Charu Kaiwar

533 total citations
10 papers, 103 citations indexed

About

Charu Kaiwar is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Charu Kaiwar has authored 10 papers receiving a total of 103 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Pathology and Forensic Medicine and 2 papers in Molecular Biology. Recurrent topics in Charu Kaiwar's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). Charu Kaiwar is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). Charu Kaiwar collaborates with scholars based in United States and Germany. Charu Kaiwar's co-authors include Eric W. Klee, Raúl Urrutia, Michael T. Zimmermann, Zhiyv Niu, Matthew J. Ferber, Dusica Babovic‐Vuksanovic, Pavel N. Pichurin, Ralitza H. Gavrilova, Joel A. Morales‐Rosado and Radhika Dhamija and has published in prestigious journals such as Blood, Clinical Immunology and American Journal of Medical Genetics Part A.

In The Last Decade

Charu Kaiwar

10 papers receiving 103 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Charu Kaiwar United States 6 61 56 11 11 11 10 103
Samantha Penney United States 5 76 1.2× 68 1.2× 9 0.8× 10 0.9× 5 0.5× 5 157
Newell Belnap United States 7 49 0.8× 84 1.5× 7 0.6× 8 0.7× 7 0.6× 12 126
Sebastian Röner Germany 3 68 1.1× 84 1.5× 13 1.2× 7 0.6× 12 1.1× 5 160
Lucile Pinson France 6 34 0.6× 68 1.2× 22 2.0× 11 1.0× 7 0.6× 8 116
Theresa Brunet Germany 7 47 0.8× 54 1.0× 8 0.7× 9 0.8× 9 0.8× 24 110
Rena A. Godfrey United States 4 54 0.9× 30 0.5× 18 1.6× 7 0.6× 7 0.6× 8 96
Jianhong Hu United States 10 80 1.3× 136 2.4× 5 0.5× 10 0.9× 10 0.9× 17 206
Nuria García Segarra Switzerland 7 45 0.7× 78 1.4× 18 1.6× 24 2.2× 5 0.5× 10 148
Laura Schultz‐Rogers United States 8 60 1.0× 79 1.4× 5 0.5× 6 0.5× 8 0.7× 11 128
Daisuke Ieda Japan 8 101 1.7× 103 1.8× 8 0.7× 12 1.1× 4 0.4× 16 164

Countries citing papers authored by Charu Kaiwar

Since Specialization
Citations

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

Fields of papers citing papers by Charu Kaiwar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charu Kaiwar

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

All Works

10 of 10 papers shown
1.
Ferrer, Alejandro, Laura Schultz‐Rogers, Charu Kaiwar, et al.. (2019). Three rare disease diagnoses in one patient through exome sequencing. Molecular Case Studies. 5(6). a004390–a004390. 7 indexed citations
2.
Kaiwar, Charu, Teresa Kruisselbrink, Yogish C. Kudva, Eric W. Klee, & Pavel N. Pichurin. (2018). Exome sequencing confirms diagnosis of kabuki syndrome in an-adult with hodgkin lymphoma and unusually severe multisystem phenotype. Clinical Immunology. 207. 55–57. 6 indexed citations
3.
Morales‐Rosado, Joel A., Charu Kaiwar, Benn E. Smith, Eric W. Klee, & Radhika Dhamija. (2018). A case of YY1‐associated syndromic learning disability or Gabriele‐de Vries syndrome with myasthenia gravis. American Journal of Medical Genetics Part A. 176(12). 2846–2849. 17 indexed citations
4.
Kaiwar, Charu, Sarah Macklin, Jennifer Gass, et al.. (2017). Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1. Hereditary Cancer in Clinical Practice. 15(1). 10–10. 1 indexed citations
5.
6.
Vairo, Filippo Pinto e, Nicole J. Boczek, Margot A. Cousin, et al.. (2017). The prevalence of diseases caused by lysosome-related genes in a cohort of undiagnosed patients. Molecular Genetics and Metabolism Reports. 13. 46–51. 17 indexed citations
7.
Blackburn, Patrick R., Sarah Barnett, Michael T. Zimmermann, et al.. (2017). Novel de novo variant in EBF3 is likely to impact DNA binding in a patient with a neurodevelopmental disorder and expanded phenotypes: patient report, in silico functional assessment, and review of published cases. Molecular Case Studies. 3(3). a001743–a001743. 18 indexed citations
8.
Kaiwar, Charu, Tammy M. McAllister, Konstantinos N. Lazaridis, & Eric W. Klee. (2017). Preemptive sequencing in the genomic medicine era. Expert Review of Precision Medicine and Drug Development. 2(2). 91–98. 4 indexed citations
9.
Engle, Elizabeth K., et al.. (2013). The JAK Inhibitor Ruxolitinib Elicits Hematologic and Symptomatic Improvement In Patients With Chuvash Polycythemia. Blood. 122(21). 4051–4051. 3 indexed citations
10.
Fisher, Daniel A.C., Christopher A. Miller, Michael D. McLellan, et al.. (2012). Clonal Evolution Revealed by Whole Genome Sequencing in a Case of Primary Myelofibrosis Transformed to Secondary Acute Myeloid Leukemia. Blood. 120(21). 706–706. 2 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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