Claudia Ruivenkamp

10.2k citations

79 papers · 3.4k indexed · h-index 31

Molecular Biology top 5%
Genetics top 1%
Pediatrics, Perinatology and Child Health top 5%
Immunology top 10%
Endocrinology, Diabetes and Metabolism top 5%

Co-authors: Sarina G. Kant Monique Losekoot Martijn H. Breuning Jan M. Wit Gijs W.E. Santen Wilma Oostdijk Arie van Haeringen Hermine A. van Duyvenvoorde
Topics: Genomic variations and chromosomal abnormalities (36 papers)Genomics and Rare Diseases (15 papers)Chromosomal and Genetic Variations (14 papers)
Cited by: Genetics Ophthalmology Molecular Biology
Journals: Nature GeneticsSHILAP Revista de lepidopterologíaPLoS ONE
Partner nations: Netherlands United States Germany

In The Last Decade

Claudia Ruivenkamp

77 papers receiving 3.3k citations

Peers

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

#	Work	Indexed citations
1	Proximal Deletions of 14q32.2 Result in Severe Neurodevelopmental Outcomes, Congenital Anomalies, and Dysmorphic Features 2025 ·American Journal of Medical Genetics Part A ·(unknown),Robert Roger Lebel,(unknown),Marvyn T. Koning,Claudia Ruivenkamp,Himanshu Goel,Scott C. Smith	0
2	A Deep Intronic Splice Variant in COL1A1 Causing Osteogenesis Imperfecta Type II 2024 ·American Journal of Medical Genetics Part A ·(unknown),Claudia Ruivenkamp,Tamara T. Koopmann,Gijs W.E. Santen,Peter G. J. Nikkels,Karin van der Tuin	0
3	Reanalysis of whole-exome sequencing (WES) data of children with neurodevelopmental disorders in a standard patient care context 2023 ·European Journal of Pediatrics ·(unknown),Arie van Haeringen,Lisenka E.L.M. Vissers,Emilia K. Bijlsma,Julie W. Rutten,Manon Suerink,Esther Nibbeling,Claudia Ruivenkamp,Saskia Koene	8
4	Diagnostic Value of a Protocolized In-Depth Evaluation of Pediatric Bone Marrow Failure: A Multi-Center Prospective Cohort Study 2022 ·Frontiers in Immunology ·(unknown),Claudia Ruivenkamp,(unknown),Esther Nibbeling,Corien L. Eckhardt,(unknown),Arjan C. Lankester,Marije Bartels,Gijs W.E. Santen,Frans J. Smiers,Mirjam van der Burg,Alexander B. Mohseny	5
5	Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family 2021 ·SHILAP Revista de lepidopterología ·Youssef Elhaji,(unknown),Claudia Ruivenkamp,Mathew Nightingale,Gijs W.E. Santen,(unknown),Peter Hull	2
6	A missense variant in the nuclear export signal of the FMR1 gene causes intellectual disability 2020 ·Gene ·(unknown),(unknown),Helen de Boer,(unknown),Claudia Ruivenkamp,Emilia K. Bijlsma,Rob Willemsen	6
7	From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care 2019 ·Genetics in Medicine ·(unknown),Monique C. Haak,P. N. Adama van Scheltema,Cacha Peeters‐Scholte,Tamara T. Koopmann,Esther Nibbeling,Emmelien Aten,Nicolette S. den Hollander,Claudia Ruivenkamp,Mariëtte J.V. Hoffer,Gijs W.E. Santen	39
8	The Prognostic Value of AJCC Staging in Uveal Melanoma Is Enhanced by Adding Chromosome 3 and 8q Status 2017 ·Investigative Ophthalmology & Visual Science ·Mehmet Doğrusöz,Mette Bagger,Sjoerd G. van Duinen,Wilma G. M. Kroes,Claudia Ruivenkamp,Stefan Böhringer,Klaus Kaae Andersen,Gregorius P. M. Luyten,Jens Folke Kiilgaard,Martine J. Jager	76
9	Parent-of-origin tumourigenesis is mediated by an essential imprinted modifier inSDHD-linked paragangliomas:SLC22A18andCDKN1Care candidate tumour modifiers 2016 ·Human Molecular Genetics ·Attje S. Hoekstra,Ruben D. Addie,Cor Ras,Reza M. Seifar,Claudia Ruivenkamp,Inge H. Briaire‐de Bruijn,Frederik J. Hes,Jeroen C. Jansen,Eleonora P.M. Corssmit,Willem E. Corver,Hans Morreau,Judith V.M.G. Bovée,Jean‐Pierre Bayley,Peter Devilee	13
10	Digital PCR Validates 8q Dosage as Prognostic Tool in Uveal Melanoma 2015 ·PLoS ONE ·Mieke Versluis,Mark J. de Lange,(unknown),Claudia Ruivenkamp,Wilma G. M. Kroes,Jinfeng Cao,Martine J. Jager,Gré P.M. Luyten,Pieter A. van der Velden	84
11	Copy number variants in patients with short stature 2013 ·European Journal of Human Genetics ·Hermine A. van Duyvenvoorde,Julian C. Lui,Sarina G. Kant,Wilma Oostdijk,Antoinet C.J. Gijsbers,Mariëtte J.V. Hoffer,Marcel Karperien,M.J.E. Walenkamp,C. Noordam,Paul G. Voorhoeve,Verónica Mericq,Alberto M. Pereira,(unknown),(unknown),Martijn H. Breuning,Monique Losekoot,Jeffrey Baron,Claudia Ruivenkamp,Jan M. Wit	57
12	Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocation 2011 ·European Journal of Medical Genetics ·Antoinet C.J. Gijsbers,Johannes G. Dauwerse,Cathy A.J. Bosch,Elles M. J. Boon,(unknown),Sarina G. Kant,(unknown),Martijn H. Breuning,Egbert Bakker,Claudia Ruivenkamp	8
13	Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome 2010 ·Nature Genetics ·Johannes G. Dauwerse,Jill Dixon,Saskia Seland,Claudia Ruivenkamp,Arie van Haeringen,Lies H. Hoefsloot,Dorien J.M. Peters,(unknown),Cornelia Daumer‐Haas,Robert Maiwald,Christiane Zweier,Bronwyn Kerr,Ana María Cobo,Joaquín Fernández Toral,A. Jeannette M. Hoogeboom,Dietmar Lohmann,Ute Hehr,Michael J. Dixon,Martijn H. Breuning,Dagmar Wieczorek	243
14	A 7 Mb region within 11q13 may contain a high penetrance gene for breast cancer 2009 ·Breast Cancer Research and Treatment ·Juan Manuel Rosa-Rosa,Guillermo Pita,Anna González‐Neira,Roger L. Milne,María Victoria Fernández,Claudia Ruivenkamp,Christi J. van Asperen,Peter Devilee,Javier Benı́tez	20
15	A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first 2009 ·European Journal of Human Genetics ·Antoinet C.J. Gijsbers,(unknown),Cathy A.J. Bosch,Janneke Schuurs-Hoeijmakers,Arie van Haeringen,Nicolette S. den Hollander,Sarina G. Kant,Emilia K. Bijlsma,Martijn H. Breuning,Egbert Bakker,Claudia Ruivenkamp	55
16	Split hand‐foot malformation, tetralogy of Fallot, mental retardation and a 1 Mb 19p deletion—evidence for further heterogeneity? 2009 ·American Journal of Medical Genetics Part A ·Emmelien Aten,Nicolette S. den Hollander,Claudia Ruivenkamp,Jeroen Knijnenburg,Hans van Bokhoven,Johan T. den Dunnen,Martijn H. Breuning	17
17	Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting 2008 ·Cytogenetic and Genome Research ·Sharan Goobie,Jeroen Knijnenburg,David Fitzpatrick,Freddie H. Sharkey,Anath C. Lionel,Christian R. Marshall,(unknown),Mary Shago,Kelly K. Chong,Roberto Mendoza‐Londono,Nicolette S. den Hollander,Claudia Ruivenkamp,E.R. Maher,Hans J. Tanke,Károly Szuhai,Richard F. Wintle,Stephen W. Scherer	30
18	A 400 kb duplication, 2.4 Mb triplication and 130 kb duplication of 9q34.3 in a patient with severe mental retardation 2008 ·European Journal of Medical Genetics ·Antoinet C.J. Gijsbers,Emilia K. Bijlsma,Marjan M. Weiss,Egbert Bakker,Martijn H. Breuning,(unknown),Claudia Ruivenkamp	10
19	Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant 2008 ·Journal of Medical Genetics ·Femke Hannes,Andrew J. Sharp,Heather C. Mefford,Thomy de Ravel,Claudia Ruivenkamp,M.H. Breuning,JP Fryns,Koenraad Devriendt,Griet Van Buggenhout,Annick Vogels,Helen Stewart,Raoul C. M. Hennekam,Gregory M. Cooper,Regina Regan,Samantha J.L. Knight,Evan E. Eichler,Joris Vermeesch	207
20	LOH of PTPRJ occurs early in colorectal cancer and is associated with chromosomal loss of 18q12–21 2003 ·Oncogene ·Claudia Ruivenkamp,Mario Hermsen,Cindy Postma,Anita Klous,Jan P. Baak,Gerrit A. Meijer,Peter Démant	67

About Claudia Ruivenkamp

Claudia Ruivenkamp is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 79 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (36 papers), Genomics and Rare Diseases (15 papers) and Chromosomal and Genetic Variations (14 papers). The work is most often cited by research in Genetics (1.8k citations), Ophthalmology (268 citations) and Molecular Biology (1.8k citations). Claudia Ruivenkamp has collaborated with scholars based in Netherlands, United States and Germany. Frequent 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. Their work appears in journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

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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