C. Prasad

887 total citations
30 papers, 431 citations indexed

About

C. Prasad is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, C. Prasad has authored 30 papers receiving a total of 431 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 10 papers in Genetics. Recurrent topics in C. Prasad's work include Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). C. Prasad is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). C. Prasad collaborates with scholars based in Canada, United States and Sri Lanka. C. Prasad's co-authors include Asuri N. Prasad, C. Anthony Rupar, Louise A. Dilling, Cheryl R. Greenberg, J. C. Haworth, L.E. Seargeant, B. Martin, Burkhardt Seifert, Frances Booth and C. R. Greenberg and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genetics in Medicine and American Journal of Medical Genetics.

In The Last Decade

C. Prasad

29 papers receiving 413 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Prasad Canada 13 233 160 108 80 55 30 431
Inderneel Sahai United States 12 187 0.8× 191 1.2× 122 1.1× 134 1.7× 64 1.2× 34 530
S. B. van der Meer Netherlands 14 207 0.9× 202 1.3× 91 0.8× 77 1.0× 76 1.4× 19 564
J. Leonard United Kingdom 6 215 0.9× 223 1.4× 68 0.6× 68 0.8× 184 3.3× 8 503
Néji Tebib Tunisia 14 164 0.7× 89 0.6× 112 1.0× 47 0.6× 89 1.6× 66 537
Catherine Lynn T. Silao Philippines 9 79 0.3× 124 0.8× 45 0.4× 85 1.1× 61 1.1× 33 287
T Momoi Japan 11 166 0.7× 56 0.3× 78 0.7× 63 0.8× 23 0.4× 16 498
Barry H. Thompson United States 9 291 1.2× 420 2.6× 195 1.8× 204 2.5× 131 2.4× 15 870
Debra Day‐Salvatore United States 11 51 0.2× 63 0.4× 82 0.8× 166 2.1× 55 1.0× 25 350
S. Kling United States 5 442 1.9× 246 1.5× 193 1.8× 141 1.8× 31 0.6× 7 631
Yuqi Yang China 9 138 0.6× 74 0.5× 81 0.8× 150 1.9× 22 0.4× 32 367

Countries citing papers authored by C. Prasad

Since Specialization
Citations

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

Fields of papers citing papers by C. Prasad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Prasad

This figure shows the co-authorship network connecting the top 25 collaborators of C. Prasad. A scholar is included among the top collaborators of C. Prasad 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 C. Prasad. C. Prasad 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.
Balcı, Tuğçe B., C. Prasad, Joseph Andrews, et al.. (2020). BCL11B-related disorder in two canadian children: Expanding the clinical phenotype. European Journal of Medical Genetics. 63(9). 104007–104007. 17 indexed citations
2.
Rupar, C. Anthony, et al.. (2016). The expanding phenotype of MELAS caused by the m.3291T > C mutation in the MT-TL1 gene. Molecular Genetics and Metabolism Reports. 6. 64–69. 10 indexed citations
3.
Raja, Veena, et al.. (2015). Sirenomelia - Mermaid Syndrome with Oesophageal Atresia: A Rare Case Report. SHILAP Revista de lepidopterología. 3(3). 113–113. 1 indexed citations
4.
5.
Prasad, Asuri N., C. Anthony Rupar, Michael J. Strong, et al.. (2013). Recurrent Encephalopathy: NAGS (N-Acetylglutamate Synthase) Deficiency in Adults. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 40(1). 3–9. 17 indexed citations
6.
Prasad, Asuri N. & C. Prasad. (2010). Genetic evaluation of the floppy infant. Seminars in Fetal and Neonatal Medicine. 16(2). 99–108. 34 indexed citations
7.
Haas, Dorothea, Petra Niklowitz, Friederike Hörster, et al.. (2009). Coenzyme Q10 is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria. Journal of Inherited Metabolic Disease. 32(4). 570–575. 24 indexed citations
8.
Korotchkina, Lioubov G., C. Prasad, Tony Rupar, et al.. (2008). Mutations of the E1β subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiency. Molecular Genetics and Metabolism. 93(4). 371–380. 34 indexed citations
9.
Seabrook, Jamie A., et al.. (2006). RISK FACTORS FOR THE DEVELOPMENT OF HOLOPROSENCEPHALY: A MANITOBA-BASED CASE-CONTROL STUDY. Neuropediatrics. 37(S 1). 1 indexed citations
10.
Prasad, C., et al.. (2005). Sir Archibald Garrod and Alkaptonuria –‘story of metabolic genetics’. Clinical Genetics. 68(3). 199–203. 11 indexed citations
11.
Dawson, Angelika J., et al.. (2003). Interstitial deletion of chromosome 2p16.2p21. Clinical Dysmorphology. 12(3). 183–185. 6 indexed citations
12.
Dawson, Angelika J., et al.. (2003). Interstitial deletion of chromosome 2p16.2p21. Clinical Dysmorphology. 12(3). 183–185. 1 indexed citations
13.
Schultz, Jack C., et al.. (2002). Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features. Clinical Genetics. 62(6). 488–494. 30 indexed citations
14.
Prasad, C. & AE Chudley. (2002). History of genetics through philately: Sir William Osler (1849–1919) and the Osler–Weber–Rendu syndrome. Clinical Genetics. 61(6). 404–407. 2 indexed citations
15.
Bowman, Natalie M., et al.. (2002). Telemedicine diagnosis for fetal alcohol syndrome – The Manitoba experience. Paediatrics & Child Health. 7(3). 147–151. 14 indexed citations
16.
Greenberg, Cheryl R., Asuri N. Prasad, Louise A. Dilling, et al.. (2002). Outcome of the First 3-Years of a DNA-Based Neonatal Screening Program for Glutaric Acidemia Type 1 in Manitoba and Northwestern Ontario, Canada. Molecular Genetics and Metabolism. 75(1). 70–78. 64 indexed citations
17.
18.
Y, Sree Sudha T, et al.. (2001). De novo interstitial long arm deletion of chromosome 3 with facial dysmorphism, Dandy-Walker variant malformation and hydrocephalus. Clinical Dysmorphology. 10(3). 193–196. 14 indexed citations
19.
Prasad, C., et al.. (2000). Kyphomelic dysplasia: a rare form of semilethal skeletal dysplasia. Clinical Genetics. 58(5). 390–395. 11 indexed citations
20.
Prasad, C., Elizabeth J. Quackenbush, David Whiteman, & Bruce R. Korf. (1997). Limb anomalies in DiGeorge and CHARGE syndromes. American Journal of Medical Genetics. 68(2). 179–181. 20 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Inderneel Sahai Breakdown of academic impact, for papers by S. B. van der Meer Breakdown of academic impact, for papers by J. Leonard Breakdown of academic impact, for papers by Néji Tebib Breakdown of academic impact, for papers by Catherine Lynn T. Silao Breakdown of academic impact, for papers by T Momoi Breakdown of academic impact, for papers by Barry H. Thompson Breakdown of academic impact, for papers by Debra Day‐Salvatore Breakdown of academic impact, for papers by S. Kling Breakdown of academic impact, for papers by Yuqi Yang
Rankless by CCL
2026