Nils Peeters

493 total citations
16 papers, 310 citations indexed

About

Nils Peeters is a scholar working on Sensory Systems, Molecular Biology and Genetics. According to data from OpenAlex, Nils Peeters has authored 16 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Sensory Systems, 6 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Nils Peeters's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Connective tissue disorders research (4 papers) and Aortic aneurysm repair treatments (4 papers). Nils Peeters is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Connective tissue disorders research (4 papers) and Aortic aneurysm repair treatments (4 papers). Nils Peeters collaborates with scholars based in Belgium, Netherlands and Denmark. Nils Peeters's co-authors include Wim Wuyts, Lut Van Laer, Guy Van Camp, Bart Loeys, Marlies Kempers, Ronald V. Lacro, Simone Salemink, Dan M. Roden, Geert Mortier and Johan Saenen and has published in prestigious journals such as Bioinformatics, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Nils Peeters

16 papers receiving 304 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nils Peeters Belgium 10 145 115 112 74 37 16 310
Yosra Bouyacoub Tunisia 12 103 0.7× 26 0.2× 222 2.0× 85 1.1× 12 0.3× 27 381
Ann Muilenburg United States 8 138 1.0× 133 1.2× 45 0.4× 41 0.6× 40 1.1× 9 271
Alisha Wilkens United States 13 255 1.8× 23 0.2× 239 2.1× 61 0.8× 8 0.2× 20 438
Joy Samanich United States 10 88 0.6× 12 0.1× 141 1.3× 86 1.2× 12 0.3× 17 289
MaryPat Jones United States 9 144 1.0× 113 1.0× 153 1.4× 31 0.4× 5 0.1× 9 326
Polona Le Quesne Stabej United Kingdom 14 167 1.2× 14 0.1× 348 3.1× 123 1.7× 93 2.5× 18 535
Catherine Bromhead Australia 8 150 1.0× 14 0.1× 169 1.5× 37 0.5× 12 0.3× 8 287
L Korniszewski Poland 12 249 1.7× 18 0.2× 274 2.4× 85 1.1× 5 0.1× 26 498
Carina Frykholm Sweden 10 56 0.4× 10 0.1× 100 0.9× 94 1.3× 17 0.5× 15 276
Laima Ambrozaitytė Lithuania 10 205 1.4× 20 0.2× 145 1.3× 19 0.3× 11 0.3× 38 313

Countries citing papers authored by Nils Peeters

Since Specialization
Citations

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

Fields of papers citing papers by Nils Peeters

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nils Peeters. 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 Nils Peeters. The network helps show where Nils Peeters may publish in the future.

Co-authorship network of co-authors of Nils Peeters

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

All Works

16 of 16 papers shown
1.
Boudewyns, An, Jenneke van den Ende, Nils Peeters, et al.. (2023). Targeted Next-Generation Sequencing in Children With Bilateral Sensorineural Hearing Loss: Diagnostic Yield and Predictors of a Genetic Cause. Otology & Neurotology. 44(4). 360–366. 2 indexed citations
2.
Kumar, Ajay, Bart Loeys, Gerarda van de Beek, et al.. (2022). varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data. Bioinformatics. 39(1). 2 indexed citations
3.
Krebsová, Alice, Birgitte Rode Diness, Steven Laga, et al.. (2021). Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings. International Journal of Molecular Sciences. 22(13). 7111–7111. 9 indexed citations
4.
Boudewyns, An, Jenneke van den Ende, Frank Declau, et al.. (2020). Etiological Work-up in Referrals From Neonatal Hearing Screening: 20 Years of Experience. Otology & Neurotology. 41(9). 1240–1248. 9 indexed citations
5.
Boudewyns, An, Jenneke van den Ende, Manou Sommen, et al.. (2018). Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children. Otology & Neurotology. 39(6). 732–738. 9 indexed citations
6.
Camp, Guy Van, Nils Peeters, Ellen Elinck, et al.. (2018). Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment. European Journal of Human Genetics. 26(4). 587–591. 23 indexed citations
7.
Kempers, Marlies, Alessandra Maugeri, Carlo Marcelis, et al.. (2018). Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: further delineation of the phenotype. Journal of Medical Genetics. 56(4). 220–227. 28 indexed citations
8.
Vandeweyer, Geert, Josephina Meester, Simone Salemink, et al.. (2015). Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm Genes. Human Mutation. 36(8). 808–814. 78 indexed citations
9.
Wischmeijer, Anita, Lut Van Laer, Nikhita Bolar, et al.. (2013). Thoracic Aortic Aneurysm in Infancy in Aneurysms–Osteoarthritis Syndrome Due to a Novel SMAD3 Mutation: Further Delineation of the Phenotype. American Journal of Medical Genetics Part A. 161(5). 1028–1035. 47 indexed citations
10.
Alasti, Fatemeh, Nils Peeters, Wim Wuyts, Mohammad Hossein Sanati, & Guy Van Camp. (2010). Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive.. PubMed. 127(1). 116–116. 1 indexed citations
11.
Konings, Annelies, Guy Van Camp, Els Van Eyken, et al.. (2008). Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients. Mitochondrion. 8(5-6). 377–382. 31 indexed citations
12.
Courtens, Winnie, Stefan Vermeulen, Wim Wuyts, et al.. (2005). An interstitial deletion of chromosome 7 at band q21: A case report and review. American Journal of Medical Genetics Part A. 134A(1). 12–23. 17 indexed citations
13.
Bygum, Anette, Regina C. Betz, Knud Kragballe, et al.. (2004). KID Syndrome: Report of a Scandinavian Patient with Connexin‐26 Gene Mutation. Acta Dermato Venereologica. 85(2). 152–155. 14 indexed citations
14.
Massa, Guy, et al.. (2003). Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene. European Journal of Pediatrics. 162(10). 674–677. 8 indexed citations
15.
Wuyts, Wim, Ignacio del Castillo, Nils Peeters, et al.. (2002). Low frequency of the GJB6 342 Kb deletion in the belgian deaf population.. The American Journal of Human Genetics. 71(4). 510. 2 indexed citations
16.
Reyniers, Edwin, Patrick Van Bogaert, Nils Peeters, et al.. (1999). A New Neurological Syndrome with Mental Retardation, Choreoathetosis, and Abnormal Behavior Maps to Chromosome Xp11. The American Journal of Human Genetics. 65(5). 1406–1412. 30 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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