Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi‐registry cohort studyMichele Santoro, Joan K. Morris, Hermien E. K. de Walle et al.|Paediatric and Perinatal Epidemiology|2022Cited by 18
Information needs of parents of children with congenital anomalies across Europe: a EUROlinkCAT surveyElena Marcus, Joan K. Morris, Anna Latos‐Bieleńska et al.|BMC Pediatrics|2022Cited by 13
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 qualityMaria Loane, Joan K. Morris, Joanne Given et al.|PLoS ONE|2023Cited by 9
COVID-19 and children with congenital anomalies: a European survey of parents’ experiences of healthcare servicesAnna Latos‐Bieleńska, Joan K. Morris, Elena Marcus et al.|BMJ Open|2022Cited by 4
Information needs of parents of children with congenital anomalies across Europe: a EUROlinkCAT surveyElena Marcus, Joan K. Morris, Anna Latos‐Bieleńska et al.|Research Square|2022Cited by 1