Use of hierarchical models to analyse European trends in congenital anomaly prevalence -н Cavadino, A, Prieto-Merino, D, Addor, M, Arriola, L, Draper, E, Garne, E, Greenlees, R, Haeusler, M, Khoshnood, B, Kurinczuk, J, McDonnell, B, Nelen, V, O'Mahoney, M, Randrianaivo, H, Rankin, J, Rissman, A, Tucker, D, Verrelen-Dumouli, C, de Walle, H, Wellesley, D, Morris, J, Bianchi, F

Mutations in MAP3K7 that alter the activity of the TAK1 signaling complex cause frontometaphyseal dysplasia. -н Wade, E, Daniel, P, Jenkins, Z, McInerney-Leo, A, Morgan, T, Addor, M, Ades, L, Bertola, D, Bohring, A, Carter, E, Cho, T, Duba, H, Fletcher, E, Kim, C, Krakow, D, Morava, E, Neuhann, T, Superti-Furga, A, Veenstra-Knol, I, Wieczorek, D, Wilson, L, Hennekam, R, Sutherland-Smith, A, Strom, T, Wilkie, A, Brown, M, Duncan, E, Markie, D, Robertson, S

Mutations in MAP3K7 that alter the activity of the TAK1 signaling complex cause frontometaphyseal dysplasia -н Wade, E, Daniel, P, Jenkins, Z, McInerney-Leo, A, Leo, P, Morgan, T, Addor, M, Adès, L, Bertola, D, Bohring, A, Carter, E, Cho, T, Duba, H, Fletcher, E, Kim, C, Krakow, D, Morava, E, Neuhann, T, Superti-Furga, A, Veenstra-Knol, I, Wieczorek, D, Wilson, L, Hennekam, R, Sutherland-Smith, A, Strom, T, Wilkie, A, Brown, M, Duncan, E, Markie, D, Robertson, S

Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study -н Morris, JK, Wellesley, DG, Barisic, I, Addor, M-C, Bergman, JEH, Braz, P, Cavero-Carbonell, C, Draper, ES, Gatt, M, Haeusler, M, Klungsoyr, K, Kurinczuk, JJ, Lelong, N, Luyt, K, Lynch, C, O'Mahony, MT, Mokoroa, O, Nelen, V, Neville, AJ, Pierini, A, Randrianaivo, H, Rankin, J, Rissmann, A, Rouget, F, Schaub, B, Tucker, DF, Verellen-Dumoulin, C, Wiesel, A, Zymak-Zakutnia, N, Lanzoni, M, Garne, E

Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study -н Garne, E, Rissmann, A, Addor, M, Barisic, I, Bergman, J, Braz, P, Cavero-Carbonell, C, Draper, E, Gatt, M, Haeusler, M, Klungsoyr, K, Kurinczuk, J, Lelong, N, Luyt, K, Lynch, C, O'Mahony, M, Mokoroa, O, Nelen, V, Neville, A, Pierini, A, Randrianaivo, H, Rankin, J, Rouget, F, Schaub, B, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Wiesel, A, Zymak-Zakutnia, N, Lanzoni, M, Morris, J

Trends in congenital anomalies in Europe from 1980 to 2012 -н Morris, J, Springett, A, Greenlees, R, Loane, M, Addor, M, Arriola, L, Barisic, I, Bergman, J, Csaky-Szunyogh, M, Dias, C, Draper, E, Garne, E, Gatt, M, Khoshnood, B, Klungsoyr, K, Lynch, C, McDonnell, R, Nelen, V, Neville, A, O'Mahony, M, Pierini, A, Queisser-Luft, A, Randrianaivo, H, Rankin, J, Rissmann, A, Kurinczuk, J, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Dolk, H

Prevalence of microcephaly in Europe : a population based study -н Morris, J, Rankin, J, Garne, E, Loane, M, Greenlees, R, Addor, M, Arriola, L, Barisic, I, Bergman, J, Csaky-Szunyogh, M, Dias, C, Draper, E, Gatt, M, Khoshnood, B, Klungsoyr, K, Kurinczuk, J, Lynch, C, McDonnell, R, Nelen, V, Neville, A, O'Mahony, M, Pierini, A, Randrianaivo, H, Rissmann, A, Tucker, D, Verellen-Dumoulin, C, de Walle, H, Wellesley, D, Wiesel, A, Dolk, H

Epidemiology of achondroplasia: a population-based study in Europe -н Coi, A, Santoro, M, Garne, E, Pierini, A, Addor, M, Alessandri, J, Bergman, J, Bianchi, F, Boban, L, Braz, P, Cavero-Carbonell, C, Gatt, M, Haeusler, M, Klungsøyr, K, Kurinczuk, J, Lanzoni, M, Lelong, N, Luyt, K, Mokoroa, O, Mullaney, C, Nelen, V, Neville, A, O'Mahony, M, Perthus, I, Rankin, J, Rissmann, A, Rouget, F, Schaub, B, Tucker, D, Wellesley, D, Wisniewska, K, Zymak-Zakutnia, N, Barišić, I

Epidemiology of aplasia cutis congenita: a population-based study in Europe -н Coi, A, Barisic, I, Garne, E, Pierini, A, Addor, M-C, Aizpurua Atxega, A, Ballardini, E, Braz, P, Broughan, JM, Cavero-Carbonell, C, de Walle, HEK, Draper, ES, Gatt, M, Häusler, M, Kinsner-Ovaskainen, A, Kurinczuk, JJ, Lelong, N, Luyt, K, Mezzasalma, L, Mullaney, C, Nelen, V, Odak, L, O'Mahony, MT, Perthus, I, Randrianaivo, H, Rankin, J, Rissmann, A, Rouget, F, Schaub, B, Tucker, D, Wellesley, D, Wiśniewska, K, Yevtushok, L, Santoro, M

Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study -н van de Putte, R, van Rooij, IALM, Marcelis, CLM, Guo, M, Brunner, HG, Addor, M-C, Cavero-Carbonell, C, Dias, CM, Draper, ES, Etxebarriarteun, L, Gatt, M, Haeusler, M, Khoshnood, B, Klungsoyr, K, Kurinczuk, JJ, Lanzoni, M, Latos-Bielenska, A, Luyt, K, O'Mahony, MT, Miller, N, Mullaney, C, Nelen, V, Neville, AJ, Perthus, I, Pierini, A, Randrianaivo, H, Rankin, J, Rissmann, A, Rouget, F, Schaub, B, Tucker, D, Wellesley, D, Wiesel, A, Zymak-Zakutnia, N, Loane, M, Barisic, I, de Walle, HEK, Roeleveld, N, Bergman, JEH

Maternal risk factors for the VACTERL association: A EUROCAT case-control study -н van de Putte, R, van Rooij, IALM, Haanappel, CP, Marcelis, CLM, Brunner, HG, Addor, M-C, Cavero-Carbonell, C, Dias, CM, Draper, ES, Etxebarriarteun, L, Gatt, M, Khoshnood, B, Kinsner-Ovaskainen, A, Klungsoyr, K, Kurinczuk, JJ, Latos-Bielenska, A, Luyt, K, O'Mahony, MT, Miller, N, Mullaney, C, Nelen, V, Neville, AJ, Perthus, I, Pierini, A, Randrianaivo, H, Rankin, J, Rissmann, A, Rouget, F, Schaub, B, Tucker, D, Wellesley, D, Wiesel, A, Zymak-Zakutnia, N, Loane, M, Barisic, I, de Walle, HEK, Bergman, JEH, Roeleveld, N

PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution -н Mirzaa, G, Timms, A, Conti, V, Boyle, E, Girisha, K, Martin, B, Kircher, M, Olds, C, Juusola, J, Collins, S, Park, K, Carter, M, Glass, I, Krägeloh-Mann, I, Chitayat, D, Parikh, A, Bradshaw, R, Torti, E, Braddock, S, Burke, L, Ghedia, S, Stephan, M, Stewart, F, Prasad, C, Napier, M, Saitta, S, Straussberg, R, Gabbett, M, O'Connor, B, Keegan, C, Yin, L, Lai, A, Martin, N, McKinnon, M, Addor, M, Boccuto, L, Schwartz, C, Lanoel, A, Conway, R, Devriendt, K, Tatton-Brown, K, Pierpont, M, Painter, M, Worgan, L, Reggin, J, Hennekam, R, Tsuchiya, K, Pritchard, C, Aracena, M, Gripp, K, Cordisco, M, Esch, H, Garavelli, L, Curry, C, Goriely, A, Kayserilli, H, Shendure, J, Graham, J, Guerrini, R, Dobyns, W