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Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene

Acta neuropathologica communications, 2017-06, Vol.5 (1), p.43-43, Article 43

2017

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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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Confirmation of high frequency of C9orf72 mutations in patients with frontotemporal dementia from Sweden

Neurobiology of aging, 2019-12, Vol.84, p.241.e21-241.e25

2019

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Phenotypic variability and neuropsychological findings associated with C9orf72 repeat expansions in a Bulgarian dementia cohort

PloS one, 2018-12, Vol.13 (12), p.e0208383-e0208383

2018

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APOE genotypes and disease severity in multiple sclerosis

Multiple sclerosis, 2002-04, Vol.8 (2), p.98-103

2002

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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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No common founder for C9orf72 expansion mutation in Sweden

Journal of human genetics, 2017-02, Vol.62 (2), p.321-324

2017

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Progressive neuropathology and cognitive decline in a single Arctic APP transgenic mouse model

Neurobiology of aging, 2011-02, Vol.32 (2), p.280-292

2011

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Increased frequency of a new polymorphism in the cell division cycle 2 (cdc2) gene in patients with Alzheimer's disease and frontotemporal dementia

Neuroscience letters, 2003-04, Vol.340 (1), p.69-73

2003

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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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Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration

European journal of human genetics : EJHG, 2013-11, Vol.21 (11), p.1260-1265

2013

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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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Biochemical studies of poly-T variants in the Alzheimer's disease associated TOMM40 gene

Journal of Alzheimer's disease, 2012-01, Vol.31 (3), p.527

2012

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Linkage to the 8p21.1 region Including the CLU gene in age at onset stratified alzheimer's disease families

Journal of Alzheimer's disease, 2011-01, Vol.23 (1), p.13

2011

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A DLST genotype associated with reduced risk for Alzheimer's disease

Neurology, 1999-04, Vol.52 (7), p.1505

1999

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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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Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia

Journal of human genetics, 2010-10, Vol.55 (10), p.649-655

2010

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Frequency of low erythrocyte porphobilinogen deaminase activity in Finland

Journal of internal medicine, 1992-04, Vol.231 (4), p.389-395

1992

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Old-age hippocampal sclerosis associates with GRN and TMEM106B but not with ABCC9 variation in population-based cohorts

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2016, Vol.42, p.35

2016

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Frequency and contribution of variants in 17 dementia related genes in a Bulgarian dementia cohort

JOURNAL OF NEUROCHEMISTRY, 2016, Vol.138, p.321

2016

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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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No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a swiss early-onset Alzheimer's disease family with a dominant mode of inheritance

Dementia and geriatric cognitive disorders, 1999-11, Vol.10 (6), p.431

1999

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Linkage analysis of autopsy-confirmed familial Alzheimer disease supports an Alzheimer disease locus in 8q24

Dementia and geriatric cognitive disorders, 2011-01, Vol.31 (2), p.109

2011

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Prevalence, phenotypic variability and neuropsychological findings of C9orf72 mutations in a Bulgarian dementia cohort

JOURNAL OF NEUROCHEMISTRY, 2016, Vol.138, p.321

2016

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Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene

Genome scan on Swedish Alzheimer's disease families

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

Confirmation of high frequency of C9orf72 mutations in patients with frontotemporal dementia from Sweden

Phenotypic variability and neuropsychological findings associated with C9orf72 repeat expansions in a Bulgarian dementia cohort

APOE genotypes and disease severity in multiple sclerosis

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

No common founder for C9orf72 expansion mutation in Sweden

Progressive neuropathology and cognitive decline in a single Arctic APP transgenic mouse model

Increased frequency of a new polymorphism in the cell division cycle 2 (cdc2) gene in patients with Alzheimer's disease and frontotemporal dementia

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

Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration

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

Biochemical studies of poly-T variants in the Alzheimer's disease associated TOMM40 gene

Linkage to the 8p21.1 region Including the CLU gene in age at onset stratified alzheimer's disease families

A DLST genotype associated with reduced risk for Alzheimer's disease

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

Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia

Frequency of low erythrocyte porphobilinogen deaminase activity in Finland

Old-age hippocampal sclerosis associates with GRN and TMEM106B but not with ABCC9 variation in population-based cohorts

Frequency and contribution of variants in 17 dementia related genes in a Bulgarian dementia cohort

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

No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a swiss early-onset Alzheimer's disease family with a dominant mode of inheritance

Linkage analysis of autopsy-confirmed familial Alzheimer disease supports an Alzheimer disease locus in 8q24

Prevalence, phenotypic variability and neuropsychological findings of C9orf72 mutations in a Bulgarian dementia cohort

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