René Mulder

403 total citations
18 papers, 241 citations indexed

About

René Mulder is a scholar working on Hematology, Genetics and Internal Medicine. According to data from OpenAlex, René Mulder has authored 18 papers receiving a total of 241 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Hematology, 5 papers in Genetics and 4 papers in Internal Medicine. Recurrent topics in René Mulder's work include Blood Coagulation and Thrombosis Mechanisms (12 papers), Venous Thromboembolism Diagnosis and Management (4 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (3 papers). René Mulder is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (12 papers), Venous Thromboembolism Diagnosis and Management (4 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (3 papers). René Mulder collaborates with scholars based in Netherlands, United Kingdom and Belgium. René Mulder's co-authors include André B. Mulder, Min Ki ten Kate, Michaël V. Lukens, Jan van der Meer, Willem M. Lijfering, Karina Meijer, F. Nanne Croles, Nic J.G.M. Veeger, James A. Huntington and Gerry A. F. Nicolaes and has published in prestigious journals such as Blood, British Journal of Haematology and Thrombosis and Haemostasis.

In The Last Decade

René Mulder

17 papers receiving 234 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
René Mulder 154 75 68 44 27 18 241
Simona Raso 114 0.7× 54 0.7× 84 1.2× 38 0.9× 51 1.9× 37 251
Hubert Galinat 112 0.7× 61 0.8× 107 1.6× 66 1.5× 34 1.3× 34 277
A. Tuinenburg 322 2.1× 37 0.5× 114 1.7× 102 2.3× 35 1.3× 11 400
Virginia Reyes‐Núñez 169 1.1× 46 0.6× 66 1.0× 35 0.8× 72 2.7× 23 271
Evdoxia Rapti 135 0.9× 87 1.2× 25 0.4× 43 1.0× 26 1.0× 11 234
Christian Pfrepper 164 1.1× 71 0.9× 48 0.7× 63 1.4× 24 0.9× 49 272
F. A. Scaraggi 424 2.8× 40 0.5× 110 1.6× 41 0.9× 36 1.3× 17 505
Lena Hau 218 1.4× 65 0.9× 41 0.6× 39 0.9× 21 0.8× 15 295
John Francis 143 0.9× 76 1.0× 21 0.3× 66 1.5× 47 1.7× 12 279
Emmanuel Arnaud 271 1.8× 156 2.1× 48 0.7× 123 2.8× 25 0.9× 11 374

Countries citing papers authored by René Mulder

Since Specialization
Citations

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

Fields of papers citing papers by René Mulder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of René Mulder

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

All Works

18 of 18 papers shown
1.
Johansson, Lennart, Bart Charbon, Dennis Hendriksen, et al.. (2025). MOLGENIS VIP: an end-to-end DNA variant interpretation pipeline for research and diagnostics configurable to support rapid implementation of new methods. NAR Genomics and Bioinformatics. 7(2). lqaf087–lqaf087.
2.
Graaf, Aniek O. de, René Mulder, Laura Bungener, et al.. (2022). Clonal hematopoiesis in patients with stem cell mobilization failure: a nested case-control study. Blood Advances. 7(7). 1269–1278. 5 indexed citations
3.
Mulder, René, Karina Meijer, & Michaël V. Lukens. (2020). Genetic testing of hereditary antithrombin deficiency in a large US pedigree using saliva samples. International Journal of Laboratory Hematology. 43(3). e101–e103. 2 indexed citations
4.
Wouters, Hanneke J. C. M., René Mulder, Isabelle A. van Zeventer, et al.. (2020). Erythrocytosis in the general population: clinical characteristics and association with clonal hematopoiesis. Blood Advances. 4(24). 6353–6363. 40 indexed citations
5.
Croles, F. Nanne, Michaël V. Lukens, René Mulder, et al.. (2019). Monitoring of heparins in antithrombin-deficient patients. Thrombosis Research. 175. 8–12. 23 indexed citations
6.
Mulder, René, et al.. (2018). High protein S activity due to C4b‐binding protein deficiency in a 34‐year‐old Surinamese female with ischemic retinopathy. Clinical Case Reports. 6(5). 935–938. 5 indexed citations
7.
Croles, F. Nanne, René Mulder, André B. Mulder, Michaël V. Lukens, & Karina Meijer. (2018). β-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study. Thrombosis Research. 168. 47–52. 2 indexed citations
8.
Kanhai, Danny A, René Mulder, Hans Kristian Ploos van Amstel, et al.. (2018). Familial macrothrombocytopenia due to a double mutation in cis in the alpha‐actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura. Pediatric Blood & Cancer. 65(12). e27418–e27418. 6 indexed citations
9.
Mulder, René, F. Nanne Croles, André B. Mulder, et al.. (2017). SERPINC1 gene mutations in antithrombin deficiency. British Journal of Haematology. 178(2). 279–285. 29 indexed citations
10.
Mulder, André B., et al.. (2017). Factor 11 single-nucleotide variants in women with heavy menstrual bleeding. Journal of Obstetrics and Gynaecology. 37(7). 912–918. 5 indexed citations
11.
Studer, Romain A., Fred R. Opperdoes, Gerry A. F. Nicolaes, André B. Mulder, & René Mulder. (2014). Understanding the functional difference between growth arrest-specific protein 6 and protein S: an evolutionary approach. Open Biology. 4(10). 140121–140121. 12 indexed citations
12.
Mahmoodi, Bakhtawar K., André B. Mulder, Femke Waanders, et al.. (2011). The impact of antiproteinuric therapy on the prothrombotic state in patients with overt proteinuria. Journal of Thrombosis and Haemostasis. 9(12). 2416–2423. 11 indexed citations
13.
Mulder, René, et al.. (2010). Relationship between cytomegalovirus infection and procoagulant changes in human immunodeficiency virus‐infected patients. Clinical Microbiology and Infection. 17(5). 747–749. 12 indexed citations
14.
Mulder, René, Bakhtawar K. Mahmoodi, Nic J.G.M. Veeger, et al.. (2010). Associations between high factor VIII and low free protein S levels with traditional arterial thrombotic risk factors and their risk on arterial thrombosis: Results from a retrospective family cohort study. Thrombosis Research. 126(4). e249–e254. 8 indexed citations
15.
Kate, Min Ki ten, Hanneke C. Kluin‐Nelemans, André B. Mulder, & René Mulder. (2010). Low cut-off values increase diagnostic performance of protein S assays. Thrombosis and Haemostasis. 104(9). 618–625. 12 indexed citations
16.
Kate, Min Ki ten, Mathieu Platteel, René Mulder, et al.. (2008). PROS1analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations. Human Mutation. 29(7). 939–947. 23 indexed citations
17.
Lijfering, Willem M., René Mulder, Min Ki ten Kate, et al.. (2008). Clinical relevance of decreased free protein S levels: results from a retrospective family cohort study involving 1143 relatives. Blood. 113(6). 1225–1230. 44 indexed citations
18.
Kate, Min Ki ten, René Mulder, Mathieu Platteel, et al.. (2006). Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency.. PubMed. 91(8). 1151–2. 2 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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