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| 23552688 | Neuropathologic basis of age-associated brain atrophy. | JAMA Neurol | 2013 |
| 23407718 | APOE ε4 increases risk for dementia in pure synucleinopathies. | JAMA Neurol | 2013 |
| 23407718 | APOE ε4 increases risk for dementia in pure synucleinopathies. | JAMA Neurol | 2013 |
| 22156576 | Variants in ASB10 are associated with open-angle glaucoma. | Hum Mol Genet | 2012 |
| 22722634 | Novel late-onset Alzheimer disease loci variants associate with brain gene expression. | Neurology | 2012 |
| 23102128 | Review of selected databases of longitudinal aging studies. | Alzheimers Dement | 2012 |
| 23035075 | GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology. | Neurology | 2012 |
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| 23035075 | GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology. | Neurology | 2012 |
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| 21460841 | Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. | Nat Genet | 2011 |
| 20452100 | Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study. | Neurobiol Aging | 2011 |
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| 21460841 | Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. | Nat Genet | 2011 |
| 19766542 | The FAS gene, brain volume, and disease progression in Alzheimer's disease. | Alzheimers Dement | 2010 |
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| 20697030 | Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. | Arch Neurol | 2010 |
| 20107173 | Association of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population. | Invest Ophthalmol Vis Sci | 2010 |
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| 20697030 | Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. | Arch Neurol | 2010 |
| 20361857 | Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases. | Stat Appl Genet Mol Biol | 2010 |
| 20237253 | The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness. | Invest Ophthalmol Vis Sci | 2010 |
| 20107173 | Association of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population. | Invest Ophthalmol Vis Sci | 2010 |
| 19566620 | Exceptional brain aging in a rural population-based cohort. | J Rural Health | 2009 |
| 19349605 | Etiology of musician's dystonia: familial or environmental? | Neurology | 2009 |
| 19666518 | A loss-of-function nonsynonymous polymorphism in the osmoregulatory TRPV4 gene is associated with human hyponatremia. | Proc Natl Acad Sci U S A | 2009 |
| 19566620 | Exceptional brain aging in a rural population-based cohort. | J Rural Health | 2009 |
| 19666518 | A loss-of-function nonsynonymous polymorphism in the osmoregulatory TRPV4 gene is associated with human hyponatremia. | Proc Natl Acad Sci U S A | 2009 |
| 19349605 | Etiology of musician's dystonia: familial or environmental? | Neurology | 2009 |
| 17174450 | Translational gene mapping of cognitive decline. | Neurobiol Aging | 2008 |
| 17174450 | Translational gene mapping of cognitive decline. | Neurobiol Aging | 2008 |
| 18032746 | Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci? | Neurology | 2008 |
| 18381645 | Childhood-onset restless legs syndrome: clinical and genetic features of 22 families. | Mov Disord | 2008 |
| 18381645 | Childhood-onset restless legs syndrome: clinical and genetic features of 22 families. | Mov Disord | 2008 |
| 18032746 | Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci? | Neurology | 2008 |
| 17702011 | Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites. | Am J Med Genet A | 2007 |
| 17565750 | Linear trend tests for case-control genetic association that incorporate random phenotype and genotype misclassification error. | Genet Epidemiol | 2007 |