Mary E. Velthuizen

614 total citations
23 papers, 248 citations indexed

About

Mary E. Velthuizen is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Oncology. According to data from OpenAlex, Mary E. Velthuizen has authored 23 papers receiving a total of 248 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 8 papers in Oncology. Recurrent topics in Mary E. Velthuizen's work include BRCA gene mutations in cancer (20 papers), Prenatal Screening and Diagnostics (7 papers) and Global Cancer Incidence and Screening (5 papers). Mary E. Velthuizen is often cited by papers focused on BRCA gene mutations in cancer (20 papers), Prenatal Screening and Diagnostics (7 papers) and Global Cancer Incidence and Screening (5 papers). Mary E. Velthuizen collaborates with scholars based in Netherlands, Norway and Germany. Mary E. Velthuizen's co-authors include Margreet G.E.M. Ausems, Eveline M. A. Bleiker, Sandra van Dulmen, E. van Riel, Daniela Hahn, Neil K. Aaronson, Marco J. Koudijs, Lizet E. van der Kolk, Ronald P. Zweemer and Mirjam P. Fransen and has published in prestigious journals such as Journal of Clinical Oncology, Annals of Surgical Oncology and Gynecologic Oncology.

In The Last Decade

Mary E. Velthuizen

23 papers receiving 248 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mary E. Velthuizen Netherlands 11 176 80 65 46 35 23 248
Robin Lee United States 9 198 1.1× 39 0.5× 46 0.7× 44 1.0× 30 0.9× 15 305
Wendy Kohlmann United States 10 185 1.1× 112 1.4× 54 0.8× 52 1.1× 46 1.3× 23 338
Hetal S. Vig United States 7 213 1.2× 48 0.6× 57 0.9× 51 1.1× 25 0.7× 9 267
Amanda Brandt United States 9 198 1.1× 48 0.6× 69 1.1× 41 0.9× 36 1.0× 19 292
Eliza Courtney Singapore 11 185 1.1× 57 0.7× 44 0.7× 60 1.3× 19 0.5× 27 319
Jenna Scott Canada 6 155 0.9× 79 1.0× 33 0.5× 75 1.6× 38 1.1× 9 283
Anna von Wachenfeldt Sweden 6 134 0.8× 109 1.4× 30 0.5× 96 2.1× 45 1.3× 14 270
Erica M. Bednar United States 8 286 1.6× 50 0.6× 68 1.0× 82 1.8× 21 0.6× 17 360
Sherry Grumet United States 6 322 1.8× 75 0.9× 84 1.3× 59 1.3× 56 1.6× 13 428
Hildegunn Høberg‐Vetti Norway 7 124 0.7× 27 0.3× 29 0.4× 28 0.6× 20 0.6× 17 197

Countries citing papers authored by Mary E. Velthuizen

Since Specialization
Citations

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

Fields of papers citing papers by Mary E. Velthuizen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary E. Velthuizen. 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 Mary E. Velthuizen. The network helps show where Mary E. Velthuizen may publish in the future.

Co-authorship network of co-authors of Mary E. Velthuizen

This figure shows the co-authorship network connecting the top 25 collaborators of Mary E. Velthuizen. A scholar is included among the top collaborators of Mary E. Velthuizen 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 Mary E. Velthuizen. Mary E. Velthuizen 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.
Bleiker, Eveline M. A., Mary E. Velthuizen, Arjan P. Schouten van der Velden, et al.. (2023). Patients’ experiences with pre-test genetic counseling provided by breast cancer healthcare professionals: Results from a large prospective multicenter study. The Breast. 69. 349–357. 4 indexed citations
2.
Bleiker, Eveline M. A., Cora M. Aalfs, Thijs van Dalen, et al.. (2023). Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling. Annals of Surgical Oncology. 30(6). 3248–3258. 7 indexed citations
3.
Bleiker, Eveline M. A., Jacob P. Hoogendam, Mary E. Velthuizen, et al.. (2022). Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing. Hereditary Cancer in Clinical Practice. 20(1). 33–33. 13 indexed citations
4.
Frederix, G. W. J., Mary E. Velthuizen, Maaike A. van der Aa, et al.. (2022). Mainstream germline genetic testing for patients with epithelial ovarian cancer leads to higher testing rates and a reduction in genetics-related healthcare costs from a healthcare payer perspective. Gynecologic Oncology. 167(1). 115–122. 8 indexed citations
5.
Zweemer, Ronald P., et al.. (2021). Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer. Familial Cancer. 21(3). 295–304. 22 indexed citations
6.
Dulmen, Sandra van, Mary E. Velthuizen, Maria van den Muijsenbergh, et al.. (2021). Effect of a health literacy training program for surgical oncologists and specialized nurses on disparities in referral to breast cancer genetic testing. The Breast. 58. 80–87. 10 indexed citations
7.
Velthuizen, Mary E., Rob B. van der Luijt, B.J. de Vries, et al.. (2021). Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences. Hereditary Cancer in Clinical Practice. 19(1). 9–9. 4 indexed citations
8.
Vlaskamp, Danique R.M., Patrick Rump, Petra M.C. Callenbach, et al.. (2021). Changes in empowerment and anxiety of patients and parents during genetic counselling for epilepsy. European Journal of Paediatric Neurology. 32. 128–135. 4 indexed citations
9.
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Velthuizen, Mary E., Hans F. A. Vasen, G. Johan A. Offerhaus, et al.. (2020). Increased prevalence of Barrett’s esophagus in patients with MUTYH-associated polyposis (MAP). Familial Cancer. 19(2). 183–187. 3 indexed citations
11.
Plantinga, Mirjam, Margreet G.E.M. Ausems, Nine V.A.M. Knoers, et al.. (2020). Cognitive and affective outcomes of genetic counselling in the Netherlands at group and individual level: a personalized approach seems necessary. European Journal of Human Genetics. 28(9). 1187–1195. 7 indexed citations
12.
Hogervorst, Frans B.L., Mary E. Velthuizen, Mariëlle Ruijs, et al.. (2019). TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort. Familial Cancer. 18(2). 273–280. 22 indexed citations
13.
Helsper, Charles W., Liesbeth M. van Vliet, Mary E. Velthuizen, et al.. (2018). Identifying patients with a history of ovarian cancer for referral for genetic counselling: non-randomised comparison of two case-finding strategies in primary care. British Journal of General Practice. 68(676). e750–e756. 3 indexed citations
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Riel, E. van, et al.. (2017). Referral to cancer genetic counseling: do migrant status and patients’ educational background matter?. Journal of Community Genetics. 8(4). 303–310. 15 indexed citations
17.
Vasen, Hans F. A., Mary E. Velthuizen, Jan H. Kleibeuker, et al.. (2016). Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry. Familial Cancer. 15(3). 429–435. 20 indexed citations
18.
Dulmen, Sandra van, Mary E. Velthuizen, E. Theunissen, et al.. (2016). Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study. Familial Cancer. 15(2). 163–171. 9 indexed citations
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20.
Bleiker, Eveline M. A., Margreet G.E.M. Ausems, Lizet E. van der Kolk, et al.. (2014). Routine assessment of psychosocial problems after cancer genetic counseling: results from a randomized controlled trial. Clinical Genetics. 87(5). 419–427. 10 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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