Jean Muller

15.7k total citations · 2 hit papers
93 papers, 8.4k citations indexed

About

Jean Muller is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Jean Muller has authored 93 papers receiving a total of 8.4k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 53 papers in Genetics and 8 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Jean Muller's work include Genetic and Kidney Cyst Diseases (22 papers), Genetic Syndromes and Imprinting (20 papers) and Genomics and Phylogenetic Studies (16 papers). Jean Muller is often cited by papers focused on Genetic and Kidney Cyst Diseases (22 papers), Genetic Syndromes and Imprinting (20 papers) and Genomics and Phylogenetic Studies (16 papers). Jean Muller collaborates with scholars based in France, Germany and United States. Jean Muller's co-authors include Peer Bork, Tobias Doerks, Michael Kuhn, Christian von Mering, Lars Juhl Jensen, Alexander Röth, Mitchell Stark, Milan Simonovic, Damian Szklarczyk and P. Julien and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Bioinformatics.

In The Last Decade

Jean Muller

86 papers receiving 8.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored

2010 2.8k citations Tobias Doerks, Jean Muller et al. Nucleic Acids Research profile →
STRING 8--a global view on proteins and their functional interactions in 630 organisms

2008 1.9k citations Jean Muller, Tobias Doerks et al. Nucleic Acids Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean Muller France	31	5.7k	1.8k	702	567	533	93	8.4k
Pablo Mínguez Spain	27	6.3k 1.1×	1.0k 0.6×	1.2k 1.6×	860 1.5×	601 1.1×	79	9.0k
Frank C. P. Holstege Netherlands	54	8.9k 1.5×	1.1k 0.6×	835 1.2×	801 1.4×	722 1.4×	156	11.1k
Ralf Herwig Germany	43	4.7k 0.8×	1.1k 0.6×	850 1.2×	342 0.6×	262 0.5×	180	7.5k
Marilyn Safran Israel	25	5.4k 0.9×	1.3k 0.7×	1.3k 1.9×	780 1.4×	419 0.8×	32	8.8k
Keiichiro Ono United States	15	4.7k 0.8×	896 0.5×	921 1.3×	400 0.7×	699 1.3×	29	6.8k
Elspeth A. Bruford United Kingdom	35	5.5k 1.0×	1.4k 0.8×	1.0k 1.4×	1.1k 2.0×	250 0.5×	57	8.4k
Helen Cook Denmark	11	6.1k 1.1×	985 0.6×	1.1k 1.5×	816 1.4×	1.5k 2.8×	14	10.9k
Yixue Li China	57	8.7k 1.5×	1.2k 0.7×	1.7k 2.5×	569 1.0×	731 1.4×	443	11.9k
Michael Smoot United States	9	5.9k 1.0×	1.1k 0.6×	819 1.2×	500 0.9×	2.0k 3.7×	11	9.1k
Michael J. Campbell United States	25	5.7k 1.0×	965 0.5×	495 0.7×	799 1.4×	502 0.9×	83	8.3k

Countries citing papers authored by Jean Muller

Since Specialization

Citations

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

Fields of papers citing papers by Jean Muller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jean Muller

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

Gérard, Bénédicte, et al.. (2025). PIK3C2A ‐Related Clinical Phenotype and Cellular Charaterization Linked to Functional SHH Primary Cilia Defect. Clinical Genetics. 108(6). 696–707.

Ravel, Jean‐Marie, M. Renaud, Jean Muller, et al.. (2023). Clinical utility of periodic reinterpretation of CNVs of uncertain significance: an 8-year retrospective study. Genome Medicine. 15(1). 39–39. 7 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.

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

Muller, Jean, Charchit Kumar, Anik Kumar Ghosh, et al.. (2022). Spray-Deposited Anisotropic Assemblies of Plasmonic Nanowires for Direction-Sensitive Strain Measurement. ACS Applied Materials & Interfaces. 14(48). 54073–54080. 5 indexed citations

Okutman, Özlem, Julien Tarabeux, Jean Muller, & Stéphane Viville. (2021). Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility. Genes. 12(3). 410–410. 7 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

Kousi, Maria, Onuralp Söylemez, Niki Mourtzi, et al.. (2020). Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy. Nature Genetics. 52(11). 1145–1150. 21 indexed citations

10.

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

11.

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

12.

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

13.

Guissart, Claire, Nathalie Drouot, İbrahim Öncel, et al.. (2015). Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2). European Journal of Human Genetics. 24(8). 1154–1159. 15 indexed citations

14.

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

15.

Cowling, Belinda S., Anne Toussaint, Jean Muller, & Jocelyn Laporte. (2012). Defective Membrane Remodeling in Neuromuscular Diseases: Insights from Animal Models. PLoS Genetics. 8(4). e1002595–e1002595. 43 indexed citations

16.

Trachana, Kalliopi, Tomas Larsson, Sean Powell, et al.. (2011). Orthology prediction methods: A quality assessment using curated protein families. BioEssays. 33(10). 769–780. 97 indexed citations

17.

Kaplan, Cécile, Jean Muller, B. Branger, et al.. (2010). Fetal alloimmune thrombocytopenia: is less invasive antenatal management safe?. The Journal of Maternal-Fetal & Neonatal Medicine. 24(4). 564–567. 11 indexed citations

18.

Vetter, Guillaume, Antony Le Béchec, Jean Muller, et al.. (2009). Time-resolved analysis of transcriptional events during SNAI1-triggered epithelial to mesenchymal transition. Biochemical and Biophysical Research Communications. 385(4). 485–491. 18 indexed citations

19.

Chalmel, Frédéric, Aurélie Lardenois, Julie Thompson, et al.. (2005). GOAnno: GO annotation based on multiple alignment. Computer applications in the biosciences. 21(9). 2095–2096. 26 indexed citations

20.

Muller, Jean & K. P. Hadeler. (2000). Monotonicity of the Number of Passages in Linear Chains and of the Basic Reproduction Number in Epidemic Models. Zeitschrift für Analysis und ihre Anwendungen. 19(1). 61–75. 5 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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