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For: Haghshenas S, Bhai P, Aref-Eshghi E, Sadikovic B. Diagnostic Utility of Genome-Wide DNA Methylation Analysis in Mendelian Neurodevelopmental Disorders. Int J Mol Sci 2020;21:E9303. [PMID: 33291301 DOI: 10.3390/ijms21239303] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Kalyakulina A, Yusipov I, Bacalini MG, Franceschi C, Vedunova M, Ivanchenko M. Disease classification for whole-blood DNA methylation: Meta-analysis, missing values imputation, and XAI. GigaScience 2022;11. [DOI: 10.1093/gigascience/giac097] [Reference Citation Analysis]
2 Di Risi T, Cuomo M, Vinciguerra R, Ferraro S, Della Monica R, Costabile D, Buonaiuto M, Trio F, Capoluongo E, Visconti R, Riccio E, Pisani A, Chiariotti L. Methylome Profiling in Fabry Disease in Clinical Practice: A Proof of Concept. Int J Mol Sci 2022;23. [PMID: 36292965 DOI: 10.3390/ijms232012110] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Kalyakulina A, Yusipov I, Bacalini MG, Franceschi C, Vedunova M, Ivanchenko M. Disease classification for whole blood DNA methylation: meta-analysis, missing values imputation, and XAI.. [DOI: 10.1101/2022.05.10.491404] [Reference Citation Analysis]
4 Nothof SA, Magdinier F, Van-gils J. Chromatin Structure and Dynamics: Focus on Neuronal Differentiation and Pathological Implication. Genes 2022;13:639. [DOI: 10.3390/genes13040639] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Wong MM, Kampen RA, Braden RO, Alagöz G, Hildebrand MS, Barnett C, Barnett M, Brusco A, Carli D, de Vries BB, Dingemans AJ, Elmslie F, Ferrero GB, Jansen NA, van de Laar IM, Moroni A, Mowat D, Murray L, Novara F, Peron A, Scheffer IE, Sirchia F, Turner SJ, Vignoli A, Vino A, Weber S, Chung WK, Gerard M, López-gonzález V, Palmer E, Morgan AT, van Bon BW, Fisher SE. SETBP1 variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental disorder.. [DOI: 10.1101/2022.03.04.22271462] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Kadlubowska MK, Schrauwen I. Methods to Improve Molecular Diagnosis in Genomic Cold Cases in Pediatric Neurology. Genes 2022;13:333. [DOI: 10.3390/genes13020333] [Reference Citation Analysis]
7 Levy MA, McConkey H, Kerkhof J, Barat-Houari M, Bargiacchi S, Biamino E, Bralo MP, Cappuccio G, Ciolfi A, Clarke A, DuPont BR, Elting MW, Faivre L, Fee T, Fletcher RS, Cherik F, Foroutan A, Friez MJ, Gervasini C, Haghshenas S, Hilton BA, Jenkins Z, Kaur S, Lewis S, Louie RJ, Maitz S, Milani D, Morgan AT, Oegema R, Østergaard E, Pallares NR, Piccione M, Pizzi S, Plomp AS, Poulton C, Reilly J, Relator R, Rius R, Robertson S, Rooney K, Rousseau J, Santen GWE, Santos-Simarro F, Schijns J, Squeo GM, St John M, Thauvin-Robinet C, Traficante G, van der Sluijs PJ, Vergano SA, Vos N, Walden KK, Azmanov D, Balci T, Banka S, Gecz J, Henneman P, Lee JA, Mannens MMAM, Roscioli T, Siu V, Amor DJ, Baynam G, Bend EG, Boycott K, Brunetti-Pierri N, Campeau PM, Christodoulou J, Dyment D, Esber N, Fahrner JA, Fleming MD, Genevieve D, Kerrnohan KD, McNeill A, Menke LA, Merla G, Prontera P, Rockman-Greenberg C, Schwartz C, Skinner SA, Stevenson RE, Vitobello A, Tartaglia M, Alders M, Tedder ML, Sadikovic B. Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders. HGG Adv 2022;3:100075. [PMID: 35047860 DOI: 10.1016/j.xhgg.2021.100075] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
8 Mubarak G, Zahir FR. Methionine Is a Major Methyl Donor Whose Dietary Intake Likely Plays a Causative Role for Neurodevelopmental Disorders via Epigenomic Profile Alterations. Nutritional Neurosciences 2022. [DOI: 10.1007/978-981-15-9781-7_4] [Reference Citation Analysis]
9 Nicolini H, Genis-mendoza AD, Martínez-magaña JJ. Epigenetics in Epidemiology. Principles of Genetics and Molecular Epidemiology 2022. [DOI: 10.1007/978-3-030-89601-0_4] [Reference Citation Analysis]
10 Thomsen M. Episignaturen als neues Werkzeug für die Diagnostik. DGNeurologie 2022;5:71-73. [DOI: 10.1007/s42451-021-00402-x] [Reference Citation Analysis]
11 Thomsen M, Lohmann K. Importance of Methylation Pattern: Episignatures as a Novel Instrument in Diagnostics. Mov Disord 2021. [PMID: 34817105 DOI: 10.1002/mds.28877] [Reference Citation Analysis]
12 Kerkhof J, Squeo GM, McConkey H, Levy MA, Piemontese MR, Castori M, Accadia M, Biamino E, Della Monica M, Di Giacomo MC, Gervasini C, Maitz S, Melis D, Milani D, Piccione M, Prontera P, Selicorni A, Sadikovic B, Merla G. DNA methylation episignature testing improves molecular diagnosis of Mendelian chromatinopathies. Genet Med 2021:S1098-3600(21)01121-7. [PMID: 34906459 DOI: 10.1016/j.gim.2021.08.007] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
13 Nogueira E, Garma C, Lobo C, Del Olmo B, Arroyo JM, Gómez I. Severe developmental expressive language disorder due to a frameshift mutation in exon 18 of SRCAP gene, far away from the mutational hotspot in exons 33 and 34 associated to the Floating-Harbor syndrome. Neurol Sci 2021;42:4349-52. [PMID: 34213696 DOI: 10.1007/s10072-021-05423-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
14 Velasco G, Ulveling D, Rondeau S, Marzin P, Unoki M, Cormier-Daire V, Francastel C. Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders. Int J Mol Sci 2021;22:3735. [PMID: 33916664 DOI: 10.3390/ijms22073735] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]