| Enhanced detection of circulating tumor DNA by fragment size analysis F Mouliere, D Chandrananda, AM Piskorz, EK Moore, J Morris, ... Science translational medicine 10 (466), eaat4921, 2018 | 872 | 2018 |
| Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) ER Maher, LA Brueton, SC Bowdin, A Luharia, W Cooper, TR Cole, ... Journal of medical genetics 40 (1), 62-64, 2003 | 762 | 2003 |
| Role of the Ras-association domain family 1 tumor suppressor gene in human cancers A Agathanggelou, WN Cooper, F Latif Cancer research 65 (9), 3497-3508, 2005 | 543 | 2005 |
| Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis–renal dysfunction–cholestasis (ARC) syndrome P Gissen, CA Johnson, NV Morgan, JM Stapelbroek, T Forshew, ... Nature genetics 36 (4), 400-404, 2004 | 366 | 2004 |
| Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome WN Cooper, A Luharia, GA Evans, H Raza, AC Haire, R Grundy, ... European journal of human genetics 13 (9), 1025-1032, 2005 | 339 | 2005 |
| The role of RASSF1A methylation in cancer LB Hesson, WN Cooper, F Latif Disease markers 23 (1-2), 73-87, 2007 | 292 | 2007 |
| Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility D Astuti, MR Morris, WN Cooper, RHJ Staals, NC Wake, GA Fews, H Gill, ... Nature genetics 44 (3), 277-284, 2012 | 269 | 2012 |
| Evaluation of the 3p21. 3 tumour-suppressor gene cluster LB Hesson, WN Cooper, F Latif Oncogene 26 (52), 7283-7301, 2007 | 219 | 2007 |
| Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome N Diaz-Meyer, CD Day, K Khatod, ER Maher, W Cooper, W Reik, ... Journal of medical genetics 40 (11), 797-801, 2003 | 203 | 2003 |
| An association between variants in the IGF2 gene and Beckwith–Wiedemann syndrome: interaction between genotype and epigenotype A Murrell, S Heeson, WN Cooper, E Douglas, S Apostolidou, GE Moore, ... Human molecular genetics 13 (2), 247-255, 2004 | 189 | 2004 |
| Periconceptional maternal micronutrient supplementation is associated with widespread gender related changes in the epigenome: a study of a unique resource in the Gambia B Khulan, WN Cooper, BM Skinner, J Bauer, S Owens, AM Prentice, ... Human molecular genetics 21 (9), 2086-2101, 2012 | 167 | 2012 |
| Residual ctDNA after treatment predicts early relapse in patients with early-stage non-small cell lung cancer D Gale, K Heider, A Ruiz-Valdepenas, S Hackinger, M Perry, G Marsico, ... Annals of oncology 33 (5), 500-510, 2022 | 163 | 2022 |
| Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour D Astuti, F Latif, K Wagner, D Gentle, WN Cooper, D Catchpoole, ... British journal of cancer 92 (8), 1574-1580, 2005 | 163 | 2005 |
| An obesogenic diet during mouse pregnancy modifies maternal nutrient partitioning and the fetal growth trajectory AN Sferruzzi‐Perri, OR Vaughan, M Haro, WN Cooper, B Musial, ... The FASEB journal 27 (10), 3928-3937, 2013 | 156 | 2013 |
| ctDNA monitoring using patient-specific sequencing and integration of variant reads JCM Wan, K Heider, D Gale, S Murphy, E Fisher, F Mouliere, ... Science translational medicine 12 (548), eaaz8084, 2020 | 153 | 2020 |
| DNA methylation profiling at imprinted loci after periconceptional micronutrient supplementation in humans: results of a pilot randomized controlled trial WN Cooper, B Khulan, S Owens, CE Elks, V Seidel, AM Prentice, ... The FASEB Journal 26 (5), 1782-1790, 2012 | 134 | 2012 |
| The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemias LB Hesson, TL Dunwell, WN Cooper, D Catchpoole, AT Brini, ... Molecular cancer 8, 1-10, 2009 | 127 | 2009 |
| Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma MR Morris, LB Hesson, KJ Wagner, NV Morgan, D Astuti, RD Lees, ... Oncogene 22 (43), 6794-6801, 2003 | 125 | 2003 |
| Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer KJ Wagner, WN Cooper, RG Grundy, G Caldwell, C Jones, RB Wadey, ... Oncogene 21 (47), 7277-7282, 2002 | 118 | 2002 |
| Beckwith Weidemann syndrome: a behavioral phenotype–genotype study L Kent, S Bowdin, GA Kirby, WN Cooper, ER Maher American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008 | 114 | 2008 |
