N. Logghe
Impact in
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- Genomic variations and chromosomal abnormalities
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- Acute Myeloid Leukemia Research
Papers in
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- RNA regulation and disease 3
- Genomics and Chromatin Dynamics 2
- DNA and Nucleic Acid Chemistry 2
- Protein Tyrosine Phosphatases 1
- Genetics 7
- Genomic variations and chromosomal abnormalities 5
- Connective tissue disorders research 1
- Co-authors
- M. van Eygen (6 shared papers)Herman Van den Berghe (5 shared papers)J. P. Fryns (4 shared papers)J P Fryns (1 shared paper)M Dumoulin (1 shared paper)Lucas G. Van Der Hauwaert (1 shared paper)Jean‐Jacques Martin (1 shared paper)Jacques Libert (1 shared paper)
- Journals
- Human Genetics (3 papers)European Journal of Pediatrics (2 papers)Drug Safety (1 paper)Pediatric Research (1 paper)Acta Neuropathologica (1 paper)
- Partner nations
- BelgiumNetherlandsUnited Kingdom
In The Last Decade
N. Logghe
13 papers receiving 234 citations
Peers
Comparison fields: 5 of 47
- Genetics 85
- Hematology 30
- Neurology 16
- Pediatrics, Perinatology and Child Health 37
- Molecular Biology 104
Countries citing papers authored by N. Logghe
This map shows the geographic impact of N. Logghe'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 N. Logghe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N. Logghe more than expected).
Fields of papers citing papers by N. Logghe
This network shows the impact of papers produced by N. Logghe. 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 N. Logghe. The network helps show where N. Logghe may publish in the future.
Co-authors
The 25 scholars most cited alongside N. Logghe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1978 | 47 | |
| 2 | 1981 | 39 | |
| 3 | 2006 | 30 | |
| 4 | 1983 | 25 | |
| 5 | 1979 | 23 | |
| 6 | 1979 | 22 | |
| 7 | 1978 | 14 | |
| 8 | Haemorrhagic disease of the newborn in the offspring of rifampicin and isoniazid treated mothers. | 1977 | 14 |
| 9 | 1979 | 11 | |
| 10 | 2016 | 6 | |
| 11 | 1989 | 6 | |
| 12 | Congenital hyperparathyroidism. Case report and review of the literature. | 1977 | 5 |
| 13 | New chromosomal syndromes. I. Partial trisomy of the distal portion of the long arm of chromosome number 10 (10q24 leads to 10qter): a clinical entity. | 1979 | 1 |
| 14 | 1980 | 0 |
About N. Logghe
N. Logghe is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Infectious Diseases, having authored 14 papers that have together received 243 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), RNA regulation and disease (3 papers), Genomics and Chromatin Dynamics (2 papers), DNA and Nucleic Acid Chemistry (2 papers), Hereditary Neurological Disorders (1 paper), Connective tissue disorders research (1 paper), Protein Tyrosine Phosphatases (1 paper) and Neonatal and fetal brain pathology (1 paper). The work is most often cited by research in Genetics (85 citations), Hematology (30 citations), Neurology (16 citations), Pediatrics, Perinatology and Child Health (37 citations) and Molecular Biology (104 citations). N. Logghe has collaborated with scholars based in Belgium, Netherlands and United Kingdom. Frequent co-authors include M. van Eygen, Herman Van den Berghe, J. P. Fryns, J P Fryns, M Dumoulin, Lucas G. Van Der Hauwaert, Jean‐Jacques Martin, Jacques Libert, J. G. Leroy and Sabrina Laroche. Their work appears in journals such as Human Genetics, European Journal of Pediatrics, Drug Safety, Pediatric Research and Acta Neuropathologica.
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.