Martine Borghgraef
- Genetics top 2%
- Cognitive Neuroscience top 5%
- Molecular Biology
- Developmental Neuroscience top 5%
- Pediatrics, Perinatology and Child Health
- Co-authors
- J. P. FrynsHerman Van den BergheJean‐Pierre FrynsJean SteyaertEric LegiusA. M. WiegersL.M.G. CurfsAnnick Vogels
- Topics
- Genetics and Neurodevelopmental Disorders (30 papers)Autism Spectrum Disorder Research (14 papers)Genomic variations and chromosomal abnormalities (7 papers)
- Journals
- The American Journal of Human GeneticsJournal of Autism and Developmental DisordersJournal of Medical Genetics
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Martine Borghgraef
52 papers receiving 891 citations
Peers
Comparison fields: 5 of 60
- Genetics 780
- Cognitive Neuroscience 408
- Molecular Biology 381
- Developmental Neuroscience 84
- Pediatrics, Perinatology and Child Health 76
Countries citing papers authored by Martine Borghgraef
This map shows the geographic impact of Martine Borghgraef'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 Martine Borghgraef with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martine Borghgraef more than expected).
Fields of papers citing papers by Martine Borghgraef
This network shows the impact of papers produced by Martine Borghgraef. 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 Martine Borghgraef. The network helps show where Martine Borghgraef may publish in the future.
Co-authorship network of co-authors of Martine Borghgraef
This figure shows the co-authorship network connecting the top 25 collaborators of Martine Borghgraef. A scholar is included among the top collaborators of Martine Borghgraef 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 Martine Borghgraef. Martine Borghgraef is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 53 | |
| 2 | Investigating neurocognitive endophenotypes of autism spectrum disorders (ASD) by including an ASD sample with co-occuring neurofibromatosis type 1 | 1 |
| 3 | 8 | |
| 4 | 47 | |
| 5 | 24 | |
| 6 | 31 | |
| 7 | Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study | 0 |
| 8 | Comparison of visual abilities in Williams-Beuren syndrome, Down syndrome and Turner syndrome: A pilot study | 1 |
| 9 | Trisomy 9p and triploidy: The changing phenotype with age, psychological profile and speech development | 1 |
| 10 | 26 | |
| 11 | 7 | |
| 12 | Adults with Williams syndrome: Evaluation of the medical, psychological and behavioural aspects | 2 |
| 13 | 16 | |
| 14 | 10 | |
| 15 | 3 | |
| 16 | 24 | |
| 17 | 70 | |
| 18 | 20 | |
| 19 | 21 | |
| 20 | 6 |
About Martine Borghgraef
Martine Borghgraef is a scholar working on Genetics, Structural Biology and Developmental Neuroscience, having authored 54 papers that have together received 925 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (30 papers), Autism Spectrum Disorder Research (14 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Genetics (780 citations), Cognitive Neuroscience (408 citations) and Developmental Neuroscience (84 citations). Martine Borghgraef has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include J. P. Fryns, Herman Van den Berghe, Jean‐Pierre Fryns, Jean Steyaert, Eric Legius, A. M. Wiegers, L.M.G. Curfs, Annick Vogels, Gene S. Fisch and Mie‐Jef Descheemaeker. Their work appears in journals such as The American Journal of Human Genetics, Journal of Autism and Developmental Disorders and 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.