Peter Marynen
About
In The Last Decade
Peter Marynen
285 papers receiving 14.5k citations
Hit Papers
Peers
Comparison fields: 5 of 153
- Molecular Biology 6.8k
- Genetics 3.1k
- Hematology 2.6k
- Oncology 2.3k
- Pathology and Forensic Medicine 2.2k
Countries citing papers authored by Peter Marynen
This map shows the geographic impact of Peter Marynen'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 Peter Marynen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Marynen more than expected).
Fields of papers citing papers by Peter Marynen
This network shows the impact of papers produced by Peter Marynen. 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 Peter Marynen. The network helps show where Peter Marynen may publish in the future.
Co-authorship network of co-authors of Peter Marynen
This figure shows the co-authorship network connecting the top 25 collaborators of Peter Marynen. A scholar is included among the top collaborators of Peter Marynen 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 Peter Marynen. Peter Marynen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 33 | |
| 2 | 68 | |
| 3 | A novel t(4;9)(q21;p24) fuses SEC31A to JAK2 in nodular-sclerosis Hodgkin lymphoma | 2 |
| 4 | 58 | |
| 5 | 92 | |
| 6 | Functional characterization of the T-ALL associated EML1-ABL1 and NUP214-ABL1 oncogenes | 1 |
| 7 | 57 | |
| 8 | Duplication of the MECP2 region is a frequent cause of severe mental retardation and neurological symptoms in males | 1 |
| 9 | Molecular karkyotyping detecs structural low grade mosaics in 4 % of patietns with idiopathic mental retardation and multiple congenital aberrations | 2 |
| 10 | Micro-array CGH analysis of 4p microdeletions refines the genotype-phenotype map of the region and pinpoints low copy repeats as susceptibility sites for terminal chromosomal deletions | 0 |
| 11 | The TET RNA-binding proteins, EWSR1 and TAF15, are involved in acute lymphoblastic leukemia, through fusion with a new transcription factor, CIZ/NMP4 | 2 |
| 12 | Molecular characterization of a t(2;3)(p23;q26): A recurrent translocation involving the EVI1 gene | 2 |
| 13 | Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive ALK tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesis | 2 |
| 14 | Fusion between the apoptosis inhibitor gene AP12 and a novel 18q gene MLT , rearranged in the t(11,18)(q21;q21), marks half of the gastro-intestinal MALT type lymphomas without large cell proliferation | 4 |
| 15 | Telomere length regulation in telomerase positive murine cell line | 1 |
| 16 | 213 | |
| 17 | Identification and characterisation of BTL, a new fusion partner of ETV6 in 1 T-ALL case and 2 AML cases with a translocation t(4;12) (q11;p13) | 1 |
| 18 | A form of non-specific mental retardation is probably caused by a microdeletion in a Belgian family | 12 |
| 19 | FISH analysis of typical t(5;12) (q32;p12) and variant t(10;12)(q23;p12) translocation in four patients with chronic myeloid disorders | 4 |
| 20 | 18 |
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.