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A practical approach to detect ancestral haplotypes in livestock populations.

Sánchez-Molano E, Tsiokos D, Chatziplis D, Jorjani H, Degano L, Diaz C, Rossoni A, Schwarzenbacher H, Seefried F, Varona L, Vicario D, Nicolazzi EL, Banos G.

BMC Genet. 2016 Jun 24;17(1):91. doi: 10.1186/s12863-016-0405-2.


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(1):400. doi: 10.1186/s12864-016-2742-y.


Clinical and biochemical signs in Fleckvieh cattle with genetically confirmed Fanconi-Bickel syndrome (cattle homozygous for Fleckvieh haplotype 2).

Burgstaller J, Url A, Pausch H, Schwarzenbacher H, Egerbacher M, Wittek T.

Berl Munch Tierarztl Wochenschr. 2016 Mar-Apr;129(3-4):132-7.


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.


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.

Genet Sel Evol. 2016 Mar 18;48:21. doi: 10.1186/s12711-016-0201-5.


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.

Genet Sel Evol. 2016 Feb 16;48:14. doi: 10.1186/s12711-016-0190-4.


A comparison of methods to calculate a total merit index using stochastic simulation.

Pfeiffer C, Fuerst-Waltl B, Schwarzenbacher H, Steininger F, Fuerst C.

Genet Sel Evol. 2015 May 2;47:36. doi: 10.1186/s12711-015-0118-4.


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.

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


Genomic regions influencing coat color saturation and facial markings in Fleckvieh cattle.

Mészáros G, Petautschnig E, Schwarzenbacher H, Sölkner J.

Anim Genet. 2015 Feb;46(1):65-8. doi: 10.1111/age.12249. Epub 2014 Dec 16.


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.

BMC Genomics. 2014 Jul 22;15:623. doi: 10.1186/1471-2164-15-623.


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. Epub 2014 Jan 2.


Short-term intermittent hypoxia reduces the severity of acute mountain sickness.

Wille M, Gatterer H, Mairer K, Philippe M, Schwarzenbacher H, Faulhaber M, Burtscher M.

Scand J Med Sci Sports. 2012 Oct;22(5):e79-85. doi: 10.1111/j.1600-0838.2012.01499.x. Epub 2012 Aug 1.


Hot topic: Effect of breeding strategies using genomic information on fitness and health.

Egger-Danner C, Willam A, Fuerst C, Schwarzenbacher H, Fuerst-Waltl B.

J Dairy Sci. 2012 Aug;95(8):4600-9. doi: 10.3168/jds.2012-5323.


Recording of direct health traits in Austria--experience report with emphasis on aspects of availability for breeding purposes.

Egger-Danner C, Fuerst-Waltl B, Obritzhauser W, Fuerst C, Schwarzenbacher H, Grassauer B, Mayerhofer M, Koeck A.

J Dairy Sci. 2012 May;95(5):2765-77. doi: 10.3168/jds.2011-4876.


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.


A novel mutation in the maternally imprinted PEG3 domain results in a loss of MIMT1 expression and causes abortions and stillbirths in cattle (Bos taurus).

Flisikowski K, Venhoranta H, Nowacka-Woszuk J, McKay SD, Flyckt A, Taponen J, Schnabel R, Schwarzenbacher H, Szczerbal I, Lohi H, Fries R, Taylor JF, Switonski M, Andersson M.

PLoS One. 2010 Nov 30;5(11):e15116. doi: 10.1371/journal.pone.0015116.


Haplotypes of the porcine peroxisome proliferator-activated receptor delta gene are associated with backfat thickness.

Meidtner K, Schwarzenbacher H, Scharfe M, Severitt S, Blöcker H, Fries R.

BMC Genet. 2009 Nov 30;10:76. doi: 10.1186/1471-2156-10-76.


Characterization of the porcine AMPK alpha 2 catalytic subunitgene (PRKAA2): genomic structure, polymorphism detection and association study.

Lin L, Flisikowski K, Schwarzenbacher H, Scharfe M, Severitt S, Blöcker H, Fries R.

Anim Genet. 2010 Apr;41(2):203-7. doi: 10.1111/j.1365-2052.2009.01971.x. Epub 2009 Sep 29.


Variation in neighbouring genes of the dopaminergic and serotonergic systems affects feather pecking behaviour of laying hens.

Flisikowski K, Schwarzenbacher H, Wysocki M, Weigend S, Preisinger R, Kjaer JB, Fries R.

Anim Genet. 2009 Apr;40(2):192-9. doi: 10.1111/j.1365-2052.2008.01821.x. Epub 2008 Dec 18.

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