List of works - Gerard D Schellenberg

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

scientific article

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

scientific article published on 14 January 2016

Research goals in progressive supranuclear palsy

Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

scientific article

Genome-wide, high-content siRNA screening identifies the Alzheimer's genetic risk factor FERMT2 as a major modulator of APP metabolism

scientific article

Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals

scientific article

Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records

scientific article

Sex-specific genetic predictors of Alzheimer's disease biomarkers

scientific article published on 02 July 2018

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

scientific article

Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport

scientific article

Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease

scientific article

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

scientific article

Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants

scientific article published on 6 October 2017

Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease

article

Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease

scientific article published on 13 March 2018

A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains

scientific article published on 18 January 2017

One for all and all for One: Improving replication of genetic studies through network diffusion

scientific article published on 23 April 2018

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

scientific article published on 27 February 2018

Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease

scientific article published on 08 July 2019

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Correction: SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians

scientific article published on 8 July 2013

Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

scholarly article by Monica Y Sanchez-Contreras published in July 2018

Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease

Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease

scientific article published on 20 February 2018

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

Activity of the poly(A) binding protein MSUT2 determines susceptibility to pathological tau in the mammalian brain

scientific article published on 01 December 2019

Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis

scientific article published on 19 October 2020

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

scientific article published on 21 October 2019

Examining the Performance of Polygenic Risk Scores for Alzheimer Disease Within and Across Populations Using k -Fold Cross-Validation

scientific article published in December 2024

Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells

scientific article published on 8 March 2025

TSC1 loss increases risk for tauopathy by inducing tau acetylation and preventing tau clearance via chaperone-mediated autophagy

scientific article published on 5 November 2021

Protein phosphatase 2A, complement component 4, and APOE genotype linked to Alzheimer’s disease using a systems biology approach

Genetic association of progressive supranuclear palsy (PSP) risk loci variants with brain gene expression and neuropathology endophenotypes

article

Sex differences in the genetic predictors of Alzheimer's pathology

scientific article published on 01 September 2019

Genetic variants and functional pathways associated with resilience to Alzheimer's disease

scientific article published on 01 August 2020

Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

scientific article published on 7 June 2021

A comparative study of structural variant calling in WGS from Alzheimer’s disease families

scientific article published on 28 February 2024

List of works by Gerard D Schellenberg

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

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

Research goals in progressive supranuclear palsy

Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

Genome-wide, high-content siRNA screening identifies the Alzheimer's genetic risk factor FERMT2 as a major modulator of APP metabolism

Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals

Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records

Sex-specific genetic predictors of Alzheimer's disease biomarkers

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport

Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants

Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease

Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease

A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains

One for all and all for One: Improving replication of genetic studies through network diffusion

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Correction: SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians

Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease

Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

Activity of the poly(A) binding protein MSUT2 determines susceptibility to pathological tau in the mammalian brain

Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

Examining the Performance of Polygenic Risk Scores for Alzheimer Disease Within and Across Populations Using k -Fold Cross-Validation

Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells

TSC1 loss increases risk for tauopathy by inducing tau acetylation and preventing tau clearance via chaperone-mediated autophagy

Protein phosphatase 2A, complement component 4, and APOE genotype linked to Alzheimer’s disease using a systems biology approach

Genetic association of progressive supranuclear palsy (PSP) risk loci variants with brain gene expression and neuropathology endophenotypes

Sex differences in the genetic predictors of Alzheimer's pathology

Genetic variants and functional pathways associated with resilience to Alzheimer's disease

Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

A comparative study of structural variant calling in WGS from Alzheimer’s disease families

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as novel risk factors for Alzheimer’s Disease