H. Holl

发表

Whole genome detection of sequence and structural polymorphism in six diverse horses

N. Sutter, M. Abri, H. Holl, 2019, bioRxiv.

Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.

T. Leeb, B. Haase, M. Penedo, 2013, Animal genetics.

Use of principle component analysis to quantitatively score the equine metabolic syndrome phenotype in an Arabian horse population

M. Mallicote, H. Holl, S. Brooks, 2018, PloS one.

Transcriptome diversity and differential expression in supporting limb laminitis.

H. Galantino-Homer, H. Holl, S. Brooks, 2021, Veterinary immunology and immunopathology.

Genome Diversity and the Origin of the Arabian Horse

Elissa J. Cosgrove, S. R. Miraei-Ashtiani, A. Clark, 2020, Scientific Reports.

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

T. Leeb, V. Jagannathan, H. Holl, 2022 .

A Frameshift Mutation in KIT is Associated with White Spotting in the Arabian Camel

D. Antczak, Y. Mohamoud, F. Almathen, 2017, Genes.

Genomewide association study reveals a risk locus for equine metabolic syndrome in the Arabian horse.

M. Mallicote, N. Place, H. Holl, 2017, Journal of animal science.

Construction of two whole genome radiation hybrid panels for dromedary (Camelus dromedarius): 5000RAD and 15000RAD

D. Larkin, P. Perelman, T. Raudsepp, 2018, Scientific Reports.

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

H. Holl, S. Brooks, D. Cook, 2019, Animal genetics.

De novo mutation of KIT discovered as a result of a non-hereditary white coat colour pattern

H. Holl, S. Brooks, E. Bailey, 2010 .

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

C. Bustamante, M. Carpenter, H. Holl, 2017, Animal genetics.

Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse

Arne Ludwig, David L. Adelson, Padmanabhan Mahadevan, 2013, PloS one.

Single nucleotide polymorphisms for DNA typing in the domestic horse

C. Bustamante, R. E. Everts, M. Carpenter, 2017, Animal genetics.

Generation of a de novo transcriptome from equine lamellar tissue

Z. Fei, Shan Gao, C. Andrews, 2015, BMC Genomics.

Leveraging Emerging Genomic Technologies For The Benefit Of The Domestic Horse

Heather Holl, H. Holl, 2014 .

Variant in the RFWD3 gene associated with PATN1, a modifier of leopard complex spotting.

M. Penedo, R. Bellone, H. Holl, 2016, Animal genetics.

PUBLISHED VERSION

M. Hofreiter, D. Adelson, A. Ludwig, 2013 .

Detection of two equine trisomies using SNP-CGH

H. Holl, S. Brooks, T. Lear, 2013, Mammalian Genome.

Generation of a de novo transcriptome from equine lamellar tissue

Z. Fei, Shan Gao, C. Andrews, 2015, BMC Genomics.

Variant in the RFWD3 gene associated with PATN1, a modifier of leopard complex spotting.

M. Penedo, R. Bellone, H. Holl, 2016, Animal genetics.

Genome Diversity and the Origin of the Arabian Horse

Elissa J. Cosgrove, S. R. Miraei-Ashtiani, J. Malek, 2020, Scientific Reports.

Genomewide association study reveals a risk locus for equine metabolic syndrome in the Arabian horse.

M. Mallicote, N. Place, H. Holl, 2017, Journal of animal science.