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Items: 1 to 20 of 248

1.

Comprehensive characterization of horse genome variation by whole-genome sequencing of 88 horses.

Jagannathan V, Gerber V, Rieder S, Tetens J, Thaller G, Drögemüller C, Leeb T.

Anim Genet. 2018 Dec 7. doi: 10.1111/age.12753. [Epub ahead of print]

PMID:
30525216
2.

A non-coding regulatory variant in the 5'-region of the MITF gene is associated with white-spotted coat in Brown Swiss cattle.

Hofstetter S, Seefried F, Häfliger IM, Jagannathan V, Leeb T, Drögemüller C.

Anim Genet. 2018 Dec 2. doi: 10.1111/age.12751. [Epub ahead of print]

PMID:
30506810
3.

A COL2A1 de novo variant in a Holstein bulldog calf.

Häfliger IM, Behn H, Freick M, Jagannathan V, Drögemüller C.

Anim Genet. 2018 Oct 31. doi: 10.1111/age.12735. [Epub ahead of print] No abstract available.

PMID:
30378686
4.

Genetic risk for squamous cell carcinoma of the nictitating membrane parallels that of the limbus in Haflinger horses.

Singer-Berk M, Knickelbein KE, Vig S, Liu J, Bentley E, Nunnery C, Reilly C, Dwyer A, Drögemüller C, Unger L, Gerber V, Lassaline M, Bellone RR.

Anim Genet. 2018 Oct;49(5):457-460. doi: 10.1111/age.12695. Epub 2018 Jul 12.

PMID:
29999543
5.

A Missense Mutation in the Vacuolar Protein Sorting 11 (VPS11) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs.

Lucot KL, Dickinson PJ, Finno CJ, Mansour TA, Letko A, Minor KM, Mickelson JR, Drögemüller C, Brown CT, Bannasch DL.

G3 (Bethesda). 2018 Jul 31;8(8):2773-2780. doi: 10.1534/g3.118.200376.

6.

Evaluation of HOXC8 in crested Swiss chicken.

Joller S, Ammann P, Flury C, Drögemüller C.

Anim Genet. 2018 Aug;49(4):334-336. doi: 10.1111/age.12674. Epub 2018 May 18.

PMID:
29774580
7.

[Bovine dilated cardiomyopathy: Almost forgotten but still present].

Riedi A, Drögemüller C, Gurtner C, Meylan M.

Schweiz Arch Tierheilkd. 2018 May;160(5):289-293. doi: 10.17236/sat00158. German.

8.

Canine NAPEPLD-associated models of human myelin disorders.

Minor KM, Letko A, Becker D, Drögemüller M, Mandigers PJJ, Bellekom SR, Leegwater PAJ, Stassen QEM, Putschbach K, Fischer A, Flegel T, Matiasek K, Ekenstedt KJ, Furrow E, Patterson EE, Platt SR, Kelly PA, Cassidy JP, Shelton GD, Lucot K, Bannasch DL, Martineau H, Muir CF, Priestnall SL, Henke D, Oevermann A, Jagannathan V, Mickelson JR, Drögemüller C.

Sci Rep. 2018 Apr 11;8(1):5818. doi: 10.1038/s41598-018-23938-7.

9.

[Fanconi-Bickel-Syndrom: a novel genetic disease in Original Braunvieh].

Joller S, Stettler M, Locher I, Dettwiler M, Seefried F, Meylan M, Drögemüller C.

Schweiz Arch Tierheilkd. 2018 Mar;160(3):179-184. doi: 10.17236/sat00152. German.

10.

Crossed beaks in a local Swiss chicken breed.

Joller S, Bertschinger F, Kump E, Spiri A, von Rotz A, Schweizer-Gorgas D, Drögemüller C, Flury C.

BMC Vet Res. 2018 Mar 5;14(1):68. doi: 10.1186/s12917-018-1398-z.

11.

Meta-analysis of genome-wide association studies for cattle stature identifies common genes that regulate body size in mammals.

Bouwman AC, Daetwyler HD, Chamberlain AJ, Ponce CH, Sargolzaei M, Schenkel FS, Sahana G, Govignon-Gion A, Boitard S, Dolezal M, Pausch H, Brøndum RF, Bowman PJ, Thomsen B, Guldbrandtsen B, Lund MS, Servin B, Garrick DJ, Reecy J, Vilkki J, Bagnato A, Wang M, Hoff JL, Schnabel RD, Taylor JF, Vinkhuyzen AAE, Panitz F, Bendixen C, Holm LE, Gredler B, Hozé C, Boussaha M, Sanchez MP, Rocha D, Capitan A, Tribout T, Barbat A, Croiseau P, Drögemüller C, Jagannathan V, Vander Jagt C, Crowley JJ, Bieber A, Purfield DC, Berry DP, Emmerling R, Götz KU, Frischknecht M, Russ I, Sölkner J, Van Tassell CP, Fries R, Stothard P, Veerkamp RF, Boichard D, Goddard ME, Hayes BJ.

Nat Genet. 2018 Mar;50(3):362-367. doi: 10.1038/s41588-018-0056-5. Epub 2018 Feb 19.

PMID:
29459679
12.

Differential distribution of Y-chromosome haplotypes in Swiss and Southern European goat breeds.

Vidal O, Drögemüller C, Obexer-Ruff G, Reber I, Jordana J, Martínez A, Bâlteanu VA, Delgado JV, Eghbalsaied S, Landi V, Goyache F, Traoré A, Pazzola M, Vacca GM, Badaoui B, Pilla F, D'Andrea M, Álvarez I, Capote J, Sharaf A, Pons À, Amills M.

Sci Rep. 2017 Nov 23;7(1):16161. doi: 10.1038/s41598-017-15593-1.

13.

Two brown coat colour-associated TYRP1 variants (bc and bd ) occur in Leonberger dogs.

Letko A, Drögemüller C.

Anim Genet. 2017 Dec;48(6):732-733. doi: 10.1111/age.12612. Epub 2017 Oct 5. No abstract available.

PMID:
28983931
14.

A genome-wide significant association on chromosome 2 for footrot resistance/susceptibility in Swiss White Alpine sheep.

Niggeler A, Tetens J, Stäuble A, Steiner A, Drögemüller C.

Anim Genet. 2017 Dec;48(6):712-715. doi: 10.1111/age.12614. Epub 2017 Oct 5.

PMID:
28983925
15.

Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species.

Bourneuf E, Otz P, Pausch H, Jagannathan V, Michot P, Grohs C, Piton G, Ammermüller S, Deloche MC, Fritz S, Leclerc H, Péchoux C, Boukadiri A, Hozé C, Saintilan R, Créchet F, Mosca M, Segelke D, Guillaume F, Bouet S, Baur A, Vasilescu A, Genestout L, Thomas A, Allais-Bonnet A, Rocha D, Colle MA, Klopp C, Esquerré D, Wurmser C, Flisikowski K, Schwarzenbacher H, Burgstaller J, Brügmann M, Dietschi E, Rudolph N, Freick M, Barbey S, Fayolle G, Danchin-Burge C, Schibler L, Bed'Hom B, Hayes BJ, Daetwyler HD, Fries R, Boichard D, Pin D, Drögemüller C, Capitan A.

Sci Rep. 2017 Sep 13;7(1):11466. doi: 10.1038/s41598-017-11523-3.

16.

Liver transcriptome analysis reveals important factors involved in the metabolic adaptation of the transition cow.

Ha NT, Drögemüller C, Reimer C, Schmitz-Hsu F, Bruckmaier RM, Simianer H, Gross JJ.

J Dairy Sci. 2017 Nov;100(11):9311-9323. doi: 10.3168/jds.2016-12454. Epub 2017 Aug 31.

PMID:
28865861
17.

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

Joller S, Berenguer Veiga I, Drögemüller C.

Anim Genet. 2017 Dec;48(6):729-730. doi: 10.1111/age.12591. Epub 2017 Aug 30. No abstract available.

PMID:
28856769
18.

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs.

Becker D, Minor KM, Letko A, Ekenstedt KJ, Jagannathan V, Leeb T, Shelton GD, Mickelson JR, Drögemüller C.

BMC Genomics. 2017 Aug 25;18(1):662. doi: 10.1186/s12864-017-4081-z.

19.

A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle.

Agerholm JS, McEvoy FJ, Heegaard S, Charlier C, Jagannathan V, Drögemüller C.

BMC Genet. 2017 Aug 2;18(1):74. doi: 10.1186/s12863-017-0541-3.

20.

A de novo germline mutation of DLX3 in a Brown Swiss calf with tricho-dento-osseus-like syndrome.

Hofstetter S, Welle M, Gorgas D, Balmer P, Roosje P, Mock T, Meylan M, Jagannathan V, Drögemüller C.

Vet Dermatol. 2017 Dec;28(6):616-e150. doi: 10.1111/vde.12462. Epub 2017 Jul 2.

PMID:
28670783

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