Nicole Maas

698 total citations
13 papers, 455 citations indexed

About

Nicole Maas is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Nicole Maas has authored 13 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Nicole Maas's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (4 papers) and Genomics and Rare Diseases (3 papers). Nicole Maas is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (4 papers) and Genomics and Rare Diseases (3 papers). Nicole Maas collaborates with scholars based in Belgium, Netherlands and United States. Nicole Maas's 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 and has published in prestigious journals such as Movement Disorders, Journal of Histochemistry & Cytochemistry and Journal of Medical Genetics.

In The Last Decade

Nicole Maas

10 papers receiving 432 citations

Peers

Nicole Maas
Heidi A. Heilstedt United States
T. Lukusa Belgium
Courtney Sebold United States
Anna Capalbo Italy
Joanna Wiszniewska United States
Katherine Rojas United States
Mónica Rosello Spain
Joo Wook Ahn United Kingdom
M. Chery France
Mauro Pierluigi Italy
Heidi A. Heilstedt United States
Nicole Maas
Citations per year, relative to Nicole Maas Nicole Maas (= 1×) peers Heidi A. Heilstedt

Countries citing papers authored by Nicole Maas

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

13 of 13 papers shown
1.
Iwanowski, Piotr, Barbara Panasiuk, Griet Van Buggenhout, et al.. (2011). Wolf–Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter. American Journal of Medical Genetics Part A. 155(8). 1833–1847. 4 indexed citations
2.
Maas, Nicole, Tom Van de Putte, Cindy Melotte, et al.. (2009). TheC20orf133gene is disrupted in a patient with Kabuki syndrome. BMJ Case Reports. 2009. bcr0620091994–bcr0620091994. 3 indexed citations
3.
Maas, Nicole, Griet Van Buggenhout, Femke Hannes, et al.. (2007). Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH). Journal of Medical Genetics. 45(2). 71–80. 99 indexed citations
4.
Maas, Nicole, Steven Van Vooren, Femke Hannes, et al.. (2007). The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random.. PubMed. 18(4). 357–65. 16 indexed citations
5.
Maas, Nicole, Tom Van de Putte, Cindy Melotte, et al.. (2007). The C20orf133 gene is disrupted in a patient with Kabuki syndrome. Journal of Medical Genetics. 44(9). 562–569. 46 indexed citations
6.
Buggenhout, Griet Van, Conny M.A. van Ravenswaaij‐Arts, Nicole Maas, et al.. (2005). The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients. European Journal of Medical Genetics. 48(3). 276–289. 100 indexed citations
7.
Vermeesch, Joris, Maria Dêbiec‐Rychter, Cindy Melotte, et al.. (2005). Molecular karyotyping: Towards improved pre- and postnatal diagnosis.
8.
Vermeesch, Joris, Cindy Melotte, Guy Froyen, et al.. (2005). Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis. Journal of Histochemistry & Cytochemistry. 53(3). 413–422. 118 indexed citations
9.
Vermeesch, Joris, Nicole Maas, Cindy Melotte, et al.. (2004). 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. European Journal of Human Genetics. 12. 145.
10.
Dimitrov, Boyan, et al.. (2004). Mesomelic form of short stature, congenital cataract, patent ductus arteriosus and muscular hypotonia associated with de novo translocation (13;18)(q14;q23). 15(1). 130–130.
11.
Buggenhout, Griet Van, Nicole Maas, Jean‐Pierre Fryns, & Joris Vermeesch. (2004). A dysmorphic boy with 4qter deletion and 4q32.3‐34.3 duplication: Clinical, cytogenetic, and molecular findings. American Journal of Medical Genetics Part A. 131A(2). 186–189. 26 indexed citations
12.
Dimitrov, Boyan, Koenraad Devriendt, Nicole Maas, et al.. (2004). Mesomelic form of chondrodysplasia and congenital glaucoma associated with de novo translocation (13;18)(q14;q23).. PubMed. 15(2). 191–7. 1 indexed citations
13.

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.

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