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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.


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 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.


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.


The Epigenomic Landscape of Prokaryotes.

Blow MJ, Clark TA, Daum CG, Deutschbauer AM, Fomenkov A, Fries R, Froula J, Kang DD, Malmstrom RR, Morgan RD, Posfai J, Singh K, Visel A, Wetmore K, Zhao Z, Rubin EM, Korlach J, Pennacchio LA, Roberts RJ.

PLoS Genet. 2016 Feb 12;12(2):e1005854. doi: 10.1371/journal.pgen.1005854. eCollection 2016 Feb. Erratum in: PLoS Genet. 2016 May;12(5):e1006064.


Severe hyperkalemia presenting with wide-complex tachycardia in a puppy with acute kidney injury secondary to leptospirosis.

Rubanick JV, Fries RC, Waugh CE, Pashmakova MB.

J Vet Emerg Crit Care (San Antonio). 2016 Feb 10. doi: 10.1111/vec.12454. [Epub ahead of print]


Isolation of Multidrug-Resistant Escherichia coli O157 from Goats in the Somali Region of Ethiopia: A Cross-Sectional, Abattoir-Based Study.

Dulo F, Feleke A, Szonyi B, Fries R, Baumann MP, Grace D.

PLoS One. 2015 Nov 11;10(11):e0142905. doi: 10.1371/journal.pone.0142905. eCollection 2015.


Copy number variation in the region harboring SOX9 gene in dogs with testicular/ovotesticular disorder of sex development (78,XX; SRY-negative).

Marcinkowska-Swojak M, Szczerbal I, Pausch H, Nowacka-Woszuk J, Flisikowski K, Dzimira S, Nizanski W, Payan-Carreira R, Fries R, Kozlowski P, Switonski M.

Sci Rep. 2015 Oct 1;5:14696. doi: 10.1038/srep14696.


Influence of two catching methods on the occurrence of lesions in broilers.

Langkabel N, Baumann MP, Feiler A, Sanguankiat A, Fries R.

Poult Sci. 2015 Aug;94(8):1735-41. doi: 10.3382/ps/pev164. Epub 2015 Jun 18.


Microbiological load and zoonotic agents in beef mortadella from Addis Ababa city supermarkets.

Hiko A, Ameni G, Langkabel N, Fries R.

J Food Prot. 2015 May;78(5):1043-5. doi: 10.4315/0362-028X.JFP-14-395.


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.


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. Epub 2015 Apr 16.


Evaluation of variant identification methods for whole genome sequencing data in dairy cattle.

Baes CF, Dolezal MA, Koltes JE, Bapst B, Fritz-Waters E, Jansen S, Flury C, Signer-Hasler H, Stricker C, Fernando R, Fries R, Moll J, Garrick DJ, Reecy JM, Gredler B.

BMC Genomics. 2014 Nov 1;15:948. doi: 10.1186/1471-2164-15-948.


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.


A powerful tool for genome analysis in maize: development and evaluation of the high density 600 k SNP genotyping array.

Unterseer S, Bauer E, Haberer G, Seidel M, Knaak C, Ouzunova M, Meitinger T, Strom TM, Fries R, Pausch H, Bertani C, Davassi A, Mayer KF, Schön CC.

BMC Genomics. 2014 Sep 29;15:823. doi: 10.1186/1471-2164-15-823.


Quantification of water as a potential risk factor for cross-contamination with Salmonella, Campylobacter and Listeria in a poultry abattoir.

Hamidi A, Irsigler H, Jaeger D, Muschaller A, Fries R.

Br Poult Sci. 2014;55(5):585-91. doi: 10.1080/00071668.2014.949622. Epub 2014 Oct 17.


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.


Whole-genome sequencing of 234 bulls facilitates mapping of monogenic and complex traits in cattle.

Daetwyler HD, Capitan A, Pausch H, Stothard P, van Binsbergen R, Brøndum RF, Liao X, Djari A, Rodriguez SC, Grohs C, Esquerré D, Bouchez O, Rossignol MN, Klopp C, Rocha D, Fritz S, Eggen A, Bowman PJ, Coote D, Chamberlain AJ, Anderson C, VanTassell CP, Hulsegge I, Goddard ME, Guldbrandtsen B, Lund MS, Veerkamp RF, Boichard DA, Fries R, Hayes BJ.

Nat Genet. 2014 Aug;46(8):858-65. doi: 10.1038/ng.3034. Epub 2014 Jul 13.

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