Lista de obras -

A standard operating procedure for King's ALS clinical staging

artículo científico publicado en 2019

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

artículo científico publicado en 2019

An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates

artículo científico publicado en 2021

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

artículo científico publicado en 2021

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

artículo científico publicado en 2022

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

artículo científico

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

artículo científico

Comparison of the King's and MiToS staging systems for ALS.

artículo científico publicado en 2017

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

artículo científico publicado en 2017

Harnessing the potential of machine learning and artificial intelligence for dementia research

artículo científico publicado en 2023

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

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

artículo científico publicado en 2022

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

artículo científico publicado en 2019

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

UK case control study of smoking and risk of amyotrophic lateral sclerosis

artículo científico publicado en 2020

What causes amyotrophic lateral sclerosis?

artículo científico publicado en 2017

Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment bias

artículo científico publicado en 2018

Lista de obras de

A standard operating procedure for King's ALS clinical staging

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

An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

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

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

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

Comparison of the King's and MiToS staging systems for ALS.

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

Harnessing the potential of machine learning and artificial intelligence for dementia research

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

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

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

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

UK case control study of smoking and risk of amyotrophic lateral sclerosis

What causes amyotrophic lateral sclerosis?

Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment bias