A. M. Wiegers
- Genetics top 10%
- Cognitive Neuroscience top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health
- Clinical Psychology
- Co-authors
- J. P. FrynsL.M.G. CurfsMartine BorghgraefLmg CurfsB. A. OostraSerieta MohkamsingDicky HalleyMartinus F. Niermeijer
- Topics
- Genetics and Neurodevelopmental Disorders (7 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers)Autism Spectrum Disorder Research (2 papers)
- Journals
- Journal of Medical GeneticsJournal of Intellectual Disability ResearchAmerican Journal of Medical Genetics
- Partner nations
- BelgiumNetherlandsUnited Kingdom
In The Last Decade
A. M. Wiegers
10 papers receiving 305 citations
Peers
Comparison fields: 5 of 34
- Genetics 297
- Cognitive Neuroscience 190
- Molecular Biology 134
- Pediatrics, Perinatology and Child Health 18
- Clinical Psychology 17
Countries citing papers authored by A. M. Wiegers
This map shows the geographic impact of A. M. Wiegers'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 A. M. Wiegers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. M. Wiegers more than expected).
Fields of papers citing papers by A. M. Wiegers
This network shows the impact of papers produced by A. M. Wiegers. 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 A. M. Wiegers. The network helps show where A. M. Wiegers may publish in the future.
Co-authorship network of co-authors of A. M. Wiegers
This figure shows the co-authorship network connecting the top 25 collaborators of A. M. Wiegers. A scholar is included among the top collaborators of A. M. Wiegers 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 A. M. Wiegers. A. M. Wiegers is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | Mental status of females with an FMR1 gene full mutation. | 166 |
| 2 | Personality profiles of children and adolescents with Williams syndrome and children and adolescents visiting regular schools | 1 |
| 3 | A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features. | 6 |
| 4 | 17 | |
| 5 | A longitudinal study of intelligence in Dutch fragile X boys. | 3 |
| 6 | 70 | |
| 7 | 14 | |
| 8 | 12 | |
| 9 | Strengths and weaknesses in the cognitive profile of fra(X) patients. | 10 |
| 10 | A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experience. | 14 |
About A. M. Wiegers
A. M. Wiegers is a scholar working on Structural Biology, Genetics and Developmental Neuroscience, having authored 10 papers that have together received 313 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Autism Spectrum Disorder Research (2 papers). The work is most often cited by research in Genetics (297 citations), Cognitive Neuroscience (190 citations) and Developmental Neuroscience (16 citations). A. M. Wiegers has collaborated with scholars based in Belgium, Netherlands and United Kingdom. Frequent co-authors include J. P. Fryns, L.M.G. Curfs, Martine Borghgraef, Lmg Curfs, B. A. Oostra, Serieta Mohkamsing, Dicky Halley, Martinus F. Niermeijer, H.J. Duivenvoorden and Ans MW van den Ouweland. Their work appears in journals such as Journal of Medical Genetics, Journal of Intellectual Disability Research and American Journal of Medical Genetics.
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.