Annick Vogels
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 33
- Genetic Syndromes and Imprinting 16
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 9
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- Congenital heart defects research 16
- Co-authors
- Koenraad Devriendt (21 shared papers)Ann Swillen (15 shared papers)Jean‐Pierre Fryns (8 shared papers)Eric Legius (16 shared papers)J P Fryns (4 shared papers)J. P. Fryns (8 shared papers)Griet Van Buggenhout (11 shared papers)Joris Vermeesch (10 shared papers)
- Journals
- Journal of Intellectual Disability Research (5 papers)European Journal of Medical Genetics (3 papers)Clinical Genetics (3 papers)Human Mutation (2 papers)The British Journal of Psychiatry (2 papers)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Annick Vogels
60 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 86
- Genetics 1.2k
- Pediatrics, Perinatology and Child Health 269
- Molecular Biology 947
- Developmental Biology 27
- Cognitive Neuroscience 215
Countries citing papers authored by Annick Vogels
This map shows the geographic impact of Annick Vogels'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 Annick Vogels with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annick Vogels more than expected).
Fields of papers citing papers by Annick Vogels
This network shows the impact of papers produced by Annick Vogels. 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 Annick Vogels. The network helps show where Annick Vogels may publish in the future.
Co-authors
The 25 scholars most cited alongside Annick Vogels, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 209 | |
| 2 | 2000 | 146 | |
| 3 | The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. | 1999 | 143 |
| 4 | 2003 | 137 | |
| 5 | 2007 | 132 | |
| 6 | 2005 | 100 | |
| 7 | 2013 | 90 | |
| 8 | 2006 | 84 | |
| 9 | 2004 | 81 | |
| 10 | 2012 | 77 | |
| 11 | 2014 | 54 | |
| 12 | Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience. | 1999 | 51 |
| 13 | 2018 | 50 | |
| 14 | 2002 | 49 | |
| 15 | 2013 | 47 | |
| 16 | 2016 | 39 | |
| 17 | 2007 | 38 | |
| 18 | 2008 | 32 | |
| 19 | 1998 | 31 | |
| 20 | Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:). | 1989 | 30 |
About Annick Vogels
Annick Vogels is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 63 papers that have together received 2.1k indexed citations. Recurring topics across this work include Congenital heart defects research (16 papers), Genetic Syndromes and Imprinting (16 papers), Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (9 papers), Autism Spectrum Disorder Research (6 papers), Prenatal Screening and Diagnostics (6 papers), Congenital Heart Disease Studies (5 papers) and Neurofibromatosis and Schwannoma Cases (4 papers). The work is most often cited by research in Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (269 citations), Molecular Biology (947 citations), Developmental Biology (27 citations) and Cognitive Neuroscience (215 citations). Annick Vogels has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Koenraad Devriendt, Ann Swillen, Jean‐Pierre Fryns, Eric Legius, J P Fryns, J. P. Fryns, Griet Van Buggenhout, Joris Vermeesch, Thomy de Ravel and Mie‐Jef Descheemaeker. Their work appears in journals such as Journal of Intellectual Disability Research, European Journal of Medical Genetics, Clinical Genetics, Human Mutation and The British Journal of Psychiatry.
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.