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Spatial centrosome proteome of human neural cells uncovers disease-relevant heterogeneity.
O'Neill AC, Uzbas F, Antognolli G, Merino F, Draganova K, Jäck A, Zhang S, Pedini G, Schessner JP, Cramer K, Schepers A, Metzger F, Esgleas M, Smialowski P, Guerrini R, Falk S, Feederle R, Freytag S, Wang Z, Bahlo M, Jungmann R, Bagni C, Borner GHH, Robertson SP, Hauck SM, Götz M. O'Neill AC, et al. Among authors: freytag s. Science. 2022 Jun 17;376(6599):eabf9088. doi: 10.1126/science.abf9088. Epub 2022 Jun 17. Science. 2022. PMID: 35709258
brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasets.
Freytag S, Burgess R, Oliver KL, Bahlo M. Freytag S, et al. Genome Med. 2017 Jun 8;9(1):55. doi: 10.1186/s13073-017-0444-y. Genome Med. 2017. PMID: 28595657 Free PMC article.
Using a subset of the curated SFARI autism gene collection we show that brain-coX's prioritisations are most similar to SFARI's own curated gene classifications. CONCLUSIONS: brain-coX is the first prioritisation and visualisation web-tool targeted to the human brai …
Using a subset of the curated SFARI autism gene collection we show that brain-coX's prioritisations are most similar to SFARI's …
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.
Heinzen EL, O'Neill AC, Zhu X, Allen AS, Bahlo M, Chelly J, Chen MH, Dobyns WB, Freytag S, Guerrini R, Leventer RJ, Poduri A, Robertson SP, Walsh CA, Zhang M; Epi4K Consortium; Epilepsy Phenome/Genome Project. Heinzen EL, et al. Among authors: freytag s. PLoS Genet. 2018 May 8;14(5):e1007281. doi: 10.1371/journal.pgen.1007281. eCollection 2018 May. PLoS Genet. 2018. PMID: 29738522 Free PMC article.
dtangle: accurate and robust cell type deconvolution.
Hunt GJ, Freytag S, Bahlo M, Gagnon-Bartsch JA. Hunt GJ, et al. Among authors: freytag s. Bioinformatics. 2019 Jun 1;35(12):2093-2099. doi: 10.1093/bioinformatics/bty926. Bioinformatics. 2019. PMID: 30407492
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2.
Henden L, Freytag S, Afawi Z, Baldassari S, Berkovic SF, Bisulli F, Canafoglia L, Casari G, Crompton DE, Depienne C, Gecz J, Guerrini R, Helbig I, Hirsch E, Keren B, Klein KM, Labauge P, LeGuern E, Licchetta L, Mei D, Nava C, Pippucci T, Rudolf G, Scheffer IE, Striano P, Tinuper P, Zara F, Corbett M, Bahlo M. Henden L, et al. Among authors: freytag s. Hum Genet. 2016 Oct;135(10):1117-25. doi: 10.1007/s00439-016-1700-8. Epub 2016 Jul 1. Hum Genet. 2016. PMID: 27368338
146 results