Frank Declau

2.2k total citations
58 papers, 1.5k citations indexed

About

Frank Declau is a scholar working on Sensory Systems, Otorhinolaryngology and Surgery. According to data from OpenAlex, Frank Declau has authored 58 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Sensory Systems, 21 papers in Otorhinolaryngology and 20 papers in Surgery. Recurrent topics in Frank Declau's work include Hearing, Cochlea, Tinnitus, Genetics (25 papers), Ear Surgery and Otitis Media (20 papers) and Nasal Surgery and Airway Studies (11 papers). Frank Declau is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (25 papers), Ear Surgery and Otitis Media (20 papers) and Nasal Surgery and Airway Studies (11 papers). Frank Declau collaborates with scholars based in Belgium, United States and Netherlands. Frank Declau's co-authors include Paul Van de Heyning, Guy Van Camp, Jenneke van den Ende, An Boudewyns, Richard J. Smith, Erik Fransén, Cor W. R. J. Cremers, Agnete Parving, Valerie Newton and Manuela Mazzoli and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Frank Declau

54 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frank Declau Belgium 20 721 618 342 323 271 58 1.5k
István Sziklai Hungary 26 685 1.0× 699 1.1× 465 1.4× 335 1.0× 316 1.2× 88 1.7k
Armağan İncesulu Türkiye 19 547 0.8× 544 0.9× 249 0.7× 263 0.8× 311 1.1× 59 1.3k
Lukas D. Landegger United States 21 528 0.7× 390 0.6× 251 0.7× 309 1.0× 273 1.0× 58 1.5k
Shin Kariya Japan 22 431 0.6× 557 0.9× 343 1.0× 165 0.5× 145 0.5× 177 1.7k
Kunihiro Fukushima Japan 28 824 1.1× 362 0.6× 335 1.0× 1.1k 3.4× 381 1.4× 121 2.3k
Samuel P. Gubbels United States 20 701 1.0× 295 0.5× 696 2.0× 185 0.6× 347 1.3× 64 1.8k
Christopher Zalewski United States 24 420 0.6× 160 0.3× 307 0.9× 371 1.1× 288 1.1× 59 1.5k
C. Eduardo Corrales United States 20 758 1.1× 244 0.4× 222 0.6× 345 1.1× 274 1.0× 79 1.4k
Markus Pfister Germany 27 1.1k 1.5× 272 0.4× 429 1.3× 842 2.6× 335 1.2× 85 2.0k
Mark Praetorius Germany 23 828 1.1× 511 0.8× 354 1.0× 253 0.8× 429 1.6× 83 1.5k

Countries citing papers authored by Frank Declau

Since Specialization
Citations

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

Fields of papers citing papers by Frank Declau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frank Declau

This figure shows the co-authorship network connecting the top 25 collaborators of Frank Declau. A scholar is included among the top collaborators of Frank Declau 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 Frank Declau. Frank Declau 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.
2.
Declau, Frank, et al.. (2024). The Body Dysmorphic Disorder Questionnaire—Aesthetic Surgery: Are We Screening the Troublesome Patients?. Facial Plastic Surgery. 40(5). 571–580. 2 indexed citations
3.
Most, Sam P., et al.. (2022). Translation and Validation of the Standardized Cosmesis and Health Nasal Outcomes Survey in Dutch. SHILAP Revista de lepidopterología. 18(3). 170–175. 1 indexed citations
4.
Ende, Jenneke van den, Frank Declau, Wim Wuyts, et al.. (2022). Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresia. European Archives of Oto-Rhino-Laryngology. 280(2). 623–631. 6 indexed citations
5.
Rompaey, Vincent Van, Paul Van de Heyning, Laure Jacquemin, et al.. (2020). EMDR in the Treatment of Chronic Subjective Tinnitus: A Systematic Review. Journal of EMDR Practice and Research. 14(3). 135–149. 4 indexed citations
6.
Foer, Bert De, et al.. (2020). Epineurial pseudocyst of the facial nerve: prevalence and clinics. Institutional Repository University of Antwerp (University of Antwerp). 16(2). 109–114.
7.
8.
Goovaerts, G., et al.. (2016). Vascular leiomyoma of the nasal cavity: case report and literature review. European Archives of Oto-Rhino-Laryngology. 274(1). 579–583. 6 indexed citations
9.
Kerschaver, Erwin Van, An Boudewyns, Frank Declau, Paul Van de Heyning, & Floris L. Wuyts. (2012). Socio-demographic determinants of hearing impairment studied in 103 835 term babies. European Journal of Public Health. 23(1). 55–60. 26 indexed citations
10.
Boudewyns, An, Frank Declau, Koenraad Smets, et al.. (2009). Cytomegalovirus DNA Detection in Guthrie Cards. Otology & Neurotology. 30(7). 943–949. 21 indexed citations
11.
Declau, Frank, et al.. (2007). Prevalence of Histologic Otosclerosis: An Unbiased Temporal Bone Study in Caucasians. Advances in oto-rhino-laryngology. 65. 6–16. 44 indexed citations
12.
Camp, Guy Van, Rikkert L. Snoeckx, Nele Hilgert, et al.. (2006). A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene. The American Journal of Human Genetics. 79(3). 449–457. 120 indexed citations
13.
Govaerts, Paul, Els De Leenheer, Isabelle Schatteman, et al.. (2002). Otosclerosis: a genetically heterogeneous disease involving at least three different genes. Bone. 30(4). 624–630. 41 indexed citations
14.
Bogaert, Kris Van Den, Paul Govaerts, Isabelle Schatteman, et al.. (2001). A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36. The American Journal of Human Genetics. 68(2). 495–500. 78 indexed citations
15.
Declau, Frank, et al.. (2001). Prevalence of Otosclerosis in an Unselected Series of Temporal Bones. Otology & Neurotology. 22(5). 596–602. 102 indexed citations
16.
Verstreken, Margriet, Frank Declau, Floris L. Wuyts, et al.. (2001). Hereditary Otovestibular Dysfunction and M??ni??re's Disease in a Large Belgian Family Is Caused by a Missense Mutation in the COCH Gene. Otology & Neurotology. 22(6). 874–881. 35 indexed citations
17.
Declau, Frank, Cor W. R. J. Cremers, & Paul Van de Heyning. (1999). Diagnosis and Management Strategies in Congenital Atresia of the External Auditory Canal. British Journal of Audiology. 33(5). 313–327. 55 indexed citations
18.
Schepper, A. De, et al.. (1996). Subcutaneous diffuse neurofibroma of the neck: a case report. The Journal of Laryngology & Otology. 110(2). 182–184. 15 indexed citations
19.
Declau, Frank, et al.. (1991). Dehiscence of the facial canal: developmental aspects. International Journal of Pediatric Otorhinolaryngology. 21(1). 21–32. 13 indexed citations
20.
Declau, Frank, et al.. (1989). Early ossification within the human fetal otic capsule: morphological and microanalytical findings. The Journal of Laryngology & Otology. 103(12). 1113–1121. 1 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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