(Q37559492)

21 August 2017

1 reference

title

Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future (English)

1 reference

21 August 2017

0 references

1 reference

Maaike Alaerts

1

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21 August 2017

Jurgen Del-Favero

series ordinal

2

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21 August 2017

publication date

1 August 2009

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21 August 2017

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21 August 2017

volume

30

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21 August 2017

issue

8

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21 August 2017

page(s)

1139-1152

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Differential diagnoses and management strategies in patients with schizophrenia and bipolar disorder

21 August 2017

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7 January 2021

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7 January 2021

Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms

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7 January 2021

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

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7 January 2021

Evaluating coverage of genome-wide association studies

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7 January 2021

Schizophrenia and 22q11.2 deletion syndrome

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Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

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7 January 2021

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

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7 January 2021

Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement

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7 January 2021

Evidence for shared susceptibility in bipolar disorder and schizophrenia

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7 January 2021

Dysregulation of miRNA 181b in the temporal cortex in schizophrenia.

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7 January 2021

Increased LIS1 expression affects human and mouse brain development

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7 January 2021

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

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7 January 2021

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

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https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Common and rare variants in multifactorial susceptibility to common diseases

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7 January 2021

Population genetics--making sense out of sequence

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7 January 2021

The DISC locus in psychiatric illness

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7 January 2021

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

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7 January 2021

Problems of reporting genetic associations with complex outcomes

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7 January 2021

A high-resolution survey of deletion polymorphism in the human genome

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7 January 2021

Copy-number variations associated with neuropsychiatric conditions

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7 January 2021

Mutational and selective effects on copy-number variants in the human genome

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https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The beginning of the end for the Kraepelinian dichotomy.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The genetics of schizophrenia and bipolar disorder: dissecting psychosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Phenotypic and genetic complexity of psychosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A continuum of psychosis, one human gene, and not much else--the case for homogeneity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

How and why genetic linkage has not solved the problem of psychosis: review and hypothesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Efficiency and power in genetic association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Small deletion variants have stable breakpoints commonly associated with alu elements.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Association study of CHRFAM7A copy number and 2bp deletion polymorphisms with schizophrenia and bipolar affective disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The copy number variant involving part of the alpha7 nicotinic receptor gene contains a polymorphic inversion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Bipolar illness and schizophrenia as oligogenic diseases: implications for the future

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

An SNP-guided microRNA map of fifteen common human disorders identifies a consensus disease phenocode aiming at principal components of the nuclear import pathway

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The endophenotype concept in psychiatry: etymology and strategic intentions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Mechanisms for human genomic rearrangements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Brain expressed microRNAs implicated in schizophrenia etiology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genome-wide association studies for common diseases and complex traits

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The genetic basis of complex traits: rare variants or "common gene, common disease"?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genotype, haplotype and copy-number variation in worldwide human populations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Disruption of the neuronal PAS3 gene in a family affected with schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Efficient control of population structure in model organism association mapping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Mapping and sequencing of structural variation from eight human genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Paired-end mapping reveals extensive structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Increase inGSK3β gene copy number variation in bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Improved correction for population stratification in genome-wide association studies by identifying hidden population structures

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Assessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21q

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

An analysis of human microRNA and disease associations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A new multipoint method for genome-wide association studies by imputation of genotypes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Common deletion polymorphisms in the human genome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Extending genome-wide association studies to copy-number variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Integrated detection and population-genetic analysis of SNPs and copy number variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Schizophrenia: a common disease caused by multiple rare alleles

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Epigenomic profiling reveals DNA-methylation changes associated with major psychosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Disruption of two novel genes by a translocation co-segregating with schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Disrupted in schizophrenia 1 and phosphodiesterase 4B: towards an understanding of psychiatric illness

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

An initial map of insertion and deletion (INDEL) variation in the human genome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Identification of DNA copy-number aberrations by array-comparative genomic hybridization in patients with schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Schizophrenia and velo-cardio-facial syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A genome-wide investigation of SNPs and CNVs in schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Bias of selection on human copy-number variants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Identification of loci associated with schizophrenia by genome-wide association and follow-up

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Microarray-based genomic selection for high-throughput resequencing.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Evaluating and improving power in whole-genome association studies using fixed marker sets.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Simulations provide support for the common disease-common variant hypothesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The fine-scale and complex architecture of human copy-number variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The NPAS3 gene--emerging evidence for a role in psychiatric illness

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Somatic mosaicism for copy number variation in differentiated human tissues

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Common and rare alleles as causes of complex phenotypes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Are rare variants responsible for susceptibility to complex diseases?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The allelic architecture of human disease genes: common disease-common variant... or not?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

On the allelic spectrum of human disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The genetics of bipolar disorder: genome ‘hot regions,’ genes, new potential candidates and future directions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Logistic regression protects against population structure in genetic association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Shared gene expression alterations in schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Segmental duplications and copy-number variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Emerging themes and new challenges in defining the role of structural variation in human disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Whole-genome association study of bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

On the mechanism of gene amplification induced under stress in Escherichia coli

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

The allelic structure of common disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genome architecture, rearrangements and genomic disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Large recurrent microdeletions associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Statistical significance for genomewide studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Relative impact of nucleotide and copy number variation on gene expression phenotypes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Genomewide association for schizophrenia in the CATIE study: results of stage 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Gene copy number variation in schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Schizophrenia, "just the facts" what we know in 2008. 2. Epidemiology and etiology

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https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Are schizophrenia and affective disorder related?: the problem of schizoaffective disorder and the discrimination of the psychoses by signs and symptoms

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Epigenetic regulation in psychiatric disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Fine-scale structural variation of the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Frequency of new copy number variation in humans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Epigenetic mechanisms in the context of complex diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Chasing genes for mood disorders and schizophrenia in genetically isolated populations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Is COMT a susceptibility gene for schizophrenia?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Strong evidence that GNB1L is associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A comprehensive analysis of common copy-number variations in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Strong association of de novo copy number mutations with sporadic schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

How many genes underlie the occurrence of common complex diseases in the population?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

A unified mixed-model method for association mapping that accounts for multiple levels of relatedness

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Leveraging the HapMap correlation structure in association studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Singleton deletions throughout the genome increase risk of bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Germ-line DNA copy number variation frequencies in a large North American population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21042

7 January 2021

Identifiers

DOI

10.1002/HUMU.21042

1 reference

21 August 2017

1 reference