User profiles for Beben Benyamin
Beben BenyaminAssociate Professor, University of South Australia Verified email at unisa.edu.au Cited by 13806 |
Meta-analysis of the heritability of human traits based on fifty years of twin studies
TJC Polderman, B Benyamin, CA De Leeuw… - Nature …, 2015 - nature.com
Despite a century of research on complex traits in humans, the relative importance and specific
nature of the influences of genes and environment on human traits remain controversial. …
nature of the influences of genes and environment on human traits remain controversial. …
Common SNPs explain a large proportion of the heritability for human height
J Yang, B Benyamin, BP McEvoy, S Gordon… - Nature …, 2010 - nature.com
SNPs discovered by genome-wide association studies (GWASs) account for only a small
fraction of the genetic variation of complex traits in human populations. Where is the remaining …
fraction of the genetic variation of complex traits in human populations. Where is the remaining …
Comparative genetic architectures of schizophrenia in East Asian and European populations
Schizophrenia is a debilitating psychiatric disorder with approximately 1% lifetime risk globally.
Large-scale schizophrenia genetic studies have reported primarily on European ancestry …
Large-scale schizophrenia genetic studies have reported primarily on European ancestry …
Common variants in TMPRSS6 are associated with iron status and erythrocyte volume
We report a genome-wide association study to iron status. We identify an association of SNPs
in TPMRSS6 to serum iron (rs855791, combined P = 1.5 × 10 −20 ), transferrin saturation (…
in TPMRSS6 to serum iron (rs855791, combined P = 1.5 × 10 −20 ), transferrin saturation (…
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
…, M Begemann, RA Belliveau, J Bene, B Benyamin… - Nature, 2022 - nature.com
Schizophrenia has a heritability of 60–80% 1 , much of which is attributable to common risk
alleles. Here, in a two-stage genome-wide association study of up to 76,755 individuals with …
alleles. Here, in a two-stage genome-wide association study of up to 76,755 individuals with …
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
We identify common genetic variants associated with cognitive performance using a two-stage
approach, which we call the proxy-phenotype method. First, we conduct a genome-wide …
approach, which we call the proxy-phenotype method. First, we conduct a genome-wide …
[HTML][HTML] Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis
Cross-ethnic genetic studies can leverage power from differences in disease epidemiology
and population-specific genetic architecture. In particular, the differences in linkage …
and population-specific genetic architecture. In particular, the differences in linkage …
[HTML][HTML] EigenGWAS: finding loci under selection through genome-wide association studies of eigenvectors in structured populations
We develop a novel approach to identify regions of the genome underlying population genetic
differentiation in any genetic data where the underlying population structure is unknown, …
differentiation in any genetic data where the underlying population structure is unknown, …
Seventy-five genetic loci influencing the human red blood cell
Anaemia is a chief determinant of global ill health, contributing to cognitive impairment,
growth retardation and impaired physical capacity. To understand further the genetic factors …
growth retardation and impaired physical capacity. To understand further the genetic factors …
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L
Intelligence in childhood, as measured by psychometric cognitive tests, is a strong predictor
of many important life outcomes, including educational attainment, income, health and …
of many important life outcomes, including educational attainment, income, health and …