| Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans TJ Aitman, R Dong, TJ Vyse, PJ Norsworthy, MD Johnson, J Smith, ... Nature 439 (7078), 851-855, 2006 | 820 | 2006 |
| The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles RA Fisher, MD Hodges, HC Rees, NJ Sebire, MJ Seckl, ES Newlands, ... Human molecular genetics 11 (26), 3267-3272, 2002 | 190 | 2002 |
| Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region CM Wang, PH Dixon, S Decordova, MD Hodges, NJ Sebire, S Ozalp, ... Journal of medical genetics 46 (8), 569-575, 2009 | 168 | 2009 |
| Familial recurrent hydatidiform mole RA Fisher, MD Hodges, ES Newlands a review 2004, 49, 2004 | 124 | 2004 |
| The Human Achaete-Scute Homologue 2 (ASCL2, HASH2) Maps to Chromosome 11p15.5, Close to IGF2 and is Expressed in Extravillus Trophoblasts M Alders, M Hodges, AK Hadjantonakis, J Postmus, I Van Wijk, J Bliek, ... Human molecular genetics 6 (6), 859-867, 1997 | 114 | 1997 |
| Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development. LC Bibb, JKL Holt, EE Tarttelin, MD Hodges, K Gregory-Evans, ... Human Molecular Genetics 10 (15), 1571-1579, 2001 | 111 | 2001 |
| Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degeneration K Gregory-Evans, F Chang, MD Hodges, CY Gregory-Evans Molecular vision 15, 962, 2009 | 74 | 2009 |
| Genomic imprinting in gestational trophoblastic disease—a review RA Fisher, MD Hodges Placenta 24, S111-S118, 2003 | 71 | 2003 |
| Combining immunolabeling and surface-enhanced Raman spectroscopy on cell membranes MD Hodges, JG Kelly, AJ Bentley, S Fogarty, II Patel, FL Martin, ... ACS nano 5 (12), 9535-9541, 2011 | 64 | 2011 |
| Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome M Alders, A Ryan, M Hodges, J Bliek, AP Feinberg, O Privitera, ... The American Journal of Human Genetics 66 (5), 1473-1484, 2000 | 63 | 2000 |
| Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa K Guerin, CY Gregory-Evans, MD Hodges, M Moosajee, DS Mackay, ... Experimental eye research 87 (3), 197-207, 2008 | 60 | 2008 |
| Genetic refinement and physical mapping of a biparental complete hydatidiform mole locus on chromosome 19q13. 4. MD Hodges, HC Rees, MJ Seckl, ES Newlands, RA Fisher Journal of Medical Genetics 40 (8), e95-e95, 2003 | 58 | 2003 |
| SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma CY Gregory-Evans, M Moosajee, MD Hodges, DS Mackay, L Game, ... Human Molecular Genetics 16 (20), 2482-2493, 2007 | 54 | 2007 |
| Artificial intelligence-assisted loop mediated isothermal amplification (AI-LAMP) for rapid detection of SARS-CoV-2 MA Rohaim, E Clayton, I Sahin, J Vilela, ME Khalifa, MQ Al-Natour, ... Viruses 12 (9), 972, 2020 | 45 | 2020 |
| Immunogenicity and protective efficacy of an intranasal live-attenuated vaccine against SARS-CoV-2 JG Park, FS Oladunni, MA Rohaim, J Whittingham-Dowd, J Tollitt, ... Iscience 24 (9), 2021 | 34 | 2021 |
| The Drosophila insulin receptor independently modulates lifespan and locomotor senescence MZBH Ismail, MD Hodges, M Boylan, R Achall, A Shirras, SJ Broughton PLoS One 10 (5), e0125312, 2015 | 34 | 2015 |
| A Human p57KIP2 Transgene Is Not Activated by Passage Through the Maternal Mouse Germline RM John, M Hodges, P Little, SC Barton, M Azim Surani Human Molecular Genetics 8 (12), 2211-2219, 1999 | 33 | 1999 |
| Evaluation of deletions in 7q11. 2 and 8p12–p21 as prognostic indicators of tumour development following molar pregnancy B Burke, NJ Sebire, J Moss, MD Hodges, MJ Seckl, ES Newlands, ... Gynecologic oncology 103 (2), 642-648, 2006 | 22 | 2006 |
| Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15. 5 and a pseudogene to 10q11. 2 MA Nesbit, MD Hodges, L Campbell, T De Meulemeester, M Alders, ... Genomics 42 (2), 284-294, 1997 | 22 | 1997 |
| Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouse MD Hodges, H Vieira, K Gregory-Evans, CY Gregory-Evans Genomics 80 (5), 531-542, 2002 | 12 | 2002 |
