Nature Search

Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

Danny Antaki
James Guevara
Jonathan Sebat
Amendments and Corrections29 Jun 2022
Nature Genetics

Volume: 54, P: 1259
Action initiation and punishment learning differ from childhood to adolescence while reward learning remains stable

Adolescence is often associated with heightened reward learning and impulsivity. Here the authors show in 742 people aged 9-18 that reward learning in fact remains stable with age, whilst punishment learning increases and action initiation decreases.

Ruth Pauli
Inti A. Brazil
Patricia L. Lockwood
ResearchOpen Access14 Sept 2023
Nature Communications

Volume: 14, P: 1-15
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

Integrated analyses in a large collection of families provide insights into the combined effects of rare variants and polygenic risk on autism spectrum disorder.

Danny Antaki
James Guevara
Jonathan Sebat
Research02 Jun 2022
Nature Genetics

Volume: 54, P: 1284-1292
Autism risk in offspring can be assessed through quantification of male sperm mosaicism

Genetic analysis of paternal sperm from families with a child affected by autism reveals that the recurrent risk for transmitting disease-associated de novo mutations to future offspring is near 0% for most couples but is substantially higher for a small fraction of couples.

Martin W. Breuss
Danny Antaki
Joseph G. Gleeson
Research23 Dec 2019
Nature Medicine

Volume: 26, P: 143-150
Preclinical models for prediction of immunotherapy outcomes and immune evasion mechanisms in genetically heterogeneous multiple myeloma

New experimental models provide much-needed tools for understanding how genetically diverse multiple myeloma progresses and evolves in response to therapy.

Marta Larrayoz
Maria J. Garcia-Barchino
Jose A. Martinez-Climent
ResearchOpen Access16 Mar 2023
Nature Medicine

Volume: 29, P: 632-645
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

ADHD is often found to be comorbid with disruptive behavior disorders, but the genetic loci underlying this comorbidity are unknown. Here, the authors have performed a GWAS meta-analysis of ADHD with disruptive behavior disorders, finding three genome-wide significant loci in Europeans, and replicating one in a Chinese cohort.

Ditte Demontis
Raymond K. Walters
Anders D. Børglum
ResearchOpen Access25 Jan 2021
Nature Communications

Volume: 12, P: 1-12
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 signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan

Jenny van Dongen
Fiona A. Hagenbeek
Dorret I. Boomsma
ResearchOpen Access08 Jan 2021
Molecular Psychiatry

Volume: 26, P: 2148-2162
Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability

Bàrbara Torrico
Noèlia Fernàndez-Castillo
Claudio Toma
Research18 Mar 2015
European Journal of Human Genetics

Volume: 23, P: 1694-1701
Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

Ditte Demontis
Raymond K. Walters
Anders D. Børglum
Amendments and CorrectionsOpen Access15 Feb 2021
Nature Communications

Volume: 12, P: 1

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Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

Action initiation and punishment learning differ from childhood to adolescence while reward learning remains stable

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

Autism risk in offspring can be assessed through quantification of male sperm mosaicism

Preclinical models for prediction of immunotherapy outcomes and immune evasion mechanisms in genetically heterogeneous multiple myeloma

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

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

DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan

Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability

Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

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