Vedam L. Ramprasad

3.0k total citations
61 papers, 1.1k citations indexed

About

Vedam L. Ramprasad is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Vedam L. Ramprasad has authored 61 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 19 papers in Genetics and 11 papers in Ophthalmology. Recurrent topics in Vedam L. Ramprasad's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Glaucoma and retinal disorders (5 papers). Vedam L. Ramprasad is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Glaucoma and retinal disorders (5 papers). Vedam L. Ramprasad collaborates with scholars based in India, United States and United Kingdom. Vedam L. Ramprasad's co-authors include Govindasamy Kumaramanickavel, Nagasamy Soumittra, Sakthivel Murugan, Rama Rajagopal, Sarangapani Sripriya, Eranga N. Vithana, Tin Aung, Donald Tan, Victor H. K. Yong and Pradeep Paul George and has published in prestigious journals such as Blood, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Vedam L. Ramprasad

56 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vedam L. Ramprasad India 18 534 382 277 207 111 61 1.1k
Victor H. K. Yong Singapore 13 351 0.7× 508 1.3× 480 1.7× 91 0.4× 27 0.2× 19 920
Denise A. Hatala United States 13 488 0.9× 327 0.9× 114 0.4× 48 0.2× 91 0.8× 16 1.1k
Deborah Wallace Ireland 22 711 1.3× 578 1.5× 219 0.8× 71 0.3× 18 0.2× 46 1.2k
Haicheng She China 15 629 1.2× 780 2.0× 351 1.3× 47 0.2× 27 0.2× 38 1.3k
Ningpu Liu China 18 276 0.5× 490 1.3× 338 1.2× 70 0.3× 46 0.4× 57 792
Wenzhen Yu China 21 503 0.9× 556 1.5× 391 1.4× 44 0.2× 33 0.3× 69 1.1k
Souska Zandi Switzerland 23 440 0.8× 738 1.9× 492 1.8× 27 0.1× 63 0.6× 59 1.4k
Gezhi Xu China 19 376 0.7× 623 1.6× 341 1.2× 26 0.1× 49 0.4× 77 1.1k
Marin L. Gantner United States 11 377 0.7× 258 0.7× 109 0.4× 89 0.4× 17 0.2× 18 671
Norman A. Zabriskie United States 14 934 1.7× 1.4k 3.8× 703 2.5× 93 0.4× 38 0.3× 19 1.9k

Countries citing papers authored by Vedam L. Ramprasad

Since Specialization
Citations

This map shows the geographic impact of Vedam L. Ramprasad'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 Vedam L. Ramprasad with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vedam L. Ramprasad more than expected).

Fields of papers citing papers by Vedam L. Ramprasad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vedam L. Ramprasad. 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 Vedam L. Ramprasad. The network helps show where Vedam L. Ramprasad may publish in the future.

Co-authorship network of co-authors of Vedam L. Ramprasad

This figure shows the co-authorship network connecting the top 25 collaborators of Vedam L. Ramprasad. A scholar is included among the top collaborators of Vedam L. Ramprasad 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 Vedam L. Ramprasad. Vedam L. Ramprasad 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.
Nampoothiri, Sheela, Jayesh Sheth, Frenny Sheth, et al.. (2024). KBG Syndrome in 16 Indian Individuals. American Journal of Medical Genetics Part A. 197(2). e63907–e63907. 1 indexed citations
2.
Ramprasad, Vedam L., Aby Abraham, Vivi M. Srivastava, et al.. (2023). Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis. Journal of Medical Genetics. 60(8). 801–809. 3 indexed citations
3.
Olszewska, Diana A., et al.. (2022). Oculogyric Crisis Phenotype of Levodopa‐Induced Ocular Dyskinesia. Movement Disorders Clinical Practice. 9(3). 390–393. 2 indexed citations
4.
5.
Bardhan, Mainak, Kiran Polavarapu, Veeramani Preethish‐Kumar, et al.. (2022). Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > C. Neurogenetics. 23(3). 187–202. 7 indexed citations
6.
Polavarapu, Kiran, Mainak Bardhan, Seena Vengalil, et al.. (2021). Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review. Journal of Clinical Neurology. 17(3). 409–409. 1 indexed citations
7.
Kukkle, Prashanth Lingappa, Vinay Goyal, Rukmini Mridula Kandadai, et al.. (2021). Clinical Study of 668 Indian Subjects with Juvenile, Young, and Early Onset Parkinson’s Disease. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 49(1). 93–101. 13 indexed citations
8.
Gupta, Himika, Sivasankar Malaichamy, Ashwin Mallipatna, et al.. (2021). Retinoblastoma genetics screening and clinical management. BMC Medical Genomics. 14(1). 188–188. 9 indexed citations
9.
Abbas, Muhammad, et al.. (2021). Chorea-acanthocytosis. Annals of Indian Academy of Neurology. 24(3). 452–456. 1 indexed citations
10.
Kukkle, Prashanth Lingappa, et al.. (2020). A Case of Autosomal Dominant Ataxia with Vocal Cord Palsy Attributed to a Mutation in the PRNP Gene. Movement Disorders Clinical Practice. 7(6). 688–692. 3 indexed citations
11.
Kukkle, Prashanth Lingappa, et al.. (2020). Reply to: Fatal Familial Insomnia: A Rare Disease with Unique Clinico‐Neurophysiological Features. Movement Disorders Clinical Practice. 8(1). 164–165. 1 indexed citations
12.
Attri, Savita Verma, Arushi Gahlot Saini, Naveen Sankhyan, et al.. (2020). Seven novel genetic variants in a North Indian cohort with classical homocystinuria. Scientific Reports. 10(1). 17299–17299. 6 indexed citations
13.
Choughule, Anuradha, Vanita Noronha, Amit Joshi, et al.. (2018). Validation of liquid biopsy: plasma cell-free DNA testing in clinical management of advanced non-small cell lung cancer. PubMed. Volume 9. 1–11. 55 indexed citations
14.
Aluri, Jahnavi, Maya Gupta, Aparna Dalvi, et al.. (2018). Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India. Frontiers in Immunology. 9. 188–188. 23 indexed citations
15.
Puri, Ratna Dua, et al.. (2017). Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation. 2(3-4). 157–164. 6 indexed citations
16.
Ramprasad, Vedam L., et al.. (2011). Gene Mapping in a Highly Inbred Consanguineous Foveal Hypoplasia Family to cytonenetic region 16q24.1. Investigative Ophthalmology & Visual Science. 52(14). 3290–3290.
17.
Ramprasad, Vedam L., et al.. (2008). Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India.. PubMed. 14. 318–22. 87 indexed citations
18.
Vithana, Eranga N., Patricio E. Morgan, Vedam L. Ramprasad, et al.. (2007). SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Human Molecular Genetics. 17(5). 656–666. 202 indexed citations
19.
Ramprasad, Vedam L., Jagadeesan Madhavan, Sakthivel Murugan, et al.. (2007). Retinoblastoma in India. Molecular Diagnosis & Therapy. 11(1). 63–70. 12 indexed citations
20.
Ramprasad, Vedam L., Sarangapani Sripriya, Ronnie George, et al.. (2005). Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.. PubMed. 11. 934–40. 9 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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