Sullivan P, Yao S, Hjerling-Leffler J
Nat Rev Neurosci. 2024; 25(9):611-624.
PMID: 39030273
DOI: 10.1038/s41583-024-00837-7.
Loe-Mie Y, Plancon C, Dubertret C, Yoshikawa T, Yalcin B, Collins S
Life (Basel). 2024; 14(2).
PMID: 38398753
PMC: 10890674.
DOI: 10.3390/life14020244.
Hu T, Wu C, Hsu S, Tsai H, Cheng F, Cheng M
J Pers Med. 2022; 12(5).
PMID: 35629206
PMC: 9144110.
DOI: 10.3390/jpm12050783.
Andlauer T, Guzman-Parra J, Streit F, Strohmaier J, Gonzalez M, Gil Flores S
Mol Psychiatry. 2019; 26(4):1286-1298.
PMID: 31712721
PMC: 7985020.
DOI: 10.1038/s41380-019-0558-2.
Glahn D, Nimgaonkar V, Raventos H, Contreras J, McIntosh A, Thomson P
Mol Psychiatry. 2018; 24(4):523-535.
PMID: 29955165
PMC: 7028329.
DOI: 10.1038/s41380-018-0073-x.
The effect of the DISC1 Ser704Cys polymorphism on striatal dopamine synthesis capacity: an [18F]-DOPA PET study.
Dahoun T, Pardinas A, Veronese M, Bloomfield M, Jauhar S, Bonoldi I
Hum Mol Genet. 2018; 27(20):3498-3506.
PMID: 29945223
PMC: 6168972.
DOI: 10.1093/hmg/ddy242.
De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activity.
Nishi A, Numata S, Tajima A, Zhu X, Ito K, Saito A
Sci Rep. 2017; 7(1):2887.
PMID: 28588275
PMC: 5460159.
DOI: 10.1038/s41598-017-02792-z.
Missing heritability of complex diseases: Enlightenment by genetic variants from intermediate phenotypes.
Blanco-Gomez A, Castillo-Lluva S, Saez-Freire M, Hontecillas-Prieto L, Hua Mao J, Castellanos-Martin A
Bioessays. 2016; 38(7):664-73.
PMID: 27241833
PMC: 5064854.
DOI: 10.1002/bies.201600084.
Systems psychopharmacology: A network approach to developing novel therapies.
Gebicke-Haerter P
World J Psychiatry. 2016; 6(1):66-83.
PMID: 27014599
PMC: 4804269.
DOI: 10.5498/wjp.v6.i1.66.
Cancer genomic research at the crossroads: realizing the changing genetic landscape as intratumoral spatial and temporal heterogeneity becomes a confounding factor.
Li S, Tachiki L, Kabeer M, Dethlefs B, Anthony M, Loudon W
Cancer Cell Int. 2014; 14(1):115.
PMID: 25411563
PMC: 4236490.
DOI: 10.1186/s12935-014-0115-7.
A Neuregulin-1 schizophrenia susceptibility variant causes perihippocampal fiber tract anomalies in healthy young subjects.
Nickl-Jockschat T, Stocker T, Krug A, Markov V, Huang R, Schneider F
Brain Behav. 2014; 4(2):215-26.
PMID: 24683514
PMC: 3967537.
DOI: 10.1002/brb3.203.
Transcription factor 4 (TCF4) and schizophrenia: integrating the animal and the human perspective.
Quednow B, Brzozka M, Rossner M
Cell Mol Life Sci. 2014; 71(15):2815-35.
PMID: 24413739
PMC: 11113759.
DOI: 10.1007/s00018-013-1553-4.
The genomics of schizophrenia: update and implications.
Giusti-Rodriguez P, Sullivan P
J Clin Invest. 2013; 123(11):4557-63.
PMID: 24177465
PMC: 3809776.
DOI: 10.1172/JCI66031.
A comprehensive family-based replication study of schizophrenia genes.
Aberg K, Liu Y, Bukszar J, McClay J, Khachane A, Andreassen O
JAMA Psychiatry. 2013; 70(6):573-81.
PMID: 23894747
PMC: 5297889.
DOI: 10.1001/jamapsychiatry.2013.288.
High loading of polygenic risk for ADHD in children with comorbid aggression.
Hamshere M, Langley K, Martin J, Agha S, Stergiakouli E, Anney R
Am J Psychiatry. 2013; 170(8):909-16.
PMID: 23599091
PMC: 3935265.
DOI: 10.1176/appi.ajp.2013.12081129.
A genome-wide association study of depressive symptoms.
Hek K, Demirkan A, Lahti J, Terracciano A, Teumer A, Cornelis M
Biol Psychiatry. 2013; 73(7):667-78.
PMID: 23290196
PMC: 3845085.
DOI: 10.1016/j.biopsych.2012.09.033.
Identifying bipolar disorder susceptibility loci in a densely affected pedigree.
Collins A, Kim Y, Szatkiewicz J, Bloom R, Hilliard C, Quackenbush C
Mol Psychiatry. 2012; 18(12):1245-6.
PMID: 23247078
PMC: 3899577.
DOI: 10.1038/mp.2012.176.
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.
Lee S, Harold D, Nyholt D, Goddard M, Zondervan K, Williams J
Hum Mol Genet. 2012; 22(4):832-41.
PMID: 23193196
PMC: 3554206.
DOI: 10.1093/hmg/dds491.
Genetics of schizophrenia from a clinicial perspective.
Kukshal P, Thelma B, Nimgaonkar V, Deshpande S
Int Rev Psychiatry. 2012; 24(5):393-404.
PMID: 23057976
PMC: 5445022.
DOI: 10.3109/09540261.2012.709178.
De novo mutations in human genetic disease.
Veltman J, Brunner H
Nat Rev Genet. 2012; 13(8):565-75.
PMID: 22805709
DOI: 10.1038/nrg3241.
