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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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Microsatellite evolution: polarity of substitutions within repeats and neutrality of flanking sequences

Proceedings of the Royal Society. B, Biological sciences, 1999-04, Vol.266 (1421), p.825-833

1999

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A DNA Methylation Study of the Amyloid Precursor Protein Gene in Several Brain Regions from Patients with Familial Alzheimer Disease

Journal of neurogenetics, 2010-12, Vol.24 (4), p.179-181

2010

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Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference

Genomics (San Diego, Calif.), 2007-09, Vol.90 (3), p.291-296

2007

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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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Heterogeneity in the rate and pattern of germline mutation at individual microsatellite loci

Nucleic acids research, 2002-05, Vol.30 (9), p.1997

2002

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PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays

Nucleic acids research, 2005-01, Vol.33 (17), p.e142

2005

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P4‐116: Methylation studies in brains from patients with familial Alzheimer's disease

Alzheimer's & dementia, 2009-07, Vol.5 (4S_Part_15), p.P465-P465

2009

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Evidence of linkage to chromosomes 10p15.3-p15.1, 14q24.3-q31.1 and 9q33.3-q34.3 in non-syndromic colorectal cancer families

European journal of human genetics : EJHG, 2012-01, Vol.20 (1), p.91-96

2012

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Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray

Prenatal diagnosis, 2007-12, Vol.27 (13), p.1197-1204

2007

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Methylation studies in brains from patients with familial Alzheimer's disease

Alzheimer's & dementia, 2009, Vol.5 (4), p.P465-P465

2009

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Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease

European journal of human genetics : EJHG, 2009-03, Vol.17 (3), p.368-377

2009

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Evolutionary evidence suggests that CpG island-associated Alus are frequently unmethylated in human germline

Human genetics, 2006-05, Vol.119 (4), p.457-458

2006

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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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Linkage analysis on autopsy-confirmed familial Alzheimer's disease supports an Alzheimer locus in 8q24

Alzheimer's & dementia, 2010-07, Vol.6 (4), p.S191-S192

2010

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P1‐063: Linkage analysis on autopsy‐confirmed familial Alzheimer's disease supports an Alzheimer locus in 8q24

Alzheimer's & dementia, 2010-07, Vol.6 (4S_Part_6), p.S191-S192

2010

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Fine mapping in 20p13 with families having a mixed phenotype of Alzheimer's disease and vascular dementia

Alzheimer's & dementia, 2010-07, Vol.6 (4), p.S196-S197

2010

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P1‐078: Fine mapping in 20p13 with families having a mixed phenotype of Alzheimer's disease and vascular dementia

Alzheimer's & dementia, 2010-07, Vol.6 (4S_Part_6), p.S196-S197

2010

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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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S1986 Evidence for a New Susceptibility Region on Chromosome 9 From a Genome-Wide Linkage Study in Non-Syndromic Colorectal Cancer Families

Gastroenterology (New York, N.Y. 1943), 2010, Vol.138 (5), p.S-295-S-295

2010

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A range of simple summary genome-wide statistics for detecting genetic linkage using high density marker data

Genetic epidemiology, 2007-09, Vol.31 (6), p.565-576

2007

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Rates and patterns of mutation in microsatellite DNA

Brohede, Jesper

2003

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Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association

Clinical dysmorphology, 2006-01, Vol.15 (1), p.1

2006

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Individual variation in microsatellite mutation rate in barn swallows

Mutation research, 2004-01, Vol.545 (1), p.73-80

2004

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

Microsatellite evolution: polarity of substitutions within repeats and neutrality of flanking sequences

A DNA Methylation Study of the Amyloid Precursor Protein Gene in Several Brain Regions from Patients with Familial Alzheimer Disease

Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference

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

Heterogeneity in the rate and pattern of germline mutation at individual microsatellite loci

PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays

P4‐116: Methylation studies in brains from patients with familial Alzheimer's disease

Evidence of linkage to chromosomes 10p15.3-p15.1, 14q24.3-q31.1 and 9q33.3-q34.3 in non-syndromic colorectal cancer families

Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray

Methylation studies in brains from patients with familial Alzheimer's disease

Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease

Evolutionary evidence suggests that CpG island-associated Alus are frequently unmethylated in human germline

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

Linkage analysis on autopsy-confirmed familial Alzheimer's disease supports an Alzheimer locus in 8q24

P1‐063: Linkage analysis on autopsy‐confirmed familial Alzheimer's disease supports an Alzheimer locus in 8q24

Fine mapping in 20p13 with families having a mixed phenotype of Alzheimer's disease and vascular dementia

P1‐078: Fine mapping in 20p13 with families having a mixed phenotype of Alzheimer's disease and vascular dementia

Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family

S1986 Evidence for a New Susceptibility Region on Chromosome 9 From a Genome-Wide Linkage Study in Non-Syndromic Colorectal Cancer Families

A range of simple summary genome-wide statistics for detecting genetic linkage using high density marker data

Rates and patterns of mutation in microsatellite DNA

Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association

Individual variation in microsatellite mutation rate in barn swallows

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