Lista de obras -

A full genome scan for late onset Alzheimer's disease.

artículo científico publicado en 1999

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

artículo científico publicado en 2007

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease

artículo científico publicado en 2005

ABCA1 polymorphisms and Alzheimer's disease.

artículo científico publicado en 2007

Alpha-2 macroglobulin gene and Alzheimer disease.

artículo científico publicado en 1999

Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.

artículo científico publicado en 2004

ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

artículo científico publicado en 2002

Association at LRP gene locus with sporadic late-onset Alzheimer's disease.

artículo científico publicado en 1998

Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease.

artículo científico publicado en 1999

Association between the low density lipoprotein receptor-related protein (LRP) and Alzheimer's disease.

artículo científico publicado en 1997

Candidate gene polymorphisms for ischemic stroke

artículo científico publicado en 2009

Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's disease

artículo científico publicado en 2004

Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer's disease

artículo científico publicado en 2005

Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: a two-stage study

artículo científico publicado en 2005

Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease

artículo científico publicado en 2007

Contribution of APOE promoter polymorphisms to Alzheimer's disease risk

artículo científico publicado en 2002

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression

artículo científico publicado en 2006

Determination of the gene structure of human GFAP and absence of coding region mutations associated with frontotemporal dementia with parkinsonism linked to chromosome 17.

artículo científico publicado en 1998

Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13?

artículo científico publicado en 2008

Full genome screen for Alzheimer disease: Stage II analysis

article

Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs

artículo científico publicado en 2009

Genetic studies on chromosome 12 in late-onset Alzheimer disease.

artículo científico publicado en 1998

Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease

artículo científico publicado en 2005

Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease.

artículo científico publicado en 1999

Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease.

artículo científico publicado en 2005

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

artículo científico publicado en 2006

Genome-wide analysis of the parkinsonism-dementia complex of Guam

artículo científico publicado en 2004

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

scientific journal article

Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease

article

IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations

artículo científico publicado en 2007

Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis.

artículo científico publicado en 2007

Insulin degrading enzyme (IDE) genetic variants and risk of Alzheimer's disease: evidence of effect modification by apolipoprotein E (APOE).

artículo científico publicado en 2003

Linkage and association analyses of type 2 diabetes/impaired glucose metabolism and adiponectin serum levels in Japanese Americans from Hawaii

artículo científico publicado en 2007

Linkage exclusion in French families with probable Parkinson's disease

article

Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?

Low frequency of alpha-synuclein mutations in familial Parkinson's disease

artículo científico publicado en 1998

Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

artículo científico publicado en 2008

Neurodegenerative diseases of Guam: Analysis of TAU

article

Neurodegenerative diseases of Guam: analysis of TAU.

No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease

artículo científico publicado en 2000

No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease.

artículo científico publicado en 1999

No association between the lipoprotein lipase S447X polymorphism and Alzheimer's disease.

artículo científico publicado en 2002

O3-02-06 Linkage analysis of AD SIB pairs indicates evidence of interaction between genes regulating beta-amyloid degradation

article

P4-070 Is APOE exclusively responsible for the AD linkage peak on chromosome 19?

P4-157 Genetic analysis of a the tau haplotype in the CEPH diversity panel and in Guam disease

artículo científico

Possible association between genetic variability at the apolipoprotein(a) locus and Alzheimer's disease in apolipoprotein E2 carriers

artículo científico publicado en 2002

Presenilin-1 polymorphism and Alzheimer's disease. The Alzheimer's Study Group

scientific article published on 01 June 1996

Problems and solutions in the genetic analysis of late-onset Alzheimer's disease

artículo científico publicado en 2004

S2-01-04 Progress toward the identification of novel genetic risk factors for late onset Alzheimer's disease

scholarly article by Alison M. Goate et al published July 2004 in Neurobiology of Aging

Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia

artículo científico publicado en 2006

Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series

artículo científico publicado en 2010

Structural genomic variation in ischemic stroke

artículo científico publicado en 2008

Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease.

artículo científico publicado en 2001

Support for association between ADHD and two candidate genes: NET1 and DRD1.

artículo científico publicado en 2005

Susceptibility locus for Alzheimer's disease on chromosome 10.

artículo científico publicado en 2000

Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations.

artículo científico publicado en 2007

The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases

artículo científico publicado en 2005

The tau H2 haplotype is almost exclusively Caucasian in origin

scientific article published on 01 October 2004

Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease

artículo científico publicado en 2009

Lista de obras de

A full genome scan for late onset Alzheimer's disease.

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease

ABCA1 polymorphisms and Alzheimer's disease.

Alpha-2 macroglobulin gene and Alzheimer disease.

Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.

ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

Association at LRP gene locus with sporadic late-onset Alzheimer's disease.

Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease.

Association between the low density lipoprotein receptor-related protein (LRP) and Alzheimer's disease.

Candidate gene polymorphisms for ischemic stroke

Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's disease

Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer's disease

Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: a two-stage study

Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease

Contribution of APOE promoter polymorphisms to Alzheimer's disease risk

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression

Determination of the gene structure of human GFAP and absence of coding region mutations associated with frontotemporal dementia with parkinsonism linked to chromosome 17.

Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13?

Full genome screen for Alzheimer disease: Stage II analysis

Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs

Genetic studies on chromosome 12 in late-onset Alzheimer disease.

Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease

Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease.

Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease.

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

Genome-wide analysis of the parkinsonism-dementia complex of Guam

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease

IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations

Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis.

Insulin degrading enzyme (IDE) genetic variants and risk of Alzheimer's disease: evidence of effect modification by apolipoprotein E (APOE).

Linkage and association analyses of type 2 diabetes/impaired glucose metabolism and adiponectin serum levels in Japanese Americans from Hawaii

Linkage exclusion in French families with probable Parkinson's disease

Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?

Low frequency of alpha-synuclein mutations in familial Parkinson's disease

Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

Neurodegenerative diseases of Guam: Analysis of TAU

Neurodegenerative diseases of Guam: analysis of TAU.

No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease

No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease.

No association between the lipoprotein lipase S447X polymorphism and Alzheimer's disease.

O3-02-06 Linkage analysis of AD SIB pairs indicates evidence of interaction between genes regulating beta-amyloid degradation

P4-070 Is APOE exclusively responsible for the AD linkage peak on chromosome 19?

P4-157 Genetic analysis of a the tau haplotype in the CEPH diversity panel and in Guam disease

Possible association between genetic variability at the apolipoprotein(a) locus and Alzheimer's disease in apolipoprotein E2 carriers

Presenilin-1 polymorphism and Alzheimer's disease. The Alzheimer's Study Group

Problems and solutions in the genetic analysis of late-onset Alzheimer's disease

S2-01-04 Progress toward the identification of novel genetic risk factors for late onset Alzheimer's disease

Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia

Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series

Structural genomic variation in ischemic stroke

Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease.

Support for association between ADHD and two candidate genes: NET1 and DRD1.

Susceptibility locus for Alzheimer's disease on chromosome 10.

Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations.

The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases

The tau H2 haplotype is almost exclusively Caucasian in origin

Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease