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BAP1 genetic testing among melanoma and cancer-prone families in Sweden.
Helgadottir H, Schultz K, Lapins J, Vassilaki I, All-Eriksson C, Höiom V. Helgadottir H, et al. Among authors: hoiom v. Acta Oncol. 2023 Jun;62(6):565-570. doi: 10.1080/0284186X.2023.2216338. Epub 2023 Jun 2. Acta Oncol. 2023. PMID: 37265265 No abstract available.
Hereditary uveal melanoma: a report of a germline mutation in BAP1.
Höiom V, Edsgärd D, Helgadottir H, Eriksson H, All-Ericsson C, Tuominen R, Ivanova I, Lundeberg J, Emanuelsson O, Hansson J. Höiom V, et al. Genes Chromosomes Cancer. 2013 Apr;52(4):378-84. doi: 10.1002/gcc.22035. Epub 2013 Jan 23. Genes Chromosomes Cancer. 2013. PMID: 23341325
Somatic BRAF and NRAS mutations in familial melanomas with known germline CDKN2A status: a GenoMEL study.
Zebary A, Omholt K, van Doorn R, Ghiorzo P, Harbst K, Hertzman Johansson C, Höiom V, Jönsson G, Pjanova D, Puig S, Scarra GB, Harland M, Olsson H, Egyhazi Brage S, Palmer J, Kanter-Lewensohn L, Vassilaki I, Hayward NK, Newton-Bishop J, Gruis NA, Hansson J; Melanoma Genetics Consortium (GenoMEL). Zebary A, et al. Among authors: hoiom v. J Invest Dermatol. 2014 Jan;134(1):287-290. doi: 10.1038/jid.2013.270. Epub 2013 Jun 14. J Invest Dermatol. 2014. PMID: 23771122 Free article. No abstract available.
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.
Yang XR, Rotunno M, Xiao Y, Ingvar C, Helgadottir H, Pastorino L, van Doorn R, Bennett H, Graham C, Sampson JN, Malasky M, Vogt A, Zhu B, Bianchi-Scarra G, Bruno W, Queirolo P, Fornarini G, Hansson J, Tuominen R, Burdett L, Hicks B, Hutchinson A, Jones K, Yeager M, Chanock SJ, Landi MT, Höiom V, Olsson H, Gruis N, Ghiorzo P, Tucker MA, Goldstein AM. Yang XR, et al. Among authors: hoiom v. Hum Genet. 2016 Nov;135(11):1241-1249. doi: 10.1007/s00439-016-1715-1. Epub 2016 Jul 23. Hum Genet. 2016. PMID: 27449771 Free PMC article.
The genetics of uveal melanoma: current insights.
Helgadottir H, Höiom V. Helgadottir H, et al. Among authors: hoiom v. Appl Clin Genet. 2016 Sep 6;9:147-55. doi: 10.2147/TACG.S69210. eCollection 2016. Appl Clin Genet. 2016. PMID: 27660484 Free PMC article. Review.
70 results