W. George Lanyon - Concepedia

Author

W. George Lanyon

Also Known As

W G Lanyon, W. G. LANYON, W. G. Lanyon, W. GEORGE LANYON, W. George LANYON, W. George Lanyon, W.G. Lanyon, W.George Lanyon, WG Lanyon

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Cancer Research UK Scotland Institute University of Glasgow Western Infirmary Institute of Genetics The University of Queensland

About

W. George Lanyon is an author at Cancer Research UK Scotland Institute specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	19	883
2	Natural Sciences	6	6	118
3	Biology	5	5	292
4	Health Sciences	2	2	110
5	Biochemistry	2	2	43

W. George Lanyon

Publications

Citations

H-Index

Page 1

	Year	Citations
Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion Sergio Ottolenghi, W. George Lanyon, John Paul, Nature BiologyGene DeletionHaemoglobin Gene DeletionGenetic DisorderGenetics	1974	219
δβ-Thalassemia is due to a gene deletion Sergio Ottolenghi, Paola Comi, Barbára Giglioni, Cell Gene DeletionGenetic DisorderGeneticsHematologyGenetic Mechanism	1976	98
CDKN2A Germline Mutations in U.K. Patients with Familial Melanoma and Multiple Primary Melanomas Rona M. MacKie, Nicola Andrew, W. George Lanyon, Journal of Investigative Dermatology Somatic VariantMedicineMelanomaPathologyMultiple Primary Melanomas	1998	83
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 Alaa Elshafey, W. George Lanyon, J.Mlchael Connor Human Molecular Genetics NeurogenomicsGeneticsGenetic EpidemiologyMolecular BiologyDisease Gene Identification	1994	71
Human globin gene analysis for a patient with beta-o/delta beta-thalassemia. Sergio Ottolenghi, W. George Lanyon, R. Williamson, Proceedings of the National Academy of Sciences ImmunohematologyLaboratory HematologyGene AnalysisGeneticsInherited Metabolic Disease	1975	68
Characterisation of inherited and sporadic mutations in neurofibromatosis type-1 Smita M. Purandare, W. George Lanyon, J. M. Connor Human Molecular Genetics	1994	50
Alternative sites of transcription initiation upstream of the canonical cap site in human -γ-globin and<i>β</i>-globin genes Guillermo Grindlay, W. George Lanyon, Maggi Allan, Nucleic Acids Research	1984	47
Human globin gene expression and linkage in bone marrow and fetal liver. W. George Lanyon, Sergio Ottolenghi, R. Williamson Proceedings of the National Academy of Sciences GeneticsBlood CellMolecular GeneticsEpigeneticsLaboratory Hematology	1975	42
Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyria Charles S. Mgone, W. George Lanyon, Michael Moore, Human Genetics BiologyHigh Mutation FrequencyGeneticsPathogenesisMolecular Genetics	1993	40
Studies on the Heterogeneity of Mouse‐Globin Messenger RNA W. George Lanyon, John Paul, Robert Williamson European Journal of Biochemistry GeneticsMolecular BiologyMolecular GeneticsEdta TreatmentMessenger Rna	1972	40

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