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Stephen J. Glatt - Publications

Affiliations: 
SUNY Upstate Medical University, Syracuse, Syracuse, NY 
Area:
Psychiatric Genetic Epidemiology
Website:
http://www.upstate.edu/psych/faculty.php?ID=glatts

157 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Hess JL, Radonjić NV, Patak J, Glatt SJ, Faraone SV. Autophagy, apoptosis, and neurodevelopmental genes might underlie selective brain region vulnerability in attention-deficit/hyperactivity disorder. Molecular Psychiatry. PMID 33339955 DOI: 10.1038/s41380-020-00974-2  0.725
2020 Hess JL, Nguyen NH, Suben J, Meath RM, Albert AB, Van Orman S, Anders KM, Forken PJ, Roe CA, Schulze TG, Faraone SV, Glatt SJ. Gene co-expression networks in peripheral blood capture dimensional measures of emotional and behavioral problems from the Child Behavior Checklist (CBCL). Translational Psychiatry. 10: 328. PMID 32968041 DOI: 10.1038/s41398-020-01007-w  0.721
2020 Lin PI, Glatt SJ, Tsuang MT. Methodology in the GBD study of China. Lancet (London, England). 396: 25. PMID 32622390 DOI: 10.1016/S0140-6736(20)30483-9  0.489
2020 Huckins LM, Chatzinakos C, Breen MS, Hartmann J, Klengel T, da Silva Almeida AC, Dobbyn A, Girdhar K, Hoffman GE, Klengel C, Logue MW, Lori A, Maihofer AX, Morrison FG, Nguyen HT, ... ... Glatt SJ, et al. Analysis of Genetically Regulated Gene Expression Identifies a Prefrontal PTSD Gene, SNRNP35, Specific to Military Cohorts. Cell Reports. 31: 107716. PMID 32492425 DOI: 10.1016/J.Celrep.2020.107716  0.398
2020 Albert AB, Wagner KE, Van Orman SE, Anders KM, Forken PJ, Blatt SD, Fremont WP, Faraone SV, Glatt SJ. Initial Responsiveness to Reward Attainment and Psychopathology in Children and Adults: An RDoC Study. Psychiatry Research. 289: 113021. PMID 32447091 DOI: 10.1016/J.Psychres.2020.113021  0.486
2020 Howrigan DP, Rose SA, Samocha KE, Fromer M, Cerrato F, Chen WJ, Churchhouse C, Chambert K, Chandler SD, Daly MJ, Dumont A, Genovese G, Hwu HG, Laird N, Kosmicki JA, ... ... Glatt SJ, et al. Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations. Nature Neuroscience. PMID 31932770 DOI: 10.1038/S41593-019-0564-3  0.697
2020 Zaso MJ, Maisto SA, Glatt SJ, Hess JL, Park A. Effects of Polygenic Risk and Perceived Friends’ Drinking and Disruptive Behavior on Development of Alcohol Use Across Adolescence Journal of Studies On Alcohol and Drugs. 81: 808-815. DOI: 10.15288/jsad.2020.81.808  0.621
2019 Lam M, Chen CY, Li Z, Martin AR, Bryois J, Ma X, Gaspar H, Ikeda M, Benyamin B, Brown BC, Liu R, Zhou W, Guan L, Kamatani Y, Kim SW, ... ... Glatt SJ, et al. Comparative genetic architectures of schizophrenia in East Asian and European populations. Nature Genetics. PMID 31740837 DOI: 10.1038/S41588-019-0512-X  0.698
2019 Liu C, Faraone SV, Glatt SJ. Psychiatric Genetics, Epigenetics, and Cellular Models in Coming Years. Journal of Psychiatry and Brain Science. 4. PMID 31608310 DOI: 10.20900/jpbs.20190012  0.51
2019 Hess JL, Tylee DS, Mattheisen M, Børglum AD, Als TD, Grove J, Werge T, Mortensen PB, Mors O, Nordentoft M, Hougaard DM, Byberg-Grauholm J, Bækvad-Hansen M, ... ... Glatt SJ, et al. A polygenic resilience score moderates the genetic risk for schizophrenia. Molecular Psychiatry. PMID 31492941 DOI: 10.1038/S41380-019-0463-8  0.799
2019 Hess JL, Tylee DS, Barve R, de Jong S, Ophoff RA, Kumarasinghe N, Tooney P, Schall U, Gardiner E, Beveridge NJ, Scott RJ, Yasawardene S, Perera A, Mendis J, Carr V, ... ... Glatt SJ, et al. Transcriptomic abnormalities in peripheral blood in bipolar disorder, and discrimination of the major psychoses. Schizophrenia Research. PMID 31391148 DOI: 10.1016/J.Schres.2019.07.036  0.807
2019 Wang SH, Hsiao PC, Yeh LL, Liu CM, Liu CC, Hwang TJ, Hsieh MH, Chien YL, Lin YT, Huang YT, Chen CY, Chandler SD, Faraone SV, Neale B, Glatt SJ, et al. Advanced Paternal Age and Early Onset of Schizophrenia in Sporadic Cases: Not Confounded by Parental Polygenic Risk for Schizophrenia. Biological Psychiatry. PMID 30926130 DOI: 10.1016/J.Biopsych.2019.01.023  0.674
2019 Nguyen NH, Albert AB, Van Orman S, Forken P, Blatt SD, Fremont WP, Faraone SV, Glatt SJ. Effort valuation and psychopathology in children and adults. Psychological Medicine. 1-7. PMID 30636648 DOI: 10.1017/S0033291718003884  0.491
2019 Hess J, Tylee D, Liu C, de Jong S, Ophoff R, Gardiner E, Sibille E, Turecki G, Tseng G, Tsuang MT, Faraone S, Glatt S. M14 DISCRIMINATION OF MAJOR NEUROPSYCHIATRIC DISORDERS USING BLOOD-BASED TRANSCRIPTOMIC SIGNATURES European Neuropsychopharmacology. 29: S173. DOI: 10.1016/J.Euroneuro.2019.08.114  0.774
2019 Hess J, Nguyen N, Suben J, Meath R, Albert A, Van Orman S, Roe C, Faraone S, Glatt S. S27BRAIN REGION-SPECIFIC TRANSCRIPTOMIC DYSREGULATION UNDERLYING BEHAVIORAL AND EMOTIONAL PROBLEMS IN LIVING CHILDREN: APPLICATION OF A NOVEL GENE EXPRESSION IMPUTATION ENGINE European Neuropsychopharmacology. 29: S128. DOI: 10.1016/J.Euroneuro.2019.08.028  0.717
2019 Hess J, Glatt SJ. SU29PREDICTING PSYCHOPATHOLOGY WITH POLYTRANSCRIPT RISK SCORES European Neuropsychopharmacology. 29: S1283. DOI: 10.1016/J.Euroneuro.2018.08.393  0.658
2019 Hess J, Patak J, Glatt SJ, Faraone SV. SA5GENES AND BRAIN CELL TYPES LINKED WITH SELECTIVE NEURONAL VULNERABILITY IN ADHD European Neuropsychopharmacology. 29: S1190-S1191. DOI: 10.1016/J.Euroneuro.2018.08.227  0.706
2019 Breen M, Tylee D, Maihofer A, Tsuang M, Chandler S, Mehta D, Binder E, Hess J, Baker D, Risbrough V, Nievergelt C, Buxbaum J, Glatt S. PTSD BLOOD TRANSCRIPTOME MEGA-ANALYSIS: INFLAMMATORY PATHWAYS ACROSS BIOLOGICAL SEX AND MODES OF TRAUMA European Neuropsychopharmacology. 29: S1056-S1057. DOI: 10.1016/J.Euroneuro.2018.07.073  0.759
2019 Hess J, Faraone SV, Glatt SJ. ASSOCIATION OF GENETIC RISK SCORES FOR SCHIZOPHRENIA WITH LYMPHOBLAST AND CORTICAL GENE EXPRESSION NETWORKS European Neuropsychopharmacology. 29: S1003. DOI: 10.1016/J.Euroneuro.2017.08.395  0.783
2019 Ollila H, Li M, Mindrinos M, Wang C, Fernandez-Vina M, Kuehn R, Krishnakumar S, Wilhelmy J, Tsuang MT, Glatt SJ, Mignot E, Levinson DF. Transethnic Analysis Of High-Resolution Hla Alleles And Complement 4 Structural Polymorphisms In Schizophrenia European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.278  0.565
2019 Hess J, Glatt SJ. FUNCTIONAL LD CLUMP ENRICHMENT TEST (FLEET) DETECTS ENRICHMENT OF RISK LOCI FOR SCHIZOPHRENIA AND BIPOLAR DISORDER IN REGULATORY ELEMENTS AND PATHWAYS European Neuropsychopharmacology. 29: S897-S898. DOI: 10.1016/J.Euroneuro.2017.08.209  0.724
2019 Hess J, Glatt SJ. GENE EXPRESSION SIGNATURES FROM PERIPHERAL BLOOD DISCRIMINATE THE MAJOR PSYCHOSES European Neuropsychopharmacology. 29: S832. DOI: 10.1016/J.Euroneuro.2017.08.091  0.748
2019 Patak J, Faraone S, Zhang-James Y, Hess J, Glatt S. PATHWAY INTERACTIONS FOR AUTISM-RISK GENE SLC9A9: IN VITRO CONFIRMATION OF BIOINFORMATIC ASSOCIATIONS European Neuropsychopharmacology. 29: S830-S831. DOI: 10.1016/J.Euroneuro.2017.08.088  0.742
2018 Lee SC, Quinn TP, Lai J, Kong SW, Hertz-Picciotto I, Glatt SJ, Crowley TM, Venkatesh S, Nguyen T. Solving for X: Evidence for sex-specific autism biomarkers across multiple transcriptomic studies. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30520558 DOI: 10.1002/Ajmg.B.32701  0.388
2018 Tylee DS, Sun J, Hess JL, Tahir MA, Sharma E, Malik R, Worrall BB, Levine AJ, Martinson JJ, Nejentsev S, Speed D, Fischer A, Mick E, Walker BR, Crawford A, ... ... Glatt SJ, et al. Genetic correlations among psychiatric and immune-related phenotypes based on genome-wide association data. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30325587 DOI: 10.1002/Ajmg.B.32652  0.809
2018 Zhang-James Y, Fernàndez-Castillo N, Hess JL, Malki K, Glatt SJ, Cormand B, Faraone SV. An integrated analysis of genes and functional pathways for aggression in human and rodent models. Molecular Psychiatry. PMID 29858598 DOI: 10.1038/S41380-018-0068-7  0.754
2018 Smoller JW, Andreassen OA, Edenberg HJ, Faraone SV, Glatt SJ, Kendler KS. Correction to: Psychiatric genetics and the structure of psychopathology. Molecular Psychiatry. PMID 29540840 DOI: 10.1038/S41380-018-0026-4  0.501
2018 Smoller JW, Andreassen OA, Edenberg HJ, Faraone SV, Glatt SJ, Kendler KS. Psychiatric genetics and the structure of psychopathology. Molecular Psychiatry. PMID 29317742 DOI: 10.1038/S41380-017-0010-4  0.557
2017 Hess JL, Akutagava-Martins GC, Patak JD, Glatt SJ, Faraone SV. Why is there selective subcortical vulnerability in ADHD? Clues from postmortem brain gene expression data. Molecular Psychiatry. 23: 1787-1793. PMID 29180674 DOI: 10.1038/Mp.2017.242  0.749
2017 Lin WY, Chen WJ, Liu CM, Hwu HG, McCarroll SA, Glatt SJ, Tsuang MT. Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants. Scientific Reports. 7: 13858. PMID 29066733 DOI: 10.1038/S41598-017-13177-7  0.584
2017 Breen MS, Tylee DS, Maihofer AX, Neylan TC, Mehta D, Binder E, Chandler SD, Hess JL, Kremen WS, Risbrough VB, Woelk CH, Baker DG, Nievergelt CM, Tsuang MT, Buxbaum JD, ... Glatt SJ, et al. PTSD Blood Transcriptome Mega-Analysis: Shared Inflammatory Pathways Across Biological Sex and Modes of Trauma. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 28925389 DOI: 10.1038/Npp.2017.220  0.776
2017 Bousman CA, Cropley V, Klauser P, Hess JL, Pereira A, Idrizi R, Bruggemann J, Mostaid MS, Lenroot R, Weickert TW, Glatt SJ, Everall IP, Sundram S, Zalesky A, Weickert CS, et al. Neuregulin-1 (NRG1) polymorphisms linked with psychosis transition are associated with enlarged lateral ventricles and white matter disruption in schizophrenia. Psychological Medicine. 1-9. PMID 28826413 DOI: 10.1017/S0033291717002173  0.698
2017 Tylee DS, Kikinis Z, Quinn TP, Antshel KM, Fremont W, Tahir MA, Zhu A, Gong X, Glatt SJ, Coman IL, Shenton ME, Kates WR, Makris N. Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study. Neuroimage. Clinical. 15: 832-842. PMID 28761808 DOI: 10.1016/J.Nicl.2017.04.029  0.695
2017 Wang SH, Hsiao PC, Yeh LL, Liu CM, Liu CC, Hwang TJ, Hsieh MH, Chien YL, Lin YT, Chandler SD, Faraone SV, Laird N, Neale B, McCarroll SA, Glatt SJ, et al. Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia. Genes, Brain, and Behavior. PMID 28719030 DOI: 10.1111/Gbb.12401  0.682
2017 Philibert R, Glatt SJ. Optimizing the chances of success in the search for epigenetic biomarkers: Embracing genetic variation. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28696057 DOI: 10.1002/Ajmg.B.32569  0.333
2017 Joseph J, Kremen WS, Franz CE, Glatt SJ, van de Leemput J, Chandler SD, Tsuang MT, Twamley EW. Predictors of current functioning and functional decline in schizophrenia. Schizophrenia Research. PMID 28139356 DOI: 10.1016/J.Schres.2017.01.038  0.552
2017 Tylee DS, Gray R, Glatt SJ, Bourke F. Evaluation of the reconsolidation of traumatic memories protocol for the treatment of PTSD: a randomized, wait-list-controlled trial Journal of Military, Veteran and Family Health. 3: 21-33. DOI: 10.3138/JMVFH.4120  0.644
2017 Howrigan D, Samocha K, Kosmicki J, Moran J, Chambert K, Fromer M, Chandler S, Laird N, Hwu H, Chen WJ, Faraone S, Glatt S, Tsuang M, McCarroll S, Neale B. Damaging Missense De Novo Coding Mutations Contribute To Schizophrenia Risk European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.481  0.645
2016 Quinn T, Tylee D, Glatt S. exprso: an R-package for the rapid implementation of machine learning algorithms. F1000research. 5: 2588. PMID 29560250 DOI: 10.12688/F1000Research.9893.2  0.678
2016 van de Leemput J, Hess JL, Glatt SJ, Tsuang MT. Genetics of Schizophrenia: Historical Insights and Prevailing Evidence. Advances in Genetics. 96: 99-141. PMID 27968732 DOI: 10.1016/Bs.Adgen.2016.08.001  0.771
2016 Jeffries CD, Perkins DO, Chandler SD, Stark T, Yeo E, Addington J, Bearden CE, Cadenhead KS, Cannon TD, Cornblatt BA, Mathalon DH, McGlashan TH, Seidman LJ, Walker EF, Woods SW, ... Glatt SJ, et al. Insights into psychosis risk from leukocyte microRNA expression. Translational Psychiatry. 6: e981. PMID 27959328 DOI: 10.1038/Tp.2016.148  0.543
2016 Tylee DS, Hess JL, Quinn TP, Barve R, Huang H, Zhang-James Y, Chang J, Stamova BS, Sharp FR, Hertz-Picciotto I, Faraone SV, Kong SW, Glatt SJ. Blood transcriptomic comparison of individuals with and without autism spectrum disorder: A combined-samples mega-analysis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 27862943 DOI: 10.1002/Ajmg.B.32511  0.799
2016 Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, O'Donnell-Luria AH, Ware JS, Hill AJ, Cummings BB, Tukiainen T, Birnbaum DP, Kosmicki JA, Duncan LE, Estrada K, ... ... Glatt SJ, et al. Analysis of protein-coding genetic variation in 60,706 humans. Nature. 536: 285-291. PMID 27535533 DOI: 10.1038/Nature19057  0.557
2016 Tylee DS, Espinoza AJ, Hess JL, Tahir MA, McCoy SY, Rim JK, Dhimal T, Cohen OS, Glatt SJ. RNA sequencing of transformed lymphoblastoid cells from siblings discordant for autism spectrum disorders reveals transcriptomic and functional alterations: Evidence for sex-specific effects. Autism Research : Official Journal of the International Society For Autism Research. PMID 27529825 DOI: 10.1002/Aur.1679  0.796
2016 Hess JL, Tylee DS, Barve R, de Jong S, Ophoff RA, Kumarasinghe N, Tooney P, Schall U, Gardiner E, Beveridge NJ, Scott RJ, Yasawardene S, Perera A, Mendis J, Carr V, ... ... Glatt SJ, et al. Transcriptome-wide mega-analyses reveal joint dysregulation of immunologic genes and transcription regulators in brain and blood in schizophrenia. Schizophrenia Research. PMID 27450777 DOI: 10.1016/J.Schres.2016.07.006  0.812
2016 Patak J, Hess JL, Zhang-James Y, Glatt SJ, Faraone SV. SLC9A9 Co-expression modules in autism-associated brain regions. Autism Research : Official Journal of the International Society For Autism Research. PMID 27439572 DOI: 10.1002/Aur.1670  0.766
2016 Breen MS, Uhlmann A, Nday CM, Glatt SJ, Mitt M, Metsalpu A, Stein DJ, Illing N. Candidate gene networks and blood biomarkers of methamphetamine-associated psychosis: an integrative RNA-sequencing report. Translational Psychiatry. 6: e802. PMID 27163203 DOI: 10.1038/Tp.2016.67  0.349
2016 van de Leemput J, Glatt SJ, Tsuang MT. The potential of genetic and gene expression analysis in the diagnosis of neuropsychiatric disorders. Expert Review of Molecular Diagnostics. PMID 27017833 DOI: 10.1586/14737159.2016.1171714  0.617
2016 Quinn T, Tylee D, Glatt S. exprso: an R-package for the rapid implementation of machine learning algorithms F1000research. 5: 2588. DOI: 10.12688/f1000research.9893.1  0.656
2015 Schwantes-An TH, Zhang J, Chen LS, Hartz SM, Culverhouse RC, Chen X, Coon H, Frank J, Kamens HM, Konte B, Kovanen L, Latvala A, Legrand LN, Maher BS, Melroy WE, ... ... Glatt SJ, et al. Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics. PMID 26392368 DOI: 10.1007/S10519-015-9737-3  0.575
2015 Hess JL, Kawaguchi DM, Wagner KE, Faraone SV, Glatt SJ. The influence of genes on "positive valence systems" constructs: A systematic review. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26365619 DOI: 10.1002/Ajmg.B.32382  0.753
2015 Cohen OS, Weickert TW, Hess JL, Paish LM, McCoy SY, Rothmond DA, Galletly C, Liu D, Weinberg DD, Huang XF, Xu Q, Shen Y, Zhang D, Yue W, Yan J, ... ... Glatt SJ, et al. A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples. Molecular Psychiatry. PMID 26347318 DOI: 10.1038/Mp.2015.137  0.797
2015 Takahashi S, Glatt SJ, Uchiyama M, Faraone SV, Tsuang MT. Meta-analysis of data from the Psychiatric Genomics Consortium and additional samples supports association of CACNA1C with risk for schizophrenia. Schizophrenia Research. 168: 429-33. PMID 26276307 DOI: 10.1016/J.Schres.2015.07.033  0.697
2015 Rees E, Kirov G, Walters JT, Richards AL, Howrigan D, Kavanagh DH, Pocklington AJ, Fromer M, Ruderfer DM, Georgieva L, Carrera N, Gormley P, Palta P, Williams H, Dwyer S, ... ... Glatt SJ, et al. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational Psychiatry. 5: e607. PMID 26196440 DOI: 10.1038/Tp.2015.99  0.616
2015 Manschreck TC, Chun J, Merrill AM, Maher BA, Boshes RA, Glatt SJ, Faraone SV, Tsuang MT, Seidman LJ. Impaired motor performance in adolescents at familial high-risk for schizophrenia. Schizophrenia Research. 168: 44-9. PMID 26165939 DOI: 10.1016/J.Schres.2015.06.013  0.658
2015 Joseph J, Kremen WS, Glatt SJ, Franz CE, Chandler SD, Liu X, Johnson BK, Tsuang MT, Twamley EW. Assessment of Lifespan Functioning Attainment (ALFA) scale: A quantitative interview for self-reported current and functional decline in schizophrenia. Journal of Psychiatric Research. 65: 102-7. PMID 25898804 DOI: 10.1016/J.Jpsychires.2015.04.001  0.562
2015 Breen MS, Maihofer AX, Glatt SJ, Tylee DS, Chandler SD, Tsuang MT, Risbrough VB, Baker DG, O'Connor DT, Nievergelt CM, Woelk CH. Gene networks specific for innate immunity define post-traumatic stress disorder. Molecular Psychiatry. PMID 25754082 DOI: 10.1038/Mp.2015.9  0.776
2015 Bulayeva K, Lesch KP, Bulayev O, Walsh C, Glatt S, Gurgenova F, Omarova J, Berdichevets I, Thompson PM. Genomic structural variants are linked with intellectual disability. Journal of Neural Transmission (Vienna, Austria : 1996). PMID 25626716 DOI: 10.1007/S00702-015-1366-8  0.369
2015 Hess JL, Quinn TP, Akbarian S, Glatt SJ. Bioinformatic analyses and conceptual synthesis of evidence linking ZNF804A to risk for schizophrenia and bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 14-35. PMID 25522715 DOI: 10.1002/Ajmg.B.32284  0.751
2015 Tylee DS, Chandler SD, Nievergelt CM, Liu X, Pazol J, Woelk CH, Lohr JB, Kremen WS, Baker DG, Glatt SJ, Tsuang MT. Blood-based gene-expression biomarkers of post-traumatic stress disorder among deployed marines: A pilot study. Psychoneuroendocrinology. 51: 472-94. PMID 25311155 DOI: 10.1016/J.Psyneuen.2014.09.024  0.778
2015 Manschreck TC, Chun J, Merrill AM, Maher BA, Boshes RA, Glatt SJ, Faraone SV, Tsuang MT, Seidman LJ. Impaired motor performance in adolescents at familial high-risk for schizophrenia Schizophrenia Research. DOI: 10.1016/j.schres.2015.06.013  0.613
2014 Walder DJ, Faraone SV, Glatt SJ, Tsuang MT, Seidman LJ. Genetic liability, prenatal health, stress and family environment: risk factors in the Harvard Adolescent Family High Risk for schizophrenia study. Schizophrenia Research. 157: 142-8. PMID 24836971 DOI: 10.1016/J.Schres.2014.04.015  0.667
2014 Hess JL, Glatt SJ. How might ZNF804A variants influence risk for schizophrenia and bipolar disorder? A literature review, synthesis, and bioinformatic analysis American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 165: 28-40. PMID 24123948 DOI: 10.1002/Ajmg.B.32207  0.749
2013 Bousman CA, Glatt SJ, Chandler SD, Lohr J, Kremen WS, Tsuang MT, Everall IP. Negative Symptoms of Psychosis Correlate with Gene Expression of the Wnt/β-Catenin Signaling Pathway in Peripheral Blood. Psychiatry Journal. 2013: 852930. PMID 24236287 DOI: 10.1155/2013/852930  0.514
2013 Kanazawa T, Ikeda M, Glatt SJ, Tsutsumi A, Kikuyama H, Kawamura Y, Nishida N, Miyagawa T, Hashimoto R, Takeda M, Sasaki T, Tokunaga K, Koh J, Iwata N, Yoneda H. Genome-wide association study of atypical psychosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 679-86. PMID 24132900 DOI: 10.1002/Ajmg.B.32164  0.426
2013 Tylee DS, Kawaguchi DM, Glatt SJ. On the outside, looking in: A review and evaluation of the comparability of blood and brain "-omes" American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 162: 595-603. PMID 24132893 DOI: 10.1002/Ajmg.B.32150  0.715
2013 Faraone SV, Seidman LJ, Buka S, Goldstein JM, Lyons M, Kremen WS, Glatt SJ. Festschrift celebrating the career of Ming T. Tsuang. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 551-8. PMID 24132890 DOI: 10.1002/Ajmg.B.32194  0.421
2013 Cohen OS, Varlinskaya EI, Wilson CA, Glatt SJ, Mooney SM. Acute prenatal exposure to a moderate dose of valproic acid increases social behavior and alters gene expression in rats. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 31: 740-50. PMID 24055786 DOI: 10.1016/J.Ijdevneu.2013.09.002  0.544
2013 Shiffrin ND, Gruber J, Glatt SJ, Faraone SV. No association between MspI allele of the ADRA2A polymorphism and ADHD: meta-analysis of family-based studies. Psychiatric Genetics. 23: 174-5. PMID 23751900 DOI: 10.1097/Ypg.0B013E3283631509  0.547
2013 Liu L, Chen Y, Li H, Qian Q, Yang L, Glatt SJ, Faraone SV, Wang Y. Association between SYP with attention-deficit/hyperactivity disorder in Chinese Han subjects: differences among subtypes and genders. Psychiatry Research. 210: 308-14. PMID 23726717 DOI: 10.1016/J.Psychres.2013.04.029  0.533
2013 Glatt SJ, Tylee DS, Chandler SD, Pazol J, Nievergelt CM, Woelk CH, Baker DG, Lohr JB, Kremen WS, Litz BT, Tsuang MT. Blood-based gene-expression predictors of PTSD risk and resilience among deployed marines: a pilot study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 313-26. PMID 23650250 DOI: 10.1002/Ajmg.B.32167  0.777
2013 Glatt SJ. How should we interpret and value the pursuit of blood-based biomarkers for autism spectrum disorders? Journal of the American Academy of Child and Adolescent Psychiatry. 52: 1248-1250. DOI: 10.1016/J.Jaac.2013.08.022  0.319
2012 Cohen OS, Mccoy SY, Middleton FA, Bialosuknia S, Zhang-James Y, Liu L, Tsuang MT, Faraone SV, Glatt SJ. Transcriptomic analysis of postmortem brain identifies dysregulated splicing events in novel candidate genes for schizophrenia. Schizophrenia Research. 142: 188-99. PMID 23062752 DOI: 10.1016/J.Schres.2012.09.015  0.765
2012 Pérez-Santiago J, Diez-Alarcia R, Callado LF, Zhang JX, Chana G, White CH, Glatt SJ, Tsuang MT, Everall IP, Meana JJ, Woelk CH. A combined analysis of microarray gene expression studies of the human prefrontal cortex identifies genes implicated in schizophrenia. Journal of Psychiatric Research. 46: 1464-74. PMID 22954356 DOI: 10.1016/J.Jpsychires.2012.08.005  0.623
2012 Glatt SJ, Tsuang MT, Winn M, Chandler SD, Collins M, Lopez L, Weinfeld M, Carter C, Schork N, Pierce K, Courchesne E. Blood-based gene expression signatures of infants and toddlers with autism. Journal of the American Academy of Child and Adolescent Psychiatry. 51: 934-44.e2. PMID 22917206 DOI: 10.1016/J.Jaac.2012.07.007  0.577
2012 Shayevitz C, Cohen OS, Faraone SV, Glatt SJ. A re-review of the association between the NOTCH4 locus and schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 477-83. PMID 22488909 DOI: 10.1002/Ajmg.B.32050  0.728
2012 Franz CE, Panizzon MS, Eaves LJ, Thompson W, Lyons MJ, Jacobson KC, Tsuang M, Glatt SJ, Kremen WS. Genetic and environmental multidimensionality of well- and ill-being in middle aged twin men. Behavior Genetics. 42: 579-91. PMID 22484556 DOI: 10.1007/S10519-012-9538-X  0.526
2012 Faraone SV, Spencer TJ, Kollins SH, Glatt SJ, Goodman D. Dose response effects of lisdexamfetamine dimesylate treatment in adults with ADHD: an exploratory study. Journal of Attention Disorders. 16: 118-27. PMID 21527575 DOI: 10.1177/1087054711403716  0.473
2011 Woelk CH, Singhania A, Pérez-Santiago J, Glatt SJ, Tsuang MT. The utility of gene expression in blood cells for diagnosing neuropsychiatric disorders. International Review of Neurobiology. 101: 41-63. PMID 22050848 DOI: 10.1016/B978-0-12-387718-5.00003-1  0.611
2011 Tsutsumi A, Glatt SJ, Kanazawa T, Kawashige S, Uenishi H, Hokyo A, Kaneko T, Moritani M, Kikuyama H, Koh J, Matsumura H, Yoneda H. The genetic validation of heterogeneity in schizophrenia. Behavioral and Brain Functions : Bbf. 7: 43. PMID 21981786 DOI: 10.1186/1744-9081-7-43  0.42
2011 Glatt SJ, Stone WS, Nossova N, Liew CC, Seidman LJ, Tsuang MT. Similarities and differences in peripheral blood gene-expression signatures of individuals with schizophrenia and their first-degree biological relatives. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 869-87. PMID 21972136 DOI: 10.1002/Ajmg.B.31239  0.634
2011 Liu L, Guan LL, Chen Y, Ji N, Li HM, Li ZH, Qian QJ, Yang L, Glatt SJ, Faraone SV, Wang YF. Association analyses of MAOA in Chinese Han subjects with attention-deficit/hyperactivity disorder: family-based association test, case-control study, and quantitative traits of impulsivity. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 737-48. PMID 21761555 DOI: 10.1002/Ajmg.B.31217  0.53
2011 Glatt SJ, Cohen OS, Faraone SV, Tsuang MT. Dysfunctional gene splicing as a potential contributor to neuropsychiatric disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 382-92. PMID 21438146 DOI: 10.1002/Ajmg.B.31181  0.753
2011 Waxmonsky JG, Waschbusch DA, Glatt SJ, Faraone SV. Prediction of placebo response in 2 clinical trials of lisdexamfetamine dimesylate for the treatment of ADHD. The Journal of Clinical Psychiatry. 72: 1366-75. PMID 21367347 DOI: 10.4088/Jcp.10M05979Pur  0.489
2011 Adler LA, Shaw DM, Spencer TJ, Newcorn JH, Sitt DJ, Morrill M, Davidow JV, Glatt SJ, Faraone SV. Reliability and validity of the Time-Sensitive ADHD Symptom Scale in adults. Comprehensive Psychiatry. 52: 769-73. PMID 21306705 DOI: 10.1016/J.Comppsych.2010.12.002  0.487
2011 Faraone SV, Glatt SJ, Tsuang MT. Genetic Epidemiology Textbook in Psychiatric Epidemiology: Third Edition. 31-51. DOI: 10.1002/9780470976739.ch3  0.59
2010 Bousman CA, Cherner M, Glatt SJ, Atkinson JH, Grant I, Tsuang MT, Everall IP. Impact of COMT Val158Met on executive functioning in the context of HIV and methamphetamine. Neurobehavioral Hiv Medicine. 2010: 1-11. PMID 24078782 DOI: 10.2147/NBHIV.S8245  0.453
2010 Bousman CA, Chana G, Glatt SJ, Chandler SD, May T, Lohr J, Kremen WS, Tsuang MT, Everall IP. Positive symptoms of psychosis correlate with expression of ubiquitin proteasome genes in peripheral blood. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1336-41. PMID 20552680 DOI: 10.1002/Ajmg.B.31106  0.622
2010 Bousman CA, Glatt SJ, Cherner M, Atkinson JH, Grant I, Tsuang MT, Everall IP. Preliminary evidence of ethnic divergence in associations of putative genetic variants for methamphetamine dependence. Psychiatry Research. 178: 295-8. PMID 20478633 DOI: 10.1016/J.Psychres.2009.07.019  0.569
2010 Hokyo A, Kanazawa T, Uenishi H, Tsutsumi A, Kawashige S, Kikuyama H, Glatt SJ, Koh J, Nishimoto Y, Matsumura H, Motomura N, Yoneda H. Habituation in prepulse inhibition is affected by a polymorphism on the NMDA receptor 2B subunit gene (GRIN2B). Psychiatric Genetics. 20: 191-8. PMID 20421849 DOI: 10.1097/Ypg.0B013E32833A201D  0.378
2010 Faraone SV, Spencer TJ, Kollins SH, Glatt SJ. Effects of lisdexamfetamine dimesylate treatment for ADHD on growth. Journal of the American Academy of Child and Adolescent Psychiatry. 49: 24-32. PMID 20215923 DOI: 10.1016/J.Jaac.2009.10.003  0.473
2010 Faraone SV, Glatt SJ. A comparison of the efficacy of medications for adult attention-deficit/hyperactivity disorder using meta-analysis of effect sizes. The Journal of Clinical Psychiatry. 71: 754-63. PMID 20051220 DOI: 10.4088/Jcp.08M04902Pur  0.489
2010 Bousman CA, Chana G, Glatt SJ, Chandler SD, Lucero GR, Tatro E, May T, Lohr JB, Kremen WS, Tsuang MT, Everall IP. Preliminary evidence of ubiquitin proteasome system dysregulation in schizophrenia and bipolar disorder: convergent pathway analysis findings from two independent samples. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 494-502. PMID 19582768 DOI: 10.1002/Ajmg.B.31006  0.628
2010 Faraone SV, Glatt SJ. Effects of extended-release guanfacine on ADHD symptoms and sedation-related adverse events in children with ADHD. Journal of Attention Disorders. 13: 532-8. PMID 19395648 DOI: 10.1177/1087054709332472  0.489
2009 Glatt SJ, Chandler SD, Bousman CA, Chana G, Lucero GR, Tatro E, May T, Lohr JB, Kremen WS, Everall IP, Tsuang MT. Alternatively Spliced Genes as Biomarkers for Schizophrenia, Bipolar Disorder and Psychosis: A Blood-Based Spliceome-Profiling Exploratory Study. Current Pharmacogenomics and Personalized Medicine. 7: 164-188. PMID 21532980 DOI: 10.2174/1875692110907030164  0.639
2009 Ramanathan S, Glatt SJ. Serotonergic system genes in psychosis of alzheimer dementia: Meta-Analysis American Journal of Geriatric Psychiatry. 17: 839-846. PMID 19910872 DOI: 10.1097/Jgp.0B013E3181Ab8C3F  0.354
2009 McGrath CL, Glatt SJ, Sklar P, Le-Niculescu H, Kuczenski R, Doyle AE, Biederman J, Mick E, Faraone SV, Niculescu AB, Tsuang MT. Evidence for genetic association of RORB with bipolar disorder. Bmc Psychiatry. 9: 70. PMID 19909500 DOI: 10.1186/1471-244X-9-70  0.7
2009 Kanazawa T, Glatt SJ, Faraone SV, Hwu HG, Yoneda H, Tsuang MT. Family-based association study of SELENBP1 in schizophrenia. Schizophrenia Research. 113: 268-72. PMID 19596560 DOI: 10.1016/J.Schres.2009.06.011  0.711
2009 Bousman CA, Glatt SJ, Everall IP, Tsuang MT. Genetic association studies of methamphetamine use disorders: A systematic review and synthesis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 1025-49. PMID 19219857 DOI: 10.1002/Ajmg.B.30936  0.62
2009 Faraone SV, Glatt SJ, Bukstein OG, Lopez FA, Arnold LE, Findling RL. Effects of once-daily oral and transdermal methylphenidate on sleep behavior of children with ADHD Journal of Attention Disorders. 12: 308-315. PMID 18400982 DOI: 10.1177/1087054708314844  0.447
2009 Glatt SJ, Faraone SV, Lasky-Su JA, Kanazawa T, Hwu HG, Tsuang MT. Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan. Molecular Psychiatry. 14: 885-93. PMID 18332877 DOI: 10.1038/mp.2008.30  0.669
2009 Chana G, Glatt SJ, Everall IP, Tsuang MT. Blood and brain gene expression in major psychiatric disorders: A search for biomarkers Biomarkers For Psychiatric Disorders. 1-21. DOI: 10.1007/978-0-387-79251-4_1  0.548
2009 Glatt SJ, Chandler SD, Bousman CA, Chana G, Lucero GR, Tatro E, May T, Lohr JB, Kremen WS, Everall IP, Tsuang MT. Alternatively spliced genes as biomarkers for schizophrenia, bipolar disorder and psychosis: A blood-based spliceome-profiling exploratory study Current Pharmacogenomics and Personalized Medicine. 7: 164-188.  0.583
2008 Chen C, Glatt SJ, Tsuang MT. The tryptophan hydroxylase gene influences risk for bipolar disorder but not major depressive disorder: results of meta-analyses. Bipolar Disorders. 10: 816-21. PMID 19032713 DOI: 10.1111/J.1399-5618.2008.00623.X  0.594
2008 Glatt SJ, Lasky-Su JA, Zhu SC, Zhang R, Zhang B, Li J, Yuan X, Li J, Lyons MJ, Faraone SV, Tsuang MT. Genome-wide linkage analysis of heroin dependence in Han Chinese: results from Wave Two of a multi-stage study. Drug and Alcohol Dependence. 98: 30-4. PMID 18538955 DOI: 10.1016/J.Drugalcdep.2008.04.011  0.649
2008 Jacobson KC, Beseler CL, Lasky-Su J, Faraone SV, Glatt SJ, Kremen WS, Lyons MJ, Tsuang MT. Ordered subsets linkage analysis of antisocial behavior in substance use disorder among participants in the Collaborative Study on the Genetics of Alcoholism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1258-69. PMID 18496835 DOI: 10.1002/Ajmg.B.30771  0.655
2008 Le-Niculescu H, McFarland MJ, Ogden CA, Balaraman Y, Patel S, Tan J, Rodd ZA, Paulus M, Geyer MA, Edenberg HJ, Glatt SJ, Faraone SV, Nurnberger JI, Kuczenski R, Tsuang MT, et al. Phenomic, convergent functional genomic, and biomarker studies in a stress-reactive genetic animal model of bipolar disorder and co-morbid alcoholism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 134-66. PMID 18247375 DOI: 10.1002/Ajmg.B.30707  0.67
2008 Kanazawa T, Chana G, Glatt SJ, Mizuno H, Masliah E, Yoneda H, Tsuang MT, Everall IP. The utility of SELENBP1 gene expression as a biomarker for major psychotic disorders: replication in schizophrenia and extension to bipolar disorder with psychosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 686-9. PMID 18163446 DOI: 10.1002/Ajmg.B.30664  0.641
2008 Adler LA, Faraone SV, Spencer TJ, Michelson D, Reimherr FW, Glatt SJ, Marchant BK, Biederman J. The reliability and validity of self- and investigator ratings of ADHD in adults Journal of Attention Disorders. 11: 711-719. PMID 18025250 DOI: 10.1177/1087054707308503  0.483
2008 Glatt SJ, Faraone SV, Tsuang MT. Mental health etiology: Biological and genetic determinants International Encyclopedia of Public Health. 343-350. DOI: 10.1016/B978-012373960-5.00040-X  0.578
2007 Trksak GH, Glatt SJ, Mortazavi F, Jackson D. A meta-analysis of animal studies on disruption of spatial navigation by prenatal cocaine exposure. Neurotoxicology and Teratology. 29: 570-7. PMID 17683902 DOI: 10.1016/J.Ntt.2007.06.003  0.761
2007 Kia-Keating BM, Glatt SJ, Tsuang MT. Meta-analyses suggest association between COMT, but not HTR1B, alleles, and suicidal behavior. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 1048-53. PMID 17525973 DOI: 10.1002/Ajmg.B.30551  0.561
2007 Kanazawa T, Glatt SJ, Kia-Keating B, Yoneda H, Tsuang MT. Meta-analysis reveals no association of the Val66Met polymorphism of brain-derived neurotrophic factor with either schizophrenia or bipolar disorder. Psychiatric Genetics. 17: 165-70. PMID 17417060 DOI: 10.1097/Ypg.0B013E32801Da2E2  0.632
2007 Glatt SJ, Bousman C, Wang RS, Murthy KK, Rana BK, Lasky-Su JA, Zhu SC, Zhang R, Li J, Zhang B, Li J, Lyons MJ, Faraone SV, Tsuang MT. Evaluation of OPRM1 variants in heroin dependence by family-based association testing and meta-analysis. Drug and Alcohol Dependence. 90: 159-65. PMID 17416470 DOI: 10.1016/J.Drugalcdep.2007.02.022  0.645
2007 Domschke K, Deckert J, O'Donovan MC, Glatt SJ. Meta-analysis of COMT val158met in panic disorder: Ethnic heterogeneity and gender specificity American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 144: 667-673. PMID 17357147 DOI: 10.1002/Ajmg.B.30494  0.407
2007 Glatt SJ, Chayavichitsilp P, Depp C, Schork NJ, Jeste DV. Successful aging: from phenotype to genotype. Biological Psychiatry. 62: 282-93. PMID 17210144 DOI: 10.1016/J.Biopsych.2006.09.015  0.307
2007 Bulayeva KB, Glatt SJ, Bulayev OA, Pavlova TA, Tsuang MT. Genome-wide linkage scan of schizophrenia: a cross-isolate study. Genomics. 89: 167-77. PMID 17140763 DOI: 10.1016/J.Ygeno.2006.10.001  0.583
2007 Qian Q, Wang Y, Li J, Yang L, Wang B, Zhou R, Glatt SJ, Faraone SV. Evaluation of potential gene-gene interactions for attention deficit hyperactivity disorder in the Han Chinese population American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 144: 200-206. PMID 17044099 DOI: 10.1002/Ajmg.B.30422  0.569
2007 Kanazawa T, Glatt SJ, Tsutsumi A, Kikuyama H, Koh J, Yoneda H, Tsuang MT. Schizophrenia is not associated with the functional candidate gene ERBB3: results from a case-control study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 113-6. PMID 16958035 DOI: 10.1002/Ajmg.B.30367  0.632
2006 Glatt SJ, Stone WS, Faraone SV, Seidman LJ, Tsuang MT. Psychopathology, personality traits and social development of young first-degree relatives of patients with schizophrenia. The British Journal of Psychiatry : the Journal of Mental Science. 189: 337-45. PMID 17012657 DOI: 10.1192/Bjp.Bp.105.016998  0.672
2006 Abdolmaleky HM, Cheng KH, Faraone SV, Wilcox M, Glatt SJ, Gao F, Smith CL, Shafa R, Aeali B, Carnevale J, Pan H, Papageorgis P, Ponte JF, Sivaraman V, Tsuang MT, et al. Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder. Human Molecular Genetics. 15: 3132-45. PMID 16984965 DOI: 10.1093/Hmg/Ddl253  0.715
2006 Ozdemir V, Williams-Jones B, Glatt SJ, Tsuang MT, Lohr JB, Reist C. Shifting emphasis from pharmacogenomics to theragnostics. Nature Biotechnology. 24: 942-6. PMID 16900136 DOI: 10.1038/Nbt0806-942  0.481
2006 Glatt SJ, Su JA, Zhu SC, Zhang R, Zhang B, Li J, Yuan X, Li J, Lyons MJ, Faraone SV, Tsuang MT. Genome-wide linkage analysis of heroin dependence in Han Chinese: results from wave one of a multi-stage study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 648-52. PMID 16856125 DOI: 10.1002/Ajmg.B.30361  0.664
2006 Luczak SE, Glatt SJ, Wall TJ. Meta-analyses of ALDH2 and ADH1B with alcohol dependence in asians Psychological Bulletin. 132: 607-621. PMID 16822169 DOI: 10.1037/0033-2909.132.4.607  0.345
2006 Seidman LJ, Giuliano AJ, Smith CW, Stone WS, Glatt SJ, Meyer E, Faraone SV, Tsuang MT, Cornblatt B. Neuropsychological functioning in adolescents and young adults at genetic risk for schizophrenia and affective psychoses: results from the Harvard and Hillside Adolescent High Risk Studies. Schizophrenia Bulletin. 32: 507-24. PMID 16707777 DOI: 10.1093/Schbul/Sbj078  0.668
2006 Beseler C, Jacobson KC, Kremen WS, Lyons MJ, Glatt SJ, Faraone SV, Gillespie NA, Tsuang MT. Is there heterogeneity among syndromes of substance use disorder for illicit drugs? Addictive Behaviors. 31: 929-47. PMID 16697532 DOI: 10.1016/J.Addbeh.2006.03.037  0.675
2006 Spencer TJ, Faraone SV, Michelson D, Adler LA, Reimherr FW, Glatt SJ, Biederman J. Atomoxetine and adult attention-deficit/hyperactivity disorder: The effects of comorbidity Journal of Clinical Psychiatry. 67: 415-420. PMID 16649828 DOI: 10.4088/Jcp.V67N0312  0.524
2006 Faraone SV, Lasky-Su J, Glatt SJ, Van Eerdewegh P, Tsuang MT. Early onset bipolar disorder: possible linkage to chromosome 9q34. Bipolar Disorders. 8: 144-51. PMID 16542184 DOI: 10.1111/J.1399-5618.2006.00289.X  0.654
2006 Glatt SJ, Jönsson EG. The Cys allele of the DRD2 Ser311Cys polymorphism has a dominant effect on risk for schizophrenia: Evidence from fixed- and random-effects meta-analyses American Journal of Medical Genetics - Neuropsychiatric Genetics. 141: 149-154. PMID 16402354 DOI: 10.1002/Ajmg.B.30273  0.404
2006 Tsuang M, Glatt S, Kremen W, Corbeil J, Sasik R, Khanlou N, Han M, Liew C, Everall I. S.16.05 Blood and brain gene expressions in schizophrenia European Neuropsychopharmacology. 16: S188. DOI: 10.1016/S0924-977X(06)70082-7  0.594
2006 Tsuang MT, Glatt SJ, Faraone SV. The complex genetics of psychiatric disorders Principles of Molecular Medicine. 1184-1190. DOI: 10.1007/978-1-59259-963-9_124  0.629
2005 Glatt SJ, Everall IP, Kremen WS, Corbeil J, Sásik R, Khanlou N, Han M, Liew CC, Tsuang MT. Comparative gene expression analysis of blood and brain provides concurrent validation of SELENBP1 up-regulation in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 102: 15533-8. PMID 16223876 DOI: 10.1073/Pnas.0507666102  0.616
2005 Faraone SV, Biederman J, Spencer T, Michelson D, Adler L, Reimherr F, Glatt SJ. Efficacy of atomoxetine in adult attention-deficit/hyperactivity disorder: a drug-placebo response curve analysis. Behavioral and Brain Functions : Bbf. 1: 16. PMID 16202140 DOI: 10.1186/1744-9081-1-16  0.617
2005 Abdolmaleky HM, Cheng KH, Russo A, Smith CL, Faraone SV, Wilcox M, Shafa R, Glatt SJ, Nguyen G, Ponte JF, Thiagalingam S, Tsuang MT. Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: a preliminary report. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 134: 60-6. PMID 15717292 DOI: 10.1002/Ajmg.B.30140  0.664
2005 Glatt SJ, Wang RS, Yeh YC, Tsuang MT, Faraone SV. Five NOTCH4 polymorphisms show weak evidence for association with schizophrenia: evidence from meta-analyses. Schizophrenia Research. 73: 281-90. PMID 15653273 DOI: 10.1016/J.Schres.2004.07.015  0.692
2005 Tsuang MT, Nossova N, Yager T, Tsuang MM, Guo SC, Shyu KG, Glatt SJ, Liew CC. Assessing the validity of blood-based gene expression profiles for the classification of schizophrenia and bipolar disorder: a preliminary report. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 133: 1-5. PMID 15645418 DOI: 10.1002/Ajmg.B.30161  0.62
2005 Lasky-Su JA, Faraone SV, Glatt SJ, Tsuang MT. Meta-analysis of the association between two polymorphisms in the serotonin transporter gene and affective disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 133: 110-5. PMID 15578606 DOI: 10.1002/Ajmg.B.30104  0.694
2005 Gamma F, Faraone SV, Glatt SJ, Yeh YC, Tsuang MT. Meta-analysis shows schizophrenia is not associated with the 40-base-pair repeat polymorphism of the dopamine transporter gene. Schizophrenia Research. 73: 55-8. PMID 15567077 DOI: 10.1016/J.Schres.2004.09.020  0.702
2005 Bulayeva KB, Leal SM, Pavlova TA, Kurbanov RM, Glatt SJ, Bulayev OA, Tsuang MT. Mapping genes of complex psychiatric diseases in Daghestan genetic isolates. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 132: 76-84. PMID 15389762 DOI: 10.1002/Ajmg.B.30073  0.596
2004 Glatt SJ, Faraone SV, Tsuang MT. DRD2 -141C insertion/deletion polymorphism is not associated with schizophrenia: results of a meta-analysis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 128: 21-3. PMID 15211624 DOI: 10.1002/Ajmg.B.30007  0.704
2004 Glatt SJ, Trksak GH, Cohen OS, Simeone BP, Jackson D. Prenatal cocaine exposure decreases nigrostriatal dopamine release in vitro: effects of age and sex. Synapse (New York, N.Y.). 53: 74-89. PMID 15170820 DOI: 10.1002/Syn.20036  0.76
2004 Abdolmaleky HM, Smith CL, Faraone SV, Shafa R, Stone W, Glatt SJ, Tsuang MT. Methylomics in psychiatry: Modulation of gene-environment interactions may be through DNA methylation. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 127: 51-9. PMID 15108180 DOI: 10.1002/Ajmg.B.20142  0.656
2004 Faraone SV, Glatt SJ, Su J, Tsuang MT. Three potential susceptibility loci shown by a genome-wide scan for regions influencing the age at onset of mania. The American Journal of Psychiatry. 161: 625-30. PMID 15056507 DOI: 10.1176/Appi.Ajp.161.4.625  0.684
2004 Abdolmaleky HM, Faraone SV, Glatt SJ, Tsuang MT. Meta-analysis of association between the T102C polymorphism of the 5HT2a receptor gene and schizophrenia. Schizophrenia Research. 67: 53-62. PMID 14741324 DOI: 10.1016/S0920-9964(03)00183-X  0.691
2004 GLATT SJ, FARAONE SV, TSUANG MT. Dr. Glatt and Colleagues Reply American Journal of Psychiatry. 161: 1135-1136. DOI: 10.1176/Appi.Ajp.161.6.1135  0.591
2003 Glatt SJ, Faraone SV, Tsuang MT. Meta-analysis identifies an association between the dopamine D2 receptor gene and schizophrenia. Molecular Psychiatry. 8: 911-5. PMID 14593428 DOI: 10.1038/Sj.Mp.4001321  0.691
2003 Glatt SJ, Faraone SV, Tsuang MT. Schizophrenia is not associated with DRD4 48-base-pair-repeat length or individual alleles: results of a meta-analysis. Biological Psychiatry. 54: 629-35. PMID 13129658 DOI: 10.1016/S0006-3223(03)00180-X  0.704
2003 Glatt SJ, Faraone SV, Tsuang MT. CAG-repeat length in exon 1 of KCNN3 does not influence risk for schizophrenia or bipolar disorder: a meta-analysis of association studies. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 121: 14-20. PMID 12898569 DOI: 10.1002/Ajmg.B.20048  0.717
2003 Faraone SV, Glatt SJ, Tsuang MT. The genetics of pediatric-onset bipolar disorder. Biological Psychiatry. 53: 970-7. PMID 12788242 DOI: 10.1016/S0006-3223(02)01893-0  0.683
2003 Qian Q, Wang Y, Zhou R, Li J, Wang B, Glatt S, Faraone SV. Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism American Journal of Medical Genetics - Neuropsychiatric Genetics. 118: 103-109. PMID 12627475 DOI: 10.1002/Ajmg.B.10064  0.535
2003 Glatt SJ, Faraone SV, Tsuang MT. Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies. The American Journal of Psychiatry. 160: 469-76. PMID 12611827 DOI: 10.1176/Appi.Ajp.160.3.469  0.701
2002 Faraone SV, Brown CH, Glatt SJ, Tsuang MT. Preventing schizophrenia and psychotic behaviour: definitions and methodological issues. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 47: 527-37. PMID 12211880 DOI: 10.1177/070674370204700604  0.68
2002 Connor DF, Glatt SJ, Lopez ID, Jackson D, Melloni RH. Psychopharmacology and aggression. I: A meta-analysis of stimulant effects on overt/covert aggression-related behaviors in ADHD. Journal of the American Academy of Child and Adolescent Psychiatry. 41: 253-61. PMID 11886019 DOI: 10.1097/00004583-200203000-00004  0.626
2000 Glatt SJ, Bolaños CA, Trksak GH, Jackson D. Effects of prenatal cocaine exposure on dopamine system development: a meta-analysis. Neurotoxicology and Teratology. 22: 617-29. PMID 11106856 DOI: 10.1016/S0892-0362(00)00088-X  0.768
2000 Glatt SJ, Bolaños CA, Trksak GH, Crowder-Dupont C, Jackson D. Prenatal cocaine exposure alters behavioral and neurochemical sensitization to amphetamine in adult rats. Neuropharmacology. 39: 599-610. PMID 10728881 DOI: 10.1016/S0028-3908(99)00181-1  0.758
2000 Bolaños CA, Trksak GH, Glatt SJ, Jackson D. Prenatal cocaine exposure increases serotonergic inhibition of electrically evoked acetylcholine release from rat striatal slices at adulthood. Synapse (New York, N.Y.). 36: 1-11. PMID 10700021 DOI: 10.1002/(Sici)1098-2396(200004)36:1<1::Aid-Syn1>3.0.Co;2-F  0.753
1998 Bolanos CA, Glatt SJ, Jackson D. Subsensitivity to dopaminergic drugs in periadolescent rats: a behavioral and neurochemical analysis. Brain Research. Developmental Brain Research. 111: 25-33. PMID 9804875 DOI: 10.1016/S0165-3806(98)00116-3  0.596
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