Katherine A. Benson

1.0k total citations
21 papers, 118 citations indexed

About

Katherine A. Benson is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Katherine A. Benson has authored 21 papers receiving a total of 118 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Nephrology. Recurrent topics in Katherine A. Benson's work include Renal Diseases and Glomerulopathies (6 papers), Genomics and Rare Diseases (5 papers) and Renal and related cancers (3 papers). Katherine A. Benson is often cited by papers focused on Renal Diseases and Glomerulopathies (6 papers), Genomics and Rare Diseases (5 papers) and Renal and related cancers (3 papers). Katherine A. Benson collaborates with scholars based in Ireland, United States and United Kingdom. Katherine A. Benson's co-authors include Alexander P. Maxwell, Amy Jayne McKnight, Gianpiero L. Cavalleri, Anthony Dorman, Peter J. Conlon, Susan Murray, Claire Kennedy, Kendrah Kidd, Patrick O’Kelly and Peter Lavin and has published in prestigious journals such as PLoS ONE, Journal of Cell Science and Journal of the American Society of Nephrology.

In The Last Decade

Katherine A. Benson

15 papers receiving 115 citations

Peers

Katherine A. Benson

GENET

NEPHR

TRANS

PFM

Adele Mitrotti Italy

Akemi Inagaki Japan

Irina Gillham‐Nasenya United Kingdom

Elizabeth Swan United Kingdom

Sergio Camilo Lopez-Garcia United Kingdom

Roisin Finn United Kingdom

Annika Faucon United States

Debra Jeandron United States

Alberto Casertano Italy

Naomi Issler United Kingdom

Adele Mitrotti Italy

Katherine A. Benson

40 ×0.8

37 ×0.8

GENET

43 ×1.0

NEPHR

4 ×0.2

TRANS

6 ×0.4

PFM

Citations per year, relative to Katherine A. Benson Katherine A. Benson (= 1×) peers Adele Mitrotti

Countries citing papers authored by Katherine A. Benson

Since Specialization

Citations

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

Fields of papers citing papers by Katherine A. Benson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katherine A. Benson. 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 Katherine A. Benson. The network helps show where Katherine A. Benson may publish in the future.

Co-authorship network of co-authors of Katherine A. Benson

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

All Works

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20 of 20 papers shown

Cormican, Sarah, Omri Teltsh, Matthew D. Griffin, et al.. (2025). Characterization of Monogenic Kidney Disease in Older Patients With CKD. Kidney International Reports. 10(7). 2140–2152.

Teltsh, Omri, et al.. (2024). #2412 Monoallelic NEK8-related polycystic kidney disease in an Irish ADPKD cohort. Nephrology Dialysis Transplantation. 39(Supplement_1). 1 indexed citations

Moloney, Patrick B., Hugh Kearney, Katherine A. Benson, et al.. (2023). Everolimus precision therapy for the GATOR1‐related epilepsies: A case series. European Journal of Neurology. 30(10). 3341–3346. 13 indexed citations

O’Kelly, Patrick, Omri Teltsh, Susan Murray, et al.. (2023). Familial Variability of Disease Severity in Adult Patients With ADPKD. Kidney International Reports. 9(3). 649–660. 6 indexed citations

Capelli, Irene, Valeria Aiello, Katherine A. Benson, et al.. (2023). Evaluation of the Predictive Ability and Concordance of Prognostic Scores for Rapid Progression in ADPKD: A Multicenter Cohort. Journal of the American Society of Nephrology. 34(11S). 213–213.

Moloney, Patrick B., et al.. (2022). Familial posterior predominant subcortical band heterotopia caused by a CEP85L missense mutation. Seizure. 103. 58–60. 2 indexed citations

Murphy, Mary, et al.. (2022). KBG syndrome mimicking genetic generalized epilepsy. Epilepsy & Behavior Reports. 19. 100545–100545. 4 indexed citations

Bhatia, Mehak, Gianpiero L. Cavalleri, Norman Delanty, et al.. (2022). Germline mosaicism in a family withMBD5haploinsufficiency. Molecular Case Studies. 8(7). a006253–a006253.

Benson, Katherine A., Susan Murray, Ross Doyle, et al.. (2020). Diagnostic utility of genetic testing in patients undergoing renal biopsy. Molecular Case Studies. 6(5). a005462–a005462. 8 indexed citations

10.

Cormican, Sarah, Claire Kennedy, Dervla M. Connaughton, et al.. (2020). Renal transplant outcomes in patients with autosomal dominant tubulointerstitial kidney disease. Clinical Transplantation. 34(2). e13783–e13783. 6 indexed citations

11.

Murray, Susan, Anthony Dorman, Katherine A. Benson, et al.. (2019). Utility of Genomic Testing after Renal Biopsy. American Journal of Nephrology. 51(1). 43–53. 19 indexed citations

12.

Cormican, Sarah, Dervla M. Connaughton, Claire Kennedy, et al.. (2019). Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland. Renal Failure. 41(1). 832–841. 14 indexed citations

13.

Delanty, Norman, Katherine A. Benson, Mark McCormack, et al.. (2019). Development of a genomics module within an epilepsy‐specific electronic health record: Toward genomic medicine in epilepsy care. Epilepsia. 60(8). 1670–1677. 5 indexed citations

14.

Smyth, Laura J., et al.. (2018). Validation of differentially methylated microRNAs identified from an epigenome-wide association study; Sanger and next generation sequencing approaches. BMC Research Notes. 11(1). 767–767. 8 indexed citations

15.

Benson, Katherine A., Sourabh Chand, Alexander P. Maxwell, et al.. (2017). Design and implementation of a custom next generation sequencing panel for selected vitamin D associated genes. BMC Research Notes. 10(1). 348–348. 2 indexed citations

16.

Benson, Katherine A., Alexander P. Maxwell, & Amy Jayne McKnight. (2016). A HuGE Review and Meta-Analyses of Genetic Associations in New Onset Diabetes after Kidney Transplantation. PLoS ONE. 11(1). e0147323–e0147323. 23 indexed citations

17.

Benson, Katherine A., et al.. (2014). Lithium‐induced thyrotoxicosis in a patient with treatment‐resistant bipolar type I affective disorder. The Medical Journal of Australia. 201(9). 541–542. 2 indexed citations

18.

Costanzo, Erin S., et al.. (2001). Preschoolers' Use of Reflective Properties: Identification of Reflections on Partially Transparent Surfaces. The Journal of Genetic Psychology. 162(4). 451–459. 1 indexed citations

19.

Benson, Katherine A., et al.. (1966). A histochemical analysis of the proteins in the larval fat body of Sarcophaga bullata. Journal of Cell Science. 1(1). 81–84. 3 indexed citations

20.

Benson, Katherine A., et al.. (1966). Masculinity - femininity and human alternation behavior in high school students. Psychology in the Schools. 3(3). 275–277. 1 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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