Rajini Haraksingh

4.4k total citations
12 papers, 425 citations indexed

About

Rajini Haraksingh is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Rajini Haraksingh has authored 12 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Rajini Haraksingh's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Cancer Genomics and Diagnostics (3 papers). Rajini Haraksingh is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Cancer Genomics and Diagnostics (3 papers). Rajini Haraksingh collaborates with scholars based in United States, Trinidad and Tobago and Australia. Rajini Haraksingh's co-authors include M Snyder, Alexander E. Urban, Alexej Abyzov, Bo Zhou, Xianglong Zhang, Steve S. Ho, Reenal Pattni, Mark Gerstein, Jimmy Lin and Marisa Dolled‐Filhart and has published in prestigious journals such as PLoS ONE, Journal of Molecular Biology and Child Development.

In The Last Decade

Rajini Haraksingh

12 papers receiving 415 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rajini Haraksingh United States 8 245 217 96 59 36 12 425
Sergi Villatoro Spain 11 162 0.7× 185 0.9× 62 0.6× 61 1.0× 43 1.2× 19 358
Chee Seng Ku Sweden 6 211 0.9× 322 1.5× 107 1.1× 46 0.8× 17 0.5× 6 472
Laura A. Crinnion United Kingdom 13 274 1.1× 160 0.7× 50 0.5× 45 0.8× 22 0.6× 26 413
Anna Maria Nardone Italy 13 380 1.6× 213 1.0× 33 0.3× 55 0.9× 35 1.0× 38 552
Emma Hobson United Kingdom 9 213 0.9× 256 1.2× 33 0.3× 37 0.6× 40 1.1× 24 405
Pauline A. Fujita United States 5 432 1.8× 103 0.5× 84 0.9× 55 0.9× 16 0.4× 5 537
Kênia Balbi El-Jaick Brazil 11 546 2.2× 284 1.3× 34 0.4× 40 0.7× 47 1.3× 20 675
Qian Du Australia 9 593 2.4× 123 0.6× 114 1.2× 43 0.7× 20 0.6× 16 704
Ron Hochstenbach Netherlands 11 306 1.2× 340 1.6× 47 0.5× 162 2.7× 87 2.4× 18 512
Stephanie Dallaire United States 5 274 1.1× 476 2.2× 69 0.7× 157 2.7× 96 2.7× 7 630

Countries citing papers authored by Rajini Haraksingh

Since Specialization
Citations

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

Fields of papers citing papers by Rajini Haraksingh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rajini Haraksingh

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

All Works

12 of 12 papers shown
1.
Seecheran, Naveen, et al.. (2024). Prevalence of CYP2C19*2 and CYP2C19*3 Allelic Variants and Clopidogrel Use in Patients with Cardiovascular Disease in Trinidad & Tobago. Cardiology and Therapy. 13(1). 191–203. 3 indexed citations
2.
Foster, J. E., et al.. (2021). Factors associated with breast cancer recurrence and survival at Sangre Grande Hospital, Trinidad. Cancer Causes & Control. 32(7). 763–772. 2 indexed citations
3.
Zhou, Bo, Steve S. Ho, Stephanie Greer, et al.. (2019). Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562. Genome Research. 29(3). 472–484. 60 indexed citations
4.
Zhou, Bo, Steve S. Ho, Xianglong Zhang, et al.. (2018). Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis. Journal of Medical Genetics. 55(11). 735–743. 70 indexed citations
5.
Haraksingh, Rajini, Alexej Abyzov, & Alexander E. Urban. (2017). Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans. BMC Genomics. 18(1). 321–321. 45 indexed citations
6.
Toriola, Adetunji T., et al.. (2017). A situational analysis of breast cancer early detection services in Trinidad and Tobago. Cancer Causes & Control. 29(1). 33–42. 5 indexed citations
7.
Haraksingh, Rajini, Fereshteh Jahanbani, Juan Rodriguez‐Paris, et al.. (2014). Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. BMC Genomics. 15(1). 1155–1155. 22 indexed citations
8.
Haraksingh, Rajini & M Snyder. (2013). Impacts of Variation in the Human Genome on Gene Regulation. Journal of Molecular Biology. 425(21). 3970–3977. 102 indexed citations
9.
Zhang, Ying, Rajini Haraksingh, Fabian Grubert, et al.. (2013). Child Development and Structural Variation in the Human Genome. Child Development. 84(1). 34–48. 19 indexed citations
10.
Dolled‐Filhart, Marisa, et al.. (2013). Computational and Bioinformatics Frameworks for Next‐Generation Whole Exome and Genome Sequencing. The Scientific World JOURNAL. 2013(1). 730210–730210. 36 indexed citations
11.
Dolled‐Filhart, Marisa, et al.. (2012). Personalizing Rare Disease Research: How Genomics is Revolutionizing the Diagnosis and Treatment of Rare Disease. Personalized Medicine. 9(8). 805–819. 6 indexed citations
12.
Haraksingh, Rajini, Alexej Abyzov, Mark Gerstein, Alexander E. Urban, & M Snyder. (2011). Genome-Wide Mapping of Copy Number Variation in Humans: Comparative Analysis of High Resolution Array Platforms. PLoS ONE. 6(11). e27859–e27859. 55 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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