- See Also
-
Links
- “Association of Prenatal Exposure to Benzodiazepines With Development of Autism Spectrum and Attention-Deficit/Hyperactivity Disorders”, Et Al 2022
- “Prenatal Antidepressant Exposures and Autism Spectrum Disorder or Traits: A Retrospective, Multi-Cohort Study”, Et Al 2022
- “Developmental Implications of Genetic Testing for Physical Indications”, Et Al 2022
- “Polygenic Influences Associated With Adolescent Cognitive Skills”, Et Al 2022
- “The Female Protective Effect against Autism Spectrum Disorder”, Et Al 2022
- “Genetic Architecture of the White Matter Connectome of the Human Brain”, Et Al 2022
- “Genomics, Convergent Neuroscience and Progress in Understanding Autism Spectrum Disorder”, Et Al 2022
- “Genome-wide Analyses of ADHD Identify 27 Risk Loci, Refine the Genetic Architecture and Implicate Several Cognitive Domains”, Et Al 2022
- “The Impact of Early Stages of COVID-19 on the Mental Health of Autistic Adults in the United Kingdom: A Longitudinal Mixed-methods Study”, Et Al 2022
- “Rare Schizophrenia Risk Variant Burden Is Conserved in Diverse Human Populations”, Et Al 2022
- “Patient-Driven Findings of Genetic Associations for PANS and PANDAS”, 2021
- “Familial Clustering of Psychiatric Disorders and Low IQ”, Et Al 2021
- “Studies of Autistic Traits in the General Population Are Not Studies of Autism”, Sasson & Bottema-2021
- “Dimensional Characterizations of Gender Diversity Are Associated With Higher Polygenic Propensity for Cognitive Performance in a Neurodiverse Sample”, Et Al 2021
- “Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders”, Et Al 2021
- “A Selection Pressure Landscape for 870 Human Polygenic Traits”, Et Al 2021
- “Autism-related Dietary Preferences Mediate Autism-gut Microbiome Associations”, Et Al 2021
- “Integrating De Novo And Inherited Variants in over 42,607 Autism Cases Identifies Mutations in New Moderate Risk Genes”, Et Al 2021
- “How Rare and Common Risk Variation Jointly Affect Liability for Autism Spectrum Disorder”, Et Al 2021
- “A Biomarker-based Study of Prenatal Smoking Exposure and Autism in a Finnish National Birth Cohort”, Cheslack-Et Al 2021
- “Rates of Contributory De Novo Mutation in High and Low-risk Autism Families”, Et Al 2021
- “Neurodevelopmental Disorders and Subsequent Risk of Violent Victimization: Exploring Sex Differences and Mechanisms”, Et Al 2021
- “Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis”, Et Al 2021
- “Differences in the Genetic Architecture of Common and Rare Variants in Childhood, Persistent and Late-diagnosed Attention Deficit Hyperactivity Disorder”, Et Al 2021
- “Genetic Correlates of Phenotypic Heterogeneity in Autism”, Et Al 2021
- “Enhanced Rationality in Autism Spectrum Disorder”, Et Al 2021
- “Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms”, Et Al 2021
- “Early Life Antibiotic Exposure and the Subsequent Risk of Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder: A Systematic Review and Meta-Analysis”, Et Al 2021
- “Identification of Shared and Differentiating Genetic Risk for Autism Spectrum Disorder, Attention Deficit Hyperactivity Disorder and Case Subgroups”, Et Al 2021
- “A Phenotypic Spectrum of Autism Is Attributable to the Combined Effects of Rare Variants, Polygenic Risk and Sex”, Et Al 2021
- “A Cross-disorder Dosage Sensitivity Map of the Human Genome”, Et Al 2021
- “Large Mosaic Copy Number Variations Confer Autism Risk”, Et Al 2021
- “The Landscape of Somatic Mutation in Cerebral Cortex of Autistic and Neurotypical Individuals Revealed by Ultra-deep Whole-genome Sequencing”, Et Al 2021
- “Interpersonal Similarity of Autistic Traits Predicts Friendship Quality”, Et Al 2021
- “Exploratory Study of Cat Adoption in Families of Children With Autism: Impact on Children’s Social Skills and Anxiety”, Et Al 2020
- “Exome Sequencing Identifies Rare Coding Variants in 10 Genes Which Confer Substantial Risk for Schizophrenia”, Et Al 2020
- “Mapping Genomic Loci Prioritises Genes and Implicates Synaptic Biology in Schizophrenia”, Et Al 2020
- “Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome”, Et Al 2020
- “Conditional GWAS Analysis to Identify Disorder-specific SNPs for Psychiatric Disorders”, Et Al 2020
- “Local Genetic Correlation Analysis Reveals Heterogeneous Etiologic Sharing of Complex Traits”, Et Al 2020
- “Etiology of Autism Spectrum Disorders and Autistic Traits Over Time”, Et Al 2020
- “Estimating the Effect-size of Gene Dosage on Cognitive Ability across the Coding Genome”, Et Al 2020
- “Psychometric Concerns With the 10-item Autism-Spectrum Quotient (AQ10) As a Measure of Trait Autism in the General Population”, Et Al 2020
- “What Intellectual Progress Did I Make In The 2010s?”, 2020
- “Autistic Peer-to-peer Information Transfer Is Highly Effective”, Et Al 2020
- “Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders”, 2019
- “The Myth of the Stupid Believer: The Negative Religiousness-IQ Nexus Is Not on General Intelligence (G) and Is Likely a Product of the Relations Between IQ and Autism Spectrum Traits”, Et Al 2019
- “Social and Non-social Autism Symptoms and Trait Domains Are Genetically Dissociable”, Et Al 2019
- “Genome Wide Meta-analysis Identifies Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders”, Et Al 2019
- “Whole-genome Deep-learning Analysis Identifies Contribution of Noncoding Mutations to Autism Risk”, Et Al 2019
- “Common Polygenic Variations for Psychiatric Disorders and Cognition in Relation to Brain Morphology in the General Pediatric Population”, Et Al 2019
- “The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals”, Et Al 2019
- “Schizophrenia Risk Conferred by Protein-coding De Novo Mutations”, Et Al 2018
- “Using Genetics to Examine a General Liability to Childhood Psychopathology”, Et Al 2018
- “Autistic Traits, Resting-state Connectivity and Absolute Pitch in Professional Musicians: Shared and Distinct Neural Features”, Et Al 2018
- “Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study”, Martin-Et Al 2018
- “Cues to Mental Health from Men’s Facial Appearance”, 2018
- “Common Genetic Variants Contribute to Risk of Rare Severe Neurodevelopmental Disorders”, Et Al 2018
- “An Analytical Framework for Whole-genome Sequence Association Studies and Its Implications for Autism Spectrum Disorder”, Et Al 2018
- “Common Risk Variants Identified in Autism Spectrum Disorder”, Et Al 2017
- “Linkage Disequilibrium-dependent Architecture of Human Complex Traits Shows Action of Negative Selection”, Et Al 2017
- “Genome-wide Association Analyses Identify 44 Risk Variants and Refine the Genetic Architecture of Major Depressive Disorder”, Et Al 2017
- “Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum”, Et Al 2017
- “Widespread Signatures of Positive Selection in Common Risk Alleles Associated to Autism Spectrum Disorder”, 2017
- “Polygenic Transmission Disequilibrium Confirms That Common and Rare Variation Act Additively to Create Risk for Autism Spectrum Disorders”, Et Al 2016
- “Genome-wide Analyses of Empathy and Systemizing: Heritability and Correlates With Sex, Education, and Psychiatric Risk”, Et Al 2016
- “Shared Genetic Aetiology between Cognitive Functions and Physical and Mental Health in UK Biobank (N = 112,151) and 24 GWAS Consortia”, Et Al 2016
- “Genetic Risk for Autism Spectrum Disorders and Neuropsychiatric Variation in the General Population”, Et Al 2016
- “Whole-genome Sequencing of Quartet Families With Autism Spectrum Disorder”
- “Synaptic, Transcriptional and Chromatin Genes Disrupted in Autism”, Et Al 2014
- “The Contribution Of De Novo Coding Mutations to Autism Spectrum Disorder”, Et Al 2014
- “Fecundity of Patients With Schizophrenia, Autism, Bipolar Disorder, Depression, Anorexia Nervosa, or Substance Abuse vs Their Unaffected Siblings”, Et Al 2013
- “Genetic Relationship between Five Psychiatric Disorders Estimated from Genome-wide SNPs”, Et Al 2013
- “Identification of Risk Loci With Shared Effects on Five Major Psychiatric Disorders: a Genome-wide Analysis”
- “CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics”, 2012
- “The Role of Genetic Variation in the Causation of Mental Illness: an Evolution-informed Framework”, 2009
- “Factors and Primes: a Specific Numerical Ability”, Hermelin & 1990
- “Infantile Autism: A Genetic Study Of 21 Twin Pairs”, 1977
- “Fathers Bequeath More Mutations As They Age: Genome Study May Explain Links between Paternal Age and Conditions such as Autism”
- “Monkeys Genetically Modified to Show Autism Symptoms: But It Is Unclear How Well the Results Match the Condition in Humans”
- Wikipedia
- Miscellaneous
- Link Bibliography
See Also
Links
“Association of Prenatal Exposure to Benzodiazepines With Development of Autism Spectrum and Attention-Deficit/Hyperactivity Disorders”, Et Al 2022
“Association of Prenatal Exposure to Benzodiazepines With Development of Autism Spectrum and Attention-Deficit/Hyperactivity Disorders”, 2022-11-22 ( ; similar; bibliography)
“Prenatal Antidepressant Exposures and Autism Spectrum Disorder or Traits: A Retrospective, Multi-Cohort Study”, Et Al 2022
“Prenatal Antidepressant Exposures and Autism Spectrum Disorder or Traits: A Retrospective, Multi-Cohort Study”, 2022-11-22 (similar)
“Developmental Implications of Genetic Testing for Physical Indications”, Et Al 2022
“Developmental implications of genetic testing for physical indications”, 2022-09-06 ( ; similar)
“Polygenic Influences Associated With Adolescent Cognitive Skills”, Et Al 2022
“Polygenic influences associated with adolescent cognitive skills”, 2022-09 ( ; similar; bibliography)
“The Female Protective Effect against Autism Spectrum Disorder”, Et Al 2022
“The female protective effect against autism spectrum disorder”, 2022-06-08 ( ; similar)
“Genetic Architecture of the White Matter Connectome of the Human Brain”, Et Al 2022
“Genetic architecture of the white matter connectome of the human brain”, 2022-05-11 ( ; similar)
“Genomics, Convergent Neuroscience and Progress in Understanding Autism Spectrum Disorder”, Et Al 2022
“Genomics, convergent neuroscience and progress in understanding autism spectrum disorder”, 2022-04-19 ( ; similar)
“Genome-wide Analyses of ADHD Identify 27 Risk Loci, Refine the Genetic Architecture and Implicate Several Cognitive Domains”, Et Al 2022
“Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains”, 2022-02-16 ( ; backlinks; similar)
“The Impact of Early Stages of COVID-19 on the Mental Health of Autistic Adults in the United Kingdom: A Longitudinal Mixed-methods Study”, Et Al 2022
“The impact of early stages of COVID-19 on the mental health of autistic adults in the United Kingdom: A longitudinal mixed-methods study”, 2022-01-27 ( ; similar)
“Rare Schizophrenia Risk Variant Burden Is Conserved in Diverse Human Populations”, Et Al 2022
“Rare schizophrenia risk variant burden is conserved in diverse human populations”, 2022-01-03 ( ; similar)
“Patient-Driven Findings of Genetic Associations for PANS and PANDAS”, 2021
“Patient-Driven Findings of Genetic Associations for PANS and PANDAS”, 2021-12-31 ( ; similar)
“Familial Clustering of Psychiatric Disorders and Low IQ”, Et Al 2021
“Familial clustering of psychiatric disorders and low IQ”, 2021-12-16 ( ; similar)
“Studies of Autistic Traits in the General Population Are Not Studies of Autism”, Sasson & Bottema-2021
“Studies of autistic traits in the general population are not studies of autism”, 2021-11-26 (similar)
“Dimensional Characterizations of Gender Diversity Are Associated With Higher Polygenic Propensity for Cognitive Performance in a Neurodiverse Sample”, Et Al 2021
“Dimensional characterizations of gender diversity are associated with higher polygenic propensity for cognitive performance in a neurodiverse sample”, 2021-11-24 ( ; similar)
“Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders”, Et Al 2021
“Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders”, 2021-11-24 ( ; similar)
“A Selection Pressure Landscape for 870 Human Polygenic Traits”, Et Al 2021
“A selection pressure landscape for 870 human polygenic traits”, 2021-11-15 ( ; similar; bibliography)
“Autism-related Dietary Preferences Mediate Autism-gut Microbiome Associations”, Et Al 2021
“Autism-related dietary preferences mediate autism-gut microbiome associations”, 2021-11-11 ( ; backlinks; similar)
“Integrating De Novo And Inherited Variants in over 42,607 Autism Cases Identifies Mutations in New Moderate Risk Genes”, Et Al 2021
“Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes”, 2021-10-11 ( ; similar)
“How Rare and Common Risk Variation Jointly Affect Liability for Autism Spectrum Disorder”, Et Al 2021
“How rare and common risk variation jointly affect liability for autism spectrum disorder”, 2021-10-06 ( ; similar)
“A Biomarker-based Study of Prenatal Smoking Exposure and Autism in a Finnish National Birth Cohort”, Cheslack-Et Al 2021
“A biomarker-based study of prenatal smoking exposure and autism in a Finnish national birth cohort”, 2021-09-10 ( ; similar)
“Rates of Contributory De Novo Mutation in High and Low-risk Autism Families”, Et Al 2021
“Rates of contributory de novo mutation in high and low-risk autism families”, 2021-09-01 ( ; similar)
“Neurodevelopmental Disorders and Subsequent Risk of Violent Victimization: Exploring Sex Differences and Mechanisms”, Et Al 2021
“Neurodevelopmental disorders and subsequent risk of violent victimization: exploring sex differences and mechanisms”, 2021-09-01 ( ; similar)
“Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis”, Et Al 2021
“Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis”, 2021-08-31 ( ; similar)
“Differences in the Genetic Architecture of Common and Rare Variants in Childhood, Persistent and Late-diagnosed Attention Deficit Hyperactivity Disorder”, Et Al 2021
“Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention deficit hyperactivity disorder”, 2021-08-08 ( ; similar)
“Genetic Correlates of Phenotypic Heterogeneity in Autism”, Et Al 2021
“Genetic correlates of phenotypic heterogeneity in autism”, 2021-08-05 ( ; similar)
“Enhanced Rationality in Autism Spectrum Disorder”, Et Al 2021
“Enhanced rationality in autism spectrum disorder”, 2021-08-01 ( ; similar)
“Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms”, Et Al 2021
“Genome-wide association meta-analysis of childhood and adolescent internalizing symptoms”, 2021-07-31 ( ; similar)
“Early Life Antibiotic Exposure and the Subsequent Risk of Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder: A Systematic Review and Meta-Analysis”, Et Al 2021
“Early Life Antibiotic Exposure and the Subsequent Risk of Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder: A Systematic Review and Meta-Analysis”, 2021-06-03 ( ; similar)
“Identification of Shared and Differentiating Genetic Risk for Autism Spectrum Disorder, Attention Deficit Hyperactivity Disorder and Case Subgroups”, Et Al 2021
“Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups”, 2021-05-21 ( ; similar)
“A Phenotypic Spectrum of Autism Is Attributable to the Combined Effects of Rare Variants, Polygenic Risk and Sex”, Et Al 2021
“A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex”, 2021-04-04 ( ; similar)
“A Cross-disorder Dosage Sensitivity Map of the Human Genome”, Et Al 2021
“A cross-disorder dosage sensitivity map of the human genome”, 2021-01-28 ( ; similar)
“Large Mosaic Copy Number Variations Confer Autism Risk”, Et Al 2021
“Large mosaic copy number variations confer autism risk”, 2021-01-11 ( ; similar)
“The Landscape of Somatic Mutation in Cerebral Cortex of Autistic and Neurotypical Individuals Revealed by Ultra-deep Whole-genome Sequencing”, Et Al 2021
“The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing”, 2021-01-11 ( ; similar)
“Interpersonal Similarity of Autistic Traits Predicts Friendship Quality”, Et Al 2021
“Interpersonal similarity of autistic traits predicts friendship quality”, 2021 ( ; similar)
“Exploratory Study of Cat Adoption in Families of Children With Autism: Impact on Children’s Social Skills and Anxiety”, Et Al 2020
“Exploratory study of cat adoption in families of children with autism: Impact on children's social skills and anxiety”, 2020-12-06 ( ; similar)
“Exome Sequencing Identifies Rare Coding Variants in 10 Genes Which Confer Substantial Risk for Schizophrenia”, Et Al 2020
“Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia”, 2020-09-18 ( ; similar)
“Mapping Genomic Loci Prioritises Genes and Implicates Synaptic Biology in Schizophrenia”, Et Al 2020
“Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia”, 2020-09-13 ( ; backlinks; similar)
“Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome”, Et Al 2020
“Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome”, 2020-09-11 ( ; similar)
“Conditional GWAS Analysis to Identify Disorder-specific SNPs for Psychiatric Disorders”, Et Al 2020
“Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders”, 2020-05-12 ( ; similar)
“Local Genetic Correlation Analysis Reveals Heterogeneous Etiologic Sharing of Complex Traits”, Et Al 2020
“Local genetic correlation analysis reveals heterogeneous etiologic sharing of complex traits”, 2020-05-10 ( ; similar)
“Etiology of Autism Spectrum Disorders and Autistic Traits Over Time”, Et Al 2020
“Etiology of Autism Spectrum Disorders and Autistic Traits Over Time”, 2020-05-06 ( ; similar)
“Estimating the Effect-size of Gene Dosage on Cognitive Ability across the Coding Genome”, Et Al 2020
“Estimating the effect-size of gene dosage on cognitive ability across the coding genome”, 2020-04-05 ( ; similar)
“Psychometric Concerns With the 10-item Autism-Spectrum Quotient (AQ10) As a Measure of Trait Autism in the General Population”, Et Al 2020
“Psychometric concerns with the 10-item Autism-Spectrum Quotient (AQ10) as a measure of trait autism in the general population”, 2020-03-05 (similar)
“What Intellectual Progress Did I Make In The 2010s?”, 2020
“What Intellectual Progress Did I Make In The 2010s?”, 2020-01-08 ( ; similar)
“Autistic Peer-to-peer Information Transfer Is Highly Effective”, Et Al 2020
“Autistic peer-to-peer information transfer is highly effective”, 2020 ( ; similar)
“Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders”, 2019
“Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders”, 2019-12-12 ( ; similar)
“The Myth of the Stupid Believer: The Negative Religiousness-IQ Nexus Is Not on General Intelligence (G) and Is Likely a Product of the Relations Between IQ and Autism Spectrum Traits”, Et Al 2019
“The Myth of the Stupid Believer: The Negative Religiousness-IQ Nexus is Not on General Intelligence (g) and is Likely a Product of the Relations Between IQ and Autism Spectrum Traits”, 2019-10-05 ( ; similar; bibliography)
“Social and Non-social Autism Symptoms and Trait Domains Are Genetically Dissociable”, Et Al 2019
“Social and non-social autism symptoms and trait domains are genetically dissociable”, 2019-09-03 ( ; similar)
“Genome Wide Meta-analysis Identifies Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders”, Et Al 2019
“Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders”, 2019-01-26 ( ; similar)
“Whole-genome Deep-learning Analysis Identifies Contribution of Noncoding Mutations to Autism Risk”, Et Al 2019
“Common Polygenic Variations for Psychiatric Disorders and Cognition in Relation to Brain Morphology in the General Pediatric Population”, Et Al 2019
“Common Polygenic Variations for Psychiatric Disorders and Cognition in Relation to Brain Morphology in the General Pediatric Population”, 2019-01 ( ; similar)
“The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals”, Et Al 2019
“The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals”, 2019 ( ; similar)
“Schizophrenia Risk Conferred by Protein-coding De Novo Mutations”, Et Al 2018
“Schizophrenia risk conferred by protein-coding de novo mutations”, 2018-12-13 ( ; similar)
“Using Genetics to Examine a General Liability to Childhood Psychopathology”, Et Al 2018
“Using genetics to examine a general liability to childhood psychopathology”, 2018-11-21 ( ; similar)
“Autistic Traits, Resting-state Connectivity and Absolute Pitch in Professional Musicians: Shared and Distinct Neural Features”, Et Al 2018
“Autistic traits, resting-state connectivity and absolute pitch in professional musicians: shared and distinct neural features”, 2018-10-30 ( ; similar)
“Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study”, Martin-Et Al 2018
“Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study”, 2018-08-15 ( ; similar)
“Cues to Mental Health from Men’s Facial Appearance”, 2018
“Cues to mental health from men's facial appearance”, 2018-08-01 ( ; similar)
“Common Genetic Variants Contribute to Risk of Rare Severe Neurodevelopmental Disorders”, Et Al 2018
“Common genetic variants contribute to risk of rare severe neurodevelopmental disorders”, 2018-05-04 ( ; similar)
“An Analytical Framework for Whole-genome Sequence Association Studies and Its Implications for Autism Spectrum Disorder”, Et Al 2018
“Common Risk Variants Identified in Autism Spectrum Disorder”, Et Al 2017
“Common risk variants identified in autism spectrum disorder”, 2017-11-25 ( ; backlinks; similar)
“Linkage Disequilibrium-dependent Architecture of Human Complex Traits Shows Action of Negative Selection”, Et Al 2017
“Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection”, 2017-09-11 ( ; backlinks; similar)
“Genome-wide Association Analyses Identify 44 Risk Variants and Refine the Genetic Architecture of Major Depressive Disorder”, Et Al 2017
“Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressive disorder”, 2017-07-24 ( ; similar)
“Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum”, Et Al 2017
“Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum”, 2017-06-09 ( ; similar)
“Widespread Signatures of Positive Selection in Common Risk Alleles Associated to Autism Spectrum Disorder”, 2017
“Widespread signatures of positive selection in common risk alleles associated to autism spectrum disorder”, 2017-02-07 ( ; similar)
“Polygenic Transmission Disequilibrium Confirms That Common and Rare Variation Act Additively to Create Risk for Autism Spectrum Disorders”, Et Al 2016
“Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders”, 2016-11-23 ( ; similar)
“Genome-wide Analyses of Empathy and Systemizing: Heritability and Correlates With Sex, Education, and Psychiatric Risk”, Et Al 2016
“Genome-wide analyses of empathy and systemizing: heritability and correlates with sex, education, and psychiatric risk”, 2016-04-29 ( ; similar)
“Shared Genetic Aetiology between Cognitive Functions and Physical and Mental Health in UK Biobank (N = 112,151) and 24 GWAS Consortia”, Et Al 2016
“Shared genetic aetiology between cognitive functions and physical and mental health in UK Biobank (n = 112,151) and 24 GWAS consortia”, 2016-01-26 ( ; backlinks; similar)
“Genetic Risk for Autism Spectrum Disorders and Neuropsychiatric Variation in the General Population”, Et Al 2016
“Whole-genome Sequencing of Quartet Families With Autism Spectrum Disorder”
“Synaptic, Transcriptional and Chromatin Genes Disrupted in Autism”, Et Al 2014
“Synaptic, transcriptional and chromatin genes disrupted in autism”, 2014-10-29 ( ; backlinks; similar)
“The Contribution Of De Novo Coding Mutations to Autism Spectrum Disorder”, Et Al 2014
“The contribution of de novo coding mutations to autism spectrum disorder”, 2014 ( ; backlinks; similar)
“Fecundity of Patients With Schizophrenia, Autism, Bipolar Disorder, Depression, Anorexia Nervosa, or Substance Abuse vs Their Unaffected Siblings”, Et Al 2013
“Fecundity of Patients With Schizophrenia, Autism, Bipolar Disorder, Depression, Anorexia Nervosa, or Substance Abuse vs Their Unaffected Siblings”, 2013-01 ( ; backlinks; similar)
“Genetic Relationship between Five Psychiatric Disorders Estimated from Genome-wide SNPs”, Et Al 2013
“Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs”, 2013 ( ; similar)
“CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics”, 2012
“CNVs: harbingers of a rare variant revolution in psychiatric genetics”, 2012 ( ; similar)
“The Role of Genetic Variation in the Causation of Mental Illness: an Evolution-informed Framework”, 2009
“The role of genetic variation in the causation of mental illness: an evolution-informed framework”, 2009-08-25 ( ; similar; bibliography)
“Factors and Primes: a Specific Numerical Ability”, Hermelin & 1990
“Factors and primes: a specific numerical ability”, 1990-02-01 ( )
“Infantile Autism: A Genetic Study Of 21 Twin Pairs”, 1977
“Infantile Autism: A Genetic Study Of 21 Twin Pairs”, 1977-09-01 ( ; similar)
“Fathers Bequeath More Mutations As They Age: Genome Study May Explain Links between Paternal Age and Conditions such as Autism”
“Monkeys Genetically Modified to Show Autism Symptoms: But It Is Unclear How Well the Results Match the Condition in Humans”
Wikipedia
Miscellaneous
Link Bibliography
-
https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2798872
: “Association of Prenatal Exposure to Benzodiazepines With Development of Autism Spectrum and Attention-Deficit / Hyperactivity Disorders”, Vincent Chin-Hung Chen, Shu-I Wu, Chiao-Fan Lin, Mong-Liang Lu, Yi-Lung Chen, Robert Stewart: -
2022-mitchell.pdf
: “Polygenic Influences Associated With Adolescent Cognitive Skills”, : -
2021-song.pdf
: “A Selection Pressure Landscape for 870 Human Polygenic Traits”, Weichen Song, Yueqi Shi, Weidi Wang, Weihao Pan, Wei Qian, Shunying Yu, Min Zhao, Guan Ning Lin: -
https://link.springer.com/article/10.1007/s10943-019-00926-3
: “The Myth of the Stupid Believer: The Negative Religiousness-IQ Nexus Is Not on General Intelligence (<em>g< / em>) and Is Likely a Product of the Relations Between IQ and Autism Spectrum Traits”, Edward Dutton, Jan te Nijenhuis, Daniel Metzen, Dimitri van der Linden4, Guy Madison: -
2009-uher.pdf
: “The Role of Genetic Variation in the Causation of Mental Illness: an Evolution-informed Framework”, Rudolf Uher: