A. Roses

发表

APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.

G. Schellenberg, W. Kukull, M. Ball, 1991, American journal of human genetics.

233 Complete genomic screen in late-onset familial Alzheimer disease

J. Haines, G. Small, A. Saunders, 1996, Neurobiology of Aging.

The role of apolipoprotein E in the nervous system.

W. Strittmatter, K. Weisgraber, A. Roses, 1994, Current opinion in lipidology.

Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage

C. Graffagnino, D. Marchuk, J. Davis, 1997, Annals of neurology.

RFLP analysis for APP 717 mutations associated with Alzheimer's disease.

B. Ghetti, M. Farlow, M. Benson, 1993, Journal of medical genetics.

Short Communication -Amyloid Protein-Containing Inclusions in Skeletal Muscle of Apolipoprotein-E-Deficient Mice

R. Martins, B. Kakulas, J. Papadimitriou, 2007 .

Characterization of amyloid fibril beta-peptide in familial Alzheimer's disease with APP717 mutations.

B. Ghetti, M. Farlow, J. Liepnieks, 1993, Biochemical and biophysical research communications.

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

M. Pericak-Vance, J. Hardy, M. Rossor, 1991, Nature.

Genetic studies in Alzheimer's disease with an NACP/alpha-synuclein polymorphism.

M. Pericak-Vance, L. Thal, R. Katzman., 1996, Annals of neurology.

Increased amyloid ,8-peptide deposition incerebral cortex asa consequence ofapolipoprotein E genotype inlate-onset Alzheimer disease

S. H. Joo, A. Roses, M. A. Pericaknvance, 1993 .

No association or linkage between an intronic polymorphism of presenilin‐1 and sporadic or late‐onset familial Alzheimer disease

J. Haines, M. Pericak-Vance, G. Small, 1997, Genetic epidemiology.

Familial Neuropathology and sporadic Alzheimer ’ s disease : cannot exclude a final common pathway

D. Pollen, B. Hyman, P. S. St George-Hyslop, 2007 .

Identification of Novel Genes in Late-Onset Alzheimer's Disease

P. M. Conneally, J. M. Vance, J. L. Haines, 2000, Experimental Gerontology.

Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease

J. Haines, M. Pericak-Vance, G. Small, 1998, Neurobiology of Aging.

Apolipoprotein E ε2 does not increase risk of early‐onset sporadic Alzheimer's disease

M. Pericak-Vance, W. Scott, P. Gaskell, 1997 .

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

M. Pericak-Vance, M. Spence, R. Martuza, 1987, Cell.

Relative abundance of Alzheimer A beta amyloid peptide variants in Alzheimer disease and normal aging.

P. Greengard, A. Roses, B. Winblad, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Localization of neuron-specific enolase (NSE) mRNA in human brain

E. Ginns, D. Schmechel, B. Martin, 1987, Neuroscience Letters.

Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms

I. James, F. Mastaglia, A. Saunders, 2013, Neuromuscular Disorders.

Novel amyloid precursor protein gene mutation (codon 665Asp) in a patient with late‐onset Alzheimer's disease

D. Murman, J. Fink, M. Peacock, 1994, Annals of neurology.

Apolipoprotein E Role in Maintaining the Integrity of the Aging Central Nervous System

E. Masliah, M. Mallory, M. Alford, 1996 .

The human NACP/alpha-synuclein gene: chromosome assignment to 4q21.3-q22 and TaqI RFLP analysis.

A. Roses, P. S. St George-Hyslop, P. N. Rao, 1995, Genomics.

Defective neuronal sprouting by human apolipoprotein E4 is a gain‐of‐negative function

J. Gilbert, A. Roses, D. Galasko, 2002, Journal of neuroscience research.

Apolipoprotein E genotype and oxidative stress response to traumatic brain injury

V. Mathura, R. Hayes, M. Mullan, 2010, Neuroscience.

Susceptibility of transgenic mice expressing human apolipoprotein E to closed head injury: The allele E3 is neuroprotective whereas E4 increases fatalities

D. Michaelson, R. Maronpot, E. Shohami, 2000, Neuroscience.

No association between very low density lipoprotein receptor (VLDL-R) and Alzheimer disease in American Caucasians

J. Haines, M. Pericak-Vance, G. Small, 1996, Neuroscience Letters.

Using Genetics to Enable Studies on the Prevention of Alzheimer's Disease

A. Roses, K. Welsh-Bohmer, S. Brannan, 2013, Clinical pharmacology and therapeutics.

Familial and sporadic Alzheimer's disease

D. Pollen, B. Hyman, P. S. St George-Hyslop, 1996, Neurology.

Apolipoprotein E-genotype dependent hippocampal and cortical responses to traumatic brain injury

V. Mathura, R. Hayes, V. Laporte, 2009, Neuroscience.

Interactions of Apolipoprotein E with Microtubule-Associated Proteins

A. Saunders, W. Strittmatter, A. Roses, 1996 .

Risky apolipoprotein in brain

M. Goedert, W. Strittmatter, A. Roses, 1994, Nature.

Dinucleotide repeat polymorphism at the human gene for the brain-derived neurotrophic factor (BDNF).

A. Saunders, A D Roses, M Pröschel, 1992, Human molecular genetics.

Apolipoprotein E ∈4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases

M. Pericak-Vance, A. Roses, K. Schmader, 1993, The Lancet.

Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.

M. Pericak-Vance, R. Bartlett, A. Heyman, 1991, American journal of human genetics.

Alzheimer's disease and possible gene interaction.

D. Pollen, J. Haines, M. Pericak-Vance, 1994, Science.

Sequestration of Amyloid β‐Peptide a

A. Saunders, D. Goldgaber, R. Bhasin, 1993 .

Pharmacogenetics of hypersensitivity to abacavir: from PGx hypothesis to confirmation to clinical utility

D. Burns, E. Lai, S. Hetherington, 2008, The Pharmacogenomics Journal.

Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity.

J. Haines, M. Pericak-Vance, A. Roses, 2000, American journal of human genetics.

Clinical comparison of Alzheimer's disease in pedigrees with the codon 717 Val→Ile mutation in the amyloid precursor protein gene

Toru Shimizu, A. Roses, P. Lantos, 1993, Neurobiology of Aging.

Are APOE ɛ genotype and TOMM40 poly-T repeat length associations with cognitive ageing mediated by brain white matter tract integrity?

I. Deary, M. Bastin, J. Starr, 2014, Translational Psychiatry.