Nicole de Leeuw

10.6k total citations
104 papers, 3.2k citations indexed

About

Nicole de Leeuw is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Nicole de Leeuw has authored 104 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Genetics, 44 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Nicole de Leeuw's work include Genomic variations and chromosomal abnormalities (68 papers), Genomics and Rare Diseases (34 papers) and Genetics and Neurodevelopmental Disorders (34 papers). Nicole de Leeuw is often cited by papers focused on Genomic variations and chromosomal abnormalities (68 papers), Genomics and Rare Diseases (34 papers) and Genetics and Neurodevelopmental Disorders (34 papers). Nicole de Leeuw collaborates with scholars based in Netherlands, United States and United Kingdom. Nicole de Leeuw's co-authors include Rolph Pfundt, Joris A. Veltman, Bert B.A. de Vries, Lisenka E.L.M. Vissers, Jayne Y. Hehir‐Kwa, David A. Koolen, Erik A. Sistermans, Han G. Brunner, Willy M. Nillesen and Ad Geurts van Kessel and has published in prestigious journals such as Nature Medicine, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Nicole de Leeuw

99 papers receiving 3.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Nicole de Leeuw Netherlands 30 2.4k 1.4k 744 456 191 104 3.2k
Bassem A. Bejjani United States 36 2.6k 1.1× 1.8k 1.2× 1.0k 1.3× 577 1.3× 191 1.0× 83 4.1k
Blake C. Ballif United States 36 3.2k 1.3× 1.8k 1.3× 1.3k 1.8× 776 1.7× 172 0.9× 75 4.0k
Svetlana A. Yatsenko United States 26 1.8k 0.8× 1.5k 1.1× 628 0.8× 366 0.8× 139 0.7× 110 3.0k
Laura K. Conlin United States 27 1.6k 0.6× 1.2k 0.8× 561 0.8× 257 0.6× 161 0.8× 73 2.5k
Swaroop Aradhya United States 26 1.9k 0.8× 1.2k 0.8× 590 0.8× 145 0.3× 278 1.5× 85 2.8k
Claudia Ruivenkamp Netherlands 31 1.8k 0.8× 1.8k 1.3× 393 0.5× 193 0.4× 292 1.5× 79 3.4k
Howard R. Slater Australia 32 1.8k 0.7× 1.3k 0.9× 795 1.1× 490 1.1× 206 1.1× 99 3.0k
Andreas Tzschach Germany 30 1.8k 0.8× 2.1k 1.5× 255 0.3× 206 0.5× 205 1.1× 104 3.3k
Seema R. Lalani United States 30 1.6k 0.7× 1.5k 1.1× 481 0.6× 287 0.6× 125 0.7× 98 2.9k
Angelo Selicorni Italy 29 1.8k 0.8× 2.5k 1.8× 553 0.7× 165 0.4× 83 0.4× 176 3.8k

Countries citing papers authored by Nicole de Leeuw

Since Specialization
Citations

This map shows the geographic impact of Nicole de Leeuw'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 de Leeuw with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicole de Leeuw more than expected).

Fields of papers citing papers by Nicole de Leeuw

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicole de Leeuw. 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 de Leeuw. The network helps show where Nicole de Leeuw may publish in the future.

Co-authorship network of co-authors of Nicole de Leeuw

This figure shows the co-authorship network connecting the top 25 collaborators of Nicole de Leeuw. A scholar is included among the top collaborators of Nicole de Leeuw 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 de Leeuw. Nicole de Leeuw is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Dingemans, Alexander J.M., Sandra Jansen, Jeroen van Reeuwijk, et al.. (2024). Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals. Nature Medicine. 30(7). 1994–2003. 4 indexed citations
2.
Haak, Monique C., Xiao Han, Martina Ruiterkamp‐Versteeg, et al.. (2024). De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of Medical Genetics. 61(6). 549–552. 1 indexed citations
3.
Boer, Elke de, Carlo Marcelis, Kornelia Neveling, et al.. (2023). A complex structural variant near SOX3 causes X-linked split-hand/foot malformation. Human Genetics and Genomics Advances. 4(3). 100200–100200. 1 indexed citations
4.
Winarni, Tri Indah, et al.. (2023). Genetic diagnostic approach to intellectual disability and multiple congenital anomalies in Indonesia. Intractable & Rare Diseases Research. 12(2). 104–113. 1 indexed citations
5.
6.
Winarni, Tri Indah, et al.. (2020). Pathogenic variant in NFIX gene affecting three sisters due to paternal mosaicism. American Journal of Medical Genetics Part A. 182(11). 2731–2736. 7 indexed citations
7.
Leeuw, Nicole de, et al.. (2019). Duplication of 1q31.3q41 in two affected siblings due to paternal insertional translocation. BMJ Case Reports. 12(8). e230941–e230941. 1 indexed citations
8.
Verhagen, Judith M.A., Nicole de Leeuw, Dimitri N.M. Papatsonis, et al.. (2015). Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family. Molecular Syndromology. 6(2). 71–76. 17 indexed citations
9.
Agha, Zehra, Zafar Iqbal, Maleeha Azam, et al.. (2014). A complex microcephaly syndrome in a Pakistani family associated with a novel missense mutation in RBBP8 and a heterozygous deletion in NRXN1. Gene. 538(1). 30–35. 12 indexed citations
10.
Egger, J.I.M., et al.. (2014). Neuropsychological phenotype of a patient with a de novo 970 kb interstitial deletion in the distal 16p11.2 region. Neuropsychiatric Disease and Treatment. 10. 513–513. 16 indexed citations
11.
Verhoeven, W.M.A., et al.. (2013). Kallmann syndrome and schizophrenia: Is there a relationship?. European Archives of Psychiatry and Clinical Neuroscience. 263. 1 indexed citations
12.
Smeets, Dominique, Willy M. Nillesen, Tri Indah Winarni, et al.. (2012). Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversion. Gene. 511(2). 451–454. 16 indexed citations
13.
Leeuw, Nicole de, Trijnie Dijkhuizen, Jayne Y. Hehir‐Kwa, et al.. (2012). Diagnostic interpretation of array data using public databases and internet sources. Human Mutation. 33(6). 930–940. 83 indexed citations
14.
Verhoeven, W.M.A., et al.. (2012). Phelan–McDermid syndrome: Clinical report of a 70‐year‐old woman. American Journal of Medical Genetics Part A. 161(1). 158–161. 25 indexed citations
15.
Simons, Annet, et al.. (2012). Genome-wide arrays in routine diagnostics of hematological malignancies. Human Mutation. 33(6). 941–948. 44 indexed citations
16.
Feenstra, Ilse, Birgit Sikkema‐Raddatz, Helger G. Yntema, et al.. (2011). Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis. European Journal of Human Genetics. 19(11). 1152–1160. 41 indexed citations
17.
Leeuw, Nicole de, et al.. (2010). Terminal 3p deletions in two families—Correlation between molecular karyotype and phenotype. American Journal of Medical Genetics Part A. 152A(2). 441–446. 42 indexed citations
18.
Koolen, David A., Rolph Pfundt, Nicole de Leeuw, et al.. (2008). Genomic microarrays in mental retardation: A practical workflow for diagnostic applications. Human Mutation. 30(3). 283–292. 103 indexed citations
19.
Koolen, David A., Rolph Pfundt, Nicole de Leeuw, et al.. (2006). A novel 2.3 Mb microduplication of 12q24.21q24.23 detected by genome-wide tiling-path resolution array comparative genomic hybridization in a girl with syndromic mental retardation. Clinical Dysmorphology. 15(3). 133–137. 7 indexed citations
20.
Beever, Jonathan E., Nicole de Leeuw, Harris A. Lewin, et al.. (1998). Characterization of the 3’ End of the Gene for Bovine Factor XI. Journal of Dairy Science. 81(2). 539–543. 4 indexed citations

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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