Advances in the genetics of schizophrenia: toward a network and pathway view for drug discovery

The spectacular advance in our understanding of the genetic basis of schizophrenia through genome‐wide association studies has the potential to identify new leads for drug treatment through improved understanding of disease pathophysiology. However, using these genetic associations successfully in d...

Full description

Saved in:
Bibliographic Details
Published inAnnals of the New York Academy of Sciences Vol. 1366; no. 1; pp. 61 - 75
Main Authors Collier, David A., Eastwood, Brian J., Malki, Karim, Mokrab, Younes
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.02.2016
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
Abstract The spectacular advance in our understanding of the genetic basis of schizophrenia through genome‐wide association studies has the potential to identify new leads for drug treatment through improved understanding of disease pathophysiology. However, using these genetic associations successfully in drug development and patient stratification requires further target validation, particularly in understanding which gene(s) is causal in the disease, how the risk variants alter gene function and regulation, and how they fit into disease pathways and networks. If researchers consider the disease network as the target, they need to understand which genes should be targeted and in which modality, in order to modulate pathophysiology and obtain a beneficial effect for the patient. In the present article, we review recent genetic findings in schizophrenia and discuss how these might be validated with biology and integrated with epigenetic and transcriptome data to identify targets that lie within disease networks and pathways. This new understanding of disease biology will also facilitate the development of assays that recapitulate specific aspects of the disease using model organisms and cells. These assays can then be used in screening approaches, which manipulate disease networks or pathological processes to generate and test therapeutic strategies.
AbstractList The spectacular advance in our understanding of the genetic basis of schizophrenia through genome-wide association studies has the potential to identify new leads for drug treatment through improved understanding of disease pathophysiology. However, using these genetic associations successfully in drug development and patient stratification requires further target validation, particularly in understanding which gene(s) is causal in the disease, how the risk variants alter gene function and regulation, and how they fit into disease pathways and networks. If researchers consider the disease network as the target, they need to understand which genes should be targeted and in which modality, in order to modulate pathophysiology and obtain a beneficial effect for the patient. In the present article, we review recent genetic findings in schizophrenia and discuss how these might be validated with biology and integrated with epigenetic and transcriptome data to identify targets that lie within disease networks and pathways. This new understanding of disease biology will also facilitate the development of assays that recapitulate specific aspects of the disease using model organisms and cells. These assays can then be used in screening approaches, which manipulate disease networks or pathological processes to generate and test therapeutic strategies.
Author Eastwood, Brian J.
Mokrab, Younes
Collier, David A.
Malki, Karim
Author_xml – sequence: 1
  givenname: David A.
  surname: Collier
  fullname: Collier, David A.
  email: collier_david_andrew@lilly.com
  organization: Discovery Neuroscience Research, Eli Lilly and Company Ltd, Surrey, Windlesham, United Kingdom
– sequence: 2
  givenname: Brian J.
  surname: Eastwood
  fullname: Eastwood, Brian J.
  organization: Discovery Neuroscience Research, Eli Lilly and Company Ltd, Surrey, Windlesham, United Kingdom
– sequence: 3
  givenname: Karim
  surname: Malki
  fullname: Malki, Karim
  organization: Discovery Neuroscience Research, Eli Lilly and Company Ltd, Surrey, Windlesham, United Kingdom
– sequence: 4
  givenname: Younes
  surname: Mokrab
  fullname: Mokrab, Younes
  organization: Discovery Neuroscience Research, Eli Lilly and Company Ltd, Windlesham, Surrey, United Kingdom
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27111133$$D View this record in MEDLINE/PubMed
BookMark eNqN0UFv0zAYBmALDbFucOEHIEtcEFLG5zixXW7VBANpDKQBEyfLSb6s3lK72ElD-PW4dNthQoAP9uV5P9l-D8ie8w4JecrgiKX1yk0mHjEOQjwgMyaLeSYEz_fIDEDKTM1zvk8OYrwCYLkq5COyn8ttkPMZ0YtmY1yNkVpH-yXSS3TY2zpS39JYL-1Pv14GdNa8pr0fTWiooUmMPlxT4xq6Nv1yNBPdWBxp6wNtwnBJGxtrv8EwPSYPW9NFfHJzHpIvb998Pn6XnX48eX-8OM3qQjCRKS5kY2QjRAUMasFBlqpQpSybpi4Uq_KKgWQlcsQW5jmoCtOeQ1FhhbLlh-TFbu46-O8Dxl6v0hWw64xDP0TNFCgQpZTq31QqOVd5Cf9Fi_TfAEWiz-_RKz8El96cVBJClJwn9exGDdUKG70OdmXCpG8LSeDlDtTBxxiwvSMM9Nbobdv6d9sJwz1c29701rs-GNv9OcJ2kdF2OP1luD77tji_zWS7jI09_rjLmHCtheSy1BdnJ_rrJ_7h4nwudcl_Aae3yVU
CODEN ANYAA9
CitedBy_id crossref_primary_10_1016_j_bbr_2016_11_049
crossref_primary_10_30773_pi_2022_0343
crossref_primary_10_1016_j_schres_2019_03_010
crossref_primary_10_1186_s12974_017_0938_y
crossref_primary_10_1111_acer_14233
crossref_primary_10_1155_2018_2682037
crossref_primary_10_1177_0269881117715597
crossref_primary_10_3389_fpsyt_2022_885904
crossref_primary_10_1007_s00439_019_02098_2
crossref_primary_10_1016_j_bbrc_2017_03_141
crossref_primary_10_1038_s41537_016_0001_5
Cites_doi 10.1371/journal.pgen.1004494
10.1038/nature13595
10.1016/j.cell.2013.03.030
10.1186/1755-8794-7-S1-S8
10.1002/gepi.20199
10.1038/ng.2915
10.1016/S0140-6736(12)62129-1
10.1016/j.cell.2012.02.039
10.1186/1471-2105-9-559
10.1038/ng.3406
10.1186/1471-2164-15-S4-S5
10.1038/nature12873
10.1186/s11689-015-9113-x
10.1038/mp.2014.40
10.1016/j.neurol.2013.07.017
10.2337/db14-0703
10.1186/gm543
10.1016/j.biopsych.2014.10.008
10.1038/nn.3922
10.1038/ng.3404
10.1126/science.1239101
10.1176/appi.ajp.2013.13070864
10.1371/journal.pgen.1005230
10.1016/j.neuron.2015.04.022
10.1111/jcpp.12295
10.1016/j.ajhg.2012.11.004
10.1093/bioinformatics/btu848
10.1038/nature12929
10.1038/npp.2008.156
10.1093/hmg/ddu739
10.1038/mp.2011.94
10.1038/nbt.2151
10.1126/scitranslmed.3007941
10.1016/S0140-6736(15)01124-1
10.1038/ng.803
10.1126/science.344.6185.687
10.1001/jamapsychiatry.2013.3730
10.1038/nature16549
10.1007/s00439-014-1494-5
10.1126/science.1132939
10.1016/S0140-6736(09)60072-6
10.1016/j.tig.2014.10.001
10.1016/S0140-6736(13)60733-3
10.1038/mp.2013.138
10.1080/10543400903572753
10.1038/nn.3898
10.1186/s13059-014-0483-2
10.1038/nature08185
10.1007/s00335-007-9040-6
10.1038/nrg3228
10.1002/pd.4613
10.1016/S0166-2236(00)01862-2
10.1371/journal.pone.0063812
10.1016/j.ajhg.2011.11.006
10.1038/ng.2892
10.1042/BJ20040311
10.1007/978-3-642-25761-2_2
10.1038/nature12975
10.1038/ng.3246
10.1038/nrd2519
10.1007/978-1-4939-2627-5_28
ContentType Journal Article
Copyright 2016 New York Academy of Sciences.
2016 The New York Academy of Sciences
Copyright_xml – notice: 2016 New York Academy of Sciences.
– notice: 2016 The New York Academy of Sciences
DBID BSCLL
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7QG
7QL
7QP
7QR
7ST
7T5
7T7
7TK
7TM
7TO
7U7
7U9
8FD
C1K
FR3
H94
K9.
M7N
P64
RC3
SOI
7X8
7SP
7U5
L7M
DOI 10.1111/nyas.13066
DatabaseName Istex
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Animal Behavior Abstracts
Bacteriology Abstracts (Microbiology B)
Calcium & Calcified Tissue Abstracts
Chemoreception Abstracts
Environment Abstracts
Immunology Abstracts
Industrial and Applied Microbiology Abstracts (Microbiology A)
Neurosciences Abstracts
Nucleic Acids Abstracts
Oncogenes and Growth Factors Abstracts
Toxicology Abstracts
Virology and AIDS Abstracts
Technology Research Database
Environmental Sciences and Pollution Management
Engineering Research Database
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Algology Mycology and Protozoology Abstracts (Microbiology C)
Biotechnology and BioEngineering Abstracts
Genetics Abstracts
Environment Abstracts
MEDLINE - Academic
Electronics & Communications Abstracts
Solid State and Superconductivity Abstracts
Advanced Technologies Database with Aerospace
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Virology and AIDS Abstracts
Oncogenes and Growth Factors Abstracts
Technology Research Database
Toxicology Abstracts
Nucleic Acids Abstracts
ProQuest Health & Medical Complete (Alumni)
Neurosciences Abstracts
Biotechnology and BioEngineering Abstracts
Environmental Sciences and Pollution Management
Genetics Abstracts
Animal Behavior Abstracts
Bacteriology Abstracts (Microbiology B)
Algology Mycology and Protozoology Abstracts (Microbiology C)
AIDS and Cancer Research Abstracts
Chemoreception Abstracts
Immunology Abstracts
Engineering Research Database
Industrial and Applied Microbiology Abstracts (Microbiology A)
Calcium & Calcified Tissue Abstracts
Environment Abstracts
MEDLINE - Academic
Solid State and Superconductivity Abstracts
Advanced Technologies Database with Aerospace
Electronics & Communications Abstracts
DatabaseTitleList MEDLINE - Academic
Genetics Abstracts

Virology and AIDS Abstracts
CrossRef
Solid State and Superconductivity Abstracts
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Sciences (General)
Biology
EISSN 1749-6632
EndPage 75
ExternalDocumentID 4062118281
27111133
10_1111_nyas_13066
NYAS13066
ark_67375_WNG_VP3MWS97_5
Genre article
Journal Article
Review
GroupedDBID ---
--Z
-~X
.3N
.55
.GA
.GJ
.Y3
05W
0R~
10A
1CY
1OB
1OC
23M
31~
33P
3O-
3SF
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5HH
5LA
5RE
5VS
66C
692
6J9
702
79B
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AAMDK
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABDBF
ABEML
ABJNI
ABLJU
ABPVW
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFO
ACGFS
ACIWK
ACPOU
ACPRK
ACSCC
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOJD
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEGXH
AEIGN
AEIMD
AELAQ
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFNX
AFFPM
AFGKR
AFPWT
AFRAH
AFSWV
AFZJQ
AHBTC
AHEFC
AHMBA
AI.
AIAGR
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ATUGU
AUFTA
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BIYOS
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BSCLL
BY8
C45
CAG
CO8
COF
CS3
D-E
D-F
DC6
DCZOG
DPXWK
DR2
DRFUL
DRSTM
EBD
EBS
EJD
EMOBN
ESX
F00
F01
F04
F5P
FEDTE
FZ0
G-S
G.N
GODZA
H.T
H.X
HF~
HGLYW
HVGLF
HZI
HZ~
I-F
IH2
IX1
J0M
K48
L7B
LATKE
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NHB
O66
O9-
OHT
OIG
OK1
OVD
P2P
P2W
P2X
P4D
PALCI
PQQKQ
Q.N
Q11
QB0
R.K
RAG
RIWAO
RJQFR
ROL
RX1
S10
SAMSI
SJN
SUPJJ
SV3
TEORI
TUS
UB1
UPT
V8K
VH1
W8V
W99
WBKPD
WH7
WHWMO
WIH
WIK
WOHZO
WQJ
WRC
WUP
WVDHM
WXSBR
X7M
XG1
YBU
YOC
YSK
ZGI
ZKB
ZXP
ZZTAW
~02
~IA
~KM
~WT
AAHQN
AAMMB
AAMNL
AANHP
AAYCA
ACRPL
ACUHS
ACYXJ
ADNMO
ADXHL
AEFGJ
AEYWJ
AFWVQ
AGHNM
AGQPQ
AGXDD
AGYGG
AHDLI
AIDQK
AIDYY
ALVPJ
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7QG
7QL
7QP
7QR
7ST
7T5
7T7
7TK
7TM
7TO
7U7
7U9
8FD
C1K
FR3
H94
K9.
M7N
P64
RC3
SOI
7X8
7SP
7U5
L7M
ID FETCH-LOGICAL-c4616-8367da7d66b010c63075848575ddc481b2b10715e3eef09208be920204bebe7f3
IEDL.DBID DR2
ISSN 0077-8923
IngestDate Fri Jul 11 01:18:27 EDT 2025
Fri Jul 11 11:01:33 EDT 2025
Fri Jul 11 14:48:25 EDT 2025
Sun Jul 13 03:54:31 EDT 2025
Thu Apr 03 07:02:36 EDT 2025
Tue Jul 01 04:00:51 EDT 2025
Thu Apr 24 23:12:37 EDT 2025
Wed Aug 20 07:27:28 EDT 2025
Wed Oct 30 09:55:42 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords genome-wide association
drug discovery
pharmacogenetics
psychosis
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
2016 New York Academy of Sciences.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4616-8367da7d66b010c63075848575ddc481b2b10715e3eef09208be920204bebe7f3
Notes istex:C9478003805CC734D5F79E282B03C637324494FF
ark:/67375/WNG-VP3MWS97-5
ArticleID:NYAS13066
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Article-2
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
PMID 27111133
PQID 1790066533
PQPubID 946344
PageCount 15
ParticipantIDs proquest_miscellaneous_1808065778
proquest_miscellaneous_1787982508
proquest_miscellaneous_1784749004
proquest_journals_1790066533
pubmed_primary_27111133
crossref_primary_10_1111_nyas_13066
crossref_citationtrail_10_1111_nyas_13066
wiley_primary_10_1111_nyas_13066_NYAS13066
istex_primary_ark_67375_WNG_VP3MWS97_5
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate February 2016
PublicationDateYYYYMMDD 2016-02-01
PublicationDate_xml – month: 02
  year: 2016
  text: February 2016
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: New York
PublicationTitle Annals of the New York Academy of Sciences
PublicationTitleAlternate Ann. N.Y. Acad. Sci
PublicationYear 2016
Publisher Blackwell Publishing Ltd
Wiley Subscription Services, Inc
Publisher_xml – name: Blackwell Publishing Ltd
– name: Wiley Subscription Services, Inc
References Kumar, G., S.L. Clark, J.L. McClay, et al. 2015. Refinement of schizophrenia GWAS loci using methylome-wide association data. Hum. Genet. 134: 77-87.
Ruderfer, D.M., A.H. Fanous, S. Ripke, et al. 2014. Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Mol. Psychiatry 19: 1017-1024.
Zhao, W., P. Langfelder, T. Fuller, et al. 2010. Weighted gene coexpression network analysis: state of the art. J. Biopharm. Stat. 20: 281-300.
Euesden, J., C.M. Lewis & P.F. O'Reilly. 2015. PRSice: polygenic risk score software. Bioinformatics 31: 1466-1468.
Richmond, R.C., A.J. Simpkin, G. Woodward, et al. 2014. Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC). Hum. Mol. Genet. 24: 2201-2217.
International Schizophrenia Consortium; S.M. Purcell, N.R. Wray, J.L. Stone, et al. 2009. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460: 748-752.
Maniatis, N., A. Collins, N.E. Morton 2007. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping. Genet. Epidemiol. 31: 179-188.
Elding, H., W. Lau, D.M. Swallow & N. Maniatis. 2013. Refinement in localization and identification of gene regions associated with Crohn disease. Am. J. Hum. Genet. 92: 107-113.
McCarthy, D.J., P. Humburg, A. Kanapin, et al. 2014. Choice of transcripts and software has a large effect on variant annotation. Genome Med. 6: 26.
Cao, C. & J. Moult. 2014. GWAS and drug targets. BMC Genomics 15(Suppl. 4): S5.
Kingsmore, S.F., I.E. Lindquist, J. Mudge, et al. 2008. Genome-wide association studies: progress and potential for drug discovery and development. Nat. Rev. Drug Discov. 7: 221-230.
Bulik-Sullivan, B., H.K. Finucane, V. Anttila, et al. 2015. An atlas of genetic correlations across human diseases and traits. Nat. Genet. 47: 1236-1241.
Grati, F.R., D. Molina Gomes, J.C. Ferreira, et al. 2015. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies. Prenat. Diagn. 35: 801-809.
Birnbaum, R., A.E. Jaffe, Q. Chen, et al. 2015. Investigation of the prenatal expression patterns of 108 schizophrenia-associated genetic loci. Biol. Psychiatry 77: e43-e51.
Zeilinger, S., B. Kuhnel, N. Klopp, et al. 2013. Tobacco smoking leads to extensive genome-wide changes in DNA methylation. PLoS One 8: e63812.
Schizophrenia Working Group of the Psychiatric Genomics Consortium. 2014. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511: 421-427.
Elding, H., W. Lau, D.M. Swallow & N. Maniatis. 2011. Dissecting the genetics of complex inheritance: linkage disequilibrium mapping provides insight into Crohn disease. Am. J. Hum. Genet. 89: 798-805.
Langfelder, P. & S. Horvath. 2008. WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics 9: 559.
Purcell, S.M., J.L. Moran, M. Fromer, et al. 2014. A polygenic burden of rare disruptive mutations in schizophrenia. Nature 506: 185-190.
Mills, S.M., J. Mallmann, A.M. Santacruz, et al. 2013. Preclinical trials in autosomal dominant AD: implementation of the DIAN-TU trial. Rev. Neurol. (Paris) 169: 737-743.
Grover, M.P., S. Ballouz, K.A. Mohanasundaram, et al. 2014 Identification of novel therapeutics for complex diseases from genome-wide association data. BMC Med. Genomics 7(Suppl. 1): S8.
Conn, P.J. & C.K. Jones. 2009. Promise of mGluR2/3 activators in psychiatry. Neuropsychopharmacology 34: 248-249.
Sanseau, P., P. Agarwal, M.R. Barnes, et al. 2012. Use of genome-wide association studies for drug repositioning. Nat. Biotechnol. 30: 317-320.
Horikoshi, M., R. Mӓgi, van M. de Bunt, et al. 2015. Discovery and fine-mapping of glycaemic and obesity-related trait loci using high-density imputation. PLoS Genet. 11: e1005230.
Okada, Y., D. Wu, G. Trynka, et al. 2013. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature 506: 376-381.
Mirnics, K., F.A. Middleton, D.A. Lewis & P. Levitt. 2001. Analysis of complex brain disorders with gene expression microarrays: schizophrenia as a disease of the synapse. Trends Neurosci. 24: 479-486.
Jaffe, A.E., J. Shin, L. Collado-Torres, et al. 2015. Developmental regulation of human cortex transcription and its clinical relevance at single base resolution. Nat. Neurosci. 18: 154-161.
Hollingworth, P., D. Harold, R. Sims, et al. 2011. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat. Genet. 43: 429-435.
Sieberts, S.K. & E.E. Schadt. 2007. Moving toward a system genetics view of disease. Mamm. Genome 18: 389-401.
Lichtenstein, P., B.H. Yip, C. Björk, et al. 2009. Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet 373: 234-239.
Guna, A., N.J. Butcher & A.S. Bassett. 2015. Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms. J. Neurodev. Disord. 7: 18.
Zhang, B., C. Gaiteri, L.G. Bodea, et al. 2013. Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's disease. Cell 153: 707-720.
Cross-Disorder Group of the Psychiatric Genomics Consortium. 2013. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. Lancet 381: 1371-1379.
Sperling, R.A., D.M. Rentz, K.A. Johnson, et al. 2014. The A4 study: stopping AD before symptoms begin? Sci. Transl. Med. 6: 228fs13.
Pidsley, R., J. Viana, E. Hannon, et al. 2014. Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia. Genome Biol. 15: 483.
Zhang, B., L. Tran, V. Emilsson & J. Zhu. 2016. Characterization of genetic networks associated with Alzheimer's disease. Methods Mol. Biol. 1303: 459-477.
Sullivan, P.; 96 Psychiatric Genetics Investigators. 2012. Don't give up on GWAS. Mol. Psychiatry 17: 2-3.
Szatkiewicz, J.P., C. O'Dushlaine, G. Chen, et al. 2014. Copy number variation in schizophrenia in Sweden. Mol. Psychiatry 19: 762-773.
Wei, G.H., D.P. Liu & C.C. Liang. 2004. Charting gene regulatory networks: strategies, challenges and perspectives. Biochem. J. 381(Pt. 1): 1-12.
Cohen, J.C. & H.H. Hobbs. 2013. Genetics. Simple genetics for a complex disease. Science 340: 689-690.
Ginovart, N. & S. Kapur. 2012. Role of dopamine D2 receptors for antipsychotic activity. Handb. Exp. Pharmacol. 212: 27-52.
Lim, E.T., P. Würtz, A.S. Havulinna, et al. 2014. Distribution and medical impact of loss-of-function variants in the Finnish founder population. PLoS Genet. 10: e1004494.
Sedeño-Cortés, A.E. & P. Pavlidis. 2014. Pitfalls in the application of gene-set analysis to genetics studies. Trends Genet. 30: 513-514.
Pocklington, A.J., E. Rees, J.T. Walters, et al. 2015. Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia. Neuron 86: 1203-1214.
Kaiser, J. 2014. The hunt for missing genes. Science 344: 687-689.
Sekar, A., A.R. Bialas, de H. Rivera, et al. 2016. Schizophrenia risk from complex variation of complement component 4. Nature 530: 177-183.
Segrè, A.V., N. Wei; DIAGRAM Consortium; MAGIC Investigators, D. Altshuler & J.C. Florez. 2015. Pathways targeted by antidiabetes drugs are enriched for multiple genes associated with type 2 diabetes risk. Diabetes 64: 1470-1483.
Finucane, H.K., B. Bulik-Sullivan, A. Gusev, et al. 2015. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nat. Genet. 47: 1228-1235.
Scheltens, P., K. Blennow, M.M. Breteler, et al. 2016. Alzheimer's disease. Lancet pii: S0140-6736(15)01124-1.
Kircher, M., D.M. Witten, P. Jain, et al. 2014. A general framework for estimating the relative pathogenicity of human genetic variants. Nat. Genet. 46: 310-315.
Richards, J.B., H.F. Zheng & T.D. Spector. 2012. Genetics of osteoporosis from genome-wide association studies: advances and challenges. Nat. Rev. Genet. 13: 576-588.
Flannick, J., G. Thorleifsson, N.L. Beer, et al. 2014. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat. Genet. 46: 357-363.
Aberg, K.A., J.L. McClay, S. Nerella, et al. 2014. Methylome-wide association study of schizophrenia: identifying blood biomarker signatures of environmental insults. JAMA Psychiatry 71: 255-264.
Malhotra, D. & J. Sebat. 2012. CNVs: harbingers of a rare variant revolution in psychiatric genetics. Cell 148: 1223-1241.
Smith, T.E., C.A. Weston & J.A. Lieberman. 2009. Schizophrenia (maintenance treatment). BMJ Clin. Evid. 2009: 1007.
Leucht, S., A. Cipriani, L. Spineli, et al. 2013. Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis. Lancet 382: 951-962.
Wray, N.R., S.H. Lee, D. Mehta, et al. 2014. Research review: polygenic methods and their application to psychiatric traits. J. Child Psychol. Psychiatry. 55: 1068-1087.
Lamb, J., E.D. Crawford, D. Peck, et al. 2006. The connectivity map: using gene-expression signatures to connect small molecules, genes, and disease. Science 313: 1929-1935.
Schneider, M., M. Debbané, A.S. Bassett, et al. 2014. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. Am. J. Psychiatry 171: 627-639.
Steinberg, S., H. Stefansson, T. Jonsson, et al. 2015. Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease. Nat. Genet. 47: 445-447.
Fromer, M., A.J. Pocklington, D.H. Kavanagh, et al. 2014. De novo mutations in schizophrenia implicate synaptic networks. Nature 506: 179-184.
Network and Pathway Analysis Subgroup of Psychiatric Genomics Consortium. 2015. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nat. Neurosci. 18: 199-209.
2015; 35
2015; 31
2015; 77
2008; 9
2008; 7
2013; 169
2014; 24
2012; 17
2014; 171
2007; 31
2012; 13
2013; 8
2009; 2009
2015; 47
2010; 20
2012; 212
2015; 86
2015; 134
2014; 15
2014; 19
2013; 153
2014; 7
2014; 6
2014; 55
2014; 10
2007; 18
2015; 18
2013; 506
2015; 11
2004; 381
2014; 46
2013; 92
2016; 1303
2013; 382
2013; 340
2009; 373
2012; 148
2006; 313
2001; 24
2013; 381
2015; 7
2014; 511
2012; 30
2009; 34
2014; 506
2015; 64
2016; 530
2011; 43
2016
2011; 89
2009; 460
2014; 30
2014; 71
2014; 344
e_1_2_10_23_1
e_1_2_10_46_1
e_1_2_10_21_1
e_1_2_10_44_1
e_1_2_10_42_1
e_1_2_10_40_1
e_1_2_10_4_1
e_1_2_10_18_1
e_1_2_10_53_1
e_1_2_10_6_1
e_1_2_10_16_1
e_1_2_10_39_1
e_1_2_10_55_1
e_1_2_10_8_1
e_1_2_10_14_1
e_1_2_10_37_1
e_1_2_10_57_1
e_1_2_10_58_1
e_1_2_10_13_1
e_1_2_10_34_1
e_1_2_10_11_1
e_1_2_10_32_1
e_1_2_10_30_1
e_1_2_10_51_1
Smith T.E. (e_1_2_10_2_1) 2009; 2009
e_1_2_10_61_1
e_1_2_10_29_1
e_1_2_10_63_1
e_1_2_10_27_1
e_1_2_10_25_1
e_1_2_10_48_1
e_1_2_10_24_1
e_1_2_10_45_1
e_1_2_10_22_1
e_1_2_10_43_1
e_1_2_10_20_1
e_1_2_10_41_1
e_1_2_10_52_1
e_1_2_10_3_1
e_1_2_10_19_1
e_1_2_10_54_1
e_1_2_10_5_1
e_1_2_10_17_1
e_1_2_10_38_1
e_1_2_10_56_1
e_1_2_10_7_1
e_1_2_10_15_1
e_1_2_10_36_1
e_1_2_10_12_1
e_1_2_10_35_1
e_1_2_10_9_1
e_1_2_10_59_1
e_1_2_10_10_1
e_1_2_10_33_1
e_1_2_10_31_1
e_1_2_10_50_1
e_1_2_10_60_1
e_1_2_10_62_1
e_1_2_10_28_1
e_1_2_10_49_1
e_1_2_10_26_1
e_1_2_10_47_1
References_xml – reference: Scheltens, P., K. Blennow, M.M. Breteler, et al. 2016. Alzheimer's disease. Lancet pii: S0140-6736(15)01124-1.
– reference: Horikoshi, M., R. Mӓgi, van M. de Bunt, et al. 2015. Discovery and fine-mapping of glycaemic and obesity-related trait loci using high-density imputation. PLoS Genet. 11: e1005230.
– reference: Hollingworth, P., D. Harold, R. Sims, et al. 2011. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat. Genet. 43: 429-435.
– reference: Sieberts, S.K. & E.E. Schadt. 2007. Moving toward a system genetics view of disease. Mamm. Genome 18: 389-401.
– reference: Bulik-Sullivan, B., H.K. Finucane, V. Anttila, et al. 2015. An atlas of genetic correlations across human diseases and traits. Nat. Genet. 47: 1236-1241.
– reference: Sanseau, P., P. Agarwal, M.R. Barnes, et al. 2012. Use of genome-wide association studies for drug repositioning. Nat. Biotechnol. 30: 317-320.
– reference: Mirnics, K., F.A. Middleton, D.A. Lewis & P. Levitt. 2001. Analysis of complex brain disorders with gene expression microarrays: schizophrenia as a disease of the synapse. Trends Neurosci. 24: 479-486.
– reference: Elding, H., W. Lau, D.M. Swallow & N. Maniatis. 2011. Dissecting the genetics of complex inheritance: linkage disequilibrium mapping provides insight into Crohn disease. Am. J. Hum. Genet. 89: 798-805.
– reference: Birnbaum, R., A.E. Jaffe, Q. Chen, et al. 2015. Investigation of the prenatal expression patterns of 108 schizophrenia-associated genetic loci. Biol. Psychiatry 77: e43-e51.
– reference: Cross-Disorder Group of the Psychiatric Genomics Consortium. 2013. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. Lancet 381: 1371-1379.
– reference: Purcell, S.M., J.L. Moran, M. Fromer, et al. 2014. A polygenic burden of rare disruptive mutations in schizophrenia. Nature 506: 185-190.
– reference: Guna, A., N.J. Butcher & A.S. Bassett. 2015. Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms. J. Neurodev. Disord. 7: 18.
– reference: Maniatis, N., A. Collins, N.E. Morton 2007. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping. Genet. Epidemiol. 31: 179-188.
– reference: Leucht, S., A. Cipriani, L. Spineli, et al. 2013. Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis. Lancet 382: 951-962.
– reference: Mills, S.M., J. Mallmann, A.M. Santacruz, et al. 2013. Preclinical trials in autosomal dominant AD: implementation of the DIAN-TU trial. Rev. Neurol. (Paris) 169: 737-743.
– reference: Euesden, J., C.M. Lewis & P.F. O'Reilly. 2015. PRSice: polygenic risk score software. Bioinformatics 31: 1466-1468.
– reference: Kaiser, J. 2014. The hunt for missing genes. Science 344: 687-689.
– reference: Richards, J.B., H.F. Zheng & T.D. Spector. 2012. Genetics of osteoporosis from genome-wide association studies: advances and challenges. Nat. Rev. Genet. 13: 576-588.
– reference: Zhang, B., L. Tran, V. Emilsson & J. Zhu. 2016. Characterization of genetic networks associated with Alzheimer's disease. Methods Mol. Biol. 1303: 459-477.
– reference: Sperling, R.A., D.M. Rentz, K.A. Johnson, et al. 2014. The A4 study: stopping AD before symptoms begin? Sci. Transl. Med. 6: 228fs13.
– reference: Pocklington, A.J., E. Rees, J.T. Walters, et al. 2015. Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia. Neuron 86: 1203-1214.
– reference: Sekar, A., A.R. Bialas, de H. Rivera, et al. 2016. Schizophrenia risk from complex variation of complement component 4. Nature 530: 177-183.
– reference: Segrè, A.V., N. Wei; DIAGRAM Consortium; MAGIC Investigators, D. Altshuler & J.C. Florez. 2015. Pathways targeted by antidiabetes drugs are enriched for multiple genes associated with type 2 diabetes risk. Diabetes 64: 1470-1483.
– reference: Kircher, M., D.M. Witten, P. Jain, et al. 2014. A general framework for estimating the relative pathogenicity of human genetic variants. Nat. Genet. 46: 310-315.
– reference: Cao, C. & J. Moult. 2014. GWAS and drug targets. BMC Genomics 15(Suppl. 4): S5.
– reference: Wei, G.H., D.P. Liu & C.C. Liang. 2004. Charting gene regulatory networks: strategies, challenges and perspectives. Biochem. J. 381(Pt. 1): 1-12.
– reference: Pidsley, R., J. Viana, E. Hannon, et al. 2014. Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia. Genome Biol. 15: 483.
– reference: Lim, E.T., P. Würtz, A.S. Havulinna, et al. 2014. Distribution and medical impact of loss-of-function variants in the Finnish founder population. PLoS Genet. 10: e1004494.
– reference: Fromer, M., A.J. Pocklington, D.H. Kavanagh, et al. 2014. De novo mutations in schizophrenia implicate synaptic networks. Nature 506: 179-184.
– reference: Langfelder, P. & S. Horvath. 2008. WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics 9: 559.
– reference: Finucane, H.K., B. Bulik-Sullivan, A. Gusev, et al. 2015. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nat. Genet. 47: 1228-1235.
– reference: Aberg, K.A., J.L. McClay, S. Nerella, et al. 2014. Methylome-wide association study of schizophrenia: identifying blood biomarker signatures of environmental insults. JAMA Psychiatry 71: 255-264.
– reference: Flannick, J., G. Thorleifsson, N.L. Beer, et al. 2014. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat. Genet. 46: 357-363.
– reference: Steinberg, S., H. Stefansson, T. Jonsson, et al. 2015. Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease. Nat. Genet. 47: 445-447.
– reference: Smith, T.E., C.A. Weston & J.A. Lieberman. 2009. Schizophrenia (maintenance treatment). BMJ Clin. Evid. 2009: 1007.
– reference: Schneider, M., M. Debbané, A.S. Bassett, et al. 2014. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. Am. J. Psychiatry 171: 627-639.
– reference: Zhang, B., C. Gaiteri, L.G. Bodea, et al. 2013. Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's disease. Cell 153: 707-720.
– reference: Ginovart, N. & S. Kapur. 2012. Role of dopamine D2 receptors for antipsychotic activity. Handb. Exp. Pharmacol. 212: 27-52.
– reference: Kingsmore, S.F., I.E. Lindquist, J. Mudge, et al. 2008. Genome-wide association studies: progress and potential for drug discovery and development. Nat. Rev. Drug Discov. 7: 221-230.
– reference: Sullivan, P.; 96 Psychiatric Genetics Investigators. 2012. Don't give up on GWAS. Mol. Psychiatry 17: 2-3.
– reference: Wray, N.R., S.H. Lee, D. Mehta, et al. 2014. Research review: polygenic methods and their application to psychiatric traits. J. Child Psychol. Psychiatry. 55: 1068-1087.
– reference: Ruderfer, D.M., A.H. Fanous, S. Ripke, et al. 2014. Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Mol. Psychiatry 19: 1017-1024.
– reference: Sedeño-Cortés, A.E. & P. Pavlidis. 2014. Pitfalls in the application of gene-set analysis to genetics studies. Trends Genet. 30: 513-514.
– reference: Lamb, J., E.D. Crawford, D. Peck, et al. 2006. The connectivity map: using gene-expression signatures to connect small molecules, genes, and disease. Science 313: 1929-1935.
– reference: Elding, H., W. Lau, D.M. Swallow & N. Maniatis. 2013. Refinement in localization and identification of gene regions associated with Crohn disease. Am. J. Hum. Genet. 92: 107-113.
– reference: Network and Pathway Analysis Subgroup of Psychiatric Genomics Consortium. 2015. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nat. Neurosci. 18: 199-209.
– reference: Conn, P.J. & C.K. Jones. 2009. Promise of mGluR2/3 activators in psychiatry. Neuropsychopharmacology 34: 248-249.
– reference: Zhao, W., P. Langfelder, T. Fuller, et al. 2010. Weighted gene coexpression network analysis: state of the art. J. Biopharm. Stat. 20: 281-300.
– reference: Kumar, G., S.L. Clark, J.L. McClay, et al. 2015. Refinement of schizophrenia GWAS loci using methylome-wide association data. Hum. Genet. 134: 77-87.
– reference: McCarthy, D.J., P. Humburg, A. Kanapin, et al. 2014. Choice of transcripts and software has a large effect on variant annotation. Genome Med. 6: 26.
– reference: Schizophrenia Working Group of the Psychiatric Genomics Consortium. 2014. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511: 421-427.
– reference: International Schizophrenia Consortium; S.M. Purcell, N.R. Wray, J.L. Stone, et al. 2009. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460: 748-752.
– reference: Szatkiewicz, J.P., C. O'Dushlaine, G. Chen, et al. 2014. Copy number variation in schizophrenia in Sweden. Mol. Psychiatry 19: 762-773.
– reference: Zeilinger, S., B. Kuhnel, N. Klopp, et al. 2013. Tobacco smoking leads to extensive genome-wide changes in DNA methylation. PLoS One 8: e63812.
– reference: Richmond, R.C., A.J. Simpkin, G. Woodward, et al. 2014. Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC). Hum. Mol. Genet. 24: 2201-2217.
– reference: Jaffe, A.E., J. Shin, L. Collado-Torres, et al. 2015. Developmental regulation of human cortex transcription and its clinical relevance at single base resolution. Nat. Neurosci. 18: 154-161.
– reference: Malhotra, D. & J. Sebat. 2012. CNVs: harbingers of a rare variant revolution in psychiatric genetics. Cell 148: 1223-1241.
– reference: Okada, Y., D. Wu, G. Trynka, et al. 2013. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature 506: 376-381.
– reference: Cohen, J.C. & H.H. Hobbs. 2013. Genetics. Simple genetics for a complex disease. Science 340: 689-690.
– reference: Grover, M.P., S. Ballouz, K.A. Mohanasundaram, et al. 2014 Identification of novel therapeutics for complex diseases from genome-wide association data. BMC Med. Genomics 7(Suppl. 1): S8.
– reference: Grati, F.R., D. Molina Gomes, J.C. Ferreira, et al. 2015. Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies. Prenat. Diagn. 35: 801-809.
– reference: Lichtenstein, P., B.H. Yip, C. Björk, et al. 2009. Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet 373: 234-239.
– volume: 7
  start-page: 18
  year: 2015
  article-title: Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms
  publication-title: J. Neurodev. Disord.
– volume: 506
  start-page: 376
  year: 2013
  end-page: 381
  article-title: Genetics of rheumatoid arthritis contributes to biology and drug discovery
  publication-title: Nature
– volume: 8
  start-page: e63812
  year: 2013
  article-title: Tobacco smoking leads to extensive genome‐wide changes in DNA methylation
  publication-title: PLoS One
– volume: 506
  start-page: 185
  year: 2014
  end-page: 190
  article-title: A polygenic burden of rare disruptive mutations in schizophrenia
  publication-title: Nature
– volume: 17
  start-page: 2
  year: 2012
  end-page: 3
  article-title: Don't give up on GWAS
  publication-title: Mol. Psychiatry
– volume: 34
  start-page: 248
  year: 2009
  end-page: 249
  article-title: Promise of mGluR2/3 activators in psychiatry
  publication-title: Neuropsychopharmacology
– volume: 506
  start-page: 179
  year: 2014
  end-page: 184
  article-title: mutations in schizophrenia implicate synaptic networks
  publication-title: Nature
– volume: 11
  start-page: e1005230
  year: 2015
  article-title: Discovery and fine‐mapping of glycaemic and obesity‐related trait loci using high‐density imputation
  publication-title: PLoS Genet
– volume: 47
  start-page: 445
  year: 2015
  end-page: 447
  article-title: Loss‐of‐function variants in confer risk of Alzheimer's disease
  publication-title: Nat. Genet.
– volume: 19
  start-page: 1017
  year: 2014
  end-page: 1024
  article-title: Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia
  publication-title: Mol. Psychiatry
– volume: 169
  start-page: 737
  year: 2013
  end-page: 743
  article-title: Preclinical trials in autosomal dominant AD: implementation of the DIAN‐TU trial
  publication-title: Rev. Neurol. (Paris)
– volume: 46
  start-page: 357
  year: 2014
  end-page: 363
  article-title: Loss‐of‐function mutations in protect against type 2 diabetes
  publication-title: Nat. Genet.
– volume: 31
  start-page: 179
  year: 2007
  end-page: 188
  article-title: Effects of single SNPs, haplotypes, and whole‐genome LD maps on accuracy of association mapping
  publication-title: Genet. Epidemiol.
– volume: 382
  start-page: 951
  year: 2013
  end-page: 962
  article-title: Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple‐treatments meta‐analysis
  publication-title: Lancet
– volume: 18
  start-page: 199
  year: 2015
  end-page: 209
  article-title: Psychiatric genome‐wide association study analyses implicate neuronal, immune and histone pathways
  publication-title: Nat. Neurosci.
– volume: 10
  start-page: e1004494
  year: 2014
  article-title: Distribution and medical impact of loss‐of‐function variants in the Finnish founder population
  publication-title: PLoS Genet
– volume: 64
  start-page: 1470
  year: 2015
  end-page: 1483
  article-title: Pathways targeted by antidiabetes drugs are enriched for multiple genes associated with type 2 diabetes risk
  publication-title: Diabetes
– volume: 20
  start-page: 281
  year: 2010
  end-page: 300
  article-title: Weighted gene coexpression network analysis: state of the art
  publication-title: J. Biopharm. Stat.
– volume: 30
  start-page: 317
  year: 2012
  end-page: 320
  article-title: Use of genome‐wide association studies for drug repositioning
  publication-title: Nat. Biotechnol.
– volume: 6
  start-page: 228fs13
  year: 2014
  article-title: The A4 study: stopping AD before symptoms begin
  publication-title: Sci. Transl. Med.
– volume: 460
  start-page: 748
  year: 2009
  end-page: 752
  article-title: Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
  publication-title: Nature
– volume: 71
  start-page: 255
  year: 2014
  end-page: 264
  article-title: Methylome‐wide association study of schizophrenia: identifying blood biomarker signatures of environmental insults
  publication-title: JAMA Psychiatry
– volume: 381
  start-page: 1371
  year: 2013
  end-page: 1379
  article-title: Identification of risk loci with shared effects on five major psychiatric disorders: a genome‐wide analysis
  publication-title: Lancet
– volume: 55
  start-page: 1068
  year: 2014
  end-page: 1087
  article-title: Research review: polygenic methods and their application to psychiatric traits
  publication-title: J. Child Psychol. Psychiatry.
– volume: 92
  start-page: 107
  year: 2013
  end-page: 113
  article-title: Refinement in localization and identification of gene regions associated with Crohn disease
  publication-title: Am. J. Hum. Genet.
– volume: 7
  start-page: S8
  issue: Suppl. 1
  year: 2014
  article-title: Identification of novel therapeutics for complex diseases from genome‐wide association data
  publication-title: BMC Med. Genomics
– volume: 47
  start-page: 1228
  year: 2015
  end-page: 1235
  article-title: Partitioning heritability by functional annotation using genome‐wide association summary statistics
  publication-title: Nat. Genet.
– volume: 313
  start-page: 1929
  year: 2006
  end-page: 1935
  article-title: The connectivity map: using gene‐expression signatures to connect small molecules, genes, and disease
  publication-title: Science
– volume: 18
  start-page: 154
  year: 2015
  end-page: 161
  article-title: Developmental regulation of human cortex transcription and its clinical relevance at single base resolution
  publication-title: Nat. Neurosci.
– volume: 35
  start-page: 801
  year: 2015
  end-page: 809
  article-title: Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies
  publication-title: Prenat. Diagn.
– volume: 18
  start-page: 389
  year: 2007
  end-page: 401
  article-title: Moving toward a system genetics view of disease
  publication-title: Mamm. Genome
– volume: 6
  start-page: 26
  year: 2014
  article-title: Choice of transcripts and software has a large effect on variant annotation
  publication-title: Genome Med
– volume: 89
  start-page: 798
  year: 2011
  end-page: 805
  article-title: Dissecting the genetics of complex inheritance: linkage disequilibrium mapping provides insight into Crohn disease
  publication-title: Am. J. Hum. Genet.
– volume: 381
  start-page: 1
  issue: Pt. 1
  year: 2004
  end-page: 12
  article-title: Charting gene regulatory networks: strategies, challenges and perspectives
  publication-title: Biochem. J.
– volume: 46
  start-page: 310
  year: 2014
  end-page: 315
  article-title: A general framework for estimating the relative pathogenicity of human genetic variants
  publication-title: Nat. Genet.
– volume: 530
  start-page: 177
  year: 2016
  end-page: 183
  article-title: Schizophrenia risk from complex variation of complement component 4
  publication-title: Nature
– volume: 19
  start-page: 762
  year: 2014
  end-page: 773
  article-title: Copy number variation in schizophrenia in Sweden
  publication-title: Mol. Psychiatry
– volume: 2009
  start-page: 1007
  year: 2009
  article-title: Schizophrenia (maintenance treatment)
  publication-title: BMJ Clin. Evid.
– volume: 1303
  start-page: 459
  year: 2016
  end-page: 477
  article-title: Characterization of genetic networks associated with Alzheimer's disease
  publication-title: Methods Mol. Biol.
– volume: 13
  start-page: 576
  year: 2012
  end-page: 588
  article-title: Genetics of osteoporosis from genome‐wide association studies: advances and challenges
  publication-title: Nat. Rev. Genet.
– volume: 24
  start-page: 2201
  year: 2014
  end-page: 2217
  article-title: Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC)
  publication-title: Hum. Mol. Genet.
– volume: 171
  start-page: 627
  year: 2014
  end-page: 639
  article-title: Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome
  publication-title: Am. J. Psychiatry
– volume: 511
  start-page: 421
  year: 2014
  end-page: 427
  article-title: Biological insights from 108 schizophrenia‐associated genetic loci
  publication-title: Nature
– volume: 148
  start-page: 1223
  year: 2012
  end-page: 1241
  article-title: CNVs: harbingers of a rare variant revolution in psychiatric genetics
  publication-title: Cell
– volume: 15
  start-page: S5
  issue: Suppl. 4
  year: 2014
  article-title: GWAS and drug targets
  publication-title: BMC Genomics
– volume: 7
  start-page: 221
  year: 2008
  end-page: 230
  article-title: Genome‐wide association studies: progress and potential for drug discovery and development
  publication-title: Nat. Rev. Drug Discov.
– volume: 153
  start-page: 707
  year: 2013
  end-page: 720
  article-title: Integrated systems approach identifies genetic nodes and networks in late‐onset Alzheimer's disease
  publication-title: Cell
– volume: 77
  start-page: e43
  year: 2015
  end-page: e51
  article-title: Investigation of the prenatal expression patterns of 108 schizophrenia‐associated genetic loci
  publication-title: Biol. Psychiatry
– volume: 212
  start-page: 27
  year: 2012
  end-page: 52
  article-title: Role of dopamine D receptors for antipsychotic activity
  publication-title: Handb. Exp. Pharmacol.
– volume: 373
  start-page: 234
  year: 2009
  end-page: 239
  article-title: Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population‐based study
  publication-title: Lancet
– volume: 340
  start-page: 689
  year: 2013
  end-page: 690
  article-title: Genetics. Simple genetics for a complex disease
  publication-title: Science
– volume: 24
  start-page: 479
  year: 2001
  end-page: 486
  article-title: Analysis of complex brain disorders with gene expression microarrays: schizophrenia as a disease of the synapse
  publication-title: Trends Neurosci
– volume: 43
  start-page: 429
  year: 2011
  end-page: 435
  article-title: Common variants at , / , , and are associated with Alzheimer's disease
  publication-title: Nat. Genet.
– volume: 30
  start-page: 513
  year: 2014
  end-page: 514
  article-title: Pitfalls in the application of gene‐set analysis to genetics studies
  publication-title: Trends Genet
– volume: 31
  start-page: 1466
  year: 2015
  end-page: 1468
  article-title: PRSice: polygenic risk score software
  publication-title: Bioinformatics
– volume: 47
  start-page: 1236
  year: 2015
  end-page: 1241
  article-title: An atlas of genetic correlations across human diseases and traits
  publication-title: Nat. Genet.
– volume: 86
  start-page: 1203
  year: 2015
  end-page: 1214
  article-title: Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia
  publication-title: Neuron
– volume: 134
  start-page: 77
  year: 2015
  end-page: 87
  article-title: Refinement of schizophrenia GWAS loci using methylome‐wide association data
  publication-title: Hum. Genet.
– year: 2016
  article-title: Alzheimer's disease
  publication-title: Lancet
– volume: 9
  start-page: 559
  year: 2008
  article-title: WGCNA: an R package for weighted correlation network analysis
  publication-title: BMC Bioinformatics
– volume: 344
  start-page: 687
  year: 2014
  end-page: 689
  article-title: The hunt for missing genes
  publication-title: Science
– volume: 15
  start-page: 483
  year: 2014
  article-title: Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia
  publication-title: Genome Biol
– ident: e_1_2_10_8_1
  doi: 10.1371/journal.pgen.1004494
– ident: e_1_2_10_21_1
  doi: 10.1038/nature13595
– ident: e_1_2_10_61_1
  doi: 10.1016/j.cell.2013.03.030
– ident: e_1_2_10_15_1
  doi: 10.1186/1755-8794-7-S1-S8
– ident: e_1_2_10_25_1
  doi: 10.1002/gepi.20199
– ident: e_1_2_10_7_1
  doi: 10.1038/ng.2915
– ident: e_1_2_10_42_1
  doi: 10.1016/S0140-6736(12)62129-1
– ident: e_1_2_10_52_1
  doi: 10.1016/j.cell.2012.02.039
– ident: e_1_2_10_49_1
  doi: 10.1186/1471-2105-9-559
– ident: e_1_2_10_43_1
  doi: 10.1038/ng.3406
– ident: e_1_2_10_11_1
  doi: 10.1186/1471-2164-15-S4-S5
– ident: e_1_2_10_13_1
  doi: 10.1038/nature12873
– ident: e_1_2_10_19_1
  doi: 10.1186/s11689-015-9113-x
– ident: e_1_2_10_53_1
  doi: 10.1038/mp.2014.40
– ident: e_1_2_10_16_1
  doi: 10.1016/j.neurol.2013.07.017
– ident: e_1_2_10_12_1
  doi: 10.2337/db14-0703
– ident: e_1_2_10_24_1
  doi: 10.1186/gm543
– ident: e_1_2_10_60_1
  doi: 10.1016/j.biopsych.2014.10.008
– ident: e_1_2_10_38_1
  doi: 10.1038/nn.3922
– ident: e_1_2_10_44_1
  doi: 10.1038/ng.3404
– ident: e_1_2_10_6_1
  doi: 10.1126/science.1239101
– ident: e_1_2_10_18_1
  doi: 10.1176/appi.ajp.2013.13070864
– ident: e_1_2_10_28_1
  doi: 10.1371/journal.pgen.1005230
– ident: e_1_2_10_54_1
  doi: 10.1016/j.neuron.2015.04.022
– ident: e_1_2_10_39_1
  doi: 10.1111/jcpp.12295
– ident: e_1_2_10_26_1
  doi: 10.1016/j.ajhg.2012.11.004
– ident: e_1_2_10_46_1
  doi: 10.1093/bioinformatics/btu848
– ident: e_1_2_10_57_1
  doi: 10.1038/nature12929
– ident: e_1_2_10_22_1
  doi: 10.1038/npp.2008.156
– ident: e_1_2_10_34_1
  doi: 10.1093/hmg/ddu739
– ident: e_1_2_10_58_1
  doi: 10.1038/mp.2011.94
– ident: e_1_2_10_14_1
  doi: 10.1038/nbt.2151
– ident: e_1_2_10_17_1
  doi: 10.1126/scitranslmed.3007941
– volume: 2009
  start-page: 1007
  year: 2009
  ident: e_1_2_10_2_1
  article-title: Schizophrenia (maintenance treatment)
  publication-title: BMJ Clin. Evid.
– ident: e_1_2_10_20_1
  doi: 10.1016/S0140-6736(15)01124-1
– ident: e_1_2_10_31_1
  doi: 10.1038/ng.803
– ident: e_1_2_10_5_1
  doi: 10.1126/science.344.6185.687
– ident: e_1_2_10_35_1
  doi: 10.1001/jamapsychiatry.2013.3730
– ident: e_1_2_10_29_1
  doi: 10.1038/nature16549
– ident: e_1_2_10_36_1
  doi: 10.1007/s00439-014-1494-5
– ident: e_1_2_10_62_1
  doi: 10.1126/science.1132939
– ident: e_1_2_10_41_1
  doi: 10.1016/S0140-6736(09)60072-6
– ident: e_1_2_10_47_1
  doi: 10.1016/j.tig.2014.10.001
– ident: e_1_2_10_3_1
  doi: 10.1016/S0140-6736(13)60733-3
– ident: e_1_2_10_45_1
  doi: 10.1038/mp.2013.138
– ident: e_1_2_10_48_1
  doi: 10.1080/10543400903572753
– ident: e_1_2_10_59_1
  doi: 10.1038/nn.3898
– ident: e_1_2_10_37_1
  doi: 10.1186/s13059-014-0483-2
– ident: e_1_2_10_40_1
  doi: 10.1038/nature08185
– ident: e_1_2_10_50_1
  doi: 10.1007/s00335-007-9040-6
– ident: e_1_2_10_10_1
  doi: 10.1038/nrg3228
– ident: e_1_2_10_55_1
  doi: 10.1002/pd.4613
– ident: e_1_2_10_30_1
  doi: 10.1016/S0166-2236(00)01862-2
– ident: e_1_2_10_33_1
  doi: 10.1371/journal.pone.0063812
– ident: e_1_2_10_27_1
  doi: 10.1016/j.ajhg.2011.11.006
– ident: e_1_2_10_23_1
  doi: 10.1038/ng.2892
– ident: e_1_2_10_63_1
  doi: 10.1042/BJ20040311
– ident: e_1_2_10_4_1
  doi: 10.1007/978-3-642-25761-2_2
– ident: e_1_2_10_56_1
  doi: 10.1038/nature12975
– ident: e_1_2_10_32_1
  doi: 10.1038/ng.3246
– ident: e_1_2_10_9_1
  doi: 10.1038/nrd2519
– ident: e_1_2_10_51_1
  doi: 10.1007/978-1-4939-2627-5_28
SSID ssj0012847
Score 2.2635837
SecondaryResourceType review_article
Snippet The spectacular advance in our understanding of the genetic basis of schizophrenia through genome‐wide association studies has the potential to identify new...
The spectacular advance in our understanding of the genetic basis of schizophrenia through genome-wide association studies has the potential to identify new...
SourceID proquest
pubmed
crossref
wiley
istex
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 61
SubjectTerms Antipsychotic Agents - therapeutic use
Biology
drug discovery
Drug Discovery - methods
Drug Discovery - trends
Drugs
Gene Regulatory Networks - genetics
Genes
Genetic Variation - genetics
Genetics
genome-wide association
Genome-Wide Association Study - methods
Genome-Wide Association Study - trends
Humans
Mental disorders
Networks
Pathways
Patients
pharmacogenetics
psychosis
Schizophrenia
Schizophrenia - diagnosis
Schizophrenia - drug therapy
Schizophrenia - genetics
Title Advances in the genetics of schizophrenia: toward a network and pathway view for drug discovery
URI https://api.istex.fr/ark:/67375/WNG-VP3MWS97-5/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fnyas.13066
https://www.ncbi.nlm.nih.gov/pubmed/27111133
https://www.proquest.com/docview/1790066533
https://www.proquest.com/docview/1784749004
https://www.proquest.com/docview/1787982508
https://www.proquest.com/docview/1808065778
Volume 1366
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1taxNBEB5Ki-AXtfUtWsuKIla4ci_7khO_pGosQoNYa-sHOXZvd0UqF8klaPz1zuy92EoJ6JdwkMmxuzcz90z22WcAHtsk8d64NDIi9xFPPI-M13HEvS4T7nRuSjrvfDiRB8f87ak4XYMX3VmYRh-i_8ONIiPkawpwbepzQV4tdU29jCXpbRNZixDR-147KuTdkIYVpmGEMa02KdF4_vz0wttogxb252VQ8yJyDa-e8XX43A26YZyc7S3mZq_89Zee4__O6gZcazEpGzVOtAlrrtqCK02XyuUWbLbxX7OnrUj17k0oRg15oGZfK4YgkqEj0nnImk09q88z-Z6zeaDmMs2qhnPOdGUZtUL-oZeMtiYYImdmZ4svjA4JE6l0eQuOx68_vDyI2mYNUcllIqNhJpXVykppsMQrJeYOxDbU_9PakiM4Tg1WmolwmXM-ztN4aBx-pjE36EfKZ7dhvZpW7i6wWCMM4ljp2RjLT5MZboRwwnJMOLlJ0gHsdg-tKFslc2qo8a3oKhpaxSKs4gAe9bbfG_2OS62ehGffm-jZGTHelChOJm-Kj--yw5OjXBViANudcxRtsOMtVB52sLJsAA_7rzFMae9FV266IBt0R452fKWNyrFij4crbEgHVAql0OZO45z9oFNF06JRPAsutmLCxeTT6Chc3fsX4_twFQFjy1rfhvX5bOEeICibmx3YGO2_2h_vhCD8DSykMrs
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLZgE4IXYONWGGAEQgwpUy6-NLxViFFgrRC78mTZsY3QUIqaVlB-Pec4btjQVAleqkj9EsXOOSffiT-fQ8gzm2XeG5cnhpc-YZlnifE6TZjXVcacLk2F-51HYzE8ZO9P-EnU5uBemLY-RPfBDT0jxGt0cPwgfcbL64VusJmxEJfJOrb0DhnVp656VIi8IRBLCMRAZGJ1UhTy_Dn33PtoHaf250Vk8zx3DS-f3Rtth9Um1CxEzcnpznxmdqpff1V0_O9x3STXIy2lg9aONsglV2-SK22jysUm2YghoKEvYp3q7VtEDVr9QEO_1hR4JAVbxC2RDZ142pwV872is6DOpZrWreyc6tpS7Ib8Qy8ork5QIM_UTudfKO4TRl3p4jY53H1z8HqYxH4NScVEJpJ-IaTV0gphIMurBIQPoDfYAtTaigE_zg0kmxl3hXM-LfO0bxz85ikzYErSF3fIWj2p3T1CUw1MiEGyZ1PIQE1hmOHcccsg5pQmy3tke_nUVBWLmWNPjW9qmdTgLKowiz3ytMN-b0t4XIh6Hh5-B9HTUxS9Sa6Ox2_V0cdidLxfSsV7ZGtpHSr6O1xClmERqyh65En3N3gqLr_o2k3miAF7ZIBjKzGyhKQ97a_AYClQwaUEzN3WOrubziUOC-_iZbCxFQNW48-D_XB0_1_Aj8nV4cFoT-29G394QK4Bf4wi9i2yNpvO3UPgaDPzKHjib5cmNWQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1tb9MwED6NTaB9ATZgFAYYgRBDypQXx24QXypGGS-rJsbY-IAsO7ERGkqnphWUX8-d88KGpkrwpYrUp5Ht3F2eqx_fATwuosg5Y-PApJkLeOR4YJwOA-50HnGrM5PTeee9kdg95G-P0-MleNGehanrQ3R_uJFn-HhNDn5auDNOXs51Rb2MhbgEK1yEfbLpnQ9d8SgfeH0clhiHkcc0xUlJx_Pnt-deRyu0sj8v4prnqat_9wyvwZd21LXk5GR7NjXb-a-_Cjr-77Suw9WGlLJBbUVrsGTLdbhct6mcr8NaEwAq9rSpUr11A9SgVg9U7FvJkEUytEQ6EFmxsWPVWSnfczb12lymWVmLzpkuC0a9kH_oOaO9CYbUmRWT2VdGp4RJVTq_CYfDVx9f7gZNt4Yg5yISQT8RstCyEMJgjpcLDB5IbqgBaFHkHNlxbDDVjFKbWOvCLA77xuJnHHKDhiRdcguWy3FpbwMLNfIgjqleEWL-aRLDTZratOAYcTITxT3Yah-ayptS5tRR47tqUxpaReVXsQePOuxpXcDjQtQT_-w7iJ6ckORNpupo9Fp92k_2jg4yqdIebLbGoRpvx1vIzG9hJUkPHnZfo5_S5osu7XhGGDRHjji-ECMzTNnD_gIMFQIVqZSI2aiNsxt0LGlaNIpn3sQWTFiNPg8O_NWdfwE_gCv7O0P1_s3o3V1YRfLYKNg3YXk6mdl7SNCm5r73w9_pxTQc
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Advances+in+the+genetics+of+schizophrenia%3A+toward+a+network+and+pathway+view+for+drug+discovery&rft.jtitle=Annals+of+the+New+York+Academy+of+Sciences&rft.au=Collier%2C+David+A&rft.au=Eastwood%2C+Brian+J&rft.au=Malki%2C+Karim&rft.au=Mokrab%2C+Younes&rft.date=2016-02-01&rft.eissn=1749-6632&rft.volume=1366&rft.issue=1&rft.spage=61&rft.epage=75&rft_id=info:doi/10.1111%2Fnyas.13066&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0077-8923&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0077-8923&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0077-8923&client=summon