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For: Perenthaler E, Yousefi S, Niggl E, Barakat TS. Beyond the Exome: The Non-coding Genome and Enhancers in Neurodevelopmental Disorders and Malformations of Cortical Development. Front Cell Neurosci 2019;13:352. [PMID: 31417368 DOI: 10.3389/fncel.2019.00352] [Cited by in Crossref: 26] [Cited by in F6Publishing: 17] [Article Influence: 8.7] [Reference Citation Analysis]
Number Citing Articles
1 Nabbout R, Kuchenbuch M. Impact of predictive, preventive and precision medicine strategies in epilepsy. Nat Rev Neurol 2020;16:674-88. [PMID: 33077944 DOI: 10.1038/s41582-020-0409-4] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 5.0] [Reference Citation Analysis]
2 Yousefi S, Deng R, Lanko K, Salsench EM, Nikoncuk A, van der Linde HC, Perenthaler E, van Ham TJ, Mulugeta E, Barakat TS. Comprehensive multi-omics integration identifies differentially active enhancers during human brain development with clinical relevance. Genome Med 2021;13:162. [PMID: 34663447 DOI: 10.1186/s13073-021-00980-1] [Reference Citation Analysis]
3 Loesch R, Chenane L, Colnot S. ARID2 Chromatin Remodeler in Hepatocellular Carcinoma. Cells 2020;9:E2152. [PMID: 32977645 DOI: 10.3390/cells9102152] [Reference Citation Analysis]
4 Perenthaler E, Nikoncuk A, Yousefi S, Berdowski WM, Alsagob M, Capo I, van der Linde HC, van den Berg P, Jacobs EH, Putar D, Ghazvini M, Aronica E, van IJcken WFJ, de Valk WG, Medici-van den Herik E, van Slegtenhorst M, Brick L, Kozenko M, Kohler JN, Bernstein JA, Monaghan KG, Begtrup A, Torene R, Al Futaisi A, Al Murshedi F, Mani R, Al Azri F, Kamsteeg EJ, Mojarrad M, Eslahi A, Khazaei Z, Darmiyan FM, Doosti M, Karimiani EG, Vandrovcova J, Zafar F, Rana N, Kandaswamy KK, Hertecant J, Bauer P, AlMuhaizea MA, Salih MA, Aldosary M, Almass R, Al-Quait L, Qubbaj W, Coskun S, Alahmadi KO, Hamad MHA, Alwadaee S, Awartani K, Dababo AM, Almohanna F, Colak D, Dehghani M, Mehrjardi MYV, Gunel M, Ercan-Sencicek AG, Passi GR, Cheema HA, Efthymiou S, Houlden H, Bertoli-Avella AM, Brooks AS, Retterer K, Maroofian R, Kaya N, van Ham TJ, Barakat TS. Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases. Acta Neuropathol 2020;139:415-42. [PMID: 31820119 DOI: 10.1007/s00401-019-02109-6] [Cited by in Crossref: 23] [Cited by in F6Publishing: 18] [Article Influence: 11.5] [Reference Citation Analysis]
5 D'haene E, Vergult S. Interpreting the impact of noncoding structural variation in neurodevelopmental disorders. Genet Med 2021;23:34-46. [PMID: 32973355 DOI: 10.1038/s41436-020-00974-1] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
6 Medico-Salsench E, Karkala F, Lanko K, Barakat TS. The non-coding genome in genetic brain disorders: new targets for therapy? Essays Biochem 2021;65:671-83. [PMID: 34414418 DOI: 10.1042/EBC20200121] [Reference Citation Analysis]
7 Chaudhuri T, Chintalapati J, Hosur MV. Identification of 3'-UTR single nucleotide variants and prediction of select protein imbalance in mesial temporal lobe epilepsy patients. PLoS One 2021;16:e0252475. [PMID: 34086756 DOI: 10.1371/journal.pone.0252475] [Reference Citation Analysis]
8 Oegema R, Barakat TS, Wilke M, Stouffs K, Amrom D, Aronica E, Bahi-Buisson N, Conti V, Fry AE, Geis T, Andres DG, Parrini E, Pogledic I, Said E, Soler D, Valor LM, Zaki MS, Mirzaa G, Dobyns WB, Reiner O, Guerrini R, Pilz DT, Hehr U, Leventer RJ, Jansen AC, Mancini GMS, Di Donato N. International consensus recommendations on the diagnostic work-up for malformations of cortical development. Nat Rev Neurol 2020;16:618-35. [PMID: 32895508 DOI: 10.1038/s41582-020-0395-6] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 4.5] [Reference Citation Analysis]
9 Gill PS, Clothier JL, Veerapandiyan A, Dweep H, Porter-Gill PA, Schaefer GB. Molecular Dysregulation in Autism Spectrum Disorder. J Pers Med 2021;11:848. [PMID: 34575625 DOI: 10.3390/jpm11090848] [Reference Citation Analysis]
10 Nair VD, Vasoya M, Nair V, Smith GR, Pincas H, Ge Y, Douglas CM, Esser KA, Sealfon SC. Differential analysis of chromatin accessibility and gene expression profiles identifies cis-regulatory elements in rat adipose and muscle. Genomics 2021;113:3827-41. [PMID: 34547403 DOI: 10.1016/j.ygeno.2021.09.013] [Reference Citation Analysis]
11 Hebbar M, Mefford HC. Recent advances in epilepsy genomics and genetic testing. F1000Res 2020;9:F1000 Faculty Rev-185. [PMID: 32201576 DOI: 10.12688/f1000research.21366.1] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 5.5] [Reference Citation Analysis]
12 Lambert JT, Su-Feher L, Cichewicz K, Warren TL, Zdilar I, Wang Y, Lim KJ, Haigh JL, Morse SJ, Canales CP, Stradleigh TW, Castillo Palacios E, Haghani V, Moss SD, Parolini H, Quintero D, Shrestha D, Vogt D, Byrne LC, Nord AS. Parallel functional testing identifies enhancers active in early postnatal mouse brain. Elife 2021;10:e69479. [PMID: 34605404 DOI: 10.7554/eLife.69479] [Reference Citation Analysis]
13 Wojcik MH, Agrawal PB. Deciphering congenital anomalies for the next generation. Cold Spring Harb Mol Case Stud 2020;6:a005504. [PMID: 32826208 DOI: 10.1101/mcs.a005504] [Reference Citation Analysis]
14 Swietlik EM, Prapa M, Martin JM, Pandya D, Auckland K, Morrell NW, Gräf S. 'There and Back Again'-Forward Genetics and Reverse Phenotyping in Pulmonary Arterial Hypertension. Genes (Basel) 2020;11:E1408. [PMID: 33256119 DOI: 10.3390/genes11121408] [Reference Citation Analysis]
15 Eleftheriadou M, Medici-van den Herik E, Stuurman K, van Bever Y, Hellebrekers DMEI, van Slegtenhorst M, Ruijter G, Barakat TS. Isobutyryl-CoA dehydrogenase deficiency associated with autism in a girl without an alternative genetic diagnosis by trio whole exome sequencing: A case report. Mol Genet Genomic Med 2021;9:e1595. [PMID: 33432785 DOI: 10.1002/mgg3.1595] [Reference Citation Analysis]
16 Klingler E, Francis F, Jabaudon D, Cappello S. Mapping the molecular and cellular complexity of cortical malformations. Science 2021;371:eaba4517. [PMID: 33479124 DOI: 10.1126/science.aba4517] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 9.0] [Reference Citation Analysis]
17 Monfils K, Barakat TS. Models behind the mystery of establishing enhancer-promoter interactions. Eur J Cell Biol 2021;100:151170. [PMID: 34246183 DOI: 10.1016/j.ejcb.2021.151170] [Reference Citation Analysis]
18 Liu Y, Henkel J, Beaurepaire A, Evans JD, Neumann P, Huang Q. Comparative genomics suggests local adaptations in the invasive small hive beetle. Ecol Evol 2021;11:15780-91. [PMID: 34824789 DOI: 10.1002/ece3.8242] [Reference Citation Analysis]
19 Mantsoki A, Parussel K, Joshi A. Identification and Characterisation of Putative Enhancer Elements in Mouse Embryonic Stem Cells. Bioinform Biol Insights 2021;15:1177932220974623. [PMID: 33623376 DOI: 10.1177/1177932220974623] [Reference Citation Analysis]
20 Barish S, Barakat TS, Michel BC, Mashtalir N, Phillips JB, Valencia AM, Ugur B, Wegner J, Scott TM, Bostwick B, Murdock DR, Dai H, Perenthaler E, Nikoncuk A, van Slegtenhorst M, Brooks AS, Keren B, Nava C, Mignot C, Douglas J, Rodan L, Nowak C, Ellard S, Stals K, Lynch SA, Faoucher M, Lesca G, Edery P, Engleman KL, Zhou D, Thiffault I, Herriges J, Gass J, Louie RJ, Stolerman E, Washington C, Vetrini F, Otsubo A, Pratt VM, Conboy E, Treat K, Shannon N, Camacho J, Wakeling E, Yuan B, Chen CA, Rosenfeld JA, Westerfield M, Wangler M, Yamamoto S, Kadoch C, Scott DA, Bellen HJ; Undiagnosed Diseases Network. BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms. Am J Hum Genet 2020;107:1096-112. [PMID: 33232675 DOI: 10.1016/j.ajhg.2020.11.003] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 6.5] [Reference Citation Analysis]
21 Lima Cunha D, Arno G, Corton M, Moosajee M. The Spectrum of PAX6 Mutations and Genotype-Phenotype Correlations in the Eye. Genes (Basel) 2019;10:E1050. [PMID: 31861090 DOI: 10.3390/genes10121050] [Cited by in Crossref: 30] [Cited by in F6Publishing: 23] [Article Influence: 10.0] [Reference Citation Analysis]
22 Spreafico R, Soriaga LB, Grosse J, Virgin HW, Telenti A. Advances in Genomics for Drug Development. Genes (Basel) 2020;11:E942. [PMID: 32824125 DOI: 10.3390/genes11080942] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
23 Zhao Y, Cai H, Zhang Z, Tang J, Li Y. Learning interpretable cellular and gene signature embeddings from single-cell transcriptomic data. Nat Commun 2021;12:5261. [PMID: 34489404 DOI: 10.1038/s41467-021-25534-2] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]