Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta K Le Blanc, C Götherström, O Ringdén, M Hassan, R McMahon, E Horwitz, ... Transplantation 79 (11), 1607-1614, 2005 | 570 | 2005 |
Language classification by numbers A McMahon, R McMahon Oxford University Press on Demand, 2005 | 410 | 2005 |
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence DC Rubinsztein, W Amos, J Leggo, S Goodburn, RS Ramesar, J Old, ... Nature genetics 7 (4), 525-530, 1994 | 184 | 1994 |
X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits L Kent, J Emerton, V Bhadravathi, E Weisblatt, G Pasco, LR Willatt, ... Journal of medical genetics 45 (8), 519-524, 2008 | 158 | 2008 |
Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL ER Woodward, C Eng, R McMahon, R Voutilainen, NA Affara, BAJ Ponder, ... Human molecular genetics 6 (7), 1051-1056, 1997 | 154 | 1997 |
Evolutionary linguistics A McMahon, R McMahon Cambridge University Press, 2012 | 142 | 2012 |
Mutation analysis of COL1A1 and COL1A2 in patients diagnosed with osteogenesis imperfecta type I‐IV R Pollitt, R McMahon, J Nunn, R Bamford, A Afifi, N Bishop, A Dalton Human mutation 27 (7), 716-716, 2006 | 136 | 2006 |
Finding families: Quantitative methods in language classification A McMahon, R McMahon Transactions of the Philological Society 101 (1), 7-55, 2003 | 134 | 2003 |
Genotype-phenotype analysis in X-linked Emery–Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype JRW Yates, J Bagshaw, VMA Aksmanovic, E Coomber, R McMahon, ... Neuromuscular Disorders 9 (3), 159-165, 1999 | 113 | 1999 |
Molecular genetic analysis of von Hippel-Lindau disease FM Richards, AR Webster, R McMahon, ER Woodward, S Rose, ... Journal of internal medicine 243 (6), 527-534, 1998 | 104 | 1998 |
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene L Osborne, G Santis, M Schwarz, K Klinger, T Dörk, I McIntosh, ... Human genetics 89 (6), 653-658, 1992 | 89 | 1992 |
The sound patterns of Englishes: representing phonetic similarity A McMahon, P Heggarty, R McMahon, W Maguire English Language & Linguistics 11 (1), 113-142, 2007 | 87 | 2007 |
Swadesh sublists and the benefits of borrowing: an Andean case study A McMahon, P Heggarty, R McMahon, N Slaska Transactions of the Philological Society 103 (2), 147-170, 2005 | 82 | 2005 |
LINGUISTICS, GENETICS AND ARCHAEOLOGY: INTERNAL AND EXTERNAL EVIDENCE IN THE AMERIND CONTROVERSY* A McMahon, R McMahon Transactions of the Philological Society 93 (2), 125-225, 1995 | 60 | 1995 |
Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only FJ Hes, S McKee, MJB Taphoorn, P Rehal, RB van Der Luijt, R McMahon, ... Journal of medical genetics 37 (12), 939-943, 2000 | 59 | 2000 |
Why linguists don’t do dates: evidence from Indo-European and Australian languages A McMahon, R McMahon Phylogenetic methods and the prehistory of languages, 153-160, 2006 | 49 | 2006 |
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families R McMahon, LM Mulligan, CS Healey, SJ Payne, M Ponder, ... Human molecular genetics 3 (4), 643-646, 1994 | 46 | 1994 |
Genetic–geographic correlation revealed across a broad European ecotypic sample of perennial ryegrass (Lolium perenne) using array-based SNP genotyping T Blackmore, I Thomas, R McMahon, W Powell, M Hegarty Theoretical and Applied Genetics 128 (10), 1917-1932, 2015 | 43 | 2015 |
Cystic fibrosis mutation analysis: report from 22 UK regional genetics laboratories MJ Schwarz, GM Malone, A Haworth, JP Cheadle, AL Meredith, ... Human mutation 6 (4), 326-333, 1995 | 43 | 1995 |
Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural history. MR Green, LT Weaver, AF Heeley, K Nicholson, JA Kuzemko, DE Barton, ... Archives of disease in childhood 68 (4), 464-467, 1993 | 42 | 1993 |