Area of research
Rheumatology · Pediatrics, Perinatology and Child Health
Research interest
Research focused on Epidemiology and Trisomy, with related work in Register (sociolinguistics), Population, Pregnancy. Notable publications include 'Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis', 'Twenty-year trends in the prevalence of Down syndrome and other trisomies in Europe: impact of maternal age and prenatal screening', and 'Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study'.
Use of GLP1 receptor agonists in early pregnancy and reproductive safety: a multicentre, observational, prospective cohort study based on the databases of six Teratology Information Services
Prevalence of Congenital Ocular Anomalies in 15 Countries of Europe: Results From the Medikeye Study
Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐based study
Surveillance of multiple congenital anomalies; searching for new associations
Prevalence of congenital heart defects in Europe, 2008–2015: A registry‐based study
Epidemiology of aplasia cutis congenita: A population‐based study in Europe
Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals
Amniotic band syndrome and limb body wall complex in Europe 1980–2019
Epidemiology of Pierre‐Robin sequence in Europe: A population‐based EUROCAT study
Prevention of Neural Tube Defects in Europe: A Public Health Failure
Duo Research Archive (University of Oslo) 2021cited by 0position: middle
Pregnancy outcome following first-trimester exposure to fingolimod: A collaborative ENTIS study
Maternal risk factors for the<scp>VACTERL</scp>association: A<scp>EUROCAT</scp>case–control study
Epidemiology of achondroplasia: A population‐based study in Europe
Congenital clubfoot in Europe: A population‐based study
Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study
Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study
Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study
Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis
Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study
Metformin Exposure in the First Trimester of Pregnancy and Risk of All or Specific Congenital Anomalies: Exploratory Case-Control Study
Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data
Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study
Gastroschisis in Europe – A Case‐malformed‐Control Study of Medication and Maternal Illness during Pregnancy as Risk Factors
Gastroschisis in Europe – A prevalence and case-malformed control study
Prevalence of microcephaly in Europe: population based study
EUROmediCAT signal detection: an evaluation of selected congenital anomaly‐medication associations
EUROmediCAT signal detection: a systematic method for identifying potential teratogenic medication
Lamotrigine use in pregnancy and risk of orofacial cleft and other congenital anomalies
University of Southern Denmark Research Portal (University of Southern Denmark) 2016cited by 0position: middle
Long term trends in prevalence of neural tube defects in Europe: population based study
Congenital anomalies associated with trisomy 18 or trisomy 13: A registry‐based study in 16 european countries, 2000–2011