S. Melquist

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Aliases
S Melquist, S. Melquist, Stacey Melquist
Publication record
20 papers · 4,335 citations · H-index 13

PAPERS

Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis.
20108 citationsauthor #26
Evidence for an association between KIBRA and late-onset Alzheimer's disease.
2010113 citationsauthor #27
APOE ε4 lowers age at onset and is a high risk factor for Alzheimer's disease; A case control study from central Norway
2008258 citationsauthor #2
Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1
200867 citationsauthor #2
GAB2 Alleles Modify Alzheimer's Risk in APOE ε4 Carriers
2007466 citationsauthor #31
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
200775 citationsauthor #1
GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.
2007285 citationsauthor #28
Identiﬁcation of a Novel Risk Locus for Progressive Supranuclear Palsy by a Pooled Genomewide Scan of 500,288 Single-Nucleotide Polymorphisms
20072 citationsauthor #1
Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies.
2007158 citationsauthor #5
Autosomal dominant dystonia-plus with cerebral calcifications
200636 citationsauthor #8
P3–163: Identification of a novel risk gene for progressive supranuclear palsy by a genome–wide scan of 500,288 SNPs
20060 citationsauthor #1
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
20061,978 citationsauthor #14
A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17.
2006100 citationsauthor #11
S2–02–06: The tauopathies: From genetics to animal models
20060 citationsauthor #2
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
2006580 citationsauthor #8
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
2005162 citationsauthor #2
LRRK2 mutations are not common in Alzheimer's disease.
200535 citationsauthor #3
P4-097 Determination of population structure in the mayo Alzheimer's disease patient registry
20040 citationsauthor #1
Determination of population structure in the Alzheimers disease patient registry
20030 citationsauthor #1
Title : Study of a Swiss dopa-responsive dystonia family with a deletion in GCH 1 : redefining DYT 14 as DYT 5
year unknown10 citationsauthor #2

TIMELINE

2003 0 citations

2004 0 citations

2005 197 citations

2006 2,694 citations

2007 986 citations

2008 325 citations

2010 121 citations

Unknown 10 citations

S. Melquist

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