Merel C. van Maarle

2.2k citations

29 papers · 788 indexed · h-index 16

Pediatrics, Perinatology and Child Health top 5%
Genetics top 10%
Public Health, Environmental and Occupational Health top 10%
Molecular Biology
Immunology

Co-authors: Mariëtte Goddijn Merel M. J. van den Berg Madelon van Wely Lidewij Henneman E. Redeker Marlies E. A. Stouthard Gouke J. Bonsel Eva Pajkrt
Topics: Prenatal Screening and Diagnostics (9 papers)Lipoproteins and Cardiovascular Health (5 papers)Congenital Anomalies and Fetal Surgery (4 papers)
Cited by: Pediatrics, Perinatology and Child Health Genetics Geriatrics and Gerontology
Journals: Genes & Development Journal of Bone and Mineral Research Atherosclerosis
Partner nations: Netherlands United States Denmark

In The Last Decade

Merel C. van Maarle

29 papers receiving 771 citations

Peers

Countries citing papers authored by Merel C. van Maarle

Since Specialization

Citations

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

Fields of papers citing papers by Merel C. van Maarle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Merel C. van Maarle. 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 Merel C. van Maarle. The network helps show where Merel C. van Maarle may publish in the future.

Co-authorship network of co-authors of Merel C. van Maarle

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Phenotype‐to‐Genotype Description of Prenatal Suspected and Postnatal Discovered Upper Limb Anomalies: A Retrospective Cohort Study 2024 ·Prenatal Diagnosis ·(unknown),Sandra van Dijk,(unknown),(unknown),Ingeborg H. Linskens,Elisabeth van Leeuwen,Merel C. van Maarle,Eva Pajkrt	2
2	Efficacy and Toxicity of Calcitonin Treatment in Children with Cherubism: A Single-Center Cohort Study 2023 ·Journal of Bone and Mineral Research ·Willem H. Schreuder,(unknown),Arjen H.G. Cleven,(unknown),(unknown),Ruud Schreurs,Renate T. de Jongh,Merel C. van Maarle,(unknown),Jan de Lange,Henk van den Berg	1
3	Counseling couples at risk of having a child with homozygous familial hypercholesterolemia – Clinical experience and recommendations 2022 ·Journal of clinical lipidology ·Tycho R. Tromp,M. Doortje Reijman,Albert Wiegman,G. Kees Hovingh,Joep C. Defesche,Merel C. van Maarle,Inge B. Mathijssen	2
4	Distal muscle weakness and optic atrophy without central nervous system involvement in a patient with a homozygous missense mutation in the C19ORF12-gene 2021 ·Clinical Neurology and Neurosurgery ·Reinier J. de Vries,Bregje Jaeger,Debby M.E.I. Hellebrekers,Liesbeth Reneman,Anne Verhamme,Hubert J.M. Smeets,Merel C. van Maarle,Marjolein Visser,Fonnet E. Bleeker	1
5	Mosaic maternal 10qter deletions are associated with FRA10B expansions and may cause false-positive noninvasive prenatal screening results 2018 ·Genetics in Medicine ·Karin Huijsdens–van Amsterdam,Roy Straver,Merel C. van Maarle,Alida C. Knegt,Diane Van Opstal,Frank Sleutels,Dominique Smeets,Erik A. Sistermans	13
6	Preconception carrier screening for multiple disorders: evaluation of a screening offer in a Dutch founder population 2018 ·European Journal of Human Genetics ·Inge B. Mathijssen,(unknown),(unknown),(unknown),Phillis Lakeman,Hanne Meijers‐Heijboer,Merel C. van Maarle,Lidewij Henneman	22
7	An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality 2018 ·Genes & Development ·Christina M. Ferrer,Mariëlle Alders,Alex V. Postma,(unknown),Mark A. Klein,Murat Çetinbaş,Eva Pajkrt,(unknown),Silvana van Koningsbruggen,Vincent M. Christoffels,Marcel M. A. M. Mannens,(unknown),Jean‐Pierre Etchegaray,Ruslan I. Sadreyev,John M. Denu,Gustavo Mostoslavsky,Merel C. van Maarle,Raúl Mostoslavsky	34
8	With expanded carrier screening, founder populations run the risk of being overlooked 2017 ·Journal of Community Genetics ·Inge B. Mathijssen,Merel C. van Maarle,(unknown),E. Redeker,Leo P. ten Kate,Lidewij Henneman,Hanne Meijers‐Heijboer	9
9	Women's Experience with Non‐Invasive Prenatal Testing and Emotional Well‐being and Satisfaction after Test‐Results 2017 ·Journal of Genetic Counseling ·Rachèl V. van Schendel,Godelieve C.M.L. Page‐Christiaens,Lean Beulen,Caterina M. Bilardo,Marjon A. de Boer,A. Coumans,Brigitte H. W. Faas,Irene M. van Langen,Klaske D. Lichtenbelt,Merel C. van Maarle,Merryn Macville,Dick Oepkes,Eva Pajkrt,Lidewij Henneman	37
10	Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part II—women's perspectives 2016 ·Prenatal Diagnosis ·Rachèl V. van Schendel,Godelieve C.M.L. Page‐Christiaens,Lean Beulen,Catia M. Bilardo,Marjon A. de Boer,A. Coumans,Brigitte H. W. Faas,Irene M. van Langen,Klaske D. Lichtenbelt,Merel C. van Maarle,Merryn Macville,Dick Oepkes,Eva Pajkrt,Lidewij Henneman	55
11	Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives: Table 1 2016 ·European Journal of Public Health ·(unknown),Inge B. Mathijssen,Phillis Lakeman,Merel C. van Maarle,Wybo Dondorp,Lidewij Henneman,Martina C. Cornel	25
12	Targeted carrier screening for four recessive disorders: High detection rate within a founder population 2015 ·European Journal of Medical Genetics ·Inge B. Mathijssen,Lidewij Henneman,(unknown),Phillis Lakeman,(unknown),E. Redeker,(unknown),Hanne Meijers‐Heijboer,Merel C. van Maarle	23
13	A Dutch family with autosomal recessively inherited lower motor neuron predominant motor neuron disease due to optineurin mutations 2015 ·Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Emma Beeldman,Anneke J. van der Kooi,Marianne de Visser,Merel C. van Maarle,Fred van Ruissen,Frank Baas	15
14	A new mutation for Huntington disease following maternal transmission of an intermediate allele 2014 ·European Journal of Medical Genetics ·Alicia Semaka,Chris Kay,(unknown),Emilia K. Bijlsma,Monique Losekoot,Irene M. van Langen,Merel C. van Maarle,Mayke Oosterloo,Michael R. Hayden,Martine J. van Belzen	10
15	Genetics of early miscarriage 2012 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Merel M. J. van den Berg,Merel C. van Maarle,Madelon van Wely,Mariëtte Goddijn	192
16	Genotype–phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysis 2009 ·Journal of Medical Genetics ·Yvonne J. Vos,Hermien E. K. de Walle,(unknown),Arjan Stegeman,(unknown),Monique J. Bruining,Merel C. van Maarle,Mariet W. Elting,Nicolette S. den Hollander,B Hamel,Ana María Fortuna,Lone Sunde,Irene Stolte‐Dijkstra,C. T. R. M. Schrander‐Stumpel,Robert M.W. Hofstra	61
17	DNA analysis of the SH3BP2 gene in patients with aggressive central giant cell granuloma 2006 ·British Journal of Oral and Maxillofacial Surgery ·Jan de Lange,Merel C. van Maarle,Hans P. van den Akker,E. Redeker	23
18	Risk perception of participants in a family‐based genetic screening program on familial hypercholesterolemia 2002 ·American Journal of Medical Genetics Part A ·Merel C. van Maarle,Marlies E. A. Stouthard,Gouke J. Bonsel	17
19	Follow up after a family based genetic screening programme for familial hypercholesterolaemia: is screening alone enough? 2002 ·BMJ ·Merel C. van Maarle,(unknown),(unknown),(unknown),(unknown)	10
20	How Disturbing Is It to Be Approached for a Genetic Cascade Screening Programme for Familial Hypercholesterolaemia? 2001 ·Public Health Genomics ·Merel C. van Maarle,Marlies E. A. Stouthard,(unknown),Niek Klazinga,Gouke J. Bonsel	49

About Merel C. van Maarle

Merel C. van Maarle is a scholar working on Developmental Biology, Aging and Pediatrics, Perinatology and Child Health, having authored 29 papers that have together received 788 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (9 papers), Lipoproteins and Cardiovascular Health (5 papers) and Congenital Anomalies and Fetal Surgery (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (309 citations), Genetics (199 citations) and Geriatrics and Gerontology (27 citations). Merel C. van Maarle has collaborated with scholars based in Netherlands, United States and Denmark. Frequent co-authors include Mariëtte Goddijn, Merel M. J. van den Berg, Madelon van Wely, Lidewij Henneman, E. Redeker, Marlies E. A. Stouthard, Gouke J. Bonsel, Eva Pajkrt, Phillis Lakeman and Hans P. van den Akker. Their work appears in journals such as Genes & Development, Journal of Bone and Mineral Research and Atherosclerosis.

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.

Explore authors with similar magnitude of impact