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Iain Fenton

Observed names: Fenton, I., I Fenton, I. Fenton
OpenAlex ID: A5073142295
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease
1993 · Russell G. Snell, John C. MacMillan, et al. · Nature Genetics · 710
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.
1993 · H G Harley, S A Rundle, et al. · PubMed · 377
Human Gene Mutation Database?A biomedical information and research resource
2000 · Michael Krawczak, Edward V. Ball, et al. · Human Mutation · 273
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Genotype–phenotype correlations in X-linked myotubular myopathy
2002 · Meriel McEntagart, Gretchen Parsons, et al. · Neuromuscular Disorders · 156
A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs
1999 · N. M. Williams, M. I. Rees, et al. · Human Molecular Genetics · 138
The natural history of congenital myotonic dystrophy: mortality and long term clinical aspects.
1993 · W Reardon, R Newcombe, et al. · Archives of Disease in Childhood · 132
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA 3 )
2000 · M.I. Rees, P. Watts, et al. · Human Genetics · 101
Molecular analysis and clinical correlations of the Huntington's disease mutation
1993 · J.C MacMillan, R.G Snell, et al. · The Lancet · 96
Holt–Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q
1994 · Jonathan A. Terrett, Ruth Newbury-Ecob, et al. · Nature Genetics · 85
Genetic heterogeneity in X-linked amelogenesis imperfecta
1992 · Michael J. Aldred, Peter J.M. Crawford, et al. · Genomics · 69
A genomewide linkage study of age at onset in schizophrenia*
2001 · Alastair G. Cardno, Peter A. Holmans, et al. · American Journal of Medical Genetics · 66
Autosome search for schizophrenia susceptibility genes in multiply affected families
1999 · M I Rees, I Fenton, et al. · Molecular Psychiatry · 19
Linkage Study of Chromosome 6p in Sib-Pairs With Schizophrenia
1997 · J.K. Daniels, G. Spurlock, et al. · American Journal of Medical Genetics · 16
Covariate-dependent age-at-onset distributions for Huntington disease.
1991 · M Krawczak, B Bockel, et al. · Europe PMC (PubMed Central) · 15
MEGABASE/PKD: A Genetic Database for Polycystic Kidney Disease
2015 · I. Fenton, L. A. Sandkuijl · Contributions to nephrology · 14
Genome search for schizophrenia susceptibility genes using a two-stage sib-pair approach
1996 · N. M. Williams, M. I. Rees, et al. · Psychiatric Genetics · 4
PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects
1998 · Williams, Nigel Melville, Fenton, I., et al. · ORCA Online Research @Cardiff (Cardiff University)
A clinical and genetic database for management of familial adenomatous polyposis.
1992 · I Fenton, J Sampson · Journal of Medical Genetics
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Works count: 18
Citation count: 2,271
H-index: 14
I10-index: 15
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