Publications by authors named "Vidhya Jagannathan"

100Publications

Missense Variant in Australian Shepherd Dogs with Junctional Epidermolysis Bullosa.

Genes (Basel) 2020 Sep 7;11(9). Epub 2020 Sep 7.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes11091055DOI Listing
September 2020

Novel Brown Coat Color (Cocoa) in French Bulldogs Results from a Nonsense Variant in .

Genes (Basel) 2020 Jun 9;11(6). Epub 2020 Jun 9.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes11060636DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349258PMC
June 2020

A Frameshift Variant in a Rottweiler Dog with Footpad Hyperkeratosis.

Genes (Basel) 2020 04 24;11(4). Epub 2020 Apr 24.

School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.3390/genes11040469DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230267PMC
April 2020

Missense Variant in Belgian Shepherd Dogs with Cardiomyopathy and Juvenile Mortality.

Genes (Basel) 2020 03 14;11(3). Epub 2020 Mar 14.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes11030313DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140874PMC
March 2020

The Locus is under Selection in Large-Sized Pakistani Goat Breeds.

Genes (Basel) 2020 02 5;11(2). Epub 2020 Feb 5.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes11020168DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074466PMC
February 2020

A major facilitator superfamily domain 8 frameshift variant in a cat with suspected neuronal ceroid lipofuscinosis.

J Vet Intern Med 2020 Jan 20;34(1):289-293. Epub 2019 Dec 20.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

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http://dx.doi.org/10.1111/jvim.15663DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979099PMC
January 2020

A Missense Variant in a Domestic Shorthair Cat with Testicular Hypoplasia and Persistent Primary Dentition.

Genes (Basel) 2019 10 14;10(10). Epub 2019 Oct 14.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes10100806DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826659PMC
October 2019

Dog10K: an international sequencing effort to advance studies of canine domestication, phenotypes and health.

Natl Sci Rev 2019 Jul 10;6(4):810-824. Epub 2019 Apr 10.

State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China.

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http://dx.doi.org/10.1093/nsr/nwz049DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776107PMC
July 2019

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

Anim Genet 2019 Dec 29;50(6):786-787. Epub 2019 Aug 29.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, 3001, Switzerland.

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http://dx.doi.org/10.1111/age.12843DOI Listing
December 2019

Frameshift Variant in Three Dogs with Recurrent Inflammatory Pulmonary Disease.

Genes (Basel) 2019 07 26;10(8). Epub 2019 Jul 26.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes10080567DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723478PMC
July 2019

A Nonsense Variant in Golden Retrievers with Congenital Eye Malformations.

Genes (Basel) 2019 06 14;10(6). Epub 2019 Jun 14.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes10060454DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628151PMC
June 2019

A Missense Variant in in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia.

Genes (Basel) 2019 05 10;10(5). Epub 2019 May 10.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3012 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes10050362DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562999PMC
May 2019

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

BMC Genomics 2019 May 8;20(1):349. Epub 2019 May 8.

Institute of Genetics, Department of Clinical Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109a, CH-3012, Bern, Switzerland.

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https://bmcgenomics.biomedcentral.com/articles/10.1186/s1286
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http://dx.doi.org/10.1186/s12864-019-5711-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505205PMC
May 2019

ATP13A2 missense variant in Australian Cattle Dogs with late onset neuronal ceroid lipofuscinosis.

Mol Genet Metab 2019 05 27;127(1):95-106. Epub 2019 Mar 27.

Mason Eye Institute, University of Missouri School of Medicine, Columbia, MO, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2018.11.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548654PMC
May 2019

Differentially expressed microRNAs, including a large microRNA cluster on chromosome 24, are associated with equine sarcoid and squamous cell carcinoma.

Vet Comp Oncol 2019 Jun 15;17(2):155-164. Epub 2019 Feb 15.

Department of Clinical Veterinary Medicine, Swiss Institute of Equine Medicine, Vetsuisse Faculty, University of Bern and Agroscope, Bern, Switzerland.

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http://doi.wiley.com/10.1111/vco.12458
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http://dx.doi.org/10.1111/vco.12458DOI Listing
June 2019

Complex Structural Variant Associated with Non-syndromic Canine Retinal Degeneration.

G3 (Bethesda) 2019 02 7;9(2):425-437. Epub 2019 Feb 7.

Department of Clinical Sciences & Advanced Medicine, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA

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http://dx.doi.org/10.1534/g3.118.200859DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385984PMC
February 2019

NHLRC1 dodecamer repeat expansion demonstrated by whole genome sequencing in a Chihuahua with Lafora disease.

Anim Genet 2019 Feb 7;50(1):118-119. Epub 2018 Dec 7.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1111/age.12756DOI Listing
February 2019

Differences in miRNA differential expression in whole blood between horses with sarcoid regression and progression.

J Vet Intern Med 2019 Jan 2;33(1):241-250. Epub 2018 Dec 2.

Swiss Institute of Equine Medicine, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

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http://dx.doi.org/10.1111/jvim.15375DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335546PMC
January 2019

Genetic variant in the NSDHL gene in a cat with multiple congenital lesions resembling inflammatory linear verrucous epidermal nevi.

Vet Dermatol 2019 Feb 25;30(1):64-e18. Epub 2018 Nov 25.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Länggassstrasse 120, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1111/vde.12699DOI Listing
February 2019

MicroRNA fingerprints in serum and whole blood of sarcoid-affected horses as potential non-invasive diagnostic biomarkers.

Vet Comp Oncol 2019 Mar 28;17(1):107-117. Epub 2018 Nov 28.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

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http://doi.wiley.com/10.1111/vco.12451
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http://dx.doi.org/10.1111/vco.12451DOI Listing
March 2019

A COL2A1 de novo variant in a Holstein bulldog calf.

Anim Genet 2019 Feb 31;50(1):113-114. Epub 2018 Oct 31.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1111/age.12735DOI Listing
February 2019

Exclusion of adrenoceptor alpha 2 variants in a horse insensitive to medetomidine.

Anim Genet 2018 Apr 23;49(2):141. Epub 2018 Jan 23.

Division of Anaesthesiology, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1111/age.12636DOI Listing
April 2018

Differential Expression of Serum MicroRNAs Supports CD4⁺ T Cell Differentiation into Th2/Th17 Cells in Severe Equine Asthma.

Genes (Basel) 2017 Dec 12;8(12). Epub 2017 Dec 12.

Department of Clinical Research and Veterinary Public Health, Institute of Genetics, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109A, 3012 Bern, Switzerland.

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http://dx.doi.org/10.3390/genes8120383DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748701PMC
December 2017

OCA2 splice site variant in German Spitz dogs with oculocutaneous albinism.

PLoS One 2017 3;12(10):e0185944. Epub 2017 Oct 3.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0185944PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626509PMC
October 2017

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

BMC Genomics 2017 Aug 25;18(1):662. Epub 2017 Aug 25.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1186/s12864-017-4081-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574090PMC
August 2017

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

BMC Genet 2017 08 2;18(1):74. Epub 2017 Aug 2.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109a, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1186/s12863-017-0541-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541750PMC
August 2017

A Large Deletion in the Gene in Labrador Retrievers with a Congenital Cornification Disorder.

G3 (Bethesda) 2017 09 7;7(9):3115-3121. Epub 2017 Sep 7.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Switzerland

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http://dx.doi.org/10.1534/g3.117.1124DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592936PMC
September 2017

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

Vet Dermatol 2017 Dec 2;28(6):616-e150. Epub 2017 Jul 2.

Vetsuisse Faculty, Institute of Genetics, University of Bern, Bremgartenstrasse 109a, Bern, 3001, Switzerland.

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http://dx.doi.org/10.1111/vde.12462DOI Listing
December 2017

Frame-shift variant in the CHRNE gene in a juvenile dog with suspected myasthenia gravis-like disease.

Anim Genet 2017 Oct 16;48(5):625. Epub 2017 May 16.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1111/age.12558DOI Listing
October 2017

LPS-induced modules of co-expressed genes in equine peripheral blood mononuclear cells.

BMC Genomics 2017 01 5;18(1):34. Epub 2017 Jan 5.

Department of Clinical Veterinary Medicine, Swiss Institute of Equine Medicine, Vetsuisse Faculty, University of Bern, and Agroscope, Länggassstrasse 124, 3012, Bern, Switzerland.

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http://dx.doi.org/10.1186/s12864-016-3390-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217269PMC
January 2017

A novel MITF variant in a white American Standardbred foal.

Anim Genet 2017 Feb 5;48(1):123-124. Epub 2016 Sep 5.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1111/age.12484DOI Listing
February 2017

An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture.

G3 (Bethesda) 2016 09 8;6(9):2963-70. Epub 2016 Sep 8.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Switzerland Dermfocus, Vetsuisse Faculty, University of Bern, 3001 Switzerland

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http://dx.doi.org/10.1534/g3.116.032433DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015953PMC
September 2016

A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype.

G3 (Bethesda) 2016 09 8;6(9):2949-54. Epub 2016 Sep 8.

Department of Clinical Research, Molecular Dermatology and Stem Cell Research, University of Bern, 3001, Switzerland DermFocus, University of Bern, 3001, Switzerland

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http://dx.doi.org/10.1534/g3.116.033225DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015951PMC
September 2016

A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle.

BMC Genomics 2016 06 30;17:479. Epub 2016 Jun 30.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109a, Bern, 3001, Switzerland.

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http://dx.doi.org/10.1186/s12864-016-2832-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929742PMC
June 2016

Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1.

BMC Vet Res 2016 Jun 13;12:100. Epub 2016 Jun 13.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109a, Bern, CH-3001, Switzerland.

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http://dx.doi.org/10.1186/s12917-016-0739-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906884PMC
June 2016

Initial characterization of stiff skin-like syndrome in West Highland white terriers.

Vet Dermatol 2016 Jun;27(3):210-e53

Tieraerztliche Spezialisten, Rodigallee 85, D-22043, Hamburg, Germany.

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http://dx.doi.org/10.1111/vde.12316DOI Listing
June 2016

MFSD8 single-base pair deletion in a Chihuahua with neuronal ceroid lipofuscinosis.

Anim Genet 2016 Oct 5;47(5):631. Epub 2016 May 5.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, 3001, Switzerland.

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http://dx.doi.org/10.1111/age.12449DOI Listing
October 2016

Whole-Genome Sequencing of a Canine Family Trio Reveals a FAM83G Variant Associated with Hereditary Footpad Hyperkeratosis.

G3 (Bethesda) 2016 Jan 8;6(3):521-7. Epub 2016 Jan 8.

Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden

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http://dx.doi.org/10.1534/g3.115.025643DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777115PMC
January 2016

A Non-Synonymous HMGA2 Variant Decreases Height in Shetland Ponies and Other Small Horses.

PLoS One 2015 16;10(10):e0140749. Epub 2015 Oct 16.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland; Swiss Competence Center of Animal Breeding and Genetics, University of Bern, Bern University of Applied Sciences HAFL & Agroscope, 3001, Bern, Switzerland.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0140749PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608717PMC
June 2016

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

PLoS Genet 2015 Jul 23;11(7):e1005427. Epub 2015 Jul 23.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland; DermFocus, University of Bern, Bern, Switzerland.

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http://dx.doi.org/10.1371/journal.pgen.1005427DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512707PMC
July 2015

A novel KIT variant in an Icelandic horse with white-spotted coat colour.

Anim Genet 2015 Aug 9;46(4):466. Epub 2015 Jun 9.

Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1111/age.12313DOI Listing
August 2015

DNA-based diagnosis of rare diseases in veterinary medicine: a 4.4 kb deletion of ITGB4 is associated with epidermolysis bullosa in Charolais cattle.

BMC Vet Res 2015 Mar 4;11:48. Epub 2015 Mar 4.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109a, 3001, Bern, Switzerland.

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http://dx.doi.org/10.1186/s12917-015-0366-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351973PMC
March 2015

Epidermolysis bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene.

BMC Vet Res 2015 Feb 7;11:23. Epub 2015 Feb 7.

Department of Veterinary Disease Biology, Section for Veterinary Pathology, Faculty of Health and Medical Sciences, University of Copenhagen, Ridebanevej 3, DK-1870, Frederiksberg C, Denmark.

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http://www.biomedcentral.com/1746-6148/11/23
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http://dx.doi.org/10.1186/s12917-015-0334-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4328060PMC
February 2015

A naturally occurring prfA truncation in a Listeria monocytogenes field strain contributes to reduced replication and cell-to-cell spread.

Vet Microbiol 2015 Aug 10;179(1-2):91-101. Epub 2015 Mar 10.

Division of Neurological Sciences, Department of Clinical Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern, Bern CH-3001, Switzerland. Electronic address:

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http://dx.doi.org/10.1016/j.vetmic.2015.03.002DOI Listing
August 2015

Whole genome sequencing confirms KIT insertions in a white cat.

Anim Genet 2015 Feb 16;46(1):98. Epub 2014 Dec 16.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, 3001, Switzerland; DermFocus, University of Bern, Bern, 3001, Switzerland.

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http://dx.doi.org/10.1111/age.12246DOI Listing
February 2015

A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs.

Hum Genet 2015 Jan 13;134(1):127-9. Epub 2014 Nov 13.

Vetsuisse Faculty, Institute of Genetics, University of Bern, Bremgartenstrasse 109a, 3001, Bern, Switzerland.

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http://link.springer.com/10.1007/s00439-014-1506-5
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http://dx.doi.org/10.1007/s00439-014-1506-5DOI Listing
January 2015

A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH).

PLoS Genet 2014 15;10(5):e1004370. Epub 2014 May 15.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland; DermFocus, University of Bern, Bern, Switzerland.

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http://dx.doi.org/10.1371/journal.pgen.1004370DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022470PMC
December 2014

A nonsense mutation in the IKBKG gene in mares with incontinentia pigmenti.

PLoS One 2013 4;8(12):e81625. Epub 2013 Dec 4.

Institute of Medical Genetics, Cardiff University, Cardiff, United Kingdom ; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0081625PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852476PMC
September 2014