Benjamin W. Darbro

2.9k total citations
75 papers, 1.4k citations indexed

About

Benjamin W. Darbro is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Benjamin W. Darbro has authored 75 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 19 papers in Genetics and 15 papers in Neurology. Recurrent topics in Benjamin W. Darbro's work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Neuroendocrine Tumor Research Advances (7 papers). Benjamin W. Darbro is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Neuroendocrine Tumor Research Advances (7 papers). Benjamin W. Darbro collaborates with scholars based in United States, Australia and Canada. Benjamin W. Darbro's co-authors include Aloysius J. Klingelhutz, Dawn E. Quelle, Jeffrey C. Murray, Alexander G. Bassuk, John R. Hess, Brett A. Wagner, Garry R. Buettner, Vinit B. Mahajan, Thomas J. van ‘t Erve and Thomas J. Raife and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Benjamin W. Darbro

70 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benjamin W. Darbro United States 22 598 284 242 145 137 75 1.4k
Emiliano Giardina Italy 27 905 1.5× 316 1.1× 206 0.9× 167 1.2× 101 0.7× 145 2.2k
Ronald A. Booth Canada 24 417 0.7× 178 0.6× 98 0.4× 177 1.2× 212 1.5× 61 1.8k
Susanna Ranta Finland 20 335 0.6× 183 0.6× 431 1.8× 86 0.6× 178 1.3× 93 1.6k
Denise Goh Singapore 19 485 0.8× 174 0.6× 360 1.5× 42 0.3× 85 0.6× 44 1.3k
Margarita Lianeri Poland 27 751 1.3× 362 1.3× 129 0.5× 120 0.8× 98 0.7× 98 1.9k
Jin Huang China 21 510 0.9× 177 0.6× 195 0.8× 255 1.8× 273 2.0× 70 2.2k
Luiz Marco Brazil 26 858 1.4× 346 1.2× 106 0.4× 106 0.7× 226 1.6× 111 2.1k
Gábor Papp Hungary 23 538 0.9× 208 0.7× 356 1.5× 45 0.3× 172 1.3× 69 2.0k
Carlos Alberto Longui Brazil 21 595 1.0× 413 1.5× 120 0.5× 48 0.3× 180 1.3× 109 1.5k
Matthew R. Lincoln United Kingdom 23 511 0.9× 404 1.4× 130 0.5× 133 0.9× 58 0.4× 41 2.8k

Countries citing papers authored by Benjamin W. Darbro

Since Specialization
Citations

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

Fields of papers citing papers by Benjamin W. Darbro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benjamin W. Darbro. 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 Benjamin W. Darbro. The network helps show where Benjamin W. Darbro may publish in the future.

Co-authorship network of co-authors of Benjamin W. Darbro

This figure shows the co-authorship network connecting the top 25 collaborators of Benjamin W. Darbro. A scholar is included among the top collaborators of Benjamin W. Darbro 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 Benjamin W. Darbro. Benjamin W. Darbro 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.
Stephan, Carrie, Theresa Czech, Benjamin W. Darbro, et al.. (2025). UDP‐glucose dehydrogenase variants cause dystroglycanopathy. Annals of Clinical and Translational Neurology. 12(6). 1302–1308. 1 indexed citations
2.
Darbro, Benjamin W., et al.. (2023). CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome. Human Genetics. 142(4). 523–530. 3 indexed citations
3.
Darbro, Benjamin W., et al.. (2023). Mosaicism in BRPF1-Related Neurodevelopmental Disorder: Report of Two Sisters and Literature Review. SHILAP Revista de lepidopterología. 2023. 1–6.
4.
Howe, James R., Andrew M. Bellizzi, Bruce A. Smith, et al.. (2023). Prioritization of Fluorescence In Situ Hybridization (FISH) Probes for Differentiating Primary Sites of Neuroendocrine Tumors with Machine Learning. International Journal of Molecular Sciences. 24(24). 17401–17401.
5.
Gutierrez, Wade R., Andrew P. Voigt, Vickie Knepper-Adrian, et al.. (2022). PRC2 loss drives MPNST metastasis and matrix remodeling. JCI Insight. 7(20). 11 indexed citations
6.
Chandra, Bharatendu, Cristina M. Justice, Anthony M. Musolf, et al.. (2022). TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis. Genes. 13(9). 1649–1649. 2 indexed citations
7.
Dickinson, Amanda, Huan Liu, Jennifer Standley, et al.. (2022). Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes. The American Journal of Human Genetics. 110(1). 71–91. 5 indexed citations
8.
Scott, Aaron T., Terry A. Braun, Bartley Brown, et al.. (2021). Presacral neuroendocrine tumors associated with the Currarino syndrome. American Journal of Medical Genetics Part A. 185(5). 1582–1588. 3 indexed citations
9.
Shchelochkov, Oleg A., et al.. (2021). Case report of a pseudo‐isodicentric chromosome 9 resulting in mosaic trisomy 9. SHILAP Revista de lepidopterología. 9(4). 2340–2344. 2 indexed citations
10.
Pulliam, Casey, Vickie Knepper-Adrian, Rajesh Khanna, et al.. (2020). RABL6A Is an Essential Driver of MPNSTs that Negatively Regulates the RB1 Pathway and Sensitizes Tumor Cells to CDK4/6 Inhibitors. Clinical Cancer Research. 26(12). 2997–3011. 40 indexed citations
11.
Scott, Aaron T., Patrick Breheny, Po Hien Ear, et al.. (2020). Gene Expression Signatures Identify Novel Therapeutics for Metastatic Pancreatic Neuroendocrine Tumors. Clinical Cancer Research. 26(8). 2011–2021. 40 indexed citations
12.
Uthoff, Johanna, T. Shawn Sato, Christopher S. Rogers, et al.. (2020). Longitudinal phenotype development in a minipig model of neurofibromatosis type 1. Scientific Reports. 10(1). 5046–5046. 15 indexed citations
13.
Henry, Travis S., et al.. (2019). Candidate modifier genes for immune function in 22q11.2 deletion syndrome. Molecular Genetics & Genomic Medicine. 8(1). e1057–e1057. 6 indexed citations
14.
Willer, Tobias, Benjamin W. Darbro, Hernán Gonorazky, et al.. (2018). Uniparental disomy unveils a novel recessive mutation in POMT2. Neuromuscular Disorders. 28(7). 592–596. 14 indexed citations
15.
Krasowski, Matthew D., et al.. (2015). Promoting improved utilization of laboratory testing through changes in an electronic medical record: experience at an academic medical center. BMC Medical Informatics and Decision Making. 15(1). 11–11. 79 indexed citations
16.
Hagen, Jussara, Sara M. Reed, Agshin F. Taghiyev, et al.. (2014). RABL6A Promotes G1–S Phase Progression and Pancreatic Neuroendocrine Tumor Cell Proliferation in an Rb1-Dependent Manner. Cancer Research. 74(22). 6661–6670. 28 indexed citations
17.
Sieren, Jessica C., David K. Meyerholz, Xiaojun Wang, et al.. (2014). Development and translational imaging of a TP53 porcine tumorigenesis model. Journal of Clinical Investigation. 124(9). 4052–4066. 73 indexed citations
18.
Cui, Huxing, Brittany L. Mason, Shizhong Han, et al.. (2013). Eating disorder predisposition is associated with ESRRA and HDAC4 mutations. Journal of Clinical Investigation. 123(11). 4706–4713. 59 indexed citations
19.
Boese, Erin A., Katherine N. Gibson‐Corley, Patricia Kirby, et al.. (2013). G-protein coupled receptor expression patterns delineate medulloblastoma subgroups. Acta Neuropathologica Communications. 1(1). 66–66. 21 indexed citations
20.
Fingert, John H., Benjamin W. Darbro, Richard Van Rheeden, et al.. (2013). TBK1and Flanking Genes in Human Retina. Ophthalmic Genetics. 35(1). 35–40. 15 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Emiliano Giardina Breakdown of academic impact, for papers by Ronald A. Booth Breakdown of academic impact, for papers by Susanna Ranta Breakdown of academic impact, for papers by Denise Goh Breakdown of academic impact, for papers by Margarita Lianeri Breakdown of academic impact, for papers by Jin Huang Breakdown of academic impact, for papers by Luiz Marco Breakdown of academic impact, for papers by Gábor Papp Breakdown of academic impact, for papers by Carlos Alberto Longui Breakdown of academic impact, for papers by Matthew R. Lincoln
Rankless by CCL
2026