Ishwar C. Verma

1.2k total citations
47 papers, 558 citations indexed

About

Ishwar C. Verma is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Ishwar C. Verma has authored 47 papers receiving a total of 558 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Physiology. Recurrent topics in Ishwar C. Verma's work include Lysosomal Storage Disorders Research (6 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (5 papers). Ishwar C. Verma is often cited by papers focused on Lysosomal Storage Disorders Research (6 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (5 papers). Ishwar C. Verma collaborates with scholars based in India, Pakistan and United States. Ishwar C. Verma's co-authors include Ratna Dua Puri, Renu Saxena, Mohammed A. Aldahmesh, Jawahir Y. Mohamed, Ayodele Alaiya, Hisham Alkuraya, Fowzan S. Alkuraya, William B. Rizzo, Sunita Bijarnia‐Mahay and Jyotsna Verma and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Clinica Chimica Acta.

In The Last Decade

Ishwar C. Verma

42 papers receiving 521 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ishwar C. Verma India 12 217 162 111 79 74 47 558
Eckhard Korsch Germany 16 421 1.9× 224 1.4× 63 0.6× 81 1.0× 28 0.4× 28 756
A. H. Fensom United Kingdom 14 175 0.8× 89 0.5× 103 0.9× 329 4.2× 60 0.8× 31 725
Vickie Hannig United States 12 175 0.8× 185 1.1× 83 0.7× 24 0.3× 22 0.3× 19 494
Shuan-Pei Lin Taiwan 19 239 1.1× 158 1.0× 64 0.6× 371 4.7× 40 0.5× 39 793
Sujatha Jagadeesh India 12 178 0.8× 165 1.0× 61 0.5× 72 0.9× 51 0.7× 39 456
Avinoam Adam Israel 13 148 0.7× 117 0.7× 208 1.9× 120 1.5× 115 1.6× 21 539
Dor Mohammad Kordi-Tamandani Iran 17 481 2.2× 147 0.9× 61 0.5× 49 0.6× 14 0.2× 63 895
Raquel Dodelson de Kremer Argentina 17 395 1.8× 58 0.4× 75 0.7× 266 3.4× 24 0.3× 52 735
M. R. A. LALLOZ United Kingdom 19 312 1.4× 130 0.8× 113 1.0× 105 1.3× 244 3.3× 33 1.1k
Laurie Demmer United States 16 634 2.9× 534 3.3× 167 1.5× 47 0.6× 29 0.4× 35 1.2k

Countries citing papers authored by Ishwar C. Verma

Since Specialization
Citations

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

Fields of papers citing papers by Ishwar C. Verma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ishwar C. Verma. 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 Ishwar C. Verma. The network helps show where Ishwar C. Verma may publish in the future.

Co-authorship network of co-authors of Ishwar C. Verma

This figure shows the co-authorship network connecting the top 25 collaborators of Ishwar C. Verma. A scholar is included among the top collaborators of Ishwar C. Verma 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 Ishwar C. Verma. Ishwar C. Verma 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.
Verma, Jyotsna, et al.. (2021). Levels of Lyso GL-1 in Gaucher and Lyso GL-3 in Fabry patients from India: Diagnostic aids for these lysosomal storage disorders. Clinica Chimica Acta. 521. 177–190. 3 indexed citations
2.
Bijarnia‐Mahay, Sunita, et al.. (2019). Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation. SHILAP Revista de lepidopterología. 9(4). e2019124–e2019124. 5 indexed citations
3.
Verma, Jyotsna, Sunita Bijarnia‐Mahay, & Ishwar C. Verma. (2017). Prenatal Diagnosis of Lysosomal Storage Disorders Using Chorionic Villi. Methods in molecular biology. 1594. 265–291. 5 indexed citations
4.
Verma, Jyotsna, Divya C. Thomas, David C. Kasper, et al.. (2016). Inherited Metabolic Disorders: Efficacy of Enzyme Assays on Dried Blood Spots for the Diagnosis of Lysosomal Storage Disorders. JIMD Reports. 31. 15–27. 19 indexed citations
5.
6.
Verma, Jyotsna, Divya C. Thomas, Kwang‐Jen Hsiao, et al.. (2015). Inherited metabolic disorders: Quality management for laboratory diagnosis. Clinica Chimica Acta. 447. 1–7. 7 indexed citations
7.
Rajasimha, Harsha, Preveen Ramamoorthy, Madhuri Hegde, et al.. (2014). Organization for rare diseases India (ORDI) – addressing the challenges and opportunities for the Indian rare diseases' community. Genetics Research. 96. e009–e009. 29 indexed citations
8.
Bijarnia‐Mahay, Sunita, Neerja Gupta, Deepak Sharma, et al.. (2014). Molecular Diagnosis of Hereditary Fructose Intolerance: Founder Mutation in a Community from India. JIMD Reports. 19. 85–93. 15 indexed citations
9.
Puri, Ratna Dua, et al.. (2014). Need for Fetal Autopsy and Genetic Diagnosis in Fetal Limb Anomalies. Journal of Fetal Medicine. 1(3). 151–157. 2 indexed citations
10.
Goyal, Manisha, Sunita Bijarnia‐Mahay, Stephen F. Kingsmore, et al.. (2014). Molecular Diagnosis of Infantile Neuro axonal Dystrophy by Next Generation Sequencing. The Indian Journal of Pediatrics. 82(5). 474–477. 10 indexed citations
11.
Aldahmesh, Mohammed A., Jawahir Y. Mohamed, Hisham Alkuraya, et al.. (2011). Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectual Disability, and Spastic Quadriplegia. The American Journal of Human Genetics. 89(6). 745–750. 134 indexed citations
12.
Saxena, Renu, et al.. (2000). A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACT CCT GAG-> ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing.. PubMed. 111. 24–7. 3 indexed citations
13.
Verma, Ishwar C.. (2000). Burden of genetic disorders in india. The Indian Journal of Pediatrics. 67(12). 893–898. 97 indexed citations
14.
Kumar, Amit, et al.. (2000). Biotinidase deficiency—A treatable entity. The Indian Journal of Pediatrics. 67(6). 464–466. 9 indexed citations
15.
Verma, Ishwar C.. (1997). Molecular diagnosis of neurological disorders in India. The Indian Journal of Pediatrics. 64(5). 661–666. 2 indexed citations
16.
Suri, Mohnish, et al.. (1995). A clinical and cytogenetic study of Turner syndrome.. PubMed. 32(4). 433–42. 11 indexed citations
17.
Halley, Dicky, Ans van den Ouweland, Wout H. Deelen, Ishwar C. Verma, & Ben A. Oostra. (1994). Strategy for reliable prenatal detection of normal male carriers of the fragile X syndrome. American Journal of Medical Genetics. 51(4). 471–473. 5 indexed citations
18.
Sachdev, Harshpal Singh, et al.. (1981). Physical growth of children with down syndrome in India. The Indian Journal of Pediatrics. 48(1). 85–89. 7 indexed citations
19.
Verma, Ishwar C., et al.. (1974). In vitro lymphoblastoid transformation with purified protein derivative (PPD) as a diagnostic test in tuberculosis.. PubMed. 62(4). 615–20. 2 indexed citations
20.
Verma, Ishwar C., et al.. (1970). Autoimmune hemolytic anemia in infancy and childhood. The Indian Journal of Pediatrics. 37(7). 326–331. 1 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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