SwePub - search: WFRF:(Al Chalabi Ammar)

Enumeration	Reference	Cover
1.	Sproviero, William (author) ATXN2 trinucleotide repeat length correlates with risk of ALS 2017 In: Neurobiology of Aging. - 0197-4580. ; 51, 178.e1-178.e9 swepub:Mat__t	Read full
2.	Dilliott, Allison A. (author) Clinical testing panels for ALS 2023 In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. - 2167-8421. swepub:Mat__t	Read full
3.	Marriott, Heather (author) Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS 2024 In: Annals of Clinical and Translational Neurology. swepub:Mat__t	Read full
4.	van Rheenen, Wouter (author) Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 2021 In: Nature Genetics. - 1061-4036. ; 53:12, 1636-1648 swepub:Mat__t	Read full
5.	Iacoangeli, Alfredo (author) SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed 2021 In: Brain Communications. ; 3:4 swepub:Mat__t	Read full
6.	Mehta, Puja R. (author) The impact of age on genetic testing decisions in amyotrophic lateral sclerosis 2022 In: Brain. - 0006-8950. ; 145:12, 4440-4447 swepub:Mat__t	Read full
7.	Adey, Brett N. (author) Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival 2023 In: Frontiers in Cellular Neuroscience. ; 17 swepub:Mat__t	Read full
8.	Gould, Rebecca (author) Acceptance and Commitment Therapy for people living with motor neuron disease 2023 In: Pilot and Feasibility Studies. ; 9 swepub:Mat__t	Read full
9.	Salmon, Kristiana (author) The importance of offering early genetic testing in everyone with amyotrophic lateral sclerosis 2022 In: Brain. - 0006-8950. ; 145:4, 1207-1210 swepub:Mat__t	Read full
10.	Lahrouchi, Najim (author) Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome 2020 In: Circulation. - 0009-7322. ; 142:4, 324-338 swepub:Mat__t	Read full
11.	Abel, Olubunmi (author) Credibility analysis of putative disease-causing genes using bioinformatics 2013 In: PLoS ONE. - 1932-6203. ; 8:6, e64899 swepub:Mat__t	Read full
12.	Diekstra, Frank P. (author) Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS 2012 In: PLoS ONE. - 1932-6203. ; 7:4, e35333 swepub:Mat__t	Read full
13.	Al-Chalabi, Ammar (author) July 2017 ENCALS statement on edaravone 2017 In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. - 2167-8421. ; 18:7-8, 471-474 swepub:Mat__t	Read full
14.	Abel, Olubunmi (author) Development of a Smartphone App for a Genetics Website 2013 In: JMIR mhealth and uhealth. ; 1:2 swepub:Mat__t	Read full
15.	Van Damme, Philip (author) European academy of neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European reference network for neuromuscular diseases (ERN EURO-NMD) 2024 In: European Journal of Neurology. - 1351-5101. swepub:Mat__t	Read full
16.	Bento-Abreu, Andre (author) Elongator subunit 3 (ELP3) modifies ALS through tRNA modification 2018 In: Human Molecular Genetics. - 0964-6906. ; 27:7, 1276-1289 swepub:Mat__t	Read full
17.	Weeks, Kirsty R (author) Needs and preferences for psychological interventions of people with motor neuron disease 2019 In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. - 2167-8421. ; 20:7-8, 521-531 swepub:Mat__t	Read full
18.	Moisse, Matthieu (author) The Effect of SMN Gene Dosage on ALS Risk and Disease Severity 2021 In: Annals of Neurology. - 0364-5134. swepub:Mat__t	Read full
19.	Benatar, Michael (author) Preventing amyotrophic lateral sclerosis 2022 In: Brain. - 0006-8950. ; 145:1, 27-44 swepub:Mat__t	Read full
20.	Kliest, Tessa (author) Clinical trials in pediatric ALS: a TRICALS feasibility study 2022 In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. - 2167-8421. ; 23:7-8, 481-488 swepub:Mat__t	Read full
21.	Tazelaar, Gijs H.P. (author) Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis 2023 In: Neurobiology of Aging. - 0197-4580. ; 122, 76-87 swepub:Mat__t	Read full
22.	Gould, Rebecca L. (author) A randomised controlled trial of acceptance and commitment therapy plus usual care compared to usual care alone for improving psychological health in people with motor neuron disease (COMMEND) 2022 In: BMC Neurology. ; 22 swepub:Mat__t	Read full
23.	Van Daele, Sien Hilde (author) Genetic variability in sporadic amyotrophic lateral sclerosis 2023 In: Brain. - 0006-8950. ; 146:9, 3760-3769 swepub:Mat__t	Read full
24.	Gould, Rebecca L. (author) Acceptance and Commitment Therapy plus usual care for improving quality of life in people with motor neuron disease (COMMEND) 2024 In: The Lancet. - 0140-6736. ; 403:10442, 2381-2394 swepub:Mat__t	Read full

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