Yolande van Bever

2.1k total citations
46 papers, 871 citations indexed

About

Yolande van Bever is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Yolande van Bever has authored 46 papers receiving a total of 871 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 19 papers in Genetics and 14 papers in Surgery. Recurrent topics in Yolande van Bever's work include Urological Disorders and Treatments (9 papers), Sexual Differentiation and Disorders (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Yolande van Bever is often cited by papers focused on Urological Disorders and Treatments (9 papers), Sexual Differentiation and Disorders (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Yolande van Bever collaborates with scholars based in Netherlands, Belgium and Brazil. Yolande van Bever's co-authors include K. Madan, Aggie Nieuwint, Dick Tibboel, Stefaan Scheers, R. Frank Kooy, Liesbeth Rooms, Rob van Luijk, Edwin Reyniers, J. Wauters and René Wijnen and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

Yolande van Bever

45 papers receiving 827 citations

Peers

Countries citing papers authored by Yolande van Bever

Since Specialization

Citations

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

Fields of papers citing papers by Yolande van Bever

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yolande van Bever. 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 Yolande van Bever. The network helps show where Yolande van Bever may publish in the future.

Co-authorship network of co-authors of Yolande van Bever

This figure shows the co-authorship network connecting the top 25 collaborators of Yolande van Bever. A scholar is included among the top collaborators of Yolande van Bever 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 Yolande van Bever. Yolande van Bever 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	Functional analysis of SRY variants in individuals with 46,XY differences of sex development 2025 ·Molecular and Cellular Endocrinology ·(unknown), Jocelyn van den Bergen, Gorjana Robevska, (unknown), (unknown), Marina M. L. Kizys, Magnus R. Dias‐da‐Silva, Hennie T. Brüggenwirth, Yolande van Bever, Andrew Sinclair, Katie Ayers	0
2	Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome 2023 ·Human Mutation ·Hannie Douben, Marianne Hoogeveen‐Westerveld, Mark Nellist, (unknown), (unknown), (unknown), (unknown), Leontine van Unen, Peter Elfferich, (unknown), Yolande van Bever, Margreethe van Vliet, Rianne Oostenbrink, Jasper J. Saris, Anja Wagner, Yvette van Ierland, Tjakko J. van Ham, Rick van Minkelen	2
3	Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development: a cross-sectional study 2023 ·European Journal of Endocrinology ·Martine Cools, (unknown), (unknown), Simon J. Tavernier, Petra Schelstraete, (unknown), (unknown), Elfride De Baere, Carolien Bonroy, Yolande van Bever, Hennie T. Brüggenwirth, (unknown), Sabine E Hannema, Yolanda B. de Rijke, (unknown), David Zangen, Hannah Verdin, Filomeen Haerynck	4
4	Undetectable anti‐Mullerian hormone and inhibin B do not preclude the presence of germ cell tumours in 45,X/46,XY or 46,XY gonadal dysgenesis 2023 ·Clinical Endocrinology ·Sabine E Hannema, Katja P. Wolffenbuttel, Yolande van Bever, Hennie T. Brüggenwirth, Sjoerd A.A. van den Berg, Remko Hersmus, J. Wolter Oosterhuis, Leendert H. J. Looijenga	1
5	Clinical Relevance of Rapid FOXF1-Targeted Sequencing in Patients Suspected of Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins 2023 ·Laboratory Investigation ·(unknown), Janna A. Hol, (unknown), Jan H. von der Thüsen, Yolande van Bever, Rogier C.J. de Jonge, Marianne van Tienhoven, Hennie T. Brüggenwirth, Annelies de Klein, Robbert J. Rottier	3
6	WDR37 syndrome: identification of a distinct new cluster of disease-associated variants and functional analyses of mutant proteins 2021 ·Human Genetics ·Елена А. Сорокина, Linda M. Reis, (unknown), Katherine Agre, Dusica Babovic‐Vuksanovic, Marissa S. Ellingson, Linda Hasadsri, Yolande van Bever, Elena V. Semina	6
7	Early prenatal disruption; a foetus with features of severe limb body wall sequence, body stalk anomaly and amniotic bands. 2014 ·Data Archiving and Networked Services (DANS) ·Sandra Ventorin von Zeidler, (unknown), (unknown), Yolande van Bever	6
8	An unusual presentation of Kabuki syndrome: Clinical overlap with CHARGE syndrome 2014 ·European Journal of Medical Genetics ·Judith M.A. Verhagen, Wilma Oostdijk, (unknown), Nicoline E. Schalij‐Delfos, Yolande van Bever	22
9	Clinical and etiological heterogeneity in patients with tracheo-esophageal malformations and associated anomalies 2014 ·European Journal of Medical Genetics ·Erwin Brosens, (unknown), Yolande van Bever, Anna E. Koopmans, Hanneke IJsselstijn, Robbert J. Rottier, René Wijnen, Dick Tibboel, Annelies de Klein	52
10	A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family 2012 ·European Journal of Human Genetics ·Jeroen Knijnenburg, Yolande van Bever, Lorette O. M. Hulsman, (unknown), (unknown), Rosa Laura E. van Loon, H. Berna Beverloo, Laura J. C. M. van Zutven	33
11	VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations 2012 ·Molecular Syndromology ·Erwin Brosens, H. J. Eussen, Yolande van Bever, R.M. van der Helm, Hanneke IJsselstijn, Hitisha P. Zaveri, René Wijnen, Daryl A. Scott, Dick Tibboel, Annelies de Klein	22
12	Homozygous Inactivating Mutations in the NKX3-2 Gene Result in Spondylo-Megaepiphyseal-Metaphyseal Dysplasia 2009 ·The American Journal of Human Genetics ·Jan Hellemans, Marleen Simon, Annelies Dheedene, Yasemin Alanay, Ercan Mıhçı, (unknown), Abdelaziz Sefiani, Yolande van Bever, M. Meradji, Andrea Superti‐Furga, Geert Mortier	28
13	Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): A patient report and review 2009 ·American Journal of Medical Genetics Part A ·Laura J. C. M. van Zutven, Yolande van Bever, (unknown), (unknown), Diane Van Opstal, Anne R. M. von Bergh, (unknown), Dick Tibboel, Carine Wouters, Pino J. Poddighe	12
14	Exclusion of a PAX6, FOXC1, PITX2, and MYCN mutation in another patient with apple peel intestinal atresia, ocular anomalies and microcephaly and review of the literature 2008 ·American Journal of Medical Genetics Part A ·Yolande van Bever, (unknown), Roger C. W. Wolfs, Dick Tibboel, Thelma L. van den Hoonaard, Saskia J. Gischler	13
15	Exclusion of OGDH and BMP4 as candidate genes in two siblings with autosomal recessive DOOR syndrome 2007 ·American Journal of Medical Genetics Part A ·Yolande van Bever, Wendy Balemans, E Duval, (unknown), François Eyskens, Wim Van Hul, Winnie Courtens	5
16	Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype 2005 ·American Journal of Medical Genetics Part A ·Yolande van Bever, Liesbeth Rooms, Annick Laridon, Edwin Reyniers, Rob van Luijk, Stefaan Scheers, J. Wauters, R. Frank Kooy	49
17	Waardenburg syndrome: Clinical differentiation between types I and II 2003 ·American Journal of Medical Genetics Part A ·(unknown), Yolande van Bever, Jenneke van den Ende, (unknown), Paula Iughetti, (unknown), Orozimbo Alves Costa Filho, Antônio Richieri‐Costa, Oswaldo Frota‐Pessoa, Paulo Alberto Otto	41
18	Haspeslagh syndrome without severe mental retardation and pterygia? 1995 ·Clinical Genetics ·Yolande van Bever, Raoul C. M. Hennekam	1
19	The oav - spectrum and associated anomalies in 77 patients 1993 ·Revista brasileira de genetica ·Yolande van Bever, (unknown), A. Richieri‐Costa	1
20	Marden‐Walker‐like syndrome without psychomotor retardation: Report of a Brazilian girl born to consanguineous parents 1992 ·American Journal of Medical Genetics ·(unknown), Yolande van Bever, (unknown), A. Richieri‐Costa	18

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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