Bahlo M - Search Results

1

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: bahlo m. Science. 2022 Jun 17;376(6599):eabf9088. doi: 10.1126/science.abf9088. Epub 2022 Jun 17. Science. 2022. PMID: 35709258

2

Systematic noise degrades gene co-expression signals but can be corrected.

Freytag S, Gagnon-Bartsch J, Speed TP, Bahlo M. Freytag S, et al. Among authors: bahlo m. BMC Bioinformatics. 2015 Sep 24;16:309. doi: 10.1186/s12859-015-0745-3. BMC Bioinformatics. 2015. PMID: 26403471 Free PMC article.

3

In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery.

Oliver KL, Lukic V, Freytag S, Scheffer IE, Berkovic SF, Bahlo M. Oliver KL, et al. Among authors: bahlo m. Neurol Genet. 2016 Jan 14;2(1):e51. doi: 10.1212/NXG.0000000000000051. eCollection 2016 Feb. Neurol Genet. 2016. PMID: 27066588 Free PMC article.

4

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. Among authors: bahlo m. Genome Med. 2017 Jun 8;9(1):55. doi: 10.1186/s13073-017-0444-y. Genome Med. 2017. PMID: 28595657 Free PMC article.

5

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: bahlo m. 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.

6

Comparison of clustering tools in R for medium-sized 10x Genomics single-cell RNA-sequencing data.

Freytag S, Tian L, Lönnstedt I, Ng M, Bahlo M. Freytag S, et al. Among authors: bahlo m. F1000Res. 2018 Aug 15;7:1297. doi: 10.12688/f1000research.15809.2. eCollection 2018. F1000Res. 2018. PMID: 30228881 Free PMC article.

7

dtangle: accurate and robust cell type deconvolution.

Hunt GJ, Freytag S, Bahlo M, Gagnon-Bartsch JA. Hunt GJ, et al. Among authors: bahlo m. Bioinformatics. 2019 Jun 1;35(12):2093-2099. doi: 10.1093/bioinformatics/bty926. Bioinformatics. 2019. PMID: 30407492

8

Genetic investigation into an increased susceptibility to biliary atresia in an extended New Zealand Māori family.

Cameron-Christie SR, Wilde J, Gray A, Tankard R, Bahlo M, Markie D, Evans HM, Robertson SP. Cameron-Christie SR, et al. Among authors: bahlo m. BMC Med Genomics. 2018 Dec 18;11(1):121. doi: 10.1186/s12920-018-0440-0. BMC Med Genomics. 2018. PMID: 30563518 Free PMC article.

9

Genome-wide genetic screen identifies host ubiquitination as important for Legionella pneumophila Dot/Icm effector translocation.

Ong SY, Schuelein R, Wibawa RR, Thomas DW, Handoko Y, Freytag S, Bahlo M, Simpson KJ, Hartland EL. Ong SY, et al. Among authors: bahlo m. Cell Microbiol. 2021 Oct;23(10):e13368. doi: 10.1111/cmi.13368. Epub 2021 Jun 8. Cell Microbiol. 2021. PMID: 34041837

10

A survey of RNA editing at single-cell resolution links interneurons to schizophrenia and autism.

Ansell BRE, Thomas SN, Bonelli R, Munro JE, Freytag S, Bahlo M. Ansell BRE, et al. Among authors: bahlo m. RNA. 2021 Dec;27(12):1482-1496. doi: 10.1261/rna.078804.121. Epub 2021 Sep 17. RNA. 2021. PMID: 34535545 Free PMC article.

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