Marlies Kempers

6.3k total citations
53 papers, 2.0k citations indexed

About

Marlies Kempers is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Marlies Kempers has authored 53 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 19 papers in Endocrinology, Diabetes and Metabolism and 16 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Marlies Kempers's work include Connective tissue disorders research (15 papers), Thyroid Disorders and Treatments (14 papers) and Aortic Disease and Treatment Approaches (9 papers). Marlies Kempers is often cited by papers focused on Connective tissue disorders research (15 papers), Thyroid Disorders and Treatments (14 papers) and Aortic Disease and Treatment Approaches (9 papers). Marlies Kempers collaborates with scholars based in Netherlands, Belgium and United Kingdom. Marlies Kempers's co-authors include Jan J. M. de Vijlder, A S Paul van Trotsenburg, Thomas Vulsma, Brenda M. Wiedijk, Frank Baas, Carrie Ris‐Stalpers, Hennie Bikker, J.C. Moreno, T. Vulsma and David A. van Tijn and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Annals of Internal Medicine.

In The Last Decade

Marlies Kempers

51 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marlies Kempers Netherlands	24	1.1k	537	496	455	411	53	2.0k
Sonir Roberto Rauber Antonini Brazil	24	606 0.6×	224 0.4×	494 1.0×	423 0.9×	124 0.3×	98	1.7k
Graziella Pinto France	26	873 0.8×	717 1.3×	1.0k 2.0×	324 0.7×	126 0.3×	65	2.1k
Zoran Gucev North Macedonia	19	805 0.7×	417 0.8×	820 1.7×	252 0.6×	318 0.8×	111	2.0k
Arpad von Moers Germany	22	742 0.7×	533 1.0×	1.1k 2.3×	292 0.6×	159 0.4×	58	2.3k
Milton R. Brown United States	22	922 0.9×	434 0.8×	758 1.5×	351 0.8×	79 0.2×	41	1.9k
Katsuhiko Tachibana Japan	26	856 0.8×	638 1.2×	910 1.8×	283 0.6×	120 0.3×	78	2.3k
Johnny Deladoëy Canada	25	1.3k 1.2×	703 1.3×	701 1.4×	347 0.8×	150 0.4×	63	1.8k
Jürgen Klammt Germany	18	872 0.8×	569 1.1×	526 1.1×	222 0.5×	59 0.1×	62	1.6k
Katie A. Woods United Kingdom	15	1.5k 1.4×	735 1.4×	654 1.3×	209 0.5×	55 0.1×	29	2.3k
Anatoly Tiulpakov Russia	22	790 0.7×	454 0.8×	637 1.3×	229 0.5×	83 0.2×	131	1.5k

Countries citing papers authored by Marlies Kempers

Since Specialization

Citations

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

Fields of papers citing papers by Marlies Kempers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marlies Kempers

This figure shows the co-authorship network connecting the top 25 collaborators of Marlies Kempers. A scholar is included among the top collaborators of Marlies Kempers 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 Marlies Kempers. Marlies Kempers 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

Laar, Ingrid M.B.H. van de, Marieke J.H. Baars, Annette F. Baas, et al.. (2025). Pregnancy and Delivery Outcomes in Vascular Ehlers–Danlos Syndrome: A Retrospective Multicentre Cohort Study. BJOG An International Journal of Obstetrics & Gynaecology. 133(3). 463–470.

Oud, Manon S., Dominique Smeets, Liliana Ramos, et al.. (2024). Innovative all‐in‐one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10‐month experience. Andrology. 13(5). 1078–1092. 2 indexed citations

Pals, Gerard, Aeilko H. Zwinderman, Marieke J.H. Baars, et al.. (2022). Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships. American Journal of Medical Genetics Part A. 191(2). 479–489. 3 indexed citations

Laar, Ingrid M.B.H. van de, Annette F. Baas, Julie De Backer, et al.. (2022). Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN). European Journal of Medical Genetics. 65(9). 104557–104557. 8 indexed citations

Verhagen, Judith M.A., Jos A. Bekkers, Marlies Kempers, et al.. (2022). Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort. Genetics in Medicine. 24(10). 2112–2122. 3 indexed citations

Kempers, Marlies, Koenraad Devriendt, Luc De Catte, et al.. (2021). Two novel presentations of KCNMA1‐related pathology––Expanding the clinical phenotype of a rare channelopathy. Molecular Genetics & Genomic Medicine. 9(10). 5 indexed citations

Kempers, Marlies, et al.. (2021). Challenges in diagnosis and management of neonatal hyperparathyroidism in a resource-limited country: a case series from a Sudanese family. Pan African Medical Journal. 40. 105–105. 2 indexed citations

Bever, Yolande van, Hennie T. Brüggenwirth, Katja P. Wolffenbuttel, et al.. (2020). Under-reported aspects of diagnosis and treatment addressed in the Dutch-Flemish guideline for comprehensive diagnostics in disorders/differences of sex development. Journal of Medical Genetics. 57(9). 581–589. 10 indexed citations

Bijker, Else M., et al.. (2019). Sex Assignment and Diagnostics in Infants with Ambiguous Genitalia - A Single-Center Retrospective Study. Sexual Development. 13(3). 109–117. 5 indexed citations

10.

Hiatt, Susan M., Michelle L. Thompson, Jeremy W. Prokop, et al.. (2019). Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder. The American Journal of Human Genetics. 104(4). 701–708. 15 indexed citations

11.

Timmers, Henri, Catherine Pienkowski, Birgit Köhler, et al.. (2019). Karyotype - Phenotype Associations in Patients with Turner Syndrome.. PubMed. 16(4). 431–440. 17 indexed citations

12.

Duijnhouwer, Anthonie L., Livia Kapusta, Marlies Kempers, et al.. (2018). Phenotype in girls and women with Turner syndrome: Association between dysmorphic features, karyotype and cardio-aortic malformations. European Journal of Medical Genetics. 61(6). 301–306. 18 indexed citations

13.

Verhagen, Judith M.A., Marlies Kempers, Luc Cozijnsen, et al.. (2018). Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives. International Journal of Cardiology. 258. 243–248. 40 indexed citations

14.

Demirdas, Serwet, Leema Robert, Marlies Kempers, et al.. (2016). Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients. Clinical Genetics. 91(3). 411–425. 46 indexed citations

15.

Verkerk, P.H., J. J. Gera Hoorweg-Nijman, Wilma Oostdijk, et al.. (2014). [Neonatal screening for congenital hypothyroidism: more than 30 years of experience in the Netherlands].. PubMed. 158. A6564–A6564. 7 indexed citations

16.

Kimmenade, Roland R.J. van, Marlies Kempers, Menko‐Jan de Boer, Bart Loeys, & Janneke Timmermans. (2013). A clinical appraisal of different Z-score equations for aortic root assessment in the diagnostic evaluation of Marfan syndrome. Genetics in Medicine. 15(7). 528–532. 31 indexed citations

17.

Veer, Liesbeth van der Sluijs, et al.. (2012). Health- related quality of life and self-worth in 10-year old children with congenital hypothyroidism diagnosed by neonatal screening. Child and Adolescent Psychiatry and Mental Health. 6(1). 32–32. 11 indexed citations

18.

Eijsbouts, A M M, Marlies Kempers, Maria T. E. Hopman, et al.. (2008). Effect of naproxen on the hypothalamic–pituitary– adrenal axis in healthy volunteers. British Journal of Clinical Pharmacology. 67(1). 22–28. 5 indexed citations

19.

Kempers, Marlies, C.I. Lanting, Arno van Heijst, et al.. (2006). Neonatal Screening for Congenital Hypothyroidism Based on Thyroxine, Thyrotropin, and Thyroxine-Binding Globulin Measurement: Potentials and Pitfalls. The Journal of Clinical Endocrinology & Metabolism. 91(9). 3370–3376. 73 indexed citations

20.

Moreno, J.C., Hennie Bikker, Marlies Kempers, et al.. (2002). Inactivating Mutations in the Gene for Thyroid Oxidase 2 (THOX2) and Congenital Hypothyroidism. New England Journal of Medicine. 347(2). 95–102. 351 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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