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Genome scan on Swedish Alzheimer's disease families

Molecular psychiatry, 2006-02, Vol.11 (2), p.182-186

2006

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Predicting Cognitive Decline across Four Decades in Mutation Carriers and Non-carriers in Autosomal-Dominant Alzheimer’s Disease

Journal of the International Neuropsychological Society, 2017-03, Vol.23 (3), p.195-203

2017

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The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation

Nature neuroscience, 2001-09, Vol.4 (9), p.887-893

2001

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Glucose metabolism and PIB binding in carriers of a His163Tyr presenilin 1 mutation

Neurobiology of aging, 2011-08, Vol.32 (8), p.1388-1399

2011

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A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of β-amyloid

Nature genetics, 1992-08, Vol.1 (5), p.345-347

1992

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Genetic counseling in a Swedish Alzheimer family with amyloid precursor protein mutation

American journal of human genetics, 1995-01, Vol.56 (1), p.332-335

1995

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A Unique Gene Expression Signature Discriminates Familial Alzheimer's Disease Mutation Carriers from Their Wild-Type Siblings

Proceedings of the National Academy of Sciences - PNAS, 2005-10, Vol.102 (41), p.14854-14859

2005

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Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.202-208

2008

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A mutation in Alzheimerʼs disease destroying a splice acceptor site in the presenilin-1 gene

Neuroreport, 1995-12, Vol.7 (1), p.297-301

1995

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Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family

Alzheimer's & dementia, 2008-11, Vol.4 (6), p.414-420

2008

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Interaction between estrogen receptor 1 and the ε4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

Neuroscience letters, 2000-03, Vol.282 (1), p.45-48

2000

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No evidence of linkage to chromosome 9q21–22 in a Swedish family with frontotemporal dementia and amyotrophic lateral sclerosis

Neuroscience letters, 2003-04, Vol.340 (3), p.245-247

2003

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Wide range of disease onset in a family with Alzheimer disease and a His163Tyr mutation in the presenilin-1 gene

Archives of neurology (Chicago), 1998-05, Vol.55 (5), p.698

1998

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Interaction between estrogen receptor 1 and the epsilon 4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

Neuroscience letters, 2000-03, Vol.282 (1-2), p.45-48

2000

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No association between polymorphisms in the neprilysin promoter region and Swedish Alzheimer's disease patients

Neuroscience letters, 2003-02, Vol.337 (2), p.111-113

2003

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Life situation, coping and quality of life in people with high and low risk of developing Alzheimer's disease

Dementia and geriatric cognitive disorders, 2003-01, Vol.16 (4), p.220

2003

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Tau gene polymorphisms and apolipoprotein E ε4 may interact to increase risk for Alzheimer’s disease

Neuroscience letters, 1999-12, Vol.277 (1), p.29-32

1999

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Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21

American journal of medical genetics, 1997-07, Vol.74 (4), p.380-385

1997

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Investigations of a CA repeat in the oestrogen receptor beta gene in patients with Alzheimer's disease

European journal of human genetics : EJHG, 2001-10, Vol.9 (10), p.802-804

2001

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Apolipoprotein ε4 allele in swedish twins and siblings with Alzheimer disease

Alzheimer disease and associated disorders, 1995, Vol.9 (3), p.166-169

1995

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Tau gene polymorphisms and apolipoprotein E epsilon 4 may interact to increase risk for Alzheimer's disease

Neuroscience letters, 1999-12, Vol.277 (1), p.29-32

1999

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Clinical findings in nondemented mutation carriers predisposed to Alzheimer's disease: a model of mild cognitive impairment

Acta neurologica Scandinavica, 2003, Vol.107 (s179), p.77-82

2003

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Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia

Archives of neurology (Chicago), 1997-05, Vol.54 (5), p.539

1997

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49 Variable age of onset in an alzheimer family with a His163Tyr mutation in the presenilin 1 gene

Neurobiology of aging, 1996, Vol.17 (4), p.S13-S13

1996

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Genome scan on Swedish Alzheimer's disease families

Predicting Cognitive Decline across Four Decades in Mutation Carriers and Non-carriers in Autosomal-Dominant Alzheimer’s Disease

The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation

Glucose metabolism and PIB binding in carriers of a His163Tyr presenilin 1 mutation

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of β-amyloid

Genetic counseling in a Swedish Alzheimer family with amyloid precursor protein mutation

A Unique Gene Expression Signature Discriminates Familial Alzheimer's Disease Mutation Carriers from Their Wild-Type Siblings

Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease

The structure of the presenilin 1 ( S182 ) gene and identification of six novel mutations in early onset AD families

A mutation in Alzheimerʼs disease destroying a splice acceptor site in the presenilin-1 gene

Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family

Interaction between estrogen receptor 1 and the ε4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

No evidence of linkage to chromosome 9q21–22 in a Swedish family with frontotemporal dementia and amyotrophic lateral sclerosis

Wide range of disease onset in a family with Alzheimer disease and a His163Tyr mutation in the presenilin-1 gene

Interaction between estrogen receptor 1 and the epsilon 4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

No association between polymorphisms in the neprilysin promoter region and Swedish Alzheimer's disease patients

Life situation, coping and quality of life in people with high and low risk of developing Alzheimer's disease

Tau gene polymorphisms and apolipoprotein E ε4 may interact to increase risk for Alzheimer’s disease

Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21

Investigations of a CA repeat in the oestrogen receptor beta gene in patients with Alzheimer's disease

Apolipoprotein ε4 allele in swedish twins and siblings with Alzheimer disease

Tau gene polymorphisms and apolipoprotein E epsilon 4 may interact to increase risk for Alzheimer's disease

Clinical findings in nondemented mutation carriers predisposed to Alzheimer's disease: a model of mild cognitive impairment

Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia

49 Variable age of onset in an alzheimer family with a His163Tyr mutation in the presenilin 1 gene

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