List of works - Joanne B Norton

Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

scientific article published on January 2004

An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations

scientific article published on 07 October 2019

Analysis of neurodegenerative Mendelian genes in clinically diagnosed Alzheimer Disease

scientific article published in November 2017

Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations

article

Assessment of the Genetic Architecture of Alzheimer's Disease Risk in Rate of Memory Decline.

scientific article published in January 2018

Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

scientific article

Coding variants in TREM2 increase risk for Alzheimer's disease

scientific article

Discovery and validation of autosomal dominant Alzheimer's disease mutations

scientific article published on 18 July 2018

Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease.

scientific article published on 4 April 2018

Examination of the Effect of Rare Variants in TREM2, ABI3, and PLCG2 in LOAD Through Multiple Phenotypes

scientific article published on 04 September 2020

Exome-sequencing confirms DNAJC5 mutations as cause of adult neuronal ceroid-lipofuscinosis

scientific article published in 2011

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

scientific article

Human fibroblast and stem cell resource from the Dominantly Inherited Alzheimer Network

scientific article published on 25 July 2018

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia

scientific article published on April 2008

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation

scientific article published in January 2007

No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found

scientific article published in June 2004

Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life

scientific article

Phenotypic Similarities Between Late-Onset Autosomal Dominant and Sporadic Alzheimer Disease: A Single-Family Case-Control Study

scientific article published on 25 July 2016

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

scientific article

SORL1 variants across Alzheimer's disease European American cohorts

scientific article published on 21 September 2016

TDP-43 A315T mutation in familial motor neuron disease

scientific article published on April 2008

List of works by Joanne B Norton

Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations

Analysis of neurodegenerative Mendelian genes in clinically diagnosed Alzheimer Disease

Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations

Assessment of the Genetic Architecture of Alzheimer's Disease Risk in Rate of Memory Decline.

Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

Coding variants in TREM2 increase risk for Alzheimer's disease

Discovery and validation of autosomal dominant Alzheimer's disease mutations

Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease.

Examination of the Effect of Rare Variants in TREM2, ABI3, and PLCG2 in LOAD Through Multiple Phenotypes

Exome-sequencing confirms DNAJC5 mutations as cause of adult neuronal ceroid-lipofuscinosis

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

Human fibroblast and stem cell resource from the Dominantly Inherited Alzheimer Network

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation

No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found

Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life

Phenotypic Similarities Between Late-Onset Autosomal Dominant and Sporadic Alzheimer Disease: A Single-Family Case-Control Study

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

SORL1 variants across Alzheimer's disease European American cohorts

TDP-43 A315T mutation in familial motor neuron disease