Identifying risk loci for FTD and shared genetic component with ALS: a large-scale multi-trait association analysis
出版年份 2023 全文链接
标题
Identifying risk loci for FTD and shared genetic component with ALS: a large-scale multi-trait association analysis
作者
关键词
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出版物
NEUROBIOLOGY OF AGING
Volume -, Issue -, Pages -
出版商
Elsevier BV
发表日期
2023-09-29
DOI
10.1016/j.neurobiolaging.2023.09.017
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Genetic correlation and gene-based pleiotropy analysis for four major neurodegenerative diseases with summary statistics
- (2023) Jiahao Qiao et al. NEUROBIOLOGY OF AGING
- Genetic risk factor clustering within and across neurodegenerative diseases
- (2023) Mathew J Koretsky et al. BRAIN
- Advances and controversies in frontotemporal dementia: diagnosis, biomarkers, and therapeutic considerations
- (2022) Bradley F Boeve et al. LANCET NEUROLOGY
- TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A
- (2022) X. Rosa Ma et al. NATURE
- A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer’s disease and gastrointestinal tract disorders
- (2022) Emmanuel O. Adewuyi et al. Communications Biology
- Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer’s disease risk genes
- (2021) Jeremy Schwartzentruber et al. NATURE GENETICS
- Early anterior cingulate involvement is seen in presymptomatic MAPT P301L mutation carriers
- (2021) Mica T. M. Clarke et al. Alzheimers Research & Therapy
- Pharmacotherapy for Frontotemporal Dementia
- (2021) Rita Khoury et al. CNS DRUGS
- Ultrasensitive Detection of Alzheimer’s Amyloids on a Plasmonic-Gold Platform
- (2021) Hsiao-Fen Han et al. ACS Applied Materials & Interfaces
- 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
- Widespread loss of the silencing epigenetic mark H3K9me3 in astrocytes and neurons along with hippocampal-dependent cognitive impairment in C9orf72 BAC transgenic mice
- (2020) Nur Jury et al. Clinical Epigenetics
- A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine
- (2020) Yanjun Guo et al. Nature Communications
- A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis
- (2020) Dan Zhou et al. NATURE GENETICS
- The role of glia in protein aggregation
- (2020) Qingyun Li et al. NEUROBIOLOGY OF DISEASE
- Multivariate genome-wide analyses of the well-being spectrum
- (2019) Bart M. L. Baselmans et al. NATURE GENETICS
- GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals
- (2019) Valentina Iotchkova et al. NATURE GENETICS
- An update on genetic frontotemporal dementia
- (2019) Caroline V. Greaves et al. JOURNAL OF NEUROLOGY
- Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
- (2019) Cornelis Blauwendraat et al. MOVEMENT DISORDERS
- 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
- Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
- (2019) Katrina M Moore et al. LANCET NEUROLOGY
- Pleiotropic mapping and annotation selection in genome-wide association studies with penalized Gaussian mixture models
- (2018) Ping Zeng et al. BIOINFORMATICS
- Multi-trait analysis of genome-wide association summary statistics using MTAG
- (2018) Patrick Turley et al. NATURE GENETICS
- Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum
- (2018) Celeste M. Karch et al. JAMA Neurology
- UNC13A polymorphism contributes to frontotemporal disease in sporadic amyotrophic lateral sclerosis
- (2018) Katerina Placek et al. NEUROBIOLOGY OF AGING
- Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder
- (2017) Noa Lipstein et al. JOURNAL OF CLINICAL INVESTIGATION
- Functional mapping and annotation of genetic associations with FUMA
- (2017) Kyoko Watanabe et al. Nature Communications
- Therapy and clinical trials in frontotemporal dementia: past, present, and future
- (2016) Richard M. Tsai et al. JOURNAL OF NEUROCHEMISTRY
- Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases
- (2016) Raffaele Ferrari et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Active zone scaffolds differentially accumulate Unc13 isoforms to tune Ca2+ channel–vesicle coupling
- (2016) Mathias A Böhme et al. NATURE NEUROSCIENCE
- The Anterior Cingulate Gyrus and Social Cognition: Tracking the Motivation of Others
- (2016) Matthew A.J. Apps et al. NEURON
- Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits
- (2016) Andrew Bakshi et al. Scientific Reports
- LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
- (2015) Brendan K Bulik-Sullivan et al. NATURE GENETICS
- A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia
- (2015) Raffaele Ferrari et al. NEUROBIOLOGY OF AGING
- Basal ganglia pathology in ALS is associated with neuropsychological deficits
- (2015) Judith Machts et al. NEUROLOGY
- Exposure to ALS-FTD-CSF generates TDP-43 aggregates in glioblastoma cells through exosomes and TNTs-like structure
- (2015) Xuebing Ding et al. Oncotarget
- 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
- Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy
- (2014) A. Montuschi et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Frontotemporal dementia and its subtypes: a genome-wide association study
- (2014) Raffaele Ferrari et al. LANCET NEUROLOGY
- Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
- (2014) Claudia Giambartolomei et al. PLoS Genetics
- Cardiovascular risk factors and frontotemporal dementia: a case–control study
- (2014) Angel Golimstok et al. Translational Neurodegeneration
- Cognitive Disorders and Dementia in CKD: The Neglected Kidney-Brain Axis
- (2013) J.-M. Bugnicourt et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Bradicardia en la demencia frontotemporal
- (2013) A. Robles Bayón et al. NEUROLOGIA
- A Subset-Based Approach Improves Power and Interpretation for the Combined Analysis of Genetic Association Studies of Heterogeneous Traits
- (2012) Samsiddhi Bhattacharjee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits
- (2012) Jian Yang et al. NATURE GENETICS
- Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
- (2011) Katya Rascovsky et al. BRAIN
- FTD and ALS: A Tale of Two Diseases
- (2011) R. Ferrari et al. Current Alzheimer Research
- Phenotypic signatures of genetic frontotemporal dementia
- (2011) Jonathan D. Rohrer et al. CURRENT OPINION IN NEUROLOGY
- Clinical Phenomenology and Neuroimaging Correlates in ALS-FTD
- (2011) Catherine Lomen-Hoerth JOURNAL OF MOLECULAR NEUROSCIENCE
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- GCTA: A Tool for Genome-wide Complex Trait Analysis
- (2010) Jian Yang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
- (2009) Michael A van Es et al. NATURE GENETICS
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