Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis
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Title
Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis
Authors
Keywords
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Journal
BMC Medicine
Volume 20, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2022-06-27
DOI
10.1186/s12916-022-02411-3
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Note: Only part of the references are listed.- TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A
- (2022) Anna-Leigh Brown et al. NATURE
- TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A
- (2022) X. Rosa Ma et al. NATURE
- The Effect of SMN Gene Dosage on ALS Risk and Disease Severity
- (2021) Matthieu Moisse et al. ANNALS OF NEUROLOGY
- Novel variants and cellular studies on patients’ primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis
- (2021) Serena Lattante et al. HUMAN MOLECULAR GENETICS
- NEK1 mutations and the risk of amyotrophic lateral sclerosis (ALS): a meta-analysis
- (2021) Luqing Yao et al. NEUROLOGICAL SCIENCES
- Association of Single Nucleotide Polymorphism at rs2275294 in the ZNF512B Gene with Prognosis in Amyotrophic Lateral Sclerosis
- (2021) Haixia Jiang et al. NEUROMOLECULAR MEDICINE
- Risk factors for cognitive impairment in amyotrophic lateral sclerosis: a systematic review and meta-analysis
- (2021) Tianmi Yang et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Novel STMN2 Variant Linked to Amyotrophic Lateral Sclerosis Risk and Clinical Phenotype
- (2021) Frances Theunissen et al. Frontiers in Aging Neuroscience
- Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population
- (2021) Yong-Ping Chen et al. JOURNAL OF MEDICAL GENETICS
- Genotype-phenotype correlations in a chinese population with familial amyotrophic lateral sclerosis
- (2021) WenChao Liu et al. NEUROLOGICAL RESEARCH
- Cardiac troponin T is elevated and increases longitudinally in ALS patients
- (2021) Ulf Kläppe et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Humoral response to neurofilaments and dipeptide repeats in ALS progression
- (2021) Fabiola Puentes et al. Annals of Clinical and Translational Neurology
- Influence of GSTP1 rs1695 polymorphism on survival in male patients’ amyotrophic lateral sclerosis: a genetic association study in Brazilian population
- (2021) Jéssica Barletto de Sousa Barros et al. MOLECULAR BIOLOGY REPORTS
- Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
- (2021) Wouter van Rheenen et al. NATURE GENETICS
- Predictors of survival in patients with amyotrophic lateral sclerosis: A large meta-analysis
- (2021) Wei-Ming Su et al. EBioMedicine
- Neurofilament light chain and C reactive protein explored as predictors of survival in amyotrophic lateral sclerosis
- (2020) Maxim De Schaepdryver et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Validation of serum neurofilaments as prognostic and potential pharmacodynamic biomarkers for ALS
- (2020) Michael Benatar et al. NEUROLOGY
- The Distinct Traits of the UNC13A Polymorphism in Amyotrophic Lateral Sclerosis
- (2020) Harold H. G. Tan et al. ANNALS OF NEUROLOGY
- ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of function
- (2020) Josephine J. Wu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- ALS Genetics: Gains, Losses, and Implications for Future Therapies
- (2020) Garam Kim et al. NEURON
- Comparison of Phenotypic Characteristics and Prognosis Between Black and White Patients in a Tertiary ALS Clinic
- (2020) David Brand et al. NEUROLOGY
- The complement C7 variant rs3792646 is associated with amyotrophic lateral sclerosis in a Han Chinese population
- (2020) Ji He et al. NEUROBIOLOGY OF AGING
- Artificial MicroRNAs Targeting C9orf72 Can Reduce Accumulation of Intra-nuclear Transcripts in ALS and FTD Patients
- (2019) Raygene Martier et al. Molecular Therapy-Nucleic Acids
- PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival
- (2019) Federico Verde et al. NEUROLOGICAL SCIENCES
- Comparative Analysis of C9orf72 and Sporadic Disease in a Large Multicenter ALS Population: The Effect of Male Sex on Survival of C9orf72 Positive Patients
- (2019) Francesca Trojsi et al. Frontiers in Neuroscience
- UNC13A variant rs12608932 is associated with increased risk of amyotrophic lateral sclerosis and reduced patient survival: a meta-analysis
- (2019) Baiyuan Yang et al. NEUROLOGICAL SCIENCES
- Prospective natural history study of C9orf72 ALS clinical characteristics and biomarkers
- (2019) Alexander J. Cammack et al. NEUROLOGY
- Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis
- (2019) Marcel Naumann et al. Annals of Clinical and Translational Neurology
- C9orf72expansion is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis
- (2018) Gabriel Miltenberger-Miltenyi et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications
- (2018) Ruth Chia et al. LANCET NEUROLOGY
- KATP Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis
- (2018) José M. Vidal-Taboada et al. MOLECULAR NEUROBIOLOGY
- Association between TBK1 mutations and risk of amyotrophic lateral sclerosis/frontotemporal dementia spectrum: a meta-analysis
- (2018) Rongrong Cui et al. NEUROLOGICAL SCIENCES
- Meta-analysis of the association between ZNF512B polymorphism rs2275294 and risk of amyotrophic lateral sclerosis
- (2018) Pingping Ning et al. NEUROLOGICAL SCIENCES
- NEK1 loss-of-function mutation induces DNA damage accumulation in ALS patient-derived motoneurons
- (2018) Julia Higelin et al. Stem Cell Research
- Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosis
- (2018) Elaheh Ekhtiari Bidhendi et al. ACTA NEUROPATHOLOGICA
- The clinical assessment of amyotrophic lateral sclerosis patients’ prognosis by ZNF512B gene, neck flexor muscle power score and body mass index (BMI)
- (2018) Chun-Jiang Yu et al. BMC Neurology
- Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis
- (2017) Zhang-Yu Zou et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort
- (2017) Xinglong Yang et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Liver X Receptor Genes Variants Modulate ALS Phenotype
- (2017) Kevin Mouzat et al. MOLECULAR NEUROBIOLOGY
- Common polymorphisms of chemokine (C-X3-C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population-based study
- (2017) Andrea Calvo et al. MUSCLE & NERVE
- Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice
- (2017) Lindsay A. Becker et al. NATURE
- Amyotrophic Lateral Sclerosis
- (2017) Robert H. Brown et al. NEW ENGLAND JOURNAL OF MEDICINE
- Recognition of c9orf72 Mutant RNA by Single-Stranded Silencing RNAs
- (2017) Jiaxin Hu et al. Nucleic Acid Therapeutics
- The Analysis of Two BDNF Polymorphisms G196A/C270T in Chinese Sporadic Amyotrophic Lateral Sclerosis
- (2017) Lianping Xu et al. Frontiers in Aging Neuroscience
- TBK1: a new player in ALS linking autophagy and neuroinflammation
- (2017) James A. Oakes et al. Molecular Brain
- Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden
- (2017) David Czell et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China
- (2017) Chuzheng Pan et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Prognostic value of clinical and electrodiagnostic parameters at time of diagnosis in patients with amyotrophic lateral sclerosis
- (2017) Wendeline Reniers et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- The Role of Dipeptide Repeats in C9ORF72-Related ALS-FTD
- (2017) Brian D. Freibaum et al. Frontiers in Molecular Neuroscience
- Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis
- (2016) Hajer El Oussini et al. ACTA NEUROPATHOLOGICA
- The frontotemporal syndrome of ALS is associated with poor survival
- (2016) Rosanne Govaarts et al. JOURNAL OF NEUROLOGY
- Influence of cigarette smoking on ALS outcome: a population-based study
- (2016) Andrea Calvo et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Defining SOD1 ALS natural history to guide therapeutic clinical trial design
- (2016) Taha Bali et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Multiplex analyte assays to characterize different dementias: brain inflammatory cytokines in poststroke and other dementias
- (2016) Aiqing Chen et al. NEUROBIOLOGY OF AGING
- Comparative analysis of C9orf72 and sporadic disease in an ALS clinic population
- (2016) Mfon E. Umoh et al. NEUROLOGY
- ALS-associated mutant FUS induces selective motor neuron degeneration through toxic gain of function
- (2016) Aarti Sharma et al. Nature Communications
- CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
- (2016) Kelly L. Williams et al. Nature Communications
- Association of a Locus in theCAMTA1Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis
- (2016) Isabella Fogh et al. JAMA Neurology
- The PRISMA Extension Statement for Reporting of Systematic Reviews Incorporating Network Meta-analyses of Health Care Interventions: Checklist and Explanations
- (2015) Brian Hutton et al. ANNALS OF INTERNAL MEDICINE
- UNC13A confers risk for sporadic ALS and influences survival in a Spanish cohort
- (2015) Jose Manuel Vidal-Taboada et al. JOURNAL OF NEUROLOGY
- C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis
- (2015) Jonathan D Rohrer et al. LANCET NEUROLOGY
- Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
- (2015) Axel Freischmidt et al. NATURE NEUROSCIENCE
- ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry
- (2015) Giuseppe Borghero et al. NEUROBIOLOGY OF AGING
- De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
- (2015) Annemarie Hübers et al. NEUROBIOLOGY OF AGING
- C9orf72andUNC13Aare shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome-wide meta-analysis
- (2014) Frank P. Diekstra et al. ANNALS OF NEUROLOGY
- Genetic architecture of ALS in Sardinia
- (2014) Giuseppe Borghero et al. NEUROBIOLOGY OF AGING
- Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
- (2014) Perry T.C. van Doormaal et al. NEUROBIOLOGY OF AGING
- Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers
- (2014) Marka van Blitterswijk et al. NEUROBIOLOGY OF AGING
- ATXN2 polyQ intermediate repeats are a modifier of ALS survival
- (2014) A. Chio et al. NEUROLOGY
- CX3CR1 Is a Modifying Gene of Survival and Progression in Amyotrophic Lateral Sclerosis
- (2014) Alan Lopez-Lopez et al. PLoS One
- Intermediate CAG Repeat Expansion in the ATXN2 Gene Is a Unique Genetic Risk Factor for ALS−A Systematic Review and Meta-Analysis of Observational Studies
- (2014) Ming-Dong Wang et al. PLoS One
- Indirect Treatment Comparison/Network Meta-Analysis Study Questionnaire to Assess Relevance and Credibility to Inform Health Care Decision Making: An ISPOR-AMCP-NPC Good Practice Task Force Report
- (2014) Jeroen P. Jansen et al. VALUE IN HEALTH
- Value of18Fluorodeoxyglucose–Positron-Emission Tomography in Amyotrophic Lateral Sclerosis
- (2014) Koen Van Laere et al. JAMA Neurology
- Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trial
- (2013) Merit E Cudkowicz et al. LANCET NEUROLOGY
- Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study
- (2013) Sarah Debray et al. NEUROBIOLOGY OF AGING
- UBQLN2 mutations are not a frequent cause of amyotrophic lateral sclerosis in Ireland
- (2013) Russell Lewis McLaughlin et al. NEUROBIOLOGY OF AGING
- Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
- (2012) A. Chio et al. BRAIN
- NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis
- (2012) Hylke M. Blauw et al. HUMAN MOLECULAR GENETICS
- Analysis of theC9orf72Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide
- (2012) Alberto García-Redondo et al. HUMAN MUTATION
- ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics
- (2012) Olubunmi Abel et al. HUMAN MUTATION
- Phenotype difference between ALS patients with expanded repeats inC9ORF72and patients with mutations in other ALS-related genes
- (2012) Stéphanie Millecamps et al. JOURNAL OF MEDICAL GENETICS
- Cognitive decline and reduced survival inC9orf72expansion frontotemporal degeneration and amyotrophic lateral sclerosis
- (2012) David J Irwin et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
- (2012) Susan Byrne et al. LANCET NEUROLOGY
- C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population
- (2012) Mario Sabatelli et al. NEUROBIOLOGY OF AGING
- C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect
- (2012) Antonia Ratti et al. NEUROBIOLOGY OF AGING
- UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study
- (2012) Adriano Chiò et al. NEUROBIOLOGY OF AGING
- Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease
- (2012) S. Lattante et al. NEUROLOGY
- Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations
- (2012) P. Corcia et al. NEUROLOGY
- Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases
- (2012) W. van Rheenen et al. NEUROLOGY
- ATXN2 and Its Neighbouring Gene SH2B3 Are Associated with Increased ALS Risk in the Turkish Population
- (2012) Suna Lahut et al. PLoS One
- Association of Long ATXN2 CAG Repeat Sizes With Increased Risk of Amyotrophic Lateral Sclerosis
- (2011) Hussein Daoud et al. ARCHIVES OF NEUROLOGY
- ATXN-2 CAG repeat expansions are interrupted in ALS patients
- (2011) Lucia Corrado et al. HUMAN GENETICS
- Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients
- (2011) T. Lee et al. HUMAN MOLECULAR GENETICS
- Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis
- (2011) Hélène Blasco et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
- (2011) Magdalini Polymenidou et al. NATURE NEUROSCIENCE
- Ataxin-2 intermediate-length polyglutamine: a possible risk factor for Chinese patients with amyotrophic lateral sclerosis
- (2011) YongPing Chen et al. NEUROBIOLOGY OF AGING
- UNC13A is a modifier of survival in amyotrophic lateral sclerosis
- (2011) Frank P. Diekstra et al. NEUROBIOLOGY OF AGING
- Genetic Variation in KIFAP3 Is Associated with an Upper Motor Neuron-Predominant Phenotype in Amyotrophic Lateral Sclerosis
- (2011) V. Orsetti et al. Neurodegenerative Diseases
- Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2
- (2011) P. Van Damme et al. NEUROLOGY
- Network meta-analysis on the log-hazard scale, combining count and hazard ratio statistics accounting for multi-arm trials: A tutorial
- (2010) Beth S Woods et al. BMC Medical Research Methodology
- Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses
- (2010) Andreas Stang EUROPEAN JOURNAL OF EPIDEMIOLOGY
- Graphical methods and numerical summaries for presenting results from multiple-treatment meta-analysis: an overview and tutorial
- (2010) Georgia Salanti et al. JOURNAL OF CLINICAL EPIDEMIOLOGY
- SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations
- (2010) S. Millecamps et al. JOURNAL OF MEDICAL GENETICS
- Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis
- (2010) S. Byrne et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Factors Affecting Survival of Patients with Neurodegenerative Disease
- (2010) Kyle Steenland et al. NEUROEPIDEMIOLOGY
- Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients
- (2010) B. J. Traynor et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Checking consistency in mixed treatment comparison meta-analysis
- (2010) S. Dias et al. STATISTICS IN MEDICINE
- Interaction between PON1 and population density in amyotrophic lateral sclerosis
- (2009) Frank P. Diekstra et al. NEUROREPORT
- Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis
- (2009) J. E. Landers et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Association of APOE with age at onset of sporadic amyotrophic lateral sclerosis
- (2008) Henrik Zetterberg et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
- (2008) Vivianna M Van Deerlin et al. LANCET NEUROLOGY
- Progranulin genetic variability contributes to amyotrophic lateral sclerosis
- (2008) K. Sleegers et al. NEUROLOGY
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