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Items: 12

1.

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.

BMC Genet. 2016 Dec 1;17(1):149.

PMID:
27905875
2.

Identification of a haplotype associated with cholesterol deficiency and increased juvenile mortality in Holstein cattle.

Kipp S, Segelke D, Schierenbeck S, Reinhardt F, Reents R, Wurmser C, Pausch H, Fries R, Thaller G, Tetens J, Pott J, Haas D, Raddatz BB, Hewicker-Trautwein M, Proios I, Schmicke M, Grünberg W.

J Dairy Sci. 2016 Nov;99(11):8915-8931. doi: 10.3168/jds.2016-11118.

PMID:
27614835
3.

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.

BMC Genomics. 2016 May 25;17:400. doi: 10.1186/s12864-016-2742-y.

4.

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.

Genet Sel Evol. 2016 Mar 31;48:25. doi: 10.1186/s12711-016-0207-z.

5.

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.

BMC Genet. 2016 Feb 29;17:49. doi: 10.1186/s12863-016-0356-7.

6.

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.

BMC Genomics. 2015 Apr 18;16:312. doi: 10.1186/s12864-015-1483-7.

7.

Short communication: Validation of 4 candidate causative trait variants in 2 cattle breeds using targeted sequence imputation.

Pausch H, Wurmser C, Reinhardt F, Emmerling R, Fries R.

J Dairy Sci. 2015 Jun;98(6):4162-7. doi: 10.3168/jds.2015-9402.

PMID:
25892690
8.

In frame exon skipping in UBE3B is associated with developmental disorders and increased mortality in cattle.

Venhoranta H, Pausch H, Flisikowski K, Wurmser C, Taponen J, Rautala H, Kind A, Schnieke A, Fries R, Lohi H, Andersson M.

BMC Genomics. 2014 Oct 12;15:890. doi: 10.1186/1471-2164-15-890.

9.

A nonsense mutation in TMEM95 encoding a nondescript transmembrane protein causes idiopathic male subfertility in cattle.

Pausch H, Kölle S, Wurmser C, Schwarzenbacher H, Emmerling R, Jansen S, Trottmann M, Fuerst C, Götz KU, Fries R.

PLoS Genet. 2014 Jan;10(1):e1004044. doi: 10.1371/journal.pgen.1004044.

10.

Short communication: evaluation of bovine milk residues from routine milk testing programs as DNA source for genotyping.

Krappmann K, Wurmser C, Repsilber D, Fries R, Weikard R, Kesting U, Kühn C.

J Dairy Sci. 2012 Sep;95(9):5436-41. doi: 10.3168/jds.2011-5259.

PMID:
22916950
11.

Identification and dissection of four major QTL affecting milk fat content in the German Holstein-Friesian population.

Wang X, Wurmser C, Pausch H, Jung S, Reinhardt F, Tetens J, Thaller G, Fries R.

PLoS One. 2012;7(7):e40711. doi: 10.1371/journal.pone.0040711.

12.

Combining evidence of selection with association analysis increases power to detect regions influencing complex traits in dairy cattle.

Schwarzenbacher H, Dolezal M, Flisikowski K, Seefried F, Wurmser C, Schlötterer C, Fries R.

BMC Genomics. 2012 Jan 30;13:48. doi: 10.1186/1471-2164-13-48.

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