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English
Schizophrenia: Incriminating genomic evidence
scientific article published in Nature
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
title
Schizophrenia: Incriminating genomic evidence
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
main subject
schizophrenia
1 reference
based on heuristic
inferred from title
author
James R. Lupski
series ordinal
1
object named as
James R Lupski
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
language of work or name
English
0 references
publication date
1 September 2008
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
published in
Nature
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
volume
455
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
issue
7210
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
page(s)
178-179
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
cites work
Psychiatric genetics: progress amid controversy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Large recurrent microdeletions associated with schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rare chromosomal deletions and duplications increase risk of schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strong association of de novo copy number mutations with sporadic schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic rearrangements and sporadic disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strong association of de novo copy number mutations with autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association between microdeletion and microduplication at 16p11.2 and autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrent 16p11.2 microdeletions in autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifying autism loci and genes by tracing recent shared ancestry
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F455178A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/455178A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
Dimensions Publication ID
1042638253
0 references
PubMed publication ID
18784712
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18784712
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18784712%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
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