Related references
Note: Only part of the references are listed.Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages
Jaeyoon Chung et al.
ALZHEIMERS & DEMENTIA (2018)
Tau Phosphorylation is Impacted by Rare AKAP9 Mutations Associated with Alzheimer Disease in African Americans
Tsuneya Ikezu et al.
JOURNAL OF NEUROIMMUNE PHARMACOLOGY (2018)
African American exome sequencing identifies potential risk variants at Alzheimer disease loci
Aurelie N'Songo et al.
NEUROLOGY-GENETICS (2017)
Transethnic genome-wide scan identifies novel Alzheimer's disease loci
Gyungah R. Jun et al.
ALZHEIMERS & DEMENTIA (2017)
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans
Jesse Mez et al.
ALZHEIMERS & DEMENTIA (2017)
A novel Alzheimer disease locus located near the gene encoding tau protein
G. Jun et al.
MOLECULAR PSYCHIATRY (2016)
Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models
Han Chen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
ABCA7 frameshift deletion associated with Alzheimer disease in African Americans
Holly N. Cukier et al.
NEUROLOGY-GENETICS (2016)
Expanding the genomic roadmap of Alzheimer's disease
Lindsay A. Farrer
LANCET NEUROLOGY (2015)
Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study
Elise Cuyvers et al.
LANCET NEUROLOGY (2015)
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease
Stacy Steinberg et al.
NATURE GENETICS (2015)
Second-generation PLINK: rising to the challenge of larger and richer datasets
Christopher C. Chang et al.
GIGASCIENCE (2015)
Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans
Mark W. Logue et al.
ALZHEIMERS & DEMENTIA (2014)
PLXNA4 Is Associated with Alzheimer Disease and Modulates Tau Phosphorylation
Gyungah Jun et al.
ANNALS OF NEUROLOGY (2014)
A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death
Monica K. Wetzel-Smith et al.
NATURE MEDICINE (2014)
Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ε4, and the Risk of Late-Onset Alzheimer Disease in African Americans
Christiane Reitz et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2013)
Factor V Activator from Daboia russelli russelli Venom Destabilizes β-Amyloid Aggregate, the Hallmark of Alzheimer Disease
Payel Bhattacharjee et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Jean-Charles Lambert et al.
NATURE GENETICS (2013)
Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)
C. Reitz et al.
TRANSLATIONAL PSYCHIATRY (2013)
Multiple Loci Influencing Hippocampal Degeneration Identified by Genome Scan
Scott A. Melville et al.
ANNALS OF NEUROLOGY (2012)
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3
Pablo Cingolani et al.
FLY (2012)
White Matter Predictors of Cognitive Functioning in Older Adults
Irene B. Meier et al.
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY (2012)
Identification of Alzheimer disease-associated variants in genes that regulate retromer function
Badri N. Vardarajan et al.
NEUROBIOLOGY OF AGING (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
Daniel G. MacArthur et al.
SCIENCE (2012)
Genome-wide association study of Alzheimer's disease
M. I. Kamboh et al.
TRANSLATIONAL PSYCHIATRY (2012)
The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
Guy M. McKhann et al.
ALZHEIMERS & DEMENTIA (2011)
A Comprehensive Genetic Association Study of Alzheimer Disease in African Americans
Mark W. Logue et al.
ARCHIVES OF NEUROLOGY (2011)
Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
Alkes L. Price et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Meta-analysis Confirms CR1, CLU, and PICALM as Alzheimer Disease Risk Loci and Reveals Interactions With APOE Genotypes
Gyungah Jun et al.
ARCHIVES OF NEUROLOGY (2010)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data
Bingshan Li et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study Implication of Additional Loci
Joseph H. Lee et al.
ARCHIVES OF NEUROLOGY (2008)
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
Ekaterina Rogaeva et al.
NATURE GENETICS (2007)
Association of Polymorphisms in the angiotensin-converting enzyme gene with Alzheimer disease in an Israeli Arab community
Y Meng et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
APOE epsilon 4 is not associated with Alzheimer's disease in elderly Nigerians
O Gureje et al.
ANNALS OF NEUROLOGY (2006)
Risk of dementia among white and African American relatives of patients with Alzheimer disease
RC Green et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2002)
Association between angiotensin-converting enzyme and Alzheimer disease
LA Farrer et al.
ARCHIVES OF NEUROLOGY (2000)