BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Wang W, Corominas R, Lin GN. De novo Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application. Front Genet 2019;10:258. [PMID: 31001316 DOI: 10.3389/fgene.2019.00258] [Cited by in Crossref: 25] [Cited by in F6Publishing: 20] [Article Influence: 8.3] [Reference Citation Analysis]
Number Citing Articles
1 Li W, Almirantis Y, Provata A. Revisiting the neutral dynamics derived limiting guanine-cytosine content using human de novo point mutation data. Meta Gene 2022;31:100994. [DOI: 10.1016/j.mgene.2021.100994] [Reference Citation Analysis]
2 Ittiwut C, Poonmaksatit S, Boonsimma P, Desudchit T, Suphapeetiporn K, Ittiwut R, Shotelersuk V. Novel de novo mutation substantiates ATP6V0C as a gene causing epilepsy with intellectual disability. Brain Dev 2021;43:490-4. [PMID: 33190975 DOI: 10.1016/j.braindev.2020.10.016] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Zamanpoor M. Schizophrenia in a genomic era: a review from the pathogenesis, genetic and environmental etiology to diagnosis and treatment insights. Psychiatr Genet 2020;30:1-9. [PMID: 31764709 DOI: 10.1097/YPG.0000000000000245] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 4.5] [Reference Citation Analysis]
4 Baldassari S, Musante I, Iacomino M, Zara F, Salpietro V, Scudieri P. Brain Organoids as Model Systems for Genetic Neurodevelopmental Disorders. Front Cell Dev Biol 2020;8:590119. [PMID: 33154971 DOI: 10.3389/fcell.2020.590119] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
5 Tamburri S, Conway E, Pasini D. Polycomb-dependent histone H2A ubiquitination links developmental disorders with cancer. Trends Genet 2021:S0168-9525(21)00201-8. [PMID: 34426021 DOI: 10.1016/j.tig.2021.07.011] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Singh SM, Castellani CA, Hill KA. Postzygotic Somatic Mutations in the Human Brain Expand the Threshold-Liability Model of Schizophrenia. Front Psychiatry 2020;11:587162. [PMID: 33192734 DOI: 10.3389/fpsyt.2020.587162] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Reilly J, Kerkhof J, Sadikovic B. EpiSigns. Advances in Molecular Pathology 2020;3:29-39. [DOI: 10.1016/j.yamp.2020.07.018] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Bellott DW, Page DC. Dosage-sensitive functions in embryonic development drove the survival of genes on sex-specific chromosomes in snakes, birds, and mammals. Genome Res 2021. [PMID: 33479023 DOI: 10.1101/gr.268516.120] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
9 Engelbrecht C, Urban M, Schoeman M, Paarwater B, van Coller A, Abraham DR, Cornelissen H, Glashoff R, Esser M, Möller M, Kinnear C, Glanzmann B. Clinical Utility of Whole Exome Sequencing and Targeted Panels for the Identification of Inborn Errors of Immunity in a Resource-Constrained Setting. Front Immunol 2021;12:665621. [PMID: 34093558 DOI: 10.3389/fimmu.2021.665621] [Reference Citation Analysis]
10 Saraiva LC, Cappi C, Simpson HB, Stein DJ, Viswanath B, van den Heuvel OA, Reddy YJ, Miguel EC, Shavitt RG. Cutting-edge genetics in obsessive-compulsive disorder. Fac Rev 2020;9:30. [PMID: 33659962 DOI: 10.12703/r/9-30] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Pillay NS, Ross OA, Christoffels A, Bardien S. Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s Disease. Front Genet 2022;13:781816. [DOI: 10.3389/fgene.2022.781816] [Reference Citation Analysis]
12 Joo JY, Lim KH, Yang S, Kim SH, Cocco L, Suh PG. Prediction of genetic alteration of phospholipase C isozymes in brain disorders: Studies with deep learning. Adv Biol Regul 2021;82:100833. [PMID: 34773889 DOI: 10.1016/j.jbior.2021.100833] [Reference Citation Analysis]
13 Zhao G, Li K, Li B, Wang Z, Fang Z, Wang X, Zhang Y, Luo T, Zhou Q, Wang L, Xie Y, Wang Y, Chen Q, Xia L, Tang Y, Tang B, Xia K, Li J. Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans. Nucleic Acids Res 2020;48:D913-26. [PMID: 31642496 DOI: 10.1093/nar/gkz923] [Cited by in Crossref: 7] [Cited by in F6Publishing: 12] [Article Influence: 3.5] [Reference Citation Analysis]
14 Tutukova S, Tarabykin V, Hernandez-Miranda LR. The Role of Neurod Genes in Brain Development, Function, and Disease. Front Mol Neurosci 2021;14:662774. [PMID: 34177462 DOI: 10.3389/fnmol.2021.662774] [Reference Citation Analysis]
15 Lin GN, Guo S, Tan X, Wang W, Qian W, Song W, Wang J, Yu S, Wang Z, Cui D, Wang H. PsyMuKB: An Integrative De Novo Variant Knowledge Base for Developmental Disorders. Genomics Proteomics Bioinformatics 2019;17:453-64. [PMID: 31809863 DOI: 10.1016/j.gpb.2019.10.002] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
16 Rylaarsdam L, Guemez-Gamboa A. Genetic Causes and Modifiers of Autism Spectrum Disorder. Front Cell Neurosci 2019;13:385. [PMID: 31481879 DOI: 10.3389/fncel.2019.00385] [Cited by in Crossref: 67] [Cited by in F6Publishing: 49] [Article Influence: 22.3] [Reference Citation Analysis]
17 Myers SM, Challman TD, Bernier R, Bourgeron T, Chung WK, Constantino JN, Eichler EE, Jacquemont S, Miller DT, Mitchell KJ, Zoghbi HY, Martin CL, Ledbetter DH. Insufficient Evidence for "Autism-Specific" Genes. Am J Hum Genet 2020;106:587-95. [PMID: 32359473 DOI: 10.1016/j.ajhg.2020.04.004] [Cited by in Crossref: 34] [Cited by in F6Publishing: 28] [Article Influence: 17.0] [Reference Citation Analysis]
18 Wang C, Horigane S, Wakamori M, Ueda S, Kawabata T, Fujii H, Kushima I, Kimura H, Ishizuka K, Nakamura Y, Iwayama Y, Ikeda M, Iwata N, Okada T, Aleksic B, Mori D, Yoshida T, Bito H, Yoshikawa T, Takemoto-kimura S, Ozaki N. Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder. Transl Psychiatry 2022;12. [DOI: 10.1038/s41398-022-01851-y] [Reference Citation Analysis]
19 Bartoshesky LE, Wright C; FACMG1. Intellectual Developmental Disabilities:: Definitions, Diagnosis, and Delivery of Care. Dela J Public Health 2021;7:6-8. [PMID: 34467189 DOI: 10.32481/djph.2021.03.004] [Reference Citation Analysis]
20 Álvarez-mora MI, Sánchez A, Rodríguez-revenga L, Corominas J, Rabionet R, Puig S, Madrigal I. Diagnostic yield of next-generation sequencing in 87 families with neurodevelopmental disorders. Orphanet J Rare Dis 2022;17. [DOI: 10.1186/s13023-022-02213-z] [Reference Citation Analysis]
21 Salcedo-Arellano MJ, Cabal-Herrera AM, Punatar RH, Clark CJ, Romney CA, Hagerman RJ. Overlapping Molecular Pathways Leading to Autism Spectrum Disorders, Fragile X Syndrome, and Targeted Treatments. Neurotherapeutics 2021;18:265-83. [PMID: 33215285 DOI: 10.1007/s13311-020-00968-6] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
22 Andrade A, Brennecke A, Mallat S, Brown J, Gomez-Rivadeneira J, Czepiel N, Londrigan L. Genetic Associations between Voltage-Gated Calcium Channels and Psychiatric Disorders. Int J Mol Sci 2019;20:E3537. [PMID: 31331039 DOI: 10.3390/ijms20143537] [Cited by in Crossref: 14] [Cited by in F6Publishing: 9] [Article Influence: 4.7] [Reference Citation Analysis]
23 Baldwin I, Shafer RL, Hossain WA, Gunewardena S, Veatch OJ, Mosconi MW, Butler MG. Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families. Int J Mol Sci 2021;22:1660. [PMID: 33562221 DOI: 10.3390/ijms22041660] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Akgün M, Ünal AB, Ergüner B, Pfeifer N, Kohlbacher O. Identifying disease-causing mutations with privacy protection. Bioinformatics 2021;36:5205-13. [PMID: 32683440 DOI: 10.1093/bioinformatics/btaa641] [Reference Citation Analysis]
25 Wang M, Marco P, Capra V, Kibar Z. Update on the Role of the Non-Canonical Wnt/Planar Cell Polarity Pathway in Neural Tube Defects. Cells 2019;8:E1198. [PMID: 31590237 DOI: 10.3390/cells8101198] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 6.3] [Reference Citation Analysis]
26 Freitag CM, Chiocchetti AG, Haslinger D, Yousaf A, Waltes R. [Genetic risk factors and their influence on neural development in autism spectrum disorders]. Z Kinder Jugendpsychiatr Psychother 2021;:1-16. [PMID: 34128703 DOI: 10.1024/1422-4917/a000803] [Reference Citation Analysis]
27 Katsonis P, Wilhelm K, Williams A, Lichtarge O. Genome interpretation using in silico predictors of variant impact. Hum Genet 2022. [PMID: 35488922 DOI: 10.1007/s00439-022-02457-6] [Reference Citation Analysis]
28 Steinhaus R, Proft S, Schuelke M, Cooper DN, Schwarz JM, Seelow D. MutationTaster2021. Nucleic Acids Res 2021;49:W446-51. [PMID: 33893808 DOI: 10.1093/nar/gkab266] [Reference Citation Analysis]