Kathryn E. Hentges

1.9k total citations
41 papers, 1.2k citations indexed

About

Kathryn E. Hentges is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Kathryn E. Hentges has authored 41 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 16 papers in Genetics and 5 papers in Epidemiology. Recurrent topics in Kathryn E. Hentges's work include Congenital heart defects research (11 papers), RNA modifications and cancer (9 papers) and RNA Research and Splicing (6 papers). Kathryn E. Hentges is often cited by papers focused on Congenital heart defects research (11 papers), RNA modifications and cancer (9 papers) and RNA Research and Splicing (6 papers). Kathryn E. Hentges collaborates with scholars based in United Kingdom, United States and France. Kathryn E. Hentges's co-authors include Monica J. Justice, Andrew S. Peterson, David L. Robertson, Paolo Sassone‐Corsi, Elena Zanaria, Giovanna Camerino, Amanda Swain, Robin Lovell‐Badge, K L Parker and Enzo Lalli and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Journal of Immunology.

In The Last Decade

Kathryn E. Hentges

40 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kathryn E. Hentges United Kingdom 17 895 457 75 74 73 41 1.2k
Jean‐Pierre Desvignes France 17 603 0.7× 324 0.7× 48 0.6× 72 1.0× 52 0.7× 31 1.0k
Toshiyuki Kobayashi Japan 18 720 0.8× 265 0.6× 64 0.9× 67 0.9× 36 0.5× 48 1.2k
Yacine Chérifi France 11 825 0.9× 282 0.6× 65 0.9× 71 1.0× 34 0.5× 21 1.0k
Mikiko Fukuda Japan 7 2.0k 2.2× 400 0.9× 41 0.5× 95 1.3× 23 0.3× 9 2.2k
Arnaud Krebs Switzerland 18 2.0k 2.2× 339 0.7× 48 0.6× 157 2.1× 25 0.3× 27 2.2k
Naihong Yan China 17 611 0.7× 151 0.3× 49 0.7× 38 0.5× 128 1.8× 56 1.1k
Anne Harrington United States 13 1.1k 1.2× 289 0.6× 69 0.9× 102 1.4× 34 0.5× 20 1.5k
Evica Rajcan‐Separovic Canada 24 775 0.9× 770 1.7× 79 1.1× 178 2.4× 24 0.3× 58 1.6k
Bernd Dworniczak Germany 18 1.2k 1.3× 1.1k 2.4× 48 0.6× 74 1.0× 206 2.8× 38 1.5k

Countries citing papers authored by Kathryn E. Hentges

Since Specialization
Citations

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

Fields of papers citing papers by Kathryn E. Hentges

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kathryn E. Hentges. 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 Kathryn E. Hentges. The network helps show where Kathryn E. Hentges may publish in the future.

Co-authorship network of co-authors of Kathryn E. Hentges

This figure shows the co-authorship network connecting the top 25 collaborators of Kathryn E. Hentges. A scholar is included among the top collaborators of Kathryn E. Hentges 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 Kathryn E. Hentges. Kathryn E. Hentges 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.
Hartill, Verity, M. Shahjahan Kabir, Sunayna Best, et al.. (2024). Molecular diagnoses and candidate gene identification in the congenital heart disease cohorts of the 100,000 genomes project. European Journal of Human Genetics. 33(6). 793–802. 1 indexed citations
2.
Qureshi, Wasay Mohiuddin Shaikh & Kathryn E. Hentges. (2023). Functions of cilia in cardiac development and disease. Annals of Human Genetics. 88(1). 4–26. 3 indexed citations
3.
Kabir, M. Shahjahan, Helen M. Stuart, Filipa M. Lopes, et al.. (2023). Predicting congenital renal tract malformation genes using machine learning. Scientific Reports. 13(1). 13204–13204. 1 indexed citations
4.
Hentges, Kathryn E., et al.. (2022). Genetic insights into non-syndromic Tetralogy of Fallot. Frontiers in Physiology. 13. 1012665–1012665. 12 indexed citations
5.
O’Keefe, Raymond T., et al.. (2021). The role of splicing factors in retinitis pigmentosa: links to cilia. Biochemical Society Transactions. 49(3). 1221–1231. 5 indexed citations
6.
Clowes, Christopher, Samantha C. Lean, Yinhui Lu, et al.. (2020). A missense mutation of ErbB2 produces a novel mouse model of stillbirth associated with a cardiac abnormality but lacking abnormalities of placental structure. PLoS ONE. 15(6). e0233007–e0233007. 1 indexed citations
7.
Villeneuve, Louis, et al.. (2020). Filamentous nestin and nonmuscle myosin IIB are associated with a migratory phenotype in neonatal rat cardiomyocytes. Journal of Cellular Physiology. 236(2). 1281–1294. 7 indexed citations
8.
Kabir, M. Shahjahan, et al.. (2019). The Essentiality Status of Mouse Duplicate Gene Pairs Correlates with Developmental Co-Expression Patterns. Scientific Reports. 9(1). 3224–3224. 6 indexed citations
9.
Kabir, M. Shahjahan, et al.. (2018). Identifying mouse developmental essential genes using machine learning. Disease Models & Mechanisms. 11(12). 13 indexed citations
10.
Kabir, M. Shahjahan, Ana Barradas, George T. Tzotzos, Kathryn E. Hentges, & Andrew J. Doig. (2017). Properties of genes essential for mouse development. PLoS ONE. 12(5). e0178273–e0178273. 17 indexed citations
11.
Burgess, Matthew, et al.. (2016). Enforced Expression of Hoxa3 Inhibits Classical and Promotes Alternative Activation of Macrophages In Vitro and In Vivo. The Journal of Immunology. 197(3). 872–884. 22 indexed citations
12.
Hentges, Kathryn E., et al.. (2016). Zfp521 promotes B-cell viability and cyclin D1 gene expression in a B cell culture system. Leukemia Research. 46. 10–17. 8 indexed citations
13.
Tenin, Gennadiy, Christopher Clowes, Eliška Krejčí, et al.. (2014). Erbb2 Is Required for Cardiac Atrial Electrical Activity during Development. PLoS ONE. 9(9). e107041–e107041. 7 indexed citations
14.
Dickerson, Jonathan E., Ana Zhu, David L. Robertson, & Kathryn E. Hentges. (2011). Defining the Role of Essential Genes in Human Disease. PLoS ONE. 6(11). e27368–e27368. 69 indexed citations
15.
Hentges, Kathryn E.. (2011). Mediator complex proteins are required for diverse developmental processes. Seminars in Cell and Developmental Biology. 22(7). 769–775. 14 indexed citations
16.
Kamp, Anna, Michael Peterson, Karen L. Svenson, et al.. (2010). Genome-wide identification of mouse congenital heart disease loci. Human Molecular Genetics. 19(16). 3105–3113. 15 indexed citations
17.
Clowes, Christopher, et al.. (2010). The Mediator complex protein Med31 is required for embryonic growth and cell proliferation during mammalian development. Developmental Biology. 342(2). 146–156. 23 indexed citations
18.
Lovell, Simon C., et al.. (2009). Correlation of microsynteny conservation and disease gene distribution in mammalian genomes. BMC Genomics. 10(1). 521–521. 4 indexed citations
19.
Liu, Bin, Gwenn M. Hansen, Darlene G. Skapura, et al.. (2007). Retroviral insertions in the VISION database identify molecular pathways in mouse lymphoid leukemia and lymphoma. Mammalian Genome. 18(10). 709–722. 12 indexed citations
20.
Hentges, Kathryn E., et al.. (2002). Tnfrsf13c (Baffr) is Mis-expressed in Tumors with Murine Leukemia Virus Insertions at Lvis22. Genomics. 80(2). 204–212. 5 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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