Nature Search

De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems

Erik A Ehli
Abdel Abdellaoui
Gareth E Davies
ResearchOpen Access11 Apr 2012
European Journal of Human Genetics

Volume: 20, P: 1037-1043
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

Genome-wide association meta-analyses of attention-deficit/hyperactivity disorder symptom measures and clinical diagnoses identify new risk loci, highlight putative effector genes and yield improved polygenic risk scores.

Camiel M. van der Laan
Hill F. Ip
Dorret I. Boomsma
Research17 Sept 2025
Nature Genetics

Volume: 57, P: 2427-2435
Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

Camiel M. van der Laan
Hill F. Ip
Dorret I. Boomsma
Amendments and Corrections29 Sept 2025
Nature Genetics

Volume: 57, P: 2604
Genetic and environmental influences interact with age and sex in shaping the human methylome

Differential impact of genetic and environmental influences on DNA methylation may result in sex- and age-related physiological variation and disease susceptibility. By analysing DNA methylome of 2,603 individuals from twin families, here, the authors establish a catalogue of between-individual variation in DNA methylation.

Jenny van Dongen
Michel G. Nivard
Dorret I. Boomsma
ResearchOpen Access07 Apr 2016
Nature Communications

Volume: 7, P: 1-13
Identical twins carry a persistent epigenetic signature of early genome programming

The mechanisms underlying how monozygotic (or identical) twins arise are yet to be determined. Here, the authors investigate this in an epigenome-wide association study, showing that monozygotic twinning has a characteristic DNA methylation signature in adult somatic tissues.

Jenny van Dongen
Scott D. Gordon
Dorret I. Boomsma
ResearchOpen Access28 Sept 2021
Nature Communications

Volume: 12, P: 1-14
A method to customize population-specific arrays for genome-wide association testing

Erik A Ehli
Abdel Abdellaoui
Jouke J Hottenga
Research23 Nov 2016
European Journal of Human Genetics

Volume: 25, P: 267-270
Genome-wide identification and differential analysis of translational initiation

Translation initiation sequencing (TI-seq) has revealed unexpected diversity in protein isoforms. Here, Zhang et al. present Ribo-TISH, a computational toolkit that can detect and compare TIs across conditions and improve open reading frame prediction from different types of ribosome profiling data.

Peng Zhang
Dandan He
Yiwen Chen
ResearchOpen Access23 Nov 2017
Nature Communications

Volume: 8, P: 1-14
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

A genome-wide association study for attention deficit/hyperactivity disorder (ADHD) identifies 12 loci and implicates neurodevelopmental pathways and conserved regions of the genome as being involved in underlying ADHD biology.

Ditte Demontis
Raymond K. Walters
Benjamin M. Neale
Research26 Nov 2018
Nature Genetics

Volume: 51, P: 63-75
DNA methylation in peripheral tissues and left-handedness

Veronika V. Odintsova
Matthew Suderman
Jenny van Dongen
ResearchOpen Access04 Apr 2022
Scientific Reports

Volume: 12, P: 1-16
Clinical utility of pharmacogenetics in a psychiatric and primary care population

Krista N. Bohlen
Julie M. Kittelsrud
Erik A. Ehli
Research27 Oct 2022
The Pharmacogenomics Journal

Volume: 23, P: 21-27
Genetic association study of childhood aggression across raters, instruments, and age

Hill F. Ip
Camiel M. van der Laan
Dorret I. Boomsma
ResearchOpen Access30 Jul 2021
Translational Psychiatry

Volume: 11, P: 1-9
Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait

Sanja Franić
Maria M Groen-Blokhuis
Dorret I Boomsma
Research25 Feb 2015
European Journal of Human Genetics

Volume: 23, P: 1378-1383
Biological insights into multiple birth: genetic findings from UK Biobank

Hamdi Mbarek
Margot P. van de Weijer
Dorret I. Boomsma
Research13 Feb 2019
European Journal of Human Genetics

Volume: 27, P: 970-979
Altered mechanisms of genital development identified through integration of DNA methylation and genomic measures in hypospadias

Melissa A. Richard
Pagna Sok
Philip J. Lupo
ResearchOpen Access29 Jul 2020
Scientific Reports

Volume: 10, P: 1-12
Integrative transcriptomic analysis for linking acute stress responses to squamous cell carcinoma development

Tran N. Nguyen
Kimal Rajapakshe
Kenneth Y. Tsai
ResearchOpen Access14 Oct 2020
Scientific Reports

Volume: 10, P: 1-14
Population structure, migration, and diversifying selection in the Netherlands

Abdel Abdellaoui
Jouke-Jan Hottenga
Dorret I Boomsma
Research27 Mar 2013
European Journal of Human Genetics

Volume: 21, P: 1277-1285
Intergenerational transmission of complex traits and the offspring methylome

Fiona A. Hagenbeek
René Pool
Dorret I. Boomsma
ResearchOpen Access03 Apr 2025
Molecular Psychiatry

Volume: 30, P: 3338-3347
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes

Liz Rietschel
Fabian Streit
Marcella Rietschel
ResearchOpen Access10 Nov 2017
Scientific Reports

Volume: 7, P: 1-15

Search

De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems

Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

Genetic and environmental influences interact with age and sex in shaping the human methylome

Identical twins carry a persistent epigenetic signature of early genome programming

A method to customize population-specific arrays for genome-wide association testing

Genome-wide identification and differential analysis of translational initiation

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

DNA methylation in peripheral tissues and left-handedness

Clinical utility of pharmacogenetics in a psychiatric and primary care population

Genetic association study of childhood aggression across raters, instruments, and age

Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait

Biological insights into multiple birth: genetic findings from UK Biobank

Altered mechanisms of genital development identified through integration of DNA methylation and genomic measures in hypospadias

Integrative transcriptomic analysis for linking acute stress responses to squamous cell carcinoma development

Population structure, migration, and diversifying selection in the Netherlands

Intergenerational transmission of complex traits and the offspring methylome

Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes

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