| Population genomics of the Viking world A Margaryan, DJ Lawson, M Sikora, F Racimo, S Rasmussen, I Moltke, ... Nature 585 (7825), 390-396, 2020 | 290 | 2020 |
| Refined genetic maps reveal sexual dimorphism in human meiotic recombination at multiple scales C Bhérer, CL Campbell, A Auton Nature communications 8 (1), 14994, 2017 | 130 | 2017 |
| Deep human genealogies reveal a selective advantage to be on an expanding wave front C Moreau, C Bhérer, H Vézina, M Jomphe, D Labuda, L Excoffier Science 334 (6059), 1148-1150, 2011 | 113 | 2011 |
| Genomic and genealogical investigation of the French Canadian founder population structure MH Roy-Gagnon, C Moreau, C Bherer, P St-Onge, D Sinnett, C Laprise, ... Human genetics 129, 521-531, 2011 | 98 | 2011 |
| From target discovery to clinical drug development with human genetics K Trajanoska, C Bhérer, D Taliun, S Zhou, JB Richards, V Mooser Nature 620 (7975), 737-745, 2023 | 75 | 2023 |
| Admixed ancestry and stratification of Quebec regional populations C Bherer, D Labuda, MH Roy‐Gagnon, L Houde, M Tremblay, H Vézina American journal of physical anthropology 144 (3), 432-441, 2011 | 69 | 2011 |
| A pedigree-based map of recombination in the domestic dog genome CL Campbell, C Bhérer, BE Morrow, AR Boyko, A Auton G3: Genes, Genomes, Genetics 6 (11), 3517-3524, 2016 | 67 | 2016 |
| A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21 M Tetreault, A Duquette, I Thiffault, C Bherer, J Jarry, L Loisel, B Banwell, ... Brain 129 (8), 2077-2084, 2006 | 39 | 2006 |
| Native American admixture in the Quebec founder population C Moreau, JF Lefebvre, M Jomphe, C Bherer, A Ruiz-Linares, H Vezina, ... PLoS One 8 (6), e65507, 2013 | 25 | 2013 |
| Carriers of recessive WNK1/HSN2 mutations for hereditary sensory and autonomic neuropathy type 2 (HSAN2) are more sensitive to thermal stimuli ML Loggia, MC Bushnell, M Tétreault, I Thiffault, C Bhérer, ... Journal of Neuroscience 29 (7), 2162-2166, 2009 | 22 | 2009 |
| Estimated prevalence of Niemann–Pick type C disease in Quebec M Labrecque, L Touma, C Bhérer, A Duquette, M Tétreault Scientific reports 11 (1), 22621, 2021 | 10 | 2021 |
| Detection of sexually antagonistic transmission distortions in trio datasets EA Lucotte, C Albiñana, R Laurent, C Bhérer, ... Evolution Letters 6 (2), 203-216, 2022 | 6 | 2022 |
| Refined genetic maps reveal sexual dimorphism in human meiotic recombination at multiple scales. Nat. Commun. 8, 14994 C Bhérer, CL Campbell, A Auton | 6 | 2017 |
| A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome C Bhérer, R Eveleigh, K Trajanoska, J St-Cyr, A Paccard, ... NPJ genomic medicine 9 (1), 8, 2024 | 5 | 2024 |
| Impact des récentes transformations démographiques liées à l’urbanisation sur le bassin génétique de la région de Lanaudière C Bherer, B Brais, H Vézina Cahiers québécois de démographie 37 (2), 211-235, 2008 | 5 | 2008 |
| Pathogenic variants carrier screening in New Brunswick: Acadians reveal high carrier frequency for multiple genetic disorders PP Robichaud, EP Allain, S Belbraouet, C Bhérer, J Mamelona, ... BMC Medical Genomics 15 (1), 98, 2022 | 2 | 2022 |
| Biased Gene Conversion and Its Impact on Genome Evolution C Bhérer, A Auton eLS, 2014 | 2* | 2014 |
| Caractérisation du pool génique de Lanaudière: analyse démogénétique et étude épidémiogénétique de la névrite héréditaire NHSA2 C Bherer Université Laval, 2006 | 2 | 2006 |
| Characterization of the Y Chromosome in Newfoundland and Labrador: Evidence of a founder effect H Zurel, C Bhérer, R Batten, ME MacMillan, S Demiriz, S Mirhendi, ... bioRxiv, 2022.08. 01.502327, 2022 | 1 | 2022 |
| Characterization of Y chromosome diversity in newfoundland and labrador: evidence for a structured founding population H Zurel, C Bhérer, R Batten, ME MacMillan, S Demiriz, S Mirhendi, ... European Journal of Human Genetics, 1-10, 2024 | | 2024 |
