Burden of rare variants in ALS genes influences survival in familial and sporadic ALS-Reference-Cited by-同舟云学术

Burden of rare variants in ALS genes influences survival in familial and sporadic ALS

Published:2017-10 Issue: Volume:58 Page:238.e9-238.e15
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Pang Shirley Yin-Yu,Hsu Jacob Shujui^ORCID,Teo Kay-Cheong,Li Yan,Kung Michelle H.W.,Cheah Kathryn S.E.,Chan Danny,Cheung Kenneth M.C.,Li Miaoxin,Sham Pak-Chung,Ho Shu-Leong

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference35 articles.

1. ALSoD: a user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics;Abel;Hum. Mutat.,2012

2. Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study;Al-Chalabi;Lancet Neurol.,2014

3. An estimate of amyotrophic lateral sclerosis heritability using twin data;Al-Chalabi;J. Neurol. Neurosurg. Psychiatry,2010

4. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis;Brooks;Amyotroph. Lateral Scler. Other Mot. Neuron Disord,2000

5. ALS onset is influenced by the burden of rare variants in known ALS genes;Cady;Ann. Neurol.,2015

Cited by 45 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unraveling the Heterogeneity of ALS—A Call to Redefine Patient Stratification for Better Outcomes in Clinical Trials;Cells;2024-03-05

2. AMPA receptor neurotransmission and therapeutic applications: A comprehensive review of their multifaceted modulation;European Journal of Medicinal Chemistry;2024-02

3. Genetics screening in an Italian cohort of patients with Amyotrophic Lateral Sclerosis: the importance of early testing and its implication;Journal of Neurology;2023-12-19

4. Genomic and transcriptomic advances in amyotrophic lateral sclerosis;Ageing Research Reviews;2023-12

5. Incidence of amyotrophic lateral sclerosis-associated genetic variants: a clinic-based study;Neurological Sciences;2023-11-11