| Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour O Ogawa, MR Eccles, J Szeto, LA McNoe, K Yun, MA Maw, PJ Smith, ... Nature 362 (6422), 749-751, 1993 | 820 | 1993 |
| Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux P Sanyanusin, LA Schimmenti, LA McNoe, TA Ward, MEM Pierpont, ... Nature genetics 9 (4), 358-364, 1995 | 752 | 1995 |
| Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2 EW Jabs, X Li, AF Scott, G Meyers, W Chen, M Eccles, J Mao, LR Charnas, ... Nature genetics 8 (3), 275-279, 1994 | 562 | 1994 |
| Conjugate for efficient delivery of short interfering RNA (siRNA) into mammalian cells A Muratovska, MR Eccles FEBS letters 558 (1-3), 63-68, 2004 | 536 | 2004 |
| Expression of insulin-like growth factor-II transcripts in Wilms' tumour AE Reeve, MR Eccles, RJ Wilkins, GI Bell, LJ Millow Nature 317 (6034), 258-260, 1985 | 410 | 1985 |
| A PANorama of PAX genes in cancer and development EJD Robson, SJ He, MR Eccles Nature Reviews Cancer 6 (1), 52-62, 2006 | 341 | 2006 |
| Paired-Box genes are frequently expressed in cancer and often required for cancer cell survival A Muratovska, C Zhou, S He, P Goodyer, MR Eccles Oncogene 22 (39), 7989-7997, 2003 | 322 | 2003 |
| Application of circularly polarized light for non‐invasive diagnosis of cancerous tissues and turbid tissue‐like scattering media B Kunnen, C Macdonald, A Doronin, S Jacques, M Eccles, I Meglinski Journal of biophotonics 8 (4), 317-323, 2015 | 279 | 2015 |
| Epigenetic drivers of tumourigenesis and cancer metastasis A Chatterjee, EJ Rodger, MR Eccles Seminars in cancer biology 51, 149-159, 2018 | 261 | 2018 |
| A third Wilms' tumor locus on chromosome 16q MA Maw, PE Grundy, LJ Millow, MR Eccles, RS Dunn, PJ Smith, ... Cancer research 52 (11), 3094-3098, 1992 | 248 | 1992 |
| Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux W Lu, AM Van Eerde, X Fan, F Quintero-Rivera, S Kulkarni, H Ferguson, ... The American Journal of Human Genetics 80 (4), 616-632, 2007 | 237 | 2007 |
| Primary renal hypoplasiain humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax21Neu +/– mutant mice S Porteous, E Torban, NP Cho, H Cunliffe, L Chua, L McNoe, T Ward, ... Human molecular genetics 9 (1), 1-11, 2000 | 223 | 2000 |
| Mutation of PAX2 in two siblings with renal-coloboma syndrome P Sanyanusin, LA McNoe, MJ Sullivan, RG Weaver, MR Eccles Human molecular genetics 4 (11), 2183-2184, 1995 | 192 | 1995 |
| Expression of the PAX2 gene in human fetal kidney and Wilms' tumor MR Eccles, LJ Wallis, AE Fidler, NK Spurr, PJ Goodfellow, AE Reeve Cell Growth Differ 3 (5), 279-289, 1992 | 177 | 1992 |
| Renal‐coloboma syndrome: a multi‐system developmental disorder caused by PAX2 mutations MR Eccles, LA Schimmenti Clinical genetics 56 (1), 1-9, 1999 | 173 | 1999 |
| Targeting DNA methylation and EZH2 activity to overcome melanoma resistance to immunotherapy A Al Emran, A Chatterjee, EJ Rodger, JC Tiffen, SJ Gallagher, MR Eccles, ... Trends in immunology 40 (4), 328-344, 2019 | 167 | 2019 |
| Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy HF Otto EA, Ramaswami G, Janssen S, Chaki M, Allen SJ, Zhou W, Airik R, Hurd ... J Med. Genet. 48 (2), 105-116, 2011 | 155 | 2011 |
| Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. LA Schimmenti, HE Cunliffe, LA McNoe, TA Ward, MC French, HH Shim, ... American journal of human genetics 60 (4), 869, 1997 | 153 | 1997 |
| Biallelic DICER1 mutations occur in Wilms tumours MK Wu, N Sabbaghian, B Xu, S Addidou‐Kalucki, C Bernard, D Zou, ... The Journal of pathology 230 (2), 154-164, 2013 | 147 | 2013 |
| Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus‐specific database M Bower, R Salomon, J Allanson, C Antignac, F Benedicenti, E Benetti, ... Human mutation 33 (3), 457-466, 2012 | 144 | 2012 |
Associate Professor Aniruddha Chatte...Rutherford Discovery Fellow, Associate Professor, University of OtagoVerified email at otago.ac.nz
