Genetics of Alzheimer's disease: a centennial review.
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[1] S. Younkin,et al. Correlative Memory Deficits, Aβ Elevation, and Amyloid Plaques in Transgenic Mice , 1996, Science.
[2] L. Feuk,et al. SNP association studies in Alzheimer's disease highlight problems for complex disease analysis. , 2001, Trends in genetics : TIG.
[3] K. Engedal,et al. The role of heredity in late-onset Alzheimer disease and vascular dementia. A twin study. , 1997, Archives of general psychiatry.
[4] M. Anagnostouli,et al. Novel mutations and repeated findings of mutations in familial Alzheimer disease , 2005, Neurogenetics.
[5] S. Bassett,et al. Linkage to chromosome 14q in Alzheimer's disease (AD) patients without psychotic symptoms , 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[6] Miguel Ángel Martínez,et al. Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex. , 1997, American journal of human genetics.
[7] M. Lerman,et al. Characterization and chromosomal localization of a cDNA encoding brain amyloid of Alzheimer's disease. , 1987, Science.
[8] L. Farrer,et al. Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community. , 2003, Human molecular genetics.
[9] P. Kehoe,et al. Current knowledge of chromosome 12 susceptibility genes for late-onset Alzheimer's disease , 2006, Neurobiology of Aging.
[10] J. Haines,et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. , 1993, Science.
[11] M. Adams,et al. Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease , 1996, Neuroreport.
[12] J. Gilbert,et al. Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22. , 2003, American journal of human genetics.
[13] J. Rommens,et al. Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. , 1996, Human molecular genetics.
[14] Y. Agid,et al. Apolipoprotein E ϵ4 Allele and Familial Aggregation of Alzheimer Disease , 1998 .
[15] S. Younkin,et al. An increased percentage of long amyloid beta protein secreted by familial amyloid beta protein precursor (beta APP717) mutants. , 1994, Science.
[16] J. H. Lee,et al. Chromosome-12 mapping of late-onset Alzheimer disease among Caribbean Hispanics. , 2002, American journal of human genetics.
[17] D. Kovacs. α2-Macroglobulin in late-onset Alzheimer's disease , 2000, Experimental Gerontology.
[18] O. Gureje,et al. APOE ε4 is not associated with Alzheimer's disease in elderly Nigerians , 2006 .
[19] K P Offord,et al. Prevalence of medically diagnosed dementia in a defined United States population , 1989, Neurology.
[20] J. Haines,et al. Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis , 1997 .
[21] J. Kere,et al. Genome scan on Swedish Alzheimer's disease families , 2006, Molecular Psychiatry.
[22] Eden R Martin,et al. Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease. , 2003, Human molecular genetics.
[23] O. Hill. A Twin Study , 1968, British Journal of Psychiatry.
[24] M. Pericak-Vance,et al. Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[25] D. Blacker,et al. Family-based association between Alzheimer's disease and variants in UBQLN1. , 2005, The New England journal of medicine.
[26] J. Hardy,et al. Increased amyloid-β42(43) in brains of mice expressing mutant presenilin 1 , 1996, Nature.
[27] O. Gureje,et al. Association of apolipoprotein E genotype and Alzheimer disease in African Americans. , 2006, Archives of neurology.
[28] P. M. Conneally,et al. Identification of Novel Genes in Late-Onset Alzheimer's Disease , 2000, Experimental Gerontology.
[29] J. Haines,et al. A genome‐wide linkage analysis of dementia in the Amish , 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[30] D. Munoz,et al. A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes. , 2005, Brain : a journal of neurology.
[31] S. Sorbi,et al. Insulin degrading enzyme and alpha-3 catenin polymorphisms in Italian patients with Alzheimer disease. , 2005, Alzheimer disease and associated disorders.
[32] D. Bennett,et al. Incidence of Alzheimer disease in a biracial urban community: relation to apolipoprotein E allele status. , 2003, Archives of neurology.
[33] L. Lannfelt,et al. New Alzheimer’s disease locus on chromosome 8 , 2006, Journal of Medical Genetics.
[34] J. Haines,et al. The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid β-protein gene , 1987, Nature.
[35] E. Kojro,et al. Constitutive and regulated alpha-secretase cleavage of Alzheimer's amyloid precursor protein by a disintegrin metalloprotease. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[36] Carl D Langefeld,et al. Ordered subset analysis in genetic linkage mapping of complex traits , 2004, Genetic epidemiology.
[37] S. M. Sumi,et al. Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease. , 1988, Science.
[38] C. Broeckhoven,et al. Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3 , 1992, Nature Genetics.
[39] Colin L Masters,et al. Alzheimer's centennial legacy: prospects for rational therapeutic intervention targeting the Abeta amyloid pathway. , 2006, Brain : a journal of neurology.
[40] R. Nussbaum,et al. Alzheimer's disease and Parkinson's disease. , 2003, The New England journal of medicine.
[41] P. Lansbury,et al. A century-old debate on protein aggregation and neurodegeneration enters the clinic , 2006, Nature.
[42] K. Hall,et al. International Studies in Dementia With Particular Emphasis on Populations of African Origin , 2006, Alzheimer disease and associated disorders.
[43] J. Haines,et al. Apolipoprotein E genotype in patients with alzheimer's disease: Implications for the risk of dementia among relatives , 1995, Annals of neurology.
[44] R. Barbour,et al. Purification and cloning of amyloid precursor protein β-secretase from human brain , 1999, Nature.
[45] S. Lovestone,et al. Premorbid cognitive testing predicts the onset of dementia and Alzheimer’s disease better than and independently of APOE genotype , 2004, Journal of Neurology, Neurosurgery & Psychiatry.
[46] D. Pollen,et al. Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14 , 1992, Nature Genetics.
[47] C. Masters,et al. Amyloid plaque core protein in Alzheimer disease and Down syndrome. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[48] D. Pollen,et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease , 1995, Nature.
[49] J. Haines,et al. Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. , 1997, JAMA.
[50] C. van Broeckhoven,et al. Presenilin mutations in Alzheimer's disease , 1998, Human mutation.
[51] D. Pollen,et al. The genetic defect causing familial Alzheimer's disease maps on chromosome 21. , 1987, Science.
[52] K. Marder,et al. Influence of APOE genotype on familial aggregation of AD in an urban population , 1999, Neurology.
[53] A D Roses,et al. Utility of the apolipoprotein E genotype in the diagnosis of Alzheimer's disease. Alzheimer's Disease Centers Consortium on Apolipoprotein E and Alzheimer's Disease. , 1998, The New England journal of medicine.
[54] Taylor J. Maxwell,et al. DAPK1 variants are associated with Alzheimer's disease and allele-specific expression. , 2006, Human molecular genetics.
[55] J. Growdon,et al. Risk of dementia among relatives of Alzheimer's disease patients in the MIRAGE study , 1996, Neurology.
[56] A. Paterson,et al. Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity. , 1998, JAMA.
[57] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[58] K. Sleegers,et al. Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample. , 2005, American journal of human genetics.
[59] B. Tycko,et al. Familial Alzheimer disease among Caribbean Hispanics: a reexamination of its association with APOE. , 2002, Archives of neurology.
[60] J. Gilbert,et al. Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease , 2006, Neurology.
[61] Nick C Fox,et al. Early onset familial Alzheimer’s disease , 2002, Neurology.
[62] Yaakov Stern,et al. The APOE-∊4 Allele and the Risk of Alzheimer Disease Among African Americans, Whites, and Hispanics , 1998 .
[63] D. Blacker,et al. Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database , 2007, Nature Genetics.
[64] S. Younkin,et al. Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. , 2003, Human molecular genetics.
[65] P. Scheltens,et al. Recommendations for the diagnosis and management of Alzheimer's disease and other disorders associated with dementia: EFNS guideline , 2007, European journal of neurology.
[66] R. Petersen,et al. Genetic variants in a haplotype block spanning IDE are significantly associated with plasma Aβ42 levels and risk for Alzheimer disease , 2004, Human mutation.
[67] J. Weber,et al. Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14. , 1992, Science.
[68] E. Génin,et al. ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease , 2005, Neurobiology of Disease.
[69] K. Welsh-Bohmer,et al. APOE and AD concordance in twin pairs as predictors of AD in first-degree relatives , 2000, Neurology.
[70] J. Ioannidis,et al. Replication validity of genetic association studies , 2001, Nature Genetics.
[71] Taylor J. Maxwell,et al. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. , 2006, American journal of human genetics.
[72] Ilana S. Hairston,et al. Environmental Enrichment Reduces Aβ Levels and Amyloid Deposition in Transgenic Mice , 2005, Cell.
[73] B. Dubois,et al. Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum. , 1999, American journal of human genetics.
[74] J. Rommens,et al. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene , 1995, Nature.
[75] D. Borchelt,et al. Environmental Enrichment Mitigates Cognitive Deficits in a Mouse Model of Alzheimer's Disease , 2005, The Journal of Neuroscience.
[76] M. Adams,et al. The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families , 1995, Nature Genetics.
[77] J. Haines,et al. An autosomal genomic screen for dementia in an extended Amish family , 2005, Neuroscience Letters.
[78] D. Selkoe,et al. Mutation of the β-amyloid precursor protein in familial Alzheimer's disease increases β-protein production , 1992, Nature.
[79] K. Blennow,et al. Genetic variation in CTNNA3 encoding alpha-3 catenin and Alzheimer's disease , 2004, Neuroscience Letters.
[80] M. Owen,et al. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease , 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[81] M. Owen,et al. α-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer’s disease , 2007, NeuroMolecular Medicine.
[82] Robert C Green,et al. Association between apolipoprotein E genotype and Alzheimer disease in African American subjects. , 2002, Archives of neurology.
[83] A. Bernstein,et al. Presenilins are required for γ-secretase cleavage of β-APP and transmembrane cleavage of Notch-1 , 2000, Nature Cell Biology.
[84] J. Haines,et al. Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease , 1998, Neurobiology of Aging.
[85] G. Jervis. Early senile dementia in mongoloid idiocy. , 1948, The American journal of psychiatry.
[86] M. Albert,et al. Results of a high-resolution genome screen of 437 Alzheimer's disease families. , 2003, Human molecular genetics.
[87] A. Hofman,et al. Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study. , 1998, Archives of neurology.
[88] K. Welsh-Bohmer,et al. APOE-ε4 count predicts age when prevalence of AD increases, then declines , 1999, Neurology.
[89] M. Kamboh,et al. Molecular Genetics of Late‐Onset Alzheimer's Disease , 2004, Annals of human genetics.
[90] J. Haines,et al. Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity. , 2000, American journal of human genetics.
[91] J. Hirschhorn,et al. Genetic association studies of complex traits: design and analysis issues. , 2005, Mutation research.
[92] J. Palmgren,et al. Genetic variants of ABCA1 modify Alzheimer disease risk and quantitative traits related to β‐amyloid metabolism , 2004, Human mutation.
[93] G. Schellenberg,et al. Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type. , 1987, Journal of neurogenetics.
[94] E M Wijsman,et al. The number of trait loci in late-onset Alzheimer disease. , 2000, American journal of human genetics.
[95] H. Soininen,et al. Linkage disequilibrium in the 13q12 region in Finnish late onset Alzheimer's disease patients , 1999, European Journal of Human Genetics.
[96] Richard Mayeux,et al. Epidemiology of neurodegeneration. , 2003, Annual review of neuroscience.
[97] G. Schellenberg,et al. Secreted amyloid β–protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease , 1996, Nature Medicine.
[98] John Hardy,et al. Amyloid, the presenilins and Alzheimer's disease , 1997, Trends in Neurosciences.
[99] Steven J. Schrodi,et al. Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[100] J. Treanor,et al. Beta-secretase cleavage of Alzheimer's amyloid precursor protein by the transmembrane aspartic protease BACE. , 1999, Science.
[101] M. Pericak-Vance,et al. Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage. , 1991, American journal of human genetics.
[102] G. Zubenko,et al. A genome survey for novel Alzheimer disease risk loci: results at 10-cM resolution. , 1998, Genomics.
[103] Martin Farrall,et al. PREDISPOSING LOCUS FOR ALZHEIMER'S DISEASE ON CHROMOSOME 21 , 1989, The Lancet.
[104] J. Yunis,et al. Apolipoprotein E genotyping in a sample of Colombian patients with Alzheimer's disease , 2001, Neuroscience Letters.
[105] D. Blacker,et al. Is α-T catenin (VR22) an Alzheimer’s disease risk gene? , 2006, Journal of Medical Genetics.
[106] U. Finckh,et al. The future of genetic association studies in Alzheimer disease , 2003, Journal of Neural Transmission.
[107] R Brookmeyer,et al. Projections of Alzheimer's disease in the United States and the public health impact of delaying disease onset. , 1998, American journal of public health.
[108] C. V. van Duijn,et al. Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia. , 2000, American journal of human genetics.
[109] J. Hardy,et al. A locus for familial early–onset Alzhelmer's disease on the long arm of chromosome 14, proximal to the α1–antichymotrypsin gene , 1992, Nature Genetics.
[110] R. Harris. Genetics of Alzheimer's disease. , 1982, British medical journal.
[111] M. Owen,et al. Full genome screen for Alzheimer disease: stage II analysis. , 2002, American journal of medical genetics.
[112] D. Easton,et al. Genome-wide linkage disequilibrium mapping of late-onset Alzheimer’s disease in Finland , 2001, Neurology.
[113] K. Jellinger. Down Syndrome and Alzheimer's Disease Biological Correlates , 2007 .
[114] E. Lander,et al. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease , 2003, Nature Genetics.
[115] B. Devlin,et al. Linkage analysis of Alzheimer disease with psychosis , 2002, Neurology.
[116] M. Citron,et al. Aβ-Generating Enzymes Recent Advances in β- and γ-Secretase Research , 2000, Neuron.
[117] C. Broeckhoven,et al. Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families , 1987, Nature.
[118] M. Owen,et al. A full genome scan for late onset Alzheimer's disease , 1999 .
[119] Margaret A. Pericak-Vance,et al. Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease , 1997 .
[120] E M Wijsman,et al. A familial Alzheimer's disease locus on chromosome 1 , 1995, Science.
[121] G. Schellenberg,et al. Candidate gene for the chromosome 1 familial Alzheimer's disease locus , 1995, Science.
[122] D. Y. Lee,et al. Combination of clinical and neuropsychologic information as a better predictor of the progression to Alzheimer disease in questionable dementia individuals. , 2006, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.
[123] R. Green,et al. Risk of dementia among white and African American relatives of patients with Alzheimer disease. , 2002, JAMA.
[124] J. Mortimer,et al. Early-Life Risk Factors for Alzheimer Disease , 2006, Alzheimer disease and associated disorders.
[125] L. Lannfelt,et al. Apolipoprotein E type ε4 allele, heritability and age at onset in twins with Alzheimer disease and vascular dementia , 1997, Clinical genetics.
[126] J. Growdon,et al. Multiple etiologies for Alzheimer disease are revealed by segregation analysis. , 1994, American journal of human genetics.
[127] B. Strooper,et al. Alzheimer dementia caused by a novel mutation located in the APP C‐terminal intracytosolic fragment , 2006, Human mutation.
[128] D. Knopman,et al. Prevalence, costs, and treatment of Alzheimer's disease and related dementia: a managed care perspective. , 2001, The American journal of managed care.
[129] P. Sham,et al. A novel method of two‐locus linkage analysis applied to a genome scan for late onset Alzheimer's disease , 2001, Annals of human genetics.
[130] R. Tanzi,et al. Alzheimer's disease: one disorder, too many genes? , 2004, Human molecular genetics.
[131] F. Struwe. Histopathologische Untersuchungen über Entstehung und Wesen der senilen Plaques , 1929 .
[132] M. Tsolaki,et al. Genetic association of acyl-coenzyme A: cholesterol acyltransferase with cerebrospinal fluid cholesterol levels, brain amyloid load, and risk for Alzheimer's disease , 2003, Molecular Psychiatry.
[133] Katrina A B Goddard,et al. A second locus for very-late-onset Alzheimer disease: a genome scan reveals linkage to 20p and epistasis between 20p and the amyloid precursor protein region. , 2002, American journal of human genetics.
[134] Johannes Kornhuber,et al. Therapeutic approaches to Alzheimer's disease. , 2006, Brain : a journal of neurology.
[135] P. Rosenberg,et al. Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2 , 2006, Journal of Medical Genetics.
[136] G. Mcclearn,et al. Use of twin cohorts for research in Alzheimer's disease* , 1993, Neurology.
[137] E. Otomo,et al. Apolipoprotein E immunoreactivity in cerebral amyloid deposits and neurofibrillary tangles in Alzheimer's disease and kuru plaque amyloid in Creutzfeldt-Jakob disease , 1991, Brain Research.
[138] I. Kanazawa,et al. Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease , 1995, Nature Genetics.
[139] J. Hardy,et al. A new pathogenic mutation in the APP gene (I716V) increases the relative proportion of A beta 42(43). , 1997, Human molecular genetics.
[140] Kaj Blennow,et al. Towards compendia of negative genetic association studies: an example for Alzheimer disease , 2006, Human Genetics.
[141] K. Lunetta,et al. The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease , 2007, Nature Genetics.
[142] R. Mayeux,et al. Predictive utility of apolipoprotein E genotype for Alzheimer disease in outpatients with mild cognitive impairment. , 2005, Archives of neurology.
[143] Takashi Asada,et al. Dynamin-binding protein gene on chromosome 10q is associated with late-onset Alzheimer's disease. , 2006, Human molecular genetics.
[144] S. Younkin,et al. Presenilins as therapeutic targets for the treatment of Alzheimer's disease. , 2001, Trends in molecular medicine.
[145] J. Growdon,et al. Segregation analysis reveals evidence of a major gene for Alzheimer disease. , 1991, American journal of human genetics.
[146] B. Tycko,et al. Apolipoprotein E ε4 and Age at Onset of Sporadic and Familial Alzheimer Disease in Caribbean Hispanics , 2006 .
[147] R. Green,et al. Conversion to dementia from mild cognitive disorder , 2006, Neurology.
[148] M G McInnis,et al. Evidence for genetic linkage of Alzheimer's disease to chromosome 10q. , 2000, Science.
[149] J. Kaprio,et al. Alzheimer's disease in Finnish twins , 1996, The Lancet.
[150] J. Hardy,et al. The presenilins and Alzheimer's disease. , 1997, Human molecular genetics.
[151] Janice E. Knoefel,et al. Apolipoprotein E element 4 association with dementia in a population-based study , 1996, Neurology.
[152] L. Feuk,et al. Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene. , 2005, Human molecular genetics.
[153] K. Davis,et al. Familial aggregation in Alzheimer's disease , 1988, Neurology.
[154] L. Feuk,et al. Genetic variation in a haplotype block spanning IDE influences Alzheimer disease , 2003, Human mutation.
[155] Alfredo G. Tomasselli,et al. Membrane-anchored aspartyl protease with Alzheimer's disease β-secretase activity , 1999, Nature.
[156] B. Schoenberg,et al. Severe dementia. Prevalence and clinical features in a biracial US population. , 1985, Archives of neurology.
[157] L. Fratiglioni,et al. Role of genes and environments for explaining Alzheimer disease. , 2006, Archives of general psychiatry.
[158] A. Hofman,et al. Genetic transmission of Alzheimer's disease among families in a Dutch population based study. , 1993, Journal of medical genetics.
[159] J. Growdon,et al. Transmission and age‐at‐onset patterns in familial Alzheimer's disease , 1990, Neurology.
[160] M. Owen,et al. Susceptibility locus for Alzheimer's disease on chromosome 10. , 2000, Science.
[161] P. S. St George-Hyslop,et al. Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus. , 1987, Science.
[162] J. Haines,et al. Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12. , 1997, JAMA.
[163] Allan I. Levey,et al. Familial Alzheimer's Disease–Linked Presenilin 1 Variants Elevate Aβ1–42/1–40 Ratio In Vitro and In Vivo , 1996, Neuron.
[164] J. M. Vance,et al. Genetic linkage studies in Alzheimer's disease families , 1988, Experimental Neurology.
[165] M. Pericak-Vance,et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease , 1991, Nature.
[166] A Hofman,et al. Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease. , 1998, Human molecular genetics.
[167] J. Blangero,et al. Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. , 2000, Science.
[168] V. Lehtinen,et al. Prevalence of severe dementia in Finland , 1985, Neurology.
[169] J. Gilbert,et al. Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer’s disease , 2005, Journal of Medical Genetics.
[170] G. Glenner,et al. Alzheimer's disease and Down's syndrome: sharing of a unique cerebrovascular amyloid fibril protein. , 1984, Biochemical and biophysical research communications.
[171] J. H. Lee,et al. Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics , 2004, Molecular Psychiatry.
[172] D. Schaid,et al. Apolipoprotein E status as a predictor of the development of Alzheimer's disease in memory-impaired individuals. , 1995, JAMA.
[173] J. Kaprio,et al. Alzheimer's disease in twins. , 1997, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[174] K. Sleegers,et al. Familial clustering and genetic risk for dementia in a genetically isolated Dutch population. , 2004, Brain : a journal of neurology.
[175] J. Haines,et al. Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases , 2006, Neurobiology of Aging.
[176] G. Schellenberg,et al. The utility of apolipoprotein E genotyping in the diagnosis of Alzheimer disease in a community-based case series. , 1999, Archives of neurology.
[177] H. Feldman,et al. Apolipoprotein E ε4 genotype as a risk factor for cognitive decline and dementia: data from the Canadian Study of Health and Aging , 2004, Canadian Medical Association Journal.
[178] Rajesh Pahwa,et al. Age at onset in two common neurodegenerative diseases is genetically controlled. , 2002, American journal of human genetics.
[179] L. Whalley,et al. A life-course approach to the aetiology of late-onset dementias , 2006, The Lancet Neurology.