Comparative transcriptome analysis of matched primary and distant metastatic ovarian carcinoma by Sallinen, H, Janhonen, S, Pölönen, P, Niskanen, H, Liu, O H, Kivelä, A, Hartikainen, J M, Anttila, M, Heinäniemi, M, Ylä-Herttuala, S, Kaikkonen, M U

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Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer by Mantere, T., Haanpää, M., Hanenberg, H., Schleutker, J., Kallioniemi, A., Kähkönen, M., Parto, K., Avela, K., Aittomäki, K., von Koskull, H., Hartikainen, J.M., Kosma, V.-M., Laasanen, S.-L., Mannermaa, A., Pylkäs, K., Winqvist, R.

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Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families by Hartikainen, JM, Kataja, V, Pirskanen, M, Arffman, A, Ristonmaa, U, Vahteristo, P, Ryynänen, M, Heinonen, S, Kosma, V-M, Mannermaa, A

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Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions by Solyom, Szilvia, Aressy, Bernadette, Pylkäs, Katri, Patterson-Fortin, Jeffrey, Hartikainen, Jaana M, Kallioniemi, Anne, Kauppila, Saila, Nikkilä, Jenni, Kosma, Veli-Matti, Mannermaa, Arto, Greenberg, Roger A, Winqvist, Robert

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Distinction Between Arrhythmic and Nonarrhythmic Death After Acute Myocardial Infarction Based on Heart Rate Variability, Signal-Averaged Electrocardiogram, Ventricular Arrhythmias... by Hartikainen, MD, Phd, J

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FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium by Agarwal, D, Herranz, J, Moreno, L T, Alonso, M R, Wang, Q, Bolla, M K, Meyer, K B, Hardisson, D, Mendiola, M, Swerdlow, A, Orr, N, Jones, M, Matsuo, K, Ito, H, Iwata, H, Hui, M, Sawyer, E, Miller, N, Choi, J-Y, Noh, D-Y, Schmidt, D F, Makalic, E, Southey, M C, Teo, S H, Yip, C H, Sivanandan, K, Brauch, H, Brüning, T, Hamann, U, Shah, M, Andrulis, I L, Knight, J A, Tchatchou, S, Broeks, A, Rosenberg, E H, van't Veer, L J, Fasching, P A, Beckmann, M W, Cai, Q, Tseng, C-C, Cox, A, Muir, K, Lophatananon, A, Siriwanarangsan, P, Zheng, W, Deming-Halverson, S, Shrubsole, M J, Long, J, Shu, X-O, Lu, W, Gao, Y-T, Zhang, B, Manoukian, S, Mariette, F, Sangrajrang, S, McKay, J, Couch, F J, Yannoukakos, D, Johnson, N, Marme, F, Burwinkel, B, Guénel, P, Bojesen, S E, Nordestgaard, B G, Arndt, V, Stegmaier, C, Mannermaa, A, Kataja, V, Lambrechts, D, Yesilyurt, B T, Rudolph, A, Seibold, P, Wang, X, Olson, J E, Purrington, K, Giles, G G, Baglietto, L, Haiman, C A, Schumacher, F, Le Marchand, L, Labrèche, F, Jukkola-Vuorinen, A, Devilee, P, García-Closas, M, Lissowska, J, Czene, K, Hooning, M J, Kriege, M, Li, J, Durda, K, Nevanlinna, H, Muranen, T A, Aittomäki, K, Bogdanova, N, Dörk, T, Hall, P, Chenevix-Trench, G, Easton, D F, Pharoah, P D P, Arias-Perez, J I

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Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility by Vuorela, Mikko, Pylkäs, Katri, Hartikainen, Jaana M., Sundfeldt, Karin, Lindblom, Annika, von Wachenfeldt Wäppling, Anna, Haanpää, Maria, Puistola, Ulla, Rosengren, Annika, Anttila, Maarit, Kosma, Veli-Matti, Mannermaa, Arto, Winqvist, Robert

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A Finnish BRCA1 exon 12 4216-2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation by Hartikainen, Jaana M., Pirskanen, Mia M., Arffman, Airi H., Ristonmaa, Ulla K., Mannermaa, Arto J.

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Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2 by Orr, N., Dudbridge, F., Dryden, N., Maguire, S., Novo, D., Perrakis, E., Johnson, N., Ghoussaini, M., Hopper, J. L., Southey, M. C., Apicella, C., Stone, J., Schmidt, M. K., Broeks, A., Van't Veer, L. J., Hogervorst, F. B., Fasching, P. A., Haeberle, L., Ekici, A. B., Beckmann, M. W., Gibson, L., Aitken, Z., Warren, H., Sawyer, E., Tomlinson, I., Kerin, M. J., Miller, N., Burwinkel, B., Marme, F., Schneeweiss, A., Sohn, C., Guenel, P., Truong, T., Cordina-Duverger, E., Sanchez, M., Bojesen, S. E., Nordestgaard, B. G., Nielsen, S. F., Flyger, H., Benitez, J., Zamora, M. P., Arias Perez, J. I., Menendez, P., Anton-Culver, H., Neuhausen, S. L., Brenner, H., Dieffenbach, A. K., Arndt, V., Stegmaier, C., Hamann, U., Brauch, H., Justenhoven, C., Bruning, T., Ko, Y.-D., Nevanlinna, H., Aittomaki, K., Blomqvist, C., Khan, S., Bogdanova, N., Dork, T., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V.-M., Hartikainen, J. M., Chenevix-Trench, G., Beesley, J., Lambrechts, D., Moisse, M., Floris, G., Beuselinck, B., Chang-Claude, J., Rudolph, A., Seibold, P., Flesch-Janys, D., Radice, P., Peterlongo, P., Peissel, B., Pensotti, V., Couch, F. J., Olson, J. E., Slettedahl, S., Vachon, C., Giles, G. G., Milne, R. L., McLean, C., Haiman, C. A., Henderson, B. E., Schumacher, F., Le Marchand, L., Simard, J., Goldberg, M. S., Labreche, F., Dumont, M., Kristensen, V., Alnaes, G. G., Nord, S., Borresen-Dale, A.-L., Zheng, W.

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Late Infantile Neuronal Ceroid Lipofuscinosis Is Due to Splicing Mutations in the CLN2 Gene by Hartikainen, Jaana M., Ju, Weina, Wisniewski, Krystyna E., Moroziewicz, Dorota N., Kaczmarski, Alexandra L., McLendon, Lucille, Zhong, David, Suarez, Carolin T., Brown, W.Ted, Zhong, Nan

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A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients by Seibold, Petra, Schmezer, Peter, Behrens, Sabine, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Flesch-Janys, Dieter, Nevanlinna, Heli, Fagerholm, Rainer, Aittomäki, Kristiina, Blomqvist, Carl, Margolin, Sara, Mannermaa, Arto, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M, Lambrechts, Diether, Wildiers, Hans, Kristensen, Vessela, Alnæs, Grethe Grenaker, Nord, Silje, Borresen-Dale, Anne-Lise, Hooning, Maartje J, Hollestelle, Antoinette, Jager, Agnes, Seynaeve, Caroline, Li, Jingmei, Liu, Jianjun, Humphreys, Keith, Dunning, Alison M, Rhenius, Valerie, Shah, Mitul, Kabisch, Maria, Torres, Diana, Ulmer, Hans-Ulrich, Hamann, Ute, Schildkraut, Joellen M, Purrington, Kristen S, Couch, Fergus J, Hall, Per, Pharoah, Paul, Easton, Doug F, Schmidt, Marjanka K, Chang-Claude, Jenny, Popanda, Odilia

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Refinement of the 22q12-q13 Breast Cancer–Associated Region: Evidence of TMPRSS6 as a Candidate Gene in an Eastern Finnish Population by Hartikainen, Jaana M, Tuhkanen, Hanna, Kataja, Vesa, Eskelinen, Matti, Uusitupa, Matti, Kosma, Veli-Matti, Mannermaa, Arto

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PO-350 MiRNAs and their relation to biological pathways in left- and right-sided colorectal cancer by Sundaramoorthy, S, Heikkinen, S, Hartikainen, JM, Kuopio, T, Mecklin, JP, Kosma, VM, Mannermaa, A

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A BRCA2 Mutation, 4088insA, in a Finnish Breast and Ovarian Cancer Family Associated with Favourable Clinical Course by HARTIKAINEN, Jaana M, MANNERMAA, Arto, HEINONEN, Seppo, KOSMA, Veli-Matti, KATAJA, Vesa

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An Autosome-Wide Scan for Linkage Disequilibrium–Based Association in Sporadic Breast Cancer Cases in Eastern Finland: Three Candidate Regions Found by HARTIKAINEN, Jaana M, TUHKANEN, Hanna, UUSITUPA, Matti, KOSMA, Veli-Matti, MANNERMAA, Arto, KATAJA, Vesa, DUNNING, Alison M, ANTONIOU, Antonis, SMITH, Paula, ARFFMAN, Airi, PIRSKANEN, Mia, EASTON, Douglas F, ESKELINEN, Matti

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Original Article: Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families by Hartikainen, J M, Kataja, V, Pirskanen, M, Arffman, A, Ristonmaa, U, Vahteristo, P, Ryynänen, M, Heinonen, S, V-M Kosma, Mannermaa, A

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The UGT1A6_19_GG genotype is associated with increased breast cancer risk based on a two-stage study by Obazee, OM, Justenhoven, C, Winter, S, Rabstein, S, Lotz, A, Harth, V, Pesch, B, Bruning, T, Baisch, C, Hartikainen, JM, Mannermaa, A, Winqvist, R, Fasching, P, Hall, P, Chang-Claude, J, Hamann, U, Ko, YD, Brauch, H

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Effect of Conscious Sedation on Cardiac Autonomic Regulation during Colonoscopy by RISTIKANKARE, M, JULKUNEN, R, LAITINEN, T, WANG, S.-X, HEIKKINEN, M, JANATUINEN, E, HARTIKAINEN, J

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Infant Vitamin D Supplementation and Allergic Conditions in Adulthood: Northern Finland Birth Cohort 1966 by HYPPöNEN, ELINA, SOVIO, ULLA, WJST, MATTHIAS, PATEL, SWATEE, PEKKANEN, JUHA, HARTIKAINEN, ANNA-LIISA, JäRVELINB, MARJO-RIITTA

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Reperfusion therapy for ST elevation acute myocardial infarction in Europe: description of the current situation in 30 countries by Widimsky, Petr, Wijns, William, Fajadet, Jean, de Belder, Mark, Knot, Jiri, Aaberge, Lars, Andrikopoulos, George, Baz, Jose Antonio, Betriu, Amadeo, Claeys, Marc, Danchin, Nicholas, Djambazov, Slaveyko, Erne, Paul, Hartikainen, Juha, Huber, Kurt, Kala, Petr, Klinčeva, Milka, Kristensen, Steen Dalby, Ludman, Peter, Ferre, Josephina Mauri, Merkely, Bela, Miličić, Davor, Morais, Joao, Noč, Marko, Opolski, Grzegorz, Ostojić, Miodrag, Radovanovič, Dragana, De Servi, Stefano, Stenestrand, Ulf, Studenčan, Martin, Tubaro, Marco, Vasiljević, Zorana, Weidinger, Franz, Witkowski, Adam, Zeymer, Uwe

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