C. Yu

发表

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.

G. Schellenberg, T. Montine, V. Lee, 2007, Brain : a journal of neurology.

Homozygosity mapping of the Werner syndrome locus (WRN).

J. Weber, G. Schellenberg, E. Wijsman, 1994, Genomics.

Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2).

B. Trask, J. Weber, G. Schellenberg, 1994, Genomics.

APP Processing Genes and Cerebrospinal Fluid APP Cleavage Product Levels in Alzheimer’s Disease

Leverenz, D. Galasko, C. Clark, 2011 .

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

E M Wijsman, G. Schellenberg, E. Wijsman, 1996, American journal of human genetics.

p53-mediated apoptosis is attenuated in Werner syndrome cells.

G. Schellenberg, C. Harris, A. Robles, 1999, Genes & development.

Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

G. Schellenberg, E. Wijsman, J. Nakura, 1997, American journal of human genetics.

Homozygous and compound heterozygous mutations at the Werner syndrome locus.

G. Schellenberg, T. Ogihara, J. Nakura, 1996, Human molecular genetics.

Apolipoprotein E in Alzheimer's disease risk and case detection: a case-control study.

G. Schellenberg, W. Kukull, E. Larson, 1996, Journal of clinical epidemiology.

Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease

E M Wijsman, E B Larson, G. Schellenberg, 1995, Neurology.

Apolipoprotein E genotypes and Alzheimer's disease in a community study of elderly African Americans

G. Schellenberg, O. Gureje, K. Hall, 1995, Annals of neurology.

Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women.

E M Wijsman, T D Bird, G. Schellenberg, 1996, American journal of human genetics.

Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.

G. Schellenberg, E. Wijsman, T. Ogihara, 1994, American journal of human genetics.

Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease

G. Schellenberg, D. Galasko, C. Clark, 2011, Neurobiology of Aging.

Integrated mapping analysis of the Werner syndrome region of chromosome 8.

J. Weber, C. Disteche, M. Boehnke, 1994, Genomics.

The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease.

E. Wijsman, M. Boehnke, K. Goddard, 1994, American journal of human genetics.

Alzheimer's disease, apolipoprotein E4, and gender.

G. Schellenberg, E. Wijsman, J. Kaye, 1994, JAMA.

A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.

B. Trask, G. Schellenberg, F. Hisama, 1996, Genomics.

A panel of radiation hybrids for human chromosome 8.

X. Gu, M. Wagner, D. Wells, 1994, Genomics.

Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.

G. Schellenberg, E. Wijsman, T. Ogihara, 1996, Genomics.