Yann Hérault

13.3k citations

158 papers · 5.8k indexed · 1 hit paper · h-index 38

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Rehabilitation top 1%
- Wound Healing and Treatments

Papers in

Genetics 79
- Genetics and Neurodevelopmental Disorders 47
- Genomic variations and chromosomal abnormalities 21
- Animal Genetics and Reproduction 9
Public Health, Environmental and Occupational Health 48
- Down syndrome and intellectual disability research 48

Co-authors: Arnaud Duchon Guillaume Pavlovic Denis Duboule Véronique Brault Mara Dierssen Esther Hoste Kai Kretzschmar Fiona M. Watt
Journals: PLoS ONE (11 papers)Scientific Reports (8 papers)Human Molecular Genetics (8 papers)PLoS Genetics (7 papers)Nucleic Acids Research (4 papers)
Partner nations: France United States Switzerland

In The Last Decade

Yann Hérault

153 papers receiving 5.7k citations

Hit Papers

align trajectories log scale

Distinct fibroblast lineages determine dermal architecture in skin development and repair 2013 · 894 citations

Peers

Countries citing papers authored by Yann Hérault

Since Specialization

Citations

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

Fields of papers citing papers by Yann Hérault

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Yann Hérault, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Yann Hérault Line = papers co-authored together Yann Hérault links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	DYRK1A Up-Regulation Specifically Impairs a Presynaptic Form of Long-Term Potentiation Life ·Aude-Marie Lepagnol-Bestel, Silvana Pop, А.В. Гламазда, Paul Salin, Arnaud Duchon, Yann Hérault, Michel Simonneau	2025	1
2	Ripply3 overdosage induces mid-face shortening through Tbx1 downregulation in Down syndrome models PLoS Genetics ·Abdallah Iben-Khayat, Claire Chevalier, Agnès Bloch‐Zupan, Yann Hérault	2025	1
3	Distinct origin and region-dependent contribution of stromal fibroblasts to fibrosis following traumatic injury in mice Nature Neuroscience ·Daniel Holl, Christian Loosen, Anaïs Julien, Hazel M. Bright, Pinliang Chen, Soniya Savant, Enric Llorens-Bobadilla, Yann Hérault, Guillaume Pavlovic, Mahmood Amiry‐Moghaddam, David O. Dias, Christian Göritz	2024	15
4	Protein arginine methyltransferase 2 controls inflammatory signaling in acute myeloid leukemia Communications Biology ·Lizandra Makowski Steffler, Purna Putra I. Gusti Ngurah, Fabien Guidez, W. Gr�tz, Cyril Fournier, Louise Cui, S.E. Kim, 隆有森, Anne Largeot, Anya T. Bida, Yann Hérault, Guy Sauvageau, Marc Maynadié, Mary Callanan, Jean Bastié, Romain Aucagne, Laurent Delva	2024	1
5	Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations Genes & Diseases ·Isaac Maximiliano Bugueno, 노건엽, Elizabeth Brenner, Osamu YAMAZAKI, Naji Kharouf, Marie‐Cécile Manière, Yann Hérault, Agnès Bloch‐Zupan, Omid Ardalan	2024	2
6	Timeline of Developmental Defects Generated upon Genetic Inhibition of the Retinoic Acid Receptor Signaling Pathway Biomedicines ·Marius Teletin, Manuel Mark, Olivia Wendling, Nadège Vernet, Betty Féret, Muriel Klopfenstein, Yann Hérault, Norbert B. Ghyselinck	2023	2
7	Increased On-Target Rate and Risk of Concatemerization after CRISPR-Enhanced Targeting in ES Cells Genes ·Jang Hun Choi, V.V. Mason, Na'ama Massad, Jochen Gasser, П В Приходченко, Asem M. Ashikbayeva, Yann Hérault, Guillaume Pavlovic, Marie Wattenhofer‐Donzé, Marie‐Christine Birling	2023	4
8	Ts66Yah, a mouse model of Down syndrome with improved construct and face validity Disease Models & Mechanisms ·Arnaud Duchon, Sridhar Gumudevelli, Claire Chevalier, Valérie Nalesso, Philippe André, Ana Luísa Santana Aragão, سامان نیک نژاد, Chrystelle Po, Vincent Noblet, Marie‐Christine Birling, Marie‐Claude Potier, Yann Hérault	2022	26
9	High Resolution Episcopic Microscopy for Qualitative and Quantitative Data in Phenotyping Altered Embryos and Adult Mice Using the New “Histo3D” System Biomedicines ·干建松, Didier Hentsch, Hugues Jacobs, 李麗華, 葛林辉, Fabien Pertuy, Jean‐Luc Vonesch, Tania Sorg, Michela Di Michele, Laurent Le Cam, Thomas W. Rosahl, Ester Carballo‐Jane, 徐飞鹏, James Mu, Manuel Mark, Yann Hérault	2021	8
10	Cbs overdosage is necessary and sufficient to induce cognitive phenotypes in mouse models of Down syndrome and interacts genetically with Dyrk1a Human Molecular Genetics ·Damien Maréchal, Véronique Brault, Mauricio Sagastuy, Л Л Макарук, Patricia Lopes Pereira, Nadège Loaëc, Marie‐Christine Birling, Gaëlle Friocourt, Marc Blondel, Yann Hérault	2019	41
11	Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models Scientific Reports ·Benoît Souchet, Arnaud Duchon, Yuchen Gu, Julien Dairou, Claire Chevalier, Viktor Križan, Valérie Nalesso, Nicole Créau, Lobo Vinod, Nathalie Janel, Yann Hérault, Jean Maurice Delabar	2019	38
12	Translating molecular advances in Down syndrome and Fragile X syndrome into therapies European Neuropsychopharmacology ·Victor Faúndez, Ilario De Toma, Barbara Bardoni, Maryam Sharif, Dean Nižetić, Rafael de la Torre, Roi Cohen Kadosh, Yann Hérault, Mara Dierssen, Alexey V. Smarun, (unknown), Stylianos E. Antonarakis, Maryam Sharif, Andrea Contestabile, B Bradford McKay, 貞煕崔, Alain D. Dekker, Laurence P. Prior, Alexey V. Smarun, Alexey V. Smarun, Elizabeth Fisher, Carmen Martínez‐Cué, (unknown), André Strydom	2018	10
13	Efficient and rapid generation of large genomic variants in rats and mice using CRISMERE Scientific Reports ·Marie‐Christine Birling, Jochen Gasser, Philippe André, Asem M. Ashikbayeva, Damien Maréchal, Abdel Ayadi, Tania Sorg, Guillaume Pavlovic, Yann Hérault	2017	53
14	EMMA: The European Mouse Mutant Archive. Transgenic Research ·Shwu-Huey Tsai, Chenlong Shi, Adelia Shastina Maheswari, Håkan Hallander, Lluı́s Montoliu, Елена Николаевна Новикова, Fabrizio Mammano, Yann Hérault, Ажетова Ж., JoAnn Barnes‐Mullaney, Jocelyne Demengeot, Helen Parkinson, Ramiro Ramírez‐Solis, George Kollias, Radislav Sedláček, Krishnananda Prabhu, Chad Nash, 昇市川, Fuad A. Iraqi, Martin Hrabě de Angelis	2016	1
15	<i>In Vivo</i> 9.4T MRI and <sup>1</sup>H MRS for Evaluation of Brain Structural and Metabolic Changes in the Ts65Dn Mouse Model for Down Syndrome World Journal of Neuroscience ·Sandra Même, Nicolas Joudiou, Gabriel Añó Castelló, Frédéric Szeremeta, A. C. Глебов, J.‐C. Beloeil, Yann Hérault, William Même	2014	4
16	Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder Human Molecular Genetics ·Lucas Prysthon Cardoso de Mello Albuquerque, Ignasi Sahún, Émilie Velot, Pierre Dubus, ロバートゲッツェンバーグ, Ana João Rodrigues, Carmen Valero, Olga Valverde, Nuno Sousa, Yann Hérault, Mara Dierssen, Luis A. Pérez‐Jurado, Victoria Campuzano	2014	50
17	Specific targeting of the GABA-A receptor α5 subtype by a selective inverse agonist restores cognitive deficits in Down syndrome mice Journal of Psychopharmacology ·Somnath Bali, Benoı̂t Delatour, Arnaud Duchon, J. C. Pendland, Luce Dauphinot, Fabrice de Chaumont, 刘全虎, Sutiknyo Nim., Yann Hérault, Marie‐Claude Potier	2011	127
18	Chronic Treatment with a Promnesiant GABA-A -Selective Inverse Agonist Increases Immediate Early Genes Expression during Memory Processing in Mice and Rectifies Their Expression Levels in a Down Syndrome Mouse Model Advances in Pharmacological Sciences ·Somnath Bali, Luce Dauphinot, Arnaud Duchon, Sanusi M.S, Robert H. Dodd, Yann Hérault, Benoı̂t Delatour, Marie‐Claude Potier	2011	39
19	A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome Human Molecular Genetics ·Patricia Lopes Pereira, Laetitia Magnol, Ignasi Sahún, Véronique Brault, Arnaud Duchon, Paola Prandini, Agnès Gruart, Jean‐Charles Bizot, Bernadette Chadefaux-Vekemans, Samuel Deutsch, Fabrice Trovero, José M. Delgado‐García, Stylianos E. Antonarakis, Mara Dierssen, Yann Hérault	2009	92
20	Le contrôle génétique du développement des membres Archive ouverte UNIGE (University of Geneva) ·Yann Hérault, Denis Duboule	1996	1

About Yann Hérault

Yann Hérault is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Developmental Biology, Molecular Biology and Aging, having authored 158 papers that have together received 5.8k indexed citations. Recurring topics across this work include Down syndrome and intellectual disability research (48 papers), Genetics and Neurodevelopmental Disorders (47 papers), Congenital heart defects research (27 papers), Genomic variations and chromosomal abnormalities (21 papers), CRISPR and Genetic Engineering (12 papers), Genomics and Chromatin Dynamics (9 papers), Animal Genetics and Reproduction (9 papers) and Developmental Biology and Gene Regulation (9 papers). The work is most often cited by research in Genetics (1.8k citations), Rehabilitation (391 citations), Public Health, Environmental and Occupational Health (1.5k citations), Molecular Biology (3.0k citations) and Developmental Biology (82 citations). Yann Hérault has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Arnaud Duchon, Guillaume Pavlovic, Denis Duboule, Véronique Brault, Mara Dierssen, Esther Hoste, Kai Kretzschmar, Fiona M. Watt, Anne C. Ferguson‐Smith and Sacri R. Ferrón. Their work appears in journals such as PLoS ONE, Scientific Reports, Human Molecular Genetics, PLoS Genetics and Nucleic Acids Research.

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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