Sarah Kiener - Search Results

Year	Number of Results
2020	6
2021	3
2022	6
2023	2

1

A COL5A2 In-Frame Deletion in a Chihuahua with Ehlers-Danlos Syndrome.

Kiener S, Chevallier L, Jagannathan V, Briand A, Cochet-Faivre N, Reyes-Gomez E, Leeb T. Kiener S, et al. Genes (Basel). 2022 May 23;13(5):934. doi: 10.3390/genes13050934. Genes (Basel). 2022. PMID: 35627319 Free PMC article.

2

ABHD5 frameshift deletion in Golden Retrievers with ichthyosis.

Kiener S, Wiener DJ, Hopke K, Diesel AB, Jagannathan V, Mauldin EA, Casal ML, Leeb T. Kiener S, et al. G3 (Bethesda). 2022 Feb 4;12(2):jkab397. doi: 10.1093/g3journal/jkab397. G3 (Bethesda). 2022. PMID: 34791225 Free PMC article.

3

Independent COL5A1 Variants in Cats with Ehlers-Danlos Syndrome.

Kiener S, Apostolopoulos N, Schissler J, Hass PK, Leuthard F, Jagannathan V, Schuppisser C, Soto S, Welle M, Mayer U, Leeb T, Fischer NM, Kaessmeyer S. Kiener S, et al. Genes (Basel). 2022 Apr 29;13(5):797. doi: 10.3390/genes13050797. Genes (Basel). 2022. PMID: 35627182 Free PMC article.

4

Independent DSG4 frameshift variants in cats with hair shaft dystrophy.

Kiener S, Rostaher A, Rüfenacht S, Jagannathan V, Sundberg JP, Welle M, Leeb T. Kiener S, et al. Mol Genet Genomics. 2022 Jan;297(1):147-154. doi: 10.1007/s00438-021-01842-6. Epub 2021 Dec 8. Mol Genet Genomics. 2022. PMID: 34878611 Free PMC article.

5

KRT5 missense variant in a Cardigan Welsh Corgi with epidermolysis bullosa simplex.

Kiener S, Mauldin EA, Jagannathan V, Casal ML, Leeb T. Kiener S, et al. Anim Genet. 2022 Dec;53(6):892-896. doi: 10.1111/age.13257. Epub 2022 Aug 25. Anim Genet. 2022. PMID: 36004757 Free PMC article.

6

A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis.

Affolter VK, Kiener S, Jagannathan V, Nagle T, Leeb T. Affolter VK, et al. Among authors: kiener s. PLoS One. 2022 Oct 17;17(10):e0275367. doi: 10.1371/journal.pone.0275367. eCollection 2022. PLoS One. 2022. PMID: 36251712 Free PMC article.

7

A Missense Variant in SLC39A4 in a Litter of Turkish Van Cats with Acrodermatitis Enteropathica.

Kiener S, Cikota R, Welle M, Jagannathan V, Åhman S, Leeb T. Kiener S, et al. Genes (Basel). 2021 Aug 25;12(9):1309. doi: 10.3390/genes12091309. Genes (Basel). 2021. PMID: 34573291 Free PMC article.

8

Variants Affecting the C-Terminal Tail of UNC93B1 Are Not a Common Risk Factor for Systemic Lupus Erythematosus.

Kiener S, Ribi C, Keller I, Chizzolini C, Trendelenburg M, Huynh-Do U, von Kempis J, On Behalf Of Swiss Sle Cohort Study Sscs, Leeb T. Kiener S, et al. Genes (Basel). 2021 Aug 19;12(8):1268. doi: 10.3390/genes12081268. Genes (Basel). 2021. PMID: 34440442 Free PMC article.

9

A DSG1 Frameshift Variant in a Rottweiler Dog with Footpad Hyperkeratosis.

Backel KA, Kiener S, Jagannathan V, Casal ML, Leeb T, Mauldin EA. Backel KA, et al. Among authors: kiener s. Genes (Basel). 2020 Apr 24;11(4):469. doi: 10.3390/genes11040469. Genes (Basel). 2020. PMID: 32344723 Free PMC article.

10

LAMB3 Missense Variant in Australian Shepherd Dogs with Junctional Epidermolysis Bullosa.

Kiener S, Laprais A, Mauldin EA, Jagannathan V, Olivry T, Leeb T. Kiener S, et al. Genes (Basel). 2020 Sep 7;11(9):1055. doi: 10.3390/genes11091055. Genes (Basel). 2020. PMID: 32906717 Free PMC article.

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