(Q35569496)

8 August 2017

1 reference

title

The molecular genetics of schizophrenia: new findings promise new insights (English)

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8 August 2017

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3

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8 August 2017

Owen MJ

1

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PubMed ID

14581932

8 August 2017

Williams NM

series ordinal

2

1 reference

PubMed ID

14581932

8 August 2017

language of work or name

English

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publication date

1 January 2004

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8 August 2017

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8 August 2017

9

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8 August 2017

14-27

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8 August 2017

1

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001444

8 August 2017

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cites work

Searching for schizophrenia genes

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

21 January 2018

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Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

21 January 2018

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Candidate gene for the chromosome 1 familial Alzheimer's disease locus

21 January 2018

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A polygenic theory of schizophrenia

21 January 2018

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Psychiatric genetics: back to the future

21 January 2018

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Is there really a split in schizophrenia? The genetic evidence

21 January 2018

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Twin concordance for DSM-III schizophrenia. Scrutinizing the validity of the definition.

21 January 2018

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Evaluating the spectrum concept of schizophrenia in the Roscommon Family Study

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

The structure of psychosis: latent class analysis of probands from the Roscommon Family Study

21 January 2018

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A twin study of genetic relationships between psychotic symptoms

21 January 2018

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The endophenotype concept in psychiatry: etymology and strategic intentions

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

The future of genetic studies of complex human diseases

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

The structure of haplotype blocks in the human genome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

High density synthetic oligonucleotide arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Lifetime prevalence, demographic risk factors, and diagnostic validity of nonaffective psychosis as assessed in a US community sample. The National Comorbidity Survey

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Neuregulin 1 and susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Replication of linkage studies of complex traits: an examination of variation in location estimates

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A schizophrenia locus may be located in region 10p15-p11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Finding the molecular basis of quantitative traits: successes and pitfalls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Large upward bias in estimation of locus-specific effects from genomewide scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Candidate-gene association studies of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Chromosomal abnormalities and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genetics of schizophrenia and the new millennium: progress and pitfalls

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Chromosomal abnormalities and mental illness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association within a family of a balanced autosomal translocation with major mental illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Functional polymorphism of -141C Ins/Del in the dopamine D2 receptor gene promoter and schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Transmission disequilibrium analysis of a triplet repeat within the hKCa3 gene using family trios with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

-141 C del/ins polymorphism of the dopamine receptor 2 gene is associated with schizophrenia in a British population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association between schizophrenia and homozygosity at the dopamine D3 receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

How many diseases does it take to map a gene with SNPs?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Replication validity of genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Glial growth factor/neuregulin inhibits Schwann cell myelination and induces demyelination

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Cell death in the Schwann cell lineage and its regulation by neuregulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

GGF/neuregulin is a neuronal signal that promotes the proliferation and survival and inhibits the differentiation of oligodendrocyte progenitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

White matter changes in schizophrenia: evidence for myelin-related dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

d -serine and serine racemase are present in the vertebrate retina and contribute to the physiological activation of NMDA receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Free D-serine in post-mortem brains and spinal cords of individuals with and without neuropsychiatric diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association and linkage analyses of RGS4 polymorphisms in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Analysis of complex brain disorders with gene expression microarrays: schizophrenia as a disease of the synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Disease-specific changes in regulator of G-protein signaling 4 (RGS4) expression in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Soluble and particulate forms of rat catechol-O-methyltransferase distinguished by gel electrophoresis and immune fixation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association analysis of a functional catechol-o-methyltransferase gene polymorphism in schizophrenic patients in Taiwan

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A highly significant association between a COMT haplotype and schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association between PRODH and schizophrenia is not confirmed

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Quantitative trait loci in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genes for schizophrenia? Recent findings and their pathophysiological implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Association studies in psychiatric genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

Genomic scan for genes predisposing to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

A single dominant gene still cannot account for the transmission of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Finnish adoptive family study: sample selection and adoptee DSM-III-R diagnoses

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Expression profiling using cDNA microarrays

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

An international two-stage genome-wide search for schizophrenia susceptibility genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

6p24-22 region and major psychoses in the Eastern Quebec population. Le Groupe IREP

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Genome scan of European-American schizophrenia pedigrees: Results of the NIMH genetics initiative and millennium consortium

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

The replication requirement

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

The serotonin-2A receptor gene locus does not contain common polymorphism affecting mRNA levels in adult brain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Cis-acting variation in the expression of a high proportion of genes in human brain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Characterization of membrane-bound and soluble catechol-O-methyltransferase from human frontal cortex

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Preferential transmission of the high activity allele of COMT in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001444

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001444

1 reference

8 August 2017

1 reference

PubMed ID

14581932