Bert A. van der Reijden

8.5k citations
93 papers · 3.7k indexed · 2 hit papers · h-index 29
  • Hematology top 0.5%
    • Acute Myeloid Leukemia Research 55
  • Genetics top 1%
    • Blood disorders and treatments 11
    • Myeloproliferative Neoplasms: Diagnosis and Treatment 11
    • Cancer Genomics and Diagnostics 8
    • Ubiquitin and proteasome pathways 10
    • Epigenetics and DNA Methylation 10
    • Protein Degradation and Inhibitors 8
    • Retinoids in leukemia and cellular processes 7
  • Immunology top 10%

Bert A. van der Reijden

90 papers receiving 3.7k citations

Hit Papers

Somatic mutations of the histone methyltransferase gene E...5412009202620142020100200300400500

Peers

Bert A. van der Reijden
Comparison fields: 5 of 121
  • Hematology 1.8k
  • Genetics 634
  • Cancer Research 554
  • Molecular Biology 2.5k
  • Immunology 413
Replace Thomas Prébet with:
Thomas Prébet France
Josée Hébert Canada
Jan Jacob Schuringa Netherlands
Joop H. Jansen Netherlands
Lydia Campos France
Norihiko Kawamata Japan
Marc Loriaux United States
Hironori Harada Japan
Johan Richter Sweden
Hetty E. Carraway United States
Bert A. van der Reijden relative to Thomas Prébet France Thomas Prébet's profile →
Citations per field
00.5×1.7×
Thomas Prébet · 1×
Citations per year

Countries citing papers authored by Bert A. van der Reijden

Since Specialization
Citations

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

Fields of papers citing papers by Bert A. van der Reijden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bert A. van der Reijden. 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 Bert A. van der Reijden. The network helps show where Bert A. van der Reijden may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Bert A. van der Reijden, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bert A. van der Reijden Line = papers co-authored together Bert A. van der Reijden links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20251
2 20241
3 20242
4 20240
5 20232
6 20235
7 20236
8 202338
9 20203
10 2017121
11 201615
12
ANALYSIS OF NEW GFI1B VARIANTS IN PATIENTS WITH INHERITED BLEEDING AND PLATELET DISORDERS
20152
13 20141
14 201034
15 200983
16 200927
17 200612
18 200483
19 200227
20 200119

About Bert A. van der Reijden

Bert A. van der Reijden is a scholar working on Hematology, Genetics and Family Practice, having authored 93 papers that have together received 3.7k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (55 papers), Blood disorders and treatments (11 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (11 papers), Ubiquitin and proteasome pathways (10 papers), Epigenetics and DNA Methylation (10 papers), Cancer Genomics and Diagnostics (8 papers), Protein Degradation and Inhibitors (8 papers) and Retinoids in leukemia and cellular processes (7 papers). The work is most often cited by research in Hematology (1.8k citations), Genetics (634 citations) and Cancer Research (554 citations). Bert A. van der Reijden has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Joop H. Jansen, Théo de Witte, Ruth Knops, Marion Massop, Saskia Langemeijer, Roland P. Kuiper, Peter Vandenberghe, Gorica Nikoloski, Reinier Raymakers and Laurens T. van der Meer. Their work appears in journals such as Nature Genetics, Journal of Clinical Oncology and The EMBO Journal.

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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