Clinical genetics in transition—a comparison of genetic services in Estonia, Finland, and the Netherlands von Vrijenhoek, T., Tonisson, N., Kääriäinen, H., Leitsalu, L., Rigter, T.

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Prolonged survival in a patient with a novel pyrroline‐5‐carboxylase reductase 2 genetic variant von Spagnoli, C., Pavlidis, E., Salerno, G. G., Koskinen, L., Kääriäinen, H., Frattini, D., Koskenvuo, J. W., Fusco, C.

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The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia von Hannula-Jouppi, Katariina, Kaminen-Ahola, Nina, Taipale, Mikko, Eklund, Ranja, Nopola-Hemmi, Jaana, Kääriäinen, Helena, Kere, Juha

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The Return of Unexpected Research Results in a Biobank Study and Referral to Health Care for Heritable Long QT Syndrome von Haukkala, A., Kujala, E., Alha, P., Salomaa, V., Koskinen, S., Swan, H., Kääriäinen, H.

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“I would like to discuss it further with an expert”: a focus group study of Finnish adults’ perspectives on genetic secondary findings von Vornanen, M., Aktan-Collan, K., Hallowell, N., Konttinen, H., Kääriäinen, H., Haukkala, A.

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Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing von Aktan-Collan, K, Haukkala, A, Pylvänäinen, K, Järvinen, H J, Aaltonen, L A, Peltomäki, P, Rantanen, E, Kääriäinen, H, Mecklin, J-P

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APOE and AGT in the Finnish p.Arg133Cys CADASIL population von Siitonen, M, Mykkanen, K, Pescini, F, Rovio, S, Kaariainen, H, Baumann, M, Poyhonen, M, Viitanen, M

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Population-Based Molecular Detection of Hereditary Nonpolyposis Colorectal Cancer von 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

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Cancer in Patients With Ataxia-Telangiectasia and in Their Relatives in the Nordic Countries von 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

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Valproate embryopathy in three sets of siblings: Further proof of hereditary susceptibility von MALM, H, KAJANTIE, E, KIVIRIKKO, S, KÄÄRIÄINEN, H, PEIPPO, M, SOMER, M

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Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease von CACHEUX, Valère, DASTOT-LE MOAL, Florence, KÄÄRIÄINEN, Helena, BONDURAND, Nadège, RINTALA, Risto, BOISSIER, Brigitte, WILSON, Meredith, MOWAT, David, GOOSSENS, Michel

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Localization of a Susceptibility Gene for Familial Nonmedullary Thyroid Carcinoma to Chromosome 2q21 von 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

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Breast and other cancers in 1445 blood relatives of 75 Nordic patients with ataxia telangiectasia von 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

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Comprehension of cancer risk one and 12 months after predictive genetic testing for hereditary non-polyposis colorectal cancer von Aktan-Collan, Katja, Haukkala, Ari, Mecklin, Jukka-Pekka, Uutela, Antti, Kääriäinen, Helena

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Psychological consequences of predictive genetic testing for hereditary non‐polyposis colorectal cancer (HNPCC): A prospective follow‐up study von Aktan‐Collan, Katja, Haukkala, Ari, Mecklin, Jukka‐Pekka, Uutela, Antti, Kääriäinen, Helena

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Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen von 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

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New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene von Zerres, K, Senderek, J, Rudnik-Schöneborn, S, Eggermann, T, Kunze, J, Mononen, T, Kääriäinen, H, Kirfel, J, Moser, M, Buettner, R, Bergmann, C

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Genetic Screening in Europe von Javaher, P., Nyoungui, E., Kääriäinen, H., Kristoffersson, U., Nippert, I., Sequeiros, J., Schmidtke, J.

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Predictive genetic testing for hereditary non‐polyposis colorectal cancer: Uptake and long‐term satisfaction von Aktan‐Collan, Katja, Mecklin, Jukka‐Pekka, Järvinen, Heikki, Nyström‐Lahti, Minna, Peltomäki, Päivi, Söderling, Ismo, Uutela, Antti, de la Chapelle, Albert, Kääriäinen, Helena

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Correspondence between the molecular genetic analysis and electron microscopic detection of granular osmiophilic material in CADASIL von Mykkänen, K, Ihalainen, S, Ruchoux, M.M, Baumann, M, Bergholm, R, Junna, M, Kääriäinen, H, Pöyhönen, M, Viitanen, M, Kalimo, H

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