Jason L. Stein, Ph.D. - Related publications

University of California, Los Angeles, Los Angeles, CA 
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50 most relevant papers in past 60 days:
Year Citation  Score
2020 Elsheikh SSM, Chimusa ER, Mulder NJ, Crimi A. Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease. Scientific Reports. 10: 1433. PMID 31996736 DOI: 10.1038/s41598-020-58291-1   
2020 Córdova-Palomera A, van der Meer D, Kaufmann T, Bettella F, Wang Y, Alnæs D, Doan NT, Agartz I, Bertolino A, Buitelaar JK, Coynel D, Djurovic S, Dørum ES, Espeseth T, Fazio L, et al. Genetic control of variability in subcortical and intracranial volumes. Molecular Psychiatry. PMID 32047264 DOI: 10.1038/s41380-020-0664-1   
2020 Guelfi S, D'Sa K, Botía JA, Vandrovcova J, Reynolds RH, Zhang D, Trabzuni D, Collado-Torres L, Thomason A, Quijada Leyton P, Gagliano Taliun SA, Nalls MA, , , Small KS, et al. Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information. Nature Communications. 11: 1041. PMID 32098967 DOI: 10.1038/s41467-020-14483-x   
2020 Biton A, Traut N, Poline JB, Aribisala BS, Bastin ME, Bülow R, Cox SR, Deary IJ, Fukunaga M, Grabe HJ, Hagenaars S, Hashimoto R, Kikuchi M, Muñoz Maniega S, Nauck M, ... , et al. Polygenic Architecture of Human Neuroanatomical Diversity. Cerebral Cortex (New York, N.Y. : 1991). PMID 32109272 DOI: 10.1093/cercor/bhz241   
2020 Barbu MC, Spiliopoulou A, Colombo M, McKeigue P, Clarke TK, Howard DM, Adams MJ, Shen X, Lawrie SM, McIntosh AM, Whalley HC. Expression quantitative trait loci-derived scores and white matter microstructure in UK Biobank: a novel approach to integrating genetics and neuroimaging. Translational Psychiatry. 10: 55. PMID 32066731 DOI: 10.1038/s41398-020-0724-y   
2020 Foo H, Mather KA, Jiang J, Thalamuthu A, Wen W, Sachdev PS. Genetic influence on ageing-related changes in resting-state brain functional networks in healthy adults: a systematic review. Neuroscience and Biobehavioral Reviews. PMID 32169413 DOI: 10.1016/j.neubiorev.2020.03.011   
2020 Schottlaender LV, Abeti R, Jaunmuktane Z, Macmillan C, Chelban V, O'Callaghan B, McKinley J, Maroofian R, Efthymiou S, Athanasiou-Fragkouli A, Forbes R, Soutar MPM, Livingston JH, Kalmar B, Swayne O, ... , et al. Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification. American Journal of Human Genetics. 106: 412-421. PMID 32142645 DOI: 10.1016/j.ajhg.2020.02.007   
2020 Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAB, Shatokhina N, Zsembik LCP, Thomopoulos SI, Zhu AH, Strike LT, ... , ... , ... , ... , ... , ... , ... , et al. The genetic architecture of the human cerebral cortex. Science (New York, N.Y.). 367. PMID 32193296 DOI: 10.1126/science.aay6690   
2020 Pishva E, Creese B, Smith AR, Viechtbauer W, Proitsi P, van den Hove DLA, Ballard C, Mill J, Lunnon K. Psychosis-associated DNA methylomic variation in Alzheimer's disease cortex. Neurobiology of Aging. PMID 32007278 DOI: 10.1016/j.neurobiolaging.2020.01.001   
2020 Zhang Y, Peng P, Ju Y, Li G, Calhoun VD, Wang YP. Canonical Correlation Analysis of Imaging Genetics Data Based on Statistical Independence and Structural Sparsity. Ieee Journal of Biomedical and Health Informatics. PMID 32071012 DOI: 10.1109/JBHI.2020.2972581   
2020 Guo Z, Fan C, Li T, Gesang L, Yin W, Wang N, Weng X, Gong Q, Zhang J, Wang J. Neural network correlates of high-altitude adaptive genetic variants in Tibetans: A pilot, exploratory study. Human Brain Mapping. PMID 32128935 DOI: 10.1002/hbm.24954   
2020 Paramonova N, Trapina I, Dokane K, Kalnina J, Sjakste T, Sjakste N. An Intergenic rs9275596 Polymorphism on Chr. 6p21 Is Associated with Multiple Sclerosis in Latvians. Medicina (Kaunas, Lithuania). 56. PMID 32244438 DOI: 10.3390/medicina56040154   
2020 Jia X, Shi N, Feng Y, Li Y, Tan J, Xu F, Wang W, Sun C, Deng H, Yang Y, Shi X. Identification of 67 Pleiotropic Genes Associated With Seven Autoimmune/Autoinflammatory Diseases Using Multivariate Statistical Analysis. Frontiers in Immunology. 11: 30. PMID 32117227 DOI: 10.3389/fimmu.2020.00030   
2020 Theunissen F, Flynn LL, Anderton RS, Mastaglia F, Pytte J, Jiang L, Hodgetts S, Burns DK, Saunders A, Fletcher S, Wilton SD, Akkari PA. Structural Variants May Be a Source of Missing Heritability in sALS. Frontiers in Neuroscience. 14: 47. PMID 32082115 DOI: 10.3389/fnins.2020.00047   
2020 Bi XA, Hu X, Wu H, Wang Y. Multimodal Data Analysis of Alzheimer's Disease Based on Clustering Evolutionary Random Forest. Ieee Journal of Biomedical and Health Informatics. PMID 32071013 DOI: 10.1109/JBHI.2020.2973324   
2020 Ray JP, de Boer CG, Fulco CP, Lareau CA, Kanai M, Ulirsch JC, Tewhey R, Ludwig LS, Reilly SK, Bergman DT, Engreitz JM, Issner R, Finucane HK, Lander ES, Regev A, et al. Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features. Nature Communications. 11: 1237. PMID 32144282 DOI: 10.1038/s41467-020-15022-4   
2020 Sasazaki S, Kawaguchi F, Nakajima A, Yamamoto R, Akiyama T, Kohama N, Yoshida E, Kobayashi E, Honda T, Oyama K, Mannen H. Detection of candidate polymorphisms around the QTL for fat area ratio to rib eye area on BTA7 using whole-genome resequencing in Japanese Black cattle. Animal Science Journal = Nihon Chikusan Gakkaiho. 91: e13335. PMID 32219932 DOI: 10.1111/asj.13335   
2020 Fernando MB, Ahfeldt T, Brennand KJ. Modeling the complex genetic architectures of brain disease. Nature Genetics. PMID 32203467 DOI: 10.1038/s41588-020-0596-3   
2020 Jiang N, Lee S, Park T. Hierarchical structural component model for pathway analysis of common variants. Bmc Medical Genomics. 13: 26. PMID 32093692 DOI: 10.1186/s12920-019-0650-0   
2020 Moore JH, Olson RS, Schmitt P, Chen Y, Manduchi E. How Computational Experiments Can Improve Our Understanding of the Genetic Architecture of Common Human Diseases. Artificial Life. 1-15. PMID 32027528 DOI: 10.1162/artl_a_00308   
2020 Steardo L, Manchia M, Carpiniello B, Pisanu C, Steardo L, Squassina A. Clinical, genetic, and brain imaging predictors of risk for bipolar disorder in high-risk individuals. Expert Review of Molecular Diagnostics. 1-7. PMID 32054361 DOI: 10.1080/14737159.2020.1727743   
2020 MacQueen AH, White JW, Lee R, Osorno JM, Schmutz J, Miklas PN, Myers J, McClean PE, Juenger TE. Genetic Associations in Four Decades of Multi-environment Trials Reveal Agronomic Trait Evolution in Common Bean. Genetics. PMID 32205398 DOI: 10.1534/genetics.120.303038   
2020 Arloth J, Eraslan G, Andlauer TFM, Martins J, Iurato S, Kühnel B, Waldenberger M, Frank J, Gold R, Hemmer B, Luessi F, Nischwitz S, Paul F, Wiendl H, Gieger C, et al. DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. Plos Computational Biology. 16: e1007616. PMID 32012148 DOI: 10.1371/journal.pcbi.1007616   
2020 Liang B, Ding H, Huang L, Luo H, Zhu X. GWAS in cancer: progress and challenges. Molecular Genetics and Genomics : Mgg. PMID 32048005 DOI: 10.1007/s00438-020-01647-z   
2020 Wang H, Vanyukov MM, Xing EP, Wu W. Discovering weaker genetic associations guided by known associations. Bmc Medical Genomics. 13: 19. PMID 32093702 DOI: 10.1186/s12920-020-0667-4   
2020 van der Burg NC, Al Hadithy AFY, van Harten PN, van Os J, Bakker PR. The genetics of drug-related movement disorders, an umbrella review of meta-analyses. Molecular Psychiatry. PMID 32020047 DOI: 10.1038/s41380-020-0660-5   
2020 Yang S, Wen J, Eckert ST, Wang Y, Liu DJ, Wu R, Li R, Zhan X. Prioritizing genetic variants in GWAS with lasso using permutation-assisted tuning. Bioinformatics (Oxford, England). PMID 32246825 DOI: 10.1093/bioinformatics/btaa229   
2020 Cornetti L, Tschirren B. Combining GWAS and F -based approaches to identify targets of Borrelia-mediated selection in natural rodent hosts. Molecular Ecology. PMID 32163646 DOI: 10.1111/mec.15410   
2020 Forstner AJ, Fischer SB, Schenk LM, Strohmaier J, Maaser-Hecker A, Reinbold CS, Sivalingam S, Hecker J, Streit F, Degenhardt F, Witt SH, Schumacher J, Thiele H, Nürnberg P, Guzman-Parra J, et al. Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families. Translational Psychiatry. 10: 57. PMID 32066727 DOI: 10.1038/s41398-020-0732-y   
2020 Lacaze P, Ronaldson KJ, Zhang EJ, Alfirevic A, Shah H, Newman L, Strahl M, Smith M, Bousman C, Francis B, Morris AP, Wilson T, Rossello F, Powell D, Vasic V, et al. Genetic associations with clozapine-induced myocarditis in patients with schizophrenia. Translational Psychiatry. 10: 37. PMID 32066683 DOI: 10.1038/s41398-020-0722-0   
2020 Cheng S, Wu C, Qi X, Liu L, Ma M, Zhang L, Cheng B, Liang C, Li P, Kafle OP, Wen Y, Zhang F. A Large-Scale Genetic Correlation Scan Between Intelligence and Brain Imaging Phenotypes. Cerebral Cortex (New York, N.Y. : 1991). PMID 32108233 DOI: 10.1093/cercor/bhaa043   
2020 Sharafeldin N, Richman J, Bosworth A, Chen Y, Singh P, Patel SK, Wang X, Francisco L, Forman SJ, Wong FL, Bhatia S. Clinical and Genetic Risk Prediction of Cognitive Impairment After Blood or Marrow Transplantation for Hematologic Malignancy. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. JCO1901085. PMID 32083992 DOI: 10.1200/JCO.19.01085   
2020 Sanchez-Mut JV, Glauser L, Monk D, Gräff J. Comprehensive analysis of PM20D1 QTL in Alzheimer's disease. Clinical Epigenetics. 12: 20. PMID 32014019 DOI: 10.1186/s13148-020-0814-y   
2020 Kepler LD, McDiarmid TA, Rankin CH. Habituation in high-throughput genetic model organisms as a tool to investigate the mechanisms of neurodevelopmental disorders. Neurobiology of Learning and Memory. 171: 107208. PMID 32147587 DOI: 10.1016/j.nlm.2020.107208   
2020 Chang YC, Wu JT, Hong MY, Tung YA, Hsieh PH, Yee SW, Giacomini KM, Oyang YJ, Chen CY, . GenEpi: gene-based epistasis discovery using machine learning. Bmc Bioinformatics. 21: 68. PMID 32093643 DOI: 10.1186/s12859-020-3368-2   
2020 Fabbri C, Montgomery S, Lewis CM, Serretti A. Genetics and major depressive disorder: clinical implications for disease risk, prognosis and treatment. International Clinical Psychopharmacology. PMID 32084067 DOI: 10.1097/YIC.0000000000000305   
2020 Guo Y, Shen XN, Hou XH, Ou YN, Huang YY, Dong Q, Tan L, Yu JT, . Genome-wide association study of white matter hyperintensity volume in elderly persons without dementia. Neuroimage. Clinical. 26: 102209. PMID 32062564 DOI: 10.1016/j.nicl.2020.102209   
2020 Curtis D, Bakaya K, Sharma L, Bandyopadhyay S. Weighted burden analysis of exome-sequenced late-onset Alzheimer's cases and controls provides further evidence for a role for PSEN1 and suggests involvement of the PI3K/Akt/GSK-3β and WNT signalling pathways. Annals of Human Genetics. PMID 32020597 DOI: 10.1111/ahg.12375   
2020 Maniwa K, Yano S, Sheikh AM, Onoda K, Mitaki S, Isomura M, Mishima S, Yamaguchi S, Nabika T, Nagai A. Association between cystatin C gene polymorphism and the prevalence of white matter lesion in elderly healthy subjects. Scientific Reports. 10: 4688. PMID 32170118 DOI: 10.1038/s41598-020-61383-7   
2020 Hussain S, Umm-E-Kalsoom, Irfanullah, Liaqat K, Nawaz S, Ahmad W. A Novel Missense Variant in the Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous Family. Genetic Testing and Molecular Biomarkers. PMID 32216639 DOI: 10.1089/gtmb.2019.0203   
2020 Ramdhani S, Navarro E, Udine E, Efthymiou AG, Schilder BM, Parks M, Goate A, Raj T. Tensor decomposition of stimulated monocyte and macrophage gene expression profiles identifies neurodegenerative disease-specific trans-eQTLs. Plos Genetics. 16: e1008549. PMID 32012164 DOI: 10.1371/journal.pgen.1008549   
2020 Li S, Li Y, Li X, Liu J, Huo Y, Wang J, Liu Z, Li M, Luo XJ. Regulatory mechanisms of major depressive disorder risk variants. Molecular Psychiatry. PMID 32214206 DOI: 10.1038/s41380-020-0715-7   
2020 Hou PS, hAilín DÓ, Vogel T, Hanashima C. Transcription and Beyond: Delineating FOXG1 Function in Cortical Development and Disorders. Frontiers in Cellular Neuroscience. 14: 35. PMID 32158381 DOI: 10.3389/fncel.2020.00035   
2020 Li C, Cai W, Liu S, Zhou C, Yin H, Sun D, Zhang S. gene identified in RNA-Seq showed strong association with milk protein concentration in Chinese Holstein cows. Peerj. 8: e8460. PMID 32140298 DOI: 10.7717/peerj.8460   
2020 Adam KM, Mohammed AM, Elamin AA. Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene. Medicine. 99: e18722. PMID 32011449 DOI: 10.1097/MD.0000000000018722   
2020 Ocarez N, Jiménez N, Núñez R, Perniola R, Marsico AD, Cardone MF, Bergamini C, Mejía N. Unraveling the Deep Genetic Architecture for Seedlessness in Grapevine and the Development and Validation of a New Set of Markers for VviAGL11-Based Gene-Assisted Selection. Genes. 11. PMID 32019199 DOI: 10.3390/genes11020151   
2020 Wang X, Ren M, Liu D, Zhang D, Zhang C, Lang Z, Macho AP, Zhang M, Zhu JK. Large-scale eQTL identification in Arabidopsis reveals novel candidate regulators of immune responses and other processes. Journal of Integrative Plant Biology. PMID 32246811 DOI: 10.1111/jipb.12930   
2020 Lutz MW, Sprague D, Barrera J, Chiba-Falek O. Shared genetic etiology underlying Alzheimer's disease and major depressive disorder. Translational Psychiatry. 10: 88. PMID 32152295 DOI: 10.1038/s41398-020-0769-y   
2020 Mahboubi M, Mehrabi R, Naji AM, Talebi R. Whole-genome diversity, population structure and linkage disequilibrium analysis of globally diverse wheat genotypes using genotyping-by-sequencing DArTseq platform. 3 Biotech. 10: 48. PMID 32002339 DOI: 10.1007/s13205-019-2014-z   
2020 González-Giraldo Y, Forero DA. A functional SNP in the synaptic gene is associated with impulsivity in a Colombian sample. 3 Biotech. 10: 134. PMID 32154047 DOI: 10.1007/s13205-020-2110-0