Prevalence of Fetal Alcohol Syndrome and Maternal Characteristics in a Sample of Schoolchildren from a Rural Province of Croatia

por Petković, Giorgie, Barišić, Ingeborg
Publicado 2013

Multiplex ligation-dependent probe amplification workflow for the detection of submicroscopic chromosomal abnormalities in patients with developmental delay/intellectual disability

por Pohovski, Leona Morozin, Dumic, Katja K, Odak, Ljubica, Barisic, Ingeborg
Publicado 2013

Novel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report

por Odak, Ljubica, Barišić, Ingeborg, Morožin Pohovski, Leona, Riegel, Mariluce, Schinzel, Albert
Publicado 2011

Chromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability

por Sansović, Ivona, Ivankov, Ana-Maria, Bobinec, Adriana, Kero, Mijana, Barišić, Ingeborg
Publicado 2017

Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11β-Hydroxylase Deficiency

por Dumic, Katja, Yuen, Tony, Grubic, Zorana, Kusec, Vesna, Barisic, Ingeborg, New, Maria I.
Publicado 2014

EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies

por Morris, Joan K, Garne, Ester, Loane, Maria, Barisic, Ingeborg, Densem, James, Latos-Bieleńska, Anna, Neville, Amanda, Pierini, Anna, Rankin, Judith, Rissmann, Anke, de Walle, Hermien, Tan, Joachim, Given, Joanne Emma, Claridge, Hugh
Publicado 2021

Global birth defects app: An innovative tool for describing and coding congenital anomalies at birth in low resource settings

por Dolk, Helen, Leke, Aminkeng Zawuo, Whitfield, Phil, Moore, Rebecca, Karnell, Katy, Barišić, Ingeborg, Barlow-Mosha, Linda, Botto, Lorenzo D., Garne, Ester, Guatibonza, Pilar, Godfred-Cato, Shana, Halleux, Christine M., Holmes, Lewis B., Moore, Cynthia A., Orioli, Ieda, Raina, Neena, Valencia, Diana
Publicado 2021

The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers

por Tylki-Szymańska, Anna, Almássy, Zsuzsanna, Christophidou-Anastasiadou, Violetta, Avdjieva-Tzavella, Daniela, Barisic, Ingeborg, Cerkauskiene, Rimante, Cuturilo, Goran, Djiordjevic, Maja, Gucev, Zoran, Hlavata, Anna, Kieć-Wilk, Beata, Magner, Martin, Pecin, Ivan, Plaiasu, Vasilica, Samardzic, Mira, Zafeiriou, Dimitrios, Zaganas, Ioannis, Lampe, Christina
Publicado 2022

Information needs of parents of children with congenital anomalies across Europe: a EUROlinkCAT survey

por Marcus, Elena, Latos-Bielenska, Anna, Jamry-Dziurla, Anna, Barišić, Ingeborg, Cavero-Carbonell, Clara, Den Hond, Elly, Garne, Ester, Genard, Lucas, Santos, Ana João, Lutke, LRenée, Matias Dias, Carlos, Neergaard Pedersen, Christina, Neville, Amanda J., Niemann, Annika, Odak, Ljubica, Pierini, Anna, Rico, Juan, Rissmann, Anke, Rankin, Judith, Morris, Joan K.
Publicado 2022

Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies

por Claridge, Hugh, Tan, Joachim, Loane, Maria, Garne, Ester, Barisic, Ingeborg, Cavero-Carbonell, Clara, Dias, Carlos, Gatt, Miriam, Jordan, Susan, Khoshnood, Babak, Kiuru-Kuhlefelt, Sonja, Klungsoyr, Kari, Mokoroa Carollo, Olatz, Nelen, Vera, Neville, Amanda J, Pierini, Anna, Randrianaivo, Hanitra, Rissmann, Anke, Tucker, David, de Walle, Hermien, Wertelecki, Wladimir, Morris, Joan K
Publicado 2023

COVID-19 and children with congenital anomalies: a European survey of parents’ experiences of healthcare services

por Latos-Bieleńska, Anna, Marcus, Elena, Jamry-Dziurla, Anna, Rankin, Judith, Barisic, Ingeborg, Cavero- Carbonell, Clara, Den Hond, Elly, Garne, Ester, Genard, Lucas, João Santos, Ana, Lutke, L Renée, Matias Dias, Carlos, Neergaard Pedersen, Christina, Neville, Amanda, Niemann, Annika, Odak, Ljubica, Páramo-Rodríguez, Lucía, Pierini, Anna, Rissmann, Anke, Morris, Joan K
Publicado 2022

Creating a population-based cohort of children born with and without congenital anomalies using birth data matched to hospital discharge databases in 11 European regions: Assessmen...

por Loane, Maria, Given, Joanne E., Tan, Joachim, Barišić, Ingeborg, Barrachina-Bonet, Laia, Cavero-Carbonell, Clara, Coi, Alessio, Densem, James, Garne, Ester, Gissler, Mika, Heino, Anna, Jordan, Sue, Lutke, Renee, Neville, Amanda J., Odak, Ljubica, Puccini, Aurora, Santoro, Michele, Scanlon, Ieuan, Urhoj, Stine K., de Walle, Hermien E. K., Wellesley, Diana, Morris, Joan K.
Publicado 2023

Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study

por Bergman, Jorieke E. H., Lutke, L. Renée, Gans, Rijk O. B., Addor, Marie-Claude, Barisic, Ingeborg, Cavero-Carbonell, Clara, Garne, Ester, Gatt, Miriam, Klungsoyr, Kari, Lelong, Nathalie, Lynch, Catherine, Mokoroa, Olatz, Nelen, Vera, Neville, Amanda J., Pierini, Anna, Randrianaivo, Hanitra, Rissmann, Anke, Tucker, David, Wiesel, Awi, Dolk, Helen, Loane, Maria, Bakker, Marian K.
Publicado 2017

Hospital length of stay among children with and without congenital anomalies across 11 European regions—A population-based data linkage study

por Urhoj, Stine Kjaer, Tan, Joachim, Morris, Joan K., Given, Joanne, Astolfi, Gianni, Baldacci, Silvia, Barisic, Ingeborg, Brigden, Joanna, Cavero-Carbonell, Clara, Evans, Hannah, Gissler, Mika, Heino, Anna, Jordan, Sue, Lutke, Renée, Odak, Ljubica, Puccini, Aurora, Santoro, Michele, Scanlon, Ieuan, de Walle, Hermien E. K., Wellesley, Diana, Zurriaga, Óscar, Loane, Maria, Garne, Ester
Publicado 2022

EUROmediCAT signal detection: an evaluation of selected congenital anomaly‐medication associations

por Given, Joanne E., Loane, Maria, Luteijn, Johannes M., Morris, Joan K., de Jong van den Berg, Lolkje T.W., Garne, Ester, Addor, Marie‐Claude, Barisic, Ingeborg, de Walle, Hermien, Gatt, Miriam, Klungsoyr, Kari, Khoshnood, Babak, Latos‐Bielenska, Anna, Nelen, Vera, Neville, Amanda J., O'Mahony, Mary, Pierini, Anna, Tucker, David, Wiesel, Awi, Dolk, Helen
Publicado 2016

Holt Oram syndrome: a registry-based study in Europe

por Barisic, Ingeborg, Boban, Ljubica, Greenlees, Ruth, Garne, Ester, Wellesley, Diana, Calzolari, Elisa, Addor, Marie-Claude, Arriola, Larraitz, Bergman, Jorieke EH, Braz, Paula, Budd, Judith LS, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, McDonnell, Bob, Nelen, Vera, Pierini, Anna, Queisser-Wahrendorf, Annette, Rankin, Judith, Rissmann, Anke, Rounding, Catherine, Tucker, David, Verellen-Dumoulin, Christine, Dolk, Helen
Publicado 2014

Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion

por van Schie, Janne J. M., Faramarz, Atiq, Balk, Jesper A., Stewart, Grant S., Cantelli, Erika, Oostra, Anneke B., Rooimans, Martin A., Parish, Joanna L., de Almeida Estéves, Cynthia, Dumic, Katja, Barisic, Ingeborg, Diderich, Karin E. M., van Slegtenhorst, Marjon A., Mahtab, Mohammad, Pisani, Francesca M., te Riele, Hein, Ameziane, Najim, Wolthuis, Rob M. F., de Lange, Job
Publicado 2020

Lamotrigine use in pregnancy and risk of orofacial cleft and other congenital anomalies

por Dolk, Helen, Wang, Hao, Loane, Maria, Morris, Joan, Garne, Ester, Addor, Marie-Claude, Arriola, Larraitz, Bakker, Marian, Barisic, Ingeborg, Doray, Berenice, Gatt, Miriam, Kallen, Karin, Khoshnood, Babak, Klungsoyr, Kari, Lahesmaa-Korpinen, Anna-Maria, Latos-Bielenska, Anna, Mejnartowicz, Jan P., Nelen, Vera, Neville, Amanda, O'Mahony, Mary, Pierini, Anna, Rißmann, Anke, Tucker, David, Wellesley, Diana, Wiesel, Awi, de Jong-van den Berg, Lolkje T.W.
Publicado 2016

Prevalence of congenital heart defects in Europe, 2008–2015: A registry‐based study

por Mamasoula, Chrysovalanto, Addor, Marie‐Claude, Carbonell, Clara Cavero, Dias, Carlos M., Echevarría‐González‐de‐Garibay, Luis‐Javier, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Randall, Kay, Stoianova, Sylvia, Haeusler, Martin, Nelen, Vera, Neville, Amanda J., Perthus, Isabelle, Pierini, Anna, Bertaut‐Nativel, Bénédicte, Rissmann, Anke, Rouget, Florence, Schaub, Bruno, Tucker, David, Wellesley, Diana, Zymak‐Zakutnia, Natalya, Barisic, Ingeborg, de Walle, Hermien E. K., Lanzoni, Monica, Mullaney, Carmel, Pennington, Lindsay, Rankin, Judith
Publicado 2022

Prevalence of vascular disruption anomalies and association with young maternal age: A EUROCAT study to compare the United Kingdom with other European countries

por Morris, Joan K., Wellesley, Diana, Limb, Elizabeth, Bergman, Jorieke E. H., Kinsner‐Ovaskainen, Agnieszka, Addor, Marie Claude, Broughan, Jennifer M., Cavero‐Carbonell, Clara, Dias, Carlos M., Echevarría‐González‐de‐Garibay, Luis‐Javier, Gatt, Miriam, Haeusler, Martin, Barisic, Ingeborg, Klungsoyr, Kari, Lelong, Nathalie, Materna‐Kiryluk, Anna, Neville, Amanda, Nelen, Vera, O'Mahony, Mary T., Perthus, Isabelle, Pierini, Anna, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Sayers, Geraldine, Stevens, Sarah, Tucker, David, Garne, Ester
Publicado 2022