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Cited by in F6Publishing
For: Catusi I, Garzo M, Capra AP, Briuglia S, Baldo C, Canevini MP, Cantone R, Elia F, Forzano F, Galesi O, Grosso E, Malacarne M, Peron A, Romano C, Saccani M, Larizza L, Recalcati MP. 8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature. Genes (Basel) 2021;12:652. [PMID: 33925474 DOI: 10.3390/genes12050652] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Hsieh MY, Tuan LH, Chang HC, Wang YC, Chen CH, Shy HT, Lee LJ, Gau SS. Altered synaptic protein expression, aberrant spine morphology, and impaired spatial memory in Dlgap2 mutant mice, a genetic model of autism spectrum disorder. Cereb Cortex 2022:bhac379. [PMID: 36169576 DOI: 10.1093/cercor/bhac379] [Reference Citation Analysis]
2 Jima DD, Skaar DA, Planchart A, Motsinger-Reif A, Cevik SE, Park SS, Cowley M, Wright F, House J, Liu A, Jirtle RL, Hoyo C. Genomic map of candidate human imprint control regions: the imprintome. Epigenetics 2022;:1-24. [PMID: 35786392 DOI: 10.1080/15592294.2022.2091815] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
3 An Y, Tsai C, Liang C, Lin Y, Lin G, Tsai C, Liu Y, Chen S, Tsai S, Hung K, Yang F. Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity. NSS 2022;Volume 14:1075-87. [DOI: 10.2147/nss.s365988] [Reference Citation Analysis]
4 Redaelli S, Conconi D, Sala E, Villa N, Crosti F, Roversi G, Catusi I, Valtorta C, Recalcati MP, Dalprà L, Lavitrano M, Bentivegna A. Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region. IJMS 2022;23:3347. [DOI: 10.3390/ijms23063347] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Kaymak D, Alpay V, Başıbüyük Z, Davutoğlu EA, Madazlı R. Prenatal Diagnosis of 8p23 Deletion Syndrome by Single Nucleotide Polymorphism Microarray. J Fetal Med 2021;8:315-9. [DOI: 10.1007/s40556-021-00322-6] [Reference Citation Analysis]