Schizophrenia: a common disease caused by multiple rare alleles

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Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

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Finishing the euchromatic sequence of the human genome

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Cancer genes and the pathways they control

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Epigenetic differences arise during the lifetime of monozygotic twins

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The History and Geography of Human Genes

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Large-scale copy number polymorphism in the human genome

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Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence

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The UCSC Genome Browser Database: update 2006

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History and Geography of Human Genes

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A population-based association study of 2q32.3 and 8q21.3 loci with schizophrenia in Han Chinese

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Increased paternal age and the influence on burden of genomic copy number variation in the general population

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The National Institute of Mental Health Research Domain Criteria

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Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia

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A biological network-based regularized artificial neural network model for robust phenotype prediction from gene expression data

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Role of the DLGAP2 Gene Encoding the SAP90/PSD-95-Associated Protein 2 in Schizophrenia

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Modeling motivational deficits in mouse models of schizophrenia: Behavior analysis as a guide for neuroscience

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Systematic Prioritization and Integrative Analysis of Copy Number Variations in Schizophrenia Reveal Key Schizophrenia Susceptibility Genes

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Dopamine genes and schizophrenia: case closed or evidence pending?

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Ion channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing

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Genetic studies of schizophrenia: an update

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Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia

Carrera, N., Sanjuán, J., Moltó, M. D., Carracedo, Á., & Costas, J. (2008) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30823 · Cited by 35

Psychiatric research: psychoproteomics, degradomics and systems biology

Kobeissy, F. H., Sadasivan, S., Liu, J., Gold, M. S., & Wang, K. (2008) · Expert Review of Proteomics · doi:10.1586/14789450.5.2.293 · Cited by 34

Gene variations in the cholecystokinin system in patients with panic disorder

Koefoed, P., Woldbye, D. P. D., Hansen, T. V. O., Hansen, E. S., Knudsen, G. M., Bolwig, T. G., & Rehfeld, J. F. (2010) · Psychiatric Genetics · doi:10.1097/ypg.0b013e32833511a8 · Cited by 33

Neural Plasticity, Human Genetics, and Risk for Alcohol Dependence

Hill, S. Y. (2010) · International review of neurobiology · doi:10.1016/s0074-7742(10)91003-9 · Cited by 31

Application of systems biology approach identifies and validates GRB2 as a risk gene for schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample

Sun, J., Wan, C., Jia, P., Fanous, A. H., Kendler, K. S., Riley, B. P., & Zhao, Z. (2010) · Schizophrenia Research · doi:10.1016/j.schres.2010.12.002 · Cited by 29

Evidence for involvement of GNB1L in autism

Chen, Y., Matsushita, M. M., Girirajan, S., Lisowski, M., Sun, E., Sul, Y., Bernier, R., Estes, A. M., Dawson, G., Minshew, N. J., et al. (2011) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32002 · Cited by 29

Discovering Schizophrenia Endophenotypes in Randomly Ascertained Pedigrees

Glahn, D. C., Williams, J. T., McKay, D., Knowles, E. E. M., Sprooten, E., Mathias, S. R., Curran, J. E., Kent, J. W., Carless, M. A., Göring, H. H. H., et al. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.06.027 · Cited by 30

Linkage and association on 8p21.2-p21.1 in schizophrenia

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Schizophrenia-Like Phenotype Inherited by the F2 Generation of a Gestational Disruption Model of Schizophrenia

Perez, S. M., Aguilar, D. D., Neary, J. L., Carless, M. A., Giuffrida, A., & Lodge, D. J. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.169 · Cited by 27

Âge paternel élevé et risque de schizophrénie

Hubert, A., Szöke, A., Leboyer, M., & Schürhoff, F. (2011) · L Encéphale · doi:10.1016/j.encep.2010.12.005 · Cited by 27

Paternal and maternal age as risk factors for schizophrenia: a case–control study

Fountoulakis, K. Ν., Gonda, X., Siamouli, M., Panagiotidis, P., Moutou, K., Nimatoudis, I., & Kasper, S. F. (2017) · International Journal of Psychiatry in Clinical Practice · doi:10.1080/13651501.2017.1391292 · Cited by 28

Evidence for association between structural variants in lissencephaly-related genes and executive deficits in schizophrenia or bipolar patients from a Spanish isolate population

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The Evolutionary Persistence of Genes That Increase Mental Disorders Risk

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Advanced paternal age and risk of schizophrenia in offspring – Review of epidemiological findings and potential mechanisms

Khachadourian, V., Zaks, N., Lin, E. S., Reichenberg, A., & Janecka, M. (2021) · Schizophrenia Research · doi:10.1016/j.schres.2021.06.016 · Cited by 27

Adjuvant chemotherapy for breast cancer in patients with schizophrenia

Johnson, F. (2012) · Oncology Letters · doi:10.3892/ol.2012.560 · Cited by 28

A genome‐wide CNV analysis of schizophrenia reveals a potential role for a multiple‐hit model

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Following the genes: a framework for animal modeling of psychiatric disorders

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The Origins of Human Modernity

Bednarik, R. G. (2011) · Humanities · doi:10.3390/h1010001 · Cited by 25

Expression of Behavioral Phenotypes in Genetic and Environmental Mouse Models of Schizophrenia

Sultana, R., & Lee, C. C. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.00029 · Cited by 23

Analytical strategies for large imaging genetic datasets: experiences from the IMAGEN study

Nymberg, C., Jia, T., Ruggeri, B., & Schumann, G. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12088 · Cited by 25

Genetic analysis of the DLGAP1 gene as a candidate gene for schizophrenia

Li, J., Lu, C.-L., Cheng, M.-C., Luu, S.-U., Hsu, S.-H., & Chen, C. (2012) · Psychiatry Research · doi:10.1016/j.psychres.2012.08.014 · Cited by 24

Dopamine in socioecological and evolutionary perspectives: implications for psychiatric disorders

Yamaguchi, Y., Lee, Y., & Goto, Y. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00219 · Cited by 26

No evidence that rare coding variants inZNF804Aconfer risk of schizophrenia

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Association of estrogen receptor alpha gene polymorphism with age at onset, general psychopathology symptoms, and therapeutic effect of schizophrenia

Wang, S., Li, W., Zhao, J., Zhang, H., Yang, Y., Wang, X., Ge, Y., & Lv, L. (2013) · Behavioral and Brain Functions · doi:10.1186/1744-9081-9-12 · Cited by 23

Strategies for Integrated Analysis of Genetic, Epigenetic, and Gene Expression Variation in Cancer: Addressing the Challenges

Thingholm, L. B., Andersen, L. V. B., Makalic, E., Southey, M. C., Thomassen, M., & Hansen, L. L. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00002 · Cited by 23

Schizophrenia: From genes to phenes to disease

Allan, C. L., Cardno, A. G., & McGuffin, P. (2008) · Current Psychiatry Reports · doi:10.1007/s11920-008-0054-x · Cited by 24

Schizophrenia and cortical blindness: protective effects and implications for language

Leivada, E., & Boeckx, C. A. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00940 · Cited by 23

Disrupted-in-Schizophrenia-1 (DISC1) protein disturbs neural function in multiple disease-risk pathways

Shao, L., Lu, B., Wen, Z., Teng, S., Wang, L., Zhao, Y. C., Wang, L., Ishizuka, K., Xu, X., Sawa, A., et al. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx147 · Cited by 22

Endophenotypes, Dimensions, Risks: Is Psychosis Analogous to Common Inherited Medical Illnesses?

Pearlson, G. D., & Folley, B. S. (2008) · Clinical EEG and Neuroscience · doi:10.1177/155005940803900210 · Cited by 21

Literature-related discovery: common factors for Parkinson’s Disease and Crohn’s Disease

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Polymorphisms in the FK506 binding protein 5 gene are associated with attention deficit hyperactivity disorder and diurnal cortisol levels

Isaksson, J., Allen, M., Nilsson, K. W., & Lindblad, F. (2015) · Acta Paediatrica · doi:10.1111/apa.13056 · Cited by 20

Basic helix–loop–helix transcription factor NEUROG1 and schizophrenia: Effects on illness susceptibility, MRI brain morphometry and cognitive abilities☆

Ho, B., Epping, E. A., WANG, K., Andreasen, N. C., Librant, A. L., & Wassink, T. H. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.08.009 · Cited by 21

The Genetic Architecture of Neurodevelopmental Disorders

Mitchell, K. J. (2015) · Wiley eBooks · doi:10.1002/9781118524947.ch1 · Cited by 20

Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia

EDWARDS, T., Wang, X., Chen, Q., WORMLY, B., Riley, B. P., O’Neill, F. A., WALSH, D., Ritchie, M. D., Kendler, K. S., & CHEN, X. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.07.022 · Cited by 20

Progress in Cytogenetics: Implications for Child Psychopathology

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A Preliminary Genetic Analysis of Complement 3 Gene and Schizophrenia

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Hypo- or hyper-mentalizing: It all depends upon what one means by “mentalizing”

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Functional and Structural Consequence of Rare Exonic Single Nucleotide Polymorphisms: One Story, Two Tales

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GWAS for psychiatric disease: is the framework built on a solid foundation?

Mitchell, K. J., & Porteous, D. J. (2009) · Molecular Psychiatry · doi:10.1038/mp.2009.17 · Cited by 18

Schizophrenia: Maternal inheritance and heteroplasmy of mtDNA mutations

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Exonic resequencing of the DLGAP3 gene as a candidate gene for schizophrenia

Li, J.-M., Lu, C.-L., Cheng, M.-C., Luu, S.-U., Hsu, S.-H., & Chen, C. (2013) · Psychiatry Research · doi:10.1016/j.psychres.2012.12.015 · Cited by 17

A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia

Costas, J., Carrera, N., Domínguez, E., Vilella, E., Martorell, L., Valero, J., Gutiérrez‐Zotes, A., Labad, A., & Carracedo, Á. (2008) · Human Genetics · doi:10.1007/s00439-008-0584-7 · Cited by 17

Genetic and functional analyses of the gene encoding synaptophysin in schizophrenia

Shen, Y., Tsai, H.-M., Ruan, J., Liao, Y., Chen, S.-F., & Chen, C. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.01.028 · Cited by 18

Searching for the true genetic vulnerability for schizophrenia

DeLisi, L. E. (2009) · Genome Medicine · doi:10.1186/gm14 · Cited by 17

Autism Spectrum Disorders: The Role of Genetics in Diagnosis and Treatment

Deutsch, S. I. (2011) · InTech eBooks · doi:10.5772/976 · Cited by 16

Exomic sequencing of the glutamate receptor, ionotropic, N-methyl-d-aspartate 3A gene (GRIN3A) reveals no association with schizophrenia

Shen, Y., Liao, D., Chen, J., Wang, Y.-C., Lai, I., Liou, Y., Chen, Y.-J., Luu, S.-U., & Chen, C. (2009) · Schizophrenia Research · doi:10.1016/j.schres.2009.07.005 · Cited by 16

Genetic and functional analysis of the gene encoding neurogranin in schizophrenia

Shen, Y., Tsai, H.-M., Cheng, M.-C., Hsu, S.-H., Chen, S., & Chen, C. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.01.011 · Cited by 17

Comparative Linkage Meta-Analysis Reveals Regionally-Distinct, Disparate Genetic Architectures: Application to Bipolar Disorder and Schizophrenia

Tang, B., Thornton‐Wells, T. A., & Askland, K. D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019073 · Cited by 15

A Case for Returning to Multiplex Families for Further Understanding the Heritability of Schizophrenia: A Psychiatrist's Perspective

DeLisi, L. E. (2016) · Complex Psychiatry · doi:10.1159/000442820 · Cited by 14

The DAO Gene Is Associated with Schizophrenia and Interacts with Other Genes in the Taiwan Han Chinese Population

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Genetic hypotheses for schizophrenia

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Genetic analysis of GABRB3 at 15q12 as a candidate gene of schizophrenia

Huang, C.-C., Cheng, M.-C., Tsai, H.-M., Lai, C.-H., & Chen, C. (2014) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000032 · Cited by 13

Resequencing and association study of the NFKB activating protein-like gene (NKAPL) in schizophrenia

Chen, S., Chao, Y.-L., Shen, Y., Chen, C., & Weng, C. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.05.038 · Cited by 13

Cortical plasticity: A proposed mechanism by which genomic factors lead to the behavioral and neurological phenotype of autism spectrum and psychotic-spectrum disorders

Oberman, L. M., & Pascual‐Leone, Á. (2008) · Behavioral and Brain Sciences · doi:10.1017/s0140525x08004378 · Cited by 13

Unheard voices: outcomes of tertiary care for treatment-refractory psychosis

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Polymorphisms of the TCF4 gene are associated with the risk of schizophrenia in the Han Chinese

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Schizophrenia in the genetic era: a review from development history, clinical features and genomic research approaches to insights of susceptibility genes

Lv, Y., Wen, L., Hu, W.-J., Deng, C., Ren, H., Bao, Y.-N., Su, B.-W., Gao, P., Man, Z., Luo, Y.-Y., et al. (2023) · Metabolic Brain Disease · doi:10.1007/s11011-023-01271-x · Cited by 13

Relationship between Single Nucleotide Polymorphisms of GRHL3 and Schizophrenia Susceptibility: A Preliminary Case-Control Study and Bioinformatics Analysis.

Sargazi, S., Nia, M. H., Sheervalilou, R., Mirinejad, S., Harati‐Sadegh, M., Moudi, M., Saravani, R., & Shakiba, M. (2020) · PubMed Central · doi:10.22088/ijmcm.bums.9.2.154 · Cited by 12

Why is creativity attractive in a potential mate?

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Whole Genome Prediction of Bladder Cancer Risk With the Bayesian LASSO

de Maturana, E. L., Chanok, S. J., Picornell, A. C., Rothman, N., Herránz, J., Calle, M. L., García‐Closas, M., Marenne, G., Brand, A. M., Tardón, A., et al. (2014) · Genetic Epidemiology · doi:10.1002/gepi.21809 · Cited by 12

Resequencing of the vesicular glutamate transporter 2 gene (VGLUT2) reveals some rare genetic variants that may increase the genetic burden in schizophrenia

Shen, Y., Liao, D., Lu, C.-L., Chen, J., Liou, Y., Chen, T., & Chen, C.-H. (2010) · Schizophrenia Research · doi:10.1016/j.schres.2010.05.015 · Cited by 11

A preliminary study of the relationship between breast cancer metastasis and loss of heterozygosity by using exome sequencing

Li, H., Yang, B., Xing, K., Yuan, N., Wang, B., Chen, Z., He, W., & Zhou, J. (2014) · Scientific Reports · doi:10.1038/srep05460 · Cited by 11

Genetic and functional analysis of the gene encoding GAP-43 in schizophrenia

Shen, Y., Tsai, H.-M., Cheng, M.-C., Hsu, S.-H., Chen, S., & Chen, C.-H. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2011.11.016 · Cited by 11

Genomic Variation, Evolvability, and the Paradox of Mental Illness

Gualtieri, C. T. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.593233 · Cited by 11

Metastatic breast cancer in patients with schizophrenia

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Screening for Mutations in the TBX1 Gene on Chromosome 22q11.2 in Schizophrenia

Ping, L.-Y., Chuang, Y.-A., Hsu, S.-H., Tsai, H.-Y., & Cheng, M.-C. (2016) · Genes · doi:10.3390/genes7110102 · Cited by 10

Exploring the Genetic Patterns of Complex Diseases via the Integrative Genome-Wide Approach

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Multiple Rare Risk Coding Variants in Postsynaptic Density-Related Genes Associated With Schizophrenia Susceptibility

Hu, T., Wang, Y.-C., Wu, C., Hsu, S.-H., Tsai, H.-Y., & Cheng, M.-C. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.524258 · Cited by 10

Resequencing and association study of vesicular glutamate transporter 1 gene (VGLUT1) with schizophrenia

Shen, Y., Liao, D., Chen, J., Wang, Y.-C., Lai, I., Liou, Y., Chen, Y.-J., Luu, S.-U., & Chen, C. (2009) · Schizophrenia Research · doi:10.1016/j.schres.2009.08.003 · Cited by 10

Approaches to psychiatric assessment in epidemiological studies of children: Table 1

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The Singapore flagship programme in translational and clinical research in psychosis

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A case-control study of paternal and maternal age as risk factors in mood disorders

Fountoulakis, K. Ν., Gonda, X., Siamouli, M., Panagiotidis, P., Moutou, K., Nimatoudis, I., & Kasper, S. F. (2019) · International Journal of Psychiatry in Clinical Practice · doi:10.1080/13651501.2018.1519079 · Cited by 10

Genome-wide investigation of rare structural variants identifiesVIPR2as a new candidate gene for schizophrenia

Nieratschker, V., Meyer‐Lindenberg, A., & Witt, S. H. (2011) · Expert Review of Neurotherapeutics · doi:10.1586/ern.11.84 · Cited by 9

The Year in Human and Medical Genetics

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Rare-Allele Detection Using Compressed Se(que)nsingPreprint

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Further evidence for the association between the LSM1 gene and schizophrenia

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Genetic Heterogeneity of Autism Spectrum Disorders

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