Feuk L - Search Results

1

Long-read whole-genome analysis of human single cells.

Hård J, Mold JE, Eisfeldt J, Tellgren-Roth C, Häggqvist S, Bunikis I, Contreras-Lopez O, Chin CS, Nordlund J, Rubin CJ, Feuk L, Michaëlsson J, Ameur A. Hård J, et al. Among authors: feuk l. Nat Commun. 2023 Aug 24;14(1):5164. doi: 10.1038/s41467-023-40898-3. Nat Commun. 2023. PMID: 37620373 Free PMC article.

2

Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity.

Höijer I, Johansson J, Gudmundsson S, Chin CS, Bunikis I, Häggqvist S, Emmanouilidou A, Wilbe M, den Hoed M, Bondeson ML, Feuk L, Gyllensten U, Ameur A. Höijer I, et al. Among authors: feuk l. Genome Biol. 2020 Dec 1;21(1):290. doi: 10.1186/s13059-020-02206-w. Genome Biol. 2020. PMID: 33261648 Free PMC article.

3

CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations.

Höijer I, Emmanouilidou A, Östlund R, van Schendel R, Bozorgpana S, Tijsterman M, Feuk L, Gyllensten U, den Hoed M, Ameur A. Höijer I, et al. Among authors: feuk l. Nat Commun. 2022 Feb 2;13(1):627. doi: 10.1038/s41467-022-28244-5. Nat Commun. 2022. PMID: 35110541 Free PMC article.

4

SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population.

Ameur A, Dahlberg J, Olason P, Vezzi F, Karlsson R, Martin M, Viklund J, Kähäri AK, Lundin P, Che H, Thutkawkorapin J, Eisfeldt J, Lampa S, Dahlberg M, Hagberg J, Jareborg N, Liljedahl U, Jonasson I, Johansson Å, Feuk L, Lundeberg J, Syvänen AC, Lundin S, Nilsson D, Nystedt B, Magnusson PK, Gyllensten U. Ameur A, et al. Among authors: feuk l. Eur J Hum Genet. 2017 Nov;25(11):1253-1260. doi: 10.1038/ejhg.2017.130. Epub 2017 Aug 23. Eur J Hum Genet. 2017. PMID: 28832569 Free PMC article.

5

De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data.

Ameur A, Che H, Martin M, Bunikis I, Dahlberg J, Höijer I, Häggqvist S, Vezzi F, Nordlund J, Olason P, Feuk L, Gyllensten U. Ameur A, et al. Among authors: feuk l. Genes (Basel). 2018 Oct 9;9(10):486. doi: 10.3390/genes9100486. Genes (Basel). 2018. PMID: 30304863 Free PMC article.

6

Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human Genomes.

Fatima N, Petri A, Gyllensten U, Feuk L, Ameur A. Fatima N, et al. Among authors: feuk l. Genes (Basel). 2020 Nov 30;11(12):1444. doi: 10.3390/genes11121444. Genes (Basel). 2020. PMID: 33266238 Free PMC article.

7

Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier.

Eisfeldt J, Pettersson M, Petri A, Nilsson D, Feuk L, Lindstrand A. Eisfeldt J, et al. Among authors: feuk l. Hum Genet. 2021 May;140(5):775-790. doi: 10.1007/s00439-020-02242-3. Epub 2020 Dec 14. Hum Genet. 2021. PMID: 33315133 Free PMC article.

8

Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain.

Ameur A, Zaghlool A, Halvardson J, Wetterbom A, Gyllensten U, Cavelier L, Feuk L. Ameur A, et al. Among authors: feuk l. Nat Struct Mol Biol. 2011 Nov 6;18(12):1435-40. doi: 10.1038/nsmb.2143. Nat Struct Mol Biol. 2011. PMID: 22056773

9

Splicing in the human brain.

Zaghlool A, Ameur A, Cavelier L, Feuk L. Zaghlool A, et al. Among authors: feuk l. Int Rev Neurobiol. 2014;116:95-125. doi: 10.1016/B978-0-12-801105-8.00005-9. Int Rev Neurobiol. 2014. PMID: 25172473 Review.

10

Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing.

Höijer I, Tsai YC, Clark TA, Kotturi P, Dahl N, Stattin EL, Bondeson ML, Feuk L, Gyllensten U, Ameur A. Höijer I, et al. Among authors: feuk l. Hum Mutat. 2018 Sep;39(9):1262-1272. doi: 10.1002/humu.23580. Epub 2018 Jul 12. Hum Mutat. 2018. PMID: 29932473 Free PMC article.

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