List of works - Beben Benyamin

A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality

scientific article

Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

scientific article

Age- and sex-specific causal effects of adiposity on cardiovascular risk factors

scientific article published on 23 February 2015

Are there common genetic and environmental factors behind the endophenotypes associated with the metabolic syndrome?

Association of CamK2A genetic variants with transition time from occasional to regular heroin use in a sample of heroin-dependent individuals

scientific article published on 01 February 2019

Association of rs1344706 in the ZNF804A gene with schizophrenia in a case/control sample from Indonesia ⬇️

scientific article published on April 13, 2013

Associations of genetically determined iron status across the phenome: A mendelian randomization study.

scientific article published on 20 June 2019

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

scientific article

Bodyweight QTL on mouse chromosomes 4 and 11 by selective genotyping: regressionv. maximum likelihood

article by Beben Benyamin et al published 2007 in Australian Journal of Experimental Agriculture

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis.

scientific article

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

scientific article

Cognitive function in adolescence: testing for interactions between breast-feeding and FADS2 polymorphisms

scientific article

Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci

scientific article

Common Genetic Components of Obesity Traits and Serum Leptin

scholarly article by Ann L. Hasselbalch et al published December 2008 in Obesity

Common SNPs explain a large proportion of the heritability for human height

scientific article (publication date: July 2010)

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

preprint

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

scholarly article

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

scientific article

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

scientific article

Comparative genetic architectures of schizophrenia in East Asian and European populations

scientific article published on 18 November 2019

Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study.

scientific article

Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

scientific article published on 30 March 2015

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

scientific article published on 20 September 2017

EigenGWAS: finding loci under selection through genome-wide association studies of eigenvectors in structured populations

scientific article published on 4 May 2016

Family-based genome-wide association studies

scientific article published on February 2009

GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors

scientific article

Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins

scientific article published on 15 September 2011

Genome partitioning of genetic variation for height from 11,214 sibling pairs

scientific article published in October 2007

Genome-wide association meta-analysis of childhood and adolescent internalising symptoms

scientific article

Genome-wide association study identifies two loci strongly affecting transferrin glycosylation

scientific article

Identification of novel loci affecting circulating chromogranins and related peptides.

scientific article

Investigating the relationship between iron and depression

scientific article published on 08 July 2017

Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?

scientific article published on 11 July 2015

Large, consistent estimates of the heritability of cognitive ability in two entire populations of 11-year-old twins from Scottish mental surveys of 1932 and 1947.

scientific article published on September 2005

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

scientific article published on 12 July 2017

Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations

scientific article published on 18 October 2011

Meta-analysis of the heritability of human traits based on fifty years of twin studies

scientific article

Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression.

scientific article published on 4 June 2019

Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci

scientific article

No Genetic Overlap Between Circulating Iron Levels and Alzheimer's Disease

scientific article published on 30 May 2017

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

scientific article

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

scientific article

Precision and bias of a normal finite mixture distribution model to analyze twin data when zygosity is unknown: simulations and application to IQ phenotypes on a large sample of twin pairs

scientific article

Serum iron level and kidney function: a Mendelian randomization study.

scientific article published in February 2017

Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

scientific article

Seventy-five genetic loci influencing the human red blood cell

scientific article published on 5 December 2012

Sharing a Placenta is Associated With a Greater Similarity in DNA Methylation in Monochorionic Versus Dichorionic Twin Pars in Blood at Age 14.

scientific article published in December 2015

Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

scientific article published on 27 February 2020

The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation

scientific article

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

scientific article (publication date: 2013)

The use of linear mixed models to estimate variance components from data on twin pairs by maximum likelihood

scientific article

Transferrin saturation and mortality

scientific article published on 22 February 2011

Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study

scientific article

Variance decomposition of apolipoproteins and lipids in Danish twins

scientific article published on 26 May 2006

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels

scientific article published on 11 December 2008

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.

scientific article published on 17 November 2017

Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs

scientific article

List of works by Beben Benyamin

A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality

Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

Age- and sex-specific causal effects of adiposity on cardiovascular risk factors

Are there common genetic and environmental factors behind the endophenotypes associated with the metabolic syndrome?

Association of CamK2A genetic variants with transition time from occasional to regular heroin use in a sample of heroin-dependent individuals

Association of rs1344706 in the ZNF804A gene with schizophrenia in a case/control sample from Indonesia ⬇️

Associations of genetically determined iron status across the phenome: A mendelian randomization study.

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Bodyweight QTL on mouse chromosomes 4 and 11 by selective genotyping: regressionv. maximum likelihood

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis.

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

Cognitive function in adolescence: testing for interactions between breast-feeding and FADS2 polymorphisms

Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci

Common Genetic Components of Obesity Traits and Serum Leptin

Common SNPs explain a large proportion of the heritability for human height

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

Comparative genetic architectures of schizophrenia in East Asian and European populations

Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study.

Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

EigenGWAS: finding loci under selection through genome-wide association studies of eigenvectors in structured populations

Family-based genome-wide association studies

GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors

Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins

Genome partitioning of genetic variation for height from 11,214 sibling pairs

Genome-wide association meta-analysis of childhood and adolescent internalising symptoms

Genome-wide association study identifies two loci strongly affecting transferrin glycosylation

Identification of novel loci affecting circulating chromogranins and related peptides.

Investigating the relationship between iron and depression

Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?

Large, consistent estimates of the heritability of cognitive ability in two entire populations of 11-year-old twins from Scottish mental surveys of 1932 and 1947.

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations

Meta-analysis of the heritability of human traits based on fifty years of twin studies

Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression.

Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci

No Genetic Overlap Between Circulating Iron Levels and Alzheimer's Disease

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

Precision and bias of a normal finite mixture distribution model to analyze twin data when zygosity is unknown: simulations and application to IQ phenotypes on a large sample of twin pairs

Serum iron level and kidney function: a Mendelian randomization study.

Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

Seventy-five genetic loci influencing the human red blood cell

Sharing a Placenta is Associated With a Greater Similarity in DNA Methylation in Monochorionic Versus Dichorionic Twin Pars in Blood at Age 14.

Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

The use of linear mixed models to estimate variance components from data on twin pairs by maximum likelihood

Transferrin saturation and mortality

Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study

Variance decomposition of apolipoproteins and lipids in Danish twins

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.

Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs