Isabelle Schatteman

1.5k total citations
28 papers, 1.1k citations indexed

About

Isabelle Schatteman is a scholar working on Sensory Systems, Otorhinolaryngology and Molecular Biology. According to data from OpenAlex, Isabelle Schatteman has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Sensory Systems, 8 papers in Otorhinolaryngology and 7 papers in Molecular Biology. Recurrent topics in Isabelle Schatteman's work include Hearing, Cochlea, Tinnitus, Genetics (16 papers), Ear Surgery and Otitis Media (8 papers) and Hearing Loss and Rehabilitation (4 papers). Isabelle Schatteman is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (16 papers), Ear Surgery and Otitis Media (8 papers) and Hearing Loss and Rehabilitation (4 papers). Isabelle Schatteman collaborates with scholars based in Belgium, United States and Netherlands. Isabelle Schatteman's co-authors include Paul Govaerts, Thomas Somers, Guy Van Camp, Paul Van de Heyning, F. Erwin Offeciers, Richard J. Smith, Geert De Ceulaer, Kristin Daemers, Paul Coucke and Carina De Beukelaer and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Isabelle Schatteman

28 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Isabelle Schatteman Belgium	15	651	365	304	257	252	28	1.1k
Umberto Ambrosetti Italy	24	842 1.3×	338 0.9×	443 1.5×	433 1.7×	204 0.8×	81	1.6k
Hideaki Moteki Japan	22	987 1.5×	426 1.2×	521 1.7×	276 1.1×	417 1.7×	68	1.4k
István Sziklai Hungary	26	685 1.1×	335 0.9×	316 1.0×	465 1.8×	699 2.8×	88	1.7k
Selena E. Heman‐Ackah United States	11	639 1.0×	316 0.9×	230 0.8×	405 1.6×	233 0.9×	25	1.0k
Satoshi Iwasaki Japan	21	927 1.4×	260 0.7×	528 1.7×	365 1.4×	432 1.7×	102	1.3k
Carla Nishimura United States	24	1.0k 1.6×	828 2.3×	246 0.8×	402 1.6×	355 1.4×	33	2.3k
Xue Zhong Liu United States	23	1.3k 1.9×	750 2.1×	406 1.3×	445 1.7×	274 1.1×	70	1.8k
A. Eliot Shearer United States	17	1.0k 1.6×	638 1.7×	369 1.2×	330 1.3×	325 1.3×	30	1.4k
R Charachon France	14	282 0.4×	332 0.9×	195 0.6×	117 0.5×	421 1.7×	87	1.1k
Miguel A. Moreno‐Pelayo Spain	19	1.2k 1.8×	1.4k 3.7×	302 1.0×	384 1.5×	164 0.7×	59	2.3k

Countries citing papers authored by Isabelle Schatteman

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Schatteman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Schatteman

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

All Works

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20 of 20 papers shown

1.

Acke, Frederic, Annelies Keymeulen, Els De Leenheer, et al.. (2023). Risk Factors for Natural Hearing Evolution in Newborns With Congenital Cytomegalovirus Infection. JAMA Otolaryngology–Head & Neck Surgery. 150(1). 30–30. 5 indexed citations

2.

Schrauwen, Isabelle, Manou Sommen, Vedat Topsakal, et al.. (2021). A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis. Human Genetics. 141(3-4). 951–963. 3 indexed citations

3.

Goderis, Julie, Frederic Acke, Annelies Keymeulen, et al.. (2020). Congenital CMV-Associated Hearing Loss: Can Brain Imaging Predict Hearing Outcome?. Ear and Hearing. 42(2). 373–380. 16 indexed citations

4.

Sommen, Manou, Matthias Beyens, Geert Vandeweyer, et al.. (2019). Insufficient evidence for a role of SERPINF1 in otosclerosis. Molecular Genetics and Genomics. 294(4). 1001–1006. 6 indexed citations

5.

Goderis, Julie, Annelies Keymeulen, Koenraad Smets, et al.. (2016). Hearing in Children with Congenital Cytomegalovirus Infection: Results of a Longitudinal Study. The Journal of Pediatrics. 172. 110–115.e2. 85 indexed citations

6.

Rompaey, Vincent Van, et al.. (2012). Transmeatal procurement of allograft tympano-ossicular systems : preliminary report. The Journal of International Advanced Otology. 8(2). 154–157. 3 indexed citations

7.

Schrauwen, Isabelle, Koen Venken, Kathleen Vanderstraeten, et al.. (2010). Involvement of T-cell receptor-β alterations in the development of otosclerosis linked to OTSC2. Genes and Immunity. 11(3). 246–253. 10 indexed citations

8.

Somers, Thomas, et al.. (2007). Transient Depression of Inner Ear Function after Stapedotomy: Skeeter versus CO<sub>2</sub> Laser Technique. Advances in oto-rhino-laryngology. 65. 267–272. 9 indexed citations

9.

Govaerts, Paul, Carina De Beukelaer, Kristin Daemers, et al.. (2002). Outcome of Cochlear Implantation at Different Ages from 0 to 6 Years. Otology & Neurotology. 23(6). 885–890. 184 indexed citations

10.

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

11.

Cryns, Kim, Markus Pfister, Ronald J. E. Pennings, et al.. (2002). Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Human Genetics. 110(5). 389–394. 71 indexed citations

12.

Govaerts, Paul, Kristin Daemers, K. Verhoeven, et al.. (2002). Clinical Presentation of DFNA8-DFNA12. Advances in oto-rhino-laryngology. 61. 60–65. 3 indexed citations

13.

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

14.

Verhoeven, Kristien, Toril Fagerheim, Sai Prasad, et al.. (2000). Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment. Human Genetics. 107(1). 7–11. 10 indexed citations

15.

Verhoeven, Kristien, Toril Fagerheim, Sai Prasad, et al.. (2000). Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment. Human Genetics. 107(1). 7–11. 4 indexed citations

16.

Verstreken, Margriet, Frank Declau, Isabelle Schatteman, et al.. (2000). Audiometric analysis of a Belgian family linked to the DFNA10 locus.. PubMed. 21(5). 675–81. 15 indexed citations

17.

Verhoeven, Kristien, Valeria Tiranti, P.L.M. Huygen, et al.. (1999). Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene. European Journal of Human Genetics. 7(1). 45–51. 68 indexed citations

18.

Camp, Guy Van, Ed Green, Margriet Verstreken, et al.. (1998). Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea.. PubMed. 5(6). 397–405. 18 indexed citations

19.

Lench, Nicholas, Alex Markham, R Mueller, et al.. (1998). A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).. Journal of Medical Genetics. 35(2). 151–152. 29 indexed citations

20.

Verhoeven, Kristien, Karin Kirschhofer, P. Kevin Legan, et al.. (1998). Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nature Genetics. 19(1). 60–62. 253 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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