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Elisabeth Dietschi

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Articles 14
Citations 254
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Recent Articles
1.
Jenkins C, De Risio L, Dietschi E, Leeb T, Rytz U, Schawalder P, et al.
Anim Genet . 2024 Oct; 55(6):914-917. PMID: 39394913
No abstract available.
2.
Gurtner C, Hug P, Kleiter M, Kohler K, Dietschi E, Jagannathan V, et al.
Genes (Basel) . 2020 Mar; 11(3). PMID: 32183361
Dog puppy loss by the age of six to eight weeks after normal development is relatively uncommon. Necropsy findings in two spontaneously deceased Belgian Shepherd puppies indicated an abnormal accumulation...
3.
Marchant T, Dietschi E, Rytz U, Schawalder P, Jagannathan V, Rasouliha S, et al.
PLoS Genet . 2019 May; 15(5):e1008102. PMID: 31095560
In flat-faced dog breeds, air resistance caused by skull conformation is believed to be a major determinant of Brachycephalic Obstructive Airway Syndrome (BOAS). The clinical presentation of BOAS is heterogeneous,...
4.
Letko A, Dietschi E, Nieburg M, Jagannathan V, Gurtner C, Oevermann A, et al.
Genes (Basel) . 2019 May; 10(5). PMID: 31083464
Spinocerebellar ataxias is an umbrella term for clinically- and neuropathologically-heterogeneous early-onset hereditary neurodegenerative diseases affecting several dog breeds. The purpose of this study is to identify the causative genetic variant...
5.
Brenig B, Steingraber L, Shan S, Xu F, Hirschfeld M, Andag R, et al.
Haematologica . 2019 Mar; 104(11):2307-2313. PMID: 30846504
Hemophilia B is a classical monogenic, X-chromosomal, recessively transmitted bleeding disorder caused by genetic variants within the coagulation factor IX gene (). Although hemophilia B has been described in dogs,...
6.
Mauri N, Kleiter M, Dietschi E, Leschnik M, Hogler S, Wiedmer M, et al.
G3 (Bethesda) . 2017 Jun; 7(8):2729-2737. PMID: 28620085
Spongy degeneration with cerebellar ataxia (SDCA) is a genetically heterogeneous neurodegenerative disorder with autosomal recessive inheritance in Malinois dogs, one of the four varieties of the Belgian Shepherd breed. Using...
7.
Bauer A, Waluk D, Galichet A, Timm K, Jagannathan V, Sayar B, et al.
PLoS Genet . 2017 Mar; 13(3):e1006651. PMID: 28249031
Ichthyoses are a heterogeneous group of inherited cornification disorders characterized by generalized dry skin, scaling and/or hyperkeratosis. Ichthyosis vulgaris is the most common form of ichthyosis in humans and caused...
8.
Wielaender F, Sarviaho R, James F, Hytonen M, Cortez M, Kluger G, et al.
Proc Natl Acad Sci U S A . 2017 Feb; 114(10):2669-2674. PMID: 28223533
The clinical and electroencephalographic features of a canine generalized myoclonic epilepsy with photosensitivity and onset in young Rhodesian Ridgeback dogs (6 wk to 18 mo) are described. A fully penetrant...
9.
Mauri N, Kleiter M, Leschnik M, Hogler S, Dietschi E, Wiedmer M, et al.
G3 (Bethesda) . 2016 Dec; 7(2):663-669. PMID: 28007838
Spongy degeneration with cerebellar ataxia (SDCA) is a severe neurodegenerative disease with monogenic autosomal recessive inheritance in Malinois dogs, one of the four varieties of the Belgian Shepherd breed. We...
10.
Frischknecht M, Jagannathan V, Plattet P, Neuditschko M, Signer-Hasler H, Bachmann I, et al.
PLoS One . 2015 Oct; 10(10):e0140749. PMID: 26474182
The identification of quantitative trait loci (QTL) such as height and their underlying causative variants is still challenging and often requires large sample sizes. In humans hundreds of loci with...