Leo P. ten Kate

5.9k total citations
137 papers, 3.3k citations indexed

About

Leo P. ten Kate is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Leo P. ten Kate has authored 137 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 46 papers in Pediatrics, Perinatology and Child Health and 37 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Leo P. ten Kate's work include Cystic Fibrosis Research Advances (33 papers), Prenatal Screening and Diagnostics (31 papers) and BRCA gene mutations in cancer (20 papers). Leo P. ten Kate is often cited by papers focused on Cystic Fibrosis Research Advances (33 papers), Prenatal Screening and Diagnostics (31 papers) and BRCA gene mutations in cancer (20 papers). Leo P. ten Kate collaborates with scholars based in Netherlands, United States and Germany. Leo P. ten Kate's co-authors include Lidewij Henneman, Martina C. Cornel, Gerrit van der Wal, Marieke J.H. Baars, Daniëlle R. M. Timmermans, Matthijs van den Berg, J. M. G. van Vugt, Gerard J. te Meerman, Gerard Pals and Jan G. Aarnoudse and has published in prestigious journals such as Cancer, Annals of the New York Academy of Sciences and Kidney International.

In The Last Decade

Leo P. ten Kate

133 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leo P. ten Kate Netherlands 34 1.1k 1.1k 655 602 437 137 3.3k
Gad Barkai Israel 33 1.6k 1.4× 742 0.7× 314 0.5× 564 0.9× 655 1.5× 122 3.6k
P. Cox United Kingdom 34 1.5k 1.3× 419 0.4× 385 0.6× 575 1.0× 396 0.9× 99 3.1k
Jaime L. Frías United States 34 689 0.6× 1.4k 1.3× 258 0.4× 816 1.4× 287 0.7× 119 3.3k
Deborah E. McFadden Canada 33 1.7k 1.5× 1.0k 0.9× 783 1.2× 1.4k 2.4× 724 1.7× 79 3.9k
Karin J. Blakemore United States 28 1.3k 1.2× 565 0.5× 213 0.3× 299 0.5× 425 1.0× 162 2.7k
Frank Louwen Germany 35 1.1k 1.0× 327 0.3× 443 0.7× 920 1.5× 600 1.4× 196 4.0k
Diego F. Wyszynski United States 35 1.2k 1.1× 1.4k 1.2× 170 0.3× 643 1.1× 818 1.9× 101 4.2k
Norman D. Rosenblum Canada 42 1.1k 1.0× 1.2k 1.1× 862 1.3× 2.8k 4.7× 581 1.3× 150 5.2k
Mark I. Evans United States 36 4.0k 3.5× 763 0.7× 498 0.8× 666 1.1× 996 2.3× 309 5.6k
B. Modell United Kingdom 32 1.4k 1.3× 755 0.7× 209 0.3× 383 0.6× 267 0.6× 81 3.7k

Countries citing papers authored by Leo P. ten Kate

Since Specialization
Citations

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

Fields of papers citing papers by Leo P. ten Kate

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leo P. ten Kate. 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 Leo P. ten Kate. The network helps show where Leo P. ten Kate may publish in the future.

Co-authorship network of co-authors of Leo P. ten Kate

This figure shows the co-authorship network connecting the top 25 collaborators of Leo P. ten Kate. A scholar is included among the top collaborators of Leo P. ten Kate 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 Leo P. ten Kate. Leo P. ten Kate 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.
Kate, Leo P. ten. (2012). Genetic risk. Journal of Community Genetics. 3(3). 159–166. 4 indexed citations
2.
Borry, Pascal, Lidewij Henneman, Phillis Lakeman, et al.. (2011). Preconceptional genetic carrier testing and the commercial offer directly-to-consumers. Human Reproduction. 26(5). 972–977. 63 indexed citations
3.
Challen, Kirsty, Hilary Harris, Ulf Kristoffersson, et al.. (2010). General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices. Journal of Community Genetics. 1(2). 83–90. 6 indexed citations
4.
Kate, Leo P. ten, Lihadh Al‐Gazali, Sonia S. Anand, et al.. (2010). Community genetics. Its definition 2010. Journal of Community Genetics. 1(1). 19–22. 17 indexed citations
5.
Plass, Anne Marie, Marieke J.H. Baars, Martina C. Cornel, et al.. (2009). Testing the Children: Do Non-Genetic Health-Care Providers Differ in Their Decision to Advise Genetic Presymptomatic Testing on Minors? A Cross-Sectional Study in Five Countries in the European Union. Genetic Testing and Molecular Biomarkers. 13(3). 367–376. 6 indexed citations
6.
Lakeman, Phillis, Gilles Thomas, J.E. Dankert-Roelse, et al.. (2008). CFTR Mutations in Turkish and North African Cystic Fibrosis Patients in Europe: Implications for Screening. Genetic Testing. 12(1). 25–35. 13 indexed citations
7.
Berg, Matthijs van den, Daniëlle R. M. Timmermans, Leo P. ten Kate, J. M. G. van Vugt, & Gerrit van der Wal. (2005). Informed decision making in the context of prenatal screening. Patient Education and Counseling. 63(1-2). 110–117. 127 indexed citations
8.
Wildhagen, Mark F., et al.. (2005). Preconception Cystic Fibrosis Carrier Screening: Costs and Consequences. Genetic Testing. 9(2). 158–166. 11 indexed citations
9.
Challen, Kirsty, Hilary Harris, Claire Julian‐Reynier, et al.. (2005). Genetic education and nongenetic health professionals: Educational providers and curricula in Europe. Genetics in Medicine. 7(5). 302–310. 32 indexed citations
10.
Poppelaars, Francis A.M., Lidewij Henneman, Herman J. Adèr, et al.. (2004). Preconceptional Cystic Fibrosis Carrier Screening: Attitudes and Intentions of the Target Population. Genetic Testing. 8(2). 80–89. 34 indexed citations
11.
Baars, Marieke J.H., Lidewij Henneman, & Leo P. ten Kate. (2004). Preconceptional Cystic Fibrosis Carrier Screening: Opinions of General Practitioners, Gynecologists, and Pediatricians in the Netherlands. Genetic Testing. 8(4). 431–436. 11 indexed citations
12.
Poppelaars, Francis A.M., Gerrit van der Wal, Jozé Braspenning, et al.. (2003). Possibilities and barriers in the implementation of a preconceptional screening programme for cystic fibrosis carriers: a focus group study. Public Health. 117(6). 396–403. 32 indexed citations
13.
Lachmeijer, Augusta M.A., et al.. (2002). Searching for preeclampsia genes: the current position. European Journal of Obstetrics & Gynecology and Reproductive Biology. 105(2). 94–113. 118 indexed citations
14.
Henneman, Lidewij, Inge Bramsen, Henk M. van der Ploeg, & Leo P. ten Kate. (2002). Preconception Cystic Fibrosis Carrier Couple Screening: Impact, Understanding, and Satisfaction. Genetic Testing. 6(3). 195–202. 41 indexed citations
15.
Kate, Leo P. ten, et al.. (2000). Community Genetics in The Netherlands. Public Health Genomics. 3(3). 131–133. 3 indexed citations
16.
17.
Cobben, Jan M., Hans Scheffer, Marjolein Visser, et al.. (1993). Linkage and apparent heterogeneity in proximal spinal muscular atrophies. Neuromuscular Disorders. 3(4). 327–333. 8 indexed citations
18.
Plukker, John Th. M., Heimen Schraffordt Koops, Ineke Molenaar, et al.. (1988). Malignant hemangiopericytoma in three kindred members of one family. Cancer. 61(4). 841–844. 15 indexed citations
19.
Dankert-Roelse, J.E., Gerard J. te Meerman, K Knol, & Leo P. ten Kate. (1987). Effect of screening for cystic fibrosis on the influence of genetic counseling. Clinical Genetics. 32(4). 271–275. 15 indexed citations
20.
Nauta, Maarten, et al.. (1987). Family Distances and Human Lymphocyte Antigens. Human Heredity. 37(6). 359–364. 17 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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