| Exercise training and DNA methylation in humans S Voisin, N Eynon, X Yan, DJ Bishop Acta Physiologica 213 (1), 39-59, 2015 | 274 | 2015 |
| Making sense of the ageing methylome K Seale, S Horvath, A Teschendorff, N Eynon, S Voisin Nature Reviews Genetics 23 (10), 585-605, 2022 | 181 | 2022 |
| Acute sleep loss induces tissue-specific epigenetic and transcriptional alterations to circadian clock genes in men J Cedernaes, ME Osler, S Voisin, JE Broman, H Vogel, SL Dickson, ... The Journal of Clinical Endocrinology & Metabolism 100 (9), E1255-E1261, 2015 | 181 | 2015 |
| Many obesity-associated SNPs strongly associate with DNA methylation changes at proximal promoters and enhancers S Voisin, MS Almén, GY Zheleznyakova, L Lundberg, S Zarei, S Castillo, ... Genome medicine 7, 1-16, 2015 | 156 | 2015 |
| A Multi-Center Comparison of O2peak Trainability Between Interval Training and Moderate Intensity Continuous Training CJ Williams, BJ Gurd, JT Bonafiglia, S Voisin, Z Li, N Harvey, I Croci, ... Frontiers in physiology 10, 19, 2019 | 135 | 2019 |
| Acute sleep loss results in tissue-specific alterations in genome-wide DNA methylation state and metabolic fuel utilization in humans J Cedernaes, M Schönke, JO Westholm, J Mi, A Chibalin, S Voisin, ... Science advances 4 (8), eaar8590, 2018 | 125 | 2018 |
| DNA methylation across the genome in aged human skeletal muscle tissue and muscle-derived cells: the role of HOX genes and physical activity DC Turner, PP Gorski, MF Maasar, RA Seaborne, P Baumert, AD Brown, ... Scientific Reports 10 (1), 15360, 2020 | 111 | 2020 |
| Epigenetic changes in healthy human skeletal muscle following exercise–a systematic review M Jacques, D Hiam, J Craig, R Barrès, N Eynon, S Voisin Epigenetics 14 (7), 633-648, 2019 | 110 | 2019 |
| An epigenetic clock for human skeletal muscle S Voisin, NR Harvey, LM Haupt, LR Griffiths, KJ Ashton, VG Coffey, ... Journal of cachexia, sarcopenia and muscle 11 (4), 887-898, 2020 | 105 | 2020 |
| Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents S Voisin, MS Almén, G Moschonis, GP Chrousos, Y Manios, HB Schiöth European Journal of Human Genetics 23 (5), 654-662, 2015 | 94 | 2015 |
| ACTN3 R577X polymorphism is associated with the incidence and severity of injuries in professional football players M Massidda, S Voisin, C Culigioni, F Piras, P Cugia, X Yan, N Eynon, ... Clinical Journal of Sport Medicine 29 (1), 57-61, 2019 | 92 | 2019 |
| No association between ACTN3 R577X and ACE I/D polymorphisms and endurance running times in 698 Caucasian athletes ID Papadimitriou, SJ Lockey, S Voisin, AJ Herbert, F Garton, ... BMC genomics 19, 1-9, 2018 | 91 | 2018 |
| Recent advances in understanding the role of FOXO3 RJ Stefanetti, S Voisin, A Russell, S Lamon F1000Research 7, 2018 | 90 | 2018 |
| ACTN3 R577X gene variant is associated with muscle-related phenotypes in elite Chinese sprint/power athletes R Yang, X Shen, Y Wang, S Voisin, G Cai, Y Fu, W Xu, N Eynon, ... The Journal of Strength & Conditioning Research 31 (4), 1107-1115, 2017 | 84 | 2017 |
| Expression of epigenetic machinery genes is sensitive to maternal obesity and weight loss in relation to fetal growth in mice PE Panchenko, S Voisin, M Jouin, L Jouneau, A Prézelin, S Lecoutre, ... Clinical epigenetics 8, 1-19, 2016 | 81 | 2016 |
| Physiological and molecular sex differences in human skeletal muscle in response to exercise training S Landen, D Hiam, S Voisin, M Jacques, S Lamon, N Eynon The Journal of physiology 601 (3), 419-434, 2023 | 80 | 2023 |
| Genetic and epigenetic sex-specific adaptations to endurance exercise S Landen, S Voisin, JM Craig, SL McGee, S Lamon, N Eynon Epigenetics 14 (6), 523-535, 2019 | 70 | 2019 |
| Meta‐analysis of genome‐wide DNA methylation and integrative omics of age in human skeletal muscle S Voisin, M Jacques, S Landen, NR Harvey, LM Haupt, LR Griffiths, ... Journal of Cachexia, Sarcopenia and Muscle 12 (4), 1064-1078, 2021 | 64 | 2021 |
| Positive selection of protective variants for type 2 diabetes from the Neolithic onward: a case study in Central Asia L Ségurel, F Austerlitz, B Toupance, M Gautier, JL Kelley, P Pasquet, ... European Journal of Human Genetics 21 (10), 1146-1151, 2013 | 61 | 2013 |
| Genome-wide analysis shows association of epigenetic changes in regulators of Rab and Rho GTPases with spinal muscular atrophy severity GY Zheleznyakova, S Voisin, AV Kiselev, M Sällman Almén, MJ Xavier, ... European Journal of Human Genetics 21 (9), 988-993, 2013 | 46 | 2013 |
Helgi SchiöthProfessor at Department of Neuroscience, Functional Pharmacology, Uppsala Universityneuro.uu.se의 이메일 확인됨