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Rebecca Renee Bellone

TitleASSOC ADJ PROF-FY
InstitutionUniversity of California Davis
DepartmentVM: POPULATION HLTH & REPROD
AddressONE SHIELDS AVE.
CA 95616
Phone530-752-9299
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Singer-Berk M, Knickelbein KE, Vig S, Liu J, Bentley E, Nunnery C, Reilly C, Dwyer A, Drögemüller C, Unger L, Gerber V, Lassaline M, Bellone R. Genetic risk for squamous cell carcinoma of the nictitating membrane parallels that of the limbus in Haflinger horses. Anim Genet. 2018 Jul 12. PMID: 29999543.
      View in: PubMed
    2. Bellone R. Genetic Testing as a Tool to Identify Horses with or at Risk for Ocular Disorders. Vet Clin North Am Equine Pract. 2017 Dec; 33(3):627-645. PMID: 29103563.
      View in: PubMed
    3. Mack M, Kowalski E, Grahn R, Bras D, Penedo MCT, Bellone R. Two Variants in SLC24A5 Are Associated with "Tiger-Eye" Iris Pigmentation in Puerto Rican Paso Fino Horses. G3 (Bethesda). 2017 08 07; 7(8):2799-2806. PMID: 28655738.
      View in: PubMed
    4. Scott EY, Mansour T, Bellone R, Brown CT, Mienaltowski MJ, Penedo MC, Ross PJ, Valberg SJ, Murray JD, Finno CJ. Identification of long non-coding RNA in the horse transcriptome. BMC Genomics. 2017 07 04; 18(1):511. PMID: 28676104.
      View in: PubMed
    5. Bellone R, Liu J, Petersen JL, Mack M, Singer-Berk M, Drögemüller C, Malvick J, Wallner B, Brem G, Penedo MC, Lassaline M. A missense mutation in damage-specific DNA binding protein 2 is a genetic risk factor for limbal squamous cell carcinoma in horses. Int J Cancer. 2017 07 15; 141(2):342-353. PMID: 28425625.
      View in: PubMed
    6. Mansour TA, Scott EY, Finno CJ, Bellone R, Mienaltowski MJ, Penedo MC, Ross PJ, Valberg SJ, Murray JD, Brown CT. Tissue resolved, gene structure refined equine transcriptome. BMC Genomics. 2017 01 20; 18(1):103. PMID: 28107812.
      View in: PubMed
    7. Tuggle CK, Giuffra E, White SN, Clarke L, Zhou H, Ross PJ, Acloque H, Reecy JM, Archibald A, Bellone R, Boichard M, Chamberlain A, Cheng H, Crooijmans RP, Delany ME, Finno CJ, Groenen MA, Hayes B, Lunney JK, Petersen JL, Plastow GS, Schmidt CJ, Song J, Watson M. GO-FAANG meeting: a Gathering On Functional Annotation of Animal Genomes. Anim Genet. 2016 Oct; 47(5):528-33. PMID: 27453069.
      View in: PubMed
    8. Scott ML, John EE, Bellone R, Ching JC, Loewen ME, Sandmeyer LS, Grahn BH, Forsyth GW. Redundant contribution of a Transient Receptor Potential cation channel Member 1 exon 11 single nucleotide polymorphism to equine congenital stationary night blindness. BMC Vet Res. 2016 Jun 21; 12(1):121. PMID: 27329127; PMCID: PMC4915136.
      View in: PubMed, PubMed Central
    9. Holl HM, Brooks SA, Archer S, Brown K, Malvick J, Penedo MC, Bellone R. Variant in the RFWD3 gene associated with PATN1, a modifier of leopard complex spotting. Anim Genet. 2016 Feb; 47(1):91-101. PMID: 26568529.
      View in: PubMed
    10. Ludwig A, Reissmann M, Benecke N, Bellone R, Sandoval-Castellanos E, Cieslak M, Fortes GG, Morales-Muñiz A, Hofreiter M, Pruvost M. Twenty-five thousand years of fluctuating selection on leopard complex spotting and congenital night blindness in horses. Philos Trans R Soc Lond B Biol Sci. 2015 Jan 19; 370(1660):20130386. PMID: 25487337; PMCID: PMC4275893.
      View in: PubMed, PubMed Central
    11. Lassaline M, Cranford TL, Latimer CA, Bellone R. Limbal squamous cell carcinoma in Haflinger horses. Vet Ophthalmol. 2015 Sep; 18(5):404-8. PMID: 25312447.
      View in: PubMed
    12. Fritz KL, Kaese HJ, Valberg SJ, Hendrickson JA, Rendahl AK, Bellone R, Dynes KM, Wagner ML, Lucio MA, Cuomo FM, Brinkmeyer-Langford CL, Skow LC, Mickelson JR, Rutherford MS, McCue ME. Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horses. Anim Genet. 2014 Jun; 45(3):392-9. PMID: 24467435.
      View in: PubMed
    13. Promerová M, Andersson LS, Juras R, Penedo MC, Reissmann M, Tozaki T, Bellone R, Dunner S, Horín P, Imsland F, Imsland P, Mikko S, Modrý D, Roed KH, Schwochow D, Vega-Pla JL, Mehrabani-Yeganeh H, Yousefi-Mashouf N, G Cothran E, Lindgren G, Andersson L. Worldwide frequency distribution of the 'Gait keeper' mutation in the DMRT3 gene. Anim Genet. 2014 Apr; 45(2):274-82. PMID: 24444049.
      View in: PubMed
    14. Bellone R, Holl H, Setaluri V, Devi S, Maddodi N, Archer S, Sandmeyer L, Ludwig A, Foerster D, Pruvost M, Reissmann M, Bortfeldt R, Adelson DL, Lim SL, Nelson J, Haase B, Engensteiner M, Leeb T, Forsyth G, Mienaltowski MJ, Mahadevan P, Hofreiter M, Paijmans JL, Gonzalez-Fortes G, Grahn B, Brooks SA. Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse. PLoS One. 2013; 8(10):e78280. PMID: 24167615; PMCID: PMC3805535.
      View in: PubMed, PubMed Central
    15. Haase B, Signer-Hasler H, Binns MM, Obexer-Ruff G, Hauswirth R, Bellone R, Burger D, Rieder S, Wade CM, Leeb T. Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses. PLoS One. 2013; 8(9):e75071. PMID: 24098679; PMCID: PMC3787084.
      View in: PubMed, PubMed Central
    16. Hauswirth R, Jude R, Haase B, Bellone R, Archer S, Holl H, Brooks SA, Tozaki T, Penedo MC, Rieder S, Leeb T. Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes. Anim Genet. 2013 Dec; 44(6):763-5. PMID: 23659293.
      View in: PubMed
    17. Makvandi-Nejad S, Hoffman GE, Allen JJ, Chu E, Gu E, Chandler AM, Loredo AI, Bellone R, Mezey JG, Brooks SA, Sutter NB. Four loci explain 83% of size variation in the horse. PLoS One. 2012; 7(7):e39929. PMID: 22808074; PMCID: PMC3394777.
      View in: PubMed, PubMed Central
    18. Pruvost M, Bellone R, Benecke N, Sandoval-Castellanos E, Cieslak M, Kuznetsova T, Morales-Muñiz A, O'Connor T, Reissmann M, Hofreiter M, Ludwig A. Genotypes of predomestic horses match phenotypes painted in Paleolithic works of cave art. Proc Natl Acad Sci U S A. 2011 Nov 15; 108(46):18626-30. PMID: 22065780; PMCID: PMC3219153.
      View in: PubMed, PubMed Central
    19. Sandmeyer LS, Bellone R, Archer S, Bauer BS, Nelson J, Forsyth G, Grahn BH. Congenital stationary night blindness is associated with the leopard complex in the Miniature Horse. Vet Ophthalmol. 2012 Jan; 15(1):18-22. PMID: 22051042.
      View in: PubMed
    20. Brooks SA, Makvandi-Nejad S, Chu E, Allen JJ, Streeter C, Gu E, McCleery B, Murphy BA, Bellone R, Sutter NB. Morphological variation in the horse: defining complex traits of body size and shape. Anim Genet. 2010 Dec; 41 Suppl 2:159-65. PMID: 21070291.
      View in: PubMed
    21. Bellone R. Pleiotropic effects of pigmentation genes in horses. Anim Genet. 2010 Dec; 41 Suppl 2:100-10. PMID: 21070283.
      View in: PubMed
    22. Bellone R, Forsyth G, Leeb T, Archer S, Sigurdsson S, Imsland F, Mauceli E, Engensteiner M, Bailey E, Sandmeyer L, Grahn B, Lindblad-Toh K, Wade CM. Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses. Brief Funct Genomics. 2010 May; 9(3):193-207. PMID: 20353955.
      View in: PubMed
    23. Wade CM, Giulotto E, Sigurdsson S, Zoli M, Gnerre S, Imsland F, Lear TL, Adelson DL, Bailey E, Bellone R, Blöcker H, Distl O, Edgar RC, Garber M, Leeb T, Mauceli E, MacLeod JN, Penedo MC, Raison JM, Sharpe T, Vogel J, Andersson L, Antczak DF, Biagi T, Binns MM, Chowdhary BP, Coleman SJ, Della Valle G, Fryc S, Guérin G, Hasegawa T, Hill EW, Jurka J, Kiialainen A, Lindgren G, Liu J, Magnani E, Mickelson JR, Murray J, Nergadze SG, Onofrio R, Pedroni S, Piras MF, Raudsepp T, Rocchi M, Røed KH, Ryder OA, Searle S, Skow L, Swinburne JE, Syvänen AC, Tozaki T, Valberg SJ, Vaudin M, White JR, Zody MC. Genome sequence, comparative analysis, and population genetics of the domestic horse. Science. 2009 Nov 06; 326(5954):865-7. PMID: 19892987.
      View in: PubMed
    24. Cook D, Brooks S, Bellone R, Bailey E. Missense mutation in exon 2 of SLC36A1 responsible for champagne dilution in horses. PLoS Genet. 2008 Sep 19; 4(9):e1000195. PMID: 18802473; PMCID: PMC2535566.
      View in: PubMed, PubMed Central
    25. Bellone R, Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B. Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus). Genetics. 2008 Aug; 179(4):1861-70. PMID: 18660533; PMCID: PMC2516064.
      View in: PubMed, PubMed Central
    26. Grahn BH, Pinard C, Archer S, Bellone R, Forsyth G, Sandmeyer LS. Congenital ocular anomalies in purebred and crossbred Rocky and Kentucky Mountain horses in Canada. Can Vet J. 2008 Jul; 49(7):675-81. PMID: 18827844; PMCID: PMC2430397.
      View in: PubMed, PubMed Central
    27. Bellone R, Lawson S, Hunter N, Archer S, Bailey E. Analysis of a SNP in exon 7 of equine OCA2 and its exclusion as a cause for appaloosa spotting. Anim Genet. 2006 Oct; 37(5):525. PMID: 16978190.
      View in: PubMed
    28. Bellone R, Lear T, Adelson DL, Bailey E. Comparative mapping of oculocutaneous albinism type II (OCA2), transient receptor potential cation channel, subfamily M member 1 (TRPM1) and two equine microsatellites, ASB08 and 1CA43, among four equid species by fluorescence in situ hybridization. Cytogenet Genome Res. 2006; 114(1):93A. PMID: 16717457.
      View in: PubMed
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