标题
Rare and low-frequency coding variants alter human adult height
作者
关键词
-
出版物
NATURE
Volume 542, Issue 7640, Pages 186-190
出版商
Springer Nature
发表日期
2017-01-31
DOI
10.1038/nature21039
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。- Mutations in pregnancy-associated plasma protein A2 cause short stature due to low IGF-I availability
- (2016) A. Dauber et al. EMBO Molecular Medicine
- The genetic architecture of type 2 diabetes
- (2016) Christian Fuchsberger et al. NATURE
- Fast and Rigorous Computation of Gene and Pathway Scores from SNP-Based Summary Statistics
- (2016) David Lamparter et al. PLoS Computational Biology
- Loss of SFRP4 Alters Body Size, Food Intake, and Energy Expenditure in Diet-Induced Obese Male Mice
- (2015) Jason Mastaitis et al. ENDOCRINOLOGY
- Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels
- (2015) Fabrice Danjou et al. NATURE GENETICS
- Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers
- (2015) Carlo Sidore et al. NATURE GENETICS
- A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
- (2015) Majid Nikpay et al. NATURE GENETICS
- Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
- (2015) Jian Yang et al. NATURE GENETICS
- Gene expression analysis identifies global gene dosage sensitivity in cancer
- (2015) Rudolf S N Fehrmann et al. NATURE GENETICS
- LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
- (2015) Brendan K Bulik-Sullivan et al. NATURE GENETICS
- Efficient Bayesian mixed-model analysis increases association power in large cohorts
- (2015) Po-Ru Loh et al. NATURE GENETICS
- Biological interpretation of genome-wide association studies using predicted gene functions
- (2015) Tune H. Pers et al. Nature Communications
- RAREMETAL: fast and powerful meta-analysis for rare variants
- (2014) S. Feng et al. BIOINFORMATICS
- Fast and accurate imputation of summary statistics enhances evidence of functional enrichment
- (2014) Bogdan Pasaniuc et al. BIOINFORMATICS
- Stanniocalcin-2 Inhibits Mammalian Growth by Proteolytic Inhibition of the Insulin-like Growth Factor Axis
- (2014) Malene R. Jepsen et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- A polygenic burden of rare disruptive mutations in schizophrenia
- (2014) Shaun M. Purcell et al. NATURE
- Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes
- (2014) Valgerdur Steinthorsdottir et al. NATURE GENETICS
- Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
- (2014) Jason Flannick et al. NATURE GENETICS
- Defining the role of common variation in the genomic and biological architecture of adult human height
- (2014) Andrew R Wood et al. NATURE GENETICS
- Quality control and conduct of genome-wide association meta-analyses
- (2014) Thomas W Winkler et al. Nature Protocols
- Searching for missing heritability: Designing rare variant association studies
- (2014) O. Zuk et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Glycosyltransferase GLT8D2 Positively Regulates ApoB100 Protein Expression in Hepatocytes
- (2013) Hong-Shan Wei et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Meta-analysis of gene-level tests for rare variant association
- (2013) Dajiang J Liu et al. NATURE GENETICS
- Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium
- (2013) Megan L. Grove et al. PLoS One
- zCall: a rare variant caller for array-based genotyping
- (2012) Jacqueline I. Goldstein et al. BIOINFORMATICS
- Cohort Profile: TwinsUK and Healthy Ageing Twin Study
- (2012) A. Moayyeri et al. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
- Cohort Profile: The ‘Children of the 90s’—the index offspring of the Avon Longitudinal Study of Parents and Children
- (2012) Andy Boyd et al. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
- A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer
- (2012) Julius Gudmundsson et al. NATURE GENETICS
- Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits
- (2012) Jian Yang et al. NATURE GENETICS
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- (2012) J. A. Tennessen et al. SCIENCE
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genomic inflation factors under polygenic inheritance
- (2011) Jian Yang et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
- (2010) Alkes L. Price et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height
- (2010) Matthew B. Lanktree et al. AMERICAN JOURNAL OF HUMAN GENETICS
- METAL: fast and efficient meta-analysis of genomewide association scans
- (2010) C. J. Willer et al. BIOINFORMATICS
- Hundreds of variants clustered in genomic loci and biological pathways affect human height
- (2010) Hana Lango Allen et al. NATURE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started