Nature Genetics Journal

Overview

publication venue for

The Ruminant Telomere-to-Telomere (RT2T) Consortium. 2024
Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes 2023
Discovery of 42 genome-wide significant loci associated with dyslexia 2022
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. 2022
Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis 2022
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects 2022
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. 2021
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. 2021
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction 2021
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale 2020
RNA is essential for PRC2 chromatin occupancy and function in human pluripotent stem cells 2020
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk 2019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use 2019
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 2019
A map of constrained coding regions in the human genome 2019
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 2018
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence 2018
Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. 2018
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects 2017
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index 2015
Targeted disruption of DNMT1, DNMT3A and DNMT3B in human embryonic stem cells 2015
Population genomics of Populus trichocarpa identifies signatures of selection and adaptive trait associations 2014
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs 2013
Endogenous retroviruses function as species-specific enhancer elements in the placenta 2013
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs (vol 44, pg 247, 2012) 2012
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs 2012
Genome-wide association study identifies five new schizophrenia loci 2011
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation 2011
Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells 2010
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy 2010
Lin28a transgenic mice manifest size and puberty phenotypes identified in human genetic association studies 2010
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database 2008
Tissue-specific transcriptional regulation has diverged significantly between human and mouse 2007
On the parsing of statistical information in family-based association testing 2007
Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database 2007
Morphogenesis in skin is governed by discrete sets of differentially expressed microRNAs 2006
A stress-sensitive reporter predicts longevity in isogenic populations of Caenorhabditis elegans 2005
Exploring nematode diversity 2004
The Collaborative Cross, a community resource for the genetic analysis of complex traits 2004
The tail does not always wag the dog 2002
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia 2002
Hypoxia and Lou Gehrig 2001
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy 2001
Plzf regulates limb and axial skeletal patterning 2000
Assembling a time bomb - cytochrome c oxidase and disease 1998
Parsing age, mutations and time 1997
Genetic analysis of ageing: Role of oxidative damage and environmental stresses 1996

Research

keywords

11 Medical and Health Sciences, 06 Biological Sciences