| A DNA methylation fingerprint of 1628 human samples AF Fernandez, Y Assenov, JI Martin-Subero, B Balint, R Siebert, ... Genome research 22 (2), 407-419, 2012 | 471 | 2012 |
| Diagnosis and management of Silver–Russell syndrome: first international consensus statement EL Wakeling, F Brioude, O Lokulo-Sodipe, SM O'Connell, J Salem, J Bliek, ... Nature Reviews Endocrinology 13 (2), 105-124, 2017 | 463 | 2017 |
| DNA methylation contributes to natural human variation H Heyn, S Moran, I Hernando-Herraez, S Sayols, A Gomez, J Sandoval, ... Genome research 23 (9), 1363-1372, 2013 | 433 | 2013 |
| Genomic imprinting disorders: lessons on how genome, epigenome and environment interact D Monk, DJG Mackay, T Eggermann, ER Maher, A Riccio Nature Reviews Genetics 20 (4), 235-248, 2019 | 335 | 2019 |
| Limited evolutionary conservation of imprinting in the human placenta D Monk, P Arnaud, S Apostolidou, FA Hills, G Kelsey, P Stanier, R Feil, ... Proceedings of the National Academy of Sciences 103 (17), 6623-6628, 2006 | 300 | 2006 |
| Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment C Tayama, V Romanelli, A Martin-Trujillo, I Iglesias-Platas, K Okamura, ... Genome research 24 (4), 554-569, 2014 | 273 | 2014 |
| Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement G Mantovani, M Bastepe, D Monk, L De Sanctis, S Thiele, A Usardi, ... Nature Reviews Endocrinology 14 (8), 476-500, 2018 | 271 | 2018 |
| The genetic aetiology of Silver–Russell syndrome S Abu-Amero, D Monk, J Frost, M Preece, P Stanier, GE Moore Journal of medical genetics 45 (4), 193-199, 2008 | 230 | 2008 |
| Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci T Eggermann, G Perez de Nanclares, ER Maher, IK Temple, Z Tümer, ... Clinical epigenetics 7, 1-18, 2015 | 187 | 2015 |
| Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark P Arnaud, D Monk, M Hitchins, E Gordon, W Dean, CV Beechey, J Peters, ... Human molecular genetics 12 (9), 1005-1019, 2003 | 179 | 2003 |
| The geometry of flag manifolds D Monk Proceedings of the London Mathematical Society 3 (2), 253-286, 1959 | 172 | 1959 |
| Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human D Monk, R Sanches, P Arnaud, S Apostolidou, FA Hills, S Abu-Amero, ... Human molecular genetics 15 (8), 1259-1269, 2006 | 170 | 2006 |
| Duplication of 7p11. 2-p13, including GRB10, in Silver-Russell syndrome D Monk, EL Wakeling, V Proud, M Hitchins, SN Abu-Amero, P Stanier, ... The American Journal of Human Genetics 66 (1), 36-46, 2000 | 170 | 2000 |
| The role and interaction of imprinted genes in human fetal growth GE Moore, M Ishida, C Demetriou, L Al-Olabi, LJ Leon, AC Thomas, ... Philosophical Transactions of the Royal Society B: Biological Sciences 370 …, 2015 | 169 | 2015 |
| Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies H Zhou, M Brockington, H Jungbluth, D Monk, P Stanier, CA Sewry, ... The American Journal of Human Genetics 79 (5), 859-868, 2006 | 131 | 2006 |
| Intrauterine growth restriction—genetic causes and consequences D Monk, GE Moore Seminars in Fetal and Neonatal Medicine 9 (5), 371-378, 2004 | 131 | 2004 |
| Preoperative risk factors for conversion from laparoscopic to open cholecystectomy: a validated risk score derived from a prospective UK database of 8820 patients RP Sutcliffe, M Hollyman, J Hodson, G Bonney, RS Vohra, EA Griffiths, ... Hpb 18 (11), 922-928, 2016 | 126 | 2016 |
| A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation AJ Wood, RG Roberts, D Monk, GE Moore, R Schulz, RJ Oakey PLoS Genetics 3 (2), e20, 2007 | 126 | 2007 |
| Genomic imprinting in the human placenta D Monk American journal of obstetrics and gynecology 213 (4), S152-S162, 2015 | 123 | 2015 |
| Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett’s esophagus C Palles, L Chegwidden, X Li, JM Findlay, G Farnham, FC Giner, ... Gastroenterology 148 (2), 367-378, 2015 | 119 | 2015 |
