Vidhya Jagannathan
Overview
Explore the profile of Vidhya Jagannathan including associated specialties, affiliations and a list of published articles.
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192
Citations
2144
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Recent Articles
1.
Rietmann S, Loderstedt S, Matiasek K, Kiefer I, Jagannathan V, Leeb T
Anim Genet
. 2024 Oct;
55(6):801-809.
PMID: 39434657
Neuronal ceroid lipofuscinosis (NCL) represents a heterogenous group of lysosomal storage diseases resulting in progressive neurodegeneration. We investigated two Small Swiss Hound littermates that showed progressive ataxia and loss of...
2.
Schwarz C, Jagannathan V, Schelling C, Leeb T
Anim Genet
. 2024 Sep;
55(6):849-853.
PMID: 39307576
Muscular dystrophies represent a group of disorders characterized by progressive muscle degeneration and weakness. An important subgroup are the dystrophin-related muscular dystrophies caused by variants in the DMD gene. They...
3.
Cook S, Schwarz C, Guevar J, Assenmacher C, Sheehy M, Fanzone N, et al.
Mov Disord
. 2024 Aug;
39(11):2049-2057.
PMID: 39177409
Background: Neuroaxonal dystrophy (NAD) is a group of inherited neurodegenerative disorders characterized primarily by the presence of spheroids (swollen axons) throughout the central nervous system. In humans, NAD is heterogeneous,...
4.
Kiener S, Lehner G, Jagannathan V, Welle M, Leeb T
Anim Genet
. 2024 Aug;
55(5):725-732.
PMID: 39136317
Ichthyoses comprise a large heterogeneous group of skin disorders, characterized by generalized scaly and hyperkeratotic skin. We investigated a miniature poodle with early onset generalized scaling, dry and irregularly thickened...
5.
Rietmann S, Cochet-Faivre N, Dropsy H, Jagannathan V, Chevallier L, Leeb T
Genes (Basel)
. 2024 Jul;
15(7).
PMID: 39062633
Hypohidrotic ectodermal dysplasia is a developmental defect characterized by sparse or absent hair, missing or malformed teeth and defects in eccrine glands. Loss-of-function variants in the X-chromosomal gene have been...
6.
Rietmann S, Nowell S, Keating M, Bauer C, Jagannathan V, Leeb T
Anim Genet
. 2024 May;
55(4):705-707.
PMID: 38745376
No abstract available.
7.
Rietmann S, Lange A, Soto S, Thom N, Manz E, Jagannathan V, et al.
Anim Genet
. 2024 May;
55(4):692-696.
PMID: 38742646
Split paw pad disease is a scarcely defined phenotype characterized by skin lesions on the paw pads of dogs. We studied a family of German Shepherd dogs, in which four...
8.
Christen M, Gregor K, Bottcher-Kunneke A, Lombardo M, Baumgartner W, Jagannathan V, et al.
Anim Genet
. 2024 May;
55(4):588-598.
PMID: 38712841
Neuronal ceroid lipofuscinoses (NCL) are among the most prevalent neurodegenerative disorders of early life in humans. Disease-causing variants have been described for 13 different NCL genes. In this study, a...
9.
Mizukami K, Dorsey-Oresto A, Raj K, Eringis A, Furrow E, Martin E, et al.
Sci Rep
. 2024 May;
14(1):10346.
PMID: 38710903
Mammals are generally resistant to Mycobacterium avium complex (MAC) infections. We report here on a primary immunodeficiency disorder causing increased susceptibility to MAC infections in a canine breed. Adult Miniature...
10.
Letko A, Gurtner C, Jagannathan V, Drogemuller C
Anim Genet
. 2024 May;
55(4):700-701.
PMID: 38692855
No abstract available.