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Page 1
Comprehensive molecular profiling of multiple myeloma identifies refined copy number and expression subtypes.
Skerget S, Penaherrera D, Chari A, Jagannath S, Siegel DS, Vij R, Orloff G, Jakubowiak A, Niesvizky R, Liles D, Berdeja J, Levy M, Wolf J, Usmani SZ; MMRF CoMMpass Network; Christofferson AW, Nasser S, Aldrich JL, Legendre C, Benard B, Miller C, Turner B, Kurdoglu A, Washington M, Yellapantula V, Adkins JR, Cuyugan L, Boateng M, Helland A, Kyman S, McDonald J, Reiman R, Stephenson K, Tassone E, Blanski A, Livermore B, Kirchhoff M, Rohrer DC, D'Agostino M, Gamella M, Collison K, Stumph J, Kidd P, Donnelly A, Zaugg B, Toone M, McBride K, DeRome M, Rogers J, Craig D, Liang WS, Gutierrez NC, Jewell SD, Carpten J, Anderson KC, Cho HJ, Auclair D, Lonial S, Keats JJ. Skerget S, et al. Among authors: adkins jr. Nat Genet. 2024 Sep;56(9):1878-1889. doi: 10.1038/s41588-024-01853-0. Epub 2024 Aug 19. Nat Genet. 2024. PMID: 39160255 Free PMC article.
Genomic analysis across 53 canine cancer types reveals novel mutations and high clinical actionability potential.
Sakthikumar S, Warrier M, Whitley D, Facista S, Adkins J, Aman S, Tsinajinnie D, Duran N, Siravegna G, Ahmed Z, Day K, Jenkins B, Patel N, Ryden K, Nadai J, Banovich K, Powers B, Edwards J, Steinberg J, Fielder S, Wong S, Byron SA, Izatt T, Zismann V, Boateng M, Zhu Z, Chuang HY, Trent JM, Haworth D, Chon E, Hendricks W, Wang G. Sakthikumar S, et al. Vet Comp Oncol. 2024 Mar;22(1):30-41. doi: 10.1111/vco.12944. Epub 2023 Dec 5. Vet Comp Oncol. 2024. PMID: 38053317
Primary nodular chest amyloidoma: A case report and review of literature.
Crain MA, Vasilakis GM, Adkins JR, Adelanwa A, Hogg JP, Lakhani DA, Kim C. Crain MA, et al. Among authors: adkins jr. Radiol Case Rep. 2021 Dec 21;17(3):631-637. doi: 10.1016/j.radcr.2021.11.048. eCollection 2022 Mar. Radiol Case Rep. 2021. PMID: 35027986 Free PMC article.
Remembered: Elisabeth G. Kaveggia.
Opitz JM, Adkins WN Jr. Opitz JM, et al. Among authors: adkins wn jr. Am J Med Genet A. 2015 Apr;167A(4):681-2. doi: 10.1002/ajmg.a.36885. Epub 2015 Feb 13. Am J Med Genet A. 2015. PMID: 25676741 No abstract available.
Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy.
Collie AM, Landsverk ML, Ruzzo E, Mefford HC, Buysse K, Adkins JR, Knutzen DM, Barnett K, Brown RH Jr, Parry GJ, Yum SW, Simpson DA, Olney RK, Chinnery PF, Eichler EE, Chance PF, Hannibal MC. Collie AM, et al. Among authors: adkins jr. J Med Genet. 2010 Sep;47(9):601-7. doi: 10.1136/jmg.2009.072348. Epub 2009 Nov 25. J Med Genet. 2010. PMID: 19939853
121 results