Sabine Duchatelet

1.9k total citations
22 papers, 1.0k citations indexed

About

Sabine Duchatelet is a scholar working on Dermatology, Surgery and Molecular Biology. According to data from OpenAlex, Sabine Duchatelet has authored 22 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Dermatology, 6 papers in Surgery and 6 papers in Molecular Biology. Recurrent topics in Sabine Duchatelet's work include Hidradenitis Suppurativa and Treatments (7 papers), Anorectal Disease Treatments and Outcomes (4 papers) and Skin and Cellular Biology Research (3 papers). Sabine Duchatelet is often cited by papers focused on Hidradenitis Suppurativa and Treatments (7 papers), Anorectal Disease Treatments and Outcomes (4 papers) and Skin and Cellular Biology Research (3 papers). Sabine Duchatelet collaborates with scholars based in France, United States and Denmark. Sabine Duchatelet's co-authors include Alain Hovnanian, Cécile Julier, Claude Chelala, M. Delage, Aude Nassif, Hervé Blanc, Olivier Join‐Lambert, Pascal Boileau, Valérie Senée and Daorong Feng and has published in prestigious journals such as Nature Genetics, Diabetes and Clinical Infectious Diseases.

In The Last Decade

Sabine Duchatelet

21 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sabine Duchatelet France 16 392 371 338 336 138 22 1.0k
L. Overbergh Belgium 17 204 0.5× 162 0.4× 154 0.5× 205 0.6× 123 0.9× 28 918
S. Baba Japan 15 193 0.5× 187 0.5× 43 0.1× 88 0.3× 89 0.6× 42 620
Christine Wai United States 20 59 0.2× 370 1.0× 151 0.4× 28 0.1× 165 1.2× 49 1.0k
Stéphanie Leclerc‐Mercier France 14 33 0.1× 221 0.6× 129 0.4× 110 0.3× 19 0.1× 59 896
Stefan Blunder Austria 17 76 0.2× 211 0.6× 288 0.9× 54 0.2× 10 0.1× 28 784
Masato Matsuki Japan 9 32 0.1× 294 0.8× 144 0.4× 68 0.2× 29 0.2× 10 1.0k
Naoko Ozawa Japan 16 145 0.4× 179 0.5× 78 0.2× 28 0.1× 100 0.7× 25 763
Dae Ho Cho South Korea 16 30 0.1× 236 0.6× 193 0.6× 29 0.1× 35 0.3× 22 724
Silvia Pellegrini Italy 19 518 1.3× 294 0.8× 14 0.0× 312 0.9× 264 1.9× 44 869
Kamaldeen Muili United States 13 213 0.5× 134 0.4× 21 0.1× 91 0.3× 20 0.1× 17 528

Countries citing papers authored by Sabine Duchatelet

Since Specialization
Citations

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

Fields of papers citing papers by Sabine Duchatelet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine Duchatelet

This figure shows the co-authorship network connecting the top 25 collaborators of Sabine Duchatelet. A scholar is included among the top collaborators of Sabine Duchatelet 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 Sabine Duchatelet. Sabine Duchatelet 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.
Duchatelet, Sabine, Stéphanie Leclerc‐Mercier, Francis Palisson, et al.. (2024). Novel variants impairing Sp1 transcription factor binding in the COL7A1 promoter cause mild cases of recessive dystrophic epidermolysis bullosa. European Journal of Human Genetics. 33(3). 344–350. 1 indexed citations
2.
Guet‐Revillet, Hélène, Jean-Philippe Jaı̈s, Marie‐Noëlle Ungeheuer, et al.. (2020). The Surface Microbiome of Clinically Unaffected Skinfolds in Hidradenitis Suppurativa: A Cross-Sectional Culture-Based and 16S rRNA Gene Amplicon Sequencing Study in 60 Patients. Journal of Investigative Dermatology. 140(9). 1847–1855.e6. 50 indexed citations
3.
Guenin‐Macé, Laure, Jean‐David Morel, Jean‐Marc Doisne, et al.. (2020). Dysregulation of tryptophan catabolism at the host-skin microbiota interface in hidradenitis suppurativa. JCI Insight. 5(20). 40 indexed citations
4.
Duchatelet, Sabine, Christian Osterburg, S. Mallet, et al.. (2019). A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia. Journal of Investigative Dermatology. 140(5). 1103–1106.e4. 2 indexed citations
5.
Duchatelet, Sabine, Olivier Join‐Lambert, M. Delage, et al.. (2019). Remission of chronic acne fulminans and severe hidradenitis suppurativa with targeted antibiotherapy. JAAD Case Reports. 5(6). 525–528. 11 indexed citations
6.
Duchatelet, Sabine, Lynn M. Boyden, Akemi Ishida‐Yamamoto, et al.. (2018). Mutations in PERP Cause Dominant and Recessive Keratoderma. Journal of Investigative Dermatology. 139(2). 380–390. 21 indexed citations
7.
Guet‐Revillet, Hélène, Jean-Philippe Jaı̈s, Marie‐Noëlle Ungeheuer, et al.. (2017). The Microbiological Landscape of Anaerobic Infections in Hidradenitis Suppurativa: A Prospective Metagenomic Study. Clinical Infectious Diseases. 65(2). 282–291. 94 indexed citations
8.
Join‐Lambert, Olivier, Hélène Coignard-Biehler, Jean-Philippe Jaı̈s, et al.. (2015). Efficacy of ertapenem in severe hidradenitis suppurativa: a pilot study in a cohort of 30 consecutive patients. Journal of Antimicrobial Chemotherapy. 71(2). 513–520. 70 indexed citations
9.
Join‐Lambert, Olivier, Sabine Duchatelet, M. Delage, et al.. (2015). Remission of refractory pyoderma gangrenosum, severe acne, and hidradenitis suppurativa (PASH) syndrome using targeted antibiotic therapy in 4 patients. Journal of the American Academy of Dermatology. 73(5). S66–S69. 28 indexed citations
10.
Duchatelet, Sabine & Alain Hovnanian. (2015). Olmsted syndrome: clinical, molecular and therapeutic aspects. Orphanet Journal of Rare Diseases. 10(1). 33–33. 62 indexed citations
11.
Clatot, Jérôme, Sabine Duchatelet, Estelle Gandjbakhch, et al.. (2014). A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation. Heart Rhythm. 11(6). 1015–1023. 37 indexed citations
12.
Duchatelet, Sabine, S. Miskinyte, M. Delage, et al.. (2014). Coexistence d’une acné fulminante et d’une hidrosadénite suppurée : syndrome ASH, une nouvelle entité ?. Annales de Dermatologie et de Vénéréologie. 141(12). S381–S382.
13.
Duchatelet, Sabine, Solenn Pruvost, Simon J. de Veer, et al.. (2014). A NewTRPV3Missense Mutation in a Patient With Olmsted Syndrome and Erythromelalgia. JAMA Dermatology. 150(3). 303–303. 40 indexed citations
14.
Clatot, Jérôme, Sabine Duchatelet, Estelle Gandjbakhch, et al.. (2013). Different Atrial and Ventricular Resting Membrane Potentials May Explain the Phenotypical Variability of a Truncating SCN5A Mutation. Heart Rhythm. 10(11). 1746–1746. 2 indexed citations
15.
Aliferis, Konstantinos A., Sophie Hellé, Gàbor Gyapay, et al.. (2011). Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencing. Ophthalmic Genetics. 33(1). 18–22. 28 indexed citations
16.
Bartos, Daniel C., Sabine Duchatelet, Don E. Burgess, et al.. (2010). R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation. Heart Rhythm. 8(1). 48–55. 57 indexed citations
17.
Duchatelet, Sabine, Sophie Caillat‐Zucman, Danièle Dubois‐Laforgue, et al.. (2007). FCRL3 −169CT functional polymorphism in type 1 diabetes and autoimmunity traits. Biomedicine & Pharmacotherapy. 62(3). 153–157. 15 indexed citations
18.
Chelala, Claude, Sabine Duchatelet, Marie‐Line Joffret, et al.. (2007). PTPN22 R620W Functional Variant in Type 1 Diabetes and Autoimmunity Related Traits. Diabetes. 56(2). 522–526. 58 indexed citations
19.
Senée, Valérie, Claude Chelala, Sabine Duchatelet, et al.. (2006). Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. Nature Genetics. 38(6). 682–687. 270 indexed citations
20.
Duchatelet, Sabine, Elsebet Østergaard, Dina Cortes, Arnaud Lemainque, & Cécile Julier. (2004). Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes. Human Molecular Genetics. 14(1). 1–5. 83 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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