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 — A (Enhanced Table)

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

Name	h						Papers	Cites
Yolande van Bever Netherlands	18	441	297	218	191	134	46	871
Mark J. Stephan United States	15	263 0.6×	279 0.9×	230 1.1×	131 0.7×	142 1.1×	23	762
James V. Higgins United States	18	414 0.9×	332 1.1×	241 1.1×	182 1.0×	52 0.4×	39	927
Marie‐France Portnoï France	19	574 1.3×	446 1.5×	71 0.3×	166 0.9×	57 0.4×	29	908
Anna Latos‐Bieleńska Poland	15	504 1.1×	501 1.7×	117 0.5×	76 0.4×	109 0.8×	50	895
Diana García‐Cruz Mexico	16	356 0.8×	272 0.9×	131 0.6×	112 0.6×	37 0.3×	81	727
Naomi Fitch Canada	22	585 1.3×	479 1.6×	262 1.2×	186 1.0×	81 0.6×	44	1.1k
R M Winter United Kingdom	14	402 0.9×	276 0.9×	165 0.8×	94 0.5×	60 0.4×	32	683
R. Sid Wilroy United States	21	778 1.8×	635 2.1×	166 0.8×	275 1.4×	60 0.4×	53	1.3k
Kosuke Izumi United States	19	635 1.4×	606 2.0×	169 0.8×	185 1.0×	145 1.1×	77	1.1k
Trijnie Dijkhuizen Netherlands	24	677 1.5×	801 2.7×	127 0.6×	201 1.1×	382 2.9×	62	1.6k

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

Bergen, Jocelyn van den, Gorjana Robevska, Marina M. L. Kizys, et al.. (2025). Functional analysis of SRY variants in individuals with 46,XY differences of sex development. Molecular and Cellular Endocrinology. 598. 112458–112458.

Douben, Hannie, Marianne Hoogeveen‐Westerveld, Mark Nellist, et al.. (2023). Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome. Human Mutation. 2023. 1–14. 2 indexed citations

Cools, Martine, Simon J. Tavernier, Petra Schelstraete, et al.. (2023). Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development: a cross-sectional study. European Journal of Endocrinology. 190(1). 34–43. 4 indexed citations

Hannema, Sabine E, Katja P. Wolffenbuttel, Yolande van Bever, et al.. (2023). 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. Clinical Endocrinology. 99(1). 58–63. 1 indexed citations

Hol, Janna A., Jan H. von der Thüsen, Yolande van Bever, et al.. (2023). Clinical Relevance of Rapid FOXF1-Targeted Sequencing in Patients Suspected of Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins. Laboratory Investigation. 103(11). 100233–100233. 3 indexed citations

Сорокина, Елена А., Linda M. Reis, Katherine Agre, et al.. (2021). WDR37 syndrome: identification of a distinct new cluster of disease-associated variants and functional analyses of mutant proteins. Human Genetics. 140(12). 1775–1789. 6 indexed citations

Zeidler, Sandra Ventorin von, et al.. (2014). Early prenatal disruption; a foetus with features of severe limb body wall sequence, body stalk anomaly and amniotic bands.. Data Archiving and Networked Services (DANS). 25(3). 315–20. 6 indexed citations

Verhagen, Judith M.A., et al.. (2014). An unusual presentation of Kabuki syndrome: Clinical overlap with CHARGE syndrome. European Journal of Medical Genetics. 57(9). 510–512. 22 indexed citations

Brosens, Erwin, Yolande van Bever, Anna E. Koopmans, et al.. (2014). Clinical and etiological heterogeneity in patients with tracheo-esophageal malformations and associated anomalies. European Journal of Medical Genetics. 57(8). 440–452. 52 indexed citations

10.

Knijnenburg, Jeroen, Yolande van Bever, Lorette O. M. Hulsman, et al.. (2012). A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family. European Journal of Human Genetics. 20(9). 986–989. 33 indexed citations

11.

Brosens, Erwin, H. J. Eussen, Yolande van Bever, et al.. (2012). VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations. Molecular Syndromology. 4(1-2). 20–26. 22 indexed citations

12.

Hellemans, Jan, Marleen Simon, Annelies Dheedene, et al.. (2009). Homozygous Inactivating Mutations in the NKX3-2 Gene Result in Spondylo-Megaepiphyseal-Metaphyseal Dysplasia. The American Journal of Human Genetics. 85(6). 916–922. 28 indexed citations

13.

Zutven, Laura J. C. M. van, Yolande van Bever, Diane Van Opstal, et al.. (2009). Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): A patient report and review. American Journal of Medical Genetics Part A. 149A(7). 1468–1475. 12 indexed citations

14.

Bever, Yolande van, et al.. (2008). 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. American Journal of Medical Genetics Part A. 146A(4). 500–504. 13 indexed citations

15.

Bever, Yolande van, Wendy Balemans, E Duval, et al.. (2007). Exclusion of OGDH and BMP4 as candidate genes in two siblings with autosomal recessive DOOR syndrome. American Journal of Medical Genetics Part A. 143A(7). 763–767. 5 indexed citations

16.

Bever, Yolande van, Liesbeth Rooms, Annick Laridon, et al.. (2005). Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype. American Journal of Medical Genetics Part A. 135A(1). 91–95. 49 indexed citations

17.

Bever, Yolande van, Jenneke van den Ende, Paula Iughetti, et al.. (2003). Waardenburg syndrome: Clinical differentiation between types I and II. American Journal of Medical Genetics Part A. 117A(3). 223–235. 41 indexed citations

18.

Bever, Yolande van & Raoul C. M. Hennekam. (1995). Haspeslagh syndrome without severe mental retardation and pterygia?. Clinical Genetics. 47(5). 263–266. 1 indexed citations

19.

Bever, Yolande van, et al.. (1993). The oav - spectrum and associated anomalies in 77 patients. Revista brasileira de genetica. 16(3). 811–817. 1 indexed citations

20.

Bever, Yolande van, et al.. (1992). Marden‐Walker‐like syndrome without psychomotor retardation: Report of a Brazilian girl born to consanguineous parents. American Journal of Medical Genetics. 42(4). 467–469. 18 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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