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ASD and ADHD have a similar burden of rare protein-truncating variants

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archgenpsychiatry.2011.76openalex-snapshot

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

inferredcites →https://doi.org/10.1007/s00787-010-0092-xopenalex-snapshot

Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder

inferredcites →https://doi.org/10.1016/j.biopsych.2004.11.024openalex-snapshot

Molecular Genetics of Attention-Deficit/Hyperactivity Disorder

inferredcites →https://doi.org/10.1016/j.jaac.2014.03.004openalex-snapshot

Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants

inferredcites →https://doi.org/10.1016/j.neuron.2015.09.016openalex-snapshot

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

inferredcites →https://doi.org/10.1016/j.resp.2008.07.003openalex-snapshot

PHOX2B mutations and ventilatory control

inferredcites →https://doi.org/10.1016/j.ymgme.2013.06.004openalex-snapshot

Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing

inferredcites →https://doi.org/10.1017/s0033291713002493openalex-snapshot

The heritability of clinically diagnosed attention deficit hyperactivity disorder across the lifespan

inferredcites →https://doi.org/10.1038/mp.2017.17openalex-snapshot

The familial co-aggregation of ASD and ADHD: a register-based cohort study

inferredcites →https://doi.org/10.1038/mp.2017.196openalex-snapshot

The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders

inferredcites →https://doi.org/10.1038/nature13772openalex-snapshot

Synaptic, transcriptional and chromatin genes disrupted in autism

inferredcites →https://doi.org/10.1038/nature13908openalex-snapshot

The contribution of de novo coding mutations to autism spectrum disorder

inferredcites →https://doi.org/10.1038/nature19057openalex-snapshot

Analysis of protein-coding genetic variation in 60,706 humans

inferredcites →https://doi.org/10.1038/ng.3039openalex-snapshot

Most genetic risk for autism resides with common variation

inferredcites →https://doi.org/10.1038/ng.3050openalex-snapshot

A framework for the interpretation of de novo mutation in human disease

inferredcites →https://doi.org/10.1038/ng.3789openalex-snapshot

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

inferredcites →https://doi.org/10.1038/s41588-018-0269-7openalex-snapshot

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

inferredcites →https://doi.org/10.1038/s41598-017-00208-6openalex-snapshot

Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies

inferredcites →https://doi.org/10.1093/bioinformatics/btq559openalex-snapshot

Robust relationship inference in genome-wide association studies

inferredcites →https://doi.org/10.1101/148353openalex-snapshot

Regional missense constraint improves variant deleteriousness prediction

inferredcites →https://doi.org/10.1101/224774openalex-snapshot

Common risk variants identified in autism spectrum disorder

inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

inferredcites →https://doi.org/10.1111/j.1469-7610.2007.01857.xopenalex-snapshot

Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample

inferredcites →https://doi.org/10.1126/scitranslmed.3002464openalex-snapshot

Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

inferredcites →https://doi.org/10.1186/1471-2156-12-58openalex-snapshot

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

inferredcites →https://doi.org/10.1186/s13059-016-0974-4openalex-snapshot

The Ensembl Variant Effect Predictor

inferredcites →https://doi.org/10.1186/s13229-017-0153-9openalex-snapshot

ADHD-related symptoms and attention profiles in the unaffected siblings of probands with autism spectrum disorder: focus on the subtypes of autism and Asperger’s disorder

inferredcites →https://doi.org/10.1371/journal.pgen.1001318openalex-snapshot

A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing

inferredcites →https://doi.org/10.1371/journal.pgen.1001322openalex-snapshot

Testing for an Unusual Distribution of Rare Variants

inferredcites →https://doi.org/10.1371/journal.pone.0153253openalex-snapshot

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/7854_2022_338openalex-snapshot

Genetics of Attention-Deficit Hyperactivity Disorder

inferred← citeshttps://doi.org/10.1007/s11920-020-1141-xopenalex-snapshot

Genetics of ADHD: What Should the Clinician Know?

inferred← citeshttps://doi.org/10.1016/j.cell.2018.06.016openalex-snapshot

The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders

inferred← citeshttps://doi.org/10.1016/j.cell.2019.01.015openalex-snapshot

Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders

inferred← citeshttps://doi.org/10.1016/j.cell.2019.12.036openalex-snapshot

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

inferred← citeshttps://doi.org/10.1016/j.celrep.2018.08.082openalex-snapshot

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

inferred← citeshttps://doi.org/10.1016/j.ygeno.2020.09.022openalex-snapshot

Autism spectrum disorder genomics: The progress and potential of genomic technologies

inferred← citeshttps://doi.org/10.1016/s2215-0366(19)30163-4openalex-snapshot

Mapping genotype to phenotype in neurodevelopmental copy number variants

inferred← citeshttps://doi.org/10.1038/s41380-020-00974-2openalex-snapshot

Autophagy, apoptosis, and neurodevelopmental genes might underlie selective brain region vulnerability in attention-deficit/hyperactivity disorder

inferred← citeshttps://doi.org/10.1038/s41380-020-01006-9openalex-snapshot

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

inferred← citeshttps://doi.org/10.1038/s41386-020-0664-5openalex-snapshot

Shared genetic background between children and adults with attention deficit/hyperactivity disorder

inferred← citeshttps://doi.org/10.1038/s41398-019-0599-yopenalex-snapshot

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder

inferred← citeshttps://doi.org/10.1038/s41586-020-2329-2openalex-snapshot

Transcript expression-aware annotation improves rare variant interpretation

inferred← citeshttps://doi.org/10.1038/s41598-018-37336-6openalex-snapshot

HSPA12A targets the cytoplasmic domain and affects the trafficking of the Amyloid Precursor Protein receptor SorLA

inferred← citeshttps://doi.org/10.1055/a-0962-1001openalex-snapshot

Genetische Grundlagen der Aufmerksamkeitsdefizit-/Hyperaktivitätsstörung

inferred← citeshttps://doi.org/10.1093/braincomms/fcad004openalex-snapshot

The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvement

inferred← citeshttps://doi.org/10.1097/yco.0000000000000852openalex-snapshot

Update on genetics of attention deficit/hyperactivity disorder: current status 2023

inferred← citeshttps://doi.org/10.1101/531210openalex-snapshot

The mutational constraint spectrum quantified from variation in 141,456 humans

inferred← citeshttps://doi.org/10.1101/554444openalex-snapshot

Transcript expression-aware annotation improves rare variant discovery and interpretation

inferred← citeshttps://doi.org/10.1101/580365openalex-snapshot

Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD

inferred← citeshttps://doi.org/10.1101/652792openalex-snapshot

Spatial organization of cells and variable expression of autophagy, apoptosis, and neurodevelopmental genes might underlie selective brain region vulnerability in Attention-Deficit/Hyperactivity Disorder

inferred← citeshttps://doi.org/10.1101/671453openalex-snapshot

Predicting Functional Effects of Missense Variants in Voltage-Gated Sodium and Calcium Channels

inferred← citeshttps://doi.org/10.1101/730952openalex-snapshot

Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify candidate risk genes and biological pathways

inferred← citeshttps://doi.org/10.1146/annurev-biodatasci-072018-021148openalex-snapshot

Analytic and Translational Genetics

inferred← citeshttps://doi.org/10.3410/f.738024165.793584912openalex-snapshot

Faculty Opinions recommendation of Transcript expression-aware annotation improves rare variant interpretation.

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