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Iain Fenton

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Meriel McEntagart; Gretchen Parsons; Anna Buj-Bello; Valérie Biancalana; Iain Fenton; Mark Little; Michael Krawczak; Nick Thomas; Gail Herman; Angus Clarke; Carina Wallgren-Pettersson
Genotype-phenotype correlations in X-linked myotubular myopathy.
Alastair G Cardno; Peter Holmans; Mark I Rees; Lisa Anne Jones; Geraldine M McCarthy; Marian Hamshere; Nigel M Williams; Nadine Norton; Hywel J Williams; Iain Fenton; Kieran C Murphy; Robert D Sanders; MY Gray; Michael C O'Donovan; Peter McGuffin; Michael J Owen
A genomewide linkage study of age at onset in schizophrenia.
Mark I Rees; P Watts; Iain Fenton; Angus Clarke; Russell G Snell; Michael J Owen; J Gray
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3).

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All Publications

2002: Meriel McEntagart; Gretchen Parsons; Anna Buj-Bello; Valérie Biancalana; Iain Fenton; Mark Little; Michael Krawczak; Nick Thomas; Gail Herman; Angus Clarke; Carina Wallgren-Pettersson
Genotype-phenotype correlations in X-linked myotubular myopathy.
Neuromuscular disorders : NMD 2002;12(10):939-46.
2001: Alastair G Cardno; Peter Holmans; Mark I Rees; Lisa Anne Jones; Geraldine M McCarthy; Marian Hamshere; Nigel M Williams; Nadine Norton; Hywel J Williams; Iain Fenton; Kieran C Murphy; Robert D Sanders; MY Gray; Michael C O'Donovan; Peter McGuffin; Michael J Owen
A genomewide linkage study of age at onset in schizophrenia.
American journal of medical genetics 2001;105(5):439-45.
2000: Mark I Rees; P Watts; Iain Fenton; Angus Clarke; Russell G Snell; Michael J Owen; J Gray
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3).
Human genetics 2000;106(2):206-9.
2000: Michael Krawczak; Edward V Ball; Iain Fenton; Peter D Stenson; Shaun S Abeysinghe; N Thomas; David N Cooper
Human gene mutation database-a biomedical information and research resource.
Human mutation 2000;15(1):45-51.
1999: Nigel M Williams; Mark I Rees; Peter Holmans; Nadine Norton; Alastair G Cardno; Lisa Anne Jones; Kieran C Murphy; Robert D Sanders; G McCarthy; MY Gray; Iain Fenton; Peter McGuffin; Michael J Owen
A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs.
Human molecular genetics 1999;8(9):1729-39.
1999: Mark I Rees; Iain Fenton; Nigel M Williams; Peter Holmans; Nadine Norton; Alastair G Cardno; Philip Asherson; Gillian Spurlock; E Roberts; E Parfitt; R Mant; Homero Vallada; E Dawson; M W Li; DA Collier; John F Powell; S Nanko; Michael Gill; Peter McGuffin; Michael J Owen
Autosome search for schizophrenia susceptibility genes in multiply affected families.
Molecular psychiatry 1999;4(4):353-9.
1999: Pat Kehoe; Fabienne Wavrant De-Vrieze; Richard Crook; W S Wu; Peter Holmans; Iain Fenton; Gillian Spurlock; Nadine Norton; Hywel Williams; Nigel Williams; Simon Lovestone; Jordi Perez-Tur; Michael Hutton; Marie-Christine Chartier-Harlin; Shantia Shears; K Roehl; Jeremy Booth; W Van Voorst; Dzanan Ramic; Julie Williams; Alison Goate; John Hardy; Michael J Owen
A full genome scan for late onset Alzheimer's disease.
Human molecular genetics 1999;8(2):237-45.
1998: W S Wu; Peter Holmans; F Wavrant-DeVrièze; Shantia Shears; Pat Kehoe; Richard Crook; Jeremy Booth; Nigel Williams; Jordi Pérez-Tur; K Roehl; Iain Fenton; Marie-Christine Chartier-Harlin; Simon Lovestone; Julie Williams; Michael Hutton; John Hardy; Michael J Owen; Alison Goate
Genetic studies on chromosome 12 in late-onset Alzheimer disease.
JAMA : the journal of the American Medical Association 1998;280(7):619-22.
1997: johanna k macpherson; Gillian Spurlock; Nigel M Williams; Alastair G Cardno; Lisa Anne Jones; Kieran C Murphy; Philip Asherson; Peter Holmans; Iain Fenton; Peter McGuffin; Michael J Owen
Linkage study of chromosome 6p in sib-pairs with schizophrenia.
American journal of medical genetics 1997;74(3):319-23.
1995: Andrew G Roberts; Sharon D Whatley; J Daniels; Peter Holmans; Iain Fenton; Michael J Owen; P Thompson; C Long; George H Elder
Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23.
Human molecular genetics 1995;4(12):2387-90.
1994: JA Terrett; R Newbury-Ecob; G S Cross; Iain Fenton; J A Raeburn; I D Young; J David Brook
Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q.
Nature genetics 1994;6(4):401-4.
1993: J C MacMillan; R G Snell; A Tyler; G D Houlihan; Iain Fenton; Jeremy P Cheadle; Lazarus Lazarou; D J Shaw; Peter S Harper
Molecular analysis and clinical correlations of the Huntington's disease mutation.
Lancet 1993;342(8877):954-8.
1993: R G Snell; J C MacMillan; Jeremy P Cheadle; Iain Fenton; Lazarus Lazarou; Peter Davies; Marcy E MacDonald; James Gusella; Peter S Harper; D J Shaw
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.
Nature genetics 1993;4(4):393-7.
1993: H G Harley; S A Rundle; J C MacMillan; J Myring; J David Brook; S Crow; W Reardon; Iain Fenton; D J Shaw; Peter S Harper
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.
American journal of human genetics 1993;52(6):1164-74.
1993: W Reardon; R Newcombe; Iain Fenton; Jonathan R Sibert; Peter S Harper
The natural history of congenital myotonic dystrophy: mortality and long term clinical aspects.
Archives of disease in childhood 1993;68(2):177-81.
1992: M J Aldred; P J M Crawford; E Roberts; C M Gillespie; N S Thomas; Iain Fenton; Lodewijk A Sandkuijl; Peter S Harper
Genetic heterogeneity in X-linked amelogenesis imperfecta.
Genomics 1992;14(3):567-73.
1992: Iain Fenton; Lodewijk A Sandkuijl
MEGABASE/PKD: a genetic database for polycystic kidney disease.
Contributions to nephrology 1992;97():118-27.