Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

High Blood Pressure and Risk of Dementia: a Two-Sample Mendelian Randomization study in the UK Biobank

Journal article

SPROVIERO W. et al, (2020), Biological Psychiatry

C9orf72 intermediate expansions of 24-30 repeats are associated with ALS.

Journal article

Iacoangeli A. et al, (2019), Acta Neuropathol Commun, 7

The role of 3 ' UTR variants in Amyotrophic Lateral Sclerosis (ALS) etiology

Conference paper

Eitan C. et al, (2019), EUROPEAN JOURNAL OF HUMAN GENETICS, 27, 319 - 320

ALSgeneScanner: a pipeline for the analysis and interpretation of DNA sequencing data of ALS patients.

Journal article

Iacoangeli A. et al, (2019), Amyotroph Lateral Scler Frontotemporal Degener, 20, 207 - 215

Telomere length is greater in ALS than in controls: a whole genome sequencing study.

Journal article

Al Khleifat A. et al, (2019), Amyotroph Lateral Scler Frontotemporal Degener, 20, 229 - 234

DNAscan: personal computer compatible NGS analysis, annotation and visualisation.

Journal article

Iacoangeli A. et al, (2019), BMC Bioinformatics, 20

Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort.

Journal article

Tazelaar GHP. et al, (2019), Neurobiol Aging, 74, 234.e9 - 234.e15

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

Journal article

Project MinE ALS Sequencing Consortium None., (2018), Eur J Hum Genet, 26, 1537 - 1546

The multistep hypothesis of ALS revisited: The role of genetic mutations.

Journal article

Chiò A. et al, (2018), Neurology, 91, e635 - e642

CHCHD10 variants in amyotrophic lateral sclerosis: Where is the evidence?

Journal article

Project MinE ALS Sequencing Consortium None., (2018), Ann Neurol, 84, 110 - 116

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

Journal article

Nicolas A. et al, (2018), Neuron, 97, 1268 - 1283.e6

Detection of long repeat expansions from PCR-free whole-genome sequence data.

Journal article

Dolzhenko E. et al, (2017), Genome Res, 27, 1895 - 1903

Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials.

Journal article

van Eijk RPA. et al, (2017), Neurology, 89, 1915 - 1922

A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK.

Journal article

Morgan S. et al, (2017), Brain, 140, 1611 - 1618

Load More