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Strategies in Aggregation Tests for Rare Variants

Current protocols, 2023-11, Vol.3 (11), p.e931-n/a

2023

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An X Chromosome Transcriptome Wide Association Study Implicates ARMCX6 in Alzheimer’s Disease

Journal of Alzheimer's disease, 2024-04, Vol.98 (3), p.1053-1067

2024

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Estimating the regulatory potential of DNA methylation in Alzheimer's disease

Alzheimer's & dementia, 2021-12, Vol.17 (S3), p.e049365-n/a

2021

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Sex‐specific analysis of DNA methylation changes implicates new loci in Alzheimer’s disease pathology

Alzheimer's & dementia, 2021-12, Vol.17 (S3), p.e049363-n/a

2021

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Cross-Species Analyses Identify Dlgap2 as a Regulator of Age-Related Cognitive Decline and Alzheimer’s Dementia

Cell reports (Cambridge), 2020-09, Vol.32 (9), p.108091-108091, Article 108091

2020

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Characterization of an Alzheimer disease‐associated deletion in SORL1

Alzheimer's & dementia, 2021-12, Vol.17, p.e055472-n/a

2021

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Heritability analyses show partial genetic overlap between (non‐Mendelian) early and late onset Alzheimer disease due to an intriguing APOE effect

Alzheimer's & dementia, 2021-12, Vol.17 (S3), p.e056143-n/a

2021

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African locus reduces the effect of ApoE ε4 allele in Alzheimer’s disease

Alzheimer's & dementia, 2021-12, Vol.17, p.e056210-n/a

2021

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Diverse Ancestral Populations and the ADSP

Alzheimer's & dementia, 2022-12, Vol.18 (S4), p.n/a

Kunkle, Brian W.

2022

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ADSP follow‐up study: NCRAD biospecimens

Alzheimer's & dementia, 2021-12, Vol.17 (S3), p.e056242-n/a

2021

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Genome‐wide association and multi‐omics studies identify MGMT as a novel risk gene for Alzheimer disease among women

Alzheimer's & dementia, 2021-12, Vol.17, p.e054483-n/a

2021

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The Alzheimer’s Disease Sequencing Project – Follow Up Study (ADSP‐FUS): Increasing ethnic diversity in Alzheimer’s genetics research with the addition of potential new cohorts

Alzheimer's & dementia, 2021-12, Vol.17, p.e056101-n/a

2021

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Admixture mapping identifies novel regions influencing Alzheimer disease in African Americans

Alzheimer's & dementia, 2021-12, Vol.17, p.e056443-n/a

2021

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APOE‐stratified genome‐wide association analysis identifies novel Alzheimer disease candidate risk loci for African Americans

Alzheimer's & dementia, 2021-12, Vol.17 (S3), p.e056383-n/a

2021

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SORL1 mutations in early- and late-onset Alzheimer disease

Neurology. Genetics, 2016-12, Vol.2 (6), p.e116

2016

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INTEGRATIVE ANALYSIS OF GWAS SUMMARY DATA AND FUNCTIONAL ANNOTATIONS IDENTIFIES ADDITIONAL LOCI FOR LATE-ONSET ALZHEIMER'S DISEASE

Alzheimer's & dementia, 2016-07, Vol.12 (7), p.P854-P854

2016

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Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease

Alzheimer's & dementia : diagnosis, assessment & disease monitoring, 2021, Vol.13 (1), p.e12255-n/a

2021

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Professional and Amateur Pitchers’ Perspective on the Ulnar Collateral Ligament Injury Risk

Orthopaedic journal of sports medicine, 2019-06, Vol.7 (6), p.2325967119850777-2325967119850777

2019

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SECONDARY ANALYSES OF INTERNATIONAL GENOMICS OF ALZHEIMER'S PROJECT STAGE I GWAS SUMMARY DATA IDENTIFIES ADDITIONAL VARIANTS ASSOCIATED WITH LATE-ONSET ALZHEIMER'S DISEASE

Alzheimer's & dementia, 2016-07, Vol.12 (7), p.P856-P857

2016

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PATHOGENIC SORL1 MUTATIONS AND PARKINSONIAN FEATURES IN ALZHEIMER'S DISEASE

Alzheimer's & dementia, 2016-07, Vol.12 (7), p.P451-P452

2016

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Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease

Neurology. Genetics, 2016-02, Vol.2 (1), p.e41-e41

2016

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HIGH-RESOLUTION IMPUTATION IN GENOME-WIDE ASSOCIATION STUDIES OF LATE-ONSET ALZHEIMER'S DISEASE IDENTIFIES NOVEL RARE VARIANT ASSOCIATIONS

Alzheimer's & dementia, 2016-07, Vol.12 (7), p.P178-P179

2016

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WHOLE EXOME SEQUENCING OF LATE ONSET MULTIPLEX FAMILIES IDENTIFIES RARE CODING VARIANTS IN KNOWN AND NOVEL ALZHEIMER’S DISEASE GENES

Alzheimer's & dementia, 2016-07, Vol.12 (7), p.P196-P197

2016

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Strategies in Aggregation Tests for Rare Variants

An X Chromosome Transcriptome Wide Association Study Implicates ARMCX6 in Alzheimer’s Disease

Estimating the regulatory potential of DNA methylation in Alzheimer's disease

Sex‐specific analysis of DNA methylation changes implicates new loci in Alzheimer’s disease pathology

Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole-genome sequencing from the Alzheimer's Disease Sequencing Project

Cross-Species Analyses Identify Dlgap2 as a Regulator of Age-Related Cognitive Decline and Alzheimer’s Dementia

Characterization of an Alzheimer disease‐associated deletion in SORL1

Heritability analyses show partial genetic overlap between (non‐Mendelian) early and late onset Alzheimer disease due to an intriguing APOE effect

African locus reduces the effect of ApoE ε4 allele in Alzheimer’s disease

Sex‐specific genetic architecture of late‐life memory performance

Diverse Ancestral Populations and the ADSP

ADSP follow‐up study: NCRAD biospecimens

Genome‐wide association and multi‐omics studies identify MGMT as a novel risk gene for Alzheimer disease among women

The Alzheimer’s Disease Sequencing Project – Follow Up Study (ADSP‐FUS): Increasing ethnic diversity in Alzheimer’s genetics research with the addition of potential new cohorts

Admixture mapping identifies novel regions influencing Alzheimer disease in African Americans

APOE‐stratified genome‐wide association analysis identifies novel Alzheimer disease candidate risk loci for African Americans

SORL1 mutations in early- and late-onset Alzheimer disease

INTEGRATIVE ANALYSIS OF GWAS SUMMARY DATA AND FUNCTIONAL ANNOTATIONS IDENTIFIES ADDITIONAL LOCI FOR LATE-ONSET ALZHEIMER'S DISEASE

Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease

Professional and Amateur Pitchers’ Perspective on the Ulnar Collateral Ligament Injury Risk

SECONDARY ANALYSES OF INTERNATIONAL GENOMICS OF ALZHEIMER'S PROJECT STAGE I GWAS SUMMARY DATA IDENTIFIES ADDITIONAL VARIANTS ASSOCIATED WITH LATE-ONSET ALZHEIMER'S DISEASE

PATHOGENIC SORL1 MUTATIONS AND PARKINSONIAN FEATURES IN ALZHEIMER'S DISEASE

Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease

HIGH-RESOLUTION IMPUTATION IN GENOME-WIDE ASSOCIATION STUDIES OF LATE-ONSET ALZHEIMER'S DISEASE IDENTIFIES NOVEL RARE VARIANT ASSOCIATIONS

WHOLE EXOME SEQUENCING OF LATE ONSET MULTIPLEX FAMILIES IDENTIFIES RARE CODING VARIANTS IN KNOWN AND NOVEL ALZHEIMER’S DISEASE GENES

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