Dhavendra Kumar

1.6k total citations
12 papers, 143 citations indexed

About

Dhavendra Kumar is a scholar working on Genetics, Molecular Biology and History and Philosophy of Science. According to data from OpenAlex, Dhavendra Kumar has authored 12 papers receiving a total of 143 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 2 papers in Molecular Biology and 1 paper in History and Philosophy of Science. Recurrent topics in Dhavendra Kumar's work include Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Dhavendra Kumar is often cited by papers focused on Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Dhavendra Kumar collaborates with scholars based in United Kingdom, India and Poland. Dhavendra Kumar's co-authors include Catherine Lynn T. Silao, Bin Alwi Zilfalil and Shahida Moosa and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Medical Genetics and Saudi Medical Journal.

In The Last Decade

Dhavendra Kumar

10 papers receiving 133 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dhavendra Kumar United Kingdom	6	58	42	16	15	14	12	143
Narayan Chandra Saha Bangladesh	6	30 0.5×	55 1.3×	15 0.9×	49 3.3×	4 0.3×	34	192
Elly Brokamp United States	6	132 2.3×	62 1.5×	7 0.4×	25 1.7×	6 0.4×	9	177
Elaine Goh Canada	7	104 1.8×	78 1.9×	5 0.3×	31 2.1×	7 0.5×	18	186
Rachel Stapleton Nigeria	5	57 1.0×	38 0.9×	16 1.0×	11 0.7×	7 0.5×	11	136
Shruti Marwaha United States	6	123 2.1×	131 3.1×	12 0.8×	8 0.5×	7 0.5×	19	283
Abdulrahman Swaid Saudi Arabia	5	66 1.1×	59 1.4×	8 0.5×	33 2.2×	3 0.2×	6	112
Laura S. Farach United States	7	57 1.0×	71 1.7×	7 0.4×	9 0.6×	6 0.4×	22	127
Ilaria Viganò Italy	7	11 0.2×	52 1.2×	16 1.0×	15 1.0×	10 0.7×	17	125
Julie Choi United States	7	93 1.6×	105 2.5×	5 0.3×	12 0.8×	22 1.6×	11	242
Vikas Bhambhani United States	7	49 0.8×	86 2.0×	29 1.8×	8 0.5×	35 2.5×	13	194

Countries citing papers authored by Dhavendra Kumar

Since Specialization

Citations

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

Fields of papers citing papers by Dhavendra Kumar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dhavendra Kumar

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

All Works

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12 of 12 papers shown

1.

Moosa, Shahida, et al.. (2025). Advancing genetic counselling in Southern Africa. Saudi Medical Journal. 46(4). 335–344.

2.

Kumar, Dhavendra. (2023). From the Double Helix to the Personal Genomes. SHILAP Revista de lepidopterología. 20(2). 109–122. 1 indexed citations

3.

Kumar, Dhavendra. (2020). The Genomic and Precision Medicine in Clinical Practice. 6(3). 2 indexed citations

4.

Kumar, Dhavendra, et al.. (2015). An Efficient Space Partitioning Tree Approach for Indexing and Retrieving Fingerprint Databases. 1–6. 3 indexed citations

5.

Kumar, Dhavendra. (2011). The personalised medicine. A paradigm of evidence-based medicine.. SHILAP Revista de lepidopterología. 47(1). 31–40. 17 indexed citations

6.

Kumar, Dhavendra. (2008). Disorders of the genome architecture: a review. PubMed. 2(3-4). 69–76. 20 indexed citations

7.

Kumar, Dhavendra. (2008). David N. Cooper and Hildegard Kehrer-Sawatzki (eds): Handbook of Human Molecular Evolution. PubMed Central. 2(3-4). 127–127.

8.

Kumar, Dhavendra. (2007). Genome Mirror-2006. PubMed. 1(1-2). 87–90. 2 indexed citations

9.

Kumar, Dhavendra. (2007). From evidence-based medicine to genomic medicine. PubMed. 1(3-4). 95–104. 19 indexed citations

10.

Kumar, Dhavendra. (2007). Genomic medicine: a new frontier of medicine in the twenty first century. PubMed. 1(1-2). 3–7. 12 indexed citations

11.

Kumar, Dhavendra. (2004). Genetic Disorders of the Indian Subcontinent. 9 indexed citations

12.

Kumar, Dhavendra. (1998). Genetic disorders among Arab populations. American Journal of Medical Genetics. 77(3). 251–252. 58 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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