Search filters

List of works by Jonathan D Glass

50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis

article

A common haplotype within the PON1 promoter region is associated with sporadic ALS.

scientific article published on October 2008

A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis

scientific article

A proteomic network approach across the ALS-FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brain.

scientific article published on 30 November 2017

Aberrant septin 11 is associated with sporadic frontotemporal lobar degeneration ⬇️

scientific article published on November 29, 2011

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.

scientific article

Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell lines

scientific article published on 03 February 2022

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis

scientific article published on 31 May 2016

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

scientific article published on 15 April 2016

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

scientific article published on October 2010

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

preprint

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

scholarly article

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

scientific article

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

scientific article

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

scientific article published on 19 February 2015

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

scientific article published on 22 October 2014

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

scientific article published in March 2018

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

scientific article published on 09 February 2019

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

scientific article published on 25 July 2016

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

scientific article

Hypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial

scientific article

Identifying patterns in amyotrophic lateral sclerosis progression from sparse longitudinal data

scientific article published on 08 September 2022

Integrated proteomics reveals brain-based cerebrospinal fluid biomarkers in asymptomatic and symptomatic Alzheimer's disease

scientific article published on 21 October 2020

Late-stage CTE pathology in a retired soccer player with dementia

scientific article

Localization of a toxic form of superoxide dismutase 1 protein to pathologically affected tissues in familial ALS ⬇️

scientific article published on March 19, 2012

Loss of dopamine phenotype among midbrain neurons in Lesch-Nyhan disease

scientific article published on 20 June 2014

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

scientific article

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

scientific article

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

scientific article published on 26 November 2020

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis

scientific article

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

scientific article

Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

Protecting the nerve terminals.

scientific article

Quantitative Analysis of the Detergent-Insoluble Brain Proteome in Frontotemporal Lobar Degeneration Using SILAC Internal Standards ⬇️

scientific article published on April 4, 2012

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

scientific article

Reconsidering the causality of TIA1 mutations in ALS.

scientific article published on 13 December 2017

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

scientific article published on 28 January 2022

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

Transplantation of spinal cord-derived neural stem cells for ALS: Analysis of phase 1 and 2 trials

scientific article published on 29 June 2016

Very early activation of m-calpain in peripheral nerve during Wallerian degeneration

scientific article (publication date: 15 April 2002)

Paulina is supported by:

About Paulina

Help