Child development and molecular genetics: 14 years later (Q26853446)

main subject

developmental disability

3 references

20 August 2019

30 April 2021

28 October 2022

physiological phenomenon

1 reference

20 August 2019

1 reference

30 April 2021

Robert Plomin

1

0 references

language of work or name

1 reference

2013

1 reference

30 March 2012

3 references

20 August 2019

30 April 2021

28 October 2022

4 references

20 August 2019

30 April 2021

28 October 2022

84

1 reference

issue

1

1 reference

page(s)

104-20

1 reference

Creative Commons Attribution 2.5 Generic

copyright license

3 references

Europe PubMed Central

20 August 2019

Europe PubMed Central

30 April 2021

Europe PubMed Central

A map of human genome variation from population-scale sequencing

28 October 2022

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7 April 2017

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High-resolution analysis of parent-of-origin allelic expression in the mouse brain

7 April 2017

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Generalist genes analysis of DNA markers associated with mathematical ability and disability reveals shared influence across ages and abilities

7 April 2017

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7 April 2017

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7 April 2017

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Association between a literature-based genetic risk score and cardiovascular events in women

7 April 2017

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Finding the missing heritability of complex diseases

7 April 2017

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Common variants on chromosome 6p22.1 are associated with schizophrenia

7 April 2017

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Common variants conferring risk of schizophrenia

7 April 2017

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The genetic contribution to non-syndromic human obesity

7 April 2017

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

7 April 2017

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Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

7 April 2017

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Epistasis--the essential role of gene interactions in the structure and evolution of genetic systems

7 April 2017

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Large recurrent microdeletions associated with schizophrenia

7 April 2017

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Rare chromosomal deletions and duplications increase risk of schizophrenia

7 April 2017

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

7 April 2017

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Data and theory point to mainly additive genetic variance for complex traits

7 April 2017

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

7 April 2017

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Heritability in the genomics era — concepts and misconceptions

7 April 2017

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Epigenomic profiling reveals DNA-methylation changes associated with major psychosis

7 April 2017

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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

7 April 2017

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Genetic prediction of future type 2 diabetes

7 April 2017

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What is a gene, post-ENCODE? History and updated definition

7 April 2017

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

7 April 2017

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A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

7 April 2017

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Global variation in copy number in the human genome

7 April 2017

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Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings

7 April 2017

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Complement factor H polymorphism in age-related macular degeneration

7 April 2017

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Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

7 April 2017

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

7 April 2017

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7 April 2017

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Estimate of the mutation rate per nucleotide in humans

7 April 2017

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Genetic heterogeneity in human disease

7 April 2017

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

7 April 2017

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Association between microdeletion and microduplication at 16p11.2 and autism

7 April 2017

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A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

7 April 2017

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HTRA1 promoter polymorphism in wet age-related macular degeneration

7 April 2017

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Origins and functional impact of copy number variation in the human genome

7 April 2017

1 reference

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Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Common SNPs explain a large proportion of the heritability for human height

7 April 2017

1 reference

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Environmental epigenomics and disease susceptibility

7 April 2017

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The future of genetic studies of complex human diseases

7 April 2017

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Missing heritability and strategies for finding the underlying causes of complex disease

7 April 2017

1 reference

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Understanding mechanisms underlying human gene expression variation with RNA sequencing

7 April 2017

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Rare variants create synthetic genome-wide associations

7 April 2017

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Common genetic variation and human traits

7 April 2017

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Human genetic variation and its contribution to complex traits

7 April 2017

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Personal genomes: The case of the missing heritability

7 April 2017

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Common and rare variants in multifactorial susceptibility to common diseases

7 April 2017

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Genome-wide association analysis identifies 20 loci that influence adult height

7 April 2017

1 reference

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Genome-wide association studies for common diseases and complex traits

7 April 2017

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Genetical Implications of the Structure of Deoxyribonucleic Acid

7 April 2017

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7 April 2017

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Replication validity of genetic association studies

21 January 2018

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Transgenerational genetic effects

7 April 2017

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Estimating missing heritability for disease from genome-wide association studies

28 September 2017

1 reference

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Synthetic associations created by rare variants do not explain most GWAS results

28 September 2017

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A commentary on 'common SNPs explain a large proportion of the heritability for human height' by Yang et al. (2010).

28 September 2017

1 reference

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Transgenerational epigenetic inheritance: more questions than answers.

28 September 2017

1 reference

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Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Annotating non-coding regions of the genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Sex-specific parent-of-origin allelic expression in the mouse brain

28 September 2017

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Estimation of effect size distribution from genome-wide association studies and implications for future discoveries

28 September 2017

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Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics

28 September 2017

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Uncovering the roles of rare variants in common disease through whole-genome sequencing

28 September 2017

1 reference

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Reading and Generalist Genes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Epigenetics and the biological definition of gene x environment interactions

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

A three-stage genome-wide association study of general cognitive ability: hunting the small effects.

28 September 2017

1 reference

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The pursuit of genome-wide association studies: where are we now?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Allelic skewing of DNA methylation is widespread across the genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Beyond genome-wide association studies: genetic heterogeneity and individual predisposition to cancer

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Structural variation in the human genome and its role in disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

A genome-wide association study identifies multiple loci associated with mathematics ability and disability

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Parental origin of sequence variants associated with complex diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Epigenetics and the environmental regulation of the genome and its function

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Common disorders are quantitative traits

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

An evaluation of statistical approaches to rare variant analysis in genetic association studies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Epistasis and its implications for personal genetics.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Genomic copy number variation, human health, and disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Common vs. rare allele hypotheses for complex diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Duplication hotspots, rare genomic disorders, and common disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Schizophrenia genetics: new insights from new approaches

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Detecting gene-gene interactions that underlie human diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Epigenetic inheritance and the missing heritability problem

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Evidence-based public health: a fundamental concept for public health practice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Predicting human height by Victorian and genomic methods

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Population analysis of large copy number variants and hotspots of human genetic disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

DNA methylation profiles in monozygotic and dizygotic twins.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Meta-analysis of the association of the HTRA1 polymorphisms with the risk of age-related macular degeneration

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Prediction of individual genetic risk of complex disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Pre- and peri-natal environmental risks for attention-deficit hyperactivity disorder (ADHD): the potential role of epigenetic processes in mediating susceptibility

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Epigenetic mechanisms mediating the long-term effects of maternal care on development.

28 September 2017

1 reference

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Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms

28 September 2017

1 reference

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Five common gene variants identify elevated genetic risk for coronary heart disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Association between common variation in 120 candidate genes and breast cancer risk

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Gene-environment interdependence

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Systematic review and meta-analysis of the association between complement factor H Y402H polymorphisms and age-related macular degeneration

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Molecular and comparative genetics of mental retardation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

An epidemiologic assessment of genomic profiling for measuring susceptibility to common diseases and targeting interventions

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Positive psychology. An introduction

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

GWAS: heritability missing in action?

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

Neuroscience: In their nurture.

31 May 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Little epistasis for anxiety-related measures in the DeFries strains of laboratory mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Hints of hidden heritability in GWAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Personalized genomic information: preparing for the future of genetic medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Interpretation of interactions: guide for the perplexed

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Epigenetics. The seductive allure of behavioral epigenetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Epigenetics as a unifying principle in the aetiology of complex traits and diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Common disorders are quantitative traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Candidate-gene approaches for studying complex genetic traits: practical considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

A custody battle for the mind: evidence for extensive imprinting in the brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Missing heritability in genome-wide association study research

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Sizing up human height variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Proof of principle of potential clinical utility of multiple SNP analysis for prediction of recurrent venous thrombosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Prediction of Coronary Heart Disease Risk using a Genetic Risk Score: The Atherosclerosis Risk in Communities Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Genome-wide genetic association of complex traits in heterogeneous stock mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01757.X

Child development, molecular genetics, and what to do with genes once they are found.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3593231

The genetics of inflammatory bowel disease

28 November 2018

1 reference

12 December 2020

1000 Genomes Project promises closer look at variation in human genome

1 reference

12 December 2020

Genomewide association studies--illuminating biologic pathways

1 reference

12 December 2020

Polygenic susceptibility to breast cancer and implications for prevention

1 reference

12 December 2020

10.1111/J.1467-8624.2012.01757.X

Identifiers

DOI

0 references

1 reference

PubMed publication ID

22469254

1 reference