Pausch H - Search Results

1

Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs.

Nosková A, Bhati M, Kadri NK, Crysnanto D, Neuenschwander S, Hofer A, Pausch H. Nosková A, et al. Among authors: pausch h. BMC Genomics. 2021 Apr 21;22(1):290. doi: 10.1186/s12864-021-07610-5. BMC Genomics. 2021. PMID: 33882824 Free PMC article.

2

Adenylate kinase 9 is essential for sperm function and male fertility in mammals.

O'Callaghan E, Navarrete-Lopez P, Štiavnická M, Sánchez JM, Maroto M, Pericuesta E, Fernández-González R, O'Meara C, Eivers B, Kelleher MM, Evans RD, Mapel XM, Lloret-Villas A, Pausch H, Balastegui-Alarcón M, Avilés M, Sanchez-Rodriguez A, Roldan ERS, McDonald M, Kenny DA, Fair S, Gutiérrez-Adán A, Lonergan P. O'Callaghan E, et al. Among authors: pausch h. Proc Natl Acad Sci U S A. 2023 Oct 17;120(42):e2305712120. doi: 10.1073/pnas.2305712120. Epub 2023 Oct 9. Proc Natl Acad Sci U S A. 2023. PMID: 37812723 Free PMC article.

3

Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage.

Jansen S, Aigner B, Pausch H, Wysocki M, Eck S, Benet-Pagès A, Graf E, Wieland T, Strom TM, Meitinger T, Fries R. Jansen S, et al. Among authors: pausch h. BMC Genomics. 2013 Jul 4;14:446. doi: 10.1186/1471-2164-14-446. BMC Genomics. 2013. PMID: 23826801 Free PMC article.

4

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: pausch h. BMC Genomics. 2014 Jul 22;15(1):623. doi: 10.1186/1471-2164-15-623. BMC Genomics. 2014. PMID: 25052073 Free PMC article.

5

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. Unterseer S, et al. Among authors: pausch h. BMC Genomics. 2014 Sep 29;15(1):823. doi: 10.1186/1471-2164-15-823. BMC Genomics. 2014. PMID: 25266061 Free PMC article.

6

Comparison among three variant callers and assessment of the accuracy of imputation from SNP array data to whole-genome sequence level in chicken.

Ni G, Strom TM, Pausch H, Reimer C, Preisinger R, Simianer H, Erbe M. Ni G, et al. Among authors: pausch h. BMC Genomics. 2015 Oct 21;16:824. doi: 10.1186/s12864-015-2059-2. BMC Genomics. 2015. PMID: 26486989 Free PMC article.

7

Meta-analysis of sequence-based association studies across three cattle breeds reveals 25 QTL for fat and protein percentages in milk at nucleotide resolution.

Pausch H, Emmerling R, Gredler-Grandl B, Fries R, Daetwyler HD, Goddard ME. Pausch H, et al. BMC Genomics. 2017 Nov 9;18(1):853. doi: 10.1186/s12864-017-4263-8. BMC Genomics. 2017. PMID: 29121857 Free PMC article.

8

Highly accurate sequence imputation enables precise QTL mapping in Brown Swiss cattle.

Frischknecht M, Pausch H, Bapst B, Signer-Hasler H, Flury C, Garrick D, Stricker C, Fries R, Gredler-Grandl B. Frischknecht M, et al. Among authors: pausch h. BMC Genomics. 2017 Dec 29;18(1):999. doi: 10.1186/s12864-017-4390-2. BMC Genomics. 2017. PMID: 29284405 Free PMC article.

9

A splice donor variant in CCDC189 is associated with asthenospermia in Nordic Red dairy cattle.

Iso-Touru T, Wurmser C, Venhoranta H, Hiltpold M, Savolainen T, Sironen A, Fischer K, Flisikowski K, Fries R, Vicente-Carrillo A, Alvarez-Rodriguez M, Nagy S, Mutikainen M, Peippo J, Taponen J, Sahana G, Guldbrandtsen B, Simonen H, Rodriguez-Martinez H, Andersson M, Pausch H. Iso-Touru T, et al. Among authors: pausch h. BMC Genomics. 2019 Apr 11;20(1):286. doi: 10.1186/s12864-019-5628-y. BMC Genomics. 2019. PMID: 30975085 Free PMC article.

10

Accurate sequence variant genotyping in cattle using variation-aware genome graphs.

Crysnanto D, Wurmser C, Pausch H. Crysnanto D, et al. Among authors: pausch h. Genet Sel Evol. 2019 May 15;51(1):21. doi: 10.1186/s12711-019-0462-x. Genet Sel Evol. 2019. PMID: 31092189 Free PMC article.

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