Olivier Quenez

4.9k total citations
18 papers, 238 citations indexed

About

Olivier Quenez is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Olivier Quenez has authored 18 papers receiving a total of 238 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Olivier Quenez's work include Genomics and Rare Diseases (6 papers), RNA regulation and disease (4 papers) and Alzheimer's disease research and treatments (4 papers). Olivier Quenez is often cited by papers focused on Genomics and Rare Diseases (6 papers), RNA regulation and disease (4 papers) and Alzheimer's disease research and treatments (4 papers). Olivier Quenez collaborates with scholars based in France, United Kingdom and Italy. Olivier Quenez's co-authors include Gaël Nicolas, Thierry Frébourg, Dominique Campion, Anne Rovelet‐Lecrux, Anne Boland, David Wallon, Kilan Le Guennec, Camille Charbonnier, Sophie Coutant and Pranitha Jenardhanan and has published in prestigious journals such as Clinical Chemistry, Molecular Psychiatry and Movement Disorders.

In The Last Decade

Olivier Quenez

16 papers receiving 238 citations

Peers

Countries citing papers authored by Olivier Quenez

Since Specialization

Citations

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

Fields of papers citing papers by Olivier Quenez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olivier Quenez

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	RRP12 Variants Are Associated With Autosomal Recessive Brain Calcifications 2025 ·Movement Disorders ·Edoardo Monfrini, Paola Rinchetti, Mathieu Anheim, Anna Klingseisen, Ouhaïd Lagha‐Boukbiza, Zhidong Cen, Dehao Yang, Xinhui Chen, Reza Maroofian, Henry Houlden, Gioia Cappelletti, Anne‐Claire Richard, Olivier Quenez, Camilo Toro, Steven J. Frucht, Francesco Lotti, Wei Luo, David Hunt, Gaël Nicolas, Giulietta Riboldi	0
2	Bridging the Diagnostic Gap in Hereditary Cancers with Simple, Cost-Effective, High-Throughput RNA Splicing Analysis 2025 ·Journal of Molecular Diagnostics ·(unknown), (unknown), L Thibaut, (unknown), Stéphanie Vasseur, Olivier Quenez, Sophie Coutant, (unknown), Françoise Charbonnier, (unknown), Angélina Legros, (unknown), Laurent Castéra, Raphaël Leman, (unknown), Stéphanie Baert‐Desurmont, Sophie Krieger, Philippe Ruminy, Claude Houdayer	0
3	Upstream open reading frame-introducing variants in patients with primary familial brain calcification 2024 ·European Journal of Human Genetics ·Anne Rovelet‐Lecrux, (unknown), Olivier Quenez, (unknown), Kévin Cassinari, Anne‐Claire Richard, Anne Boland, Jean‐François Deleuze, Cyril Goizet, (unknown), Christophe Verny, Karine Nguyen, Magalie Lecourtois, Gaël Nicolas	2
4	High diagnostic potential of short and long read genome sequencing with transcriptome analysis in exome-negative developmental disorders 2023 ·Human Genetics ·François Lecoquierre, Olivier Quenez, (unknown), Sophie Coutant, Myriam Vézain, (unknown), Nathalie Drouot, Anne Boland, Robert Olaso, Vincent Meyer, Jean‐François Deleuze, (unknown), (unknown), (unknown), Pascale Saugier-Véber, Alice Goldenberg, Anne‐Marie Guerrot, Gaël Nicolas	4
5	uORF‐introducing variants in the 5′UTR of the NIPBL gene as a cause of Cornelia de Lange syndrome 2022 ·Human Mutation ·(unknown), Anne Rovelet‐Lecrux, Kévin Cassinari, Elise Brischoux‐Boucher, Pascale Saugier-Véber, Alice Goldenberg, François Lecoquierre, Nathalie Drouot, Anne‐Claire Richard, Gabriella Vera, Sophie Coutant, Olivier Quenez, (unknown), Céline Bonnet, Myriam Bronner, Magalie Lecourtois, Gaël Nicolas	9
6	Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease 2021 ·Acta Neuropathologica Communications ·Anne Rovelet‐Lecrux, Sébastien Feuillette, Laëtitia Miguel, Catherine Schramm, (unknown), Olivier Quenez, Isabelle Ségalas-Milazzo, Laure Guilhaudis, Stéphane Rousseau, Gaëtan Riou, Thierry Frébourg, Dominique Campion, Gaël Nicolas, Magalie Lecourtois	16
7	Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome 2020 ·Journal of Medical Genetics ·Chaker Aloui, Stéphanie Guey, Eva Pipiras, Manoëlle Kossorotoff, Sophie Guéden, (unknown), (unknown), Jean‐Michel Pédespan, Marie Husson, Dominique Hervé, Florence Riant, Markus Kraemer, Julie Steffann, Olivier Quenez, Elisabeth Tournier‐Lasserve	9
8	Haploinsufficiency of the Primary Familial Brain Calcification Gene SLC20A2 Mediated by Disruption of a Regulatory Element 2020 ·Movement Disorders ·Kévin Cassinari, Anne Rovelet‐Lecrux, (unknown), Olivier Quenez, Anne‐Claire Richard, Camille Charbonnier, Robert Olaso, Anne Boland, Jean‐François Deleuze, J.-F. Besancenot, Benoît Delpont, (unknown), François Lecoquierre, Pascal Chambon, Christel Thauvin‐Robinet, Dominique Campion, Thierry Frébourg, Jean‐Luc Battini, Gaël Nicolas	9
9	Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer’s Disease 2019 ·Journal of Alzheimer s Disease ·(unknown), (unknown), Olivier Quenez, Annie Laquerrière, Florent Marguet, Kévin Cassinari, David Wallon, Olivier Martinaud, Camille Charbonnier, Gaël Nicolas, Jean‐François Deleuze, Anne Boland, Mark Lathrop, Thierry Frébourg, Dominique Campion, Sébastien S. Hébert, Anne Rovelet‐Lecrux	17
10	A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations 2019 ·Clinical Chemistry ·Kévin Cassinari, Olivier Quenez, Géraldine Joly‐Hélas, Ludivine Beaussire, Nathalie Le Meur, Mathieu Castelain, Alice Goldenberg, Anne‐Marie Guerrot, Anne‐Claire Bréhin, Jean‐François Deleuze, Anne Boland, Anne Rovelet‐Lecrux, Dominique Campion, Pascale Saugier-Véber, Nicolas Gruchy, Thierry Frébourg, Gaël Nicolas, Nasrin Sarafan‐Vasseur, Pascal Chambon	11
11	Confirmation and further delineation of the SMG9‐deficiency syndrome, a rare and severe developmental disorder 2019 ·American Journal of Medical Genetics Part A ·François Lecoquierre, (unknown), (unknown), (unknown), (unknown), Mariette Renaux‐Petel, Jean‐Baptiste Leca, (unknown), M. Brasseur‐Daudruy, Férielle Louillet, M. Muraine, Sophie Coutant, Olivier Quenez, Anne Boland, (unknown), Thierry Frébourg, Alice Goldenberg, Pascale Saugier-Véber, Anne‐Marie Guerrot, Gaël Nicolas	7
12	Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing 2018 ·Translational Psychiatry ·(unknown), (unknown), Olivier Quenez, Camille Charbonnier, Maud Rothärmel, (unknown), (unknown), Anne‐Claire Richard, Thierry Frébourg, Jean‐François Deleuze, Anne Boland, Emmanuelle Génin, Stéphanie Debette, Christophe Tzourio, Dominique Campion, Gaël Nicolas, Olivier Guillin	12
13	Biallelic Loss of Function of SORL1 in an Early Onset Alzheimer’s Disease Patient 2018 ·Journal of Alzheimer s Disease ·Kilan Le Guennec, Hélène Tubeuf, Didier Hannequin, David Wallon, Olivier Quenez, Stéphane Rousseau, Anne‐Claire Richard, Jean‐François Deleuze, Anne Boland, Thierry Frébourg, Pascaline Gaildrat, Dominique Campion, Alexandra Martins, Gaël Nicolas	11
14	Deletion of exons 9 and 10 of the Presenilin 1 gene in a patient with Early-onset Alzheimer Disease generates longer amyloid seeds 2017 ·Neurobiology of Disease ·Kilan Le Guennec, Sarah Veugelen, Olivier Quenez, María Szaruga, Stéphane Rousseau, Gaël Nicolas, David Wallon, Frédérique Fluchère, Thierry Frébourg, Bart De Strooper, Dominique Campion, Lucía Chávez‐Gutiérrez, Anne Rovelet‐Lecrux	16
15	Clinical and pathologic features of Aicardi–Goutières syndrome due to an IFIH1 mutation: A pediatric case report 2016 ·American Journal of Medical Genetics Part A ·Florent Marguet, Annie Laquerrière, Alice Goldenberg, Anne‐Marie Guerrot, Olivier Quenez, (unknown), Catherine Vanhulle, (unknown), Françoise Charbonnier, Myriam Vézain, Soumeya Bekri, Isabelle Tournier, Thierry Frébourg, Gaël Nicolas	14
16	Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing 2016 ·European Journal of Human Genetics ·(unknown), (unknown), Olivier Quenez, Anne Rovelet‐Lecrux, Anne‐Claire Richard, Marc Vérin, Snejana Jurici, Isabelle Le Ber, Anne Boland, Jean‐François Deleuze, Thierry Frébourg, João Ricardo Mendes de Oliveira, Didier Hannequin, Dominique Campion, Gaël Nicolas	19
17	De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease 2015 ·Molecular Psychiatry ·Anne Rovelet‐Lecrux, Camille Charbonnier, David Wallon, Gaël Nicolas, Matthew Seaman, Cyril Pottier, Sophia Y. Breusegem, Premendu P. Mathur, Pranitha Jenardhanan, Kilan Le Guennec, Aamir S. Mukadam, Olivier Quenez, Sophie Coutant, Simon Rousseau, (unknown), Anne Boland, J.-F. Deleuze, Thierry Frébourg, Didier Hannequin, Dominique Campion, (unknown)	74
18	Development of genomic resources for the tick Ixodes ricinus: isolation and characterization of single nucleotide polymorphisms 2013 ·Molecular Ecology Resources ·Elsa Quillery, Olivier Quenez, Pierre Peterlongo, Olivier Plantard	8

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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