Author

Fredi Janett

University of Zurich

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 2 Genomics· 2

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Approach:statistical model· 3 Approach:experimental assay· 2 Assay:whole-genome sequencing· 2 Organism:bacteria (other)· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1 Organism:multiple species· 1 Organism:plant (other)· 1

Frequent Co-Authors

Hubert PauschiD· 4 shared Maya HiltpoldiD· 3 shared Naveen Kumar KadriiD· 2 shared Stefan NeuenschwanderiD· 2 shared Ulrich WitschiiD· 2 shared Xena Marie MapeliD· 2 shared Zih‐Hua FangiD· 2 shared Adéla NoskováiD· 1 shared

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2020-2024 · peak 1/yr

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10 top collaborators · 31 mutual co-author links

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4 shared papersGenomics

Hubert PauschORCID

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4 papers

Recent·Most cited

Wisent genome assembly uncovers extended runs of homozygosity and a large deletion that inactivates the thyroid hormone responsive gene

Chiara Bortoluzzi, Xena Marie Mapel, Stefan Neuenschwander, Fredi Janett, Hubert Pausch, Alexander S. Leonard

The paper presents a high-quality wisent genome assembly, identifies a deletion inactivating the THRSP gene, and shows its absence in bison compared to cattle and water buffalo.

bioRxiv · Apr 8, 2024 · PreprintGenomics

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

Maya Hiltpold, Fredi Janett, Xena Marie Mapel, Naveen Kumar Kadri, Zih‐Hua Fang, Hermann Schwarzenbacher, Franz R. Seefried, Mirjam Spengeler, Ulrich Witschi, Hubert Pausch

The paper identifies a 1-bp deletion in QRICH2 as a recessive cause of low sperm count and immotile sperm with morphological abnormalities in Brown Swiss bulls.

Genetics Selection Evolution · Mar 7, 2022Peer-reviewedGenetics

Autosomal recessive loci contribute significantly to quantitative variation of male fertility in a dairy cattle population

Maya Hiltpold, Naveen Kumar Kadri, Fredi Janett, Ulrich Witschi, Fritz Schmitz‐Hsu, Hubert Pausch

The paper identifies four novel recessive QTL for male fertility in dairy cattle and prioritizes a missense variant in SPATA16 as a candidate causal variant.

BMC Genomics · Mar 30, 2021Peer-reviewedGenetics

Infertility due to defective sperm flagella caused by an intronic deletion in DNAH17 that perturbs splicing

Adéla Nosková, Maya Hiltpold, Fredi Janett, Thomas Echtermann, Zih‐Hua Fang, Xaver Sidler, Christin Selige, Andreas Hofer A, Stefan Neuenschwander, Hubert Pausch

The paper identifies an intronic deletion in DNAH17 causing infertility in pigs due to defective sperm flagella by disrupting splicing and axoneme assembly.

Genetics · Dec 18, 2020Peer-reviewedGenomics