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Rudd Garces, Gabriela; Letko, Anna; Häfliger, Irene M; Müller, Jana; Herden, Christiane; Nesseler, Anne; Wagner, Henrik; Schmidt, Martin J; Drögemüller, Cord; Lühken, Gesine (2024). MFSD2A frameshift variant in Kerry Hill sheep with microcephaly. Animal genetics, 55(1), pp. 152-157. Wiley 10.1111/age.13374
Tan, K; Adeniyi, O O; Letko, A; RuddGarces, G; Manz, E; Wagner, H; Zanolari, P; Drögemüller, C; Lühken, G (2024). Identification of genomic regions associated with differences in fleece type in Huacaya and Suri alpacas (Vicugna pacos). Animal genetics, 55(1), pp. 163-167. Wiley 10.1111/age.13377
Gmel, Annik; Ricard, Anne; Gerber, Vinzenz; Neuditschko, Markus (2024). Population structure and genomic diversity of the Einsiedler horse. Animal genetics, 55(3), pp. 475-479. Wiley 10.1111/age.13421
Kiener, Sarah; Åhman, Susanne; Cikota, Robert; Jagannathan, Vidhya; Blatter, Sohvi; Cvitas, Iva; Soto, Sara; Leeb, Tosso (2024). Heterozygous ASPRV1 frameshift variant in a Pembroke Welsh Corgi with ichthyosis. Animal genetics, 55(3), pp. 490-492. Wiley 10.1111/age.13423
Kiener, Sarah; Wildermuth, Brett; Meertens, Nadine M; Jagannathan, Vidhya; Leeb, Tosso (2024). Heterozygous deletion of the NSDHL gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi. Animal genetics, 55(4), pp. 697-699. Wiley 10.1111/age.13436
Letko, Anna; Gurtner, Corinne; Jagannathan, Vidhya; Drögemüller, Cord (2024). Renal dysplasia in Leonberger dogs - An emerging recessive congenital disorder? Animal genetics, 55(4), pp. 700-701. Wiley 10.1111/age.13439
Christen, Matthias; Gregor, Katharina M; Böttcher-Künneke, Ariane; Lombardo, Mara S; Baumgärtner, Wolfgang; Jagannathan, Vidhya; Puff, Christina; Leeb, Tosso (2024). Intragenic MFSD8 duplication and histopathological findings in a rabbit with neuronal ceroid lipofuscinosis. Animal genetics, 55, pp. 588-598. Wiley 10.1111/age.13441
Rietmann, Stefan J; Lange, Anja; Soto, Sara; Thom, Nina; Manz, Eberhard; Jagannathan, Vidhya; Mayer, Ursula; Leeb, Tosso (2024). KRT5 in-frame deletion in a family of German Shepherd dogs with split paw pad disease resembling localized epidermolysis bullosa simplex in human patients. Animal genetics, 55, pp. 692-696. Wiley 10.1111/age.13444
Rietmann, Stefan J; Nowell, Sarah; Keating, M Kelly; Bauer, Cynthia; Jagannathan, Vidhya; Leeb, Tosso (2024). Heterozygous COL5A1 deletion in a cat with classical Ehlers-Danlos syndrome. Animal genetics, 55(4), pp. 705-707. Wiley 10.1111/age.13446
Kiener, Sarah; Lehner, Georg; Jagannathan, Vidhya; Welle, Monika; Leeb, Tosso (2024). Heterozygous DSP in-frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalities. (In Press). Animal genetics Wiley 10.1111/age.13467
Abitbol, Marie; Jagannathan, Vidhya; Lopez, Marie; Courtin, Ambre; Dufaure de Citres, Caroline; Gache, Vincent; Leeb, Tosso (2023). A CDH23 missense variant in Beauceron dogs with non-syndromic deafness. Animal genetics, 54(1), pp. 73-77. Wiley 10.1111/age.13273
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 (2023). Genomic regions underlying positive selection in local, Alpine cattle breeds. Animal genetics, 54(3), pp. 239-253. Blackwell 10.1111/age.13295
Christen, Matthias; Ludwig-Peisker, Odette; Jagannathan, Vidhya; Hetzel, Udo; Schönball, Ulrike; Leeb, Tosso (2023). STK36 splice site variant in an Australian Shepherd dog with primary ciliary dyskinesia. Animal genetics, 54(3), pp. 412-415. Wiley 10.1111/age.13306
Kiener, Sarah; Yang, Ching; Rich, Naomi; Jagannathan, Vidhya; Mauldin, Elizabeth A; Leeb, Tosso (2023). Heterozygous ATP2A2 missense variant identified in a Shih Tzu with Darier disease. Animal genetics, 54(4), pp. 558-561. Wiley 10.1111/age.13314
Jacinto, Joana G P; Schiavon, Eliana; Häfliger, Irene M; Coin, Patrizio; Seefried, Franz R; Drögemüller, Cord (2023). MYH3-associated non-syndromic palatoschisis (cleft palate, CP) in Limousine cattle. Animal genetics, 54(4), pp. 581-582. Wiley 10.1111/age.13317
Kiener, Sarah; Castilla, Eloy; Jagannathan, Vidhya; Welle, Monika; Leeb, Tosso (2023). SDR9C7 missense variant in a Chihuahua with non-epidermolytic ichthyosis. Animal genetics, 54(4), pp. 562-565. Wiley 10.1111/age.13319
Lindtke, Dorothea; Seefried, Franz R; Drögemüller, Cord; Neuditschko, Markus (2023). Increased heterozygosity in low-pass sequencing data allows identification of blood chimeras in cattle. Animal genetics, 54(5), pp. 613-618. Wiley 10.1111/age.13334
Littlejohn, Mathew D; Sneddon, Nick; Dittmer, Keren; Keehan, Mike; Stephen, Melissa; Drögemüller, Michaela; Garrick, Dorian (2023). A frameshift-deletion mutation in Reelin causes cerebellar hypoplasia in White Swiss Shepherd dogs. Animal genetics, 54(5), pp. 632-636. Wiley 10.1111/age.13336
Kiener, Sarah; Åhman, Susanne; Jagannathan, Vidhya; Soto, Sara; Leeb, Tosso (2023). Heterozygous KRT10 missense variant in a Chihuahua with severe epidermolytic ichthyosis. Animal genetics, 54(5), pp. 652-654. Wiley 10.1111/age.13341
Jacinto, Joana G P; Bolcato, Marilena; Häfliger, Irene M; Oevermann, Anna; Gentile, Arcangelo; Drögemüller, Cord (2023). DYRK1B haploinsufficiency in a Holstein cattle with epilepsy. Animal genetics, 54(5), pp. 623-627. Wiley 10.1111/age.13348
Graber, Jennifer Kalinka; Signer-Hasler, Heidi; Burren, Alexander; Drögemüller, Cord (2022). Evaluation of truncating variants in the LCORL gene in relation to body size of goats from Switzerland. Animal genetics, 53(2), pp. 237-239. Wiley 10.1111/age.13177
Häfliger, Irene M.; Wolf-Hofstetter, Sonja; Casola, Christina; Hetzel, Udo; Seefried, Franz R.; Drögemüller, Cord (2022). A de novo variant in the bovine ADAMTSL4 gene in an Original Braunvieh calf with congenital cataract. Animal genetics, 53(3), pp. 416-421. Wiley 10.1111/age.13178
Hauser, Miriam; Signer-Hasler, Heidi; Küttel, Luzia; Capitan, Aurélien; Guldbrandtsen, Bernt; Hinrichs, Dirk; Flury, Christine; Seefried, Franz R; Drögemüller, Cord (2022). Identification of two new recessive MC1R alleles in red-coloured Evolèner cattle and other breeds. Animal genetics, 53(3), pp. 427-435. Blackwell 10.1111/age.13206
Jacinto, Joana G P; Häfliger, Irene M; Baes, Christine F; de Oliveira, Hinayah R; Drögemüller, Cord (2022). A de novo start-lost variant in ANKRD28 in a Holstein calf with dwarfism. Animal genetics, 53(3), pp. 470-471. 10.1111/age.13204
Jacinto, Joana G P; Häfliger, Irene M; Christen, Matthias; Paris, Julia M; Seefried, Franz R; Drögemüller, Cord (2022). Is a heterozygous missense variant in SGSH the cause of a syndromic form of congenital amastia in an Original Braunvieh calf? Animal genetics, 53(4), pp. 530-531. Wiley 10.1111/age.13207
Widmer, Sarah; Seefried, Franz R; von Rohr, Peter; Häfliger, Irene M; Spengeler, Mirjam; Drögemüller, Cord (2022). Associated regions for multiple birth in Brown Swiss and Original Braunvieh cattle on chromosomes 15 and 11. Animal genetics, 53(5), pp. 557-569. Wiley 10.1111/age.13229
Tan, Kirsty; Roy, Mia; Manz, Eberhard; Wagner, Henrik; Zanolari, Patrik; Drögemüller, Cord; Lühken, Gesine (2022). The KIT:c.376G>A variant in German and Swiss alpacas (Vicugna pacos) with different coat colors. Animal genetics, 53(5), pp. 718-720. Wiley 10.1111/age.13231
Jacinto, Joana G P; Häfliger, Irene M; Caivano, Domenico; Drögemüller, Cord (2022). A germline de novo variant in NUMB associated with a double-outlet right ventricle in Chianina cattle. Animal genetics, 53(5), pp. 713-714. Wiley 10.1111/age.13236
Abitbol, Marie; Jagannathan, Vidhya; Laurent, Nelly; Noblet, Eglantine; Dutil, Guillaume F.; Troupel, Thibaut; de Dufaure de Citres, Caroline; Gache, Vincent; Blot, Stéphane; Escriou, Catherine; Leeb, Tosso (2022). A PNPLA8 frameshift variant in Australian shepherd dogs with hereditary ataxia. Animal genetics, 53(5), pp. 709-712. Wiley 10.1111/age.13245
Kinsey, Nathan A.; Belanger, Janelle M.; Dog Biomedical Variant Database, Consortium; Oberbauer, Anita M. (2022). Canine reference genome accuracy impacts variant calling: Lessons learned from investigating embryonic lethal variants. Animal genetics, 53(5), pp. 706-708. Wiley 10.1111/age.13241
Kiener, Sarah; Mauldin, Elizabeth A; Jagannathan, Vidhya; Casal, Margret L; Leeb, Tosso (2022). KRT5 missense variant in a Cardigan Welsh Corgi with epidermolysis bullosa simplex. Animal genetics, 53(6), pp. 892-896. Wiley 10.1111/age.13257
Christen, Matthias; Gutierrez-Quintana, Rodrigo; Vandenberghe, Helene; Kaczmarska, Adriana; Penderis, Jacques; José-López, Roberto; Rupp, Angie; Griffiths, Ian R; Jagannathan, Vidhya; Leeb, Tosso (2022). Mitochondrial fission factor (MFF) frameshift variant in Bullmastiffs with mitochondrial fission encephalopathy. Animal genetics, 53(6), pp. 814-820. Wiley 10.1111/age.13263
Jacinto, Joana G P; Häfliger, Irene M.; Gentile, Arcangelo; Drögemüller, Cord; Bolcato, Marilena (2021). A 6.7 kb deletion in the COL2A1 gene in a Holstein calf with achondrogenesis type II and perosomus elumbis. Animal genetics, 52(2), pp. 244-245. Wiley 10.1111/age.13033
Eager, Katie L.M.; Cauchi, Monique; Willet, Cali E.; Häfliger, Irene M.; Drögemüller, Cord; O’Rourke, Brendon A.; Tammen, Imke (2021). The previously reported LRP4 c.4940C>T variant is not associated with syndactyly in cattle. Animal genetics, 52(3), pp. 380-381. Wiley 10.1111/age.13061
Letko, Anna; Bützberger, Charis; Hirter, Nathalie; Paris, Julia M.; Abril, Carlos; Drögemüller, Cord (2021). Genetic evaluation of small ruminant lentivirus susceptibility in Valais blacknose sheep. Animal genetics, 52(5), pp. 781-782. Wiley 10.1111/age.13108
Jenkins, Christopher A.; Dog Biomedical Variant Database, Consortium; Schofield, Ellen C.; Mellersh, Cathryn S.; De Risio, Luisa; Ricketts, Sally L. (2021). Improving the resolution of canine genome-wide association studies using genotype imputation: A study of two breeds. Animal genetics, 52(5), pp. 703-713. Wiley 10.1111/age.13117
Bauer, A.; Hadji Rasouliha, S.; Brunner, M. T.; Jagannathan, V.; Bucher, I.; Bannoehr, J.; Varjonen, K.; Bond, R.; Bergvall, K.; Welle, M. M.; Roosje, P.; Leeb, T. (2021). Corrigendum: A second KRT71 allele in curly coated dogs. Animal genetics, 52(4), p. 575. Wiley 10.1111/age.13098
Christen, Matthias; Reineking, Wencke; Beineke, Andreas; Jagannathan, Vidhya; Baumgärtner, Wolfgang; Leeb, Tosso (2021). Polyadenine insertion disrupting the G6PC1 gene in German Pinschers with glycogen storage disease type Ia (GSD1A). Animal genetics, 52(6), pp. 900-902. Wiley 10.1111/age.13146
Letko, A.; Ammann, B.; Jagannathan, V.; Henkel, J.; Leuthard, F.; Schelling, C.; Carneiro, M.; Drögemüller, C.; Leeb, T. (2020). A deletion spanning the promoter and first exon of the hair cycle-specific ASIP transcript isoform in black and tan rabbits. Animal genetics, 51(1), pp. 137-140. Wiley 10.1111/age.12881
Torrecilha, R B P; Milanesi, M; Gallana, M; Falbo, A-K; Reichler, I M; Hug, Petra; Jagannathan, Vidya; Trigo, B B; Paulan, S C; Bruno, D B; Garcia, S D; Scaramele, N F; Lopes, F L; Dolf, Gaudenz; Leeb, Tosso; Sölkner, J; Garcia, J F; Pieńkowska-Schelling, A; Schelling, C and Utsunomiya, Y T (2020). Association of missense variants in GDF9 with litter size in Entlebucher Mountain dogs. Animal genetics, 51(1), pp. 78-86. Wiley 10.1111/age.12882
Hirter, Nathalie; Letko, Anna; Häfliger, Irene Monika; Becker, Doreen; Greber, Deborah; Drögemüller, Cord (2020). A genome-wide significant association on chromosome 15 for congenital entropion in Swiss White Alpine sheep. Animal genetics, 51(2), pp. 278-283. Wiley 10.1111/age.12903
Simon, R; Lischer, H. E. L.; Pieńkowska-Schelling, A.; Keller, I.; Häfliger, I. M.; Letko, A.; Schelling, C; Lühken, G; Drögemüller, C. (2020). New genomic features of the polled intersex syndrome variant in goats unraveled by long-read whole-genome sequencing. Animal genetics, 51(3), pp. 439-448. Wiley 10.1111/age.12918
Häfliger, I. M.; Hirter, N.; Paris, J. M.; Wolf Hofstetter, S.; Seefried, F R; Drögemüller, C. (2020). A de novo germline mutation of KIT in a white-spotted Brown Swiss cow. Animal genetics, 51(3), pp. 449-452. Wiley 10.1111/age.12920
Häfliger, I. M.; Wiedemar, N.; Švara, T; Starič, J; Cociancich, V; Šest, K; Gombač, M; Paller, T; Agerholm, J S; Drögemüller, C. (2020). Identification of small and large genomic candidate variants in bovine pulmonary hypoplasia and anasarca syndrome. Animal genetics, 51(3), pp. 382-390. Wiley 10.1111/age.12923
Häfliger, Irene Monika; Seefried, Franz; Drögemüller, Cord (2020). Trisomy 29 in a stillborn Swiss Original Braunvieh calf. Animal genetics, 51(3), pp. 483-484. Wiley 10.1111/age.12929
Häfliger, I. M.; Letko, A.; Murgiano, L.; Drögemüller, C. (2020). De novo stop-lost germline mutation in FGFR3 causes severe chondrodysplasia in the progeny of a Holstein bull. Animal genetics, 51(3), pp. 466-469. Wiley 10.1111/age.12934
Dettwiler, M.; Leuthard, F.; Bauer, A.; Jagannathan, V.; Lourenço, A. M.; Pereira, H.; Leeb, T.; Welle, M. M. (2020). A nonsense variant in the KRT14 gene in a domestic shorthair cat with epidermolysis bullosa simplex. Animal genetics, 51(5), pp. 829-832. Wiley 10.1111/age.12979
Paris, J. M.; Letko, A.; Häfliger, I. M.; Ammann, P.; Drögemüller, C. (2020). Ear type in sheep is associated with the MSRB3 locus. Animal genetics, 51(6), pp. 968-972. Wiley 10.1111/age.12994
Häfliger, Irene Monika; Agerholm, Jørgen Steen; Drögemüller, Cord (2020). Constitutional trisomy 20 in an aborted Holstein fetus with pulmonary hypoplasia and anasarca syndrome. Animal genetics, 51(6), pp. 988-989. Wiley 10.1111/age.13008
Abdalla, E. A.; Id-Lahoucine, S.; Cánovas, A.; Casellas, J.; Schenkel, F. S.; Wood, B. J.; Baes, C. F. (2020). Discovering lethal alleles across the turkey genome using a transmission ratio distortion approach. Animal genetics, 51(6), pp. 876-889. Wiley 10.1111/age.13003
Häfliger, Irene Monika; Behn, Holger; Freick, Markus; Jagannathan, Vidhya; Drögemüller, Cord (2019). A COL2A1 de novo variant in a Holstein bulldog calf. Animal genetics, 50(1), pp. 113-114. Blackwell 10.1111/age.12735
Bauer, Anina; Hadji Rasouliha, Sheida; Brunner, Magdalena; Jagannathan, Vidya; Bucher, I; Bannöhr, Jeanette; Varjonen, K; Bond, R; Bergvall, K; Welle, Monika Maria; Roosje, Petra; Leeb, Tosso (2019). A second KRT71 allele in curly coated dogs. Animal genetics, 50(1), pp. 97-100. Blackwell 10.1111/age.12743
Hofstetter, Sonja; Seefried, F; Häfliger, Irene Monika; Jagannathan, Vidya; Leeb, Tosso; Drögemüller, Cord (2019). A non-coding regulatory variant in the 5'-region of the MITF gene is associated with white-spotted coat in Brown Swiss cattle. Animal genetics, 50(1), pp. 27-32. Blackwell 10.1111/age.12751
Barrientos, Laura Soledad; Maiolini, Arianna; Häni, Anna Katrin; Jagannathan, Vidya; Leeb, Tosso (2019). NHLRC1 dodecamer repeat expansion demonstrated by whole genome sequencing in a Chihuahua with Lafora disease. Animal genetics, 50(1), pp. 118-119. Blackwell 10.1111/age.12756
Jagannathan, Vidya; Gerber, Vinzenz; Rieder, S; Tetens, J; Thaller, G; Drögemüller, Cord; Leeb, Tosso (2019). Comprehensive characterization of horse genome variation by whole-genome sequencing of 88 horses. Animal genetics, 50(1), pp. 74-77. Blackwell 10.1111/age.12753
Henkel, Jan Wolfgang; Lafayette, C; Brooks, S A; Martin, K; Patterson-Rosa, L; Cook, D; Jagannathan, Vidya; Leeb, Tosso (2019). Whole-genome sequencing reveals a large deletion in the MITF gene in horses with white spotted coat colour and increased risk of deafness. Animal genetics, 50(2), pp. 172-174. Wiley 10.1111/age.12762
Häfliger, Irene Monika; Hofstetter, Sonja; Mock, Thomas; Stettler, Manuela Hanna; Meylan, Mireille; Mehinagic, Kemal; Stokar von Neuforn, Nadine; Drögemüller, Cord (2019). APOB-associated cholesterol deficiency in Holstein cattle is not a simple recessive disease. Animal genetics, 50(4), pp. 372-375. Wiley 10.1111/age.12801
Küttel, Luzia Marlis; Letko, Anna; Häfliger, Irene Monika; Signer-Hasler, Heidi; Joller, Sara; Hirsbrunner, Gabriela; Mészáros, G; Sölkner, J; Flury, C; Leeb, Tosso; Drögemüller, C. (2019). A complex structural variant at the KIT locus in cattle with the Pinzgauer spotting pattern. Animal genetics, 50(5), pp. 423-429. Wiley 10.1111/age.12821
Signer-Hasler, Heidi; Burren, A; Ammann, P; Drögemüller, Cord; Flury, C (2019). Runs of homozygosity and signatures of selection: a comparison among eight local Swiss sheep breeds. Animal genetics, 50(5), pp. 512-525. Wiley 10.1111/age.12828
Bauer, Anina; de Lucia, M; Leuthard, Fabienne Nadja; Jagannathan, Vidya; Leeb, Tosso (2019). Compound heterozygosity for TNXB genetic variants in a mixed-breed dog with Ehlers-Danlos syndrome. Animal genetics, 50(5), pp. 546-549. Wiley 10.1111/age.12830
Letko, Anna; Zdora, Isabel; Hitzler, Valerie; Jagannathan, Vidya; Beineke, Andreas; Möhrke, Carola; Drögemüller, Cord (2019). A de novo in-frame duplication in the COL1A2 gene in a Lagotto Romagnolo dog with osteogenesis imperfecta. Animal genetics, 50(6), pp. 786-787. Blackwell 10.1111/age.12843
Paris, Julia Maria; Letko, Anna; Häfliger, Irene Monika; Ammann, P; Flury, C; Drögemüller, Cord (2019). Identification of two TYRP1 loss-of-function alleles in Valais Red sheep. Animal genetics, 50(6), pp. 778-782. Wiley 10.1111/age.12863
Woolley, S A; Eager, K L M; Häfliger, Irene Monika; Bauer, Anina; Drögemüller, Cord; Leeb, Tosso; O'Rourke, B A; Tammen, I (2019). An ABCA12 missense variant in a Shorthorn calf with ichthyosis fetalis. Animal genetics, 50(6), pp. 749-752. Wiley 10.1111/age.12856
Leuthard, Fabienne; Lehner, G; Jagannathan, Vidya; Leeb, Tosso; Welle, Monika Maria (2019). A missense variant in the NSDHL gene in a Chihuahua with a congenital cornification disorder resembling inflammatory linear verrucous epidermal nevi. Animal genetics, 50(6), pp. 768-771. Wiley 10.1111/age.12862
Hug, Petra; Jude, R; Henkel, Jan Wolfgang; Jagannathan, Vidya; Leeb, Tosso (2019). A novel KIT deletion variant in a German Riding Pony with white-spotting coat colour phenotype. Animal genetics, 50(6), pp. 761-763. Wiley 10.1111/age.12840
Jagannathan, V.; Drögemüller, C.; Leeb, T. (2019). A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves. Animal genetics, 50(6), pp. 695-704. Wiley 10.1111/age.12834
Felkel, S; Vogl, C; Rigler, D; Jagannathan, Vidhya; Leeb, Tosso; Fries, R; Neuditschko, M; Rieder, S; Velie, B; Lindgren, G; Rubin, C-J; Schlötterer, C; Rattei, T; Brem, G; Wallner, B (2018). Asian horses deepen the MSY phylogeny. Animal genetics, 49(1), pp. 90-93. Blackwell 10.1111/age.12635
Bauer, Anina; Kehl, A; Jagannathan, Vidhya; Leeb, Tosso (2018). A novel MLPH variant in dogs with coat colour dilution. Animal genetics, 49(1), pp. 94-97. Blackwell 10.1111/age.12632
Schmutz, Isabelle; Jagannathan, Vidhya; Dìez Bernal, Sabina; Lanz, Simone; Kalbfleisch, Ted; Leeb, Tosso; Spadavecchia, Claudia (2018). Exclusion of adrenoceptor alpha 2 variants in a horse insensitive to medetomidine. Animal genetics, 49(2), p. 141. Blackwell 10.1111/age.12636
Bauer, Anina; Nimmo, J; Newman, R; Brunner, Magdalena Anna Theresa; Welle, Monika Maria; Jagannathan, Vidhya; Leeb, Tosso (2018). A splice site variant in the SUV39H2 gene in Greyhounds with nasal parakeratosis. Animal genetics, 49(2), pp. 137-140. Blackwell 10.1111/age.12643
Joller, Sara; Ammann, P.; Flury, C.; Drögemüller, Cord (2018). Evaluation of HOXC8 in crested Swiss chicken. Animal genetics, 49(4), pp. 334-336. Blackwell 10.1111/age.12674
Dürig, Nicole; Letko, Anna; Lepori, Vincent; Hadji Rasouliha, Sheida; Loechel, R; Kehl, A; Hytönen, M K; Lohi, H; Mauri, Nico; Dietrich, Sara Joëlle; Wiedmer, Michaela; Drögemüller, Michaela; Jagannathan, Vidhya; Schmutz, S M; Leeb, Tosso (2018). Two MC1R loss-of-function alleles in cream-coloured Australian Cattle Dogs and white Huskies. Animal genetics, 49(4), pp. 284-290. Blackwell 10.1111/age.12660
Singer-Berk, M.; Knickelbein, K. E.; Vig, S.; Liu, J.; Bentley, E.; Nunnery, C.; Reilly, C.; Dwyer, A.; Drögemüller, Cord; Unger, Lucia; Gerber, Vinzenz; Lassaline, M.; Bellone, R. R. (2018). Genetic risk for squamous cell carcinoma of the nictitating membrane parallels that of the limbus in Haflinger horses. Animal genetics, 49(5), pp. 457-460. Blackwell 10.1111/age.12695
Spycher, M; Bauer, Anina; Jagannathan, Vidhya; Frizzi, M; De Lucia, M; Leeb, Tosso (2018). A frameshift variant in the COL5A1 gene in a cat with Ehlers-Danlos syndrome. Animal genetics, 49(6), pp. 641-644. Wiley 10.1111/age.12727
Hadji Rasouliha, S; Bauer, Anina; Dettwiler, Martina Andrea; Welle, Monika Maria; Leeb, Tosso (2018). A frameshift variant in the EDA gene in Dachshunds with X-linked hypohidrotic ectodermal dysplasia. Animal genetics, 49(6), pp. 651-654. Wiley 10.1111/age.12729
Gallana, M; Utsunomiya, Y T; Dolf, Gaudenz; Pintor Torrecilha, R B; Falbo, A-K; Jagannathan, Vidhya; Leeb, Tosso; Reichler, I; Sölkner, J; Schelling, C (2018). Genome-wide association study and heritability estimate for ectopic ureters in Entlebucher mountain dogs. Animal genetics, 49(6), pp. 645-650. Wiley 10.1111/age.12728
Burns, E N; Bordbari, M H; Mienaltowski, M J; Affolter, V K; Barro, M V; Gianino, F; Gianino, G; Giulotto, E; Kalbfleisch, T S; Katzman, S A; Lassaline, M; Leeb, Tosso; Mack, M; Müller, Eliane Jasmine; MacLeod, J N; Ming-Whitfield, B; Alanis, C R; Raudsepp, T; Scott, E; Vig, S; ... (2018). Generation of an equine biobank to be used for Functional Annotation of Animal Genomes project. Animal genetics, 49(6), pp. 564-570. Wiley 10.1111/age.12717
Larsen, H.; Hemsworth, P. H.; Cronin, G. M.; Gebhardt, Sabine; Smith, C. L.; Rault, J.-L. (2018). Relationship between welfare and individual ranging behaviour in commercial free-range laying hens. Animal genetics, 12(11), pp. 2356-2364. Cambridge University Press 10.1017/S1751731118000022
Dürig, Nicole; Jude, Rony; Jagannathan, Vidhya; Leeb, Tosso (2017). A novel MITF variant in a white American Standardbred foal. Animal genetics, 48(1), pp. 123-124. Blackwell 10.1111/age.12484
Dürig, Nicole; Jude, R; Holl, H; Brooks, S A; Lafayette, C; Jagannathan, Vidhya; Leeb, Tosso (2017). Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes. Animal genetics, 48(4), pp. 483-485. Blackwell 10.1111/age.12556
Herder, Vanessa; Ciurkiewicz, Malgorzata; Baumgärtner, Wolfgang; Jagannathan, Vidhya; Leeb, Tosso (2017). Frame-shift variant in the CHRNE gene in a juvenile dog with suspected myasthenia gravis-like disease. Animal genetics, 48(5), p. 625. Blackwell 10.1111/age.12558
Schnider, Debora; Rieder, S; Leeb, Tosso; Gerber, Vinzenz; Neuditschko, M (2017). A genome-wide association study for equine recurrent airway obstruction in European Warmblood horses reveals a suggestive new quantitative trait locus on chromosome 13. Animal genetics, 48(6), pp. 691-693. Blackwell 10.1111/age.12583
Caduff, M; Bauer, Anina; Jagannathan, Vidhya; Leeb, Tosso (2017). A single base deletion in the SLC45A2 gene in a Bullmastiff with oculocutaneous albinism. Animal genetics, 48(5), pp. 619-621. Blackwell 10.1111/age.12582
Joller, Sara; Berenguer Veiga, Inês Margarida; Drögemüller, Cord (2017). Dermatosparaxis in White Dorper sheep: confirmation of a causative nonsense mutation in ADAMTS2. Animal genetics, 48(6), pp. 729-730. Blackwell 10.1111/age.12591
Letko, Anna; Drögemüller, Cord (2017). Two brown coat colour-associated TYRP1 variants (b(c) and b(d)) occur in Leonberger dogs. Animal genetics, 48(6), pp. 732-733. Blackwell 10.1111/age.12612
Niggeler, Allegra; Tetens, Jens; Stäuble, Anna; Steiner, Adrian; Drögemüller, Cord (2017). A genome-wide significant association on chromosome 2 for footrot resistance/susceptibility in Swiss White Alpine sheep. Animal genetics, 48(6), pp. 712-715. Blackwell 10.1111/age.12614
Frischknecht, Mirjam; Signer-Hasler, Heidi; Leeb, Tosso; Rieder, S; Neuditschko, M (2016). Genome-wide association studies based on sequence-derived genotypes reveal new QTL associated with conformation and performance traits in the Franches-Montagnes horse breed. Animal genetics, 47(2), pp. 227-229. Blackwell 10.1111/age.12406
Menzi, Fiona; Besuchet Schmutz, Nathalie; Fragnière, Muriel; Hofstetter, S; Jagannathan, Vidhya; Mock, Thomas; Raemy, Andreas; Studer, Eveline; Mehinagic, Kemal; Regenscheit, Nadine; Meylan, Mireille; Schmitz-Hsu, F; Drögemüller, Cord (2016). A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle. Animal genetics, 47(2), pp. 253-257. Blackwell 10.1111/age.12410
Frischknecht, Mirjam; Flury, C; Leeb, Tosso; Rieder, S; Neuditschko, M (2016). Selection signatures in Shetland ponies. Animal genetics, 47(3), pp. 370-372. Blackwell 10.1111/age.12416
Karli, Philemon; Oevermann, Anna; Bauer, Anina Estrella; Jagannathan, Vidhya; Leeb, Tosso (2016). MFSD8 single-base pair deletion in a Chihuahua with neuronal ceroid lipofuscinosis. Animal genetics, 47(5), p. 631. Blackwell 10.1111/age.12449
Burren, A; Neuditschko, Markus; Signer-Hasler, Heidi; Frischknecht, Mirjam; Reber, Irene; Menzi, Fiona; Drögemüller, Cord; Flury, C (2016). Genetic diversity analyses reveal first insights into breed-specific selection signatures within Swiss goat breeds. Animal genetics, 47(6), pp. 727-739. Blackwell 10.1111/age.12476
Ghosh, S.; Das, P. J.; McQueen, C. M.; Gerber, Vinzenz; Swiderski, C. E.; Lavoie, J.-P.; Chowdhary, B. P; Raudsepp, T. (2016). Analysis of genomic copy number variation in equine recurrent airway obstruction (heaves). Animal genetics, 47(3), pp. 334-344. Blackwell 10.1111/age.12426
Becker, Doreen; Otto, Mandy; Ammann, P; Keller, Irene; Drögemüller, Cord; Leeb, Tosso (2015). The brown coat colour of Coppernecked goats is associated with a non-synonymous variant at the TYRP1 locus on chromosome 8. Animal genetics, 46(1), pp. 50-54. Blackwell 10.1111/age.12240
Tetens, J; Wiedemar, Natalie; Menoud, Annie; Thaller, G; Drögemüller, Cord (2015). Association mapping of the scurs locus in polled Simmental cattle - evidence for genetic heterogeneity. Animal genetics, 46(2), pp. 224-225. Blackwell 10.1111/age.12237
Reber, Irene; Keller, Irene; Becker, Doreen; Flury, C; Welle, Monika Maria; Drögemüller, Cord (2015). Wattles in goats are associated with the FMN1/GREM1 region on chromosome 10. Animal genetics, 46(3), pp. 316-320. Blackwell 10.1111/age.12279
Haase, Bianca; Rieder, S; Leeb, Tosso (2015). Two variants in the KIT gene as candidate causative mutations for a dominant white and a white spotting phenotype in the donkey. Animal genetics, 46(3), pp. 321-324. Blackwell 10.1111/age.12282
Dietrich, Joëlle; Menzi, Fiona; Ammann, Philippe; Drögemüller, Cord; Leeb, Tosso (2015). A breeding experiment confirms the dominant mode of inheritance of the brown coat colour associated with the (496) Asp TYRP1 allele in goats. Animal genetics, 46(5), pp. 587-588. Blackwell 10.1111/age.12320
Haase, Bianca; Jagannathan, Vidhya; Rieder, Stefan; Leeb, Tosso (2015). A novel KIT variant in an Icelandic horse with white-spotted coat colour. Animal genetics, 46(4), p. 466. Blackwell 10.1111/age.12313
Wiedemar, Natalie; Drögemüller, Cord (2015). A 1.8-kb insertion in the 3'-UTR of RXFP2 is associated with polledness in sheep. Animal genetics, 46(4), pp. 457-461. Blackwell 10.1111/age.12309
Becker, Doreen; Luther, Henning; Hofer, Andreas; Leeb, Tosso (2014). A variant in MYO10 is associated with hind limb conformation in Swiss Large White boars. Animal genetics, 45(2), p. 308. Blackwell 10.1111/age.12111
Drögemüller, Michaela; Jagannathan, Vidhya; Howard, J.; Bruggmann, Rémy; Drögemüller, Cord; Ruetten, Maja; Leeb, Tosso; Kook, Peter H. (2014). A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption). Animal genetics, 45(1), pp. 148-150. Blackwell 10.1111/age.12094
Frischknecht, Mirjam; Jagannathan, Vidhya; Leeb, Tosso (2014). Whole genome sequencing confirms KIT insertions in a white cat. Animal genetics, 46(1), p. 98. Blackwell 10.1111/age.12246
Tetens, J L; Qanbari, S; Drögemüller, Cord; Pimentel, E C G; Bennewitz, J; Thaller, G; Tetens, J (2014). Bos indicus introgression into (peri-)alpine cattle breeds - evidence from the analysis of bovine whey protein variants. Animal genetics, 45(4), pp. 585-588. Blackwell 10.1111/age.12185
Wiedemar, Natalie; Drögemüller, Cord (2014). A 19-Mb de novo deletion on BTA 22 including MITF leads to microphthalmia and the absence of pigmentation in a Holstein calf. Animal genetics, 45(6), pp. 868-870. Blackwell 10.1111/age.12213
Shakhsi Niaei, Mostafa; Drögemüller, Michaela; Jagannathan, Vidhya; Gerber, Vinzenz; Leeb, Tosso (2013). IL26 gene inactivation in Equidae. Animal genetics, 44(6), pp. 770-772. Blackwell 10.1111/age.12069
Hauswirth, Regula; Jude, Rony; Haase, Bianca; Bellone, Rebecca R; Archer, Sheila; Holl, Heather; Brooks, Samantha A; Tozaki, Teruaki; Penedo, Maria Cecilia T; Rieder, Stefan; Leeb, Tosso (2013). Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes. Animal genetics, 44(6), pp. 763-765. Blackwell 10.1111/age.12057
Owczarek-Lipska, Marta; Mausberg, Theresa-Bernadette; Stephenson, Hannah; Dukes-McEwan, Joanna; Wess, Gerhard; Leeb, Tosso (2013). A 16-bp deletion in the canine PDK4 gene is not associated with dilated cardiomyopathy in a European cohort of Doberman Pinschers. Animal genetics, 44(2), p. 239. Blackwell 10.1111/j.1365-2052.2012.02396.x
Klukowska-Rötzler, Jolanta; Swinburne, J.E.; Drögemüller, Cord; Dolf, Gaudenz; Janda, Jozef; Leeb, Tosso; Gerber, Vinzenz (2012). The interleukin 4 receptor gene and its role in recurrent airway obstruction in Swiss Warmblood horses. Animal genetics, 43(4), pp. 450-453. Oxford: Blackwell 10.1111/j.1365-2052.2011.02277.x
Shakhsi-Niaei, M; Klukowska-Rötzler, Jolanta; Drögemüller, Cord; Swinburne, J; Ehrmann, C; Saftic, Dounia; Ramseyer, Alessandra; Gerber, Vinzenz; Dolf, Gaudenz; Leeb, Tosso (2012). Replication and fine-mapping of a QTL for recurrent airway obstruction in European Warmblood horses. Animal genetics, 43(5), pp. 627-631. Blackwell 10.1111/j.1365-2052.2011.02315.x
Haase, Bianca; Rieder, S.; Tozaki, T.; Hasegawa, T.; Penedo, M.C.; Jude, R.; Leeb, Tosso (2011). Five novel KIT mutations in horses with white coat colour phenotypes. Animal genetics, 42(3), pp. 337-9. Oxford: Blackwell 10.1111/j.1365-2052.2011.02173.x
Klukowska-Rotzler, Jolanta; Gerber, Vinzenz; Leeb, Tosso (2011). Association analysis of SNPs in the IL21R gene with recurrent airway obstruction (RAO) in Swiss Warmblood horses. Animal genetics, 43(4), pp. 475-476. Oxford: Blackwell 10.1111/j.1365-2052.2011.02289.x
Scharrenberg, A.; Gerber, V.; Swinburne, J.E.; Wilson, A.D.; Klukowska-Rotzler, J.; Laumen, E.; Marti, E. (2010). IgE, IgGa, IgGb and IgG(T) serum antibody levels in offspring of two sires affected with equine recurrent airway obstruction. Animal genetics, 41(s2), pp. 131-137. Oxford: Blackwell 10.1111/j.1365-2052.2010.02122.x
Morina, R.; Knorr, C.; Haase, Bianca; Leeb, Tosso; Seuberlich, Torsten; Zurbriggen, Andreas; Brem, G.; Schutz, E.; Brenig, B. (2010). Molecular analysis of carbohydrate N-acetylgalactosamine 4-O sulfotransferase 8 (CHST8) as a candidate gene for bovine spongiform encephalopathy susceptibility. Animal genetics, 41(1), pp. 85-8. Oxford: Blackwell 10.1111/j.1365-2052.2009.01951.x
Danilowicz, E.; Martinez-Arias, R.; Dolf, Gaudenz; Singh, M.; Probst, I.; Tummler, B.; Holtig, D.; Waldmann, K.H.; Gerlach, G.F.; Stanke, F.; Leeb, Tosso (2010). Characterization of the porcine transferrin gene (TF) and its association with disease severity following an experimental Actinobacillus pleuropneumoniae infection. Animal genetics, 41(4), pp. 424-7. Oxford: Blackwell 10.1111/j.1365-2052.2009.02012.x
Drögemüller, Cord; Demmel, Steffi; Engensteiner, M.; Rieder, S.; Leeb, Tosso (2010). A shared 336 kb haplotype associated with the belt pattern in three divergent cattle breeds. Animal genetics, 41(3), pp. 304-7. Oxford: Blackwell 10.1111/j.1365-2052.2009.01987.x
Schmitz, Andrea; Demmel, Steffi; Peters, Laureen Michèle; Leeb, Tosso; Mevissen, Meike; Haase, Bianca (2010). Comparative human-horse sequence analysis of the CYP3A subfamily gene cluster. Animal genetics, 41(s2), pp. 72-79. Oxford: Blackwell 10.1111/j.1365-2052.2010.02111.x
Shakhsi-Niaei, Mostafa; Klukowska-Rötzler, Jolanta; Drögemüller, Cord; Swinburne, J.E.; Gerber, Vinzenz; Leeb, Tosso (2010). Characterization of the equine ITGAX gene and its association with recurrent airway obstruction in European Warmblood horses. Animal genetics, 41(5), pp. 559-60. Oxford: Blackwell 10.1111/j.1365-2052.2010.02066.x
Haase, Bianca; Brooks, S.A.; Tozaki, T.; Burger, D.; Poncet, P.A.; Rieder, S.; Hasegawa, T.; Penedo, C.; Leeb, Tosso (2009). Seven novel KIT mutations in horses with white coat colour phenotypes. Animal genetics, 40(5), pp. 623-9. Oxford: Blackwell 10.1111/j.1365-2052.2009.01893.x
Drögemüller, Cord; Engensteiner, M.; Moser, S.; Rieder, S.; Leeb, Tosso (2009). Genetic mapping of the belt pattern in Brown Swiss cattle to BTA3. Animal genetics, 40(2), pp. 225-9. Oxford: Blackwell 10.1111/j.1365-2052.2008.01826.x
Anistoroaei, R; Fredholm, M; Christensen, K; Leeb, Tosso (2008). Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation. Animal genetics, 39(6), pp. 645-648. Blackwell 10.1111/j.1365-2052.2008.01788.x
Haase, Bianca; Jude, R; Brooks, S A; Leeb, Tosso (2008). An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds. Animal genetics, 39(3), pp. 306-309. Blackwell 10.1111/j.1365-2052.2008.01715.x
Mömke, S; Fink, S; Wöhlke, A; Drögemüller, C.; Distl, O (2008). Linkage of bilateral convergent strabismus with exophthalmus (BCSE) to BTA5 and BTA18 in German Brown cattle. Animal genetics, 39(5), pp. 544-549. Wiley 10.1111/j.1365-2052.2008.01771.x
Prause, Andrea; Guionaud, C T; Klukowska-Rötzler, J; Giulotto, E; Magnani, E; Chowdhary, B P; Philipp, U; Leeb, Tosso; Mevissen, Meike (2007). Chromosomal assignment of five equine HTR genes by FISH and RH mapping. Animal genetics, 38(1), pp. 83-4. Oxford: Blackwell 10.1111/j.1365-2052.2006.01546.x
Wittwer, C; Löhring, K; Drögemüller, Cord; Hamann, H; Rosenberger, E; Distl, O (2007). Mapping quantitative trait loci for osteochondrosis in fetlock and hock joints and palmar/plantar osseus fragments in fetlock joints of South German Coldblood horses. Animal genetics, 38(4), pp. 350-7. Oxford: Blackwell 10.1111/j.1365-2052.2007.01610.x
Drögemüller, Cord; Rüfenacht, S; Wichert, B; Leeb, Tosso (2007). Mutations within the FGF5 gene are associated with hair length in cats. Animal genetics, 38(3), pp. 218-21. Oxford: Blackwell 10.1111/j.1365-2052.2007.01590.x
Tetens, J; Goldammer, T; Maddox, J F; Cockett, N E; Leeb, Tosso; Drögemüller, Cord (2007). A radiation hybrid map of sheep chromosome 23 based on ovine BAC-end sequences. Animal genetics, 38(2), pp. 132-40. Oxford: Blackwell 10.1111/j.1365-2052.2007.01572.x
Hamann, H; Jude, R; Sieme, H; Mertens, U; Töpfer-Petersen, E; Distl, O; Leeb, Tosso (2007). A polymorphism within the equine CRISP3 gene is associated with stallion fertility in Hanoverian warmblood horses. Animal genetics, 38(3), pp. 259-64. Oxford: Blackwell 10.1111/j.1365-2052.2007.01594.x
Guziewicz, K E; Owczarek, Marta; Küffer, J; Schelling, C; Tontis, A; Denis, C; Eggen, A; Leeb, Tosso; Dolf, Gaudenz; Braunschweig, Martin (2007). The locus for bovine dilated cardiomyopathy maps to chromosome 18. Animal genetics, 38(3), pp. 265-9. Oxford: Blackwell 10.1111/j.1365-2052.2007.01596.x
Glowatzki-Mullis, M L; Muntwyler, J; Gaillard, C (2007). Cost-effective parentage verification with 17-plex PCR for goats and 19-plex PCR for sheep. Animal genetics, 38(1), pp. 86-8. Oxford: Blackwell 10.1111/j.1365-2052.2006.01550.x
Zabek, T; Bugno, M; Klukowska-Rötzler, J; Uhlmann, B; Gerber, V; S¿ota, E (2007). Chromosomal assignment of five equine genes responsible for the development of the skeletal and nervous systems. Animal genetics, 38(4), pp. 425-6. Oxford: Blackwell 10.1111/j.1365-2052.2007.01624.x
Peter, C; Bruford, M; Perez, T; Dalamitra, S; Hewitt, G; Erhardt, G; Obexer-Rugg, Gaby; ECONOGENE, Consortium (2007). Genetic diversity and subdivision of 57 European and Middle-Eastern sheep breeds. Animal genetics, 38(1), pp. 37-44. Oxford: Blackwell 10.1111/j.1365-2052.2007.01561.x
Dierks, C; Mömke, S; Drögemüller, Cord; Leeb, Tosso; Chowdhary, B P; Distl, O (2006). A high-resolution comparative radiation hybrid map of equine chromosome 4q12-q22. Animal genetics, 37(5), pp. 513-7. Oxford: Blackwell 10.1111/j.1365-2052.2006.01510.x
Klukowska-Rötzler, Jolanta; Jost, U; Schelling, C; Dolf, Gaudenz; Chowdhary, B P; Leeb, Tosso; Gerber, Vinzenz (2006). Characterization and RH mapping of six gene-associated equine microsatellite markers. Animal genetics, 37(3), pp. 305-6. Oxford: Blackwell 10.1111/j.1365-2052.2006.01445.x
Meadows, J R S; Hanotte, O; Drögemüller, Cord; Calvo, J; Godfrey, R; Coltman, D; Maddox, J F; Marzanov, N; Kantanen, J; Kijas, J W (2006). Globally dispersed Y chromosomal haplotypes in wild and domestic sheep. Animal genetics, 37(5), pp. 444-53. Oxford: Blackwell 10.1111/j.1365-2052.2006.01496.x
Cañón, J; García, D; García-Atance, MA; Obexer-Ruff, Gaby; Lenstra, JA; Ajmone-Marsan, P; Dunner, S; ECONOGENE, Consortium (2006). Geographical partitioning of goat diversity in Europe and the Middle East. Animal genetics, 37(4), pp. 327-34. Oxford: Blackwell 10.1111/j.1365-2052.2006.01461.x
Karlskov-Mortensen, P; Bruun, C S; Braunschweig, M H; Sawera, M; Markljung, E; Enfält, A C; Hedebro-Velander, I; Josell, A; Lindahl, G; Lundström, K; von Seth, G; Jørgensen, C B; Andersson, L; Fredholm, M (2006). Genome-wide identification of quantitative trait loci in a cross between Hampshire and Landrace I: carcass traits. Animal genetics, 37(2), pp. 156-62. Oxford: Blackwell 10.1111/j.1365-2052.2005.01405.x
Glowatzki-Mullis, M L; Muntwyler, J; Pfister, W; Marti, E; Rieder, S; Poncet, P A; Gaillard, C (2006). Genetic diversity among horse populations with a special focus on the Franches-Montagnes breed. Animal genetics, 37(1), pp. 33-9. Oxford: Blackwell 10.1111/j.1365-2052.2005.01376.x
Pariset, L; Cappuccio, I; Joost, S; D'Andrea, M; Marletta, D; Ajmone Marsan, P; Valentini, A; Obexer-Rugg, Gaby; ECONOGENE, Consortium (2006). Characterization of single nucleotide polymorphismus in sheep and their variation as evidence of selection. Animal genetics, 37(3), pp. 290-2. Oxford: Blackwell 10.1111/j.1365-2052.2006.01441.x
Leeb, Tosso; Brenig, B; Rohrer, G A (2005). Characterization and linkage mapping of four gene-associated porcine microsatellites. Animal genetics, 36(3), pp. 279-280. Blackwell 10.1111/j.1365-2052.2005.01291.x
Sander, P; Drögemüller, Cord; Cadieu, E; André, C; Leeb, Tosso (2005). Analysis of the canine EDAR gene and exclusion as a candidate for the hairless phenotype in the Chinese Crested dog. Animal genetics, 36(2), pp. 168-171. Blackwell 10.1111/j.1365-2052.2005.01242.x
Solinas, S; Pauli, U; Kuhnert, Peter; Peterhans, Ernst; Fries, R (1992). Assignment of the porcine tumour necrosis factor alpha and beta genes to the chromosome region 7p11-q11 by in situ hybridization. Animal genetics, 23(3), pp. 267-271. Blackwell
