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Partitioning the genetic architecture of amyotrophic lateral sclerosis

https://doi.org/10.1101/505693
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Progressive Supranuclear Palsy
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Resequencing of 29 Candidate Genes in Patients With Familial and Sporadic Amyotrophic Lateral Sclerosis
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Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum
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Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior
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A Functional SNP Catalog of Overlapping miRNA-Binding Sites in Genes Implicated in Prion Disease and Other Neurodegenerative Disorders
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The role of de novo mutations in the development of amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1002/mus.21683openalex-snapshot
Discovery and verification of amyotrophic lateral sclerosis biomarkers by proteomics
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Statistical Analysis of Network Data with R
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FUS-mediated alternative splicing in the nervous system: consequences for ALS and FTLD
inferredcites →https://doi.org/10.1007/s00401-017-1693-yopenalex-snapshot
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia
inferredcites →https://doi.org/10.1007/s10048-008-0164-yopenalex-snapshot
Familial risks for amyotrophic lateral sclerosis and autoimmune diseases
inferredcites →https://doi.org/10.1007/s10522-015-9575-yopenalex-snapshot
Human aging in the post-GWAS era: further insights reveal potential regulatory variants
inferredcites →https://doi.org/10.1016/j.ajhg.2012.02.020openalex-snapshot
Combined Analysis of Genome-wide Association Studies for Crohn Disease and Psoriasis Identifies Seven Shared Susceptibility Loci
inferredcites →https://doi.org/10.1016/j.ajhg.2013.01.001openalex-snapshot
Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors
inferredcites →https://doi.org/10.1016/j.conb.2015.10.008openalex-snapshot
New statistical approaches exploit the polygenic architecture of schizophrenia — implications for the underlying neurobiology
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2017.10.010openalex-snapshot
Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes
inferredcites →https://doi.org/10.1016/j.neuron.2018.02.027openalex-snapshot
Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene
inferredcites →https://doi.org/10.1016/s0140-6736(10)62345-8openalex-snapshot
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
inferredcites →https://doi.org/10.1016/s1474-4422(07)70037-6openalex-snapshot
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
inferredcites →https://doi.org/10.1016/s1474-4422(11)70261-7openalex-snapshot
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
inferredcites →https://doi.org/10.1016/s1474-4422(14)70065-1openalex-snapshot
Frontotemporal dementia and its subtypes: a genome-wide association study
inferredcites →https://doi.org/10.1038/30918openalex-snapshot
Collective dynamics of ‘small-world’ networks
inferredcites →https://doi.org/10.1038/mp.2016.244openalex-snapshot
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium
inferredcites →https://doi.org/10.1038/mp.2016.45openalex-snapshot
Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151)
inferredcites →https://doi.org/10.1038/mp.2017.153openalex-snapshot
Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117)
inferredcites →https://doi.org/10.1038/nature09320openalex-snapshot
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
inferredcites →https://doi.org/10.1038/nature10251openalex-snapshot
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
inferredcites →https://doi.org/10.1038/nature10405openalex-snapshot
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
inferredcites →https://doi.org/10.1038/nature12873openalex-snapshot
Genetics of rheumatoid arthritis contributes to biology and drug discovery
inferredcites →https://doi.org/10.1038/nature13595openalex-snapshot
Biological insights from 108 schizophrenia-associated genetic loci
inferredcites →https://doi.org/10.1038/nature14101openalex-snapshot
Common genetic variants influence human subcortical brain structures
inferredcites →https://doi.org/10.1038/nature14132openalex-snapshot
New genetic loci link adipose and insulin biology to body fat distribution
inferredcites →https://doi.org/10.1038/nature14177openalex-snapshot
Genetic studies of body mass index yield new insights for obesity biology
inferredcites →https://doi.org/10.1038/nature17671openalex-snapshot
Genome-wide association study identifies 74 loci associated with educational attainment
inferredcites →https://doi.org/10.1038/nature18642openalex-snapshot
The genetic architecture of type 2 diabetes
inferredcites →https://doi.org/10.1038/nchembio.118openalex-snapshot
Network pharmacology: the next paradigm in drug discovery
inferredcites →https://doi.org/10.1038/ncomms14774openalex-snapshot
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
inferredcites →https://doi.org/10.1038/ncomms8247openalex-snapshot
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy
inferredcites →https://doi.org/10.1038/ncomms9739openalex-snapshot
Correction: Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci
inferredcites →https://doi.org/10.1038/ng.2560openalex-snapshot
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
inferredcites →https://doi.org/10.1038/ng.2563openalex-snapshot
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
inferredcites →https://doi.org/10.1038/ng.2797openalex-snapshot
Discovery and refinement of loci associated with lipid levels
inferredcites →https://doi.org/10.1038/ng.2802openalex-snapshot
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
inferredcites →https://doi.org/10.1038/ng.3097openalex-snapshot
Defining the role of common variation in the genomic and biological architecture of adult human height
inferredcites →https://doi.org/10.1038/ng.3396openalex-snapshot
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
inferredcites →https://doi.org/10.1038/ng.3412openalex-snapshot
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
inferredcites →https://doi.org/10.1038/ng.3552openalex-snapshot
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
inferredcites →https://doi.org/10.1038/ng.3622openalex-snapshot
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/ng.3680openalex-snapshot
Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants
inferredcites →https://doi.org/10.1038/ng.3736openalex-snapshot
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
inferredcites →https://doi.org/10.1038/ng.3760openalex-snapshot
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
inferredcites →https://doi.org/10.1038/ng.3841openalex-snapshot
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
inferredcites →https://doi.org/10.1038/ng.3888openalex-snapshot
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
inferredcites →https://doi.org/10.1038/ng.543openalex-snapshot
Multiple common variants for celiac disease influencing immune gene expression
inferredcites →https://doi.org/10.1038/ng.571openalex-snapshot
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
inferredcites →https://doi.org/10.1038/ng.859openalex-snapshot
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
inferredcites →https://doi.org/10.1038/ng1017-1558copenalex-snapshot
Erratum: Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence
inferredcites →https://doi.org/10.1038/nn.3801openalex-snapshot
Genetic variability in the regulation of gene expression in ten regions of the human brain
inferredcites →https://doi.org/10.1038/nn.4000openalex-snapshot
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
inferredcites →https://doi.org/10.1038/nrneurol.2011.152openalex-snapshot
Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/nrneurol.2016.182openalex-snapshot
Gene discovery in amyotrophic lateral sclerosis: implications for clinical management
inferredcites →https://doi.org/10.1038/s41467-017-00471-1openalex-snapshot
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/s41467-017-01261-5openalex-snapshot
Functional mapping and annotation of genetic associations with FUMA
inferredcites →https://doi.org/10.1038/s41576-018-0018-xopenalex-snapshot
The personal and clinical utility of polygenic risk scores
inferredcites →https://doi.org/10.1038/s41588-018-0090-3openalex-snapshot
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
inferredcites →https://doi.org/10.1038/s41588-018-0152-6openalex-snapshot
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
inferredcites →https://doi.org/10.1038/s41588-018-0269-7openalex-snapshot
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
inferredcites →https://doi.org/10.1038/s41588-019-0397-8openalex-snapshot
Genome-wide association study identifies 30 loci associated with bipolar disorder
inferredcites →https://doi.org/10.1038/tp.2017.115openalex-snapshot
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia
inferredcites →https://doi.org/10.1056/nejme1709904openalex-snapshot
Targeting Inflammation in Coronary Artery Disease
inferredcites →https://doi.org/10.1056/nejmra1603471openalex-snapshot
Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1073/pnas.0902505106openalex-snapshot
Role of mutant SOD1 disulfide oxidation and aggregation in the pathogenesis of familial ALS
inferredcites →https://doi.org/10.1074/mcp.m500431-mcp200openalex-snapshot
Informatics-assisted Protein Profiling in a Transgenic Mouse Model of Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1080/21678421.2017.1418006openalex-snapshot
An association study between SCFD1 rs10139154 variant and amyotrophic lateral sclerosis in a Chinese cohort
inferredcites →https://doi.org/10.1093/brain/awv268openalex-snapshot
Common polygenic variation enhances risk prediction for Alzheimer’s disease
inferredcites →https://doi.org/10.1093/hmg/ddm361openalex-snapshot
A genome-wide association study of sporadic ALS in a homogenous Irish population
inferredcites →https://doi.org/10.1093/hmg/ddn375openalex-snapshot
Variants of the elongator protein 3 ( ELP3 ) gene are associated with motor neuron degeneration
inferredcites →https://doi.org/10.1093/hmg/dds199openalex-snapshot
Evidence for an oligogenic basis of amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1093/hmg/dds334openalex-snapshot
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls
inferredcites →https://doi.org/10.1093/hmg/ddt587openalex-snapshot
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1093/nar/gkq537openalex-snapshot
The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function
inferredcites →https://doi.org/10.1111/neup.12240openalex-snapshot
Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP‐43‐negative inclusions of C9ORF72‐ALS
inferredcites →https://doi.org/10.1126/science.aaa3650openalex-snapshot
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
inferredcites →https://doi.org/10.1136/jnnp-2016-314411openalex-snapshot
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases
inferredcites →https://doi.org/10.1137/s003614450342480openalex-snapshot
The Structure and Function of Complex Networks
inferredcites →https://doi.org/10.1152/physiolgenomics.00087.2001openalex-snapshot
Molecular signature of late-stage human ALS revealed by expression profiling of postmortem spinal cord gray matter
inferredcites →https://doi.org/10.1161/circulationaha.110.948570openalex-snapshot
Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels
inferredcites →https://doi.org/10.1161/circulationaha.115.015489openalex-snapshot
Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease
inferredcites →https://doi.org/10.1186/gb-2008-9-s1-s4openalex-snapshot
GeneMANIA: a real-time multiple association network integration algorithm for predicting gene function
inferredcites →https://doi.org/10.1186/s13024-018-0270-8openalex-snapshot
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases
inferredcites →https://doi.org/10.1186/s13229-017-0137-9openalex-snapshot
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
inferredcites →https://doi.org/10.1212/wnl.0b013e3182a6cc13openalex-snapshot
Autoimmune disease preceding amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1371/journal.pgen.1003455openalex-snapshot
Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate
inferredcites →https://doi.org/10.1371/journal.pgen.1006125openalex-snapshot
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci
inferredcites →https://doi.org/10.1371/journal.pmed.1002487openalex-snapshot
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies
inferredcites →https://doi.org/10.1371/journal.pmed.1002504openalex-snapshot
Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies
inferredcites →https://doi.org/10.1371/journal.pone.0002051openalex-snapshot
Network ‘Small-World-Ness’: A Quantitative Method for Determining Canonical Network Equivalence
inferredcites →https://doi.org/10.1371/journal.pone.0032768openalex-snapshot
A High-Density Genome-Wide Association Screen of Sporadic ALS in US Veterans
inferredcites →https://doi.org/10.1371/journal.pone.0042956openalex-snapshot
ATXN2 and Its Neighbouring Gene SH2B3 Are Associated with Increased ALS Risk in the Turkish Population
inferredcites →https://doi.org/10.3109/17482960802635397openalex-snapshot
A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.3978/j.issn.2305-5839.2016.01.16openalex-snapshot
Toward precision medicine in amyotrophic lateral sclerosis.
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