| Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping A Vaysse, A Ratnakumar, T Derrien, E Axelsson, G Rosengren Pielberg, ... PLoS genetics 7 (10), e1002316, 2011 | 406 | 2011 |
| Targeting of the EphA4 tyrosine kinase receptor affects dorsal/ventral pathfinding of limb motor axons F Helmbacher, S Schneider-Maunoury, P Topilko, L Tiret, P Charnay Development 127 (15), 3313-3324, 2000 | 304 | 2000 |
| SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs M Pelé, L Tiret, JL Kessler, S Blot, JJ Panthier Human Molecular Genetics 14 (11), 1417-1427, 2005 | 189 | 2005 |
| Increased apoptosis of motoneurons and altered somatotopic maps in the brachial spinal cord of Hoxc-8-deficient mice L Tiret, H Le Mouellic, M Maury, P Brulet Development 125 (2), 279-291, 1998 | 153 | 1998 |
| Absence of SARS-CoV-2 infection in cats and dogs in close contact with a cluster of COVID-19 patients in a veterinary campus S Temmam, A Barbarino, D Maso, S Behillil, V Enouf, C Huon, A Jaraud, ... One health 10, 100164, 2020 | 151 | 2020 |
| MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers AH Beggs, J Böhm, E Snead, M Kozlowski, M Maurer, K Minor, ... Proceedings of the National Academy of Sciences 107 (33), 14697-14702, 2010 | 138 | 2010 |
| A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis M Abitbol, JL Thibaud, NJ Olby, C Hitte, JP Puech, M Maurer, ... Proceedings of the National Academy of Sciences 107 (33), 14775-14780, 2010 | 122 | 2010 |
| Feline low-grade alimentary lymphoma: an emerging entity and a potential animal model for human disease MV Paulin, L Couronné, J Beguin, S Le Poder, M Delverdier, MO Semin, ... BMC veterinary research 14, 1-19, 2018 | 95 | 2018 |
| Necroptosis mediates myofibre death in dystrophin-deficient mice JE Morgan, A Prola, V Mariot, V Pini, J Meng, C Hourde, J Dumonceaux, ... Nature communications 9 (1), 3655, 2018 | 83 | 2018 |
| Inhibited gastrulation in mouse embryos overexpressing the leukemia inhibitory factor. F Conquet, N Peyrieras, L Tiret, P Brûlet Proceedings of the National Academy of Sciences 89 (17), 8195-8199, 1992 | 75 | 1992 |
| Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy J Böhm, N Vasli, M Maurer, B Cowling, GD Shelton, W Kress, A Toussaint, ... PLoS genetics 9 (6), e1003430, 2013 | 74 | 2013 |
| Myod and H19-Igf2 locus interactions are required for diaphragm formation in the mouse M Borensztein, P Monnier, F Court, Y Louault, MA Ripoche, L Tiret, Z Yao, ... Development 140 (6), 1231-1239, 2013 | 68 | 2013 |
| Breed differences in natriuretic peptides in healthy dogs K Sjöstrand, G Wess, I Ljungvall, J Häggström, AC Merveille, M Wiberg, ... Journal of Veterinary Internal Medicine 28 (2), 451-457, 2014 | 63 | 2014 |
| Uterine contractions depend on KIT-positive interstitial cells in the mouse: genetic and pharmacological evidence S Allix, E Reyes-Gomez, G Aubin-Houzelstein, D Noël, L Tiret, JJ Panthier, ... Biology of reproduction 79 (3), 510-517, 2008 | 55 | 2008 |
| HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth J Blondelle, Y Ohno, V Gache, S Guyot, S Storck, N Blanchard-Gutton, ... Journal of molecular cell biology 7 (5), 429-440, 2015 | 52 | 2015 |
| The cnm locus, a canine homologue of human autosomal forms of centronuclear myopathy, maps to chromosome 2 L Tiret, S Blot, JL Kessler, H Gaillot, M Breen, JJ Panthier Human genetics 113, 297-306, 2003 | 51 | 2003 |
| Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice F Redelsperger, N Raddi, A Bacquin, C Vernochet, V Mariot, V Gache, ... PLoS Genetics 12 (9), e1006289, 2016 | 50 | 2016 |
| Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys R Legrand, L Tiret, M Abitbol Genetics Selection Evolution 46, 1-7, 2014 | 40 | 2014 |
| Centronuclear Myopathy in Labrador Retrievers: A Recent Founder Mutation in the PTPLA Gene Has Rapidly Disseminated Worldwide M Maurer, J Mary, L Guillaud, M Fender, M Pele, T Bilzer, N Olby, ... Public Library of Science 7 (10), e46408, 2012 | 34 | 2012 |
| A deletion in FOXN1 is associated with a syndrome characterized by congenital hypotrichosis and short life expectancy in Birman cats M Abitbol, P Bossé, A Thomas, L Tiret PLoS One 10 (3), e0120668, 2015 | 32 | 2015 |
Jens HäggströmProfessor Internal Medicine, Companion AnimalsVerified email at slu.se
