| Genome-wide association study between copy number variants and hoof health traits in Holstein dairy cattle AM Butty, TCS Chud, DF Cardoso, LSF Lopes, F Miglior, FS Schenkel, ... Journal of dairy science 104 (7), 8050-8061, 2021 | 23 | 2021 |
| A non‐coding regulatory variant in the 5′‐region of the MITF gene is associated with white‐spotted coat in Brown Swiss cattle S Hofstetter, F Seefried, IM Häfliger, V Jagannathan, T Leeb, ... Animal genetics 50 (1), 27-32, 2019 | 22 | 2019 |
| Identification of small and large genomic candidate variants in bovine pulmonary hypoplasia and anasarca syndrome IM Häfliger, N Wiedemar, T Švara, J Starič, V Cociancich, K Šest, ... Animal genetics 51 (3), 382-390, 2020 | 21 | 2020 |
| New genomic features of the polled intersex syndrome variant in goats unraveled by long‐read whole‐genome sequencing R Simon, HEL Lischer, A Pieńkowska‐Schelling, I Keller, IM Häfliger, ... Animal genetics 51 (3), 439-448, 2020 | 21 | 2020 |
| Chromosomal imbalance in pigs showing a syndromic form of cleft palate A Grahofer, A Letko, IM Häfliger, V Jagannathan, A Ducos, O Richard, ... BMC genomics 20, 1-11, 2019 | 20 | 2019 |
| Evaluation of an investigative model in dairy herds with high calf perinatal mortality rates in Switzerland T Mock, JF Mee, M Dettwiler, S Rodriguez-Campos, J Hüsler, B Michel, ... Theriogenology 148, 48-59, 2020 | 19 | 2020 |
| A complex structural variant at the KIT locus in cattle with the Pinzgauer spotting pattern L Küttel, A Letko, IM Häfliger, H Signer‐Hasler, S Joller, G Hirsbrunner, ... Animal genetics 50 (5), 423-429, 2019 | 19 | 2019 |
| A major QTL at the LHCGR/FSHR locus for multiple birth in Holstein cattle S Widmer, FR Seefried, P von Rohr, IM Häfliger, M Spengeler, ... Genetics selection evolution 53 (1), 57, 2021 | 17 | 2021 |
| High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data AM Butty, TCS Chud, F Miglior, FS Schenkel, A Kommadath, K Krivushin, ... Scientific reports 10 (1), 8044, 2020 | 17 | 2020 |
| Identification of two TYRP1 loss‐of‐function alleles in Valais Red sheep JM Paris, A Letko, IM Häfliger, P Ammann, C Flury, C Drögemüller Animal genetics 50 (6), 778-782, 2019 | 15 | 2019 |
| Four novel candidate causal variants for deficient homozygous haplotypes in Holstein cattle IM Häfliger, M Spengeler, FR Seefried, C Drögemüller Scientific reports 12 (1), 5435, 2022 | 14 | 2022 |
| APOB‐associated cholesterol deficiency in Holstein cattle is not a simple recessive disease IM Häfliger, S Hofstetter, T Mock, MH Stettler, M Meylan, K Mehinagic, ... Animal genetics 50 (4), 372-375, 2019 | 13 | 2019 |
| Ear type in sheep is associated with the MSRB3 locus JM Paris, A Letko, IM Häfliger, P Ammann, C Drögemüller Animal genetics 51 (6), 968-972, 2020 | 11 | 2020 |
| A Heterozygous Missense Variant in the COL5A2 in Holstein Cattle Resembling the Classical Ehlers–Danlos Syndrome JGP Jacinto, IM Häfliger, IMB Veiga, A Letko, C Benazzi, M Bolcato, ... Animals 10 (11), 2002, 2020 | 11 | 2020 |
| An ABCA12 missense variant in a Shorthorn calf with ichthyosis fetalis SA Woolley, KLM Eager, IM Häfliger, A Bauer, C Drögemüller, T Leeb, ... Animal genetics 50 (6), 749-752, 2019 | 10 | 2019 |
| KCNG1-Related Syndromic Form of Congenital Neuromuscular Channelopathy in a Crossbred Calf JGP Jacinto, IM Häfliger, EE Akyürek, R Sacchetto, C Benazzi, A Gentile, ... Genes 12 (11), 1792, 2021 | 9 | 2021 |
| Mining massive genomic data of two Swiss Braunvieh cattle populations reveals six novel candidate variants that impair reproductive success IM Häfliger, FR Seefried, M Spengeler, C Drögemüller Genetics Selection Evolution 53, 1-16, 2021 | 8 | 2021 |
| Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy A Letko, B Strugnell, IM Häfliger, JM Paris, K Waine, C Drögemüller, ... Molecular Genetics and Genomics 296 (1), 235-242, 2021 | 8 | 2021 |
| Trisomy 29 in a stillborn Swiss Original Braunvieh calf. IM Häfliger, F Seefried, C Drögemüller Animal genetics 51 (3), 2020 | 8 | 2020 |
| A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle JGP Jacinto, IM Häfliger, IMB Veiga, A Letko, A Gentile, C Drögemüller Molecular Genetics and Genomics 296 (6), 1313-1322, 2021 | 7 | 2021 |
Cord DrögemüllerProfessor of Animal Genetics, University of Bern, SwitzerlandVerified email at unibe.ch
