“I would like to discuss it further with an expert”: a focus group study of Finnish adults’ perspectives on genetic secondary findings
Vornanen, M., Aktan-Collan, K., Hallowell, N., Konttinen, H., Kääriäinen, H., Haukkala, A.
Published in Journal of community genetics (01.07.2018)
Published in Journal of community genetics (01.07.2018)
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APOE and AGT in the Finnish p.Arg133Cys CADASIL population
Siitonen, M., Mykkänen, K., Pescini, F., Rovio, S., Kääriäinen, H., Baumann, M., Pöyhönen, M., Viitanen, M.
Published in Acta neurologica Scandinavica (01.12.2015)
Published in Acta neurologica Scandinavica (01.12.2015)
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Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing
Aktan-Collan, K, Haukkala, A, Pylvänäinen, K, Järvinen, H J, Aaltonen, L A, Peltomäki, P, Rantanen, E, Kääriäinen, H, Mecklin, J-P
Published in Journal of medical genetics (01.11.2007)
Published in Journal of medical genetics (01.11.2007)
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Population-Based Molecular Detection of Hereditary Nonpolyposis Colorectal Cancer
Salovaara, R, Loukola, A, Kristo, P, Kääriäinen, H, Ahtola, H, Eskelinen, M, Härkönen, N, Julkunen, R, Kangas, E, Ojala, S, Tulikoura, J, Valkamo, E, Järvinen, H, Mecklin, J P, Aaltonen, L A, de la Chapelle, A
Published in Journal of clinical oncology (01.06.2000)
Published in Journal of clinical oncology (01.06.2000)
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Valproate embryopathy in three sets of siblings: further proof of hereditary susceptibility
Malm, H, Kajantie, E, Kivirikko, S, Kääriäinen, H, Peippo, M, Somer, M
Published in Neurology (27.08.2002)
Published in Neurology (27.08.2002)
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Cancer in Patients With Ataxia-Telangiectasia and in Their Relatives in the Nordic Countries
Olsen, Jørgen H., Hahnemann, Johanne M., Børresen-Dale, Anne-Lise, Brøndum-Nielsen, Karen, Hammarström, Lennart, Kleinerman, Ruth, Kääriäinen, Helena, Lönnqvist, Tuula, Sankila, Risto, Seersholm, Niels, Tretli, Steinar, Yuen, Jonathan, Boice, John D., Tucker, Margaret
Published in JNCI : Journal of the National Cancer Institute (17.01.2001)
Published in JNCI : Journal of the National Cancer Institute (17.01.2001)
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Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease
CACHEUX, Valère, DASTOT-LE MOAL, Florence, KÄÄRIÄINEN, Helena, BONDURAND, Nadège, RINTALA, Risto, BOISSIER, Brigitte, WILSON, Meredith, MOWAT, David, GOOSSENS, Michel
Published in Human molecular genetics (01.07.2001)
Published in Human molecular genetics (01.07.2001)
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Breast and other cancers in 1445 blood relatives of 75 Nordic patients with ataxia telangiectasia
OLSEN, J. H, HAHNEMANN, J. M. D, BRØNDUM-NIELSEN, K, YUEN, J, TUCKER, M, BØRRESEN-DALE, A.-L, TRETLI, S, KLEINERMAN, R, SANKILA, R, HAMMARSTRÖM, L, ROBSAHM, T. E, KÄÄRIÄINEN, H, BREGARD, A
Published in British journal of cancer (25.07.2005)
Published in British journal of cancer (25.07.2005)
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Comprehension of cancer risk one and 12 months after predictive genetic testing for hereditary non-polyposis colorectal cancer
Aktan-Collan, Katja, Haukkala, Ari, Mecklin, Jukka-Pekka, Uutela, Antti, Kääriäinen, Helena
Published in Journal of medical genetics (01.11.2001)
Published in Journal of medical genetics (01.11.2001)
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Localization of a Susceptibility Gene for Familial Nonmedullary Thyroid Carcinoma to Chromosome 2q21
McKay, James D., Lesueur, Fabienne, Jonard, Laurence, Pastore, Alessandro, Williamson, Jan, Hoffman, Linda, Burgess, John, Duffield, Anne, Papotti, Mauro, Stark, Markus, Sobol, Hagay, Maes, Béatrice, Murat, Arnaud, Kääriäinen, Helena, Bertholon-Grégoire, Mireille, Zini, Michele, Rossing, Mary Anne, Toubert, Marie-Elisabeth, Bonichon, Françoise, Cavarec, Marie, Bernard, Anne-Marie, Boneu, Andrée, Leprat, Frédéric, Haas, Oskar, Lasset, Christine, Schlumberger, Martin, Canzian, Federico, Goldgar, David E., Romeo, Giovanni
Published in American journal of human genetics (01.08.2001)
Published in American journal of human genetics (01.08.2001)
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Psychological consequences of predictive genetic testing for hereditary non‐polyposis colorectal cancer (HNPCC): A prospective follow‐up study
Aktan‐Collan, Katja, Haukkala, Ari, Mecklin, Jukka‐Pekka, Uutela, Antti, Kääriäinen, Helena
Published in International journal of cancer (15.08.2001)
Published in International journal of cancer (15.08.2001)
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Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen
Bachner, L, Schärer, K, Kääriäinen, H, von Mühlendahl, K. E, Zerres, K, Deschennes, G, Steinbicker, V, Eggermann, T, Rudnik-Schöneborn, S, Mücher, G, Knapp, M, Neumann, H. P. H, Wirth, B, Misselwitz, J, Pirson, Y, Lennert, T
Published in Nature genetics (01.07.1994)
Published in Nature genetics (01.07.1994)
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New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene
Zerres, K, Senderek, J, Rudnik-Schöneborn, S, Eggermann, T, Kunze, J, Mononen, T, Kääriäinen, H, Kirfel, J, Moser, M, Buettner, R, Bergmann, C
Published in Clinical genetics (01.07.2004)
Published in Clinical genetics (01.07.2004)
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Genetic Screening in Europe
Javaher, P., Nyoungui, E., Kääriäinen, H., Kristoffersson, U., Nippert, I., Sequeiros, J., Schmidtke, J.
Published in Community genetics (01.01.2010)
Published in Community genetics (01.01.2010)
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Correspondence between the molecular genetic analysis and electron microscopic detection of granular osmiophilic material in CADASIL
Mykkänen, K, Ihalainen, S, Ruchoux, M.M, Baumann, M, Bergholm, R, Junna, M, Kääriäinen, H, Pöyhönen, M, Viitanen, M, Kalimo, H
Published in JOURNAL OF THE NEUROLOGICAL SCIENCES (2009)
Published in JOURNAL OF THE NEUROLOGICAL SCIENCES (2009)
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Conference Proceeding
Predictive genetic testing for hereditary non‐polyposis colorectal cancer: Uptake and long‐term satisfaction
Aktan‐Collan, Katja, Mecklin, Jukka‐Pekka, Järvinen, Heikki, Nyström‐Lahti, Minna, Peltomäki, Päivi, Söderling, Ismo, Uutela, Antti, de la Chapelle, Albert, Kääriäinen, Helena
Published in International journal of cancer (20.01.2000)
Published in International journal of cancer (20.01.2000)
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Genetic Control of Serum IgE Levels and Asthma: Linkage and Linkage Disequilibrium Studies in an Isolated Population
Laitinen, Tarja, Kauppi, Paula, Ignatius, Jaakko, Ruotsalainen, Tarja, Daly, Mark J., Kääriäinen, Helena, Kruglyak, Leonid, Laitinen, Hannu, de la Chapelle, Albert, Lander, Eric S., Laitinen, Lauri A., Kere, Juha
Published in Human molecular genetics (01.11.1997)
Published in Human molecular genetics (01.11.1997)
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