Raman Kumar

2.5k total citations
36 papers, 919 citations indexed

About

Raman Kumar is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Raman Kumar has authored 36 papers receiving a total of 919 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Oncology. Recurrent topics in Raman Kumar's work include Genetics and Neurodevelopmental Disorders (11 papers), Epigenetics and DNA Methylation (6 papers) and Genomics and Rare Diseases (4 papers). Raman Kumar is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Epigenetics and DNA Methylation (6 papers) and Genomics and Rare Diseases (4 papers). Raman Kumar collaborates with scholars based in Australia, United States and France. Raman Kumar's co-authors include David F. Callen, Paul M. Neilsen, Jozef Gécz, Jacqueline E. Noll, Renèe B. Schulz, Fares Al‐Ejeh, Jessie Jeffery, Kum Kum Khanna, Lachlan A. Jolly and Rachel J. Suetani and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Molecular and Cellular Biology.

In The Last Decade

Raman Kumar

35 papers receiving 910 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raman Kumar Australia 16 618 242 215 151 87 36 919
Matsuyuki Shirota Japan 16 586 0.9× 172 0.7× 123 0.6× 94 0.6× 56 0.6× 49 899
Enyuan Shang United States 17 921 1.5× 190 0.8× 99 0.5× 201 1.3× 54 0.6× 27 1.2k
Scott Topper United States 12 553 0.9× 574 2.4× 98 0.5× 181 1.2× 56 0.6× 16 1.2k
Isabel Barragán Spain 21 990 1.6× 203 0.8× 166 0.8× 198 1.3× 115 1.3× 49 1.3k
Chiara Conti Italy 13 753 1.2× 62 0.3× 297 1.4× 120 0.8× 82 0.9× 28 965
Hanna Pinças United States 16 567 0.9× 161 0.7× 207 1.0× 237 1.6× 58 0.7× 36 1.0k
Salvatore Cortellino United States 13 600 1.0× 142 0.6× 149 0.7× 223 1.5× 291 3.3× 20 1.1k
Reyna Favis United States 17 644 1.0× 224 0.9× 451 2.1× 187 1.2× 33 0.4× 27 1.2k
Leon Raskin United States 21 500 0.8× 239 1.0× 479 2.2× 281 1.9× 46 0.5× 46 1.1k
JT den Dunnen Netherlands 3 402 0.7× 244 1.0× 75 0.3× 66 0.4× 48 0.6× 6 825

Countries citing papers authored by Raman Kumar

Since Specialization
Citations

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

Fields of papers citing papers by Raman Kumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raman Kumar

This figure shows the co-authorship network connecting the top 25 collaborators of Raman Kumar. A scholar is included among the top collaborators of Raman 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 Raman Kumar. Raman Kumar 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.
Kumar, Raman, Manjeet Singh, Ranjan Patra, et al.. (2025). Influence of structural diversity in Co( ii )–oxamide complexes towards single molecule magnets and electrochemical oxygen evolution reaction. New Journal of Chemistry. 49(35). 15236–15251.
2.
Kumar, Raman, Michaela Scherer, Tarin Ritchie, et al.. (2024). Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties. Open Biology. 14(4). 230383–230383. 1 indexed citations
3.
4.
Eyk, Clare L. van, Tarin Ritchie, Rikke S. Møller, et al.. (2024). Multiomic analysis implicates nuclear hormone receptor signalling in clustering epilepsy. Translational Psychiatry. 14(1). 65–65. 3 indexed citations
5.
Kumar, Raman, Karthik Shantharam Kamath, Luke Carroll, et al.. (2022). Endogenous protein interactomes resolved through immunoprecipitation-coupled quantitative proteomics in cell lines. STAR Protocols. 3(4). 101693–101693. 4 indexed citations
6.
Jolly, Lachlan A., Raman Kumar, Peter Penzes, Michael Piper, & Jozef Gécz. (2022). The DUB Club: Deubiquitinating Enzymes and Neurodevelopmental Disorders. Biological Psychiatry. 92(8). 614–625. 16 indexed citations
7.
Carroll, Renée, Marie Shaw, Maria Arvio, et al.. (2020). Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion. European Journal of Medical Genetics. 63(10). 104010–104010. 4 indexed citations
8.
Pederick, Daniel T., Kay Richards, Sandra Piltz, et al.. (2018). Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 Epilepsy. Neuron. 97(1). 59–66.e5. 87 indexed citations
9.
Carroll, Renée, Raman Kumar, Marie Shaw, et al.. (2017). Variant in the X-chromosome spliceosomal gene GPKOW causes male-lethal microcephaly with intrauterine growth restriction. European Journal of Human Genetics. 25(9). 1078–1082. 6 indexed citations
10.
Jeffery, Jessie, et al.. (2016). FBXO31 protects against genomic instability by capping FOXM1 levels at the G2/M transition. Oncogene. 36(7). 1012–1022. 29 indexed citations
11.
Kumar, Raman, Thuong Ha, Duyen Pham, et al.. (2016). A non-coding variant in the 5ʹ UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability. European Journal of Human Genetics. 24(11). 1612–1616. 8 indexed citations
12.
Homan, Claire C., Raman Kumar, Lam Son Nguyen, et al.. (2014). Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth. The American Journal of Human Genetics. 94(3). 470–478. 100 indexed citations
13.
Huang, Lingli, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, et al.. (2012). A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability. The American Journal of Human Genetics. 91(4). 694–702. 73 indexed citations
14.
Noll, Jacqueline E., Jessie Jeffery, Fares Al‐Ejeh, et al.. (2011). Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11. Oncogene. 31(23). 2836–2848. 59 indexed citations
15.
Neilsen, Paul M., et al.. (2011). The Application of Delivery Systems for DNA Methyltransferase Inhibitors. BioDrugs. 25(4). 227–242. 9 indexed citations
16.
Pishas, Kathleen I., Fares Al‐Ejeh, Irene Zinonos, et al.. (2010). Nutlin-3a Is a Potential Therapeutic for Ewing Sarcoma. Clinical Cancer Research. 17(3). 494–504. 59 indexed citations
17.
Kumar, Raman, Paul M. Neilsen, Paul Anderson, et al.. (2010). Systematic characterisation of the rat and human CYP24A1 promoter. Molecular and Cellular Endocrinology. 325(1-2). 46–53. 16 indexed citations
18.
Fraser, Cara K., Erin L. Lousberg, Raman Kumar, et al.. (2009). Dasatinib inhibits the secretion of TNF-α following TLR stimulation in vitro and in vivo. Experimental Hematology. 37(12). 1435–1444. 38 indexed citations
19.
Kumar, Raman, Marie‐Anne Lelu, & Ian Small. (1995). Purification of mitochondria and mitochondrial nucleic acids from embryogenic suspension cultures of a gymnosperm, Larix x leptoeuropaea. Plant Cell Reports. 14(8). 534–8. 12 indexed citations
20.
Kumar, Raman, et al.. (1995). Characterization of the nuclear gene encoding chloroplast ribosomal protein S13 from Arabidopsis thaliana. Current Genetics. 28(4). 346–352. 7 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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