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Journal Abstract Search

490 related items for PubMed ID: 26096145

  • 1. Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases.
    Rai K, Pilarski R, Cebulla CM, Abdel-Rahman MH.
    Clin Genet; 2016 Mar; 89(3):285-94. PubMed ID: 26096145
    [Abstract] [Full Text] [Related]

  • 2. Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide.
    Walpole S, Pritchard AL, Cebulla CM, Pilarski R, Stautberg M, Davidorf FH, de la Fouchardière A, Cabaret O, Golmard L, Stoppa-Lyonnet D, Garfield E, Njauw CN, Cheung M, Turunen JA, Repo P, Järvinen RS, van Doorn R, Jager MJ, Luyten GPM, Marinkovic M, Chau C, Potrony M, Höiom V, Helgadottir H, Pastorino L, Bruno W, Andreotti V, Dalmasso B, Ciccarese G, Queirolo P, Mastracci L, Wadt K, Kiilgaard JF, Speicher MR, van Poppelen N, Kilic E, Al-Jamal RT, Dianzani I, Betti M, Bergmann C, Santagata S, Dahiya S, Taibjee S, Burke J, Poplawski N, O'Shea SJ, Newton-Bishop J, Adlard J, Adams DJ, Lane AM, Kim I, Klebe S, Racher H, Harbour JW, Nickerson ML, Murali R, Palmer JM, Howlie M, Symmons J, Hamilton H, Warrier S, Glasson W, Johansson P, Robles-Espinoza CD, Ossio R, de Klein A, Puig S, Ghiorzo P, Nielsen M, Kivelä TT, Tsao H, Testa JR, Gerami P, Stern MH, Paillerets BB, Abdel-Rahman MH, Hayward NK.
    J Natl Cancer Inst; 2018 Dec 01; 110(12):1328-1341. PubMed ID: 30517737
    [Abstract] [Full Text] [Related]

  • 3. Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases.
    Pilarski R, Cebulla CM, Massengill JB, Rai K, Rich T, Strong L, McGillivray B, Asrat MJ, Davidorf FH, Abdel-Rahman MH.
    Genes Chromosomes Cancer; 2014 Feb 01; 53(2):177-82. PubMed ID: 24243779
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  • 4. BAP1 Syndrome - Predisposition to Malignant Mesothelioma, Skin and Uveal Melanoma, Renal and Other Cancers.
    Foretová L, Navrátilová M, Svoboda M, Házová J, Vašíčková P, Sťahlová EH, Fabian P, Schneiderová M, Macháčková E.
    Klin Onkol; 2019 Feb 01; 32(Supplementum2):118-122. PubMed ID: 31409087
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  • 7. CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma.
    Betti M, Aspesi A, Biasi A, Casalone E, Ferrante D, Ogliara P, Gironi LC, Giorgione R, Farinelli P, Grosso F, Libener R, Rosato S, Turchetti D, Maffè A, Casadio C, Ascoli V, Dianzani C, Colombo E, Piccolini E, Pavesi M, Miccoli S, Mirabelli D, Bracco C, Righi L, Boldorini R, Papotti M, Matullo G, Magnani C, Pasini B, Dianzani I.
    Cancer Lett; 2016 Aug 10; 378(2):120-30. PubMed ID: 27181379
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  • 8. Genotypic and Phenotypic Features of BAP1 Cancer Syndrome: A Report of 8 New Families and Review of Cases in the Literature.
    Haugh AM, Njauw CN, Bubley JA, Verzì AE, Zhang B, Kudalkar E, VandenBoom T, Walton K, Swick BL, Kumar R, Rana HQ, Cochrane S, McCormick SR, Shea CR, Tsao H, Gerami P.
    JAMA Dermatol; 2017 Oct 01; 153(10):999-1006. PubMed ID: 28793149
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  • 9. BAP1 Germline Mutations in Finnish Patients with Uveal Melanoma.
    Turunen JA, Markkinen S, Wilska R, Saarinen S, Raivio V, Täll M, Lehesjoki AE, Kivelä TT.
    Ophthalmology; 2016 May 01; 123(5):1112-7. PubMed ID: 26876698
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  • 10. Histomorphologic spectrum of BAP1 negative melanocytic neoplasms in a family with BAP1-associated cancer susceptibility syndrome.
    Marušić Z, Buljan M, Busam KJ.
    J Cutan Pathol; 2015 Jun 01; 42(6):406-12. PubMed ID: 25902915
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  • 11. A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma.
    Wadt KA, Aoude LG, Johansson P, Solinas A, Pritchard A, Crainic O, Andersen MT, Kiilgaard JF, Heegaard S, Sunde L, Federspiel B, Madore J, Thompson JF, McCarthy SW, Goodwin A, Tsao H, Jönsson G, Busam K, Gupta R, Trent JM, Gerdes AM, Brown KM, Scolyer RA, Hayward NK.
    Clin Genet; 2015 Sep 01; 88(3):267-72. PubMed ID: 25225168
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  • 13. Germline BAP1 mutations predispose to malignant mesothelioma.
    Testa JR, Cheung M, Pei J, Below JE, Tan Y, Sementino E, Cox NJ, Dogan AU, Pass HI, Trusa S, Hesdorffer M, Nasu M, Powers A, Rivera Z, Comertpay S, Tanji M, Gaudino G, Yang H, Carbone M.
    Nat Genet; 2011 Aug 28; 43(10):1022-5. PubMed ID: 21874000
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  • 14. Tumours associated with BAP1 mutations.
    Murali R, Wiesner T, Scolyer RA.
    Pathology; 2013 Feb 28; 45(2):116-26. PubMed ID: 23277170
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  • 15. Germline BAP1 alterations in familial uveal melanoma.
    Rai K, Pilarski R, Boru G, Rehman M, Saqr AH, Massengill JB, Singh A, Marino MJ, Davidorf FH, Cebulla CM, H Abdel-Rahman M.
    Genes Chromosomes Cancer; 2017 Feb 28; 56(2):168-174. PubMed ID: 27718540
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  • 16. BAPoma presenting as an incidental scalp papule: case report, literature review, and screening recommendations for BAP1 tumor predisposition syndrome.
    Zaayman M, Nguyen P, Silfvast-Kaiser A, Frieder J, West C, Tumminello K, Paek SY.
    J Dermatolog Treat; 2022 Jun 28; 33(4):1855-1860. PubMed ID: 34106034
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  • 17. BAP1 mutations in high-grade meningioma: implications for patient care.
    Shankar GM, Santagata S.
    Neuro Oncol; 2017 Oct 19; 19(11):1447-1456. PubMed ID: 28482042
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  • 18. A population-based analysis of germline BAP1 mutations in melanoma.
    O'Shea SJ, Robles-Espinoza CD, McLellan L, Harrigan J, Jacq X, Hewinson J, Iyer V, Merchant W, Elliott F, Harland M, Bishop DT, Newton-Bishop JA, Adams DJ.
    Hum Mol Genet; 2017 Feb 15; 26(4):717-728. PubMed ID: 28062663
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  • 19. BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy.
    Soares de Sá BC, de Macedo MP, Torrezan GT, Braga JCT, Fidalgo F, Moredo LF, Lellis R, Duprat JP, Carraro DM.
    BMC Cancer; 2019 Nov 09; 19(1):1077. PubMed ID: 31706282
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  • 20. Two unique BAP1 pathogenic variants identified in the same family by panel cascade testing.
    Byrne L, Ingalls C, Ansari A, Porteus C, Donenberg TR, Sussman DA, Cebulla CM, Abdel-Rahman MH.
    Fam Cancer; 2023 Jul 09; 22(3):307-311. PubMed ID: 36513904
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