Stacey Melquist, Ph.D.

Affiliations: 
 
Area:
Genetics
Google:
"Stacey Melquist"
Mean distance: 20.75 (cluster 28)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Webster J, Reiman EM, Zismann VL, et al. (2010) Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis. International Journal of Molecular Epidemiology and Genetics. 1: 19-30
Corneveaux JJ, Liang WS, Reiman EM, et al. (2010) Evidence for an association between KIBRA and late-onset Alzheimer's disease. Neurobiology of Aging. 31: 901-9
Ludolph AC, Kassubek J, Landwehrmeyer BG, et al. (2009) Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 16: 297-309
Sando SB, Melquist S, Cannon A, et al. (2008) Risk-reducing effect of education in Alzheimer's disease. International Journal of Geriatric Psychiatry. 23: 1156-62
Sando SB, Melquist S, Cannon A, et al. (2008) APOE epsilon 4 lowers age at onset and is a high risk factor for Alzheimer's disease; a case control study from central Norway. Bmc Neurology. 8: 9
Golan MP, Melquist S, Safranow K, et al. (2008) Analysis of UBQLN1 variants in a Polish Alzheimer's disease patient: control series. Dementia and Geriatric Cognitive Disorders. 25: 366-71
Wider C, Melquist S, Hauf M, et al. (2008) Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5. Neurology. 70: 1377-83
Reiman EM, Webster JA, Myers AJ, et al. (2007) GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. Neuron. 54: 713-20
Melquist S, Craig DW, Huentelman MJ, et al. (2007) Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. American Journal of Human Genetics. 80: 769-78
Pearson JV, Huentelman MJ, Halperin RF, et al. (2007) Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. American Journal of Human Genetics. 80: 126-39
See more...