Sophie Scheidecker

1.3k total citations
20 papers, 423 citations indexed

About

Sophie Scheidecker is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Sophie Scheidecker has authored 20 papers receiving a total of 423 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Sophie Scheidecker's work include Genetic and Kidney Cyst Diseases (9 papers), Hedgehog Signaling Pathway Studies (8 papers) and Genetic Syndromes and Imprinting (7 papers). Sophie Scheidecker is often cited by papers focused on Genetic and Kidney Cyst Diseases (9 papers), Hedgehog Signaling Pathway Studies (8 papers) and Genetic Syndromes and Imprinting (7 papers). Sophie Scheidecker collaborates with scholars based in France, Germany and United Kingdom. Sophie Scheidecker's co-authors include Hélène Dollfus, Véronique Geoffroy, Corinne Stoetzel, Jean Muller, Élise Schaefer, Christelle Etard, Uwe Strähle, Vincent Marion, Valérie Pelletier and Kirsley Chennen and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and International Journal of Molecular Sciences.

In The Last Decade

Sophie Scheidecker

19 papers receiving 419 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sophie Scheidecker France	11	321	278	55	26	25	20	423
Liliya Nazlamova United Kingdom	7	345 1.1×	271 1.0×	101 1.8×	22 0.8×	14 0.6×	10	444
Farooq Ahmad Pakistan	12	272 0.8×	227 0.8×	39 0.7×	34 1.3×	20 0.8×	38	421
Muriel Holder France	9	283 0.9×	185 0.7×	26 0.5×	18 0.7×	19 0.8×	14	408
Hannah Verdin Belgium	14	317 1.0×	268 1.0×	26 0.5×	29 1.1×	8 0.3×	29	467
Cathy Obringer France	11	308 1.0×	252 0.9×	65 1.2×	16 0.6×	16 0.6×	22	408
Chad Haldeman‐Englert United States	11	184 0.6×	204 0.7×	48 0.9×	50 1.9×	10 0.4×	21	359
Linda Manwaring United States	8	136 0.4×	175 0.6×	75 1.4×	31 1.2×	18 0.7×	15	374
Mohammed Zain Seidahmed Saudi Arabia	12	277 0.9×	227 0.8×	26 0.5×	65 2.5×	13 0.5×	21	409
Nara Sobreira United States	10	325 1.0×	323 1.2×	25 0.5×	20 0.8×	36 1.4×	27	550
Magdalena Cárdenas-Rodríguez Uruguay	8	284 0.9×	273 1.0×	54 1.0×	24 0.9×	17 0.7×	12	364

Countries citing papers authored by Sophie Scheidecker

Since Specialization

Citations

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

Fields of papers citing papers by Sophie Scheidecker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sophie Scheidecker

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

Baer, Sarah, Marguerite Miguet, Élise Schaefer, et al.. (2024). Copy Number Variation and Epilepsy: State of the Art in the Era of High-Throughput Sequencing—A Multicenter Cohort Study. Pediatric Neurology. 159. 16–25. 1 indexed citations

Geoffroy, Véronique, Thomas Guignard, Arnaud Kress, et al.. (2023). The AnnotSV webserver in 2023: updated visualization and ranking. Nucleic Acids Research. 51(W1). W39–W45. 6 indexed citations

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

Francannet, Christine, Boris Keren, Jonathan Lévy, et al.. (2023). Unexpected Inheritance Patterns in a Large Cohort of Patients with a Suspected Ciliopathy. Human Mutation. 2023. 1–7.

M’kacher, Radhia, Marguerite Miguet, Bruno Colicchio, et al.. (2022). A Central Role of Telomere Dysfunction in the Formation of a Unique Translocation within the Sub-Telomere Region Resulting in Duplication and Partial Trisomy. Genes. 13(10). 1762–1762. 1 indexed citations

Geoffroy, Véronique, Thomas Guignard, Arnaud Kress, et al.. (2021). AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysis. Nucleic Acids Research. 49(W1). W21–W28. 34 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

Stoetzel, Corinne, Élise Schaefer, Nadège Calmels, et al.. (2020). A severe case of Frank-ter Haar syndrome and literature review: Further delineation of the phenotypical spectrum. European Journal of Medical Genetics. 63(4). 103857–103857. 10 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

10.

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

11.

Lornage, Xavière, Valérie Biancalana, Tracey Willis, et al.. (2019). Clinical, histological, and genetic characterization of PYROXD1-related myopathy. Acta Neuropathologica Communications. 7(1). 138–138. 16 indexed citations

12.

Kremer, Valérie, et al.. (2018). 9q22.3 Microdeletion Syndrome with Multiple Basal Cell Carcinomas Treated with Vismodegib: Three Key Messages in One Patient. Acta Dermato Venereologica. 98(2). 287–288. 2 indexed citations

13.

Scheidecker, Sophie, M. Köhler, Anne‐Lise Delezoide, et al.. (2016). Prenatal diagnosis of focal dermal hypoplasia: Report of three fetuses and review of the literature. American Journal of Medical Genetics Part A. 173(2). 479–486. 5 indexed citations

14.

Stoetzel, Corinne, Séverine Bär, Johan‐Owen De Craene, et al.. (2016). A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi. Nature Communications. 7(1). 13586–13586. 40 indexed citations

15.

Schaefer, Élise, Corinne Stoetzel, Sophie Scheidecker, et al.. (2016). Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet–Biedl syndrome. Journal of Human Genetics. 61(5). 447–450. 57 indexed citations

16.

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

17.

Scheidecker, Sophie, Christelle Etard, Laurence Haren, et al.. (2015). Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy. The American Journal of Human Genetics. 96(4). 666–674. 50 indexed citations

18.

Herenger, Yvan, Corinne Stoetzel, Élise Schaefer, et al.. (2015). Long term follow up of two independent patients with Schinzel–Giedion carrying SETBP1 mutations. European Journal of Medical Genetics. 58(9). 479–487. 15 indexed citations

19.

Braun, Jean, Vincent Noblet, M. Durand, et al.. (2014). Olfaction evaluation and correlation with brain atrophy in Bardet‐Biedl syndrome. Clinical Genetics. 86(6). 521–529. 27 indexed citations

20.

Scheidecker, Sophie, Christelle Etard, Nathan W. Pierce, et al.. (2013). Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18). Journal of Medical Genetics. 51(2). 132–136. 104 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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