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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 4
2004 3
2006 1
2007 2
2008 1
2011 2
2012 1
2013 3
2014 3
2015 1
2016 1
2018 1
2019 1
2020 0
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24 results
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Page 1
Transcriptome and genome sequencing uncovers functional variation in humans.
Lappalainen T, Sammeth M, Friedländer MR, 't Hoen PA, Monlong J, Rivas MA, Gonzàlez-Porta M, Kurbatova N, Griebel T, Ferreira PG, Barann M, Wieland T, Greger L, van Iterson M, Almlöf J, Ribeca P, Pulyakhina I, Esser D, Giger T, Tikhonov A, Sultan M, Bertier G, MacArthur DG, Lek M, Lizano E, Buermans HP, Padioleau I, Schwarzmayr T, Karlberg O, Ongen H, Kilpinen H, Beltran S, Gut M, Kahlem K, Amstislavskiy V, Stegle O, Pirinen M, Montgomery SB, Donnelly P, McCarthy MI, Flicek P, Strom TM; Geuvadis Consortium, Lehrach H, Schreiber S, Sudbrak R, Carracedo A, Antonarakis SE, Häsler R, Syvänen AC, van Ommen GJ, Brazma A, Meitinger T, Rosenstiel P, Guigó R, Gut IG, Estivill X, Dermitzakis ET. Lappalainen T, et al. Among authors: karlberg o. Nature. 2013 Sep 26;501(7468):506-11. doi: 10.1038/nature12531. Epub 2013 Sep 15. Nature. 2013. PMID: 24037378 Free PMC article.
Imaging single DNA molecules for high precision NIPT.
Dahl F, Ericsson O, Karlberg O, Karlsson F, Howell M, Persson F, Roos F, Stenberg J, Ahola T, Alftrén I, Andersson B, Barkenäs E, Brandner B, Dahlberg J, Elfman S, Eriksson M, Forsgren PO, Francois N, Gousseva A, Hakamali F, Janfalk-Carlsson Å, Johansson H, Lundgren J, Mohsenchian A, Olausson L, Olofsson S, Qureshi A, Skarpås B, Sävneby A, Åström E, Öhman O, Westgren M, Kopp-Kallner H, Fianu-Jonasson A, Syngelaki A, Nicolaides K. Dahl F, et al. Among authors: karlberg o. Sci Rep. 2018 Mar 14;8(1):4549. doi: 10.1038/s41598-018-22606-0. Sci Rep. 2018. PMID: 29540801 Free PMC article.
Clinical validation of a novel automated cell-free DNA screening assay for trisomies 21, 13, and 18 in maternal plasma.
Ericsson O, Ahola T, Dahl F, Karlsson F, Persson F, Karlberg O, Roos F, Alftrén I, Andersson B, Barkenäs E, Boghos A, Brandner B, Dahlberg J, Forsgren PO, Francois N, Gousseva A, Hakamali F, Janfalk-Carlsson Å, Johansson H, Lundgren J, Mohsenchian A, Olausson L, Olofsson S, Qureshi A, Skarpås B, Svahn P, Sävneby A, Åström E, Sahlberg A, Fianu-Jonasson A, Gautier J, Costa JM, Jacobsson B, Nicolaides K. Ericsson O, et al. Among authors: karlberg o. Prenat Diagn. 2019 Oct;39(11):1011-1015. doi: 10.1002/pd.5528. Epub 2019 Aug 19. Prenat Diagn. 2019. PMID: 31429096 Free PMC article.
On the origin of mitochondria: a genomics perspective.
Andersson SG, Karlberg O, Canbäck B, Kurland CG. Andersson SG, et al. Among authors: karlberg o. Philos Trans R Soc Lond B Biol Sci. 2003 Jan 29;358(1429):165-77; discussion 177-9. doi: 10.1098/rstb.2002.1193. Philos Trans R Soc Lond B Biol Sci. 2003. PMID: 12594925 Free PMC article. Review.
Reproducibility of high-throughput mRNA and small RNA sequencing across laboratories.
't Hoen PA, Friedländer MR, Almlöf J, Sammeth M, Pulyakhina I, Anvar SY, Laros JF, Buermans HP, Karlberg O, Brännvall M; GEUVADIS Consortium, den Dunnen JT, van Ommen GJ, Gut IG, Guigó R, Estivill X, Syvänen AC, Dermitzakis ET, Lappalainen T. 't Hoen PA, et al. Among authors: karlberg o. Nat Biotechnol. 2013 Nov;31(11):1015-22. doi: 10.1038/nbt.2702. Epub 2013 Sep 15. Nat Biotechnol. 2013. PMID: 24037425
Mitochondrial gene history and mRNA localization: is there a correlation?
Karlberg EO, Andersson SG. Karlberg EO, et al. Nat Rev Genet. 2003 May;4(5):391-7. doi: 10.1038/nrg1063. Nat Rev Genet. 2003. PMID: 12728281 Review.
A novel splicing mutation in the IQSEC2 gene that modulates the phenotype severity in a family with intellectual disability.
Madrigal I, Alvarez-Mora MI, Rosell J, Rodríguez-Revenga L, Karlberg O, Sauer S, Syvänen AC, Mila M. Madrigal I, et al. Among authors: karlberg o. Eur J Hum Genet. 2016 Aug;24(8):1117-23. doi: 10.1038/ejhg.2015.267. Epub 2016 Jan 6. Eur J Hum Genet. 2016. PMID: 26733290 Free PMC article.
A wiring of the human nucleolus.
Hinsby AM, Kiemer L, Karlberg EO, Lage K, Fausbøll A, Juncker AS, Andersen JS, Mann M, Brunak S. Hinsby AM, et al. Among authors: karlberg eo. Mol Cell. 2006 Apr 21;22(2):285-95. doi: 10.1016/j.molcel.2006.03.012. Mol Cell. 2006. PMID: 16630896 Free article.
Efficient application of next-generation sequencing for the diagnosis of rare genetic syndromes.
Madrigal I, Alvarez-Mora MI, Karlberg O, Rodríguez-Revenga L, Elurbe DM, Rabionet R, Mur A, Pie J, Ballesta F, Sauer S, Syvänen AC, Milà M. Madrigal I, et al. Among authors: karlberg o. J Clin Pathol. 2014 Dec;67(12):1099-103. doi: 10.1136/jclinpath-2014-202537. Epub 2014 Sep 30. J Clin Pathol. 2014. PMID: 25271213
Deep origin of plastid/parasite ATP/ADP translocases.
Amiri H, Karlberg O, Andersson SG. Amiri H, et al. Among authors: karlberg o. J Mol Evol. 2003 Feb;56(2):137-50. doi: 10.1007/s00239-002-2387-0. J Mol Evol. 2003. PMID: 12574860
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