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Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.
Ghazani AA, Oliver NM, St Pierre JP, Garofalo A, Rainville IR, Hiller E, Treacy DJ, Rojas-Rudilla V, Wood S, Bair E, Parello M, Huang F, Giannakis M, Wilson FH, Stover EH, Corsello SM, Nguyen T, Rana HQ, Church AJ, Lowenstein C, Cibulskis C, Amin-Mansour A, Heng J, Brais L, Santos A, Bauer P, Waldron A, Lo P, Gorman M, Lydon CA, Welch M, McNamara P, Gabriel S, Sholl LM, Lindeman NI, Garber JE, Joffe S, Van Allen EM, Gray SW, Ja Nne PA, Garraway LA, Wagle N. Ghazani AA, et al. Among authors: rana hq. Genet Med. 2017 Jul;19(7):787-795. doi: 10.1038/gim.2016.191. Epub 2017 Jan 26. Genet Med. 2017. PMID: 28125075 Free article.
Prevalence of germline variants in inflammatory breast cancer.
Rana HQ, Sacca R, Drogan C, Gutierrez S, Schlosnagle E, Regan MM, Speare V, LaDuca H, Dolinsky J, Garber JE, Overmoyer BA. Rana HQ, et al. Cancer. 2019 Jul 1;125(13):2194-2202. doi: 10.1002/cncr.32062. Epub 2019 Apr 1. Cancer. 2019. PMID: 30933323 Free article.
Vulvar Melanoma in association with germline MITF p.E318K variant.
Koeller DR, Schwartz A, DeSimone MS, Rana HQ, Rojas-Rudilla V, Russell-Goldman E, Laga AC, Lindeman NI, Garber JE, Ghazani AA. Koeller DR, et al. Among authors: rana hq. Cancer Genet. 2022 Apr;262-263:102-106. doi: 10.1016/j.cancergen.2022.02.003. Epub 2022 Feb 15. Cancer Genet. 2022. PMID: 35220194
An optimized protocol for evaluating pathogenicity of VHL germline variants in patients suspected with von Hippel-Lindau syndrome: Using somatic genome to inform the role of germline variants.
Koeller DR, Manning DK, Schwartz A, Chittenden A, Hayes CP, Abraamyan F, Rana HQ, Lindeman NI, Garber JE, Ghazani AA. Koeller DR, et al. Among authors: rana hq. MethodsX. 2022 Jun 18;9:101761. doi: 10.1016/j.mex.2022.101761. eCollection 2022. MethodsX. 2022. PMID: 35774415 Free PMC article.
64 results