Pat R. Levitt - Related publications

Keck School of Medicine, University of Southern California, Los Angeles, CA, United States 
Molecular and Developmental Basis of Neuropsychiatric Disorders
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50 most relevant papers in past 60 days:
Year Citation  Score
2020 Cukier HN, Griswold AJ, Hofmann NK, Gomez L, Whitehead PL, Abramson RK, Gilbert JR, Cuccaro ML, Dykxhoorn DM, Pericak-Vance MA. Three Brothers With Autism Carry a Stop-Gain Mutation in the HPA-Axis Gene NR3C2. Autism Research : Official Journal of the International Society For Autism Research. PMID 32064789 DOI: 10.1002/aur.2269   
2020 Fakhro KA. Genomics of Autism. Advances in Neurobiology. 24: 83-96. PMID 32006357 DOI: 10.1007/978-3-030-30402-7_3   
2020 Asif M, Martiniano HFMC, Marques AR, Santos JX, Vilela J, Rasga C, Oliveira G, Couto FM, Vicente AM. Identification of biological mechanisms underlying a multidimensional ASD phenotype using machine learning. Translational Psychiatry. 10: 43. PMID 32066720 DOI: 10.1038/s41398-020-0721-1   
2020 Toma C. Genetic Variation across Phenotypic Severity of Autism. Trends in Genetics : Tig. PMID 32037010 DOI: 10.1016/j.tig.2020.01.005   
2020 Phan BN, Bohlen JF, Davis BA, Ye Z, Chen HY, Mayfield B, Sripathy SR, Cerceo Page S, Campbell MN, Smith HL, Gallop D, Kim H, Thaxton CL, Simon JM, Burke EE, et al. A myelin-related transcriptomic profile is shared by Pitt-Hopkins syndrome models and human autism spectrum disorder. Nature Neuroscience. PMID 32015540 DOI: 10.1038/s41593-019-0578-x   
2020 Bacchelli E, Cameli C, Viggiano M, Igliozzi R, Mancini A, Tancredi R, Battaglia A, Maestrini E. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. Scientific Reports. 10: 3198. PMID 32081867 DOI: 10.1038/s41598-020-59922-3   
2020 Kong Y, Zhou W, Sun Z. Nuclear receptor corepressors in intellectual disability and autism. Molecular Psychiatry. PMID 32034290 DOI: 10.1038/s41380-020-0667-y   
2020 Riley JD, Delahunty C, Alsadah A, Mazzola S, Astbury C. Further evidence of GABRA4 and TOP3B as autism susceptibility genes. European Journal of Medical Genetics. 103876. PMID 32028044 DOI: 10.1016/j.ejmg.2020.103876   
2020 Takahashi N, Harada T, Nishimura T, Okumura A, Choi D, Iwabuchi T, Kuwabara H, Takagai S, Nomura Y, Takei N, Tsuchiya KJ. Association of Genetic Risks With Autism Spectrum Disorder and Early Neurodevelopmental Delays Among Children Without Intellectual Disability. Jama Network Open. 3: e1921644. PMID 32031653 DOI: 10.1001/jamanetworkopen.2019.21644   
2020 Chen YJ, Chen CY, Mai TL, Chuang CF, Chen YC, Gupta SK, Yen L, Wang YD, Chuang TJ. Genome-wide integrative analysis of circular RNA dysregulation and the corresponding circular RNA-microRNA-mRNA regulatory axes in autism. Genome Research. PMID 32127416 DOI: 10.1101/gr.255463.119   
2020 Mahmuda NA, Yokoyama S, Munesue T, Hayashi K, Yagi K, Tsuji C, Higashida H. One Single Nucleotide Polymorphism of the Channel Gene Identified as a Risk Factor in Bipolar Disorder Associates with Autism Spectrum Disorder in a Japanese Population. Diseases (Basel, Switzerland). 8. PMID 32046066 DOI: 10.3390/diseases8010004   
2020 de la Cruz BM, Ding Y, McInerney V, Krawczyk J, Lu Y, Yang G, Qian X, Li W, Howard L, Allen NM, O'Brien T, Gallagher L, Shen S. Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A). Stem Cell Research. 44: 101722. PMID 32097875 DOI: 10.1016/j.scr.2020.101722   
2020 Traglia M, Windham GC, Pearl M, Poon V, Eyles D, Jones KL, Lyall K, Kharrazi M, Croen LA, Weiss LA. Genetic Contributions to Maternal and Neonatal Vitamin D Levels. Genetics. PMID 32047095 DOI: 10.1534/genetics.119.302792   
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 Price KM, Wigg KG, Feng Y, Blokland K, Wilkinson M, He G, Kerr EN, Carter TC, Guger SL, Lovett MW, Strug LJ, Barr CL. Genome-Wide Association Study of Word Reading: Overlap with Risk Genes for Neurodevelopmental Disorders. Genes, Brain, and Behavior. e12648. PMID 32108986 DOI: 10.1111/gbb.12648   
2020 Zhang Y, Chen Y, Hu T. PANDA: Prioritization of autism-genes using network-based deep-learning approach. Genetic Epidemiology. PMID 32039500 DOI: 10.1002/gepi.22282   
2020 Garrett L, Chang YJ, Niedermeier KM, Heermann T, Enard W, Fuchs H, Gailus-Durner V, Angelis MH, Huttner WB, Wurst W, Hölter SM. A truncating Aspm allele leads to a complex cognitive phenotype and region-specific reductions in parvalbuminergic neurons. Translational Psychiatry. 10: 66. PMID 32066665 DOI: 10.1038/s41398-020-0686-0   
2020 Kaczorowski JA, Smith TF, Shrewsbury AM, Thomas LR, Knopik VS, Acosta MT. Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders. Behavior Genetics. PMID 32026187 DOI: 10.1007/s10519-020-09991-x   
2020 Barbosa S, Greville-Heygate S, Bonnet M, Godwin A, Fagotto-Kaufmann C, Kajava AV, Laouteouet D, Mawby R, Wai HA, Dingemans AJM, Hehir-Kwa J, Willems M, Capri Y, Mehta SG, Cox H, ... , et al. Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders. American Journal of Human Genetics. PMID 32109419 DOI: 10.1016/j.ajhg.2020.01.018   
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 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 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 Rinaldi B, Race V, Corveleyn A, Van Hoof E, Bauters M, Van Den Bogaert K, Denayer E, de Ravel T, Legius E, Baldewijns M, Aertsen M, Lewi L, De Catte L, Breckpot J, Devriendt K. Next-generation sequencing in prenatal setting: Some examples of unexpected variant association. European Journal of Medical Genetics. 103875. PMID 32058062 DOI: 10.1016/j.ejmg.2020.103875   
2020 Berg EL, Pride MC, Petkova SP, Lee RD, Copping NA, Shen Y, Adhikari A, Fenton TA, Pedersen LR, Noakes LS, Nieman BJ, Lerch JP, Harris S, Born HA, Peters MM, et al. Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome. Translational Psychiatry. 10: 39. PMID 32066685 DOI: 10.1038/s41398-020-0720-2   
2020 Salcedo-Arellano MJ, Hagerman RJ, Martínez-Cerdeño V. Fragile X syndrome: clinical presentation, pathology and treatment. Gaceta Medica De Mexico. 156: 60-66. PMID 32026885 DOI: 10.24875/GMM.19005275   
2020 Zhang R, Song J, Isgren A, Jakobsson J, Blennow K, Sellgren CM, Zetterberg H, Bergen SE, Landén M. Genome-wide study of immune biomarkers in cerebrospinal fluid and serum from patients with bipolar disorder and controls. Translational Psychiatry. 10: 58. PMID 32066700 DOI: 10.1038/s41398-020-0737-6   
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 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 Hollander JA, Cory-Slechta DA, Jacka FN, Szabo ST, Guilarte TR, Bilbo SD, Mattingly CJ, Moy SS, Haroon E, Hornig M, Levin ED, Pletnikov MV, Zehr JL, McAllister KA, Dzierlenga AL, et al. Beyond the looking glass: recent advances in understanding the impact of environmental exposures on neuropsychiatric disease. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 32109936 DOI: 10.1038/s41386-020-0648-5   
2020 Hollander JA, Cory-Slechta DA, Jacka FN, Szabo ST, Guilarte TR, Bilbo SD, Mattingly CJ, Moy SS, Haroon E, Hornig M, Levin ED, Pletnikov MV, Zehr JL, McAllister KA, Dzierlenga AL, et al. Beyond the looking glass: recent advances in understanding the impact of environmental exposures on neuropsychiatric disease. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 32109936 DOI: 10.1038/s41386-020-0648-5   
2020 Huang S, Yang L, Zhao L, Xu R, Wu Y. Novel In-Frame Deletion Mutation in in a Chinese Sporadic Case of Adams-Oliver Syndrome. Dna and Cell Biology. PMID 32129674 DOI: 10.1089/dna.2019.5200   
2020 Jain L, Fadason T, Schierding W, Vickers M, O'Sullivan JM, Perry JK. 3D interactions with the GH locus in cellular signalling and cancer-related pathways. Journal of Molecular Endocrinology. PMID 32106092 DOI: 10.1530/JME-20-0010   
2020 Xia X, Jin J, Chen ZJ, Zhou Z, Chen H, Zhang C, Zhang L, Sun L. Unraveling the genetic causes in large pedigrees with gout by whole‑exome sequencing. International Journal of Molecular Medicine. PMID 32124961 DOI: 10.3892/ijmm.2020.4501   
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 Lessel I, Chen MJ, Lüttgen S, Arndt F, Fuchs S, Meien S, Thiele H, Jones JR, Shaw BR, Crossman DK, Nürnberg P, Korf BR, Kubisch C, Lessel D. Two novel cases further expand the phenotype of TOR1AIP1-associated nuclear envelopathies. Human Genetics. PMID 32055997 DOI: 10.1007/s00439-019-02105-6   
2020 Peng Q, Wilhelmsen KC, Ehlers CL. Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations. Addiction Biology. e12877. PMID 32027075 DOI: 10.1111/adb.12877   
2020 Wu M, Zheng X, Wang X, Zhang G, Kuang J. 4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report. Bmc Medical Genomics. 13: 31. PMID 32126996 DOI: 10.1186/s12920-020-0697-y   
2020 Li M, Shen L, Chen L, Huai C, Huang H, Wu X, Yang C, Ma J, Zhou W, Du H, Fan L, He L, Wan C, Qin S. Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients. Translational Psychiatry. 10: 5. PMID 32066673 DOI: 10.1038/s41398-020-0708-y   
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 Wang X, Wei C, Zhang Z, Liu D, Guo Y, Sun G, Wang Y, Li H, Tian Y, Kang X, Han R, Li Z. Association of growth traits with a structural variation downstream of the KCNJ11 gene: a large population-based study in chickens. British Poultry Science. PMID 32008360 DOI: 10.1080/00071668.2020.1724878   
2020 Sul JH, Service SK, Huang AY, Ramensky V, Hwang SG, Teshiba TM, Park Y, Ori APS, Zhang Z, Mullins N, Olde Loohuis LM, Fears SC, Araya C, Araya X, Spesny M, et al. Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates. Translational Psychiatry. 10: 74. PMID 32094344 DOI: 10.1038/s41398-020-0758-1   
2020 Mardy AH, Chetty SP, Norton ME. Maternal Genetic Disorders and Fetal Development. Prenatal Diagnosis. PMID 32010984 DOI: 10.1002/pd.5659   
2020 Liu X, Moncuquet P, Zhu QH, Stiller W, Zhang Z, Wilson I. Genetic Identification and Transcriptome Analysis of Lintless and Fuzzless Traits in L. International Journal of Molecular Sciences. 21. PMID 32121400 DOI: 10.3390/ijms21051675   
2020 Tekendo-Ngongang C, Dahoun S, Nguefack S, Moix I, Gimelli S, Zambo H, Morris MA, Sloan-Béna F, Wonkam A. MECP2 duplication syndrome in a patient from Cameroon. American Journal of Medical Genetics. Part A. PMID 32052928 DOI: 10.1002/ajmg.a.61510   
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 Matsunari H, Honda M, Watanabe M, Fukushima S, Suzuki K, Miyagawa S, Nakano K, Umeyama K, Uchikura A, Okamoto K, Nagaya M, Toyo-Oka T, Sawa Y, Nagashima H. Pigs with δ-sarcoglycan deficiency exhibit traits of genetic cardiomyopathy. Laboratory Investigation; a Journal of Technical Methods and Pathology. PMID 32060408 DOI: 10.1038/s41374-020-0406-7   
2020 Zaib T, Zhang C, Saleem K, Xu L, Qin Q, Wang Y, Ji W, Khan H, Yu H, Zhu S, Gao W, Huang Y, Jia X, Wu J, Song H, et al. Functional Characterization of a Missense Variant of Identified in Lynch Syndrome Pedigree. Disease Markers. 2020: 8360841. PMID 32076465 DOI: 10.1155/2020/8360841   
2020 Rodríguez-García ME, Cotrina-Vinagre FJ, Arranz-Canales E, Aragón AM, Hernández-Sánchez L, Rodríguez-Fornés F, Carnicero-Rodríguez P, Morales-Conejo M, Martín-Hernández E, Martínez-Azorín F. A novel mutation in the gene associated with a new clinical finding: large brainstem. Journal of Genetics. 99. PMID 32089526   
2020 Peretz H, Korostishevsky M, Steinberg DM, Kabha M, Usher S, Krause I, Shalev H, Landau D, Levartovsky D. An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming belt. Jimd Reports. 51: 45-52. PMID 32071838 DOI: 10.1002/jmd2.12077   
2020 Yang N, Ying P, Tian J, Wang X, Mei S, Zou D, Peng X, Gong Y, Yang Y, Zhu Y, Ke J, Zhong R, Chang J, Miao X. Genetic variants in m6A modification genes are associated with esophageal squamous-cell carcinoma in the Chinese population. Carcinogenesis. PMID 32047883 DOI: 10.1093/carcin/bgaa012