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For: [DOI: 10.1101/2020.09.12.20192922] [Cited by in Crossref: 132] [Cited by in F6Publishing: 137] [Reference Citation Analysis]
Number Citing Articles
1 Yuan K, Longchamps RJ, Pardiñas AF, Yu M, Chen TT, Lin SC, Chen Y, Lam M, Liu R, Xia Y, Guo Z, Shi W, Shen C, Daly MJ, Neale B, Feng YA, Lin YF, Chen CY, O'Donovan M, Ge T, Huang H; Schizophrenia Workgroup of Psychiatric Genomics Consortium. Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases. medRxiv 2023:2023. [PMID: 36711496 DOI: 10.1101/2023.01.07.23284293] [Reference Citation Analysis]
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6 Chen H, Liu J, Sonthalia S, Stein-o’brien G, Xiao L, Caffo B, Colantuoni C. Structured Joint Decomposition (SJD) identifies conserved molecular dynamics across collections of biologically related multi-omics data matrices.. [DOI: 10.1101/2022.11.07.515489] [Reference Citation Analysis]
7 Nøhr AK, Forsingdal A, Moltke I, Howes OD, Vitezic M, Albrechtsen A, Dalby M. Polygenic heterogeneity in antidepressant treatment and placebo response. Transl Psychiatry 2022;12:456. [PMID: 36309483 DOI: 10.1038/s41398-022-02221-4] [Reference Citation Analysis]
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11 Degiosio RA, Grubisha MJ, Macdonald ML, Mckinney BC, Camacho CJ, Sweet RA. More than a marker: potential pathogenic functions of MAP2. Front Mol Neurosci 2022;15:974890. [DOI: 10.3389/fnmol.2022.974890] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Bell N, Uffelmann E, van Walree E, de Leeuw C, Posthuma D. Using genome-wide association results to identify drug repurposing candidates.. [DOI: 10.1101/2022.09.06.22279660] [Reference Citation Analysis]
13 Bhattacharya A, Jops C, Kim M, Wen C, Vo DD, Hervoso JL, Pasaniuc B, Gandal MJ. Isoform-level transcriptome-wide association uncovers extensive novel genetic risk mechanisms for neuropsychiatric disorders in the human brain.. [DOI: 10.1101/2022.08.23.22279134] [Reference Citation Analysis]
14 Creeth HDJ, Rees E, Legge SE, Dennison CA, Holmans P, Walters JTR, O'Donovan MC, Owen MJ. Ultrarare Coding Variants and Cognitive Function in Schizophrenia. JAMA Psychiatry 2022. [PMID: 35976659 DOI: 10.1001/jamapsychiatry.2022.2289] [Reference Citation Analysis]
15 Kang J, Castro VM, Ripperger M, Venkatesh S, Burstein D, Linnér RK, Rocha DB, Hu Y, Wilimitis D, Morley T, Han L, Kim RY, Feng YA, Ge T, Heckers S, Voloudakis G, Chabris C, Roussos P, Mccoy TH, Walsh CG, Perlis RH, Ruderfer DM. Genome-wide association study of treatment resistant depression highlights shared biology with metabolic traits.. [DOI: 10.1101/2022.08.10.22278630] [Reference Citation Analysis]
16 Worf K, Matosin N, Gerstner N, Fröhlich AS, Koller AC, Degenhardt F, Thiele H, Rietschel M, Udawela M, Scarr E, Dean B, Theis FJ, Knauer-arloth J, Mueller NS. Variant-risk-exon interplay impacts on cortical cell-cell interactions in severe psychiatric disorders.. [DOI: 10.1101/2022.08.09.22278128] [Reference Citation Analysis]
17 Zhou J, Li J, Zhao Q, Ou P, Zhao W. Working memory deficits in children with schizophrenia and its mechanism, susceptibility genes, and improvement: A literature review. Front Psychiatry 2022;13:899344. [DOI: 10.3389/fpsyt.2022.899344] [Reference Citation Analysis]
18 Bauminger H, Gaisler-salomon I. Beyond NMDA Receptors: Homeostasis at the Glutamate Tripartite Synapse and Its Contributions to Cognitive Dysfunction in Schizophrenia. IJMS 2022;23:8617. [DOI: 10.3390/ijms23158617] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Wolter JM, Le BD, Matoba N, Lafferty MJ, Aygün N, Liang D, Courtney K, Song J, Piven J, Zylka MJ, Stein JL. Cellular genome-wide association study identifies common genetic variation influencing lithium induced neural progenitor proliferation. Biological Psychiatry 2022. [DOI: 10.1016/j.biopsych.2022.08.014] [Reference Citation Analysis]
20 Loughnan RJ, Palmer CE, Makowski C, Thompson WK, Barch DM, Jernigan TL, Dale AM, Fan CC. Unique prediction of developmental psychopathology from genetic and familial risk. J Child Psychol Psychiatry 2022. [PMID: 35764363 DOI: 10.1111/jcpp.13649] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 Chen C, Tian R, Ge T, Lam M, Sanchez-andrade G, Singh T, Urpa L, Liu JZ, Sanderson M, Rowley C, Ironfield H, Fang T, Daly M, Palotie A, Tsai EA, Huang H, Hurles ME, Gerety SS, Lencz T, Runz H, Biogen Biobank Team, the SUPER-Finland study, the Northern Finland Intellectual Disability study. The impact of rare protein coding genetic variation on adult cognitive function.. [DOI: 10.1101/2022.06.24.22276728] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Strom NI, Smit DJ, Silzer T, Iyegbe C, Burton CL, Pool R, Lemire M, Crowley JJ, Hottenga J, Ivanov VZ, Larsson H, Lichtenstein P, Magnusson P, Rück C, Schachar R, Wu HM, Meier SM, Crosbie J, Arnold PD, Mattheisen M, Boomsma DI, Mataix-cols D, Cath D. Meta-Analysis of Genome-Wide Association Studies of Hoarding Symptoms in 27 537 Individuals.. [DOI: 10.1101/2022.06.19.22276077] [Reference Citation Analysis]
23 Das D, Sonthalia S, Stein-o’brien G, Wahbeh M, Feuer K, Colantuoni C, Machairaki V, Avramopoulos D. Insights for disease modeling from single cell transcriptomics of iPSC-derived neurons and astrocytes across differentiation time and co-culture.. [DOI: 10.1101/2022.06.15.495952] [Reference Citation Analysis]
24 Segura AG, Mezquida G, Martínez-Pinteño A, Gassó P, Rodriguez N, Moreno-Izco L, Amoretti S, Bioque M, Lobo A, González-Pinto A, García-Alcon A, Roldán-Bejarano A, Vieta E, de la Serna E, Toll A, Cuesta MJ, Mas S, Bernardo M; PEPs Group. Link between cognitive polygenic risk scores and clinical progression after a first-psychotic episode. Psychol Med 2022;:1-14. [PMID: 35678455 DOI: 10.1017/S0033291722001544] [Reference Citation Analysis]
25 Fabbri C. Genetics in psychiatry: Methods, clinical applications and future perspectives. PCN Reports 2022;1. [DOI: 10.1002/pcn5.6] [Reference Citation Analysis]
26 Fabbri C, Leggio GM, Drago F, Serretti A. Imputed expression of schizophrenia-associated genes and cognitive measures in patients with schizophrenia. Mol Genet Genomic Med 2022;10:e1942. [PMID: 35488718 DOI: 10.1002/mgg3.1942] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Dorfschmidt L, Bethlehem RA, Seidlitz J, Váša F, White SR, Romero-García R, Kitzbichler MG, Aruldass AR, Morgan SE, Goodyer IM, Fonagy P, Jones PB, Dolan RJ, Harrison NA, Vértes PE, Bullmore ET; NSPN Consortium. Sexually divergent development of depression-related brain networks during healthy human adolescence. Sci Adv 2022;8:eabm7825. [PMID: 35622918 DOI: 10.1126/sciadv.abm7825] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
28 Li J, Ho DJ, Henault M, Yang C, Neri M, Ge R, Renner S, Mansur L, Lindeman A, Kelly B, Tumkaya T, Ke X, Soler-Llavina G, Shanker G, Russ C, Hild M, Gubser Keller C, Jenkins JL, Worringer KA, Sigoillot FD, Ihry RJ. DRUG-seq Provides Unbiased Biological Activity Readouts for Neuroscience Drug Discovery. ACS Chem Biol 2022. [PMID: 35508359 DOI: 10.1021/acschembio.1c00920] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Kamran M, Bibi F, ur. Rehman A, Morris DW. Major Depressive Disorder: Existing Hypotheses about Pathophysiological Mechanisms and New Genetic Findings. Genes 2022;13:646. [DOI: 10.3390/genes13040646] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
30 Townsley KG, Li A, Deans PM, Fullard JF, Yu A, Cartwright S, Zhang W, Wang M, Voloudakis G, Girdhar K, Stahl E, Akbarian S, Zhang B, Roussos P, Huckins LM, Brennand KJ. Convergent impact of schizophrenia risk genes.. [DOI: 10.1101/2022.03.29.486286] [Reference Citation Analysis]
31 Li M, Li T, Xiao X, Chen J, Hu Z, Fang Y. Phenotypes, mechanisms and therapeutics: insights from bipolar disorder GWAS findings. Mol Psychiatry. [DOI: 10.1038/s41380-022-01523-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
32 Harder A, Nguyen TD, Pasman JA, Mosing MA, Hägg S, Lu Y. Genetics of age-at-onset in major depression. Transl Psychiatry 2022;12:124. [PMID: 35347114 DOI: 10.1038/s41398-022-01888-z] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Liu W, Zhong W, Chen J, Huang B, Hu M, Li Y. Understanding Regulatory Mechanisms of Brain Function and Disease through 3D Genome Organization. Genes 2022;13:586. [DOI: 10.3390/genes13040586] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
34 Dumrongprechachan V, Salisbury RB, Butler L, Macdonald ML, Kozorovitskiy Y. Dynamic proteomic and phosphoproteomic atlas of corticostriatal axon neurodevelopment.. [DOI: 10.1101/2022.03.21.485234] [Reference Citation Analysis]
35 Kanai M, Elzur R, Zhou W, Daly MJ, Finucane HK, Global Biobank Meta-analysis Initiative. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution.. [DOI: 10.1101/2022.03.16.22272457] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
36 Kowalczyk M, Kucia K, Owczarek A, Suchanek-raif R, Paul-samojedny M, Choreza P, Kowalski J, Belluzzi E. HSPB1 Gene Variants and Schizophrenia: A Case-Control Study in a Polish Population. Disease Markers 2022;2022:1-9. [DOI: 10.1155/2022/4933011] [Reference Citation Analysis]
37 Mitjans M, Papiol S, Barrot C, Guardiola-ripoll M, Giménez-palomo A, Gavín P, Oraki Kohshour M, Acosta M, Pomarol-clotet E, Castellà-garcía J, Pérez-pérez RM, Gutiérrez B, Schulze TG, Fatjó-vilas M, Arias B, Benabarre A. Completed suicide is associated with a higher polygenic burden for psychiatric disorders. Eur Arch Psychiatry Clin Neurosci. [DOI: 10.1007/s00406-022-01398-5] [Reference Citation Analysis]
38 Talarico F, Costa GO, Ota VK, Santoro ML, Noto C, Gadelha A, Bressan R, Azevedo H, Belangero SI. Systems-Level Analysis of Genetic Variants Reveals Functional and Spatiotemporal Context in Treatment-resistant Schizophrenia. Mol Neurobiol. [DOI: 10.1007/s12035-022-02794-7] [Reference Citation Analysis]
39 Serretti A. Precision medicine in mood disorders. PCN Reports 2022;1. [DOI: 10.1002/pcn5.1] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
40 van der Meer D, Gurholt TP, Sønderby IE, Shadrin AA, Hindley G, Rahman Z, de Lange AG, Frei O, Leinhard OD, Linge J, Simon R, Westlye LT, Halvorsen S, Dale AM, Karlsen TH, Kaufmann T, Andreassen OA. The role of liver fat in cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition.. [DOI: 10.1101/2022.02.24.481887] [Reference Citation Analysis]
41 Grotzinger AD, Mallard TT, Liu Z, Seidlitz J, Ge T, Smoller JW. Multivariate Genomic Architecture of Cortical Thickness and Surface Area at Multiple Levels of Analysis.. [DOI: 10.1101/2022.02.19.22271223] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
42 Maury EA, Jones A, Seplyarskiy V, Rosenbluh C, Bae T, Wang Y, Abyzov A, Khoshkoo S, Chahine Y, Park PJ, Akbarian S, Lee EA, Sunyaev SR, Walsh CA, Chess A, Brain Somatic Mosaicism Network. Enrichment of somatic mutations in schizophrenia brain targets prenatally active transcription factor bindings sites.. [DOI: 10.1101/2022.02.23.481681] [Reference Citation Analysis]
43 Muntané G, Vázquez-bourgon J, Sada E, Martorell L, Papiol S, Bosch E, Navarro A, Crespo-facorro B, Vilella E. Leveraging genetics to improve Body Mass Index increase prediction in the first-episode of psychosis.. [DOI: 10.1101/2022.02.15.22270982] [Reference Citation Analysis]
44 Wilkinson ID, Mahmood T, Yasmin SF, Tomlinson A, Nazari J, Alhaj H, El Din SN, Neill J, Pandit C, Ashraf S, Cardno AG, Clapcote SJ, Inglehearn CF, Woodruff PW. In memory of Professor Iain Wilkinson: cognitive and neuroimaging endophenotypes in a consanguineous schizophrenia multiplex family. Psychol Med 2022;:1-9. [PMID: 35125130 DOI: 10.1017/S0033291721005250] [Reference Citation Analysis]
45 Fernandez-cabello S, Alnæs D, van der Meer D, Dahl A, Holm M, Kjelkenes R, Maximov II, Norbom LB, Pedersen ML, Voldsbekk I, Andreassen OA, Westlye LT. Associations between brain imaging and polygenic scores of mental health and educational attainment in children aged 9-11.. [DOI: 10.1101/2022.02.01.22270003] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
46 Wolter JM, Le BD, Matoba N, Lafferty MJ, Aygün N, Liang D, Courtney K, Piven J, Zylka MJ, Stein JL. Cellular genome wide association study identifies common genetic variation influencing lithium induced neural progenitor proliferation.. [DOI: 10.1101/2022.01.31.478307] [Reference Citation Analysis]
47 Sheardown E, Mech AM, Petrazzini MEM, Leggieri A, Gidziela A, Hosseinian S, Sealy IM, Torres-perez JV, Busch-nentwich EM, Malanchini M, Brennan CH. Translational relevance of forward genetic screens in animal models for the study of psychiatric disease. Neuroscience & Biobehavioral Reviews 2022. [DOI: 10.1016/j.neubiorev.2022.104559] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
48 Mangnier L, Joly-Beauparlant C, Droit A, Bilodeau S, Bureau A. Cis-regulatory hubs: a new 3D model of complex disease genetics with an application to schizophrenia. Life Sci Alliance 2022;5:e202101156. [PMID: 35086934 DOI: 10.26508/lsa.202101156] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
49 Johnson T, Saatci D, Handunnetthi L. Maternal immune activation induces methylation changes in schizophrenia genes.. [DOI: 10.1101/2022.01.11.22268935] [Reference Citation Analysis]
50 Kozlova A, Zhang S, Kotlar AV, Jamison B, Zhang H, Shi S, Forrest MP, Mcdaid J, Cutler DJ, Epstein MP, Zwick ME, Pang ZP, Sanders AR, Warren ST, Gejman PV, Mulle JG, Duan J. Loss-of-function of OTUD7A in the schizophrenia-associated 15q13.3 deletion impairs synapse development and function in human neurons.. [DOI: 10.1101/2022.01.06.473910] [Reference Citation Analysis]
51 Liu D, Meyer D, Fennessy B, Feng C, Cheng E, Johnson JS, Park YJ, Rieder M, Ascolillo S, de Pins A, Dobbyn A, Lebovitch D, Moya E, Nguyen T, Wilkins L, Hassan A, Burdick KE, Buxbaum JD, Domenici E, Frangou S, Hartmann AM, Malhotra D, Pato CN, Pato MT, Ressler K, Roussos P, Rujescu D, Arango C, Bertolino A, Blasi G, Bocchio-chiavetto L, Campion D, Carr V, Fullerton JM, Gennarelli M, González-peñas J, Levinson DF, Mowry B, Nimgaokar VL, Pergola G, Rampino A, Rivera-sanchez M, Schwab SG, Wildenauer DB, Daly M, Neale B, Singh T, O’donovan MC, Owen MJ, Walters JT, Ayub M, Malhotra AK, Lencz T, Sullivan PF, Sklar P, Stahl EA, Huckins LM, Charney AW, Psychiatric Genomics Consortium Phase 3 Targeted Sequencing of Schizophrenia Study Team, Schizophrenia Exome Meta-analysis Consortium. Rare schizophrenia risk variant burden is conserved in diverse human populations.. [DOI: 10.1101/2022.01.03.22268662] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
52 Medeiros GC, Goes FS. Genome-wide association study biomarkers in bipolar disorder. Biomarkers in Bipolar Disorders 2022. [DOI: 10.1016/b978-0-12-821398-8.00016-3] [Reference Citation Analysis]
53 Ryan NM, Ormond C, Brady P, Heron EA, Corvin A. Schizophrenia genomics. Psychiatric Genomics 2022. [DOI: 10.1016/b978-0-12-819602-1.00002-4] [Reference Citation Analysis]
54 Langley K, Martin J, Thapar A. Genetics of Attention-Deficit Hyperactivity Disorder. New Discoveries in the Behavioral Neuroscience of Attention-Deficit Hyperactivity Disorder 2022. [DOI: 10.1007/7854_2022_338] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
55 Golimbet V, Kostyuk G. Genotype — phenotype relationships in view of recent advances in the understanding of genetic causes of schizophrenia. Z nevrol psikhiatr im S S Korsakova 2022;122:20. [DOI: 10.17116/jnevro202212201220] [Reference Citation Analysis]
56 Alfimova M, Korovaitseva G, Gabaeva M, Plakunova V, Lezheiko T, Golimbet V. Genetic polymorphism of cytokines IL-1β, IL-4 and TNF-α as a factor modifying the impact of childhood adversity on schizophrenia symptoms. Z nevrol psikhiatr im S S Korsakova 2022;122:110. [DOI: 10.17116/jnevro2022122091110] [Reference Citation Analysis]
57 Li W, Zhang C, Liu J, Guan F, Shao M, Zhang L, Liu Q, Yang Y, Su X, Zhang Y, Xiao X, Luo X, Li M, Lv L. Identification of a Risk Locus at 7p22.3 for Schizophrenia and Bipolar Disorder in East Asian Populations. Front Genet 2021;12. [DOI: 10.3389/fgene.2021.789512] [Reference Citation Analysis]
58 Hosang GM, Martin J, Karlsson R, Lundström S, Larsson H, Ronald A, Lichtenstein P, Taylor MJ. Association of Etiological Factors for Hypomanic Symptoms, Bipolar Disorder, and Other Severe Mental Illnesses. JAMA Psychiatry 2021. [PMID: 34910090 DOI: 10.1001/jamapsychiatry.2021.3654] [Reference Citation Analysis]
59 Verdolini N, Amoretti S, Pacchiarotti I, Vieta E. P.0585 Disentangling clinical, neurobiological, and genetic correlates of first episode mania from first episode psychosis. European Neuropsychopharmacology 2021;53:S428-S429. [DOI: 10.1016/j.euroneuro.2021.10.550] [Reference Citation Analysis]
60 Alver M, Lykoskoufis N, Ramisch A, Ongen H, Dermitzakis ET. Leveraging interindividual variability of regulatory activity refines genetic regulation of gene expression in schizophrenia.. [DOI: 10.1101/2021.10.18.21264945] [Reference Citation Analysis]
61 Terrillion CE, Kang B, Melia JM. Behavioral phenotyping of Zip8 393T-KI mice for in vivo study of schizophrenia pathogenesis.. [DOI: 10.1101/2021.10.18.464839] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
62 Sun BB, Kurki MI, Foley CN, Mechakra A, Chen C, Marshall E, Wilk JB, Chahine M, Chevalier P, Christé G, Finngen, Palotie A, Daly MJ, Runz H, Biogen Biobank Team. Genetic associations of protein-coding variants in human disease.. [DOI: 10.1101/2021.10.14.21265023] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
63 Hsu YH, Nacu E, Liu R, Pintacuda G, Kim A, Tsafou K, Petrossian N, Crotty W, Suh JM, Riseman J, Martin JM, Biagini JC, Ching JK, Malolepsza E, Li T, Singh T, Ge T, Egri SB, Tanenbaum B, Stanclift CR, Apffel AM, Carr SA, Schenone M, Jaffe J, Fornelos N, Huang H, Eggan KC, Lage K, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Stanley Global Asia Initiatives. Using brain cell-type-specific protein interactomes to interpret genetic data in schizophrenia.. [DOI: 10.1101/2021.10.07.21264568] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
64 Grotzinger AD, de la Fuente J, Nivard MG, Tucker-drob EM. Pervasive Downward Bias in Estimates of Liability Scale Heritability in GWAS Meta-Analysis: A Simple Solution.. [DOI: 10.1101/2021.09.22.21263909] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
65 Nehme R, Pietiläinen O, Artomov M, Tegtmeyer M, Bell C, Ganna A, Singh T, Trehan A, Valakh V, Sherwood J, Manning D, Peirent E, Malik R, Guss EJ, Hawes D, Beccard A, Bara AM, Hazelbaker DZ, Zuccaro E, Genovese G, Loboda AA, Neumann A, Lilliehook C, Kuismin O, Hamalainen E, Kurki M, Hultman CM, Kähler AK, Paulo JA, Madison J, Cohen B, Mcphie D, Adolfsson R, Perlis R, Dolmetsch R, Farhi S, Mccarroll S, Hyman S, Neale B, Barrett LE, Harper W, Palotie A, Daly M, Eggan K. The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.. [DOI: 10.1101/2021.09.22.461360] [Reference Citation Analysis]
66 Pietiläinen O, Nehme R, Trehan A, Eggan K. Astrocytic cell adhesion genes linked to schizophrenia promote synaptic programs in neurons.. [DOI: 10.1101/2021.09.11.459765] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
67 Kouakou MR, Cameron D, Hannon E, Dempster EL, Mill J, Hill MJ, Bray NJ. Sites of active gene regulation in the prenatal frontal cortex and their role in neuropsychiatric disorders.. [DOI: 10.1101/2021.09.01.458548] [Reference Citation Analysis]
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