Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease
出版年份 2018 全文链接
标题
Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease
作者
关键词
-
出版物
Frontiers in Neuroscience
Volume 12, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2018-04-04
DOI
10.3389/fnins.2018.00209
参考文献
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。- Polygenic risk score of sporadic late-onset Alzheimer's disease reveals a shared architecture with the familial and early-onset forms
- (2018) Carlos Cruchaga et al. Alzheimers & Dementia
- Genetic Determinants of Disease Progression in Alzheimer's Disease
- (2018) Xingbin Wang et al. JOURNAL OF ALZHEIMERS DISEASE
- Leukoencephalopathy-causing CLCN2 mutations are associated with impaired Cl− channel function and trafficking
- (2017) Héctor Gaitán-Peñas et al. JOURNAL OF PHYSIOLOGY-LONDON
- Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
- (2017) Rebecca Sims et al. NATURE GENETICS
- Analysis of neurodegenerative Mendelian genes in clinically diagnosed Alzheimer Disease
- (2017) Maria Victoria Fernández et al. PLoS Genetics
- Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis
- (2016) Sek-Shir Cheong et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees
- (2016) Jae Hoon Sul et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- Assessment of the genetic variance of late-onset Alzheimer's disease
- (2016) Perry G. Ridge et al. NEUROBIOLOGY OF AGING
- A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model
- (2015) Qi Yan et al. HUMAN HEREDITY
- Rare-Variant Association Analysis: Study Designs and Statistical Tests
- (2014) Seunggeung Lee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- FARVAT: a family-based rare variant association test
- (2014) Sungkyoung Choi et al. BIOINFORMATICS
- Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias
- (2014) Gary W. Beecham et al. PLoS Genetics
- Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
- (2014) Holly N Cukier et al. Molecular Autism
- Rare-Variant Extensions of the Transmission Disequilibrium Test: Application to Autism Exome Sequence Data
- (2013) Zongxiao He et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Family-based association tests for sequence data, and comparisons with population-based association tests
- (2013) Iuliana Ionita-Laza et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Multiple Genetic Variant Association Testing by Collapsing and Kernel Methods With Pedigree or Population Structured Data
- (2013) Daniel J. Schaid et al. GENETIC EPIDEMIOLOGY
- GEE-Based SNP Set Association Test for Continuous and Discrete Traits in Family-Based Association Studies
- (2013) Xuefeng Wang et al. GENETIC EPIDEMIOLOGY
- Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
- (2013) Carlos Cruchaga et al. NATURE
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
- (2013) Jean-Charles Lambert et al. NATURE GENETICS
- Rare Variant Analysis for Family-Based Design
- (2013) Gourab De et al. PLoS One
- Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement
- (2013) Rita João Guerreiro et al. JAMA Neurology
- Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies
- (2012) Seunggeun Lee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff
- (2012) Pablo Cingolani et al. FLY
- Genome-wide efficient mixed-model analysis for association studies
- (2012) Xiang Zhou et al. NATURE GENETICS
- Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families
- (2012) Carlos Cruchaga et al. PLoS One
- NALP1/NLRP1 Genetic Variants are Associated With Alzheimer Disease
- (2011) Alessandra Pontillo et al. ALZHEIMER DISEASE & ASSOCIATED DISORDERS
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Population-based and family-based designs to analyze rare variants in complex diseases
- (2011) Rémi Kazma et al. GENETIC EPIDEMIOLOGY
- Family-based designs for genome-wide association studies
- (2011) Jurg Ott et al. NATURE REVIEWS GENETICS
- Genome-Wide Association of Familial Late-Onset Alzheimer's Disease Replicates BIN1 and CLU and Nominates CUGBP2 in Interaction with APOE
- (2011) Ellen M. Wijsman et al. PLoS Genetics
- Testing for an Unusual Distribution of Rare Variants
- (2011) Benjamin M. Neale et al. PLoS Genetics
- Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
- (2010) Alkes L. Price et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A genome-wide map of human genetic interactions inferred from radiation hybrid genotypes
- (2010) A. Lin et al. GENOME RESEARCH
- Variance component model to account for sample structure in genome-wide association studies
- (2010) Hyun Min Kang et al. NATURE GENETICS
- Statistical analysis strategies for association studies involving rare variants
- (2010) Vikas Bansal et al. NATURE REVIEWS GENETICS
- Uncovering the roles of rare variants in common disease through whole-genome sequencing
- (2010) Elizabeth T. Cirulli et al. NATURE REVIEWS GENETICS
- A Generalized Family-Based Association Test for Dichotomous Traits
- (2009) Wei-Min Chen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Two novelCLCN2mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy
- (2009) C��cile Saint-Martin et al. HUMAN MUTATION
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- Human genetic variation and its contribution to complex traits
- (2009) Kelly A. Frazer et al. NATURE REVIEWS GENETICS
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data
- (2008) Bingshan Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
- (2008) Sergio E. Baranzini et al. HUMAN MOLECULAR GENETICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search