Lafayette C - Search Results

1

A novel splice mutation within equine KIT and the W15 allele in the homozygous state lead to all white coat color phenotypes.

Holl HM, Brooks SA, Carpenter ML, Bustamante CD, Lafayette C. Holl HM, et al. Among authors: lafayette c. Anim Genet. 2017 Aug;48(4):497-498. doi: 10.1111/age.12554. Epub 2017 Apr 5. Anim Genet. 2017. PMID: 28378922 No abstract available.

2

Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes.

Dürig N, Jude R, Holl H, Brooks SA, Lafayette C, Jagannathan V, Leeb T. Dürig N, et al. Among authors: lafayette c. Anim Genet. 2017 Aug;48(4):483-485. doi: 10.1111/age.12556. Epub 2017 Apr 26. Anim Genet. 2017. PMID: 28444912

3

Single nucleotide polymorphisms for DNA typing in the domestic horse.

Holl HM, Vanhnasy J, Everts RE, Hoefs-Martin K, Cook D, Brooks SA, Carpenter ML, Bustamante CD, Lafayette C. Holl HM, et al. Among authors: lafayette c. Anim Genet. 2017 Dec;48(6):669-676. doi: 10.1111/age.12608. Epub 2017 Sep 13. Anim Genet. 2017. PMID: 28901559

4

Whole-genome sequencing reveals a large deletion in the MITF gene in horses with white spotted coat colour and increased risk of deafness.

Henkel J, Lafayette C, Brooks SA, Martin K, Patterson-Rosa L, Cook D, Jagannathan V, Leeb T. Henkel J, et al. Among authors: lafayette c. Anim Genet. 2019 Apr;50(2):172-174. doi: 10.1111/age.12762. Epub 2019 Jan 15. Anim Genet. 2019. PMID: 30644113

5

A candidate gene approach identifies variants in SLC45A2 that explain dilute phenotypes, pearl and sunshine, in compound heterozygote horses.

Holl HM, Pflug KM, Yates KM, Hoefs-Martin K, Shepard C, Cook DG, Lafayette C, Brooks SA. Holl HM, et al. Among authors: lafayette c. Anim Genet. 2019 Jun;50(3):271-274. doi: 10.1111/age.12790. Epub 2019 Apr 21. Anim Genet. 2019. PMID: 31006892

6

Identification of a novel missense variant in SLC45A2 associated with dilute snowdrop phenotype in Gypsy horses.

Bisbee D, Carpenter ML, Hoefs-Martin K, Brooks SA, Lafayette C. Bisbee D, et al. Among authors: lafayette c. Anim Genet. 2020 Mar;51(2):342-343. doi: 10.1111/age.12913. Epub 2020 Jan 21. Anim Genet. 2020. PMID: 31961951 No abstract available.

7

De novo mutation of KIT causes extensive coat white patterning in a family of Berber horses.

Martin K, Patterson Rosa L, Vierra M, Foster G, Brooks SA, Lafayette C. Martin K, et al. Among authors: lafayette c. Anim Genet. 2021 Feb;52(1):135-137. doi: 10.1111/age.13017. Epub 2020 Oct 28. Anim Genet. 2021. PMID: 33111383 No abstract available.

8

Fragile Foal Syndrome (PLOD1 c.2032G>A) occurs across diverse horse populations.

Martin K, Brooks S, Vierra M, Lafayette WT, McClure S, Carpenter M, Lafayette C. Martin K, et al. Among authors: lafayette wt, lafayette c. Anim Genet. 2021 Feb;52(1):137-138. doi: 10.1111/age.13020. Epub 2020 Nov 9. Anim Genet. 2021. PMID: 33165934 No abstract available.

9

Two Variants of KIT Causing White Patterning in Stock-Type Horses.

Patterson Rosa L, Martin K, Vierra M, Foster G, Lundquist E, Brooks SA, Lafayette C. Patterson Rosa L, et al. Among authors: lafayette c. J Hered. 2021 Aug 25;112(5):447-451. doi: 10.1093/jhered/esab033. J Hered. 2021. PMID: 34223905

10

Stock-type equine disciplines Hunter, Reining and Roping are associated with the A allele at the DMRT3 locus for gait phenotypes in the horse.

Patterson Rosa L, Staiger EA, Martin K, Vierra M, Foster G, Lundquist E, Brooks SA, Lafayette C. Patterson Rosa L, et al. Among authors: lafayette c. Anim Genet. 2021 Oct;52(5):773-774. doi: 10.1111/age.13110. Epub 2021 Jul 12. Anim Genet. 2021. PMID: 34250625 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

22 results

Search Page