publication venue for
- 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
- 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
- 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
- Insulin regulation of heart function in aging fruit flies 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