Works matching AU Drögemüller, Cord

Results: 177

Social Values, Individual Judgments and Acceptance: The Case of High-Level Radioactive Waste in Germany.

Published in:

Sustainability (2071-1050), 2025, v. 17, n. 12, p. 5373, doi. 10.3390/su17125373

By:

Drögemüller, Cord;
Seidl, Roman;
Walther, Clemens

Publication type:

Article

Imputation of sequence level genotypes in the Franches-Montagnes horse breed.

Published in:

Genetics Selection Evolution, 2014, v. 46, p. 1, doi. 10.1186/s12711-014-0063-7

By:

Frischknecht, Mirjam;
Neuditschko, Markus;
Jagannathan, Vidhya;
Drögemüller, Cord;
Tetens, Jens;
Thaller, Georg;
Leeb, Tosso;
Rieder, Stefan

Publication type:

Article

Identification of a second encephalitis-associated astrovirus in cattle.

Published in:

Emerging Microbes & Infections, 2017, v. 6, n. 1, p. 1, doi. 10.1038/emi.2017.56

By:

Seuberlich, Torsten;
Wüthrich, Daniel;
Selimovic-Hamza, Senija;
Drögemüller, Cord;
Oevermann, Anna;
Bruggmann, Rémy;
Bouzalas, Ilias

Publication type:

Article

Identification of a second encephalitis-associated astrovirus in cattle.

Published in:

Emerging Microbes & Infections, 2016, v. 5, n. 1, p. e5, doi. 10.1038/emi.2016.5

By:

Seuberlich, Torsten;
Wüthrich, Daniel;
Selimovic-Hamza, Senija;
Drögemüller, Cord;
Oevermann, Anna;
Bruggmann, Rémy;
Bouzalas, Ilias

Publication type:

Article

Identification of a de novo missense variant in the BRI3BP gene in a Holstein calf with congenital cardiac malformation and carpus valgus.

Published in:

Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13494

By:

He, Chang;
Grau‐Roma, Llorenç;
Schmid, Robin;
Häfliger, Irene M.;
Meylan, Mireille;
Drögemüller, Cord;
Jacinto, Joana G. P.

Publication type:

Article

Trisomy 26 in a Holstein calf with disorders of sex development.

Published in:

Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13489

By:

Freick, Markus;
Jacinto, Joana G. P.;
Häfliger, Irene M.;
Weber, Jim;
Behn, Holger;
Schreiter, Ruben;
Drögemüller, Cord

Publication type:

Article

Renal dysplasia in Leonberger dogs – An emerging recessive congenital disorder?

Published in:

Animal Genetics, 2024, v. 55, n. 4, p. 700, doi. 10.1111/age.13439

By:

Letko, Anna;
Gurtner, Corinne;
Jagannathan, Vidhya;
Drögemüller, Cord

Publication type:

Article

MFSD2A frameshift variant in Kerry Hill sheep with microcephaly.

Published in:

Animal Genetics, 2024, v. 55, n. 1, p. 152, doi. 10.1111/age.13374

By:

Rudd Garces, Gabriela;
Letko, Anna;
Häfliger, Irene M.;
Müller, Jana;
Herden, Christiane;
Nesseler, Anne;
Wagner, Henrik;
Schmidt, Martin J.;
Drögemüller, Cord;
Lühken, Gesine

Publication type:

Article

DYRK1B haploinsufficiency in a Holstein cattle with epilepsy.

Published in:

Animal Genetics, 2023, v. 54, n. 5, p. 623, doi. 10.1111/age.13348

By:

Jacinto, Joana G. P.;
Bolcato, Marilena;
Häfliger, Irene M.;
Oevermann, Anna;
Gentile, Arcangelo;
Drögemüller, Cord

Publication type:

Article

Increased heterozygosity in low‐pass sequencing data allows identification of blood chimeras in cattle.

Published in:

Animal Genetics, 2023, v. 54, n. 5, p. 613, doi. 10.1111/age.13334

By:

Lindtke, Dorothea;
Seefried, Franz R.;
Drögemüller, Cord;
Neuditschko, Markus

Publication type:

Article

MYH3‐associated non‐syndromic palatoschisis (cleft palate, CP) in Limousine cattle.

Published in:

Animal Genetics, 2023, v. 54, n. 4, p. 581, doi. 10.1111/age.13317

By:

Jacinto, Joana G. P.;
Schiavon, Eliana;
Häfliger, Irene M.;
Coin, Patrizio;
Seefried, Franz R.;
Drögemüller, Cord

Publication type:

Article

Genomic regions underlying positive selection in local, Alpine cattle breeds.

Published in:

Animal Genetics, 2023, v. 54, n. 3, p. 239, doi. 10.1111/age.13295

By:

Signer‐Hasler, Heidi;
Casanova, Lucas;
Barenco, Alex;
Maitre, Blaise;
Bagnato, Alessandro;
Vevey, Mario;
Berger, Beate;
Simčič, Mojca;
Boichon, Denis;
Capitan, Aurélien;
Medugorac, Ivica;
Bennewitz, Jörn;
Mészáros, Gábor;
Sölkner, Johann;
Drögemüller, Cord;
Flury, Christine

Publication type:

Article

Canine reference genome accuracy impacts variant calling: Lessons learned from investigating embryonic lethal variants.

Published in:

Animal Genetics, 2022, v. 53, n. 5, p. 706, doi. 10.1111/age.13241

By:

Kinsey, Nathan A.;
Belanger, Janelle M.;
Oberbauer, Anita M.;
Aguirre, Gustavo;
André, Catherine;
Bannasch, Danika;
Becker, Doreen;
Davis, Brian;
Drögemüller, Cord;
Ekenstedt, Kari;
Faller, Kiterie;
Forman, Oliver;
Friedenberg, Steven;
Furrow, Eva;
Giger, Urs;
Hitte, Christophe;
Hytönen, Marjo;
Jagannathan, Vidhya;
Leeb, Tosso;
Lingaas, Frode

Publication type:

Article

A germline de novo variant in NUMB associated with a double‐outlet right ventricle in Chianina cattle.

Published in:

Animal Genetics, 2022, v. 53, n. 5, p. 713, doi. 10.1111/age.13236

By:

Jacinto, Joana G. P.;
Häfliger, Irene M.;
Caivano, Domenico;
Drögemüller, Cord

Publication type:

Article

The KIT:c.376G>A variant in German and Swiss alpacas (Vicugna pacos) with different coat colors.

Published in:

Animal Genetics, 2022, v. 53, n. 5, p. 718, doi. 10.1111/age.13231

By:

Tan, Kirsty;
Roy, Mia;
Manz, Eberhard;
Wagner, Henrik;
Zanolari, Patrik;
Drögemüller, Cord;
Lühken, Gesine

Publication type:

Article

Associated regions for multiple birth in Brown Swiss and Original Braunvieh cattle on chromosomes 15 and 11.

Published in:

Animal Genetics, 2022, v. 53, n. 5, p. 557, doi. 10.1111/age.13229

By:

Widmer, Sarah;
Seefried, Franz R.;
von Rohr, Peter;
Häfliger, Irene M.;
Spengeler, Mirjam;
Drögemüller, Cord

Publication type:

Article

Is a heterozygous missense variant in SGSH the cause of a syndromic form of congenital amastia in an Original Braunvieh calf?

Published in:

Animal Genetics, 2022, v. 53, n. 4, p. 530, doi. 10.1111/age.13207

By:

Jacinto, Joana G. P.;
Häfliger, Irene M.;
Christen, Matthias;
Paris, Julia M.;
Seefried, Franz R.;
Drögemüller, Cord

Publication type:

Article

Identification of two new recessive MC1R alleles in red‐coloured Evolèner cattle and other breeds.

Published in:

Animal Genetics, 2022, v. 53, n. 3, p. 427, doi. 10.1111/age.13206

By:

Hauser, Miriam;
Signer‐Hasler, Heidi;
Küttel, Luzia;
Capitan, Aurélien;
Guldbrandtsen, Bernt;
Hinrichs, Dirk;
Flury, Christine;
Seefried, Franz R.;
Drögemüller, Cord

Publication type:

Article

A de novo start‐lost variant in ANKRD28 in a Holstein calf with dwarfism.

Published in:

Animal Genetics, 2022, v. 53, n. 3, p. 470, doi. 10.1111/age.13204

By:

Jacinto, Joana G. P.;
Häfliger, Irene M.;
Baes, Christine F.;
de Oliveira, Hinayah R.;
Drögemüller, Cord

Publication type:

Article

A de novo variant in the bovine ADAMTSL4 gene in an Original Braunvieh calf with congenital cataract.

Published in:

Animal Genetics, 2022, v. 53, n. 3, p. 416, doi. 10.1111/age.13178

By:

Häfliger, Irene M.;
Wolf‐Hofstetter, Sonja;
Casola, Christina;
Hetzel, Udo;
Seefried, Franz R.;
Drögemüller, Cord

Publication type:

Article

Evaluation of truncating variants in the LCORL gene in relation to body size of goats from Switzerland.

Published in:

Animal Genetics, 2022, v. 53, n. 2, p. 237, doi. 10.1111/age.13177

By:

Graber, Jennifer Kalinka;
Signer‐Hasler, Heidi;
Burren, Alexander;
Drögemüller, Cord

Publication type:

Article

Genetic evaluation of small ruminant lentivirus susceptibility in Valais blacknose sheep.

Published in:

Animal Genetics, 2021, v. 52, n. 5, p. 781, doi. 10.1111/age.13108

By:

Letko, Anna;
Bützberger, Charis;
Hirter, Nathalie;
Paris, Julia M.;
Abril, Carlos;
Drögemüller, Cord

Publication type:

Article

The previously reported LRP4 c.4940C>T variant is not associated with syndactyly in cattle.

Published in:

Animal Genetics, 2021, v. 52, n. 3, p. 380, doi. 10.1111/age.13061

By:

Eager, Katie L.M.;
Cauchi, Monique;
Willet, Cali E.;
Häfliger, Irene M.;
Drögemüller, Cord;
O'Rourke, Brendon A.;
Tammen, Imke

Publication type:

Article

A 6.7 kb deletion in the COL2A1 gene in a Holstein calf with achondrogenesis type II and perosomus elumbis.

Published in:

Animal Genetics, 2021, v. 52, n. 2, p. 244, doi. 10.1111/age.13033

By:

Jacinto, Joana G. P.;
Häfliger, Irene M.;
Gentile, Arcangelo;
Drögemüller, Cord;
Bolcato, Marilena

Publication type:

Article

Constitutional trisomy 20 in an aborted Holstein fetus with pulmonary hypoplasia and anasarca syndrome.

Published in:

Animal Genetics, 2020, v. 51, n. 6, p. 988, doi. 10.1111/age.13008

By:

Häfliger, Irene Monika;
Agerholm, Jørgen Steen;
Drögemüller, Cord

Publication type:

Article

Trisomy 29 in a stillborn Swiss Original Braunvieh calf.

Published in:

Animal Genetics, 2020, v. 51, n. 3, p. 483, doi. 10.1111/age.12929

By:

Häfliger, Irene Monika;
Seefried, Franz;
Drögemüller, Cord

Publication type:

Article

A de novo in‐frame duplication in the COL1A2 gene in a Lagotto Romagnolo dog with osteogenesis imperfecta.

Published in:

Animal Genetics, 2019, v. 50, n. 6, p. 786, doi. 10.1111/age.12843

By:

Letko, Anna;
Zdora, Isabel;
Hitzler, Valerie;
Jagannathan, Vidhya;
Beineke, Andreas;
Möhrke, Carola;
Drögemüller, Cord

Publication type:

Article

APOB‐associated cholesterol deficiency in Holstein cattle is not a simple recessive disease.

Published in:

Animal Genetics, 2019, v. 50, n. 4, p. 372, doi. 10.1111/age.12801

By:

Häfliger, Irene Monika;
Hofstetter, Sonja;
Mock, Thomas;
Stettler, Manuela Hanna;
Meylan, Mireille;
Mehinagic, Kemal;
Stokar‐Regenscheit, Nadine;
Drögemüller, Cord

Publication type:

Article

A COL2A1 de novo variant in a Holstein bulldog calf.

Published in:

2019

By:

Häfliger, Irene Monika;
Behn, Holger;
Freick, Markus;
Jagannathan, Vidhya;
Drögemüller, Cord

Publication type:

Abstract

Dermatosparaxis in White Dorper sheep: confirmation of a causative nonsense mutation in ADAMTS2.

Published in:

Animal Genetics, 2017, v. 48, n. 6, p. 729, doi. 10.1111/age.12591

By:

Joller, Sara;
Berenguer Veiga, Inês;
Drögemüller, Cord

Publication type:

Article

Two brown coat colour-associated TYRP1 variants ( b c and b d) occur in Leonberger dogs.

Published in:

Animal Genetics, 2017, v. 48, n. 6, p. 732, doi. 10.1111/age.12612

By:

Letko, Anna;
Drögemüller, Cord

Publication type:

Article

A breeding experiment confirms the dominant mode of inheritance of the brown coat colour associated with the 496Asp TYRP1 allele in goats.

Published in:

Animal Genetics, 2015, v. 46, n. 5, p. 587, doi. 10.1111/age.12320

By:

Dietrich, Joëlle;
Menzi, Fiona;
Ammann, Philippe;
Drögemüller, Cord;
Leeb, Tosso

Publication type:

Article

A 1.8-kb insertion in the 3′-UTR of RXFP2 is associated with polledness in sheep.

Published in:

Animal Genetics, 2015, v. 46, n. 4, p. 457, doi. 10.1111/age.12309

By:

Wiedemar, Natalie;
Drögemüller, Cord

Publication type:

Article

A 19-Mb de novo deletion on BTA 22 including MITF leads to microphthalmia and the absence of pigmentation in a Holstein calf.

Published in:

Animal Genetics, 2014, v. 45, n. 6, p. 868, doi. 10.1111/age.12213

By:

Wiedemar, Natalie;
Drögemüller, Cord

Publication type:

Article

A frameshift mutation in the cubilin gene ( CUBN) in Beagles with Imerslund- Gräsbeck syndrome (selective cobalamin malabsorption).

Published in:

Animal Genetics, 2014, v. 45, n. 1, p. 148, doi. 10.1111/age.12094

By:

Drögemüller, Michaela;
Jagannathan, Vidhya;
Howard, Judith;
Bruggmann, Rémy;
Drögemüller, Cord;
Ruetten, Maja;
Leeb, Tosso;
Kook, Peter H.

Publication type:

Article

Polymelia in a chimeric Simmental calf: nociceptive withdrawal reflex, anaesthetic and analgesic management, anatomic and genetic analysis.

Published in:

BMC Veterinary Research, 2019, v. 15, n. 1, p. N.PAG, doi. 10.1186/s12917-019-1846-4

By:

Morath-Huss, Ute;
Drögemüller, Cord;
Stoffel, Michael;
Precht, Christina;
Zanolari, Patrik;
Spadavecchia, Claudia

Publication type:

Article

A de novo germline mutation in MYH7 causes a progressive dominant myopathy in pigs.

Published in:

BMC Genetics, 2012, v. 13, n. 1, p. 99, doi. 10.1186/1471-2156-13-99

By:

Murgiano, Leonardo;
Tammen, Imke;
Harlizius, Barbara;
Drögemüller, Cord

Publication type:

Article

Selection signatures in goats reveal copy number variants underlying breed-defining coat color phenotypes.

Published in:

PLoS Genetics, 2019, v. 15, n. 12, p. 1, doi. 10.1371/journal.pgen.1008536

By:

Henkel, Jan;
Saif, Rashid;
Jagannathan, Vidhya;
Schmocker, Corinne;
Zeindler, Flurina;
Bangerter, Erika;
Herren, Ursula;
Posantzis, Dimitris;
Bulut, Zafer;
Ammann, Philippe;
Drögemüller, Cord;
Flury, Christine;
Leeb, Tosso

Publication type:

Article

Correction: Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses.

Published in:

2019

By:

Hauswirth, Regula;
Haase, Bianca;
Blatter, Marlis;
Brooks, Samantha A.;
Burger, Dominik;
Drögemüller, Cord;
Gerber, Vincent;
Henke, Diana;
Janda, Jozef;
Jude, Rony;
Magdesian, K. Gary;
Matthews, Jacqueline M.;
Poncet, Pierre-André;
Svansson, Vilhjálmur;
Tozaki, Teruaki;
Wilkinson-White, Lorna;
Penedo, M. Cecilia T.;
Rieder, Stefan;
Leeb, Tosso

Publication type:

Correction Notice

Pulmonary hypoplasia and anasarca syndrome in Cika cattle.

Published in:

Acta Veterinaria Scandinavica, 2016, p. 1, doi. 10.1186/s13028-016-0220-9

By:

Švara, Tanja;
Cociancich, Vasilij;
Šest, Katarina;
Gombač, Mitja;
Paller, Tomislav;
Starič, Jože;
Drögemüller, Cord

Publication type:

Article

Occurrence of congenital disorders in Swiss sheep.

Published in:

Acta Veterinaria Scandinavica, 2013, v. 55, n. 1, p. 1, doi. 10.1186/1751-0147-55-27

By:

Greber, Deborah;
Doherr, Marcus;
Drögemüller, Cord;
Steiner, Adrian

Publication type:

Article

Whole genome sequencing reveals candidate causal genetic variants for spastic syndrome in Holstein cattle.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-82446-z

By:

Jacinto, Joana G.P.;
Letko, Anna;
Häfliger, Irene M.;
Akyürek, Eylem Emek;
Sacchetto, Roberta;
Gentile, Arcangelo;
Drögemüller, Cord

Publication type:

Article

Novel Prion Protein in BSE-affected Cattle, Switzerland.

Published in:

2012

By:

Seuberlich, Torsten;
Gsponer, Michaela;
Drögemüller, Cord;
Polak, Miroslaw P.;
McCutcheon, Sandra;
Heim, Dagmar;
Oevermann, Anna;
Zurbriggen, Andreas

Publication type:

Case Study

A large deletion in the GP9 gene in Cocker Spaniel dogs with Bernard-Soulier syndrome.

Published in:

PLoS ONE, 2019, v. 14, n. 9, p. 1, doi. 10.1371/journal.pone.0220625

By:

Gentilini, Fabio;
Turba, Maria Elena;
Giancola, Fiorella;
Chiocchetti, Roberto;
Bernardini, Chiara;
Dajbychova, Markéta;
Jagannathan, Vidhya;
Drögemüller, Michaela;
Drögemüller, Cord

Publication type:

Article

Procedural fairness and safety in the acceptance of nuclear waste disposal in Germany: an empirical study.

Published in:

Journal of Risk Research, 2024, v. 27, n. 8, p. 969, doi. 10.1080/13669877.2024.2431896

By:

Seidl, Roman;
Drögemüller, Cord

Publication type:

Article

Chromosomal imbalance in pigs showing a syndromic form of cleft palate.

Published in:

BMC Genomics, 2019, v. 20, n. 3, p. 1, doi. 10.1186/s12864-019-5711-4

By:

Grahofer, Alexander;
Letko, Anna;
Häfliger, Irene Monika;
Jagannathan, Vidhya;
Ducos, Alain;
Richard, Olivia;
Peter, Vanessa;
Nathues, Heiko;
Drögemüller, Cord

Publication type:

Article

Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation.

Published in:

PLoS Genetics, 2015, v. 11, n. 7, p. 1, doi. 10.1371/journal.pgen.1005427

By:

Murgiano, Leonardo;
Shirokova, Vera;
Welle, Monika Maria;
Jagannathan, Vidhya;
Plattet, Philippe;
Oevermann, Anna;
Pienkowska-Schelling, Aldona;
Gallo, Daniele;
Gentile, Arcangelo;
Mikkola, Marja;
Drögemüller, Cord

Publication type:

Article

A Missense Change in the ATG4D Gene Links Aberrant Autophagy to a Neurodegenerative Vacuolar Storage Disease.

Published in:

PLoS Genetics, 2015, v. 11, n. 4, p. 1, doi. 10.1371/journal.pgen.1005169

By:

Kyöstilä, Kaisa;
Syrjä, Pernilla;
Jagannathan, Vidhya;
Chandrasekar, Gayathri;
Jokinen, Tarja S.;
Seppälä, Eija H.;
Becker, Doreen;
Drögemüller, Michaela;
Dietschi, Elisabeth;
Drögemüller, Cord;
Lang, Johann;
Steffen, Frank;
Rohdin, Cecilia;
Jäderlund, Karin H.;
Lappalainen, Anu K.;
Hahn, Kerstin;
Wohlsein, Peter;
Baumgärtner, Wolfgang;
Henke, Diana;
Oevermann, Anna

Publication type:

Article

An ARHGEF10 Deletion Is Highly Associated with a Juvenile-Onset Inherited Polyneuropathy in Leonberger and Saint Bernard Dogs.

Published in:

PLoS Genetics, 2014, v. 10, n. 10, p. 1, doi. 10.1371/journal.pgen.1004635

By:

Ekenstedt, Kari J.;
Becker, Doreen;
Minor, Katie M.;
Shelton, G. Diane;
Patterson, Edward E.;
Bley, Tim;
Oevermann, Anna;
Bilzer, Thomas;
Leeb, Tosso;
Drögemüller, Cord;
Mickelson, James R.

Publication type:

Article

A Mutation in the FAM83G Gene in Dogs with Hereditary Footpad Hyperkeratosis (HFH).

Published in:

PLoS Genetics, 2014, v. 10, n. 5, p. 1, doi. 10.1371/journal.pgen.1004370

By:

Drögemüller, Michaela;
Jagannathan, Vidhya;
Becker, Doreen;
Drögemüller, Cord;
Schelling, Claude;
Plassais, Jocelyn;
Kaerle, Cécile;
Dufaure de Citres, Caroline;
Thomas, Anne;
Müller, Eliane J.;
Welle, Monika M.;
Roosje, Petra;
Leeb, Tosso

Publication type:

Article