Corinne Stoetzel

6.9k total citations
67 papers, 3.3k citations indexed

About

Corinne Stoetzel is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Corinne Stoetzel has authored 67 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 46 papers in Genetics and 12 papers in Rheumatology. Recurrent topics in Corinne Stoetzel's work include Genetic and Kidney Cyst Diseases (28 papers), Genetic Syndromes and Imprinting (23 papers) and Hedgehog Signaling Pathway Studies (20 papers). Corinne Stoetzel is often cited by papers focused on Genetic and Kidney Cyst Diseases (28 papers), Genetic Syndromes and Imprinting (23 papers) and Hedgehog Signaling Pathway Studies (20 papers). Corinne Stoetzel collaborates with scholars based in France, United Kingdom and Germany. Corinne Stoetzel's co-authors include Fabienne Perrin‐Schmitt, Bernard Thisse, Hélène Dollfus, Christine Thisse, Jean Muller, Vincent Marion, Véronique Geoffroy, P Gerlinger, Catherine Wolf and Jean‐Louis Mandel and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Corinne Stoetzel

67 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Corinne Stoetzel France	30	2.5k	1.8k	273	235	215	67	3.3k
Elena V. Semina United States	36	3.6k 1.4×	2.0k 1.1×	416 1.5×	143 0.6×	237 1.1×	98	4.9k
Aimée Zúñiga Switzerland	25	2.9k 1.1×	833 0.5×	389 1.4×	116 0.5×	136 0.6×	45	3.9k
Sigmar Stricker Germany	36	2.6k 1.0×	825 0.5×	286 1.0×	422 1.8×	313 1.5×	74	3.5k
Hildegard Kehrer‐Sawatzki Germany	37	2.3k 0.9×	1.9k 1.0×	152 0.6×	630 2.7×	220 1.0×	126	4.6k
Wilbur R. Harrison United States	25	1.5k 0.6×	1.1k 0.6×	206 0.8×	257 1.1×	161 0.7×	49	2.7k
Pao‐Tien Chuang United States	34	4.2k 1.7×	1.5k 0.8×	480 1.8×	207 0.9×	203 0.9×	52	5.1k
Sue Malcolm United Kingdom	33	2.6k 1.0×	2.3k 1.3×	260 1.0×	175 0.7×	136 0.6×	62	4.4k
Heiko Peters United Kingdom	23	2.7k 1.1×	1.0k 0.6×	140 0.5×	277 1.2×	127 0.6×	29	3.2k
Frits Meijlink Netherlands	36	2.9k 1.1×	961 0.5×	304 1.1×	110 0.5×	237 1.1×	58	3.6k
Derk ten Berge Netherlands	28	2.9k 1.1×	834 0.5×	309 1.1×	191 0.8×	219 1.0×	38	3.7k

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

Estrada‐Cuzcano, Alejandro, Véronique Geoffroy, Julien Tarabeux, et al.. (2023). WGS Revealed Novel BBS5 Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function Defects. International Journal of Molecular Sciences. 24(10). 8729–8729. 5 indexed citations

Jacquemont, Marie‐Line, Françoise Darcel, Jean‐Luc Alessandri, et al.. (2020). High prevalence of Bardet‐Biedl syndrome in La Réunion Island is due to a founder variant in ARL6/BBS3. Clinical Genetics. 98(2). 166–171. 11 indexed citations

Scheidecker, Sophie, Séverine Bär, Corinne Stoetzel, et al.. (2019). Mutations inKARScause a severe neurological and neurosensory disease with optic neuropathy. Human Mutation. 40(10). 1826–1840. 15 indexed citations

Obringer, Cathy, Corinne Stoetzel, Michel J. Roux, et al.. (2019). In vivo phenotypic and molecular characterization of retinal degeneration in mouse models of three ciliopathies. Experimental Eye Research. 186. 107721–107721. 7 indexed citations

Estrada‐Cuzcano, Alejandro, Christelle Etard, Corinne Stoetzel, et al.. (2019). NovelIQCEvariations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish. Human Mutation. 41(1). 240–254. 5 indexed citations

Geoffroy, Véronique, Yvan Herenger, Arnaud Kress, et al.. (2018). AnnotSV: an integrated tool for structural variations annotation. Bioinformatics. 34(20). 3572–3574. 207 indexed citations

Scheidecker, Sophie, Sarah Hull, Valérie Pelletier, et al.. (2015). Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome. American Journal of Ophthalmology. 160(2). 364–372.e1. 19 indexed citations

Sen, Parveen, Umashankar Vetrivel, Neerja Gupta, et al.. (2014). Mutation spectrum in BBS genes guided by homozygosity mapping in an Indian cohort. Clinical Genetics. 87(2). 161–166. 26 indexed citations

Laugel-Haushalter, Virginie, Corinne Stoetzel, Jean Muller, et al.. (2014). A Novel Mutation in the <b><i>ROGDI</i></b> Gene in a Patient with Kohlschütter-Tönz Syndrome. Molecular Syndromology. 5(6). 293–298. 15 indexed citations

10.

Fradin, Mélanie, Bernard Aral, Jean Muller, et al.. (2013). Long-Term Follow-Up and Molecular Characterization of a Patient with a RECQL4 Mutation Spectrum Disorder. Dermatology. 226(4). 353–357. 8 indexed citations

11.

Redin, Claire, Stéphanie Le Gras, Véronique Geoffroy, et al.. (2012). Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes. Journal of Medical Genetics. 49(8). 502–512. 81 indexed citations

12.

Marion, Vincent, Cathy Obringer, Nadia Messaddeq, et al.. (2012). BBS-Induced Ciliary Defect Enhances Adipogenesis, Causing Paradoxical Higher-Insulin Sensitivity, Glucose Usage, and Decreased Inflammatory Response. Cell Metabolism. 16(3). 363–377. 71 indexed citations

13.

Aliferis, Konstantinos A., Corinne Stoetzel, Valérie Pelletier, et al.. (2011). A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype. Ophthalmic Genetics. 32(4). 250–255. 14 indexed citations

14.

Stoetzel, Corinne, Laura Liebermann, Vincent Marion, et al.. (2010). Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral Ectopia Lentis. Ophthalmic Genetics. 31(1). 47–51. 29 indexed citations

15.

Stoetzel, Corinne, Virginie Laurier, Laurence Faivre, et al.. (2005). BBS8 is rarely mutated in a cohort of 128 Bardet–Biedl syndrome families. Journal of Human Genetics. 51(1). 81–84. 22 indexed citations

16.

Dollfus, Hélène, Partha S. Biswas, Corinne Stoetzel, et al.. (2002). Saethre‐Chotzen syndrome: Notable intrafamilial phenotypic variability in a large family with Q28X TWIST mutation. American Journal of Medical Genetics. 109(3). 218–225. 14 indexed citations

17.

Yoshiba, Kunihiko, Nagako Yoshiba, Daniel Aberdam, et al.. (2000). Differential expression of laminin-5 subunits during incisor and molar development in the mouse. The International Journal of Developmental Biology. 44(3). 337–340. 18 indexed citations

18.

Stoetzel, Corinne, Anne‐Laure Bolcato‐Bellemin, Patrice Bourgeois, et al.. (1998). X-twi is expressed prior to gastrulation in presumptive neurectodermal and mesodermal cells in dorsalized and ventralized Xenopus laevis embryos. The International Journal of Developmental Biology. 42(6). 747–756. 10 indexed citations

19.

Stoetzel, Corinne, et al.. (1995). Dorso-ventral and rostro-caudal sequential expression of M-twist in the postimplantation murine embryo. Mechanisms of Development. 51(2-3). 251–263. 68 indexed citations

20.

Wolf, Catherine, Christine Thisse, Corinne Stoetzel, et al.. (1991). The M-twist gene of Mus is expressed in subsets of mesodermal cells and is closely related to the Xenopus X-twi and the Drosophila twist genes. Developmental Biology. 143(2). 363–373. 237 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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