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Author Details
Full Name
William K Scott
Affiliation
John P. Hussman Institute for Human Genomics.
ORCID
Career Start Year
1994
Papers
220
H Index
56
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36929524
Psychometric approaches to defining cognitive phenotypes in the Old Order Amish.
Int J Geriatr Psychiatry
2023
37561946
Visuospatial and Verbal Memory Differences in Amish Individuals With Alzheimer Disease and Related Dementias.
Alzheimer Dis Assoc Disord
2023
37742071
Founder population-specific weights yield improvements in performance of polygenic risk scores for Alzheimer disease in the Midwestern Amish.
HGG Adv
2023
35142102
Neuropathological lesions and their contribution to dementia and cognitive impairment in a heterogeneous clinical population.
Alzheimers Dement
2022
35857289
Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration.
Invest Ophthalmol Vis Sci
2022
35599847
The genetic architecture of Alzheimer disease risk in the Ohio and Indiana Amish.
HGG Adv
2022
35941704
Corpora amylacea are associated with tau burden and cognitive status in Alzheimer's disease.
Acta Neuropathol Commun
2022
35997131
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy.
Mov Disord
2022
35930268
Consequences of a Rare Complement Factor H Variant for Age-Related Macular Degeneration in the Amish.
Invest Ophthalmol Vis Sci
2022
33285633
Lower Levels of Education Are Associated with Cognitive Impairment in the Old Order Amish.
J Alzheimers Dis
2021
33522086
Increased APOE ε4 expression is associated with the difference in Alzheimer's disease risk from diverse ancestral backgrounds.
Alzheimers Dement
2021
34831363
Plasma Metabolomics of Intermediate and Neovascular Age-Related Macular Degeneration Patients.
Cells
2021
33938021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease.
Ann Neurol
2021
34036211
Transdisciplinary Perspectives on Precision Medicine.
Health Equity
2021
32224865
Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida.
Genes (Basel)
2020
33281709
Novel Variants in <i>LRRK2</i> and <i>GBA</i> Identified in Latino Parkinson Disease Cohort Enriched for Caribbean Origin.
Front Neurol
2020
29746403
AMISH EYE STUDY: Baseline Spectral Domain Optical Coherence Tomography Characteristics of Age-Related Macular Degeneration.
Retina
2019
31436842
Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis.
JAMA Ophthalmol
2019
31379924
Motivations for Participation in Parkinson Disease Genetic Research Among Hispanics versus Non-Hispanics.
Front Genet
2019
31403079
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease.
Neurol Genet
2019
31367973
Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish.
Hum Genet
2019
29321258
Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn's disease and Parkinson's disease.
Sci Transl Med
2018
30289878
Human genetic variation in GLS2 is associated with development of complicated Staphylococcus aureus bacteremia.
PLoS Genet
2018
30326066
The Carnitine Shuttle Pathway is Altered in Patients With Neovascular Age-Related Macular Degeneration.
Invest Ophthalmol Vis Sci
2018
29392307
Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets.
Invest Ophthalmol Vis Sci
2018
29691419
Author Correction: A population-specific reference panel empowers genetic studies of Anabaptist populations.
Sci Rep
2018
27826014
Generation of disease-specific autopsy-confirmed iPSCs lines from postmortem isolated Peripheral Blood Mononuclear Cells.
Neurosci Lett
2017
29805915
Genomics of human pulmonary tuberculosis: from genes to pathways.
Curr Genet Med Rep
2017
28332560
Evaluating genetic susceptibility to Staphylococcus aureus bacteremia in African Americans using admixture mapping.
Genes Immun
2017
28813576
Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1.
Invest Ophthalmol Vis Sci
2017
28729679
A population-specific reference panel empowers genetic studies of Anabaptist populations.
Sci Rep
2017
28594911
Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans.
PLoS One
2017
28853718
Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis.
Eur J Hum Genet
2017
28628665
A chromosome 5q31.1 locus associates with tuberculin skin test reactivity in HIV-positive individuals from tuberculosis hyper-endemic regions in east Africa.
PLoS Genet
2017
27760082
Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample.
Menopause
2017
26752265
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.
Nat Genet
2016
26450422
Polymorphisms in HLA Class II Genes Are Associated With Susceptibility to Staphylococcus aureus Infection in a White Population.
J Infect Dis
2016
27661856
Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses.
Invest Ophthalmol Vis Sci
2016
27832277
Progression Rate From Intermediate to Advanced Age-Related Macular Degeneration Is Correlated With the Number of Risk Alleles at the CFH Locus.
Invest Ophthalmol Vis Sci
2016
27625572
Whole exome sequencing of extreme age-related macular degeneration phenotypes.
Mol Vis
2016
27771146
Heritability of Choroidal Thickness in the Amish.
Ophthalmology
2016
27537254
A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium.
Invest Ophthalmol Vis Sci
2016
27123490
DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient.
Neurol Genet
2016
27116550
Genetic Association Analysis of Drusen Progression.
Invest Ophthalmol Vis Sci
2016
26942285
A Locus at 5q33.3 Confers Resistance to Tuberculosis in Highly Susceptible Individuals.
Am J Hum Genet
2016
27066581
Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants.
Neurol Genet
2016
26959068
The Application of Genetic Risk Scores in Age-Related Macular Degeneration: A Review.
J Clin Med
2016
26681389
The Relationship Between Reticular Pseudodrusen and Severity of AMD.
Ophthalmology
2016
26691988
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Nat Genet
2016
26918299
Linkage of familial essential tremor to chromosome 5q35.
Mov Disord
2016
1 - 50 of 220
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