Marlies Kempers

6.3k citations

53 papers · 2.0k indexed · h-index 24

Endocrinology, Diabetes and Metabolism top 1%
Genetics top 5%
Molecular Biology
Surgery top 10%
Pulmonary and Respiratory Medicine top 5%

Co-authors: Jan J. M. de Vijlder A S Paul van Trotsenburg Thomas Vulsma Brenda M. Wiedijk Carrie Ris‐Stalpers Frank Baas J.C. Moreno Hennie Bikker
Topics: Connective tissue disorders research (15 papers)Thyroid Disorders and Treatments (14 papers)Aortic Disease and Treatment Approaches (9 papers)
Cited by: Endocrinology, Diabetes and Metabolism Endocrine and Autonomic Systems Genetics
Journals: New England Journal of Medicine Journal of Biological Chemistry Annals of Internal Medicine
Partner nations: Netherlands Belgium United Kingdom

In The Last Decade

Marlies Kempers

51 papers receiving 1.9k citations

Peers

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

#	Work	Indexed citations
1	Innovative all‐in‐one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10‐month experience 2024 ·Andrology ·Manon S. Oud,(unknown),Dominique Smeets,Liliana Ramos,Godfried W. van der Heijden,(unknown),Maartje van de Vorst,Tom Hofste,Marlies Kempers,Marijn F. Stokman,Kathleen D’Hauwers,Brigitte H. W. Faas,Dineke Westra	2
2	Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships 2022 ·American Journal of Medical Genetics Part A ·(unknown),Gerard Pals,Aeilko H. Zwinderman,(unknown),Marieke J.H. Baars,(unknown),Yvonne Hilhorst‐Hofstee,Arjan C. Houweling,Marlies Kempers,Ingrid P.C. Krapels,Ingrid M.B.H. van de Laar,Bart Loeys,(unknown),(unknown),Vivian de Waard,Jan M. Wit,Leonie A. Menke	3
3	Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN) 2022 ·European Journal of Medical Genetics ·Ingrid M.B.H. van de Laar,Annette F. Baas,Julie De Backer,(unknown),(unknown),(unknown),Arjan C. Houweling,Marlies Kempers,Bart Loeys,Fransiska Malfait,Leema Robert,George A. Tanteles,Michael Frank	8
4	Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort 2022 ·Genetics in Medicine ·(unknown),Judith M.A. Verhagen,Jos A. Bekkers,Marlies Kempers,Arjan C. Houweling,Marieke J.H. Baars,Eline Overwater,Yvonne Hilhorst‐Hofstee,Daniela Q.C.M. Barge‐Schaapveld,(unknown),Ingrid P.C. Krapels,(unknown),Marja W. Wessels,Bart Loeys,Hence J.M. Verhagen,Alessandra Maugeri,Jolien W. Roos‐Hesselink,Hennie T. Brüggenwirth,Ingrid M.B.H. van de Laar	3
5	Two novel presentations of KCNMA1‐related pathology––Expanding the clinical phenotype of a rare channelopathy 2021 ·Molecular Genetics & Genomic Medicine ·(unknown),(unknown),Marlies Kempers,(unknown),(unknown),Koenraad Devriendt,Luc De Catte,Marcella Baldewijns,Maaike Alaerts,Josephina Meester,Aline Verstraeten,(unknown),Bart Loeys	5
6	Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings 2021 ·International Journal of Molecular Sciences ·(unknown),Alice Krebsová,Birgitte Rode Diness,Steven Laga,(unknown),Marlies Kempers,Nilesh J. Samani,Tom R. Webb,(unknown),(unknown),(unknown),Ilse Luyckx,Nils Peeters,(unknown),Milan Maçek,Josephina Meester,Lut Van Laer,Aline Verstraeten,Bart Loeys	9
7	Sex Assignment and Diagnostics in Infants with Ambiguous Genitalia - A Single-Center Retrospective Study 2019 ·Sexual Development ·(unknown),Else M. Bijker,Barbara Kortmann,Marlies Kempers,Antonius E. van Herwaarden,(unknown),Hedi L. Claahsen‐van der Grinten	5
8	Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder 2019 ·The American Journal of Human Genetics ·Susan M. Hiatt,Michelle L. Thompson,Jeremy W. Prokop,James M.J. Lawlor,Stacy W. Gray,E. Martina Bebin,Tuula Rinne,Marlies Kempers,Rolph Pfundt,Bregje W.M. van Bon,Cyril Mignot,Caroline Nava,Christel Depienne,Louisa Kalsner,Anita Rauch,Pascal Joset,Ruxandra Bachmann‐Gagescu,Ingrid M. Wentzensen,Kirsty McWalter,Gregory M. Cooper	15
9	Phenotype in girls and women with Turner syndrome: Association between dysmorphic features, karyotype and cardio-aortic malformations 2018 ·European Journal of Medical Genetics ·(unknown),Anthonie L. Duijnhouwer,Livia Kapusta,Marlies Kempers,Nel Roeleveld,Michiel Schokking,Dominique Smeets,Kim Freriks,Henri Timmers,(unknown)	18
10	Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives 2018 ·International Journal of Cardiology ·Judith M.A. Verhagen,Marlies Kempers,Luc Cozijnsen,Berto J. Bouma,Anthonie L. Duijnhouwer,Jan G. Post,Yvonne Hilhorst‐Hofstee,Sebastiaan C.A.M. Bekkers,Wilhelmina S. Kerstjens‐Frederikse,Thomas J. van Brakel,(unknown),Marja W. Wessels,Bart Loeys,Jolien W. Roos‐Hesselink,Ingrid M.B.H. van de Laar	40
11	Mutations in N-acetylglucosamine (O-GlcNAc) transferase in patients with X-linked intellectual disability 2017 ·Journal of Biological Chemistry ·(unknown),Mehmet Gundogdu,Marlies Kempers,Jacques C. Giltay,Rolph Pfundt,Martin Elferink,(unknown),Joris Fuijkschot,Andrew T. Ferenbach,Koen L.I. van Gassen,Daan M. F. van Aalten,Dirk J. Lefeber	66
12	[Neonatal screening for congenital hypothyroidism: more than 30 years of experience in the Netherlands]. 2014 ·PubMed ·P.H. Verkerk,(unknown),J. J. Gera Hoorweg-Nijman,Wilma Oostdijk,David A. van Tijn,Marlies Kempers,(unknown),J.G. Loeber,L.H. Elvers,(unknown)	7
13	A clinical appraisal of different Z-score equations for aortic root assessment in the diagnostic evaluation of Marfan syndrome 2013 ·Genetics in Medicine ·Roland R.J. van Kimmenade,Marlies Kempers,Menko‐Jan de Boer,Bart Loeys,Janneke Timmermans	31
14	Myopathy in a 20‐year‐old female patient with D4ST‐1 deficient Ehlers‐Danlos syndrome due to a homozygous CHST14 mutation 2012 ·American Journal of Medical Genetics Part A ·Nicol C. Voermans,Marlies Kempers,Martin Lammens,Nens van Alfen,Mirian C. H. Janssen,C. Bönnemann,Baziel G.M. van Engelen,Ben C.J. Hamel	27
15	Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndrome 2011 ·Clinical Genetics ·Teodora Radonic,(unknown),Maarten Groenink,(unknown),Jean‐Pierre Timmermans,(unknown),Maarten P. van den Berg,(unknown),(unknown),Marlies Kempers,(unknown),(unknown)	40
16	Effect of naproxen on the hypothalamic–pituitary– adrenal axis in healthy volunteers 2008 ·British Journal of Clinical Pharmacology ·A M M Eijsbouts,Marlies Kempers,(unknown),Maria T. E. Hopman,F.H.J. van den Hoogen,(unknown),Ad R. Hermus,Fred C.G.J. Sweep,Leo B. A. Van De Putte	5
17	Neonatal Screening for Congenital Hypothyroidism Based on Thyroxine, Thyrotropin, and Thyroxine-Binding Globulin Measurement: Potentials and Pitfalls 2006 ·The Journal of Clinical Endocrinology & Metabolism ·Marlies Kempers,C.I. Lanting,Arno van Heijst,A S Paul van Trotsenburg,Brenda M. Wiedijk,Jan J. M. de Vijlder,T. Vulsma	73
18	The Effect of Life-long Thyroxine Treatment and Physical Activity on Bone Mineral Density in Young Adult Women with Congenital Hypothyroidism 2006 ·Journal of Pediatric Endocrinology and Metabolism ·Marlies Kempers,T. Vulsma,Brenda M. Wiedijk,Jan J. M. de Vijlder,Berthe L.F. van Eck‐Smit,Hein J. Verberne	5
19	Inactivating Mutations in the Gene for Thyroid Oxidase 2 (THOX2) and Congenital Hypothyroidism 2002 ·New England Journal of Medicine ·J.C. Moreno,Hennie Bikker,Marlies Kempers,A S Paul van Trotsenburg,Frank Baas,Jan J. M. de Vijlder,Thomas Vulsma,Carrie Ris‐Stalpers	351
20	Can GnRH Agonist Treatment Cause Slipped Capital Femoral Epiphysis? 2001 ·Journal of Pediatric Endocrinology and Metabolism ·Marlies Kempers,C. Noordam,C. Rouwé,B.J. Otten	12

About Marlies Kempers

Marlies Kempers is a scholar working on Endocrinology, Diabetes and Metabolism, Endocrine and Autonomic Systems and Genetics, having authored 53 papers that have together received 2.0k indexed citations. Recurring topics across this work include Connective tissue disorders research (15 papers), Thyroid Disorders and Treatments (14 papers) and Aortic Disease and Treatment Approaches (9 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.1k citations), Endocrine and Autonomic Systems (170 citations) and Genetics (537 citations). Marlies Kempers has collaborated with scholars based in Netherlands, Belgium and United Kingdom. Frequent co-authors include Jan J. M. de Vijlder, A S Paul van Trotsenburg, Thomas Vulsma, Brenda M. Wiedijk, Carrie Ris‐Stalpers, Frank Baas, J.C. Moreno, Hennie Bikker, T. Vulsma and David A. van Tijn. Their work appears in journals such as New England Journal of Medicine, Journal of Biological Chemistry and Annals of Internal Medicine.

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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