Author details

Full Name

Peter M Visscher

Affiliation

ORCID

Career Start Year

1992

Papers

477

H Index

118

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37505983	Chromosomal inversion polymorphisms shape human brain morphology.	Cell Rep	2023
35987817	Genetic and modifiable risk factors combine multiplicatively in common disease.	Clin Res Cardiol	2023
37601976	Joint analysis of GWAS and multi-omics QTL summary statistics reveals a large fraction of GWAS signals shared with molecular phenotypes.	Cell Genom	2023
37723263	Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores.	Nat Genet	2023
37982710	Correction: Epigenetic scores for the circulating proteome as tools for disease prediction.	Elife	2023
37963177	Cross-ancestry analyses identify new genetic loci associated with 25-hydroxyvitamin D.	PLoS Genet	2023
37769091	Community-wide genome sequencing reveals 30 years of Darwin's finch evolution.		2023
36893272	Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness.	Proc Natl Acad Sci U S A	2023
36707517	Estimation and implications of the genetic architecture of fasting and non-fasting blood glucose.	Nat Commun	2023
36634672	15 years of GWAS discovery: Realizing the promise.		2023
36608683	mBAT-combo: A more powerful test to detect gene-trait associations from GWAS data.	Am J Hum Genet	2023
36790133	Rare genetic variants underlie outlying levels of DNA methylation and gene-expression.	Hum Mol Genet	2023
35113692	Discovery of genomic loci of the human cerebral cortex using genetically informed brain atlases.	Science	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
35905320	Improving GWAS discovery and genomic prediction accuracy in biobank data.	Proceedings of the National Academy of Sciences of the United States of America	2022
35508631	Genetics of cognitive performance, education and learning: from research to policy?	npj Science of Learning	2022
35817969	From Mendel to quantitative genetics in the genome era: the scientific legacy of W. G. Hill.	Nat Genet	2022
35869320	Author Correction: From Mendel to quantitative genetics in the genome era: the scientific legacy of W. G. Hill.	Nat Genet	2022
35365697	Author Correction: Assortative mating biases marker-based heritability estimators.	Nature Communications	2022
35610986	Parsimonious model for mass-univariate vertexwise analysis.	J Med Imaging (Bellingham)	2022
36253871	Local CpG density affects the trajectory and variance of age-associated DNA methylation changes.	Genome Biol	2022
33907316	Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia.	Eur J Hum Genet	2022
35217535	Australian Parkinson's Genetics Study (APGS): pilot (n=1532).	BMJ Open	2022
35023833	Epigenetic scores for the circulating proteome as tools for disease prediction.	Elife	2022
35115518	Assortative mating biases marker-based heritability estimators.	Nature Communications	2022
34475573	Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.	Nat Genet	2021
32398722	Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.	Mol Psychiatry	2021
33811805	Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals.	Am J Hum Genet	2021
33542196	Multi-omic and multi-species meta-analyses of nicotine consumption.	Transl Psychiatry	2021
34014919	Gene action, genetic variation, and GWAS: A user-friendly web tool.	PLoS Genet	2021
33961780	Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals.	Am J Hum Genet	2021
33682710	Variation in VKORC1 Is Associated with Vascular Dementia.	J Alzheimers Dis	2021
34214457	Genomic partitioning of inbreeding depression in humans.	Am J Hum Genet	2021
33568206	Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.	Mol Autism	2021
33664403	Quantifying genetic heterogeneity between continental populations for human height and body mass index.	Scientific Reports	2021
33608531	GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression.	Nat Commun	2021
33608517	Widespread signatures of natural selection across human complex traits and functional genomic categories.	Nat Commun	2021
33558551	Publisher Correction: Genome-wide analyses of behavioural traits are subject to bias by misreports and longitudinal changes.	Nat Commun	2021
34192436	Problems with Using Polygenic Scores to Select Embryos.	N Engl J Med	2021
33436567	Genome-wide analyses of behavioural traits are subject to bias by misreports and longitudinal changes.	Nat Commun	2021
33595649	Creating and Validating a DNA Methylation-Based Proxy for Interleukin-6.	J Gerontol A Biol Sci Med Sci	2021
33594080	Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals.	Nat Commun	2021
32671396	Alzheimer's disease genetic risk and sleep phenotypes in healthy young men: association with more slow waves and daytime sleepiness.	Sleep	2021
32997097	From Basic Science to Clinical Application of Polygenic Risk Scores: A Primer.	JAMA Psychiatry	2021
34848700	Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits.	Nat Commun	2021
34554790	Discovery and implications of polygenicity of common diseases.	Science	2021
34493871	Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation.	Nat Genet	2021
34381240	Retraction Note: Detection and replication of epistasis influencing transcription in humans.	Nature	2021
34381229	Phantom epistasis between unlinked loci.	Nature	2021
34767757	Autism-related dietary preferences mediate autism-gut microbiome associations.	Cell	2021