Avinash M. Veerappa

410 total citations
27 papers, 280 citations indexed

About

Avinash M. Veerappa is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Avinash M. Veerappa has authored 27 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 4 papers in Epidemiology. Recurrent topics in Avinash M. Veerappa's work include Genomic variations and chromosomal abnormalities (11 papers), Congenital heart defects research (7 papers) and Chromosomal and Genetic Variations (4 papers). Avinash M. Veerappa is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Congenital heart defects research (7 papers) and Chromosomal and Genetic Variations (4 papers). Avinash M. Veerappa collaborates with scholars based in India and United States. Avinash M. Veerappa's co-authors include Nallur B. Ramachandra, Prakash Padakannaya, Sangeetha Vishweswaraiah, Chittibabu Guda, Ray Bahado‐Singh, Nitish K. Mishra, Uppala Radhakrishna, P A Mahesh, Nallur B. Ramachandra and Rouba Ali‐Fehmi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neuroscience & Biobehavioral Reviews.

In The Last Decade

Avinash M. Veerappa

27 papers receiving 274 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Avinash M. Veerappa India 10 148 112 43 30 28 27 280
Morana Vitezic Denmark 11 251 1.7× 96 0.9× 11 0.3× 9 0.3× 14 0.5× 16 358
Elisa Biamino Italy 13 188 1.3× 204 1.8× 35 0.8× 10 0.3× 57 2.0× 25 456
Sultan Cingöz Türkiye 10 99 0.7× 60 0.5× 24 0.6× 9 0.3× 20 0.7× 18 254
Hernán Guillermo Hernández Colombia 8 188 1.3× 59 0.5× 10 0.2× 15 0.5× 16 0.6× 14 300
Louise O'Gorman Australia 9 123 0.8× 121 1.1× 25 0.6× 9 0.3× 29 1.0× 10 414
Sarah Williams United States 8 159 1.1× 64 0.6× 38 0.9× 3 0.1× 25 0.9× 10 349
Ramin Badii Qatar 12 161 1.1× 123 1.1× 16 0.4× 8 0.3× 21 0.8× 21 394
K. Naga Mohan India 11 255 1.7× 98 0.9× 7 0.2× 28 0.9× 9 0.3× 30 327
Yann Grattau France 5 112 0.8× 100 0.9× 45 1.0× 9 0.3× 28 1.0× 5 323
Heidi Mateus Colombia 11 165 1.1× 119 1.1× 18 0.4× 6 0.2× 10 0.4× 32 362

Countries citing papers authored by Avinash M. Veerappa

Since Specialization
Citations

This map shows the geographic impact of Avinash M. Veerappa's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Avinash M. Veerappa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Avinash M. Veerappa more than expected).

Fields of papers citing papers by Avinash M. Veerappa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Avinash M. Veerappa. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Avinash M. Veerappa. The network helps show where Avinash M. Veerappa may publish in the future.

Co-authorship network of co-authors of Avinash M. Veerappa

This figure shows the co-authorship network connecting the top 25 collaborators of Avinash M. Veerappa. A scholar is included among the top collaborators of Avinash M. Veerappa based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Avinash M. Veerappa. Avinash M. Veerappa is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Veerappa, Avinash M. & Chittibabu Guda. (2024). Coordination among frequent genetic variants imparts substance use susceptibility and pathogenesis. Frontiers in Neuroscience. 18. 1332419–1332419. 1 indexed citations
2.
Radhakrishna, Uppala, Swapan K. Nath, Avinash M. Veerappa, et al.. (2023). Placental microRNA methylome signatures may serve as biomarkers and therapeutic targets for prenatally opioid-exposed infants with neonatal opioid withdrawal syndrome. Frontiers in Genetics. 14. 1215472–1215472. 3 indexed citations
3.
Veerappa, Avinash M., Gurudutt Pendyala, & Chittibabu Guda. (2021). A systems omics-based approach to decode substance use disorders and neuroadaptations. Neuroscience & Biobehavioral Reviews. 130. 61–80. 3 indexed citations
4.
Radhakrishna, Uppala, Sangeetha Vishweswaraiah, Avinash M. Veerappa, et al.. (2019). Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD). PLoS ONE. 14(3). e0200229–e0200229. 39 indexed citations
5.
Veerappa, Avinash M., et al.. (2018). Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis. Multiple Sclerosis and Related Disorders. 22. 153–156. 9 indexed citations
6.
Radhakrishna, Uppala, Sangeetha Vishweswaraiah, Avinash M. Veerappa, et al.. (2018). Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF). PLoS ONE. 13(9). e0203893–e0203893. 22 indexed citations
7.
Veerappa, Avinash M., et al.. (2018). Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosis. Autoimmunity. 51(4). 147–151. 16 indexed citations
8.
Veerappa, Avinash M., et al.. (2016). High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts. Neurological Research. 38(9). 775–785. 4 indexed citations
9.
Vishweswaraiah, Sangeetha, et al.. (2015). Copy Number Variation Burden on Asthma Subgenome in Normal Cohorts Identifies Susceptibility Markers. Allergy Asthma and Immunology Research. 7(3). 265–265. 9 indexed citations
10.
Veerappa, Avinash M., et al.. (2015). Global Spectrum of Copy Number Variations Reveals Genome Organizational Plasticity and Proposes New Migration Routes. PLoS ONE. 10(4). e0121846–e0121846. 7 indexed citations
11.
Veerappa, Avinash M., et al.. (2015). Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization. Genetics Research. 97. e18–e18. 4 indexed citations
12.
Veerappa, Avinash M., et al.. (2014). Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays. Genetics Research. 96. e17–e17. 2 indexed citations
13.
Vishweswaraiah, Sangeetha, et al.. (2014). Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma. Annals of Allergy Asthma & Immunology. 113(4). 418–424.e1. 12 indexed citations
14.
Veerappa, Avinash M., et al.. (2014). Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family. Genetics Research. 96. e12–e12. 2 indexed citations
15.
Veerappa, Avinash M., et al.. (2014). Family based genome‐wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(7). 572–580. 9 indexed citations
16.
Veerappa, Avinash M., et al.. (2014). Copy Number Variations Burden on miRNA Genes Reveals Layers of Complexities Involved in the Regulation of Pathways and Phenotypic Expression. PLoS ONE. 9(2). e90391–e90391. 12 indexed citations
17.
Veerappa, Avinash M., et al.. (2013). Genome‐wide copy number scan identifies disruption of PCDH11X in developmental dyslexia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(8). 889–897. 28 indexed citations
18.
Veerappa, Avinash M., Prakash Padakannaya, & Nallur B. Ramachandra. (2013). Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome. Functional & Integrative Genomics. 13(3). 285–293. 31 indexed citations
19.
Veerappa, Avinash M., et al.. (2013). Unravelling the Complexity of Human Olfactory Receptor Repertoire by Copy Number Analysis across Population Using High Resolution Arrays. PLoS ONE. 8(7). e66843–e66843. 11 indexed citations
20.
Veerappa, Avinash M., et al.. (2013). Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity. Journal of Human Genetics. 58(8). 539–547. 38 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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