A Bröcker-Vriends

1.2k total citations
26 papers, 842 citations indexed

About

A Bröcker-Vriends is a scholar working on Hematology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, A Bröcker-Vriends has authored 26 papers receiving a total of 842 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Hematology, 8 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in A Bröcker-Vriends's work include Hemophilia Treatment and Research (16 papers), Cancer-related gene regulation (7 papers) and Prenatal Screening and Diagnostics (4 papers). A Bröcker-Vriends is often cited by papers focused on Hemophilia Treatment and Research (16 papers), Cancer-related gene regulation (7 papers) and Prenatal Screening and Diagnostics (4 papers). A Bröcker-Vriends collaborates with scholars based in Netherlands, Curacao and Belarus. A Bröcker-Vriends's co-authors include Inge Varekamp, Cees Smit, E Briët, Theo P. B. M. Suurmeijer, F.R. Rosendaal, Jan P. Vandenbroucke, Hans F. A. Vasen, Yvonne Hendriks, Andrea E. van der Meulen‐de Jong and Hans Morreau and has published in prestigious journals such as Social Science & Medicine, Annals of Oncology and CA A Cancer Journal for Clinicians.

In The Last Decade

A Bröcker-Vriends

26 papers receiving 808 citations

Peers

A Bröcker-Vriends

HEMAT

GENET

PFM

ONCOL

Dorothy L. Williams United States

NJ Chao United States

Hisaya Nakadate Japan

GD Long United States

Clare J. Twist United States

Archie Bleyer United States

Michael Lobell United States

Giuseppe Lentini Germany

Maarten Egeler Netherlands

Jutte van der Werff ten Bosch Belgium

Dorothy L. Williams United States

A Bröcker-Vriends

801 ×2.1

HEMAT

417 ×2.3

175 ×1.0

GENET

173 ×1.1

PFM

210 ×1.5

ONCOL

Citations per year, relative to A Bröcker-Vriends A Bröcker-Vriends (= 1×) peers Dorothy L. Williams

Countries citing papers authored by A Bröcker-Vriends

Since Specialization

Citations

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

Fields of papers citing papers by A Bröcker-Vriends

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A Bröcker-Vriends. 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 A Bröcker-Vriends. The network helps show where A Bröcker-Vriends may publish in the future.

Co-authorship network of co-authors of A Bröcker-Vriends

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Oostrom, Iris van, Hanne Meijers-Heijboer, H.J. Duivenvoorden, et al.. (2006). Experience of parental cancer in childhood is a risk factor for psychological distress during genetic cancer susceptibility testing. Annals of Oncology. 17(7). 1090–1095. 36 indexed citations

Hendriks, Yvonne, Andrea E. van der Meulen‐de Jong, Hans Morreau, et al.. (2006). Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians. CA A Cancer Journal for Clinicians. 56(4). 213–225. 116 indexed citations

Oostrom, Iris van, Hanne Meijers‐Heijboer, H.J. Duivenvoorden, et al.. (2006). Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study. Clinical Genetics. 71(1). 35–42. 63 indexed citations

Houtum, William H. van, Eleonora P.M. Corssmit, Pim Dekker, et al.. (2005). Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas. European Journal of Endocrinology. 152(1). 87–94. 33 indexed citations

Vasen, Hans F. A., Yvonne Hendriks, Andrea E. van der Meulen‐de Jong, et al.. (2004). Identification of HNPCC by Molecular Analysis of Colorectal and Endometrial Tumors. Disease Markers. 20(4-5). 207–213. 33 indexed citations

Hendriks, Yvonne, Jasper J. van der Smagt, Sarina G. Kant, et al.. (2003). Bannayan–Riley–Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases. Familial Cancer. 2(2). 79–85. 55 indexed citations

Cobben, J. M., A Bröcker-Vriends, & N. J. Leschot. (2002). [Prenatal diagnosis for hereditary predisposition to mammary and ovarian carcinoma--defining a position].. PubMed. 146(31). 1461–5. 2 indexed citations

Varekamp, Inge, Th.P.B.M. Suurmeijer, F.R. Rosendaal, & A Bröcker-Vriends. (1993). The use of preventive health care services: Carrier testing for the genetic disorder haemophilia. Social Science & Medicine. 37(5). 639–648. 10 indexed citations

Varekamp, Inge, Th.P.B.M. Suurmeijer, A Bröcker-Vriends, & F.R. Rosendaal. (1992). Hemophilia and the use of genetic counseling and carrier testing within family networks.. PubMed. 28(1). 139–48. 15 indexed citations

10.

Bröcker-Vriends, A, Egbert Bakker, H. H. H. Kanhai, et al.. (1992). The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B. Annals of Hematology. 64(1). 2–11. 8 indexed citations

11.

Rosendaal, F.R., Cees Smit, Inge Varekamp, et al.. (1990). Modern haemophilia treatment: medical improvements and quality of life. Journal of Internal Medicine. 228(6). 633–640. 68 indexed citations

12.

Rosendaal, Frits R., A Bröcker-Vriends, Hans C. van Houwelingen, et al.. (1990). Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis. Human Genetics. 86(2). 139–146. 27 indexed citations

13.

Varekamp, Inge, Th.P.B.M. Suurmeijer, A Bröcker-Vriends, et al.. (1990). Carrier testing and prenatal diagnosis for hemophilia: Experiences and attitudes of 549 potential and obligate carriers. American Journal of Medical Genetics. 37(1). 147–154. 47 indexed citations

14.

Smit, Cees, et al.. (1989). Physical condition, longevity, and social performance of Dutch haemophiliacs, 1972-85.. BMJ. 298(6668). 235–238. 63 indexed citations

15.

Varekamp, Inge, Cees Smit, Frits R. Rosendaal, et al.. (1989). Employment of individuals with haemophilia in the Netherlands. Social Science & Medicine. 28(3). 261–270. 19 indexed citations

16.

Rosendaal, F.R., Inge Varekamp, Cees Smit, et al.. (1989). Mortality and causes of death in Dutch haemophiliacs, 1973–86. British Journal of Haematology. 71(1). 71–76. 166 indexed citations

17.

Varekamp, Inge, et al.. (1989). [Social effects of current hemophilia treatment].. PubMed. 133(8). 404–8. 1 indexed citations

18.

Bröcker-Vriends, A, E Briët, H. H. H. Kanhai, et al.. (1988). First trimester prenatal diagnosis of haemophilia A: Two years' experience. Prenatal Diagnosis. 8(6). 411–421. 8 indexed citations

19.

Bröcker-Vriends, A, et al.. (1986). Monosomy 8p: an easily overlooked syndrome.. Journal of Medical Genetics. 23(2). 153–154. 21 indexed citations

20.

Bröcker-Vriends, A, et al.. (1984). [Detection of carrier state of hemophilia; current status].. PubMed. 128(8). 354–60. 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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