| Valproic acid monotherapy in pregnancy and major congenital malformations J Jentink, MA Loane, H Dolk, I Barisic, E Garne, JK Morris, ... New England Journal of Medicine 362 (23), 2185-2193, 2010 | 457 | 2010 |
| Prenatal diagnosis of severe structural congenital malformations in Europe E Garne, M Loane, H Dolk, C De Vigan, G Scarano, D Tucker, C Stoll, ... Ultrasound in Obstetrics and Gynecology: The Official Journal of the …, 2005 | 321 | 2005 |
| Evaluation of prenatal ultrasound diagnosis of fetal abdominal wall defects by 19 European registries I Barisic, M Clementi, M Haeusler, R Gjergja, J Kern, C Stoll Ultrasound in Obstetrics and Gynecology: The Official Journal of the …, 2001 | 241 | 2001 |
| Congenital diaphragmatic hernia: evaluation of prenatal diagnosis in 20 European regions E Garne, M Haeusler, I Barisic, R Gjergja, C Stoll, M Clementi Ultrasound in Obstetrics and Gynecology: The Official Journal of the …, 2002 | 202 | 2002 |
| Preventing neural tube defects in Europe: a missed opportunity A Busby, B Armstrong, H Dolk, N Armstrong, M Haeusler, A Berghold, ... Reproductive Toxicology 20 (3), 393-402, 2005 | 164 | 2005 |
| Long term trends in prevalence of neural tube defects in Europe: population based study B Khoshnood, M Loane, H De Walle, L Arriola, MC Addor, I Barisic, ... Bmj 351, h5949, 2015 | 151 | 2015 |
| Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study MR McGivern, KE Best, J Rankin, D Wellesley, R Greenlees, MC Addor, ... Archives of Disease in Childhood-Fetal and Neonatal Edition 100 (2), F137-F144, 2015 | 130 | 2015 |
| Congenital hydrocephalus–prevalence, prenatal diagnosis and outcome of pregnancy in four European regions E Garne, M Loane, MC Addor, PA Boyd, I Barisic, H Dolk european journal of paediatric neurology 14 (2), 150-155, 2010 | 119 | 2010 |
| Paper 1: the EUROCAT network—organization and processes PA Boyd, M Haeusler, I Barisic, M Loane, E Garne, H Dolk Birth Defects Research Part A: Clinical and Molecular Teratology 91 (S1), S2-S15, 2011 | 118 | 2011 |
| Paper 6: EUROCAT member registries: organization and activities R Greenlees, A Neville, MC Addor, E Amar, L Arriola, M Bakker, I Barisic, ... Birth Defects Research Part A: Clinical and Molecular Teratology 91 (S1 …, 2011 | 116 | 2011 |
| Prenatal ultrasonographic detection of gastrointestinal obstruction: results from 18 European congenital anomaly registries MCH Haeusler, A Berghold, C Stoll, I Barisic, M Clementi Prenatal Diagnosis: Published in Affiliation With the International Society …, 2002 | 111 | 2002 |
| Spectrum of congenital anomalies in pregnancies with pregestational diabetes E Garne, M Loane, H Dolk, I Barisic, MC Addor, L Arriola, M Bakker, ... Birth Defects Research Part A: Clinical and Molecular Teratology 94 (3), 134-140, 2012 | 100 | 2012 |
| Descriptive epidemiology of Cornelia de Lange syndrome in Europe I Barisic, V Tokic, M Loane, F Bianchi, E Calzolari, E Garne, D Wellesley, ... American Journal of Medical Genetics Part A 146 (1), 51-59, 2008 | 92 | 2008 |
| Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe E Garne, M Loane, D Wellesley, I Barisic, EUROCAT Working Group Journal of pediatric urology 5 (1), 47-52, 2009 | 78 | 2009 |
| Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2) S Schuffenhauer, P Lichtner, P Peykar-Derakhshandeh, J Murken, ... European Journal of Human Genetics 6 (3), 213, 1998 | 78 | 1998 |
| Osteogenesis imperfecta at the beginning of bone and joint decade D Primorac, DW Rowe, M Mottes, I Barisic, D Anticevic, S Mirandola, ... Croatian medical journal 42 (4), 393-415, 2001 | 75 | 2001 |
| Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe I Barisic, L Odak, M Loane, E Garne, D Wellesley, E Calzolari, H Dolk, ... European Journal of Human Genetics 22 (8), 1026, 2014 | 68 | 2014 |
| Epidemiology of hypospadias in Europe: a registry-based study JEH Bergman, M Loane, M Vrijheid, A Pierini, RJM Nijman, MC Addor, ... World journal of urology 33 (12), 2159-2167, 2015 | 61 | 2015 |
| Paper 5: Surveillance of multiple congenital anomalies: implementation of a computer algorithm in European registers for classification of cases E Garne, H Dolk, M Loane, D Wellesley, I Barisic, E Calzolari, J Densem, ... Birth Defects Research Part A: Clinical and Molecular Teratology 91 (S1 …, 2011 | 51 | 2011 |
| Genotype–phenotype spectrum of PYCR1-related autosomal recessive cutis laxa A Dimopoulou, B Fischer, T Gardeitchik, P Schröter, H Kayserili, ... Molecular genetics and metabolism 110 (3), 352-361, 2013 | 49 | 2013 |
