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。Genome-wide association study identifies 74 loci associated with educational attainment
Aysu Okbay et al.
NATURE (2016)
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek et al.
NATURE (2016)
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
Elise B. Robinson et al.
NATURE GENETICS (2016)
Directional dominance on stature and cognition in diverse human populations
Peter K. Joshi et al.
NATURE (2015)
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
Jian Yang et al.
NATURE GENETICS (2015)
Large multiallelic copy number variations in humans
Robert E. Handsaker et al.
NATURE GENETICS (2015)
Second-generation PLINK: rising to the challenge of larger and richer datasets
Christopher C. Chang et al.
GIGASCIENCE (2015)
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu
Liis Leitsalu et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2015)
Toward better understanding of artifacts in variant calling from high-coverage samples
Heng Li
BIOINFORMATICS (2014)
CNVs conferring risk of autism or schizophrenia affect cognition in controls
Hreinn Stefansson et al.
NATURE (2014)
Genome sequencing identifies major causes of severe intellectual disability
Christian Gilissen et al.
NATURE (2014)
The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov et al.
NATURE (2014)
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke et al.
NATURE (2014)
A framework for the interpretation of de novo mutation in human disease
Kaitlin E. Samocha et al.
NATURE GENETICS (2014)
The high heritability of educational achievement reflects many genetically influenced traits, not just intelligence
Eva Krapohl et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Searching for missing heritability: Designing rare variant association studies
Or Zuk et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Molecular genetic contributions to socioeconomic status and intelligence
Riccardo E. Marioni et al.
INTELLIGENCE (2014)
Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants
Iuliana Ionita-Laza et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
dbNSFP v2.0: A Database of Human Non-synonymous SNVs and Their Functional Predictions and Annotations
Xiaoming Liu et al.
HUMAN MUTATION (2013)
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Stephan Ripke et al.
NATURE GENETICS (2013)
The Genotype-Tissue Expression (GTEx) project
John Lonsdale et al.
NATURE GENETICS (2013)
Variation in the Heritability of Educational Attainment: An International Meta-Analysis
Amelia R. Branigan et al.
SOCIAL FORCES (2013)
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3
Pablo Cingolani et al.
FLY (2012)
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Luke Jostins et al.
NATURE (2012)
Using Drosophila melanogaster as a Model for Genotoxic Chemical Mutational Studies with a New Program, SnpSift
Pablo Cingolani et al.
Frontiers in Genetics (2012)
Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
Michael C. Wu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A. DePristo et al.
NATURE GENETICS (2011)
Thirty-five-year trends in cardiovascular risk factors in Finland
Erkki Vartiainen et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2010)
A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
Bo Eskerod Madsen et al.
PLOS GENETICS (2009)