Fries R - Search Results

1

A frameshift mutation in GON4L is associated with proportionate dwarfism in Fleckvieh cattle.

Schwarzenbacher H, Wurmser C, Flisikowski K, Misurova L, Jung S, Langenmayer MC, Schnieke A, Knubben-Schweizer G, Fries R, Pausch H. Schwarzenbacher H, et al. Among authors: fries r. Genet Sel Evol. 2016 Mar 31;48:25. doi: 10.1186/s12711-016-0207-z. Genet Sel Evol. 2016. PMID: 27036302 Free PMC article.

2

Imputation of high-density genotypes in the Fleckvieh cattle population.

Pausch H, Aigner B, Emmerling R, Edel C, Götz KU, Fries R. Pausch H, et al. Among authors: fries r. Genet Sel Evol. 2013 Feb 13;45(1):3. doi: 10.1186/1297-9686-45-3. Genet Sel Evol. 2013. PMID: 23406470 Free PMC article.

3

A nonsense mutation in PLD4 is associated with a zinc deficiency-like syndrome in Fleckvieh cattle.

Jung S, Pausch H, Langenmayer MC, Schwarzenbacher H, Majzoub-Altweck M, Gollnick NS, Fries R. Jung S, et al. Among authors: fries r. BMC Genomics. 2014 Jul 22;15(1):623. doi: 10.1186/1471-2164-15-623. BMC Genomics. 2014. PMID: 25052073 Free PMC article.

4

Homozygous haplotype deficiency reveals deleterious mutations compromising reproductive and rearing success in cattle.

Pausch H, Schwarzenbacher H, Burgstaller J, Flisikowski K, Wurmser C, Jansen S, Jung S, Schnieke A, Wittek T, Fries R. Pausch H, et al. Among authors: fries r. BMC Genomics. 2015 Apr 18;16(1):312. doi: 10.1186/s12864-015-1483-7. BMC Genomics. 2015. PMID: 25927203 Free PMC article.

5

A multi-trait meta-analysis with imputed sequence variants reveals twelve QTL for mammary gland morphology in Fleckvieh cattle.

Pausch H, Emmerling R, Schwarzenbacher H, Fries R. Pausch H, et al. Among authors: fries r. Genet Sel Evol. 2016 Feb 16;48:14. doi: 10.1186/s12711-016-0190-4. Genet Sel Evol. 2016. PMID: 26883850 Free PMC article.

6

A frameshift mutation in ARMC3 is associated with a tail stump sperm defect in Swedish Red (Bos taurus) cattle.

Pausch H, Venhoranta H, Wurmser C, Hakala K, Iso-Touru T, Sironen A, Vingborg RK, Lohi H, Söderquist L, Fries R, Andersson M. Pausch H, et al. Among authors: fries r. BMC Genet. 2016 Feb 29;17:49. doi: 10.1186/s12863-016-0356-7. BMC Genet. 2016. PMID: 26923438 Free PMC article.

7

Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle.

Kunz E, Rothammer S, Pausch H, Schwarzenbacher H, Seefried FR, Matiasek K, Seichter D, Russ I, Fries R, Medugorac I. Kunz E, et al. Among authors: fries r. Genet Sel Evol. 2016 Mar 18;48:21. doi: 10.1186/s12711-016-0201-5. Genet Sel Evol. 2016. PMID: 26992691 Free PMC article.

8

A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle.

Schwarzenbacher H, Burgstaller J, Seefried FR, Wurmser C, Hilbe M, Jung S, Fuerst C, Dinhopl N, Weissenböck H, Fuerst-Waltl B, Dolezal M, Winkler R, Grueter O, Bleul U, Wittek T, Fries R, Pausch H. Schwarzenbacher H, et al. Among authors: fries r. BMC Genomics. 2016 May 25;17:400. doi: 10.1186/s12864-016-2742-y. BMC Genomics. 2016. PMID: 27225349 Free PMC article.

9

A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle.

Pausch H, Ammermüller S, Wurmser C, Hamann H, Tetens J, Drögemüller C, Fries R. Pausch H, et al. Among authors: fries r. BMC Genet. 2016 Dec 1;17(1):149. doi: 10.1186/s12863-016-0458-2. BMC Genet. 2016. PMID: 27905875 Free PMC article.

10

Evaluation of the accuracy of imputed sequence variant genotypes and their utility for causal variant detection in cattle.

Pausch H, MacLeod IM, Fries R, Emmerling R, Bowman PJ, Daetwyler HD, Goddard ME. Pausch H, et al. Among authors: fries r. Genet Sel Evol. 2017 Feb 21;49(1):24. doi: 10.1186/s12711-017-0301-x. Genet Sel Evol. 2017. PMID: 28222685 Free PMC article.

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