Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer von Öfverholm, Anna, Törngren, Therese, Rosén, Anna, Arver, Brita, Einbeigi, Zakaria, Haraldsson, Karin, Ståhlbom, Anne Kinhult, Kuchinskaya, Ekaterina, Lindblom, Annika, Melin, Beatrice, Paulsson-Karlsson, Ylva, Stenmark-Askmalm, Marie, Tham, Emma, von Wachenfeldt, Anna, Kvist, Anders, Borg, Åke, Ehrencrona, Hans

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The effects of different familial Alzheimer's disease mutations on APP processing in vivo von Thordardottir, Steinunn, Kinhult Ståhlbom, Anne, Almkvist, Ove, Thonberg, Håkan, Eriksdotter, Maria, Zetterberg, Henrik, Blennow, Kaj, Graff, Caroline

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White matter changes in familial Alzheimer's disease von Li, X., Westman, E., Ståhlbom, A. K., Thordardottir, S., Almkvist, O., Blennow, K., Wahlund, L.‐O., Graff, C.

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Prospective blinded surveillance screening of Swedish women with increased hereditary risk of breast cancer von Liljegren, Annelie, von Wachenfeldt, Anna, Azavedo, Edward, Eloranta, Sandra, Grundström, Helene, Ståhlbom, Anne Kinhult, Sundbom, Ann, Sundén, Per, Svane, Gunilla, Ulitzsch, Dieter, Arver, Brita

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Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53 von Omran, Meis, Blomqvist, Lennart, Brandberg, Yvonne, Pal, Niklas, Kogner, Per, Ståhlbom, Anne Kinhult, Tham, Emma, Bajalica-Lagercrantz, Svetlana

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Evaluation of the BOADICEA risk assessment model in women with a family history of breast cancer von Ståhlbom, Anne Kinhult, Johansson, Hemming, Liljegren, Annelie, von Wachenfeldt, Anna, Arver, Brita

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The effects of different familial Alzheimer's disease mutations on APP processing in vivo von Thordardottir, S, Stahlbom, AK, Almkvist, O, Thonberg, H, Eriksdotter, M, Zetterberg, H, Blennow, K, Graff, C

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Insulin-like growth factor mRNA in Barramundi (Lates calcarifer): alternative splicing and nonresponsiveness to growth hormone von Ståhlbom, A K, Sara, V R, Hoeben, P

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Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis von Rohrer, JD, Nicholas, JM, Cash, DM, van Swieten, J, Dopper, E, Jiskoot, L, van Minkelen, R, Rombouts, SA, Cardoso, MJ, Clegg, S, Espak, M, Mead, S, Thomas, DL, De Vita, E, Masellis, M, Black, SE, Freedman, M, Keren, R, MacIntosh, BJ, Rogaeva, E, Tang-Wai, D, Tartaglia, MC, Laforce, R, Tagliavini, F, Tiraboschi, P, Redaelli, V, Prioni, S, Grisoli, M, Borroni, B, Padovani, A, Galimberti, D, Scarpini, E, Arighi, A, Fumagalli, G, Rowe, JB, Coyle-Gilchrist, I, Graff, C, Fallström, M, Jelic, V, Ståhlbom, AK, Andersson, C, Thonberg, H, Lilius, L, Frisoni, GB, Pievani, M, Bocchetta, M, Benussi, L, Ghidoni, R, Finger, E, Sorbi, S, Nacmias, B, Lombardi, G, Polito, C, Warren, JD, Ourselin, S, Fox, NC, Rossor, MN

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