Runjun D. Kumar

1.9k citations

21 papers · 626 indexed · h-index 9

Impact in

Molecular Biology
- RNA and protein synthesis mechanisms
- Ubiquitin and proteasome pathways
- RNA modifications and cancer
- Bioinformatics and Genomic Networks
- Genomics and Phylogenetic Studies
Microbiology

Papers in ⓘ

Cancer Research 5
- Cancer Genomics and Diagnostics 4
Genetics 6
- Genomics and Rare Diseases 5

Co-authors: Ron Bose (4 shared papers)Peer Bork (2 shared papers)Anne‐Claude Gavin (2 shared papers)Vera van Noort (2 shared papers)Pablo Mínguez (1 shared paper)Luca Parca (1 shared paper)Daniel R. Mende (1 shared paper)Manuela Helmer‐Citterich (1 shared paper)
Journals: Molecular Systems Biology (2 papers)Scientific Reports (1 paper)Nature Genetics (1 paper)Journal of Thoracic Oncology (1 paper)Bioinformatics (1 paper)
Partner nations: United States Germany Canada

In The Last Decade

Runjun D. Kumar

19 papers receiving 621 citations

Peers

Countries citing papers authored by Runjun D. Kumar

Since Specialization

Citations

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

Fields of papers citing papers by Runjun D. Kumar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Runjun D. Kumar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Runjun D. Kumar Line = papers co-authored together Runjun D. Kumar links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Deciphering a global network of functionally associated post‐translational modifications Molecular Systems Biology ·Pablo Mínguez, Luca Parca, Francesca Diella, Daniel R. Mende, Runjun D. Kumar, Manuela Helmer‐Citterich, Anne‐Claude Gavin, Vera van Noort, Peer Bork	2012	188
2	Cross‐talk between phosphorylation and lysine acetylation in a genome‐reduced bacterium Molecular Systems Biology ·Vera van Noort, Jan Seebacher, Samuel L. Bader, Shabaz Mohammed, Ivana Vonkova, Matthew J. Betts, Sebastian Kühner, Runjun D. Kumar, Tobias Maier, Martina O’Flaherty, Vladimir Rybin, Arne Schmeisky, Eva Yus, Jörg Stülke, Luís Serrano, Robert B. Russell, Albert J. R. Heck, Peer Bork, Anne‐Claude Gavin	2012	148
3	PoxA, YjeK, and Elongation Factor P Coordinately Modulate Virulence and Drug Resistance in Salmonella enterica Molecular Cell ·William Wiley Navarre, Shengwei Zou, Hervé Roy, Jinglin Lucy Xie, Alexei Savchenko, A.U. Singer, Elena Edvokimova, Lynne R. Prost, Runjun D. Kumar, Michael Ibba, Ferric C. Fang	2010	131
4	Statistically identifying tumor suppressors and oncogenes from pan-cancer genome-sequencing data Bioinformatics ·Runjun D. Kumar, Adam C. Searleman, S. Joshua Swamidass, Obi L. Griffith, Ron Bose	2015	39
5	Unsupervised detection of cancer driver mutations with parsimony-guided learning Nature Genetics ·Runjun D. Kumar, S. Joshua Swamidass, Ron Bose	2016	38
6	Prioritizing Potentially Druggable Mutations with dGene: An Annotation Tool for Cancer Genome Sequencing Data PLoS ONE ·Runjun D. Kumar, Li‐Wei Chang, Matthew J. Ellis, Ron Bose	2013	23
7	Analysis of somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer types Scientific Reports ·Runjun D. Kumar, Ron Bose	2017	11
8	A deep intronic variant is a common cause of OTC deficiency in individuals with previously negative genetic testing Molecular Genetics and Metabolism Reports ·Runjun D. Kumar, Lindsay C. Burrage, Jan Bartoš, Saima Ali, Eric Schmitt, Sandesh C.S. Nagamani, Cynthia LeMons	2021	9
9	A phase I study of MEDI1873, a novel GITR agonist, in advanced solid tumors Annals of Oncology ·C.S. Denlinger, Jeffrey R. Infante, Raid Aljumaily, Aung Naing, Ashish V. Chintakuntlawar, Naiyer A. Rizvi, Helen J. Ross, Michael S. Gordon, Runjun D. Kumar, Mingyang Ma, Long Yan, Paola Vicini, Nathan Standifer, Jennifer Cann, Aruna B. Perera, Nicholas M. Durham, S. Krishnan, Ani Sarkis Balmanoukian	2018	9
10	P3.04-23 Phase 1b/2 Study to Evaluate Novel Combinations With Oleclumab (MEDI9447) in Previously Treated Advanced EGFRm NSCLC Journal of Thoracic Oncology ·Naiyer A. Rizvi, Catherine A. Shu, Sarah B. Goldberg, V. Papadimitrakopoulou, D. Ross Camidge, Sandip Pravin Patel, Kristen A. Marrone, S. Kim, D. Kim, H. Hsieh, Nancy K. Mueller, Runjun D. Kumar, Judson M. Englert, K. Park	2018	6
11	A TMPRSS2‐ERG gene signature predicts prognosis of patients with prostate adenocarcinoma SHILAP Revista de lepidopterología ·Emily Zhou, Baoyi Zhang, Kenneth Zhu, Evelien Schaafsma, Runjun D. Kumar, Chao Cheng	2020	5
12	Clinical genome sequencing: Three years’ experience at a tertiary children’s hospital Genetics in Medicine ·Runjun D. Kumar, Lisa Saba, Haley Streff, Chad A. Shaw, Elizabeth Mizerik, Matthew T. Snyder, Dolores López‐Terrada, Jennifer Scull	2023	4
13	The germline p53 activation syndrome: A new patient further refines the clinical phenotype American Journal of Medical Genetics Part A ·Runjun D. Kumar, Mustafa Tosur, Seema R. Lalani, Donald H. Mahoney, Alison A. Bertuch	2022	3
14	Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis American Journal of Medical Genetics Part A ·Runjun D. Kumar, Linyan Meng, Pengfei Liu, Christina Y. Miyake, Kim C. Worley, Weimin Bi, Seema R. Lalani	2022	3
15	Insights on improving accessibility and usability of functional data to unlock their potential for variant interpretation The American Journal of Human Genetics ·Min Seon Park, Runjun D. Kumar, Cristian Ovadiuc, Andrew Folta, Abbye E. McEwen, Ashley Snyder, Rehan M. Villani, Amanda B. Spurdle, Douglas M. Fowler, Alan F. Rubin, Brian H. Shirts, Lea M. Starita, Andrew B. Stergachis	2025	3
16	Selection for or against escape from nonsense mediated decay is a novel signature for the detection of cancer genes Cancer Genetics ·Runjun D. Kumar, Briana A. Burns, Paul J. Vandeventer, Pamela N. Luna, Chad A. Shaw	2021	2
17	Facial Nerve Palsy in a Child With Fever of Unknown Origin Clinical Pediatrics ·Charmaine P. Mutucumarana, Runjun D. Kumar, Dana Foradori, Veena Ramgopal, Gail J. Demmler	2020	2
18	PRM1 Kaplan-Meier Survival Curves: A Potential Source of Data for Systematic Reviews Value in Health ·J Gupta, MK Bhutani, Runjun D. Kumar, Maninder Kaur, R. Jindal, Mohammad Khubeb Siddiqui	2012	1
19	Genomic Data and Privacy Clinical Chemistry ·Candace T. Myers, Runjun D. Kumar, Lisa Pilgram, Luca Bonomi, Mara Thomas, Obi L. Griffith, Stephanie M. Fullerton, Richard A. Gibbs	2025	1
20	P564: Genetic test stewardship for clinical exome sequencing: Review of critical care orders at Texas Children’s Hospital SHILAP Revista de lepidopterología ·Haley Streff, Lisa Saba, Runjun D. Kumar, Dolores López‐Terrada, Jennifer Scull	2023	0

About Runjun D. Kumar

Runjun D. Kumar is a scholar working on Cancer Research, Genetics, Molecular Biology, Immunology and Allergy and Parasitology, having authored 21 papers that have together received 626 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Cancer Genomics and Diagnostics (4 papers), Genomics and Phylogenetic Studies (3 papers), Ferroptosis and cancer prognosis (3 papers), RNA and protein synthesis mechanisms (3 papers), RNA modifications and cancer (2 papers), Ubiquitin and proteasome pathways (2 papers) and Metabolism and Genetic Disorders (1 paper). The work is most often cited by research in Molecular Biology (514 citations), Microbiology (31 citations), Spectroscopy (74 citations), Cancer Research (60 citations) and Geriatrics and Gerontology (15 citations). Runjun D. Kumar has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Ron Bose, Peer Bork, Anne‐Claude Gavin, Vera van Noort, Pablo Mínguez, Luca Parca, Daniel R. Mende, Manuela Helmer‐Citterich, Francesca Diella and S. Joshua Swamidass. Their work appears in journals such as Molecular Systems Biology, Scientific Reports, Nature Genetics, Journal of Thoracic Oncology and Bioinformatics.

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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