T. Bird

发表

Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

J. Gallacher, M. Fornage, I. Giegling, 2018, bioRxiv.

A familial Alzheimer's disease locus on chromosome 1

E M Wijsman, T D Bird, J. Weber, 1995, Science.

Genetic linkage evidence for heterogeneity in Charcot‐Marie‐Tooth neuropathy (HMSN type I)

S. M. Sumi, J. Ott, G. Kraft, 1983, Annals of neurology.

Variants regulating ZBTB4 are associated with age‐at‐onset of Alzheimer's disease

E. Wijsman, M. Bamshad, T. Thornton, 2018, Genes, brain, and behavior.

Familial Alzheimer's disease: Site of mutation influences clinical phenotype

D. Pollen, P. S. St George-Hyslop, D. Drachman, 2000, Annals of Neurology.

Amyloid (Aβ) deposition in chromosome 1–linked Alzheimer's disease: The volga german families

S. M. Sumi, D. Mann, T. Iwatsubo, 1997, Annals of neurology.

Amyloid β protein (Aβ) deposition in chromosome 14–linked Alzheimer's disease: Predominance of Aβ42(43)

S. M. Sumi, P. Lantos, M. Rossor, 1996 .

Phenotypic heterogeneity in familial alzheimer's disease: A study of 24 kindreds

S. M. Sumi, T D Bird, G. Schellenberg, 1989, Annals of neurology.

Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions

T D Bird, P. S. St George-Hyslop, A. Kertesz, 2000, Neurology.

Parkinson’s disease, CYP2D6 polymorphism, and age

J. Nutt, J. Kaye, R. Camicioli, 2001, Neurology.

parkin mutation analysis in clinic patients with early‐onset Parkinson's disease

Thomas D. Bird, Gerard D. Schellenberg, John G. Nutt, 2004 .

Normal glutamic acid decarboxylase activity in kidney tissue from patients with Huntington's Disease

T. Bird, 1976, Journal of neurochemistry.

Parkin mutation analysis in clinic patients with early‐onset Parkinson's disease (Am J Med Genet 129A: 44–50, 2004)

J. Nutt, H. Payami, P. Poorkaj, 2005 .