| Whole-genome sequencing of 234 bulls facilitates mapping of monogenic and complex traits in cattle HD Daetwyler, A Capitan, H Pausch, P Stothard, R Van Binsbergen, ... Nature genetics 46 (8), 858-865, 2014 | 857 | 2014 |
| Meta-analysis of genome-wide association studies for cattle stature identifies common genes that regulate body size in mammals AC Bouwman, HD Daetwyler, AJ Chamberlain, CH Ponce, M Sargolzaei, ... Nature genetics 50 (3), 362-367, 2018 | 304 | 2018 |
| Detection of haplotypes associated with prenatal death in dairy cattle and identification of deleterious mutations in GART, SHBG and SLC37A2 S Fritz, A Capitan, A Djari, SC Rodriguez, A Barbat, A Baur, C Grohs, ... PloS one 8 (6), e65550, 2013 | 245 | 2013 |
| Whole-genome analysis of introgressive hybridization and characterization of the bovine legacy of Mongolian yaks I Medugorac, A Graf, C Grohs, S Rothammer, Y Zagdsuren, E Gladyr, ... Nature genetics 49 (3), 470-475, 2017 | 133 | 2017 |
| Novel Insights into the Bovine Polled Phenotype and Horn Ontogenesis in Bovidae A Allais-Bonnet, C Grohs, I Medugorac, S Krebs, A Djari, A Graf, S Fritz, ... PloS one 8 (5), e63512, 2013 | 126 | 2013 |
| Characterization of the DGAT1 K232A and variable number of tandem repeat polymorphisms in French dairy cattle M Gautier, A Capitan, S Fritz, A Eggen, D Boichard, T Druet Journal of Dairy Science 90 (6), 2980-2988, 2007 | 116 | 2007 |
| Rapid discovery of de novo deleterious mutations in cattle enhances the value of livestock as model species E Bourneuf, P Otz, H Pausch, V Jagannathan, P Michot, C Grohs, G Piton, ... Scientific Reports 7 (1), 11466, 2017 | 89 | 2017 |
| Uncovering adaptation from sequence data: lessons from genome resequencing of four cattle breeds S Boitard, M Boussaha, A Capitan, D Rocha, B Servin Genetics 203 (1), 433-450, 2016 | 89 | 2016 |
| Genomic prediction from whole genome sequence in livestock: the 1000 bull genomes project BJ Hayes, HD Daetwyler, PJ Bowman, AJ Chamberlian, CJ Vander Jagt, ... 10th World Congress of Genetics Applied to Livestock Production, 2014 | 74 | 2014 |
| The 80-kb DNA duplication on BTA1 is the only remaining candidate mutation for the polled phenotype of Friesian origin S Rothammer, A Capitan, E Mullaart, D Seichter, I Russ, I Medugorac Genetics Selection Evolution 46, 1-5, 2014 | 73 | 2014 |
| A Newly Described Bovine Type 2 Scurs Syndrome Segregates with a Frame-Shift Mutation in TWIST1 A Capitan, C Grohs, B Weiss, MN Rossignol, P Reversé, A Eggen PloS one 6 (7), e22242, 2011 | 66 | 2011 |
| An initiator codon mutation in SDE2 causes recessive embryonic lethality in Holstein cattle S Fritz, C Hoze, E Rebours, A Barbat, M Bizard, A Chamberlain, ... Journal of dairy science 101 (7), 6220-6231, 2018 | 53 | 2018 |
| The scurs inheritance: new insights from the French Charolais breed A Capitan, C Grohs, M Gautier, A Eggen BMC genetics 10, 1-11, 2009 | 49 | 2009 |
| A splice site mutation in CENPU is associated with recessive embryonic lethality in Holstein cattle C Hozé, C Escouflaire, M Mesbah-Uddin, A Barbat, M Boussaha, ... Journal of Dairy Science 103 (1), 607-612, 2020 | 38 | 2020 |
| A reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breeds P Michot, S Chahory, A Marete, C Grohs, D Dagios, E Donzel, ... Genetics Selection Evolution 48, 1-15, 2016 | 37 | 2016 |
| Whole-genome scan to detect quantitative trait loci associated with milk protein composition in 3 French dairy cattle breeds MP Sanchez, A Govignon-Gion, M Ferrand, M Gelé, D Pourchet, ... Journal of dairy science 99 (10), 8203-8215, 2016 | 37 | 2016 |
| Rare phenotypes in domestic animals: unique resources for multiple applications G Leroy, B Besbes, P Boettcher, I Hoffmann, A Capitan, R Baumung Animal genetics 47 (2), 141-153, 2016 | 34 | 2016 |
| Experience from large scale use of the EuroGenomics custom SNP chip in cattle DA Boichard, M Boussaha, A Capitan, D Rocha, C Hoze, MP Sanchez, ... Proceedings of the World Congress on Genetics Applied to Livestock …, 2018 | 32 | 2018 |
| A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse C Morgenthaler, M Diribarne, A Capitan, R Legendre, R Saintilan, ... Genetics Selection Evolution 49, 1-10, 2017 | 32 | 2017 |
| A 3.7 Mb deletion encompassing ZEB2 causes a novel polled and multisystemic syndrome in the progeny of a somatic mosaic bull A Capitan, A Allais-Bonnet, A Pinton, B Marquant-Le Guienne, ... PloS one 7 (11), e49084, 2012 | 32 | 2012 |
