Janna Kenny

1.9k total citations
17 papers, 502 citations indexed

About

Janna Kenny is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Janna Kenny has authored 17 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in Janna Kenny's work include Genomics and Rare Diseases (7 papers), Genetic Syndromes and Imprinting (4 papers) and Prion Diseases and Protein Misfolding (4 papers). Janna Kenny is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genetic Syndromes and Imprinting (4 papers) and Prion Diseases and Protein Misfolding (4 papers). Janna Kenny collaborates with scholars based in United Kingdom, Ireland and United States. Janna Kenny's co-authors include Elizabeth Forsythe, Chiara Bacchelli, Philip L. Beales, Simon Mead, Nick C. Fox, Natalie S. Ryan, Martin N. Rossor, Gary Adamson, Bart De Strooper and Jon Beck and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Lancet Neurology and The American Journal of Human Genetics.

In The Last Decade

Janna Kenny

16 papers receiving 488 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janna Kenny United Kingdom 9 271 246 160 61 52 17 502
Kristin Barañano United States 9 228 0.8× 237 1.0× 165 1.0× 72 1.2× 42 0.8× 21 536
Carolyn Tysoe United Kingdom 13 264 1.0× 190 0.8× 206 1.3× 42 0.7× 21 0.4× 23 586
Zhongdong Lin China 10 133 0.5× 84 0.3× 51 0.3× 53 0.9× 29 0.6× 23 321
Yang Hai China 12 190 0.7× 86 0.3× 55 0.3× 20 0.3× 24 0.5× 31 447
Lisa Flint United States 8 199 0.7× 151 0.6× 99 0.6× 22 0.4× 26 0.5× 9 514
Angel On-Kei Chan China 11 115 0.4× 47 0.2× 105 0.7× 27 0.4× 14 0.3× 24 318
Joyce So Canada 13 328 1.2× 438 1.8× 59 0.4× 31 0.5× 21 0.4× 26 643
Iris Noyman Israel 9 207 0.8× 64 0.3× 72 0.5× 104 1.7× 23 0.4× 26 455
M. Pineda Spain 13 285 1.1× 118 0.5× 67 0.4× 59 1.0× 59 1.1× 26 533
Zucai Xu China 12 226 0.8× 37 0.2× 64 0.4× 94 1.5× 80 1.5× 64 491

Countries citing papers authored by Janna Kenny

Since Specialization
Citations

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

Fields of papers citing papers by Janna Kenny

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janna Kenny

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

All Works

17 of 17 papers shown
1.
Streață, Ioana, Athina Ververi, Ratna Dua Puri, et al.. (2024). Catalogue of inherited autosomal recessive disorders found amongst the Roma population of Europe. European Journal of Medical Genetics. 73. 104989–104989. 2 indexed citations
2.
Ng, Bobby G., Antonio Rubio‐del‐Campo, Matthew P. Wilson, et al.. (2023). Beyond genetics: Deciphering the impact of missense variants in CAD deficiency. Journal of Inherited Metabolic Disease. 46(6). 1170–1185. 6 indexed citations
3.
Durkie, Miranda, Christopher M. Watson, Peter R. Winship, et al.. (2023). The Common PKD1 p.(Ile3167Phe) Variant Is Hypomorphic and Associated with Very Early Onset, Biallelic Polycystic Kidney Disease. Human Mutation. 2023. 1–8. 2 indexed citations
4.
Kenny, Janna, et al.. (2022). Fontaine progeroid syndrome—A case report. SHILAP Revista de lepidopterología. 10(9). e6291–e6291. 5 indexed citations
5.
Kenny, Janna, Natalie S. Ryan, Jonathan D. Rohrer, et al.. (2020). Genetic testing in dementia — utility and clinical strategies. Nature Reviews Neurology. 17(1). 23–36. 25 indexed citations
6.
Haworth, A., Eva Serra, Janna Kenny, et al.. (2020). A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review. BJOG An International Journal of Obstetrics & Gynaecology. 128(6). 1012–1019. 29 indexed citations
7.
Kenny, Janna, et al.. (2020). Ethical Issues in Genetic Testing for Inherited Cancer Predisposition Syndromes: the Potentially Conflicting Interests of Patients and Their Relatives. St George's Online Research Archive (St George's University of London). 8(2). 72–77. 3 indexed citations
8.
Forsythe, Elizabeth, Janna Kenny, Chiara Bacchelli, & Philip L. Beales. (2018). Managing Bardet–Biedl Syndrome—Now and in the Future. Frontiers in Pediatrics. 6. 23–23. 148 indexed citations
9.
Kenny, Janna, Elizabeth Forsythe, Philip L. Beales, & Chiara Bacchelli. (2017). Toward Personalized Medicine in Bardet–Biedl Syndrome. Personalized Medicine. 14(5). 447–456. 20 indexed citations
10.
Frankó, Edit, Tim Wehner, Olivier Joly, et al.. (2016). Quantitative EEG parameters correlate with the progression of human prion diseases. Journal of Neurology Neurosurgery & Psychiatry. 87(10). 1061–1067. 19 indexed citations
11.
Adamson, Gary, Janna Kenny, Martin N. Rossor, et al.. (2016). PROBING FTD GENETICS WITH NEXT-GENERATION SEQUENCING. Journal of Neurology Neurosurgery & Psychiatry. 87(12). e1.198–e1. 1 indexed citations
12.
Ryan, Natalie S., Jennifer M. Nicholas, Philip S.J. Weston, et al.. (2016). Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series. The Lancet Neurology. 15(13). 1326–1335. 144 indexed citations
13.
Minikel, Eric Vallabh, Inga Zerr, Steven Collins, et al.. (2014). Ascertainment Bias Causes False Signal of Anticipation in Genetic Prion Disease. The American Journal of Human Genetics. 95(4). 371–382. 26 indexed citations
14.
Beck, John S., Alan Pittman, Gary Adamson, et al.. (2013). Validation of next-generation sequencing technologies in genetic diagnosis of dementia. Neurobiology of Aging. 35(1). 261–265. 47 indexed citations
15.
Vandersteen, Anthony M., Janna Kenny, Naheed L. Khan, & Alison Male. (2013). Marfan syndrome presenting with headache and coincidental ophthalmic artery aneurysm. BMJ Case Reports. 2013. bcr2012008323–bcr2012008323. 1 indexed citations
16.
Kenny, Janna, Melissa Lees, Susan Drury, et al.. (2011). Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndrome. Pediatric Nephrology. 26(8). 1331–1334. 24 indexed citations
17.

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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2026