What is complex about complex disorders? (Q42132685)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

editorial

0 references

title

What is complex about complex disorders? (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author name string

Kevin J Mitchell

series ordinal

1

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17 October 2017

23 January 2012

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

page(s)

237

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

20 January 2020

cites work

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Clan genomics and the complex architecture of human disease

29 May 2018

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Complex genetic architecture of Drosophila aggressive behavior

29 May 2018

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Unlocking Mendelian disease using exome sequencing

29 May 2018

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The functional spectrum of low-frequency coding variation

29 May 2018

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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

29 May 2018

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Pervasive sharing of genetic effects in autoimmune disease

29 May 2018

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A copy number variation morbidity map of developmental delay

29 May 2018

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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

29 May 2018

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Exome sequencing supports a de novo mutational paradigm for schizophrenia.

29 May 2018

1 reference

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Genetics of type 2 diabetes: the GWAS era and future perspectives [Review]

29 May 2018

1 reference

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Demographic history and rare allele sharing among human populations

29 May 2018

1 reference

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Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy

29 May 2018

1 reference

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Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

29 May 2018

1 reference

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

29 May 2018

1 reference

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Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders

29 May 2018

1 reference

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

29 May 2018

1 reference

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Genome partitioning of genetic variation for complex traits using common SNPs

29 May 2018

1 reference

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A genome-wide comparison of the functional properties of rare and common genetic variants in humans

29 May 2018

1 reference

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A population genetic approach to mapping neurological disorder genes using deep resequencing

29 May 2018

1 reference

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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The Importance of Synthetic Associations Will Only Be Resolved Empirically

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Synthetic associations are unlikely to account for many common disease genome-wide association signals

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

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

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Genetic modifiers of neurological disease

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

AIP mutation in pituitary adenomas in the 18th century and today

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting

29 May 2018

1 reference

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Deep resequencing reveals excess rare recent variants consistent with explosive population growth

29 May 2018

1 reference

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Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome.

29 May 2018

1 reference

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A map of human genome variation from population-scale sequencing

29 May 2018

1 reference

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Allelic diversity in human developmental neurogenetics: insights into biology and disease

29 May 2018

1 reference

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

29 May 2018

1 reference

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

29 May 2018

1 reference

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The characterization of twenty sequenced human genomes

29 May 2018

1 reference

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The genetics of neurodevelopmental disease.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Evolutionary evidence of the effect of rare variants on disease etiology

29 May 2018

1 reference

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Functional roles for noise in genetic circuits

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Achondroplasia: pathogenesis and implications for future treatment

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Genomic analysis of mental illness: a changing landscape

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

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

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The genome-wide association study--a new era for common polygenic disorders

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Functional impact of global rare copy number variation in autism spectrum disorders

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

29 May 2018

1 reference

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Strong synaptic transmission impact by copy number variations in schizophrenia

29 May 2018

1 reference

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Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

29 May 2018

1 reference

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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

29 May 2018

1 reference

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Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease

29 May 2018

1 reference

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Clinical assessment incorporating a personal genome

29 May 2018

1 reference

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Tourette syndrome is associated with recurrent exonic copy number variants

29 May 2018

1 reference

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Genetic heterogeneity in human disease

29 May 2018

1 reference

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Rethinking the genetic architecture of schizophrenia.

29 May 2018

1 reference

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Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait

29 May 2018

1 reference

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A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci

29 May 2018

1 reference

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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Evolution in health and medicine Sackler colloquium: Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Rare variants create synthetic genome-wide associations

29 May 2018

1 reference

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The Kraepelinian dichotomy - going, going... but still not gone

29 May 2018

1 reference

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Narrowing the boundaries of the genetic architecture of schizophrenia.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

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

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Common disorders are quantitative traits

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Finding the missing heritability of complex diseases

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The role of genetic variation in the causation of mental illness: an evolution-informed framework

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

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

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

A genome-wide investigation of SNPs and CNVs in schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Genetic architecture of complex traits: large phenotypic effects and pervasive epistasis

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Nature, nurture, or chance: stochastic gene expression and its consequences

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Large recurrent microdeletions associated with schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Rare chromosomal deletions and duplications increase risk of schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The 'common disease-common variant' hypothesis and familial risks

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Assessing the evolutionary impact of amino acid mutations in the human genome

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Strong association of de novo copy number mutations with sporadic schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

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

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Structural variation of chromosomes in autism spectrum disorder

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The rise and fall of the common disease-common variant (CD-CV) hypothesis: how the sickle cell disease paradigm led us all astray (or did it?).

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

New links to the pathogenesis of Crohn disease provided by genome-wide association scans

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The DISC locus in psychiatric illness

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The genetics of brain wiring: from molecule to mind

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Strong association of de novo copy number mutations with autism

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Schizophrenia: a common disease caused by multiple rare alleles

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Heritability of Threshold Characters.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Resolving the paradox of common, harmful, heritable mental disorders: which evolutionary genetic models work best?

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Genome-wide association studies for common diseases and complex traits

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Flexibility in a gene network affecting a simple behavior in Drosophila melanogaster

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

29 May 2018

Biological robustness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Noise, delays, robustness, canalization and all that

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The International HapMap Project

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Beyond Mendel: an evolving view of human genetic disease transmission

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Complex genetic diseases: controversy over the Croesus code

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

On the allelic spectrum of human disease

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Are rare variants responsible for susceptibility to complex diseases?

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Error and attack tolerance of complex networks

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

The future of genetic studies of complex human diseases

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Refutation of the general single-locus model for the etiology of schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

A polygenic theory of schizophrenia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Frequency in relatives for an all‐or‐none trait

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Resolving genetic models for the transmission of schizophrenia.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Linkage strategies for genetically complex traits. I. Multilocus models

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Genetic linkage and complex diseases, with special reference to psychiatric disorders

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Parieto-occipital lobe epilepsy caused by a POLG1 compound heterozygous A467T/W748S genotype.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

A family-based study of common polygenic variation and risk of schizophrenia

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

A de novo paradigm for mental retardation

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Digenic mutations in severe myoclonic epilepsy of infancy

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Masking epilepsy by combining two epilepsy genes.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Mina, an Il4 repressor, controls T helper type 2 bias

17 August 2018

1 reference

https://api.crossref.org/works/10.1186%2FGB-2012-13-1-237

Genome-wide association study identifies five new schizophrenia loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FGB-2012-13-1-237

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FGB-2012-13-1-237

Targeted capture and massively parallel sequencing of 12 human exomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FGB-2012-13-1-237

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FGB-2012-13-1-237

Common disorders are quantitative traits

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3334577

Familial Parkinsonism with digenic parkin and PINK1 mutations.

1 December 2018

1 reference

12 December 2020

Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters

1 reference

12 December 2020

Increased exonic de novo mutation rate in individuals with schizophrenia

1 reference

12 December 2020

A study of rare structural variants in schizophrenia patients and normal controls from Chinese Han population

1 reference

12 December 2020

Identifiers

DOI

10.1186/GB-2012-13-1-237

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

20 January 2020

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/gb-2012-13-1-237

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

PubMed publication ID

22269335

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22269335%20AND%20SRC:MED&resulttype=core&format=json