I. C. Verma

2.2k total citations
101 papers, 1.3k citations indexed

About

I. C. Verma is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Epidemiology. According to data from OpenAlex, I. C. Verma has authored 101 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 17 papers in Pediatrics, Perinatology and Child Health and 16 papers in Epidemiology. Recurrent topics in I. C. Verma's work include Hemoglobinopathies and Related Disorders (8 papers), Prenatal Screening and Diagnostics (7 papers) and Bacterial Infections and Vaccines (6 papers). I. C. Verma is often cited by papers focused on Hemoglobinopathies and Related Disorders (8 papers), Prenatal Screening and Diagnostics (7 papers) and Bacterial Infections and Vaccines (6 papers). I. C. Verma collaborates with scholars based in India, Pakistan and United States. I. C. Verma's co-authors include Sunita Bijarnia, Pawan Kumar Jain, Manjit Singh Grewal, V. Ramalingaswami, N Kochupillai, Ved Prakash Choudhry, Renu Saxena, J. B. Clegg, Anuja Premawardhena and D. J. Weatherall and has published in prestigious journals such as Nature, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

I. C. Verma

96 papers receiving 1.2k citations

Peers

I. C. Verma

PPCH

GENET

HEMAT

P.J.L. Cook United Kingdom

Ryo Sumazaki Japan

S. W. Serjeantson Australia

Alessandro Plebani Italy

J. Bruce Smith United States

Issarang Nuchprayoon Thailand

Lina Shao United States

R. Clark Brown United States

Stephen D. Litwin United States

Hans-Georg Koch Germany

P.J.L. Cook United Kingdom

I. C. Verma

673 ×1.9

185 ×0.6

PPCH

498 ×1.6

GENET

147 ×0.7

GENET

279 ×1.6

HEMAT

Citations per year, relative to I. C. Verma I. C. Verma (= 1×) peers P.J.L. Cook

Countries citing papers authored by I. C. Verma

Since Specialization

Citations

This map shows the geographic impact of I. 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 I. 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 I. C. Verma more than expected).

Fields of papers citing papers by I. C. Verma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of I. C. Verma. A scholar is included among the top collaborators of I. 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 I. C. Verma. I. C. Verma is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Danda, Sumita, Atanu Kumar Dutta, Sheela Nampoothiri, et al.. (2020). Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India. Clinical Rheumatology. 39(9). 2743–2749. 2 indexed citations

Puri, Ratna Dua, et al.. (2018). Noninvasive prenatal testing (NIPT) detects variant of Turner syndrome not detectable by fluorescent in situ hybridization. The Journal of Maternal-Fetal & Neonatal Medicine. 32(24). 4177–4180. 1 indexed citations

Puri, Ratna Dua, Narayanan Namboodiri, Mohan Nair, et al.. (2016). KCNQ1 mutations associated with Jervell and Lange–Nielsen syndrome and autosomal recessive Romano–Ward syndrome in India—expanding the spectrum of long QT syndrome type 1. American Journal of Medical Genetics Part A. 170(6). 1510–1519. 10 indexed citations

Saxena, Renu, et al.. (2014). Lack of any Association of the CTLA-4 +49 G/A Polymorphism with Breast Cancer Risk in a North Indian Population. Asian Pacific Journal of Cancer Prevention. 15(5). 2035–2038. 15 indexed citations

Pyott, Shawna M., Thao Tran, Dru F. Leistritz, et al.. (2013). WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 92(4). 590–597. 170 indexed citations

Verma, I. C., Renu Saxena, & Sudha Kohli. (2012). Hemoglobinopathies in India—Clinical and Laboratory Aspects. Clinics in Laboratory Medicine. 32(2). 249–262. 7 indexed citations

Vivante, Asaf, Danny Lotan, Naomi Pode‐Shakked, et al.. (2011). Familial Autosomal Recessive Renal Tubular Acidosis: Importance of Early Diagnosis. Nephron Physiology. 119(3). p31–p39. 8 indexed citations

Verma, I. C., Renu Saxena, J Zeman, et al.. (2007). A New Mutation within the Porphobilinogen Deaminase Gene Leading to a Truncated Protein as a Cause of Acute Intermittent Porphyria in an Extended Indian Family. Folia Biologica. 53(6). 194–201. 3 indexed citations

Puri, Ratna Dua, et al.. (2007). Spectrum of severe skeletal dysplasias in North India. The Indian Journal of Pediatrics. 74(11). 995–1002. 13 indexed citations

10.

Herrmann, F. H., et al.. (2000). Factor VIII gene polymorphisms in the Asian Indian population. Haemophilia. 6(6). 625–630. 21 indexed citations

11.

Jain, Yogesh, et al.. (1995). Juvenile chronic myelocytic leukemia—report of 10 cases. Medical and Pediatric Oncology. 24(2). 100–103. 3 indexed citations

12.

Gupta, Anupama, Manorama Berry, & I. C. Verma. (1994). Congential absence of both fibulae in four siblings. Pediatric Radiology. 24(3). 220–221. 1 indexed citations

13.

Verma, I. C., et al.. (1993). Sphingomyelinase enzyme assay in Niemann-Pick disease. The Indian Journal of Pediatrics. 60(4). 583–590. 3 indexed citations

14.

Buckshee, K., Kallol Kumar Roy, & I. C. Verma. (1993). Nomograms of fetal nuchal fold thickness for early detection of down syndrome. The Indian Journal of Pediatrics. 60(5). 655–657. 4 indexed citations

15.

Verma, I. C., et al.. (1992). Congenital heart disease in Down syndrome: an echocardiographic study.. PubMed. 29(9). 1113–6. 18 indexed citations

16.

Mehta, Lakshmi, Puneet Jain, Renu Saxena, & I. C. Verma. (1992). The tricho-rhino - Phalangeal syndromes I and II. The Indian Journal of Pediatrics. 59(3). 373–377. 1 indexed citations

17.

Kabra, S. K., Pravin Kumar, & I. C. Verma. (1991). Dexamethasone in bacterial meningitis. The Indian Journal of Pediatrics. 58(4). 421–425. 1 indexed citations

18.

Kochupillai, Vinod, Sanjeev Sharma, Sebastian Francis, et al.. (1987). Fetal liver infusion in acute myelogenous leukaemia. PubMed. 10(1-2). 117–124. 7 indexed citations

19.

Verma, I. C., et al.. (1986). Interpreting on electrocardiogram Part II, the complexes. The Indian Journal of Pediatrics. 53(5). 629–639. 1 indexed citations

20.

Verma, I. C.. (1982). Differential diagnosis of hydrops fetalis. The Indian Journal of Pediatrics. 49(1). 19–20. 2 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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