Brian W. Davis

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2007-2013 Texas A & M University, College Station, TX, United States 
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"Brian Davis"
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Publications

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Jevit MJ, Castaneda C, Paria N, et al. (2023) Trio-binning of a hinny refines the comparative organization of the horse and donkey X chromosomes and reveals novel species-specific features. Scientific Reports. 13: 20180
Meadows JRS, Kidd JM, Wang GD, et al. (2023) Author Correction: Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture. Genome Biology. 24: 255
Bredemeyer KR, Hillier L, Harris AJ, et al. (2023) Single-haplotype comparative genomics provides insights into lineage-specific structural variation during cat evolution. Nature Genetics. 55: 1953-1963
Hart SFM, Yonemitsu MA, Giersch RM, et al. (2023) Centuries of genome instability and evolution in soft-shell clam, Mya arenaria, bivalve transmissible neoplasia. Nature Cancer
Momen M, Brauer K, Patterson MM, et al. (2023) Genetic architecture and polygenic risk score prediction of degenerative suspensory ligament desmitis (DSLD) in the Peruvian Horse. Frontiers in Genetics. 14: 1201628
Meadows JRS, Kidd JM, Wang GD, et al. (2023) Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture. Genome Biology. 24: 187
Stroupe S, Martone C, McCann B, et al. (2023) Chromosome-level reference genome for North American bison (Bison bison) and variant database aids in identifying albino mutation. G3 (Bethesda, Md.)
Ott JA, Mitchell C, Sheppard M, et al. (2023) Evolution of immunogenetic components encoding ultralong CDR H3. Immunogenetics
Binversie EE, Momen M, Rosa GJM, et al. (2022) Across-breed genetic investigation of canine hip dysplasia, elbow dysplasia, and anterior cruciate ligament rupture using whole-genome sequencing. Frontiers in Genetics. 13: 913354
Castaneda C, Radovic L, Felkel S, et al. (2022) Copy number variation (CNV) of horse Y chromosome genes in normal equine populations and in horses with abnormal sex development and subfertility; Relationship of CNVs with Y haplogroups. G3 (Bethesda, Md.)
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