Clarisse Baumann

7.5k total citations
73 papers, 2.1k citations indexed

About

Clarisse Baumann is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Clarisse Baumann has authored 73 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 30 papers in Genetics and 21 papers in Surgery. Recurrent topics in Clarisse Baumann's work include Genomic variations and chromosomal abnormalities (12 papers), Congenital Ear and Nasal Anomalies (9 papers) and Urological Disorders and Treatments (8 papers). Clarisse Baumann is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Congenital Ear and Nasal Anomalies (9 papers) and Urological Disorders and Treatments (8 papers). Clarisse Baumann collaborates with scholars based in France, United Kingdom and Belgium. Clarisse Baumann's co-authors include Alain Verloès, Anne‐Lise Delezoide, Didier Lacombe, Stanislas Lyonnet, David Cohen, Sylvie Tordjman, Dominique Brémond‐Gignac, Lydie Bürglen, Yves Sznajer and Philippe Mazet and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Clarisse Baumann

71 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Clarisse Baumann France 26 969 853 495 432 330 73 2.1k
R.J.C. Admiraal Netherlands 29 1.1k 1.1× 739 0.9× 493 1.0× 859 2.0× 689 2.1× 58 2.9k
Damien Sanlaville France 33 1.6k 1.6× 2.2k 2.6× 356 0.7× 362 0.8× 263 0.8× 189 3.7k
Irene M. Janssen Netherlands 17 1.6k 1.6× 2.1k 2.5× 307 0.6× 625 1.4× 437 1.3× 23 3.4k
Muriel Holder‐Espinasse France 26 1.1k 1.1× 1.0k 1.2× 358 0.7× 169 0.4× 291 0.9× 74 2.0k
Patrick MacLeod Canada 29 1.3k 1.4× 910 1.1× 469 0.9× 125 0.3× 382 1.2× 74 3.1k
Thomy de Ravel Belgium 38 2.0k 2.1× 1.9k 2.3× 382 0.8× 387 0.9× 475 1.4× 112 4.2k
Israela Lerer Israel 29 1.2k 1.3× 972 1.1× 238 0.5× 161 0.4× 343 1.0× 77 2.5k
David Geneviève France 24 1.3k 1.4× 1.1k 1.3× 285 0.6× 168 0.4× 189 0.6× 80 2.3k
Bruno Leheup France 29 1.1k 1.1× 758 0.9× 239 0.5× 215 0.5× 225 0.7× 97 2.2k
Bronwyn Kerr United Kingdom 32 1.6k 1.6× 1.3k 1.5× 480 1.0× 170 0.4× 118 0.4× 67 3.2k

Countries citing papers authored by Clarisse Baumann

Since Specialization
Citations

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

Fields of papers citing papers by Clarisse Baumann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clarisse Baumann

This figure shows the co-authorship network connecting the top 25 collaborators of Clarisse Baumann. A scholar is included among the top collaborators of Clarisse Baumann 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 Clarisse Baumann. Clarisse Baumann 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.
Deloison, B., P. Sonigo, A. Millischer, et al.. (2018). Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome. European Journal of Medical Genetics. 61(12). 773–782. 12 indexed citations
2.
Lévy, Jonathan, Aurélie Coussement, Céline Dupont, et al.. (2017). Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome. American Journal of Medical Genetics Part A. 173(8). 2081–2087. 15 indexed citations
3.
Petit, Florence, Joris Andrieux, Geneviève Baujat, et al.. (2013). Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families. Clinical Genetics. 85(5). 464–469. 17 indexed citations
4.
Ageeli, Essam Al, Séverine Drunat, Catherine Delanöe, et al.. (2013). Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases. European Journal of Medical Genetics. 57(1). 5–14. 67 indexed citations
5.
Spaggiari, Emmanuel, Clarisse Baumann, Marianne Alison, et al.. (2013). Mowat–Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: Advocacy for standard autopsy. European Journal of Medical Genetics. 56(6). 297–300. 13 indexed citations
6.
Elmaleh, Monique, Clarisse Baumann, Vincent Couloigner, et al.. (2012). Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome andSOX10Mutations. American Journal of Neuroradiology. 34(6). 1257–1263. 77 indexed citations
7.
Gérard‐Blanluet, Marion, et al.. (2010). Unilateral agenesis of the abdominal wall musculature: An early muscle deficiency. American Journal of Medical Genetics Part A. 152A(11). 2870–2874. 5 indexed citations
8.
Borck, Guntram, Clarisse Baumann, Geneviève Baujat, et al.. (2009). Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families. Journal of Medical Genetics. 47(12). 797–802. 79 indexed citations
9.
Gérard‐Blanluet, Marion, Stéphane Serero, Clarisse Baumann, et al.. (2008). Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome. American Journal of Medical Genetics Part A. 146A(14). 1871–1874. 9 indexed citations
10.
Verloès, Alain, Dominique Brémond‐Gignac, Bertrand Isidor, et al.. (2006). Blepharophimosis‐mental retardation (BMR) syndromes: A proposed clinical classification of the so‐called Ohdo syndrome, and delineation of two new BMR syndromes, one X‐linked and one autosomal recessive. American Journal of Medical Genetics Part A. 140A(12). 1285–1296. 52 indexed citations
11.
Salomon, Laurent, Clarisse Baumann, Anne‐Lise Delezoide, et al.. (2006). Abnormal abdominal situs: what and how should we look for?. Prenatal Diagnosis. 26(3). 282–285. 7 indexed citations
12.
Guilmin‐Crépon, Sophie, Cathérine Garel, Clarisse Baumann, et al.. (2006). High Proportion of Pituitary Abnormalities and Other Congenital Defects in Children with Congenital Nasal Pyriform Aperture Stenosis. Pediatric Research. 60(4). 478–484. 30 indexed citations
13.
Delezoide, Anne‐Lise, Clarisse Baumann, E. Vuillard, et al.. (2006). Prenatal Marfan syndrome: report of one case and review of the literature. Prenatal Diagnosis. 26(8). 696–699. 16 indexed citations
14.
Karmous‐Benailly, Houda, Anne‐Claude Tabet, Olivier Dupuy, et al.. (2005). Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?. Prenatal Diagnosis. 25(3). 193–197. 3 indexed citations
15.
Sznajer, Yves, Clarisse Baumann, Albert David, et al.. (2003). Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome). European Journal of Pediatrics. 162(12). 863–867. 51 indexed citations
16.
Sanlaville, Damien, Serge Romana, Jeanne Amiel, et al.. (2002). A CGH study of 27 patients with CHARGE association. Clinical Genetics. 61(2). 135–138. 21 indexed citations
17.
Pingault, Véronique, Mathilde Girard, Nadège Bondurand, et al.. (2002). SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism. Human Genetics. 111(2). 198–206. 95 indexed citations
18.
Baumann, Clarisse, et al.. (2001). [Pregnancy outcome and infant follow-up after diagnosis of nuchal anomalies at the 1st or 2nd trimester ultrasound examination].. PubMed. 30(1 Suppl). 68–74. 5 indexed citations
19.
Sanlaville, Damien, Clarisse Baumann, Serge Romana, et al.. (1999). De novo inverted duplication 9p21pter involving telomeric repeated sequences. American Journal of Medical Genetics. 83(2). 125–131. 16 indexed citations
20.
Garel, Cathérine, et al.. (1998). Carbohydrate-deficient glycoprotein syndrome type I: a new cause of dysostosis multiplex. Skeletal Radiology. 27(1). 43–45. 21 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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