相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types
Sara Saez-Atienzar et al.
SCIENCE ADVANCES (2021)
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Wouter van Rheenen et al.
NATURE GENETICS (2021)
mTOR-mediated phosphorylation of VAMP8 and SCFD1 regulates autophagosome maturation
Hong Huang et al.
NATURE COMMUNICATIONS (2021)
Novel Insight Into the Role of Immune Dysregulation in Amyotrophic Lateral Sclerosis Based on Bioinformatic Analysis
Yongzhi Xie et al.
FRONTIERS IN NEUROSCIENCE (2021)
SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed
Alfredo Iacoangeli et al.
BRAIN COMMUNICATIONS (2021)
Novel roles of phosphoinositides in signaling, lipid transport, and disease
Gerald R. V. Hammond et al.
CURRENT OPINION IN CELL BIOLOGY (2020)
Polygenic risk scores: from research tools to clinical instruments
Cathryn M. Lewis et al.
GENOME MEDICINE (2020)
Gene Set Analysis: Challenges, Opportunities, and Future Research
Farhad Maleki et al.
FRONTIERS IN GENETICS (2020)
Molecular and Cellular Mechanisms Affected in ALS
Laura Le Gall et al.
JOURNAL OF PERSONALIZED MEDICINE (2020)
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis
Ryoichi Nakamura et al.
COMMUNICATIONS BIOLOGY (2020)
What Can Machine Learning Approaches in Genomics Tell Us about the Molecular Basis of Amyotrophic Lateral Sclerosis?
Christina Vasilopoulou et al.
JOURNAL OF PERSONALIZED MEDICINE (2020)
Summary-data-based Mendelian randomization prioritizes potential druggable targets for multiple sclerosis
Benjamin M. Jacobs et al.
BRAIN COMMUNICATIONS (2020)
Respiratory Failure in Amyotrophic Lateral Sclerosis
Shannon Niedermeyer et al.
CHEST (2019)
Genetics of amyotrophic lateral sclerosis: A review
Stephane Mathis et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2019)
Benefits and limitations of genome-wide association studies
Vivian Tam et al.
NATURE REVIEWS GENETICS (2019)
g:Profiler: a web server for functional enrichment analysis and conversions of gene lists (2019 update)
Uku Raudvere et al.
NUCLEIC ACIDS RESEARCH (2019)
A Systematic Review of Suggested Molecular Strata, Biomarkers and Their Tissue Sources in ALS
Udaya Geetha Vijayakumar et al.
FRONTIERS IN NEUROLOGY (2019)
PRSice-2: Polygenic Risk Score software for biobank-scale data
Shing Wan Choi et al.
GIGASCIENCE (2019)
Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications
Ruth Chia et al.
LANCET NEUROLOGY (2018)
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Aude Nicolas et al.
NEURON (2018)
A Genome-wide Expression Association Analysis Identifies Genes and Pathways Associated with Amyotrophic Lateral Sclerosis
Yanan Du et al.
CELLULAR AND MOLECULAR NEUROBIOLOGY (2018)
Personalized Medicine and Molecular Interaction Networks in Amyotrophic Lateral Sclerosis (ALS): Current Knowledge
Stephen Morgan et al.
JOURNAL OF PERSONALIZED MEDICINE (2018)
Polymorphism of rs3737597 in DISC1 Gene on Chromosome 1q42.2 in sALS Patients: a Chinese Han Population Case-Control Study
Libin Deng et al.
MOLECULAR NEUROBIOLOGY (2017)
Gene discovery in amyotrophic lateral sclerosis: implications for clinical management
Ammar Al-Chalabi et al.
NATURE REVIEWS NEUROLOGY (2017)
DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants
Janet Pinero et al.
NUCLEIC ACIDS RESEARCH (2017)
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)
Jacqueline MacArthur et al.
NUCLEIC ACIDS RESEARCH (2017)
KEGG: new perspectives on genomes, pathways, diseases and drugs
Minoru Kanehisa et al.
NUCLEIC ACIDS RESEARCH (2017)
Genetic screening in sporadic ALS and FTD
Martin R. Turner et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2017)
Functional mapping and annotation of genetic associations with FUMA
Kyoko Watanabe et al.
NATURE COMMUNICATIONS (2017)
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis
Beben Benyamin et al.
NATURE COMMUNICATIONS (2017)
Amyotrophic lateral sclerosis
Orla Hardiman et al.
NATURE REVIEWS DISEASE PRIMERS (2017)
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa
Laramie Duncan et al.
AMERICAN JOURNAL OF PSYCHIATRY (2017)
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Wouter van Rheenen et al.
NATURE GENETICS (2016)
The statistical properties of gene-set analysis
Christiaan A. de Leeuw et al.
NATURE REVIEWS GENETICS (2016)
Projected increase in amyotrophic lateral sclerosis from 2015 to 2040
Karissa C. Arthur et al.
NATURE COMMUNICATIONS (2016)
Gene set analysis: A step-by-step guide
Michael A. Mooney et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2015)
Genome-wide pathway analysis in amyotrophic lateral sclerosis
Y. H. Lee et al.
GENETICS AND MOLECULAR RESEARCH (2015)
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis
Po-Ru Loh et al.
NATURE GENETICS (2015)
Genome-Wide Detection and Analysis of Multifunctional Genes
Yuri Pritykin et al.
PLOS COMPUTATIONAL BIOLOGY (2015)
The Molecular Signatures Database Hallmark Gene Set Collection
Arthur Liberzon et al.
CELL SYSTEMS (2015)
Pathway Analysis of Two Amyotrophic Lateral Sclerosis GWAS Highlights Shared Genetic Signals with Alzheimer's Disease and Parkinson's Disease
Hong Shang et al.
MOLECULAR NEUROBIOLOGY (2015)
State of play in amyotrophic lateral sclerosis genetics
Alan E. Renton et al.
NATURE NEUROSCIENCE (2014)
A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations
Tong Xie et al.
NEUROBIOLOGY OF AGING (2014)
Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool
Edward Y. Chen et al.
BMC BIOINFORMATICS (2013)
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra et al.
NATURE GENETICS (2013)
Global Epidemiology of Amyotrophic Lateral Sclerosis: A Systematic Review of the Published Literature
A. Chio et al.
NEUROEPIDEMIOLOGY (2013)
WEB-based GEne SeT AnaLysis Toolkit (WebGestalt): update 2013
Jing Wang et al.
NUCLEIC ACIDS RESEARCH (2013)
Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
Peter M. Andersen et al.
NATURE REVIEWS NEUROLOGY (2011)
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Alan E. Renton et al.
NEURON (2011)
ICSNPathway: identify candidate causal SNPs and pathways from genome-wide association study by one analytical framework
Kunlin Zhang et al.
NUCLEIC ACIDS RESEARCH (2011)
Successes of Genome-wide Association Studies
Robert J. Klein et al.
CELL (2010)
Comparisons of Multi-Marker Association Methods to Detect Association Between a Candidate Region and Disease
David H. Ballard et al.
GENETIC EPIDEMIOLOGY (2010)
Prognostic factors in ALS: A critical review
Adriano Chio et al.
AMYOTROPHIC LATERAL SCLEROSIS (2009)
Strategies and issues in the detection of pathway enrichment in genome-wide association studies
Mun-Gwan Hong et al.
HUMAN GENETICS (2009)
Genetics of motor neuron disorders: new insights into pathogenic mechanisms
Patrick A. Dion et al.
NATURE REVIEWS GENETICS (2009)
Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists
Da Wei Huang et al.
NUCLEIC ACIDS RESEARCH (2009)
A genome-wide association study of sporadic ALS in a homogenous Irish population
Simon Cronin et al.
HUMAN MOLECULAR GENETICS (2008)
Pathway-based approaches for analysis of genomewide association studies
Kai Wang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Analyzing gene expression data in terms of gene sets:: methodological issues
Jelle J. Goeman et al.
BIOINFORMATICS (2007)
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls:: first stage analysis and public release of data
Jennifer C. Schymick et al.
LANCET NEUROLOGY (2007)
Depletion of reduced glutathione enhances motor neuron degeneration in vitro and in vivo
L. Chi et al.
NEUROSCIENCE (2007)
Neuratrophin-regulated signalling pathways
Louis F. Reichardt
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2006)
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
A Subramanian et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Structure-based functional analysis reveals a role for the SM protein Sly1p in retrograde transport to the endoplasmic reticulum
YJ Li et al.
MOLECULAR BIOLOGY OF THE CELL (2005)
Medical progress: Amyotrophic lateral sclerosis.
LP Rowland et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)
分享论文
