Detection of KRAS mutations in liquid biopsies from metastatic colorectal cancer patients using droplet digital PCR, Idylla, and next generation sequencing von Holm, Matilda, Andersson, Emma, Osterlund, Emerik, Ovissi, Ali, Soveri, Leena-Maija, Anttonen, Anna-Kaisa, Kytola, Soili, Aittomaki, Kristiina, Osterlund, Pia, Ristimaki, Ari

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Albert de la Chapelle (1933-2020) von Kääriäinen, Helena, Aittomäki, Kristiina

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Surrogacy: outcomes for surrogate mothers, children and the resulting families-a systematic review von Söderström-Anttila, Viveca, Wennerholm, Ulla-Britt, Loft, Anne, Pinborg, Anja, Aittomäki, Kristiina, Romundstad, Liv Bente, Bergh, Christina

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Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment von Menko, Fred H., Maher, Eamonn R., Schmidt, Laura S., Middelton, Lindsay A., Aittomäki, Kristiina, Tomlinson, Ian, Richard, Stéphane, Linehan, W. Marston

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Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer von Kiiski, Johanna I., Pelttari, Liisa M., Khan, Sofia, Freysteinsdottir, Edda S., Reynisdottir, Inga, Hart, Steven N., Shimelis, Hermela, Vilske, Sara, Kallioniemi, Anne, Schleutker, Johanna, Leminen, Arto, Bützow, Ralf, Blomqvist, Carl, Barkardottir, Rosa B., Couch, Fergus J., Aittomäki, Kristiina, Nevanlinna, Heli

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Prognostic Role of HuR in Hereditary Breast Cancer von Heinonen, Mira, Fagerholm, Rainer, Aaltonen, Kirsimari, Kilpivaara, Outi, Aittomäki, Kristiina, Blomqvist, Carl, Heikkilä, Päivi, Haglund, Caj, Nevanlinna, Heli, Ristimäki, Ari

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The Breast Cancer Susceptibility Mutation PALB2 1592delT Is Associated with an Aggressive Tumor Phenotype von Heikkinen, Tuomas, Kärkkäinen, Hanni, Aaltonen, Kirsimari, Milne, Roger L, Heikkilä, Päivi, Aittomäki, Kristiina, Blomqvist, Carl, Nevanlinna, Heli

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A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients von Wendt, Camilla, Muranen, Taru A., Mielikäinen, Lotta, Thutkawkorapin, Jessada, Blomqvist, Carl, Jiao, Xiang, Ehrencrona, Hans, Tham, Emma, Arver, Brita, Melin, Beatrice, Kuchinskaya, Ekaterina, Stenmark Askmalm, Marie, Paulsson-Karlsson, Ylva, Einbeigi, Zakaria, von Wachenfeldt Väppling, Anna, Kalso, Eija, Tasmuth, Tiina, Kallioniemi, Anne, Aittomäki, Kristiina, Nevanlinna, Heli, Borg, Åke, Lindblom, Annika

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TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia von Sandbacka, Maria, Laivuori, Hannele, Freitas, Érika, Halttunen, Mervi, Jokimaa, Varpu, Morin-Papunen, Laure, Rosenberg, Carla, Aittomäki, Kristiina

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CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population von Hallamies, Sanna, Pelttari, Liisa M, Poikonen-Saksela, Paula, Jekunen, Antti, Jukkola-Vuorinen, Arja, Auvinen, Päivi, Blomqvist, Carl, Aittomäki, Kristiina, Mattson, Johanna, Nevanlinna, Heli

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Constitutional mosaicism for a BRCA2 mutation as a cause of early-onset breast cancer von Alhopuro, Pia, Vainionpää, Reetta, Anttonen, Anna-Kaisa, Aittomäki, Kristiina, Nevanlinna, Heli, Pöyhönen, Minna

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RAD51C is a susceptibility gene for ovarian cancer von Pelttari, Liisa M., Heikkinen, Tuomas, Thompson, Deborah, Kallioniemi, Anne, Schleutker, Johanna, Holli, Kaija, Blomqvist, Carl, Aittomäki, Kristiina, Bützow, Ralf, Nevanlinna, Heli

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The Outcome of Patients With Right Atrial Isomerism is Poor von Eronen, Marianne P., Aittomäki, Kristiina A. U., Kajantie, Eero O., Sairanen, Heikki I., Pesonen, Erkki J.

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MiR-34a expression has an effect for lower risk of metastasis and associates with expression patterns predicting clinical outcome in breast cancer von Peurala, Hanna, Greco, Dario, Heikkinen, Tuomas, Kaur, Sippy, Bartkova, Jirina, Jamshidi, Maral, Aittomäki, Kristiina, Heikkilä, Päivi, Bartek, Jiri, Blomqvist, Carl, Bützow, Ralf, Nevanlinna, Heli

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Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics von Jönsson, Göran, Staaf, Johan, Vallon-Christersson, Johan, Ringnér, Markus, Holm, Karolina, Hegardt, Cecilia, Gunnarsson, Haukur, Fagerholm, Rainer, Strand, Carina, Agnarsson, Bjarni A, Kilpivaara, Outi, Luts, Lena, Heikkilä, Päivi, Aittomäki, Kristiina, Blomqvist, Carl, Loman, Niklas, Malmström, Per, Olsson, Håkan, Johannsson, Oskar Th, Arason, Adalgeir, Nevanlinna, Heli, Barkardottir, Rosa B, Borg, Ake

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A founder mutation in CERKL is a major cause of retinal dystrophy in Finland von Avela, Kristiina, Sankila, Eeva‐Marja, Seitsonen, Sanna, Kuuluvainen, Liina, Barton, Stephanie, Gillies, Stuart, Aittomäki, Kristiina

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A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis von Rafiq, Sajjad, Khan, Sofia, Tapper, William, Collins, Andrew, Upstill-Goddard, Rosanna, Gerty, Susan, Blomqvist, Carl, Aittomäki, Kristiina, Couch, Fergus J, Liu, Jianjun, Nevanlinna, Heli, Eccles, Diana

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Recurrent moderate‐risk mutations in Finnish breast and ovarian cancer patients von Nurmi, Anna, Muranen, Taru A., Pelttari, Liisa M., Kiiski, Johanna I., Heikkinen, Tuomas, Lehto, Sini, Kallioniemi, Anne, Schleutker, Johanna, Bützow, Ralf, Blomqvist, Carl, Aittomäki, Kristiina, Nevanlinna, Heli

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Outcome of Left Atrial Isomerism at a Single Institution von Eronen, Marianne P., Aittomäki, Kristiina A. U., Kajantie, Eero O., Sairanen, Heikki I.

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Circulating tumor DNA is a prognostic biomarker in metastatic melanoma patients treated with chemoimmunotherapy and BRAF inhibitor von Mattila, Kalle E., Mäkelä, Siru, Kytölä, Soili, Andersson, Emma, Vihinen, Pia, Ramadan, Susan, Skyttä, Tanja, Tiainen, Leena, Vuoristo, Meri-Sisko, Tyynelä-Korhonen, Kristiina, Koivunen, Jussi, Kohtamäki, Laura, Aittomäki, Kristiina, Hernberg, Micaela

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