M. Spengeler

A major QTL at the LHCGR/FSHR locus for multiple birth in Holstein cattle

P. von Rohr, C. Drögemüller, F. Seefried, 2021, Genetics, selection, evolution : GSE.

Four novel candidate causal variants for deficient homozygous haplotypes in Holstein cattle

C. Drögemüller, F. Seefried, I. Häfliger, 2022, Scientific Reports.

Activation of cryptic splicing in bovine WDR19 is associated with reduced semen quality and male fertility

A. Schnieke, F. Schmitz-Hsu, H. Schwarzenbacher, 2020, bioRxiv.

Christmas disease in a Hovawart family resembling human hemophilia B Leyden is caused by a single nucleotide deletion in a highly conserved transcription factor binding site of the F9 gene promoter

M. Hirschfeld, B. Brenig, T. Leeb, 2018, Haematologica.

523. Sequence-based GWAS meta-analyses for beef production traits

D. Boichard, M. Boussaha, P. Chitneedi, 2022, Proceeding of 12th World Congress on Genetics Applied to Livestock Production (WCGALP).

Mining massive genomic data of two Swiss Braunvieh cattle populations reveals six novel candidate variants that impair reproductive success

C. Drögemüller, F. Seefried, I. Häfliger, 2021, Genetics Selection Evolution.

Mining massive genomic data of two Swiss Braunvieh cattle populations reveals six novel candidate variants that impair reproductive success

C. Drögemüller, F. Seefried, I. Häfliger, 2021, Genetics, selection, evolution : GSE.

CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle

C. Drögemüller, F. Seefried, I. Häfliger, 2021, International journal of molecular sciences.

A 1-bp deletion in bovine QRICH2 causes low sperm count and immotile sperm with multiple morphological abnormalities

H. Schwarzenbacher, F. Seefried, H. Pausch, 2021, bioRxiv.