The biology of autism

Search for the Exclusive W Boson Hadronic Decays W^{±}→π^{±}γ, W^{±}→K^{±}γ and W^{±}→ρ^{±}γ with the ATLAS Detector.

Physical review letters·2024

Determination of the Relative Sign of the Higgs Boson Couplings to W and Z Bosons Using WH Production via Vector-Boson Fusion with the ATLAS Detector.

Physical review letters·2024

Statistical Combination of ATLAS Run 2 Searches for Charginos and Neutralinos at the LHC.

Physical review letters·2024

Combination of Measurements of the Top Quark Mass from Data Collected by the ATLAS and CMS Experiments at sqrt[s]=7 and 8 TeV.

Physical review letters·2024

Combination of Searches for Resonant Higgs Boson Pair Production Using pp Collisions at sqrt[s]=13 TeV with the ATLAS Detector.

Physical review letters·2024

Search for Nearly Mass-Degenerate Higgsinos Using Low-Momentum Mildly Displaced Tracks in pp Collisions at sqrt[s]=13 TeV with the ATLAS Detector.

Physical review letters·2024

Hallucinations and auditory-verbal signal detection studies: A meta-analytic review.

Psychological medicine·2026

How much is sexual minority stress confounded with familial causes? A systematic multilevel meta-analysis.

Psychological medicine·2026

Anxiety and depression subtypes and their psychotherapy response: A network analysis of 33,675 patients.

Psychological medicine·2026

Permissive and instructive causality: integrating biological and environmental factors in mental health.

Psychological medicine·2026

Autism spectrum disorder: has it lost its meaning and is it leading to misdiagnosis?

Psychological medicine·2026

Longitudinal associations among autism and ADHD traits, social maladjustment, and mental health in school-aged children.

Psychological medicine·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Molecular genetics & genomic medicine·2026

Contribution of Copy Number Variants and Cumulative Genetic Load to Autism Spectrum Disorders: Integrative Insights from Chromosomal Microarray Analysis.

International journal of molecular sciences·2026

RFX3 Pathogenic Variants as a Rare Cause of Infantile Epileptic Spasms Syndrome.

International journal of molecular sciences·2026

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Search for the Exclusive W Boson Hadronic Decays W^{±}→π^{±}γ, W^{±}→K^{±}γ and W^{±}→ρ^{±}γ with the ATLAS Detector.

Determination of the Relative Sign of the Higgs Boson Couplings to W and Z Bosons Using WH Production via Vector-Boson Fusion with the ATLAS Detector.

Statistical Combination of ATLAS Run 2 Searches for Charginos and Neutralinos at the LHC.

Combination of Measurements of the Top Quark Mass from Data Collected by the ATLAS and CMS Experiments at sqrt[s]=7 and 8 TeV.

Combination of Searches for Resonant Higgs Boson Pair Production Using pp Collisions at sqrt[s]=13 TeV with the ATLAS Detector.

Search for Nearly Mass-Degenerate Higgsinos Using Low-Momentum Mildly Displaced Tracks in pp Collisions at sqrt[s]=13 TeV with the ATLAS Detector.

Hallucinations and auditory-verbal signal detection studies: A meta-analytic review.

How much is sexual minority stress confounded with familial causes? A systematic multilevel meta-analysis.

Anxiety and depression subtypes and their psychotherapy response: A network analysis of 33,675 patients.

Permissive and instructive causality: integrating biological and environmental factors in mental health.

Autism spectrum disorder: has it lost its meaning and is it leading to misdiagnosis?

Longitudinal associations among autism and ADHD traits, social maladjustment, and mental health in school-aged children.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Contribution of Copy Number Variants and Cumulative Genetic Load to Autism Spectrum Disorders: Integrative Insights from Chromosomal Microarray Analysis.

RFX3 Pathogenic Variants as a Rare Cause of Infantile Epileptic Spasms Syndrome.

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