Claudia Ruivenkamp

10.2k total citations
79 papers, 3.4k citations indexed

About

Claudia Ruivenkamp is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Claudia Ruivenkamp has authored 79 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Genetics, 33 papers in Molecular Biology and 15 papers in Plant Science. Recurrent topics in Claudia Ruivenkamp's work include Genomic variations and chromosomal abnormalities (36 papers), Genomics and Rare Diseases (15 papers) and Chromosomal and Genetic Variations (14 papers). Claudia Ruivenkamp is often cited by papers focused on Genomic variations and chromosomal abnormalities (36 papers), Genomics and Rare Diseases (15 papers) and Chromosomal and Genetic Variations (14 papers). Claudia Ruivenkamp collaborates with scholars based in Netherlands, United States and Germany. Claudia Ruivenkamp's co-authors include Sarina G. Kant, Monique Losekoot, Martijn H. Breuning, Jan M. Wit, Gijs W.E. Santen, Wilma Oostdijk, Arie van Haeringen, Hermine A. van Duyvenvoorde, Marjolein Kriek and Antoinet C.J. Gijsbers and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Claudia Ruivenkamp

77 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Claudia Ruivenkamp Netherlands	31	1.8k	1.8k	393	341	296	79	3.4k
Marco Seri Italy	38	2.3k 1.3×	1.4k 0.8×	202 0.5×	488 1.4×	329 1.1×	193	5.3k
Andreas Winterpacht Germany	33	2.5k 1.4×	1.4k 0.8×	275 0.7×	122 0.4×	86 0.3×	85	3.7k
Guillermo Antiñolo Spain	30	2.0k 1.1×	792 0.4×	204 0.5×	94 0.3×	244 0.8×	179	3.3k
Hong Lei United States	21	5.0k 2.8×	1.8k 1.0×	584 1.5×	220 0.6×	85 0.3×	27	5.7k
Pamela R. Fain United States	37	1.9k 1.0×	1.4k 0.8×	127 0.3×	1.4k 4.2×	433 1.5×	106	5.3k
Pumin Zhang United States	27	3.8k 2.1×	762 0.4×	216 0.5×	312 0.9×	95 0.3×	51	4.6k
Michele Rubini Italy	25	1.7k 1.0×	841 0.5×	114 0.3×	333 1.0×	1.1k 3.7×	76	3.3k
Gwenaëlle Collod‐Béroud France	21	1.7k 0.9×	1.6k 0.9×	63 0.2×	134 0.4×	98 0.3×	38	3.6k
Célia Bádenas Spain	33	2.2k 1.2×	1.4k 0.8×	400 1.0×	229 0.7×	53 0.2×	139	3.9k
Jan D. Marshall United States	29	1.2k 0.7×	1.8k 1.0×	147 0.4×	487 1.4×	105 0.4×	78	3.1k

Countries citing papers authored by Claudia Ruivenkamp

Since Specialization

Citations

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

Fields of papers citing papers by Claudia Ruivenkamp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Claudia Ruivenkamp. 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 Claudia Ruivenkamp. The network helps show where Claudia Ruivenkamp may publish in the future.

Co-authorship network of co-authors of Claudia Ruivenkamp

This figure shows the co-authorship network connecting the top 25 collaborators of Claudia Ruivenkamp. A scholar is included among the top collaborators of Claudia Ruivenkamp 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 Claudia Ruivenkamp. Claudia Ruivenkamp 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

Ruivenkamp, Claudia, et al.. (2024). A Deep Intronic Splice Variant in COL1A1 Causing Osteogenesis Imperfecta Type II. American Journal of Medical Genetics Part A. 197(5). e63972–e63972.

Haeringen, Arie van, Lisenka E.L.M. Vissers, Emilia K. Bijlsma, et al.. (2023). Reanalysis of whole-exome sequencing (WES) data of children with neurodevelopmental disorders in a standard patient care context. European Journal of Pediatrics. 183(1). 345–355. 8 indexed citations

Elhaji, Youssef, et al.. (2021). Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family. SHILAP Revista de lepidopterología. 1(3). 100022–100022. 2 indexed citations

Boer, Helen de, et al.. (2020). A missense variant in the nuclear export signal of the FMR1 gene causes intellectual disability. Gene. 768. 145298–145298. 6 indexed citations

Haak, Monique C., P. N. Adama van Scheltema, Cacha Peeters‐Scholte, et al.. (2019). From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care. Genetics in Medicine. 21(10). 2303–2310. 39 indexed citations

Sollis, Elliot, Pelagia Derizioti, Hirotomo Saitsu, et al.. (2017). Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders. Human Mutation. 38(11). 1542–1554. 30 indexed citations

Doğrusöz, Mehmet, Mette Bagger, Sjoerd G. van Duinen, et al.. (2017). The Prognostic Value of AJCC Staging in Uveal Melanoma Is Enhanced by Adding Chromosome 3 and 8q Status. Investigative Ophthalmology & Visual Science. 58(2). 833–833. 76 indexed citations

Hiemstra, Yasmine L., Regina Bökenkamp, Anneke M. van Mil, et al.. (2017). A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects. Netherlands Heart Journal. 25(12). 675–681. 17 indexed citations

Versluis, Mieke, Mark J. de Lange, Claudia Ruivenkamp, et al.. (2015). Digital PCR Validates 8q Dosage as Prognostic Tool in Uveal Melanoma. PLoS ONE. 10(3). e0116371–e0116371. 84 indexed citations

10.

Duyvenvoorde, Hermine A. van, Julian C. Lui, Sarina G. Kant, et al.. (2013). Copy number variants in patients with short stature. European Journal of Human Genetics. 22(5). 602–609. 57 indexed citations

11.

Nielsen, Maartje, Clementien L. Vermont, Emmelien Aten, et al.. (2012). Deletion of the 3q26 region including the EVI1 and MDS1 genes in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia. Journal of Medical Genetics. 49(9). 598–600. 23 indexed citations

12.

Hansson, Kerstin, Antoinet C.J. Gijsbers, Wilma Oostdijk, et al.. (2012). Molecular and clinical characterization of patients with a ring chromosome 11. European Journal of Medical Genetics. 55(12). 708–714. 16 indexed citations

13.

Gijsbers, A.C.J., Jacqueline Schoumans, & Claudia Ruivenkamp. (2011). Interpretation of Array Comparative Genome Hybridization Data: A Major Challenge. Cytogenetic and Genome Research. 135(3-4). 222–227. 29 indexed citations

14.

Schoumans, Jacqueline & Claudia Ruivenkamp. (2010). Laboratory Methods for the Detection of Chromosomal Abnormalities. Methods in molecular biology. 628. 53–73. 2 indexed citations

15.

Rosa-Rosa, Juan Manuel, Guillermo Pita, Anna González‐Neira, et al.. (2009). A 7 Mb region within 11q13 may contain a high penetrance gene for breast cancer. Breast Cancer Research and Treatment. 118(1). 151–159. 20 indexed citations

16.

Hochstenbach, Ron, Ellen van Binsbergen, J.J.M. Engelen, et al.. (2009). Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands. European Journal of Medical Genetics. 52(4). 161–169. 149 indexed citations

17.

Gijsbers, Antoinet C.J., Cathy A.J. Bosch, Janneke Schuurs-Hoeijmakers, et al.. (2009). A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first. European Journal of Human Genetics. 17(11). 1394–1402. 55 indexed citations

18.

Goobie, Sharan, Jeroen Knijnenburg, David Fitzpatrick, et al.. (2008). Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting. Cytogenetic and Genome Research. 123(1-4). 65–78. 30 indexed citations

19.

Schoumans, Jacqueline, Ann Nordgren, Claudia Ruivenkamp, et al.. (2004). Genome-wide screening using array-CGH does not reveal microdeletions/microduplications in children with Kabuki syndrome. European Journal of Human Genetics. 13(2). 260–263. 23 indexed citations

20.

Ruivenkamp, Claudia, Mario Hermsen, Cindy Postma, et al.. (2003). LOH of PTPRJ occurs early in colorectal cancer and is associated with chromosomal loss of 18q12–21. Oncogene. 22(22). 3472–3474. 67 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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