John W. Nelson

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Hao Hu, Stefan A. Haas, Jamel Chelly et al. · Molecular Psychiatry · 2015 · 299 citations · Full text

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

Lesley McGregor, Ville Makela, S. M. Darling et al. · Nature Genetics · 2003 · 257 citations

Fraser Syndrome, Fibrosis, Developmental Biology +9

Mutations in PYCR1 cause cutis laxa with progeroid features

Bruno Reversade, Nathalie Escande‐Beillard, Aikaterini Dimopoulou et al. · Nature Genetics · 2009 · 252 citations

Biology, Plant Biology, Genetics +5

Incidence of the mucopolysaccharidoses in Northern Ireland

John W. Nelson · Human Genetics · 1997 · 222 citations

Zoonotic Disease, Northern Ireland, Disease Outbreak +2

Sustainable livelihoods and livelihood diversification

Karim Hussein, John W. Nelson · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · 1998 · 162 citations · Full text