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English
Rethinking the genetic architecture of schizophrenia.
scientific article published on 12 April 2010
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
Rethinking the genetic architecture of schizophrenia
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
main subject
schizophrenia
0 references
author
David J. Porteous
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
Kevin J. Mitchell
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
author name string
K J Mitchell
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1
1 reference
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Europe PubMed Central
PubMed publication ID
20380786
retrieved
22 August 2017
language of work or name
English
0 references
publication date
12 April 2010
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
published in
Psychological Medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
volume
41
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
page(s)
19-32
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol
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Noise, delays, robustness, canalization and all that
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A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression
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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
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Relation of schizophrenia prevalence to latitude, climate, fish consumption, infant mortality, and skin color: a role for prenatal vitamin d deficiency and infections?
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Rare chromosomal deletions and duplications increase risk of schizophrenia
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CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.
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Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
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Family aggregation of mental disorders in the nationwide Danish three generation study.
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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
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7 January 2021
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A framework for interpreting genome-wide association studies of psychiatric disorders
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Severe mental disorders in offspring with 2 psychiatrically ill parents.
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A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation
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Common variants on chromosome 6p22.1 are associated with schizophrenia
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The DISC locus in psychiatric illness
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7 January 2021
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Disruption of the neurexin 1 gene is associated with schizophrenia
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7 January 2021
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Advancing paternal age and the risk of schizophrenia
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7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Parkinsonism with digenic parkin and PINK1 mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Modifier genes in mice and humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrence risks in an oligogenic threshold model: the effect of alterations in allele frequency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Precursors and prodromata of schizophrenia: findings from the Edinburgh High Risk Study and their literature context
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Testing the monogenic theory of schizophrenia: An application of segregation analysis to blind family study data
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrent CNVs disrupt three candidate genes in schizophrenia patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biological robustness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A nonsense mutation in the synaptogyrin 1 gene in a family with schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Resolving genetic models for the transmission of schizophrenia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurological abnormalities among offspring of persons with schizophrenia: relation to premorbid psychopathology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Premorbid IQ in schizophrenia: a meta-analytic review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS003329171000070X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S003329171000070X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
PubMed publication ID
20380786
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20380786
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20380786%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 January 2020
ResearchGate publication ID
43097807
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