H Veenema
- Molecular Biology
- Genetics top 5%
- Genetics top 10%
- Cognitive Neuroscience
- Cardiology and Cardiovascular Medicine
- Co-authors
- P. PearsonEgbert BakkerChristine Van BroeckhovenG J van OmmenJohan T. den DunnenP.M. GrootscholtenMarten H. HofkerG.J.B. van Ommen
- Topics
- Genetics and Neurodevelopmental Disorders (11 papers)Muscle Physiology and Disorders (6 papers)Neurogenetic and Muscular Disorders Research (5 papers)
- Cited by
- GeneticsMolecular Biology
- Partner nations
- NetherlandsUnited KingdomGermany
In The Last Decade
H Veenema
24 papers receiving 700 citations
Peers
Comparison fields: 5 of 66
- Molecular Biology 470
- Genetics 396
- Genetics 114
- Cognitive Neuroscience 82
- Cardiology and Cardiovascular Medicine 81
Countries citing papers authored by H Veenema
This map shows the geographic impact of H Veenema'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 H Veenema with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H Veenema more than expected).
Fields of papers citing papers by H Veenema
This network shows the impact of papers produced by H Veenema. 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 H Veenema. The network helps show where H Veenema may publish in the future.
Co-authorship network of co-authors of H Veenema
This figure shows the co-authorship network connecting the top 25 collaborators of H Veenema. A scholar is included among the top collaborators of H Veenema 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 H Veenema. H Veenema is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | [Early diagnosis of fragile X mental retardation syndrome]. | 1 |
| 2 | Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis. | 1 |
| 3 | 16 | |
| 4 | [Clinical, cytogenetic and molecular aspects of fragile X syndrome]. | 1 |
| 5 | 10 | |
| 6 | A male carrier for Duchenne muscular dystrophy. | 2 |
| 7 | 3 | |
| 8 | 21 | |
| 9 | 155 | |
| 10 | 37 | |
| 11 | Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation. | 74 |
| 12 | 12 | |
| 13 | 39 | |
| 14 | 50 | |
| 15 | 60 | |
| 16 | 1 | |
| 17 | [Mental retardation and the fragile X syndrome]. | 1 |
| 18 | 9 | |
| 19 | [Familial mental retardation and the fragile X syndrome]. | 1 |
| 20 | 6 |
About H Veenema
H Veenema is a scholar working on Genetics, Genetics and Developmental Biology, having authored 24 papers that have together received 726 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Muscle Physiology and Disorders (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). The work is most often cited by research in Genetics (396 citations), Genetics (114 citations) and Molecular Biology (470 citations). H Veenema has collaborated with scholars based in Netherlands, United Kingdom and Germany. Frequent co-authors include P. Pearson, Egbert Bakker, Christine Van Broeckhoven, G J van Ommen, Johan T. den Dunnen, P.M. Grootscholten, Marten H. Hofker, G.J.B. van Ommen, J P Geraedts and Wim Van Hul. Their work appears in journals such as Nature, Journal of Neurology Neurosurgery & Psychiatry and Clinical Pharmacology & Therapeutics.
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.