M. Wragg

发表

Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease

M. Adams, J. Venter, J. Hardy, 1996, Neuroreport.

The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

M. Adams, N. Fox, J. Venter, 1995, Nature Genetics.

Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease. Alzheimer's Disease Collaborative Group.

M. Hutton, C. Talbot, M. Wragg, 1996, Lancet.

E280A PS‐1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles

A. Myers, A. Goate, K. Kosik, 1997, Human mutation.

A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene

M. Adams, J. Hardy, M. Rossor, 1995, Neuroreport.

Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease

A. Goate, M. Hutton, C. Talbot, 1996, The Lancet.

Autosomal dominant dementia with widespread neurofibrillary tangles

M. L. Schmidt, G. V. Van Hoesen, J. Morris, 1997, Annals of neurology.

Genetic association studies between dementia of the Alzheimer's type and three receptors for apolipoprotein E in a Caucasian population

N. Craddock, J. Morris, A. Goate, 1997, Neuroscience Letters.

No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant

J. Morris, A. Goate, C. Lendon, 1995, Neuroscience Letters.

The role of presenilin 1 in the genetics of Alzheimer's disease.

M. Adams, J. Hardy, A. Goate, 1996, Cold Spring Harbor symposia on quantitative biology.