Ingeborg Barišić

University Hospital Centre Zagreb — Croatia

Biochemistry, Genetics and Molecular Biology · Life Sciences

46h-index6.6kcitations414works3.92yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(54), Congenital Anomalies and Fetal Surgery(51), Genetics and Neurodevelopmental Disorders(35), Prenatal Screening and Diagnostics(28), Congenital heart defects research(28)

Publications413 total

Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the <scp>EUROCAT</scp> Network
Paediatric and Perinatal Epidemiology·2025Open Access
Support Needs of Parents of Children With Congenital Anomalies Across Europe: A EUROlinkCAT Survey
Child Care Health and Development·2025· 1 citedOpen Access
Health outcomes of children with Prader-Willi or Angelman syndromes: a European population-based multicentre study
Archives of Disease in Childhood·2025Open Access
Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort study
Orphanet Journal of Rare Diseases·2025· 3 citedOpen Access
Risk of Congenital Ocular Anomaly After Prenatal Exposure to Medications: A <scp>EUROmediCAT</scp> Study
Birth Defects Research·2025· 1 citedOpen Access
Prevalence of Congenital Ocular Anomalies in 15 Countries of Europe: Results From the Medikeye Study
Birth Defects Research·2024· 3 citedOpen Access
Risk of Congenital Ocular Anomaly in EUROmediCAT: Assessment of the Potential Risk of Taking Medications during Pregnancy in Europe
SPIRE - Sciences Po Institutional REpository·2024
P079 Elexacaftor/tezacaftor/ivacaftor: a first case of severe rash in Croatia and our approach to desensitization
Journal of Cystic Fibrosis·2024
The Association of Prenatal Diagnoses with Mortality and Long-Term Morbidity in Children with Specific Isolated Congenital Anomalies: A European Register-Based Cohort Study
Maternal and Child Health Journal·2024· 5 citedOpen Access
Updated <scp>EUROCAT</scp> guidelines for classification of cases with congenital anomalies
Birth Defects Research·2024· 26 citedOpen Access
Surveillance of multiple congenital anomalies; searching for new associations
European Journal of Human Genetics·2023· 9 citedOpen Access
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: Assessment of linkage success and data quality
PLoS ONE·2023· 9 citedOpen Access
Severe Congenital Heart Defects and Cerebral Palsy
The Journal of Pediatrics·2023· 3 citedOpen Access
Dose imbalance of DYRK1A kinase causes systemic progeroid status in Down syndrome by increasing the un-repaired DNA damage and reducing LaminB1 levels
EBioMedicine·2023· 23 citedOpen Access
Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies
BMJ Open·2023· 2 citedOpen Access
Causes of death in children with congenital anomalies up to age 10 in eight European countries
BMJ Paediatrics Open·2023· 14 citedOpen Access
Surveillance of multiple congenital anomalies; searching for new associations
Research Square (Research Square)·2023Open Access
Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐based study
Birth Defects Research·2023· 30 citedOpen Access
Amniotic band syndrome and limb body wall complex in Europe 1980–2019
American Journal of Medical Genetics Part A·2022· 13 citedOpen Access
Information needs of parents of children with congenital anomalies across Europe: a EUROlinkCAT survey
BMC Pediatrics·2022· 10 citedOpen Access
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Frequent Co-authors

Ester Garne(33), Anke Rißmann(26), Diana Wellesley(25), Miriam Gatt(25), Maria Loane(24), Helen Dolk(24), Marie‐Claude Addor(24), David Tucker(23), Vera Nelen(22), Judith Rankin(21), Kari Klungsøyr(21), Anna Pierini(21), Babak Khoshnood(19), Mary O’Mahony(19), Amanda J. Neville(19), Martin Haeusler(18), Larraitz Arriola(16), Christine Verellen‐Dumoulin(14), Hermien E. K. de Walle(13), Elisa Calzolari(13)