionary Biology · 19
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Catch Them Before They Fall: A Simple Test of Sight-Word and Pseudo-Word Reading in Kannada for a Quick and Early Assessment
2014 · Marita Saldanha, Anand Siddaiah, et al. · SAGE Open · 18
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Soluble Intercellular Adhesion Molecule-1 and E-selectin in Patients with Asthma Exacerbation
2009 · Mahdi Bijanzadeh, Nallur B. Ramachandra, et al. · Lung · 18
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse
2021 · Swati Agarwala, Nallur B. Ramachandra · Egyptian Journal of Medical Human Genetics · 17
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Family based genome‐wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics
2014 · Avinash M. Veerappa, Marita Saldanha, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 17
A Maiden Report on CRELD1 Single-Nucleotide Polymorphism Association in Congenital Heart Disease Patients of Mysore, South India
2011 · Lingaiah Kusuma, Sosalagere M. Dinesh, et al. · Genetic Testing and Molecular Biomarkers · 17
Single-Nucleotide Polymorphisms of NKX2.5 Found in Congenital Heart Disease Patients of Mysore, South India
2010 · S.M. Dinesh, L. Kusuma, et al. · Genetic Testing and Molecular Biomarkers · 17
Allelic variants of DYX1C1 are not associated with dyslexia in India
2008 · NallurBasappa Ramachandra, Pushpa Saviour, et al. · Indian journal of human genetics · 17
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High-risk genes involved in common septal defects of congenital heart disease
2022 · S. Chaithra, Swati Agarwala, et al. · Gene · 16
Copy Number Variation Burden on Asthma Subgenome in Normal Cohorts Identifies Susceptibility Markers
2015 · Sangeetha Vishweswaraiah, Avinash M Veerappa, et al. · Allergy Asthma and Immunology Research · 15
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Unravelling the Complexity of Human Olfactory Receptor Repertoire by Copy Number Analysis across Population Using High Resolution Arrays
2013 · Avinash M. Veerappa, Sangeetha Vishweswaraiah, et al. · PLoS ONE · 15
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GATA4 Specific Nonsynonymous Single-Nucleotide Polymorphisms in Congenital Heart Disease Patients of Mysore, India
2011 · Sosalagere M. Dinesh, Kusuma Lingaiah, et al. · Genetic Testing and Molecular Biomarkers · 15
Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with Developmental Dyslexia
2013 · Shyamala K. Venkatesh, Anand Siddaiah, et al. · Gene · 11
Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders
2020 · S. Niranjana Murthy Ashitha, Nallur B. Ramachandra · Neuroscience · 10
Works count: 77
Citation count: 763
H-index: 17
I10-index: 27
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