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For: Motahari Z, Moody SA, Maynard TM, LaMantia AS. In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects? J Neurodev Disord 2019;11:7. [PMID: 31174463 DOI: 10.1186/s11689-019-9267-z] [Cited by in Crossref: 23] [Cited by in F6Publishing: 20] [Article Influence: 7.7] [Reference Citation Analysis]
Number Citing Articles
1 Maynard TM, Horvath A, Bernot JP, Karpinski BA, Tavares ALP, Shah A, Zheng Q, Spurr L, Olender J, Moody SA, Fraser CM, LaMantia AS, Lee NH. Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome. Hum Mol Genet 2020;29:1002-17. [PMID: 32047912 DOI: 10.1093/hmg/ddaa024] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
2 Manno GC, Segal GS, Yu A, Xu F, Ray JW, Cooney E, Britt AD, Jain SK, Goldblum RM, Robinson SS, Dong J; School of Medicine, University of Texas Medical Branch, Galveston, Texas, USA, Department of Pathology, University of Texas Medical Branch, Galveston, Texas, USA, Department of Pediatrics, University of Texas Medical Branch, Galveston, Texas, USA. . AIMSMOLES 2021;8:257-74. [DOI: 10.3934/molsci.2021020] [Reference Citation Analysis]
3 Li Y, Xia Y, Zhu H, Luu E, Huang G, Sun Y, Sun K, Markx S, Leong KW, Xu B, Fu BM. Investigation of Neurodevelopmental Deficits of 22 q11.2 Deletion Syndrome with a Patient-iPSC-Derived Blood-Brain Barrier Model. Cells 2021;10:2576. [PMID: 34685556 DOI: 10.3390/cells10102576] [Reference Citation Analysis]
4 Fiksinski AM, Schneider M, Zinkstok J, Baribeau D, Chawner SJRA, Vorstman JAS. Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome. Curr Psychiatry Rep 2021;23:13. [PMID: 33625600 DOI: 10.1007/s11920-021-01225-z] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
5 Yitsege G, Stokes BA, Sabatino JA, Sugrue KF, Banyai G, Paronett EM, Karpinski BA, Maynard TM, LaMantia AS, Zohn IE. Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome. Birth Defects Res 2020;112:1194-208. [PMID: 32431076 DOI: 10.1002/bdr2.1709] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
6 Cirillo E, Prencipe MR, Giardino G, Romano R, Scalia G, Genesio R, Nitsch L, Pignata C. Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion. The Journal of Allergy and Clinical Immunology: In Practice 2020;8:3112-20. [DOI: 10.1016/j.jaip.2020.06.051] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
7 Mancini V, Rochas V, Seeber M, Grent-‘t-jong T, Rihs TA, Latrèche C, Uhlhaas PJ, Michel CM, Eliez S. Oscillatory neural signatures of visual perception across developmental stages in individuals with 22q11.2 deletion syndrome. Biological Psychiatry 2022. [DOI: 10.1016/j.biopsych.2022.02.961] [Reference Citation Analysis]
8 Räsänen N, Tiihonen J, Koskuvi M, Lehtonen Š, Koistinaho J. The iPSC perspective on schizophrenia. Trends Neurosci 2022;45:8-26. [PMID: 34876311 DOI: 10.1016/j.tins.2021.11.002] [Reference Citation Analysis]
9 Forsyth JK, Mennigen E, Lin A, Sun D, Vajdi A, Kushan-Wells L, Ching CRK, Villalon-Reina JE, Thompson PM, Bearden CE; 22q11.2 ENIGMA Consortium. Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics. Cereb Cortex 2021;31:3285-98. [PMID: 33638978 DOI: 10.1093/cercor/bhab008] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
10 Jane Tseng C, Mcdougle CJ, Hooker JM, Zu¨rcher NR. Epigenetics of Autism Spectrum Disorder: Histone deacetylases. Biological Psychiatry 2021. [DOI: 10.1016/j.biopsych.2021.11.021] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Motahari Z, Maynard TM, Popratiloff A, Moody SA, LaMantia AS. Aberrant early growth of individual trigeminal sensory and motor axons in a series of mouse genetic models of 22q11.2 deletion syndrome. Hum Mol Genet 2020;29:3081-93. [PMID: 32901287 DOI: 10.1093/hmg/ddaa199] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
12 Karpinski BA, Maynard TM, Bryan CA, Yitsege G, Horvath A, Lee NH, Moody SA, Lamantia A. Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome. Disease Models & Mechanisms 2022;15:dmm047357. [DOI: 10.1242/dmm.047357] [Reference Citation Analysis]
13 Peter B, Scherer N, Liang WS, Pophal S, Nielsen C, Grebe TA. A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocation. Am J Med Genet A 2021;185:1532-7. [PMID: 33569883 DOI: 10.1002/ajmg.a.62121] [Reference Citation Analysis]
14 Moreau CA, Raznahan A, Bellec P, Chakravarty M, Thompson PM, Jacquemont S. Dissecting autism and schizophrenia through neuroimaging genomics. Brain 2021;144:1943-57. [PMID: 33704401 DOI: 10.1093/brain/awab096] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
15 Schussler O, Gharibeh L, Mootoosamy P, Murith N, Tien V, Rougemont AL, Sologashvili T, Suuronen E, Lecarpentier Y, Ruel M. Cardiac Neural Crest Cells: Their Rhombomeric Specification, Migration, and Association with Heart and Great Vessel Anomalies. Cell Mol Neurobiol 2021;41:403-29. [PMID: 32405705 DOI: 10.1007/s10571-020-00863-w] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
16 Sandini C, Schneider M, Eliez S, Armando M. Association Between Parental Anxiety and Depression Level and Psychopathological Symptoms in Offspring With 22q11.2 Deletion Syndrome. Front Psychiatry 2020;11:646. [PMID: 32792992 DOI: 10.3389/fpsyt.2020.00646] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Lin I, Afshar Y, Goldstein J, Grossman J, Grody WW, Quintero-Rivera F. Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome. Am J Med Genet A 2021. [PMID: 34196458 DOI: 10.1002/ajmg.a.62346] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Karbarz M. Consequences of 22q11.2 Microdeletion on the Genome, Individual and Population Levels. Genes (Basel) 2020;11:E977. [PMID: 32842603 DOI: 10.3390/genes11090977] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
19 Faurschou S, Lildballe DL, Maroun LL, Helvind M, Rasmussen M. Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion. Case Rep Genet 2021;2021:5539855. [PMID: 34221520 DOI: 10.1155/2021/5539855] [Reference Citation Analysis]
20 Comer AL, Carrier M, Tremblay MÈ, Cruz-Martín A. The Inflamed Brain in Schizophrenia: The Convergence of Genetic and Environmental Risk Factors That Lead to Uncontrolled Neuroinflammation. Front Cell Neurosci 2020;14:274. [PMID: 33061891 DOI: 10.3389/fncel.2020.00274] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 8.0] [Reference Citation Analysis]
21 LaMantia AS. Why Does the Face Predict the Brain? Neural Crest Induction, Craniofacial Morphogenesis, and Neural Circuit Development. Front Physiol 2020;11:610970. [PMID: 33362582 DOI: 10.3389/fphys.2020.610970] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Maynard TM, Zohn IE, Moody SA, LaMantia AS. Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology. Annu Rev Neurosci 2020;43:315-36. [PMID: 32101484 DOI: 10.1146/annurev-neuro-100419-100636] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
23 Favicchia I, Flore G, Cioffi S, Lania G, Baldini A, Illingworth E. Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome. Front Mol Neurosci 2021;14:663598. [PMID: 34552467 DOI: 10.3389/fnmol.2021.663598] [Reference Citation Analysis]
24 Li J, Ryan SK, Deboer E, Cook K, Fitzgerald S, Lachman HM, Wallace DC, Goldberg EM, Anderson SA. Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia. Transl Psychiatry 2019;9:302. [PMID: 31740674 DOI: 10.1038/s41398-019-0643-y] [Cited by in Crossref: 24] [Cited by in F6Publishing: 21] [Article Influence: 8.0] [Reference Citation Analysis]
25 Eom TY, Han SB, Kim J, Blundon JA, Wang YD, Yu J, Anderson K, Kaminski DB, Sakurada SM, Pruett-Miller SM, Horner L, Wagner B, Robinson CG, Eicholtz M, Rose DC, Zakharenko SS. Schizophrenia-related microdeletion causes defective ciliary motility and brain ventricle enlargement via microRNA-dependent mechanisms in mice. Nat Commun 2020;11:912. [PMID: 32060266 DOI: 10.1038/s41467-020-14628-y] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
26 Tepper Á, Cuiza A, Alliende LM, Mena C, Ramirez-Mahaluf JP, Iruretagoyena B, Ornstein C, Fritsch R, Nachar R, González-Valderrama A, Undurraga J, Cruz JP, Tejos C, Fornito A, Repetto G, Crossley N. Functional Dysconnectivity in Ventral Striatocortical Systems in 22q11.2 Deletion Syndrome. Schizophr Bull 2021:sbab139. [PMID: 34931688 DOI: 10.1093/schbul/sbab139] [Reference Citation Analysis]
27 Lin A, Forsyth JK, Hoftman GD, Kushan-Wells L, Jalbrzikowski M, Dokuru D, Coppola G, Fiksinski A, Zinkstok J, Vorstman J, Nachun D, Bearden CE. Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression. Brain Behav Immun Health 2021;18:100386. [PMID: 34841284 DOI: 10.1016/j.bbih.2021.100386] [Reference Citation Analysis]