Clarisse Baumann

7.5k citations

73 papers · 2.1k indexed · h-index 26

Molecular Biology top 10%
Genetics top 2%
Surgery top 10%
Genetics top 2%
Pulmonary and Respiratory Medicine top 10%

Co-authors: Alain Verloès Anne‐Lise Delezoide Didier Lacombe Stanislas Lyonnet David Cohen Sylvie Tordjman Dominique Brémond‐Gignac Lydie Bürglen
Topics: Genomic variations and chromosomal abnormalities (12 papers)Congenital Ear and Nasal Anomalies (9 papers)Urological Disorders and Treatments (8 papers)
Cited by: Genetics Molecular Biology
Journals: Proceedings of the National Academy of Sciences PLoS ONE The Journal of Clinical Endocrinology & Metabolism
Partner nations: France United Kingdom Belgium

In The Last Decade

Clarisse Baumann

71 papers receiving 2.1k citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome 2018 ·European Journal of Medical Genetics ·B. Deloison,P. Sonigo,A. Millischer,Thibaud Quibel,Mara Cavallin,G. Benoist,Chloé Quēlin,Pierre‐Simon Jouk,Dorit Lev,Marianne Alison,Clarisse Baumann,C. Beldjord,(unknown),B. Bessières,Nathalie Boddaert,Y. Ville,L. J. Salomon,Nadia Bahi‐Buisson	12
2	Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome 2017 ·American Journal of Medical Genetics Part A ·Jonathan Lévy,Aurélie Coussement,Céline Dupont,Fabien Guimiot,Clarisse Baumann,Géraldine Viot,Sandrine Passemard,Yline Capri,Séverine Drunat,Alain Verloès,Eva Pipiras,Brigitte Benzacken,Jean‐Michel Dupont,Anne‐Claude Tabet	15
3	Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families 2013 ·Clinical Genetics ·Florence Petit,(unknown),Joris Andrieux,Geneviève Baujat,Clarisse Baumann,Claire Bénéteau,A. David,Laurence Faivre,Dominique Gaillard,Brigitte Gilbert‐Dussardier,Pierre‐Simon Jouk,Cédric Le Caignec,Philippe Loget,Laurent Pasquier,Nicole Porchet,Muriel Holder‐Espinasse,Sylvie Manouvrier‐Hanu,Fabienne Escande	17
4	Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases 2013 ·European Journal of Medical Genetics ·Essam Al Ageeli,Séverine Drunat,Catherine Delanöe,Laurence Perrin,Clarisse Baumann,Yline Capri,(unknown),Azzedine Aboura,Céline Dupont,Stéphane Auvin,Laïla El Khattabi,(unknown),Anne Moncla,Anne‐Claude Tabet,Alain Verloès	67
5	Mowat–Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: Advocacy for standard autopsy 2013 ·European Journal of Medical Genetics ·Emmanuel Spaggiari,Clarisse Baumann,Marianne Alison,Jean‐François Oury,N. Belarbi,Céline Dupont,Fabien Guimiot,Anne‐Lise Delezoide	13
6	Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome andSOX10Mutations 2012 ·American Journal of Neuroradiology ·Monique Elmaleh,Clarisse Baumann,(unknown),(unknown),Vincent Couloigner,Koenraad Devriendt,Meredith Wilson,Sandrine Marlin,G. Sebag,Véronique Pingault	77
7	Unilateral agenesis of the abdominal wall musculature: An early muscle deficiency 2010 ·American Journal of Medical Genetics Part A ·Marion Gérard‐Blanluet,(unknown),Clarisse Baumann,(unknown),(unknown),G. Audry,Anne‐Lise Delezoide,Alain Verloès	5
8	Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families 2009 ·Journal of Medical Genetics ·(unknown),(unknown),Guntram Borck,Clarisse Baumann,Geneviève Baujat,Éric Bieth,Patrick Edery,Chantal Farra,(unknown),Delphine Héron,Bruno Leheup,M Le Merrer,Stanislas Lyonnet,Dominique Martin‐Coignard,M Mathieu,Christel Thauvin‐Robinet,Alain Verloès,Laurence Colleaux,Arnold Münnich,Valérie Cormier‐Daire	79
9	Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome 2008 ·American Journal of Medical Genetics Part A ·(unknown),Marion Gérard‐Blanluet,Stéphane Serero,(unknown),Clarisse Baumann,Marie‐Line Jacquemont,Céline Dupont,(unknown),Séverine Drunat,(unknown),(unknown),Brigitte Benzacken,Alain Verloès,Anne‐Claude Tabet,Azzedine Aboura	9
10	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 2006 ·American Journal of Medical Genetics Part A ·Alain Verloès,Dominique Brémond‐Gignac,Bertrand Isidor,Albert David,Clarisse Baumann,M Leroy,René Stevens,Y. Gillerot,Delphine Héron,Bénédicte Héron,Brigitte Benzacken,Didier Lacombe,Han G. Brunner,Pierre Bitoun	52
11	Abnormal abdominal situs: what and how should we look for? 2006 ·Prenatal Diagnosis ·Laurent Salomon,Clarisse Baumann,Anne‐Lise Delezoide,Jean‐François Oury,Danièle Pariente,G. Sebag,Cathérine Garel	7
12	High Proportion of Pituitary Abnormalities and Other Congenital Defects in Children with Congenital Nasal Pyriform Aperture Stenosis 2006 ·Pediatric Research ·Sophie Guilmin‐Crépon,Cathérine Garel,Clarisse Baumann,Dominique Brémond‐Gignac,Isabelle Bailleul‐Forestier,S Magnier,Mireille Castanet,Paul Czernichow,T. Van Den Abbeele,Juliane Léger	30
13	Prenatal Marfan syndrome: report of one case and review of the literature 2006 ·Prenatal Diagnosis ·(unknown),Anne‐Lise Delezoide,Clarisse Baumann,E. Vuillard,Dominique Luton,Yvon Chitrit,A. Azancot	16
14	Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly? 2005 ·Prenatal Diagnosis ·Houda Karmous‐Benailly,Anne‐Claude Tabet,(unknown),Olivier Dupuy,(unknown),Dominique Luton,Clarisse Baumann,Anne‐Lise Delezoide	3
15	Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome) 2003 ·European Journal of Pediatrics ·Yves Sznajer,Clarisse Baumann,Albert David,Hubert Journel,Didier Lacombe,Yves Pérel,Pascale Blouin,(unknown),Jean‐Pierre Cézard,Michel Peuchmaur,(unknown),Inderjeet Dokal,Alain Verloès	51
16	A CGH study of 27 patients with CHARGE association 2002 ·Clinical Genetics ·Damien Sanlaville,Serge Romana,(unknown),Jeanne Amiel,David Geneviève,Catherine Ozilou,Marc Le Lorc’h,Sophie Brisset,Philippe Gosset,Clarisse Baumann,C Turleau,Stanislas Lyonnet,Michel Vekemans	21
17	SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism 2002 ·Human Genetics ·Véronique Pingault,Mathilde Girard,Nadège Bondurand,Huw Dorkins,Lionel Van Maldergem,David Mowat,Takashi Shimotake,Ishwar C. Verma,Clarisse Baumann,Michel Goossens	95
18	[Pregnancy outcome and infant follow-up after diagnosis of nuchal anomalies at the 1st or 2nd trimester ultrasound examination]. 2001 ·PubMed ·Clarisse Baumann,(unknown),E. Vuillard,J.F. Oury	5
19	De novo inverted duplication 9p21pter involving telomeric repeated sequences 1999 ·American Journal of Medical Genetics ·Damien Sanlaville,Clarisse Baumann,(unknown),Serge Romana,Nathalie Collot,V. Cacheux,C Turleau,Gérard Tachdjian	16
20	Carbohydrate-deficient glycoprotein syndrome type I: a new cause of dysostosis multiplex 1998 ·Skeletal Radiology ·Cathérine Garel,Clarisse Baumann,M. Besnard,H. Ogier,J. Jaeken,(unknown)	21

About Clarisse Baumann

Clarisse Baumann is a scholar working on Developmental Biology, Urology and Genetics, having authored 73 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Congenital Ear and Nasal Anomalies (9 papers) and Urological Disorders and Treatments (8 papers). The work is most often cited by research in Genetics (432 citations), Genetics (853 citations) and Molecular Biology (969 citations). Clarisse Baumann has collaborated with scholars based in France, United Kingdom and Belgium. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

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.

Explore authors with similar magnitude of impact