|
| 30820047 | Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. | Nat Genet | 2019 |
| 27030769 | ABCA7 Deficiency Accelerates Amyloid-β Generation and Alzheimer's Neuronal Pathology. | J Neurosci | 2016 |
| 26507310 | Evaluating pathogenic dementia variants in posterior cortical atrophy. | Neurobiol Aging | 2016 |
| 27727239 | Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases. | Sci Data | 2016 |
| 25189118 | Late-onset Alzheimer's risk variants in memory decline, incident mild cognitive impairment, and Alzheimer's disease. | Neurobiol Aging | 2015 |
| 26399695 | Erratum to: Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility. | Mol Neurodegener | 2015 |
| 25881291 | Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility. | Mol Neurodegener | 2015 |
| 23643458 | Evaluation of memory endophenotypes for association with CLU, CR1, and PICALM variants in black and white subjects. | Alzheimers Dement | 2014 |
| 25324900 | Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels. | Alzheimers Res Ther | 2014 |
| 24607147 | ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease. | Mol Neurodegener | 2014 |
| 24670887 | Late-onset Alzheimer disease genetic variants in posterior cortical atrophy and posterior AD. | Neurology | 2014 |
| 23724096 | Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology. | PLoS One | 2013 |
| 20864222 | Association and heterogeneity at the GAPDH locus in Alzheimer's disease. | Neurobiol Aging | 2012 |
| 22722634 | Novel late-onset Alzheimer disease loci variants associate with brain gene expression. | Neurology | 2012 |
| 22685416 | Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants. | PLoS Genet | 2012 |
| 22855871 | TMEM106B risk variant is implicated in the pathologic presentation of Alzheimer disease. | Neurology | 2012 |
| 22494505 | Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications. | Mol Neurodegener | 2012 |
| 21132329 | Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease. | Hum Genet | 2011 |
| 21798052 | Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study. | Mol Neurodegener | 2011 |
| 21731745 | Multiple insulin degrading enzyme variants alter in vitro reporter gene expression. | PLoS One | 2011 |
| 21321396 | Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions. | J Alzheimers Dis | 2011 |
| 20142614 | Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease. | Neurology | 2010 |
| 21087763 | Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma. | Am J Hum Genet | 2010 |
| 20554627 | Replication of CLU, CR1, and PICALM associations with alzheimer disease. | Arch Neurol | 2010 |
| 19158106 | Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. | Brain | 2009 |
| 19136949 | Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. | Nat Genet | 2009 |
| 15390127 | Parkinsonism, FXTAS, and FMR1 premutations. | Mov Disord | 2005 |
| 14985393 | DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function. | J Med Genet | 2004 |
| 15655258 | Multiplication of the alpha-synuclein gene is not a common disease mechanism in Lewy body disease. | J Mol Neurosci | 2004 |
| 15308306 | Alpha-synuclein missense and multiplication mutations in autosomal dominant Parkinson's disease. | Neurosci Lett | 2004 |
| 15197707 | Parkinson's disease in Ireland: clinical presentation and genetic heterogeneity in patients with parkin mutations. | Mov Disord | 2004 |
| 15354349 | Identification of the human ubiquitin specific protease 31 (USP31) gene: structure, sequence and expression analysis. | DNA Seq | 2004 |
| 12771249 | Parkin-proven disease: common founders but divergent phenotypes. | Neurology | 2003 |
| 11958849 | The tau H1 haplotype is associated with Parkinson's disease in the Norwegian population. | Neurosci Lett | 2002 |