Yvonne J. Vos

4.3k total citations
42 papers, 1.0k citations indexed

About

Yvonne J. Vos is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Yvonne J. Vos has authored 42 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Yvonne J. Vos's work include Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (6 papers) and Genetic factors in colorectal cancer (6 papers). Yvonne J. Vos is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (6 papers) and Genetic factors in colorectal cancer (6 papers). Yvonne J. Vos collaborates with scholars based in Netherlands, United States and Sweden. Yvonne J. Vos's co-authors include Robert M.W. Hofstra, Wilhelmina S. Kerstjens‐Frederikse, Gideon J. du Marchie Sarvaas, Patrick Rump, Maarten P. van den Berg, Oebele F. Brouwer, J. Peter van Tintelen, Anthonie J. van Essen, Rudi J. Planta and Johanna C. Herkert and has published in prestigious journals such as Journal of the American College of Cardiology, The Journal of Pediatrics and Gene.

In The Last Decade

Yvonne J. Vos

42 papers receiving 989 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yvonne J. Vos Netherlands 19 520 240 190 131 112 42 1.0k
Isabelle Thiffault United States 23 822 1.6× 482 2.0× 76 0.4× 100 0.8× 224 2.0× 65 1.4k
Caroline Astbury United States 17 483 0.9× 427 1.8× 85 0.4× 66 0.5× 51 0.5× 54 1.0k
Maria Lisa Dentici Italy 19 704 1.4× 459 1.9× 61 0.3× 58 0.4× 63 0.6× 74 1.1k
Andrew Norman United Kingdom 17 444 0.9× 211 0.9× 65 0.3× 38 0.3× 86 0.8× 30 825
P. Gallano Spain 20 1.0k 1.9× 287 1.2× 261 1.4× 30 0.2× 213 1.9× 65 1.4k
Stavit A. Shalev Israel 19 519 1.0× 416 1.7× 45 0.2× 49 0.4× 83 0.7× 44 962
Seung Tae Baek South Korea 17 966 1.9× 196 0.8× 386 2.0× 39 0.3× 81 0.7× 29 1.4k
Nara Sobreira United States 19 690 1.3× 671 2.8× 46 0.2× 70 0.5× 68 0.6× 61 1.3k
Carol A. Crowe United States 17 582 1.1× 318 1.3× 79 0.4× 32 0.2× 53 0.5× 28 904
Tracey Lewis United States 14 927 1.8× 306 1.3× 359 1.9× 61 0.5× 549 4.9× 23 1.4k

Countries citing papers authored by Yvonne J. Vos

Since Specialization
Citations

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

Fields of papers citing papers by Yvonne J. Vos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yvonne J. Vos. 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 Yvonne J. Vos. The network helps show where Yvonne J. Vos may publish in the future.

Co-authorship network of co-authors of Yvonne J. Vos

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

All Works

20 of 20 papers shown
1.
Vansenne, Fleur, Johanna M. Fock, Irene Stolte‐Dijkstra, et al.. (2022). Phenotypic expansion of EGP5-related Vici syndrome: 15 Dutch patients carrying a founder variant. European Journal of Paediatric Neurology. 41. 91–98. 3 indexed citations
2.
Westers, Helga, Yvonne J. Vos, K. Joeri van der Velde, et al.. (2022). Validation of New Gene Variant Classification Methods: a Field-Test in Diagnostic Cardiogenetics. Frontiers in Genetics. 13. 824510–824510. 2 indexed citations
3.
Leenders, Erika, Pauline Terhal, Katharina Löhner, et al.. (2021). TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility. European Journal of Human Genetics. 29(11). 1669–1676. 15 indexed citations
4.
Veenstra‐Knol, Hermine E., Fleur Vansenne, Erica H. Gerkes, et al.. (2020). De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability. European Journal of Human Genetics. 28(6). 763–769. 8 indexed citations
5.
Aukema, Sietse, Wim Timens, Yvonne J. Vos, et al.. (2020). A homozygous variant in growth and differentiation factor 2 (GDF2) may cause lymphatic dysplasia with hydrothorax and nonimmune hydrops fetalis. American Journal of Medical Genetics Part A. 182(9). 2152–2160. 8 indexed citations
6.
Suerink, Manon, Frederik J. Hes, Alexandra M. J. Langers, et al.. (2019). Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy. European Journal of Human Genetics. 28(2). 222–230. 12 indexed citations
7.
Vlaskamp, Danique R.M., Petra M.C. Callenbach, Patrick Rump, et al.. (2018). PRRT2-related phenotypes in patients with a 16p11.2 deletion. European Journal of Medical Genetics. 62(4). 265–269. 21 indexed citations
8.
Otter, Maarten, et al.. (2017). A novel mutation in L1CAM causes a mild form of L1 syndrome: a case report. Clinical Case Reports. 5(8). 1213–1217. 9 indexed citations
9.
Lange, Iris, Patrick Rump, Rinze F. Neuteboom, et al.. (2017). Male patients affected by mosaic PCDH19 mutations: five new cases. Neurogenetics. 18(3). 147–153. 36 indexed citations
10.
11.
Nielsen, Maartje, Renée C. Niessen, Carli M.J. Tops, et al.. (2012). Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review. Familial Cancer. 12(1). 43–50. 16 indexed citations
12.
Verhagen, Judith M.A., C. T. R. M. Schrander‐Stumpel, Jacobiene W. Weber, et al.. (2012). Adducted thumbs: A clinical clue to genetic diagnosis. European Journal of Medical Genetics. 56(3). 153–158. 9 indexed citations
13.
Riel, E. van, Margreet G.E.M. Ausems, Frans B.L. Hogervorst, et al.. (2010). A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. Hereditary Cancer in Clinical Practice. 8(1). 7–7. 16 indexed citations
14.
Vos, Yvonne J. & Robert M.W. Hofstra. (2009). An updated and upgradedL1CAMmutation database. Human Mutation. 31(1). E1102–E1109. 48 indexed citations
15.
Stulp, Rein P., et al.. (2008). Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum. Hereditary Cancer in Clinical Practice. 6(1). 15–15. 21 indexed citations
16.
Tintelen, J. Peter van, René A. Tio, Wilhelmina S. Kerstjens‐Frederikse, et al.. (2007). Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene. Journal of the American College of Cardiology. 49(25). 2430–2439. 68 indexed citations
17.
Sival, Deborah, Johannes H. van der Hoeven, Yvonne J. Vos, et al.. (2006). Shah-Waardenburg syndrome and PCWH associated with SOX10 mutations: A case report and review of the literature. European Journal of Paediatric Neurology. 10(1). 11–17. 45 indexed citations
18.
Rump, Patrick, P.M. Grootscholten, Johanna M. Fock, et al.. (2005). A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect. Neurogenetics. 6(4). 201–207. 14 indexed citations
19.
Kariola, Reetta, Robyn Otway, Tiina Raevaara, et al.. (2003). Two mismatch repair gene mutations found in a colon cancer patient – which one is pathogenic?. Human Genetics. 112(2). 105–109. 28 indexed citations
20.
Vos, Yvonne J., et al.. (1985). Repeated sequences on mitochondrial DNA ofSpirodela oligorhiza. Plant Molecular Biology. 4(4). 219–224. 6 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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