Nicole Maas
- Genetics top 5%
- Molecular Biology
- Plant Science
- Pediatrics, Perinatology and Child Health top 10%
- Genetics
- Co-authors
- Joris VermeeschGriet Van BuggenhoutKoenraad DevriendtJean‐Pierre FrynsCindy MelotteDamien SanlavilleAnnick VogelsConny M.A. van Ravenswaaij‐Arts
- Topics
- Genomic variations and chromosomal abnormalities (10 papers)Prenatal Screening and Diagnostics (4 papers)Genomics and Rare Diseases (3 papers)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Nicole Maas
10 papers receiving 432 citations
Peers
Comparison fields: 5 of 53
- Genetics 351
- Molecular Biology 191
- Plant Science 120
- Pediatrics, Perinatology and Child Health 101
- Genetics 36
Countries citing papers authored by Nicole Maas
This map shows the geographic impact of Nicole Maas'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 Nicole Maas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicole Maas more than expected).
Fields of papers citing papers by Nicole Maas
This network shows the impact of papers produced by Nicole Maas. 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 Nicole Maas. The network helps show where Nicole Maas may publish in the future.
Co-authorship network of co-authors of Nicole Maas
This figure shows the co-authorship network connecting the top 25 collaborators of Nicole Maas. A scholar is included among the top collaborators of Nicole Maas 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 Nicole Maas. Nicole Maas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 4 | |
| 2 | 3 | |
| 3 | 99 | |
| 4 | The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random. | 16 |
| 5 | 46 | |
| 6 | 100 | |
| 7 | Molecular karyotyping: Towards improved pre- and postnatal diagnosis | 0 |
| 8 | 118 | |
| 9 | Micro-array CGH analysis of 4p microdeletions refines the genotype-phenotype map of the region and pinpoints low copy repeats as susceptibility sites for terminal chromosomal deletions | 0 |
| 10 | Mesomelic form of short stature, congenital cataract, patent ductus arteriosus and muscular hypotonia associated with de novo translocation (13;18)(q14;q23) | 0 |
| 11 | 26 | |
| 12 | Mesomelic form of chondrodysplasia and congenital glaucoma associated with de novo translocation (13;18)(q14;q23). | 1 |
| 13 | 42 |
About Nicole Maas
Nicole Maas is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 13 papers that have together received 455 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (351 citations), Pediatrics, Perinatology and Child Health (101 citations) and Developmental Biology (8 citations). Nicole Maas has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Joris Vermeesch, Griet Van Buggenhout, Koenraad Devriendt, Jean‐Pierre Fryns, Cindy Melotte, Damien Sanlaville, Annick Vogels, Conny M.A. van Ravenswaaij‐Arts, J. P. Fryns and Ronald Thoelen. Their work appears in journals such as Movement Disorders, Journal of Histochemistry & Cytochemistry 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.