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Targeted next generation sequencing as a diagnostic tool in epileptic disorders.
Epilepsia. 2012 Aug;53(8):1387-98. doi: 10.1111/j.1528-1167.2012.03516.x. Epub 2012 May 21.
Epilepsia. 2012.
PMID: 22612257
Free article.
Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies.
Glöckle N, Kohl S, Mohr J, Scheurenbrand T, Sprecher A, Weisschuh N, Bernd A, Rudolph G, Schubach M, Poloschek C, Zrenner E, Biskup S, Berger W, Wissinger B, Neidhardt J.
Glöckle N, et al. Among authors: scheurenbrand t.
Eur J Hum Genet. 2014 Jan;22(1):99-104. doi: 10.1038/ejhg.2013.72. Epub 2013 Apr 17.
Eur J Hum Genet. 2014.
PMID: 23591405
Free PMC article.
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Analysis of the intestinal microbiota using SOLiD 16S rRNA gene sequencing and SOLiD shotgun sequencing.
Mitra S, Förster-Fromme K, Damms-Machado A, Scheurenbrand T, Biskup S, Huson DH, Bischoff SC.
Mitra S, et al. Among authors: scheurenbrand t.
BMC Genomics. 2013;14 Suppl 5(Suppl 5):S16. doi: 10.1186/1471-2164-14-S5-S16. Epub 2013 Oct 16.
BMC Genomics. 2013.
PMID: 24564472
Free PMC article.
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A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort.
Klein K, Tremmel R, Winter S, Fehr S, Battke F, Scheurenbrand T, Schaeffeler E, Biskup S, Schwab M, Zanger UM.
Klein K, et al. Among authors: scheurenbrand t.
Front Genet. 2019 Jan 31;10:7. doi: 10.3389/fgene.2019.00007. eCollection 2019.
Front Genet. 2019.
PMID: 30766545
Free PMC article.
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Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression.
Tremmel R, Klein K, Battke F, Fehr S, Winter S, Scheurenbrand T, Schaeffeler E, Biskup S, Schwab M, Zanger UM.
Tremmel R, et al. Among authors: scheurenbrand t.
Hum Genet. 2020 Feb;139(2):137-149. doi: 10.1007/s00439-019-02093-7. Epub 2019 Nov 30.
Hum Genet. 2020.
PMID: 31786673
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