K. Rooke

发表

A physical map of the human APP gene in YACs

J. Hardy, A. Goate, C. Talbot, 1993, Mammalian Genome.

Analysis of the KSP repeat of the neurofilament heavy subunit in familial amyotrophic lateral sclerosis

G. Rouleau, F. Han, D. Figlewicz, 1996, Neurology.

SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.

A. Clark, J. Julien, O. Suchowersky, 1996, Annals of neurology.

Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile.

J. Hardy, M. Rossor, R. Tanzi, 1992, Human molecular genetics.

Mapping of three members of the mouse protein disulfide isomerase family

A. J. Lusis, M. Mehrabian, K. Rooke, 1998, Mammalian Genome.

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.

Mapping of the gene for calreticulin (Calr) to mouse Chromosome 8

A. J. Lusis, K. Rooke, M. Doolittle, 2009, Mammalian Genome.

Genetic Factors in Atherosclerosis

T. Drake, J. Qiao, A. Lusis, 1998 .

SOD1 mutation is assosiated with accumulation of neurofilaments in amyotrophic lateral scelaries

Guy A. Rouleau, Jean-Pierre Julien, A. Clark, 1996 .

GENETIC FACTORS IN ATHEROSCLEROSIS From Humans to Mice and Back Again

T. Drake, J. Qiao, M. Mehrabian, 1996 .

Correlation between CAG repeat length and clinical features in Machado-Joseph disease.

Í. Lopes-Cendes, L. Farrer, A. DeStefano, 1995, American journal of human genetics.