Corinne Stoetzel

6.9k citations

67 papers · 3.3k indexed · h-index 30

Co-authors: Fabienne Perrin‐Schmitt Bernard Thisse Hélène Dollfus Christine Thisse Jean Muller Vincent Marion Véronique Geoffroy Catherine Wolf
Topics: Genetic and Kidney Cyst Diseases (28 papers)Genetic Syndromes and Imprinting (23 papers)Hedgehog Signaling Pathway Studies (20 papers)
Cited by: Genetics Molecular Biology Aging
Journals: Cell Proceedings of the National Academy of Sciences Journal of Biological Chemistry
Partner nations: France United Kingdom Germany

In The Last Decade

Corinne Stoetzel

67 papers receiving 3.3k citations

Peers

Countries citing papers authored by Corinne Stoetzel

Since Specialization

Citations

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

Fields of papers citing papers by Corinne Stoetzel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinne Stoetzel

This figure shows the co-authorship network connecting the top 25 collaborators of Corinne Stoetzel. A scholar is included among the top collaborators of Corinne Stoetzel 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 Corinne Stoetzel. Corinne Stoetzel 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

#	Work	Indexed citations
1	WGS Revealed Novel BBS5 Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function Defects 2023 ·International Journal of Molecular Sciences ·(unknown),(unknown),Alejandro Estrada‐Cuzcano,Véronique Geoffroy,(unknown),(unknown),(unknown),Julien Tarabeux,Corinne Stoetzel,Sophie Scheidecker,Louise F. Porter,Emmanuelle Génin,Richard Redon,(unknown),Anne Boland,Jean‐François Deleuze,Nicolas Le May,Hélène Dollfus,Jean Muller	5
2	High prevalence of Bardet‐Biedl syndrome in La Réunion Island is due to a founder variant in ARL6/BBS3 2020 ·Clinical Genetics ·(unknown),(unknown),Marie‐Line Jacquemont,Françoise Darcel,(unknown),(unknown),(unknown),Jean‐Luc Alessandri,Bérénice Doray,Paul Guéguen,(unknown),Hanitra Randrianaivo,Corinne Stoetzel,Sophie Scheidecker,Hugues Flodrops,Hélène Dollfus,Jean Muller	11
3	Atypical Retinal Phenotype in a Patient With Alström Syndrome and Biallelic Novel Pathogenic Variants in ALMS1, Including a de novo Variation 2020 ·Frontiers in Genetics ·(unknown),Louise F. Porter,Valérie Pelletier,(unknown),(unknown),(unknown),(unknown),Corinne Stoetzel,Hélène Dollfus,Jean Muller	7
4	Mutations inKARScause a severe neurological and neurosensory disease with optic neuropathy 2019 ·Human Mutation ·Sophie Scheidecker,Séverine Bär,Corinne Stoetzel,Véronique Geoffroy,Béatrice Lannes,Bruno Rinaldi,Frédéric Fischer,H. D. Becker,Valérie Pelletier,Cécile Pagan,Cécile Acquaviva,Stéphane Kremer,Marc Mirande,Christine Tranchant,Jean Muller,Sylvie Friant,Hélène Dollfus	15
5	In vivo phenotypic and molecular characterization of retinal degeneration in mouse models of three ciliopathies 2019 ·Experimental Eye Research ·(unknown),(unknown),Cathy Obringer,(unknown),(unknown),Corinne Stoetzel,Michel J. Roux,Nadia Messaddeq,Hélène Dollfus,Vincent Marion	7
6	NovelIQCEvariations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish 2019 ·Human Mutation ·Alejandro Estrada‐Cuzcano,Christelle Etard,(unknown),Corinne Stoetzel,Élise Schaefer,Sophie Scheidecker,Véronique Geoffroy,(unknown),(unknown),Francesca Mattioli,Kirsley Chennen,Sabine Sigaudy,Damien Plassard,Olivier Poch,Amélie Piton,Uwe Strähle,Jean Muller,Hélène Dollfus	5
7	AnnotSV: an integrated tool for structural variations annotation 2018 ·Bioinformatics ·Véronique Geoffroy,Yvan Herenger,Arnaud Kress,Corinne Stoetzel,Amélie Piton,Hélène Dollfus,Jean Muller	207
8	Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar 2016 ·Frontiers in Physiology ·Agnès Bloch‐Zupan,(unknown),Corinne Stoetzel,Julia Meyer,Véronique Geoffroy,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Philippe Gorry,Marie‐Cécile Manière,(unknown),Hélène Dollfus	11
9	Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome 2015 ·American Journal of Ophthalmology ·Sophie Scheidecker,Sarah Hull,(unknown),(unknown),Valérie Pelletier,Jean Muller,Corinne Stoetzel,Élise Schaefer,Sabine Defoort‐Dhellemmes,Isabelle Drumare,Graham E. Holder,Christian P. Hamel,Andrew R. Webster,Anthony T. Moore,Bernard Puech,Hélène Dollfus	19
10	Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy 2015 ·The American Journal of Human Genetics ·Sophie Scheidecker,Christelle Etard,Laurence Haren,Corinne Stoetzel,Sarah Hull,Gavin Arno,Vincent Plagnol,Séverine Drunat,Sandrine Passemard,Annick Toutain,Cathy Obringer,Mériam Koob,Véronique Geoffroy,Vincent Marion,Uwe Strähle,Pia Østergaard,Alain Verloès,Andreas Merdes,Anthony T. Moore,Hélène Dollfus	50
11	Exome sequencing identifies mutations in LZTFL1, a BBSome and smoothened trafficking regulator, in a family with Bardet–Biedl syndrome with situs inversus and insertional polydactyly 2012 ·Journal of Medical Genetics ·Vincent Marion,Fanny Stutzmann,Marion Gérard,(unknown),Élise Schaefer,(unknown),Sophie Hellé,Valérie Delague,Eric H. Souied,Catherine Barrey,Alain Verloès,Corinne Stoetzel,Hélène Dollfus	101
12	BBS-Induced Ciliary Defect Enhances Adipogenesis, Causing Paradoxical Higher-Insulin Sensitivity, Glucose Usage, and Decreased Inflammatory Response 2012 ·Cell Metabolism ·Vincent Marion,(unknown),(unknown),Cathy Obringer,(unknown),(unknown),Nadia Messaddeq,M. Durand,Luc Dupuis,Jean‐Philippe Loeffler,Peter King,Catherine Schmidt‐Mutter,Nikolai Petrovsky,Corinne Stoetzel,Hélène Dollfus	71
13	A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype 2011 ·Ophthalmic Genetics ·Konstantinos A. Aliferis,Corinne Stoetzel,Valérie Pelletier,Sophie Hellé,Karine Angioï-Duprez,Jacqueline Vigneron,Bruno Leheup,Vincent Marion,Hélène Dollfus	14
14	Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencing 2011 ·Ophthalmic Genetics ·Konstantinos A. Aliferis,Sophie Hellé,Gàbor Gyapay,Sabine Duchatelet,Corinne Stoetzel,Jean‐Louis Mandel,Hélène Dollfus	28
15	Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral Ectopia Lentis 2010 ·Ophthalmic Genetics ·(unknown),Corinne Stoetzel,(unknown),(unknown),Laura Liebermann,Vincent Marion,(unknown),Cathérine Boileau,Jean‐Louis Dufier,Hélène Dollfus	29
16	Saethre‐Chotzen syndrome: Notable intrafamilial phenotypic variability in a large family with Q28X TWIST mutation 2002 ·American Journal of Medical Genetics ·Hélène Dollfus,Partha S. Biswas,(unknown),Corinne Stoetzel,(unknown),Jyotirmay Biswas,Elisabeth Lajeunie,Dominique Rénier,Fabienne Perrin‐Schmitt	14
17	Differential expression of laminin-5 subunits during incisor and molar development in the mouse 2000 ·The International Journal of Developmental Biology ·Kunihiko Yoshiba,Nagako Yoshiba,Daniel Aberdam,Guerrino Meneguzzi,Fabienne Perrin‐Schmitt,Corinne Stoetzel,J V Ruch,H. Lesot	18
18	X-twi is expressed prior to gastrulation in presumptive neurectodermal and mesodermal cells in dorsalized and ventralized Xenopus laevis embryos 1998 ·The International Journal of Developmental Biology ·Corinne Stoetzel,Anne‐Laure Bolcato‐Bellemin,Patrice Bourgeois,Fabienne Perrin‐Schmitt,David Meyer,Michael von Wolff,P. Rémy	10
19	Expression and localization of laminin-5 subunits in the mouse incisor 1998 ·Cell and Tissue Research ·Nagako Yoshiba,Kunihiko Yoshiba,Daniel Aberdam,Guerrino Meneguzzi,Fabienne Perrin‐Schmitt,Corinne Stoetzel,J V Ruch,H. Lesot	29
20	Dorso-ventral and rostro-caudal sequential expression of M-twist in the postimplantation murine embryo 1995 ·Mechanisms of Development ·Corinne Stoetzel,Bruno Weber,Patrice Bourgeois,Anne‐Laure Bolcato‐Bellemin,(unknown)	68

About Corinne Stoetzel

Corinne Stoetzel is a scholar working on Genetics, Developmental Biology and Rheumatology, having authored 67 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (28 papers), Genetic Syndromes and Imprinting (23 papers) and Hedgehog Signaling Pathway Studies (20 papers). The work is most often cited by research in Genetics (1.8k citations), Molecular Biology (2.5k citations) and Aging (41 citations). Corinne Stoetzel has collaborated with scholars based in France, United Kingdom and Germany. Frequent co-authors include Fabienne Perrin‐Schmitt, Bernard Thisse, Hélène Dollfus, Christine Thisse, Jean Muller, Vincent Marion, Véronique Geoffroy, Catherine Wolf, P Gerlinger and Jean‐Louis Mandel. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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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