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Rob McMahon
Rob McMahon
NHS Scotland
Verified email at aber.ac.uk
Title
Cited by
Cited by
Year
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
5702005
Language classification by numbers
A McMahon, R McMahon
Oxford University Press on Demand, 2005
4102005
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
1841994
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
1582008
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
1541997
Evolutionary linguistics
A McMahon, R McMahon
Cambridge University Press, 2012
1422012
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
1362006
Finding families: Quantitative methods in language classification
A McMahon, R McMahon
Transactions of the Philological Society 101 (1), 7-55, 2003
1342003
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
1131999
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
1041998
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
891992
The sound patterns of Englishes: representing phonetic similarity
A McMahon, P Heggarty, R McMahon, W Maguire
English Language & Linguistics 11 (1), 113-142, 2007
872007
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
822005
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
601995
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
592000
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
492006
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
461994
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
432015
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
431995
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
421993
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