Update on Lynch syndrome genomics von Peltomaeki, Paeivi

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Lynch Syndrome Genetics and Clinical Implications von Peltomäki, Päivi, Nyström, Minna, Mecklin, Jukka-Pekka, Seppälä, Toni T.

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Mutations and epimutations in the origin of cancer von Peltomaeki, Paeivi

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Lynch syndrome genes von Peltomaeki, Paeivi

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LINE-1 hypomethylation in familial and sporadic cancer von Pavicic, Walter, Joensuu, Emmi I., Nieminen, Taina, Peltomäki, Päivi

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Testing for Lynch Syndrome in Endometrial Carcinoma: From Universal to Age-Selective MLH1 Methylation Analysis von Pasanen, Annukka, Loukovaara, Mikko, Kaikkonen, Elina, Olkinuora, Alisa, Pylvänäinen, Kirsi, Alhopuro, Pia, Peltomäki, Päivi, Mecklin, Jukka-Pekka, Bützow, Ralf

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Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospec... von Haupt, Saskia, Seppälä, Toni T., Sampson, Julian R., Sunde, Lone, Bernstein, Inge, Jenkins, Mark A., Engel, Christoph, Aretz, Stefan, Nielsen, Maartje, Capella, Gabriel, Balaguer, Francesc, Evans, Dafydd Gareth, Burn, John, Holinski-Feder, Elke, Bonanni, Bernardo, Lindblom, Annika, Levi, Zohar, Macrae, Finlay, Winship, Ingrid, Plazzer, John-Paul, Sijmons, Rolf, Della Valle, Adriana, Heinimann, Karl, Dębniak, Tadeusz, Fruscio, Robert, Katz, Lior H., Laish, Ido, Vainer, Elez, Carraro, Dirce Maria, Monahan, Kevin, Half, Elizabeth, Stakelum, Aine, Winter, Des, Kennelly, Rory, Gluck, Nathan, Sheth, Harsh, Abu-Freha, Naim, Greenblatt, Marc, Bohorquez, Mabel, Cavestro, Giulia Martina, Lino-Silva, Leonardo S., Horisberger, Karoline, Nascimento, Ivana do, Thomas, Huw, Rossi, Norma Teresa, Apolinário da Silva, Leandro, Zaránd, Attila, Ruiz-Bañobre, Juan, Heuveline, Vincent, Mecklin, Jukka-Pekka, Renkonen-Sinisalo, Laura, Peltomäki, Päivi, Madsen, Mia Gebauer, Burgdorf, Stefan Kobbelgaard, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane, Le Marchand, Loïc, Newcomb, Polly A., Figueiredo, Jane, Buchanan, Daniel D., Rahner, Nils, Schröck, Evelin, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Hüneburg, Robert, Redler, Silke, Büttner, Reinhard, Weitz, Jürgen, Pineda, Marta, Duenas, Nuria, Vidal, Joan Brunet, Moreira, Leticia, Sánchez, Ariadna, Hovig, Eivind, Nakken, Sigve, Green, Kate, Lalloo, Fiona, Hill, James, Crosbie, Emma, Mints, Miriam, Goldberg, Yael, Tjandra, Douglas, ten Broeke, Sanne W., Kariv, Revital, Rosner, Guy, Advani, Suresh H., Thomas, Lidiya, Shah, Pankaj, Shah, Mithun, Neffa, Florencia, Esperon, Patricia, Pavicic, Walter, Torrezan, Giovana Tardin, Bassaneze, Thiago, Moslein, Gabriela, Moller, Pål

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Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics von Lagerstedt Robinson, Kristina, Liu, Tao, Vandrovcova, Jana, Halvarsson, Britta, Clendenning, Mark, Frebourg, Thierry, Papadopoulos, Nickolas, Kinzler, Kenneth W., Vogelstein, Bert, Peltomäki, Päivi, Kolodner, Richard D., Nilbert, Mef, Lindblom, Annika

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Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents von Olkinuora, Alisa Petriina, Mayordomo, Andrea Constanza, Kauppinen, Anni Katariina, Cerliani, María Belén, Coraglio, Mariana, Collia, Ávila Karina, Gutiérrez, Alejandro, Alvarez, Karin, Cassana, Alessandra, Lopéz-Köstner, Francisco, Jauk, Federico, García-Rivello, Hernán, Ristimäki, Ari, Koskenvuo, Laura, Lepistö, Anna, Nieminen, Taina Tuulikki, Vaccaro, Carlos Alberto, Pavicic, Walter Hernán, Peltomäki, Päivi

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Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis von Pavicic, Walter, Nieminen, Taina T., Gylling, Annette, Pursiheimo, Juha-Pekka, Laiho, Asta, Gyenesei, Attila, Järvinen, Heikki J., Peltomäki, Päivi

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Reducing the risk of type 2 diabetes with nutrition and physical activity – efficacy and implementation of lifestyle interventions in Finland von Lindström, Jaana, Absetz, Pilvikki, Hemiö, Katri, Peltomäki, Päivi, Peltonen, Markku

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Distinct Genetic and Epigenetic Signatures of Colorectal Cancers According to Ethnic Origin von NIEMINEN, Taina T, SHOMAN, Soheir, EISSA, Saad, PELTOMÄKI, Päivi, ABDEL-RAHMAN, Wael M

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Epigenetic signatures of familial cancer are characteristic of tumor type and family category von Joensuu, Emmi I, Abdel-Rahman, Wael M, Ollikainen, Miina, Ruosaari, Salla, Knuutila, Sakari, Peltomäki, Päivi

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Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer von Joensuu, Emmi I., Nieminen, Taina T., Lotsari, Johanna E., Pavicic, Walter, Abdel-Rahman, Wael M., Peltomäki, Päivi

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Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases von Lotsari, Johanna E, Gylling, Annette, Abdel-Rahman, Wael M, Nieminen, Taina T, Aittomäki, Kristiina, Friman, Marjukka, Pitkänen, Reino, Aarnio, Markku, Järvinen, Heikki J, Mecklin, Jukka-Pekka, Kuopio, Teijo, Peltomäki, Päivi

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Clinicopathological Characterization and Genomic Aberrations in Subcutaneous Panniculitis-Like T-Cell Lymphoma von Hahtola, Sonja, Burghart, Elke, Jeskanen, Leila, Karenko, Leena, Abdel-Rahman, Wael M., Polzer, Bernhard, Kajanti, Mikael, Peltomäki, Päivi, Pettersson, Tom, Klein, Christoph A., Ranki, Annamari

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p53 Codon 72 and MDM2 SNP309 Polymorphisms and Age of Colorectal Cancer Onset in Lynch Syndrome von SOTAMAA, Kaisa, LIYANARACHCHI, Sandya, MECKLIN, Jukka-Pekka, JÄRVINEN, Heikki, AALTONEN, Lauri A, PELTOMÄKI, Päivi, DE LA CHAPELLE, Albert

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Somatic FGF9 mutations in colorectal and endometrial carcinomas associated with membranous β-catenin von Abdel-Rahman, Wael M, Kalinina, Juliya, Shoman, Soheir, Eissa, Saad, Ollikainen, Miina, Elomaa, Outi, Eliseenkova, Anna V, Bützow, Ralf, Mohammadi, Moosa, Peltomäki, Päivi

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Cancer-Predicting Gene Expression Changes in Colonic Mucosa of Western Diet Fed Mlh1+/- Mice: e76865 von Pussila, Marjaana, Sarantaus, Laura, Bebek, Denis Dermadi, Valo, Satu, Reyhani, Nima, Ollila, Saara, Paeivaerinta, Essi, Peltomaeki, Paeivi, Mutanen, Marja, Nystrom, Minna

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HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1 von Raevaara, Tiina E., Gerdes, Anne-Marie, Lönnqvist, Karin E., Tybjærg-Hansen, Anne, Abdel-Rahman, Wael M., Kariola, Reetta, Peltomäki, Päivi, Nyström-Lahti, Minna

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