Médéric Jeanne

510 total citations
12 papers, 72 citations indexed

About

Médéric Jeanne is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Médéric Jeanne has authored 12 papers receiving a total of 72 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Médéric Jeanne's work include Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Médéric Jeanne is often cited by papers focused on Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Médéric Jeanne collaborates with scholars based in France, United States and Netherlands. Médéric Jeanne's co-authors include Frédéric Laumonnier, Wendy K. Chung, Patrick Vourc’h, Sylviane Marouillat, Philippe Corcia, Chunhua Weng, Charlotte Veyrat‐Durebex, Marie‐Laure Vuillaume, Hélène Blasco and Annick Toutain and has published in prestigious journals such as International Journal of Molecular Sciences, Clinical Chemistry and Clinica Chimica Acta.

In The Last Decade

Médéric Jeanne

9 papers receiving 72 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Médéric Jeanne France	5	42	21	7	5	5	12	72
Muhsin Elmas Türkiye	6	47 1.1×	32 1.5×	6 0.9×	9 1.8×	2 0.4×	25	89
Abolfazl Heidari Iran	4	17 0.4×	13 0.6×	6 0.9×	6 1.2×	2 0.4×	8	59
Matt Velinder United States	5	56 1.3×	52 2.5×	4 0.6×	1 0.2×	4 0.8×	9	96
Nikolay A. Ivanov United States	6	58 1.4×	25 1.2×	12 1.7×	5 1.0×	4 0.8×	14	107
Sarah Grotto France	5	51 1.2×	26 1.2×	6 0.9×	17 3.4×	8 1.6×	12	79
Qianwen Gao China	3	49 1.2×	40 1.9×	7 1.0×	4 0.8×	4 0.8×	7	94
Cecilia E Kim United States	2	25 0.6×	32 1.5×	4 0.6×	3 0.6×		4	53
Kathleen Mommaerts Luxembourg	7	64 1.5×	9 0.4×	10 1.4×	9 1.8×	2 0.4×	11	119
Sumaiya Nazeen United States	3	66 1.6×	53 2.5×	4 0.6×	2 0.4×	22 4.4×	6	113
Janet L. Goldstein United States	4	37 0.9×	57 2.7×	7 1.0×	7 1.4×	2 0.4×	4	110

Countries citing papers authored by Médéric Jeanne

Since Specialization

Citations

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

Fields of papers citing papers by Médéric Jeanne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Médéric Jeanne

This figure shows the co-authorship network connecting the top 25 collaborators of Médéric Jeanne. A scholar is included among the top collaborators of Médéric Jeanne 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 Médéric Jeanne. Médéric Jeanne is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Moizard, Marie‐Pierre, Nathalie Ronce, Paul Guéguen, et al.. (2025). Variant Update on ASCC1 : Characterization of the First Homozygous Missense Variant Involved in Prenatal‐Onset Spinal Muscular Atrophy With Congenital Bone Fractures 2. American Journal of Medical Genetics Part A. 200(3). 744–748.

Bouvagnet, Patrice, Anne‐Claire Bréhin, Alexis Hermida, et al.. (2025). MYH6 in Congenital Heart Defects: A Genotype–Phenotype Characterization in a French Cohort. Pediatric Cardiology.

Jeanne, Médéric & Wendy K. Chung. (2025). DNA Sequencing in Newborn Screening: Opportunities, Challenges, and Future Directions. Clinical Chemistry. 71(1). 77–86. 3 indexed citations

Chung, Wendy K., et al.. (2024). Rare disease diagnosis using knowledge guided retrieval augmentation for ChatGPT. Journal of Biomedical Informatics. 157. 104702–104702. 11 indexed citations

Dohrn, Maike F., Güney Bademci, Adriana Rebelo, et al.. (2024). Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism. Annals of Clinical and Translational Neurology. 11(4). 1075–1079. 1 indexed citations

Jeanne, Médéric, et al.. (2024). A Child with a Congenital Aplasia of the Scalp: A Quiz. Acta Dermato Venereologica. 104. adv39948–adv39948. 1 indexed citations

Vourc’h, Patrick, et al.. (2023). Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders. Frontiers in Neuroscience. 17. 1154446–1154446. 12 indexed citations

Gueguen, Paul, Hélène Blasco, Isabelle Benz‐de Bretagne, et al.. (2023). Sweet ending: When genetics prevent a dramatic CDG diagnostic mistake. Clinica Chimica Acta. 551. 117620–117620. 2 indexed citations

Jeanne, Médéric, et al.. (2022). Melorheostosis or "Dripping Candle Wax" Bone Disease. The Journal of Rheumatology. 49(11). jrheum.201624–jrheum.201624.

10.

Vourc’h, Patrick, Médéric Jeanne, Sylviane Marouillat, et al.. (2022). The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration. International Journal of Molecular Sciences. 23(7). 3882–3882. 18 indexed citations

11.

Jeanne, Médéric, Marie‐Laure Vuillaume, Valerie E. Vancollie, et al.. (2021). Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth. Human Genetics. 140(6). 885–896. 14 indexed citations

12.

Vuillaume, Marie‐Laure, Benjamin Cogné, Médéric Jeanne, et al.. (2018). Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability. Clinica Chimica Acta. 485. 218–223. 10 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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