JC Oosterwijk

646 total citations
22 papers, 407 citations indexed

About

JC Oosterwijk is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, JC Oosterwijk has authored 22 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Cell Biology. Recurrent topics in JC Oosterwijk's work include BRCA gene mutations in cancer (7 papers), Skin and Cellular Biology Research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). JC Oosterwijk is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Skin and Cellular Biology Research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). JC Oosterwijk collaborates with scholars based in Netherlands, Poland and United States. JC Oosterwijk's co-authors include Rob Willemsen, B. A. Oostra, A. T. Hoogeveen, Joop Theelen, I. van der Bürgt, Anne Smits, Aad Tibben, Peter Devilee, Martinus F. Niermeijer and Petra G. Frets and has published in prestigious journals such as Journal of Clinical Oncology, Cancer Research and The American Journal of Human Genetics.

In The Last Decade

JC Oosterwijk

22 papers receiving 396 citations

Peers

JC Oosterwijk

GENET

PPCH

SPS

Antonia Paula Marques‐de‐Faria Brazil

Sophia Kitsiou‐Tzeli Greece

C E de Die-Smulders Netherlands

Kathryn A. Steinhaus United States

Shweta U. Dhar United States

Maria Michela Rinaldi Italy

Marsha Speevak Canada

Rakel Tryggvadóttir United States

Mary O’Driscoll United Kingdom

Margaret Lilley Canada

Antonia Paula Marques‐de‐Faria Brazil

JC Oosterwijk

391 ×1.2

GENET

383 ×2.0

65 ×0.8

75 ×1.4

PPCH

12 ×0.2

SPS

Citations per year, relative to JC Oosterwijk JC Oosterwijk (= 1×) peers Antonia Paula Marques‐de‐Faria

Countries citing papers authored by JC Oosterwijk

Since Specialization

Citations

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

Fields of papers citing papers by JC Oosterwijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of JC Oosterwijk

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

Beek, Irma van de, Ellen M.A. Smets, Joanne A. de Hullu, et al.. (2019). Genetic counseling of patients with ovarian carcinoma: acceptance, timing, and psychological wellbeing. Journal of Community Genetics. 11(2). 183–191. 3 indexed citations

Mann, Ritse M., Martijne van ’t Riet, Cornelis Verhoef, et al.. (2019). Abstract P6-13-01: MRI breast cancer screening compared to mammography in women with a familial risk: A multicenter randomized controlled trial. Cancer Research. 79(4_Supplement). P6–13. 2 indexed citations

Schreuder, K., P.E.R. Spronk, JC Oosterwijk, et al.. (2018). Hospital transfer after a breast cancer diagnosis: A population-based study in the Netherlands of the extent, predictive characteristics and its impact on time to treatment. European Journal of Surgical Oncology. 45(4). 560–566. 7 indexed citations

Wely, Madelon van, Frank J. Broekmans, Thea M. Mooij, et al.. (2014). BRCA1/2 mutation carriers do not have earlier natural menopause compared to proven non-carriers: report from the Dutch hereditary breast and ovarian cancer study group (HEBON). University of Groningen research database (University of Groningen / Centre for Information Technology). 1 indexed citations

Sijmons, Rolf H., et al.. (2011). The introduction of a choice to learn pre‐symptomatic DNA test results for BRCA or Lynch syndrome either face‐to‐face or by letter. Clinical Genetics. 81(5). 421–429. 6 indexed citations

Vos, Joël, JC Oosterwijk, E. Gómez, et al.. (2010). Perceiving cancer-risks and heredity-likelihood in genetic-counseling: how counselees recall and interpret BRCA 1/2-test results. Clinical Genetics. 79(3). 207–218. 34 indexed citations

Callenbach, Petra M.C., I.F.M. de Coo, R. ten Houten, et al.. (2005). Refinement of the chromosome 16 locus for benign familial infantile convulsions. Clinical Genetics. 67(6). 517–525. 20 indexed citations

Oosterwijk, JC, et al.. (1999). A new X-linked mental retardation syndrome with distal limb defects, hearing impairment, verrucosis and immunodeficiency.. Data Archiving and Networked Services (DANS). 2 indexed citations

Wu, Yuanqing, et al.. (1999). A DGGE system for comprehensive mutation screening of the complete coding regions of BRCA1 and BRCA2 outside exons 11. Data Archiving and Networked Services (DANS). 5 indexed citations

10.

Oosterwijk, JC. (1999). Genetic aspects of (gynecological) tumours. European Journal of Obstetrics & Gynecology and Reproductive Biology. 82(2). 125–128. 2 indexed citations

11.

Boerman, O.C., et al.. (1998). Two-step targeting of RCC tumors in mice : Improved tumor uptake and retention with a bivalent chelate. University of Groningen research database (University of Groningen / Centre for Information Technology). 39(5). 5 indexed citations

12.

DeBoer, Arthur, et al.. (1997). Excessive use of a single donor? And inadvertent consanguinity - Reply. Fertility and Sterility. 67(6). 1182–1183. 1 indexed citations

13.

Losekoot, Monique, E Hoogendoorn, Renske Olmer, et al.. (1997). Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.. Journal of Medical Genetics. 34(11). 924–926. 19 indexed citations

14.

Oosterwijk, JC, Gabriela Richard, Michiel J.R. van der Wielen, et al.. (1997). Molecular genetic analysis of two families with keratosis follicularis spinulosa decalvans: refinement of gene localization and evidence for genetic heterogeneity. Human Genetics. 100(5-6). 520–524. 16 indexed citations

15.

Tibben, Aad, Petra G. Frets, E.J. Meijers-Heijboer, et al.. (1997). BRCA1 in the family: A case description of the psychological implications. American Journal of Medical Genetics. 71(1). 63–71. 74 indexed citations

16.

Oosterwijk, JC, et al.. (1996). Cataracts, radiculomegaly, septal heart defects and hearing loss in two unrelated adult females with normal intelligence and similar facial appearance: confirmation of a syndrome?. Clinical Dysmorphology. 5(2). 93–103. 20 indexed citations

17.

Smits, Anne, Joop Theelen, Rob Willemsen, et al.. (1995). Normal phenotype in two brothers with a full FMR1 mutation. Human Molecular Genetics. 4(11). 2103–2108. 130 indexed citations

18.

Ris-Stalpers, C., Theo Hoogenboezem, Hein F.B.M. Sleddens, et al.. (1994). A Practical Approach to the Detection of Androgen Receptor Gene Mutations and Pedigree Analysis in Families with X-Linked Androgen Insensitivity. Pediatric Research. 36(2). 227–234. 28 indexed citations

19.

Oosterwijk, JC, et al.. (1992). Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2.. PubMed. 50(4). 801–7. 29 indexed citations

20.

Oosterwijk, JC, et al.. (1991). REGIONAL ASSIGNMENT TO XP22.2-P21.2 OF KERATOSIS FOLLICULARIS SPINULOSA DECALVANS. The American Journal of Human Genetics. 49(4). 353–353. 1 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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