Sébastien Chénier

790 total citations
17 papers, 473 citations indexed

About

Sébastien Chénier is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Sébastien Chénier has authored 17 papers receiving a total of 473 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 3 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Sébastien Chénier's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Sébastien Chénier is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Sébastien Chénier collaborates with scholars based in Canada, France and United States. Sébastien Chénier's co-authors include Dimitri J. Stavropoulos, David Chitayat, Joyce So, Sergiu Dumitriu, Hanna Faghfoury, Marta Gîrdea, M. Stephen Meyn, Peter N. Ray, Michael Brudno and Marc Fiume and has published in prestigious journals such as Biochemical Journal, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Sébastien Chénier

16 papers receiving 463 citations

Peers

Countries citing papers authored by Sébastien Chénier

Since Specialization

Citations

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

Fields of papers citing papers by Sébastien Chénier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sébastien Chénier

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

All Works

Sort: Min cites: Since: Top N: Style:

17 of 17 papers shown

#	Work	Indexed citations
1	PMS2 c.2117del ( p.Lys706Serfs19 ) is the Most Frequent Cancer‐Associated Founder Pathogenic Variant in the French‐Canadian Population of Quebec, Canada 2025 ·Clinical Genetics* ·(unknown), (unknown), Supriya Behl, (unknown), Sébastien Chénier, Bruno Maranda, Valérie Désilets, Sébastien Lévesque, (unknown), Anne‐Marie Mes‐Masson, Sylvie Giroux, François Rousseau, Nancy Hamel, George Chong, Simon Gravel, William D. Foulkes	0
2	The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study 2023 ·Journal of Child Neurology ·(unknown), (unknown), (unknown), (unknown), Luan T. Tran, (unknown), Chantal Poulin, (unknown), Myriam Srour, Bernard Rosenblatt, Sébastien Chénier, (unknown), Anne‐Marie Laberge, Daniela D’Agostino, (unknown), (unknown), Geneviève Bernard	4
3	Copy number variation in genetic epilepsy with febrile seizures plus 2020 ·European Journal of Paediatric Neurology ·(unknown), (unknown), Sébastien Chénier, (unknown), Michael Shevell, (unknown), Kenneth A. Myers	4
4	Molecular diagnosis of muscular diseases in outpatient clinics 2020 ·Neurology Genetics ·(unknown), (unknown), (unknown), (unknown), Elvy Lapointe, (unknown), Sandrine Larue, Amélie Nadeau, Sébastien Chénier, Paula J. Waters, Pierre‐Étienne Jacques, Serge Gravel, Sébastien Lévesque	15
5	Successful in vitro maturation of oocytes in a woman with gonadotropin-resistant ovary syndrome associated with a novel combination of FSH receptor gene variants: a case report 2019 ·Journal of Assisted Reproduction and Genetics ·(unknown), Chirine Toufaily, Daniel J. Bernard, Seda Ateş, Véronique Blais, Sébastien Chénier, Moncef Benkhalifa, Pierre Miron	18
6	Clinical validity of phenotype-driven analysis software PhenoVar as a diagnostic aid for clinical geneticists in the interpretation of whole-exome sequencing data 2018 ·Genetics in Medicine ·(unknown), (unknown), (unknown), Sébastien Chénier, Valérie Désilets, Bruno Maranda, Paula J. Waters, Pierre‐Étienne Jacques, Sébastien Lévesque	9
7	Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease 2018 ·Journal of Child Neurology ·Andrea Accogli, Kether Guerrero, Daniela D’Agostino, Luan T. Tran, Cécile Cieuta‐Walti, Isabelle Thiffault, Sébastien Chénier, Jeremy Schwartzentruber, Jacek Majewski, Geneviève Bernard	8
8	Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: further delineation of the phenotype 2018 ·Journal of Medical Genetics ·(unknown), Marlies Kempers, Alessandra Maugeri, Carlo Marcelis, Thatjana Gardeitchik, Julie Richer, Dimitra Micha, Luc Beauchesne, Janneke Timmermans, Paul Vermeersch, (unknown), Sébastien Chénier, Gerarda van de Beek, Nils Peeters, Maaike Alaerts, Dorien Schepers, Lut Van Laer, Aline Verstraeten, Bart Loeys	28
9	Does personal genome testing drive service utilization in an adult preventive medicine clinic? 2017 ·Journal of Community Genetics ·Ny Hoang, Robin Z. Hayeems, Janet M. Davies, Shuye Pu, Syed Wasim, Lea Velsher, (unknown), Sébastien Chénier, Dimitri J. Stavropoulos, Riyana Babul‐Hirji, Rosanna Weksberg, Cheryl Shuman	3
10	Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing 2016 ·Orphanet Journal of Rare Diseases ·Sébastien Lévesque, Christiane Auray‐Blais, (unknown), Michel Boutin, (unknown), Pierre‐Étienne Jacques, Sébastien Chénier, Sandrine Larue, Marie‐France Rioux, Walla Al‐Hertani, Amélie Nadeau, Jean Mathieu, Bruno Maranda, Valérie Désilets, Paula J. Waters, Joan Keutzer, Stephanie Austin, Priya S. Kishnani	43
11	CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems 2014 ·Journal of Neurodevelopmental Disorders ·Sébastien Chénier, Grace Yoon, Bob Argiropoulos, Julie Lauzon, Rachel Laframboise, Joo Wook Ahn, Caroline Mackie Ogilvie, Anath C. Lionel, Christian R. Marshall, Andrea K. Vaags, Bita Hashemi, (unknown), Géraldine Mathonnet, Frédérique Tihy, Joyce So, Stephen W. Scherer, Emmanuelle Lemyre, Dimitri J. Stavropoulos	63
12	Capturing the clinical utility of genomic testing: medical recommendations following pediatric microarray 2014 ·European Journal of Human Genetics ·Robin Z. Hayeems, Ny Hoang, Sébastien Chénier, Dimitri J. Stavropoulos, Shuye Pu, Rosanna Weksberg, Cheryl Shuman	17
13	PhenoTips: Patient Phenotyping Software for Clinical and Research Use 2013 ·Human Mutation ·Marta Gîrdea, Sergiu Dumitriu, Marc Fiume, Sarah Bowdin, Kym M. Boycott, Sébastien Chénier, David Chitayat, Hanna Faghfoury, M. Stephen Meyn, Peter N. Ray, Joyce So, Dimitri J. Stavropoulos, Michael Brudno	144
14	Osteopathia striata with cranial sclerosis and developmental delay in a male with a mosaic deletion in chromosome region Xq11.2 2012 ·American Journal of Medical Genetics Part A ·Sébastien Chénier, Abdul Noor, Lucie Dupuis, Dimitri J. Stavropoulos, Roberto Mendoza‐Londono	10
15	Interstitial deletion of 11q‐implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndrome 2012 ·American Journal of Medical Genetics Part A ·Andrea Guerin, Dimitri J. Stavropoulos, Yaser Diab, Sébastien Chénier, Hilary Christensen, Walter H.A. Kahr, Riyana Babul‐Hirji, David Chitayat	43
16	Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation 2011 ·BMC Medical Genomics ·Tracy Tucker, Alexandre Montpetit, David Chai, Susanna Chan, Sébastien Chénier, Bradley P. Coe, Allen Delaney, Patrice Eydoux, Wan L. Lam, Sylvie Langlois, Emmanuelle Lemyre, Marco A. Marra, Hong Qian, Guy A. Rouleau, David F. Vincent, Jacques L. Michaud, Jan M. Friedman	21
17	Subcellular distribution of GABAB receptor homo- and hetero-dimers 2005 ·Biochemical Journal ·(unknown), Lynda Adam, Nicola Bevan, (unknown), Sébastien Chénier, Michel Bouvier	43

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.

Explore authors with similar magnitude of impact