Concepedia

David Mansfield

DM

Statistics

Publications

11

Citations

640

H-Index

10

Active since

1994

Affiliations

Inverclyde Royal Hospital(Current)

Western General Hospital

St James's University Hospital

Glasgow Caledonian University

University of Leeds

David Mansfield is an author at Inverclyde Royal Hospital specializing in genetics, molecular genetics, and life sciences.

ORCID

Publications per year

1994–2021

11

Publications

11

Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta

David Parry, Alan J. Mighell, Walid El‐Sayed et al. · The American Journal of Human Genetics · 2009 · 167 citations · Full text

, , +14

Linkage Mapping in 29 Bardet–Biedl Syndrome Families Confirms Loci in Chromosomal Regions 11q13, 15q22.3–q23, and 16q21

Elspeth A. Bruford, Ruth Riise, Peter Teague et al. · Genomics · 1997 · 125 citations

, , +14

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

T J Keen, Matthew M. Hims, Arthur B. McKie et al. · European Journal of Human Genetics · 2002 · 92 citations · Full text

, , +5

A New Locus for Autosomal Dominant Familial Exudative Vitreoretinopathy Maps to Chromosome 11p12-13

Louise Downey, T J Keen, Emma Roberts et al. · The American Journal of Human Genetics · 2001 · 81 citations · Full text

, , +6

Automation of Genetic Linkage Analysis Using Fluorescent Microsatellite Markers

David Mansfield, Alastair F. Brown, Daryll K. Green et al. · Genomics · 1994 · 80 citations

, , +8

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