Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis von Fiddes, Ian T., Lodewijk, Gerrald A., Mooring, Meghan, Bosworth, Colleen M., Ewing, Adam D., Mantalas, Gary L., Novak, Adam M., van den Bout, Anouk, Bishara, Alex, Rosenkrantz, Jimi L., Lorig-Roach, Ryan, Field, Andrew R., Haeussler, Maximilian, Russo, Lotte, Bhaduri, Aparna, Nowakowski, Tomasz J., Pollen, Alex A., Dougherty, Max L., Nuttle, Xander, Addor, Marie-Claude, Zwolinski, Simon, Katzman, Sol, Kriegstein, Arnold, Eichler, Evan E., Salama, Sofie R., Jacobs, Frank M.J., Haussler, David

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Long term trends in prevalence of neural tube defects in Europe: population based study von Khoshnood, Babak, Loane, Maria, Walle, Hermien de, Arriola, Larraitz, Addor, Marie-Claude, Barisic, Ingeborg, Beres, Judit, Bianchi, Fabrizio, Dias, Carlos, Draper, Elizabeth, Garne, Ester, Gatt, Miriam, Haeusler, Martin, Klungsoyr, Kari, Latos-Bielenska, Anna, Lynch, Catherine, McDonnell, Bob, Nelen, Vera, Neville, Amanda J, O’Mahony, Mary T, Queisser-Luft, Annette, Rankin, Judith, Rissmann, Anke, Ritvanen, Annukka, Rounding, Catherine, Sipek, Antonin, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana, Dolk, Helen

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Trends in congenital anomalies in Europe from 1980 to 2012 von Morris, Joan K, Springett, Anna L, Greenlees, Ruth, Loane, Maria, Addor, Marie-Claude, Arriola, Larraitz, Barisic, Ingeborg, Bergman, Jorieke E H, Csaky-Szunyogh, Melinda, Dias, Carlos, Draper, Elizabeth S, Garne, Ester, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Lynch, Catherine, McDonnell, Robert, Nelen, Vera, Neville, Amanda J, O'Mahony, Mary, Pierini, Anna, Queisser-Luft, Annette, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Kurinczuk, Jennifer, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana, Dolk, Helen

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Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study von McGivern, Mark R, Best, Kate E, Rankin, Judith, Wellesley, Diana, Greenlees, Ruth, Addor, Marie-Claude, Arriola, Larraitz, de Walle, Hermien, Barisic, Ingeborg, Beres, Judit, Bianchi, Fabrizio, Calzolari, Elisa, Doray, Berenice, Draper, Elizabeth S, Garne, Ester, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, Latos-Bielenska, Anna, O'Mahony, Mary, Braz, Paula, McDonnell, Bob, Mullaney, Carmel, Nelen, Vera, Queisser-Luft, Anette, Randrianaivo, Hanitra, Rissmann, Anke, Rounding, Catherine, Sipek, Antonin, Thompson, Rosie, Tucker, David, Wertelecki, Wladimir, Martos, Carmen

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Twenty-year trends in the prevalence of Down syndrome and other trisomies in Europe: impact of maternal age and prenatal screening von Loane, Maria, Morris, Joan K, Addor, Marie-Claude, Arriola, Larraitz, Budd, Judith, Doray, Berenice, Garne, Ester, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsøyr Melve, Kari, Latos-Bielenska, Anna, McDonnell, Bob, Mullaney, Carmel, O'Mahony, Mary, Queisser-Wahrendorf, Annette, Rankin, Judith, Rissmann, Anke, Rounding, Catherine, Salvador, Joaquin, Tucker, David, Wellesley, Diana, Yevtushok, Lyubov, Dolk, Helen

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Epidemiology of achondroplasia: A population‐based study in Europe von Coi, Alessio, Santoro, Michele, Garne, Ester, Pierini, Anna, Addor, Marie‐Claude, Alessandri, Jean‐Luc, Bergman, Jorieke E. H., Bianchi, Fabrizio, Boban, Ljubica, Braz, Paula, Cavero‐Carbonell, Clara, Gatt, Miriam, Haeusler, Martin, Klungsøyr, Kari, Kurinczuk, Jennifer J., Lanzoni, Monica, Lelong, Nathalie, Luyt, Karen, Mokoroa, Olatz, Mullaney, Carmel, Nelen, Vera, Neville, Amanda J., O'Mahony, Mary T., Perthus, Isabelle, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Schaub, Bruno, Tucker, David, Wellesley, Diana, Wisniewska, Katarzyna, Zymak‐Zakutnia, Nataliia, Barišić, Ingeborg

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The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients von Nguyen, Ngoc Minh Phuong, Khawajkie, Yassemine, Mechtouf, Nawel, Rezaei, Maryam, Breguet, Magali, Kurvinen, Elvira, Jagadeesh, Sujatha, Solmaz, Asli Ece, Aguinaga, Monica, Hemida, Reda, Harma, Mehmet Ibrahim, Rittore, Cécile, Rahimi, Kurosh, Arseneau, Jocelyne, Hovanes, Karine, Clisham, Ronald, Lenzi, Tiffanee, Scurry, Bonnie, Addor, Marie-Claude, Bagga, Rashmi, Nendaz, Genevieve Girardet, Finci, Vildana, Poke, Gemma, Grimes, Leslie, Gregersen, Nerine, York, Kayla, Bolze, Pierre-Adrien, Patel, Chirag, Mozdarani, Hossein, Puechberty, Jacques, Scotchie, Jessica, Fardaei, Majid, Harma, Muge, Gardner, R. J. McKinlay, Sahoo, Trilochan, Dudding-Byth, Tracy, Srinivasan, Radhika, Sauthier, Philippe, Slim, Rima

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Congenital clubfoot in Europe: A population‐based study von Wang, Hao, Barisic, Ingeborg, Loane, Maria, Addor, Marie‐Claude, Bailey, Linda M., Gatt, Miriam, Klungsoyr, Kari, Mokoroa, Olatz, Nelen, Vera, Neville, Amanda J., O'Mahony, Mary, Pierini, Anna, Rissmann, Anke, Verellen‐Dumoulin, Christine, Walle, Hermien E.K., Wiesel, Awi, Wisniewska, Katarzyna, Jong‐van den Berg, Lolkje T.W., Dolk, Helen, Khoshnood, Babak, Garne, Ester

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Prevalence of microcephaly in Europe: population based study von Morris, Joan K, Rankin, Judith, Garne, Ester, Loane, Maria, Greenlees, Ruth, Addor, Marie-Claude, Arriola, Larraitz, Barisic, Ingeborg, Bergman, Jorieke E H, Csaky-Szunyogh, Melinda, Dias, Carlos, Draper, Elizabeth S, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Kurinczuk, Jennifer J, Lynch, Catherine, McDonnell, Robert, Nelen, Vera, Neville, Amanda J, O’Mahony, Mary T, Pierini, Anna, Randrianaivo, Hanitra, Rissmann, Anke, Tucker, David, Verellen-Dumoulin, Christine, de Walle, Hermien E K, Wellesley, Diana, Wiesel, Awi, Dolk, Helen

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Epidemiology of Pierre‐Robin sequence in Europe: A population‐based EUROCAT study von Santoro, Michele, Coi, Alessio, Barišić, Ingeborg, Pierini, Anna, Addor, Marie‐Claude, Baldacci, Silvia, Ballardini, Elisa, Boban, Ljubica, Braz, Paula, Cavero‐Carbonell, Clara, Walle, Hermien E. K., Draper, Elizabeth S., Gatt, Miriam, Haeusler, Martin, Klungsøyr, Kari, Kurinczuk, Jennifer J., Materna‐Kiryluk, Anna, Lanzoni, Monica, Lelong, Nathalie, Luyt, Karen, Mokoroa, Olatz, Mullaney, Carmel, Nelen, Vera, O’Mahony, Mary T., Perthus, Isabelle, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Schaub, Bruno, Tucker, David, Wellesley, Diana, Zymak‐Zakutnia, Nataliia, Garne, Ester

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Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe von WELLESLEY, Diana, DOLK, Helen, MULLANEY, Carmel, CALZOLARI, Elisa, BAKKER, Marian, SALVADOR, Joaquin, ADDOR, Marie-Claude, DRAPER, Elizabeth, RANKIN, Judith, TUCKER, David, BOYD, Patricia A, GREENLEES, Ruth, HAEUSLER, Martin, NELEN, Vera, GARNE, Ester, KHOSHNOOD, Babak, DORAY, Berenice, RISSMANN, Anke

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Pregnancy outcome following first-trimester exposure to fingolimod: A collaborative ENTIS study von Pauliat, Emmanuelle, Onken, Marlies, Weber-Schoendorfer, Corinna, Rousson, Valentin, Addor, Marie-Claude, Baud, David, Théaudin, Marie, Diav-Citrin, Orna, Cottin, Judith, Agusti, Antonia, Rollason, Victoria, Kaplan, Yusuf C, Kennedy, Debra, Kadioglu, Mine, Rothuizen, Laura E, Livio, Françoise, Buclin, Thierry, Panchaud, Alice, Winterfeld, Ursula

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Surveillance of multiple congenital anomalies; searching for new associations von Morris, Joan K, Bergman, Jorieke E H, Barisic, Ingeborg, Wellesley, Diana, Tucker, David, Limb, Elizabeth, Addor, Marie-Claude, Cavero-Carbonell, Clara, Matias Dias, Carlos, Draper, Elisabeth S, Echevarría-González-de-Garibay, Luis Javier, Gatt, Miriam, Klungsøyr, Kari, Lelong, Nathalie, Luyt, Karen, Materna-Kiryluk, Anna, Nelen, Vera, Neville, Amanda, Perthus, Isabelle, Pierini, Anna, Randrianaivo-Ranjatoelina, Hanitra, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Sayers, Geraldine, Wertelecki, Wladimir, Kinsner-Ovaskainen, Agnieszka, Garne, Ester

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Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study von van de Putte, Romy, van Rooij, Iris A. L. M., Marcelis, Carlo L. M., Guo, Michel, Brunner, Han G., Addor, Marie-Claude, Cavero-Carbonell, Clara, Dias, Carlos M., Draper, Elizabeth S., Etxebarriarteun, Larraitz, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, Kurinczuk, Jenny J., Lanzoni, Monica, Latos-Bielenska, Anna, Luyt, Karen, O’Mahony, Mary T., Miller, Nicola, Mullaney, Carmel, Nelen, Vera, Neville, Amanda J., Perthus, Isabelle, Pierini, Anna, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Schaub, Bruno, Tucker, David, Wellesley, Diana, Wiesel, Awi, Zymak-Zakutnia, Natalya, Loane, Maria, Barisic, Ingeborg, de Walle, Hermien E. K., Roeleveld, Nel, Bergman, Jorieke E. H.

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Congenital anomalies associated with trisomy 18 or trisomy 13: A registry-based study in 16 european countries, 2000-2011 von Springett, Anna, Wellesley, Diana, Greenlees, Ruth, Loane, Maria, Addor, Marie-Claude, Arriola, Larraitz, Bergman, Jorieke, Cavero-Carbonell, Clara, Csaky-Szunyogh, Melinda, Draper, Elizabeth S., Garne, Ester, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, Lynch, Catherine, Dias, Carlos Matias, McDonnell, Robert, Nelen, Vera, O'Mahony, Mary, Pierini, Anna, Queisser-Luft, Annette, Rankin, Judith, Rissmann, Anke, Rounding, Catherine, Stoianova, Sylvia, Tuckerz, David, Zymak-Zakutnia, Natalya, Morris, Joan K.

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Epidemiology of multiple congenital anomalies in Europe: A EUROCAT population-based registry study von Calzolari, Elisa, Barisic, Ingeborg, Loane, Maria, Morris, Joan, Wellesley, Diana, Dolk, Helen, Addor, Marie-Claude, Arriola, Larraitz, Bianchi, Fabrizio, Neville, Amanda J., Budd, Judith L.S., Klungsoyr, Kari, Khoshnood, Babak, McDonnell, Bob, Nelen, Vera, Queisser-Luft, Annette, Rankin, Judith, Rissmann, Anke, Rounding, Catherine, Tucker, David, Verellen-Dumoulin, Christine, de Walle, Hermien, Garne, Ester

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Use of asthma medication during pregnancy and risk of specific congenital anomalies: A European case-malformed control study von Garne, Ester, MD, Hansen, Anne Vinkel, MSc, Morris, Joan, PhD, Zaupper, Louise, MD, Addor, Marie-Claude, MD, Barisic, Ingeborg, PhD, Gatt, Miriam, MD, MSc, Lelong, Nathalie, MSc, Klungsøyr, Kari, MD, PhD, O'Mahony, Mary, MFPHMI, Nelen, Vera, MD, Neville, Amanda J., BSc, Pierini, Anna, BSc, Tucker, David, MPH, de Walle, Hermien, PhD, Wiesel, Awi, MD, MSc, Loane, Maria, PhD, Dolk, Helen, PhD

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Spectrum of congenital anomalies in pregnancies with pregestational diabetes von Garne, Ester, Loane, Maria, Dolk, Helen, Barisic, Ingeborg, Addor, Marie-Claude, Arriola, Larraitz, Bakker, Marian, Calzolari, Elisa, Matias Dias, Carlos, Doray, Berenice, Gatt, Miriam, Melve, Kari Klyungsoyr, Nelen, Vera, O'Mahony, Mary, Pierini, Anna, Randrianaivo-Ranjatoelina, Hanitra, Rankin, Judith, Rissmann, Anke, Tucker, David, Verellun-Dumoulin, Christine, Wiesel, Awi

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Gastroschisis in Europe – A Case‐malformed‐Control Study of Medication and Maternal Illness during Pregnancy as Risk Factors von Given, Joanne E., Loane, Maria, Garne, Ester, Nelen, Vera, Barisic, Ingeborg, Randrianaivo, Hanitra, Khoshnood, Babak, Wiesel, Awi, Rissmann, Anke, Lynch, Catherine, Neville, Amanda J., Pierini, Anna, Bakker, Marian, Klungsoyr, Kari, Latos Bielenska, Anna, Cavero‐Carbonell, Clara, Addor, Marie‐Claude, Zymak‐Zakutnya, Natalya, Tucker, David, Dolk, Helen

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Epidemiology of aplasia cutis congenita: A population‐based study in Europe von Coi, Alessio, Barisic, Ingeborg, Garne, Ester, Pierini, Anna, Addor, Marie‐Claude, Aizpurua Atxega, Amaia, Ballardini, Elisa, Braz, Paula, Broughan, Jennifer M., Cavero‐Carbonell, Clara, Walle, Hermien E. K., Draper, Elizabeth S., Gatt, Miriam, Häusler, Martin, Kinsner‐Ovaskainen, Agnieszka, Kurinczuk, Jennifer J., Lelong, Nathalie, Luyt, Karen, Mezzasalma, Lorena, Mullaney, Carmel, Nelen, Vera, Odak, Ljubica, O'Mahony, Mary T., Perthus, Isabelle, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Schaub, Bruno, Tucker, David, Wellesley, Diana, Wiśniewska, Katarzyna, Yevtushok, Lyubov, Santoro, Michele

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