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Page 1
Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.
Kloss-Brandstätter A, Erhart G, Lamina C, Meister B, Haun M, Coassin S, Seifert M, Klein-Franke A, Paulweber B, Kedenko L, Kollerits B, Swinkels DW, Vermeulen SH, Galesloot TE, Kronenberg F, Weiss G. Kloss-Brandstätter A, et al. Among authors: erhart g. PLoS One. 2012;7(4):e35015. doi: 10.1371/journal.pone.0035015. Epub 2012 Apr 11. PLoS One. 2012. PMID: 22509377 Free PMC article.
Polymorphisms in the gene regions of the adaptor complex LAMTOR2/LAMTOR3 and their association with breast cancer risk.
De Araujo ME, Erhart G, Buck K, Müller-Holzner E, Hubalek M, Fiegl H, Campa D, Canzian F, Eilber U, Chang-Claude J, Coassin S, Haun M, Kedenko L, Paulweber B, Reitsamer R, Himmel I, Flesch-Janys D, Lamina C, Kronenberg F, Huber LA, Kloss-Brandstätter A. De Araujo ME, et al. Among authors: erhart g. PLoS One. 2013;8(1):e53768. doi: 10.1371/journal.pone.0053768. Epub 2013 Jan 16. PLoS One. 2013. PMID: 23341997 Free PMC article.
Investigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working population.
Coassin S, Schweiger M, Kloss-Brandstätter A, Lamina C, Haun M, Erhart G, Paulweber B, Rahman Y, Olpin S, Wolinski H, Cornaciu I, Zechner R, Zimmermann R, Kronenberg F. Coassin S, et al. Among authors: erhart g. PLoS Genet. 2010 Dec 9;6(12):e1001239. doi: 10.1371/journal.pgen.1001239. PLoS Genet. 2010. PMID: 21170305 Free PMC article.
A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.
Lamina C, Friedel S, Coassin S, Rueedi R, Yousri NA, Seppälä I, Gieger C, Schönherr S, Forer L, Erhart G, Kollerits B, Marques-Vidal P, Ried J, Waeber G, Bergmann S, Dähnhardt D, Stöckl A, Kiechl S, Raitakari OT, Kähönen M, Willeit J, Kedenko L, Paulweber B, Peters A, Meitinger T, Strauch K; KORA Study Group; Lehtimäki T, Hunt SC, Vollenweider P, Kronenberg F. Lamina C, et al. Among authors: erhart g. Hum Mol Genet. 2016 Aug 15;25(16):3635-3646. doi: 10.1093/hmg/ddw211. Epub 2016 Jul 12. Hum Mol Genet. 2016. PMID: 27412012 Free PMC article.
Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma.
Kloss-Brandstätter A, Weissensteiner H, Erhart G, Schäfer G, Forer L, Schönherr S, Pacher D, Seifarth C, Stöckl A, Fendt L, Sottsas I, Klocker H, Huck CW, Rasse M, Kronenberg F, Kloss FR. Kloss-Brandstätter A, et al. Among authors: erhart g. PLoS One. 2015 Aug 11;10(8):e0135643. doi: 10.1371/journal.pone.0135643. eCollection 2015. PLoS One. 2015. PMID: 26262956 Free PMC article.
A novel but frequent variant in LPA KIV-2 is associated with a pronounced Lp(a) and cardiovascular risk reduction.
Coassin S, Erhart G, Weissensteiner H, Eca Guimarães de Araújo M, Lamina C, Schönherr S, Forer L, Haun M, Losso JL, Köttgen A, Schmidt K, Utermann G, Peters A, Gieger C, Strauch K, Finkenstedt A, Bale R, Zoller H, Paulweber B, Eckardt KU, Hüttenhofer A, Huber LA, Kronenberg F. Coassin S, et al. Among authors: erhart g. Eur Heart J. 2017 Jun 14;38(23):1823-1831. doi: 10.1093/eurheartj/ehx174. Eur Heart J. 2017. PMID: 28444229 Free PMC article.
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms.
Mack S, Coassin S, Rueedi R, Yousri NA, Seppälä I, Gieger C, Schönherr S, Forer L, Erhart G, Marques-Vidal P, Ried JS, Waeber G, Bergmann S, Dähnhardt D, Stöckl A, Raitakari OT, Kähönen M, Peters A, Meitinger T, Strauch K, Kedenko L, Paulweber B, Lehtimäki T, Hunt SC, Vollenweider P, Lamina C, Kronenberg F. Mack S, et al. Among authors: erhart g. J Lipid Res. 2017 Sep;58(9):1834-1844. doi: 10.1194/jlr.M076232. Epub 2017 May 16. J Lipid Res. 2017. PMID: 28512139 Free PMC article.
34 results