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W. Lanyon · SciRah

Researcher profile · Semantic Scholar

W. Lanyon

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W. Lanyon — researcher profile on SciRah

h-index: 16
Works: 43
Citations: 926

Most-cited papers

The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion.
S. Ottolenghi, W. Lanyon, J. Paul, Robert Williamson +5 more
1974Nature161 citations
Semantic Scholar
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.
R. MacKie, N. Andrew, W. Lanyon, J. Connor
1998Journal of Investigative Dermatology90 citations Open access
Semantic Scholar
δβ-Thalassemia is due to a gene deletion
S. Ottolenghi, P. Comi, B. Giglioni, P. Tolstoshev +11 more
197676 citations
Semantic Scholar
Identification of a new missense point mutation in exon 4 of the Cu/Zn superoxide dismutase (SOD-1) gene in a family with amyotrophic lateral sclerosis.
A. Elshafey, W. Lanyon, Jeffrey M. Connor
1994Human Molecular Genetics68 citations
Semantic Scholar
Human globin gene analysis for a patient with beta-o/delta beta-thalassemia.
Sergio Ottolenghi, W. Lanyon, Robert Williamson, D. Weatherall +2 more
1975Proceedings of the National Academy of Sciences of the United States of America55 citations Open access
Semantic Scholar
Characterisation of inherited and sporadic mutations in neurofibromatosis type-1.
S. Purandare, W. Lanyon, J. Connor
1994Human Molecular Genetics50 citations
Semantic Scholar
Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion
S. Ottolenghi, W. Lanyon, J. Paul, R. Williamson +5 more
1974Nature45 citations
Semantic Scholar
Identification of five novel mutations in the porphobilinogen deaminase gene.
C. Mgone, W. Lanyon, M. R. Moore, G. Louie +1 more
1994Human Molecular Genetics33 citations
Semantic Scholar
Human globin gene expression and linkage in bone marrow and fetal liver.
W. Lanyon, Sergio Ottolenghi, Robert Williamson
1975Proceedings of the National Academy of Sciences of the United States of America32 citations Open access
Semantic Scholar
Studies on the heterogeneity of mouse-globin messenger RNA.
W. Lanyon, John Paul, Robert Williamson
1972European Journal of Biochemistry31 citations
Semantic Scholar
Alternative sites of transcription initiation upstream of the canonical cap site in human -γ-globin and β-globin genes
G. Grindlay, W. Lanyon, M. Allan, J. Paul
198429 citations Open access
Semantic Scholar
The poly(adenylic acid) sequence of mouse globin messenger RNA.
J. Mansbridge, Jennifer Crossley, W. Lanyon, Robert Williamson
1974European Journal of Biochemistry29 citations Open access
Semantic Scholar
Characteristics of erythropoietin-induced RNA from foetal mouse liver erythropoietic cell cultures and the effects of 5-fluorodeoxyuridine.
A. Nicol, D. Conkie, W. Lanyon, Christine E. Drewienkiewicz +2 more
1972Biochimica et Biophysica Acta19 citations
Semantic Scholar
Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyria
C. Mgone, W. Lanyon, M. R. Moore, G. Louie +1 more
1993Human Genetics18 citations
Semantic Scholar
Screening for molecular pathologies in Lesch‐Nyhan syndrome
Marie Boyd, W. Lanyon, J. Connor
1993Human Mutation17 citations
Semantic Scholar
Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.
A. Cooke, W. Lanyon, D. Wilcox, E. Dornan +6 more
1990Journal of Medical Genetics17 citations Open access
Semantic Scholar
AB1 repetitive sequence near the mouse β-major globin gene
L. Coggins, J. Vass, M. Stinson, W. Lanyon +1 more
198216 citations
Semantic Scholar
Detection of four mutations in six unrelated South African patients with acute intermittent porphyria.
P. Ong, W. Lanyon, R. Hift, J. Halkett +3 more
1996Molecular and Cellular Probes13 citations
Semantic Scholar
Detection of mutations in ectopic factor VIII transcripts from nine haemophilia A patients and the correlation with phenotype
S. Bidichandani, W. Lanyon, C. Shiach, R. Shiach +2 more
1995Human Genetics13 citations
Semantic Scholar
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNA
C. Mgone, W. Lanyon, M. R. Moore, J. Connor
1992Human Genetics13 citations
Semantic Scholar
Acute intermittent porphyria: the in vitro expression of mutant hydroxymethylbilane synthase.
P. Ong, W. Lanyon, Gordon Graham, R. Hift +3 more
1997Molecular and Cellular Probes12 citations
Semantic Scholar
Scottish frequency of the common G985 mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene and the role of MCAD deficiency in sudden infant death syndrome (SIDS)
M. Dundar, W. Lanyon, J. Connor
1993Journal of Inherited Metabolic Disease11 citations
Semantic Scholar
The fractionation of ribonucleic acid on a preparative scale by polyacrylamide gel electrophoresis
W. Lanyon, J. Paul, Robert Williamson
1968FEBS Letters11 citations
Semantic Scholar
Identification of Two Novel Mutations in the Hydroxymethylbilane Synthase Gene in Three Patients from Two Unrelated Families with Acute Intermittent Porphyria
P. Ong, W. Lanyon, R. Hift, J. Halkett +3 more
1998Human Heredity9 citations
Semantic Scholar
Characterisation of a novel splice donor mutation affecting position +1 in intron 18 of the NF-1 gene.
S. Purandare, W. Lanyon, R. Arngrímsson, J. Connor
1995Human Molecular Genetics9 citations
Semantic Scholar
Multiple origins of transcription in the 4.5 Kb upstream of the epsilon-globin gene.
M. Allan, W. Lanyon, J. Paul
1983Cell7 citations
Semantic Scholar
Characterization ofAlu family repetitive sequences which flank human β-type globin genes
L. Coggins, W. Lanyon, A. A. Slater, G. Grindlay +1 more
1981Bioscience Reports7 citations
Semantic Scholar
Acute intermittent porphyria: alternative splicing of hydroxymethylbilane synthase mRNA excludes exons 3 and 12.
P. Ong, W. Lanyon, M. R. Moore, J. Connor
1998Molecular and Cellular Probes6 citations
Semantic Scholar
A novel splice donor mutation affecting position +3 in intron 6 of the factor VIII gene.
Sanjay I. Bidichandan, Caroline R. Shiach, W. Lanyon, J. Connor
1994Human Molecular Genetics6 citations
Semantic Scholar
The Polyadenylate Regions of Mouse Haemoglobin Messenger Ribonucleic Acid
J. Mansbridge, Jennifer Crossley, W. Lanyon, R. Williamson
19735 citations
Semantic Scholar
A novel insertional mutation of a single base in exon 34 of the neurofibromatosis‐1 gene
S. Purandare, H. R. Davidson, W. Lanyon, J. Connor
1994Human Mutation4 citations Open access
Semantic Scholar
Delta-beta-thalassemia is due to a gene deletion.
S. Ottolenghi, P. Comi, B. Giglioni, P. Tolstoshev +11 more
1976Cell4 citations
Semantic Scholar
Characterisation of a 5-bp deletion in exon 4 of the factor VIII gene: concordance with slipped-mispairing at DNA replication
S. Bidichandani, W. Lanyon, J. Connor
1994Human Genetics3 citations
Semantic Scholar
Evidence for involvement of a second genetic locus on chromosome 11q in porphyrin metabolism
B. Norton, W. Lanyon, M. R. Moore, M. Porteous +2 more
1993Human Genetics3 citations
Semantic Scholar
Alternative sites of transcription initiation upstream of the canonical cap site in human gamma-globin and beta-globin genes.
G. Grindlay, W. Lanyon, M. Allan, J. Paul
1984Nucleic Acids Research3 citations
Semantic Scholar
Analysis ofScottish Duchenne andBecker muscular dystrophy families withdystrophin cDNA probes
A. Cooke, W. Lanyon, D. Wilcox, A. Kataki +5 more
19901 citations
Semantic Scholar
A B1 repetitive sequence near the mouse beta-major globin gene.
L. Coggins, J. Vass, M. Stinson, W. Lanyon +1 more
1982Gene1 citations
Semantic Scholar
A novel mutation in the human ferrochelatase gene. A family study
É. Remenyik, W. Lanyon, M. Moore, G. Paragh +3 more
19980 citations
Semantic Scholar
Mutation Detection Using Unlabelled Amplification and Mismatch Detection (AMD) Analysis Technique
Munis Dündar, H. Acar, H. Yüce, W. Lanyon +1 more
1996Turkish Journal of Medical Sciences0 citations
Semantic Scholar
Analysis of mutations in the entire coding sequence of the factor VIII gene
S. I. Bidichadani, W. Lanyon, J. Connor
19940 citations
Semantic Scholar
Characterisation of three novel splice site mutations in introns 11, 18 and 30 of the NF-1 gene
S. Purandare, W. Lanyon, R. Arngrímsson
19940 citations
Semantic Scholar
Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experience.
I. Glass, R. D. Del Mastro, W. Lanyon, J. Raeburn +3 more
1992American journal of medical genetics0 citations
Semantic Scholar
Studies on the heterogeneity of mouse globin messenger ribonucleic acid.
W. Lanyon, J. Paul, Robert Williamson
1972Biochemical Journal0 citations Open access
Semantic Scholar

Frequent co-authors

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