Rebecca Bellone, BS; PhD

Title(s)Adjunct Professor, School of Veterinary Medicine
SchoolUniversity of California, Davis
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    1. Genetics of Equine Ocular Disease. Vet Clin North Am Equine Pract. 2020 Aug; 36(2):303-322. Bellone RR. PMID: 32654784.
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    2. Evidence supports white spotting in donkeys as a homozygous lethal condition. Anim Genet. 2020 Jul 13. Tanaka J, Grahn R, Bellone RR. PMID: 32657451.
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    3. Whole genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse. Equine Vet J. 2020 Jul 12. Hack YL, Crabtree EE, Avila F, Sutton RB, Grahn RA, Oh A, Gilger B, Bellone RR. PMID: 32654228.
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    4. Genetic Testing in the Horse. Vet Clin North Am Equine Pract. 2020 Jun 10. Bellone RR, Avila F. PMID: 32534857.
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    5. A De Novo MITF Deletion Explains a Novel Splashed White Phenotype in an American Paint Horse. J Hered. 2020 May 20; 111(3):287-293. Magdesian KG, Tanaka J, Bellone RR. PMID: 32242630.
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    6. Risk factors for equine recurrent uveitis in a population of Appaloosa horses in western Canada. Vet Ophthalmol. 2020 May; 23(3):515-525. Sandmeyer LS, Kingsley NB, Walder C, Archer S, Leis ML, Bellone RR, Bauer BS. PMID: 32086865.
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    7. Functionally Annotating Regulatory Elements in the Equine Genome Using Histone Mark ChIP-Seq. Genes (Basel). 2019 12 18; 11(1). Kingsley NB, Kern C, Creppe C, Hales EN, Zhou H, Kalbfleisch TS, MacLeod JN, Petersen JL, Finno CJ, Bellone RR. PMID: 31861495.
      View in: PubMed   Mentions:    Fields:    Translation:AnimalsCells
    8. Genetic investigation of equine recurrent uveitis in Appaloosa horses. Anim Genet. 2020 Feb; 51(1):111-116. Rockwell H, Mack M, Famula T, Sandmeyer L, Bauer B, Dwyer A, Lassaline M, Beeson S, Archer S, McCue M, Bellone RR. PMID: 31793009.
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    9. Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies. Genes (Basel). 2019 10 19; 10(10). Tanaka J, Leeb T, Rushton J, Famula TR, Mack M, Jagannathan V, Flury C, Bachmann I, Eberth J, McDonnell SM, Penedo MCT, Bellone RR. PMID: 31635058.
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    10. Warmblood fragile foal syndrome type 1 mutation (PLOD1 c.2032G>A) is not associated with catastrophic breakdown and has a low allele frequency in the Thoroughbred breed. Equine Vet J. 2020 May; 52(3):411-414. Bellone RR, Ocampo NR, Hughes SS, Le V, Arthur R, Finno CJ, Penedo MCT. PMID: 31502696.
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    11. Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post-genome era. Anim Genet. 2019 Dec; 50(6):569-597. Raudsepp T, Finno CJ, Bellone RR, Petersen JL. PMID: 31568563.
      View in: PubMed   Mentions: 1     Fields:    Translation:AnimalsCells
    12. Additional Evidence for DDB2 T338M as a Genetic Risk Factor for Ocular Squamous Cell Carcinoma in Horses. Int J Genomics. 2019; 2019:3610965. Singer-Berk MH, Knickelbein KE, Lounsberry ZT, Crausaz M, Vig S, Joshi N, Britton M, Settles ML, Reilly CM, Bentley E, Nunnery C, Dwyer A, Lassaline ME, Bellone RR. PMID: 31637255.
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    13. Erratum: Author Correction: Improved reference genome for the domestic horse increases assembly contiguity and composition. Commun Biol. 2019; 2:342. Kalbfleisch TS, Rice ES, DePriest MS, Walenz BP, Hestand MS, Vermeesch JR, O'Connell BL, Fiddes IT, Vershinina AO, Saremi NF, Petersen JL, Finno CJ, Bellone RR, McCue ME, Brooks SA, Bailey E, Orlando L, Green RE, Miller DC, Antczak DF, MacLeod JN. PMID: 31531403.
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    14. Author Correction: Improved reference genome for the domestic horse increases assembly contiguity and composition. Commun Biol. 2019 Sep 11; 2(1):342. Kalbfleisch TS, Rice ES, DePriest MS, Walenz BP, Hestand MS, Vermeesch JR, O'Connell BL, Fiddes IT, Vershinina AO, Saremi NF, Petersen JL, Finno CJ, Bellone RR, McCue ME, Brooks SA, Bailey E, Orlando L, Green RE, Miller DC, Antczak DF, MacLeod JN. PMID: 31925183.
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    15. Horses with equine recurrent uveitis have an activated CD4+ T-cell phenotype that can be modulated by mesenchymal stem cells in vitro. Vet Ophthalmol. 2020 Jan; 23(1):160-170. Saldinger LK, Nelson SG, Bellone RR, Lassaline M, Mack M, Walker NJ, Borjesson DL. PMID: 31441218.
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    16. A missense mutation in damage-specific DNA binding protein 2 is a genetic risk factor for ocular squamous cell carcinoma in Belgian horses. Equine Vet J. 2020 Jan; 52(1):34-40. Knickelbein KE, Lassaline ME, Singer-Berk M, Reilly CM, Clode AB, Famula TR, Michau TM, Bellone RR. PMID: 30903710.
      View in: PubMed   Mentions:    Fields:    Translation:Animals
    17. Improved reference genome for the domestic horse increases assembly contiguity and composition. Commun Biol. 2018; 1:197. Kalbfleisch TS, Rice ES, DePriest MS, Walenz BP, Hestand MS, Vermeesch JR, O Connell BL, Fiddes IT, Vershinina AO, Saremi NF, Petersen JL, Finno CJ, Bellone RR, McCue ME, Brooks SA, Bailey E, Orlando L, Green RE, Miller DC, Antczak DF, MacLeod JN. PMID: 30456315.
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    18. Effects of high fat diet-induced obesity on mammary tumorigenesis in the PyMT/MMTV murine model. Cancer Biol Ther. 2019; 20(4):487-496. Cranford TL, Velázquez KT, Enos RT, Sougiannis AT, Bader JE, Carson MS, Bellone RR, Chatzistamou I, Nagarkatti M, Murphy EA. PMID: 30388923.
      View in: PubMed   Mentions: 1     Fields:    Translation:Animals
    19. Generation of an equine biobank to be used for Functional Annotation of Animal Genomes project. Anim Genet. 2018 Dec; 49(6):564-570. Burns EN, Bordbari MH, Mienaltowski MJ, Affolter VK, Barro MV, Gianino F, Gianino G, Giulotto E, Kalbfleisch TS, Katzman SA, Lassaline M, Leeb T, Mack M, Müller EJ, MacLeod JN, Ming-Whitfield B, Alanis CR, Raudsepp T, Scott E, Vig S, Zhou H, Petersen JL, Bellone RR, Finno CJ. PMID: 30311254.
      View in: PubMed   Mentions: 2     Fields:    Translation:Animals
    20. Ruling out BGN variants as simple X-linked causative mutations for bilateral corneal stromal loss in Friesian horses. Anim Genet. 2018 Dec; 49(6):656-657. Alberi C, Hisey E, Lassaline M, Atilano A, Kalbfleisch T, Stoppini R, Hermans H, Back W, Mienaltowski MJ, Bellone RR. PMID: 30246344.
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    21. Limbal squamous cell carcinoma in a Rocky Mountain Horse: Case report and investigation of genetic contribution. Vet Ophthalmol. 2019 Mar; 22(2):201-205. Knickelbein KE, Lassaline ME, Bellone RR. PMID: 30238589.
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    22. Genetic risk for squamous cell carcinoma of the nictitating membrane parallels that of the limbus in Haflinger horses. Anim Genet. 2018 Oct; 49(5):457-460. 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 RR. PMID: 29999543.
      View in: PubMed   Mentions: 1     Fields:    Translation:AnimalsCells
    23. 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. Bellone RR. PMID: 29103563.
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    24. 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. Mack M, Kowalski E, Grahn R, Bras D, Penedo MCT, Bellone R. PMID: 28655738.
      View in: PubMed   Mentions: 1     Fields:    Translation:Animals
    25. Identification of long non-coding RNA in the horse transcriptome. BMC Genomics. 2017 07 04; 18(1):511. Scott EY, Mansour T, Bellone RR, Brown CT, Mienaltowski MJ, Penedo MC, Ross PJ, Valberg SJ, Murray JD, Finno CJ. PMID: 28676104.
      View in: PubMed   Mentions: 4     Fields:    Translation:AnimalsCells
    26. 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. Bellone RR, Liu J, Petersen JL, Mack M, Singer-Berk M, Drögemüller C, Malvick J, Wallner B, Brem G, Penedo MC, Lassaline M. PMID: 28425625.
      View in: PubMed   Mentions: 2     Fields:    Translation:AnimalsCells
    27. Tissue resolved, gene structure refined equine transcriptome. BMC Genomics. 2017 01 20; 18(1):103. Mansour TA, Scott EY, Finno CJ, Bellone RR, Mienaltowski MJ, Penedo MC, Ross PJ, Valberg SJ, Murray JD, Brown CT. PMID: 28107812.
      View in: PubMed   Mentions: 7     Fields:    Translation:AnimalsCells
    28. Inherited ocular disorders. . 2016 Dec 28; 545-566. Lynne Sheila Sandmeyer, Rebecca Bellone. .
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    29. Morphological Variation in Gaited Horse Breeds. Journal of Equine Veterinary Science. 2016 Aug 1; 43(Appl Anim Behav Sci 80 2003):55-65. Elizabeth A. Staiger, Rebecca R. Bellone, Nathan B. Sutter, Samantha A. Brooks. .
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    30. GO-FAANG meeting: a Gathering On Functional Annotation of Animal Genomes. Anim Genet. 2016 Oct; 47(5):528-33. Tuggle CK, Giuffra E, White SN, Clarke L, Zhou H, Ross PJ, Acloque H, Reecy JM, Archibald A, Bellone RR, 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. PMID: 27453069.
      View in: PubMed   Mentions: 8     Fields:    Translation:Animals
    31. 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. Scott ML, John EE, Bellone RR, Ching JC, Loewen ME, Sandmeyer LS, Grahn BH, Forsyth GW. PMID: 27329127.
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    32. Variant in the RFWD3 gene associated with PATN1, a modifier of leopard complex spotting. Anim Genet. 2016 Feb; 47(1):91-101. Holl HM, Brooks SA, Archer S, Brown K, Malvick J, Penedo MC, Bellone RR. PMID: 26568529.
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    33. 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. Ludwig A, Reissmann M, Benecke N, Bellone R, Sandoval-Castellanos E, Cieslak M, Fortes GG, Morales-Muñiz A, Hofreiter M, Pruvost M. PMID: 25487337.
      View in: PubMed   Mentions: 8     Fields:    Translation:AnimalsCells
    34. Limbal squamous cell carcinoma in Haflinger horses. Vet Ophthalmol. 2015 Sep; 18(5):404-8. Lassaline M, Cranford TL, Latimer CA, Bellone RR. PMID: 25312447.
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    35. Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horses. Anim Genet. 2014 Jun; 45(3):392-9. Fritz KL, Kaese HJ, Valberg SJ, Hendrickson JA, Rendahl AK, Bellone RR, Dynes KM, Wagner ML, Lucio MA, Cuomo FM, Brinkmeyer-Langford CL, Skow LC, Mickelson JR, Rutherford MS, McCue ME. PMID: 24467435.
      View in: PubMed   Mentions: 6     Fields:    Translation:AnimalsCells
    36. Worldwide frequency distribution of the 'Gait keeper' mutation in the DMRT3 gene. Anim Genet. 2014 Apr; 45(2):274-82. 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. PMID: 24444049.
      View in: PubMed   Mentions: 9     Fields:    Translation:Animals
    37. 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. Bellone RR, 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. PMID: 24167615.
      View in: PubMed   Mentions: 19     Fields:    Translation:AnimalsCells
    38. 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. Haase B, Signer-Hasler H, Binns MM, Obexer-Ruff G, Hauswirth R, Bellone RR, Burger D, Rieder S, Wade CM, Leeb T. PMID: 24098679.
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    39. Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes. Anim Genet. 2013 Dec; 44(6):763-5. Hauswirth R, Jude R, Haase B, Bellone RR, Archer S, Holl H, Brooks SA, Tozaki T, Penedo MC, Rieder S, Leeb T. PMID: 23659293.
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    40. Coat Color Genomics. . 2013 Apr 8; 143-153. Samantha A. Brooks, Rebecca R. Bellone. .
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    41. Four loci explain 83% of size variation in the horse. PLoS One. 2012; 7(7):e39929. Makvandi-Nejad S, Hoffman GE, Allen JJ, Chu E, Gu E, Chandler AM, Loredo AI, Bellone RR, Mezey JG, Brooks SA, Sutter NB. PMID: 22808074.
      View in: PubMed   Mentions: 47     Fields:    Translation:HumansAnimalsCells
    42. Reply to Bar-Oz and Lev-Yadun: Horse colors in time and space. Proceedings of the National Academy of Sciences of the United States of America. 2012 May 15; 109(20):e1213-e1213. Arne Ludwig, Melanie Pruvost, Rebecca Bellone, Norbert Benecke, Edson Sandoval-Castellanos, Arturo Morales-Muñiz, Terry O'Connor, Monika Reissmann, Michael Hofreiter. .
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    43. 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. 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. PMID: 22065780.
      View in: PubMed   Mentions: 9     Fields:    Translation:Animals
    44. Congenital stationary night blindness is associated with the leopard complex in the Miniature Horse. Vet Ophthalmol. 2012 Jan; 15(1):18-22. Sandmeyer LS, Bellone RR, Archer S, Bauer BS, Nelson J, Forsyth G, Grahn BH. PMID: 22051042.
      View in: PubMed   Mentions: 7     Fields:    Translation:Animals
    45. Pleiotropic effects of pigmentation genes in horses. Anim Genet. 2010 Dec; 41 Suppl 2:100-10. Bellone RR. PMID: 21070283.
      View in: PubMed   Mentions: 14     Fields:    Translation:Animals
    46. Morphological variation in the horse: defining complex traits of body size and shape. Anim Genet. 2010 Dec; 41 Suppl 2:159-65. Brooks SA, Makvandi-Nejad S, Chu E, Allen JJ, Streeter C, Gu E, McCleery B, Murphy BA, Bellone R, Sutter NB. PMID: 21070291.
      View in: PubMed   Mentions: 13     Fields:    Translation:Animals
    47. 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. Bellone RR, 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. PMID: 20353955.
      View in: PubMed   Mentions: 11     Fields:    Translation:AnimalsCells
    48. Genome sequence, comparative analysis, and population genetics of the domestic horse. Science. 2009 Nov 06; 326(5954):865-7. Wade CM, Giulotto E, Sigurdsson S, Zoli M, Gnerre S, Imsland F, Lear TL, Adelson DL, Bailey E, Bellone RR, 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, Lander ES, Lindblad-Toh K. PMID: 19892987.
      View in: PubMed   Mentions: 227     Fields:    Translation:HumansAnimalsCells
    49. Missense mutation in exon 2 of SLC36A1 responsible for champagne dilution in horses. PLoS Genet. 2008 Sep 19; 4(9):e1000195. Cook D, Brooks S, Bellone R, Bailey E. PMID: 18802473.
      View in: PubMed   Mentions: 12     Fields:    Translation:AnimalsCells
    50. 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. Bellone RR, Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B. PMID: 18660533.
      View in: PubMed   Mentions: 59     Fields:    Translation:Animals
    51. Congenital ocular anomalies in purebred and crossbred Rocky and Kentucky Mountain horses in Canada. Can Vet J. 2008 Jul; 49(7):675-81. Grahn BH, Pinard C, Archer S, Bellone R, Forsyth G, Sandmeyer LS. PMID: 18827844.
      View in: PubMed   Mentions: 10     Fields:    Translation:Animals
    52. 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. Bellone R, Lawson S, Hunter N, Archer S, Bailey E. PMID: 16978190.
      View in: PubMed   Mentions: 1     Fields:    Translation:Animals
    53. 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. Bellone R, Lear T, Adelson DL, Bailey E. PMID: 16717457.
      View in: PubMed   Mentions: 2     Fields:    Translation:Animals
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