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

Author:

Morris Joan K.1ORCID,Wellesley Diana2,Limb Elizabeth1,Bergman Jorieke E. H.3ORCID,Kinsner‐Ovaskainen Agnieszka4,Addor Marie Claude5,Broughan Jennifer M.6,Cavero‐Carbonell Clara7,Dias Carlos M.8,Echevarría‐González‐de‐Garibay Luis‐Javier9,Gatt Miriam10,Haeusler Martin11,Barisic Ingeborg12,Klungsoyr Kari1314,Lelong Nathalie15,Materna‐Kiryluk Anna16,Neville Amanda17,Nelen Vera18,O'Mahony Mary T.19,Perthus Isabelle20,Pierini Anna2122,Rankin Judith23,Rissmann Anke24ORCID,Rouget Florence25,Sayers Geraldine26,Stevens Sarah27,Tucker David28,Garne Ester29ORCID

Affiliation:

1. St George's University of London London United Kingdom

2. Clinical Genetics, University of Southampton and Wessex Clinical Genetics Service Princess Anne Hospital Southampton United Kingdom

3. University of Groningen, University Medical Center Groningen Department of Genetics Groningen The Netherlands

4. European Commission Joint Research Centre (JRC) Ispra Italy

5. Department of Woman‐Mother‐Child, University Medical Center CHUV Lausanne Switzerland

6. National Disease Registration Service, NHS Digital Leeds United Kingdom

7. Rare Diseases Research Unit Foundation for the Promotion of Health and Biomedical Research in the Valencian Region Valencia Spain

8. Department of Epidemiology Instituto Nacional de Saúde Doutor Ricardo Jorge; Av padre Cruz Lisbon Portugal

9. Ministry of Health of the Basque Government, Directorate for Healthcare Planning Organisation and Evaluation Vitoria‐Gasteiz Spain

10. Directorate for Health Information and Research Malta Congenital Anomalies Registry G'Mangia Malta

11. Medical University of Graz Austria

12. Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine Medical School University of Zagreb Zagreb Croatia

13. Department of Global Public Health and Primary Care University of Bergen Bergen Norway

14. Division of Mental and Physical Health Norwegian Institute of Public Health Bergen Norway

15. Université de Paris, INSERM U1153, CRESS Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé) Paris France

16. Polish Registry of Congenital Malformations, Department of Medical Genetics Poznan University of Medical Sciences Poznan Poland

17. Center for Clinical and Epidemiological Research University of Ferrara Ferrara Italy

18. Provincial Institute for Hygiene Antwerp Belgium

19. Department of Public Health Health Service Executive‐South Cork Ireland

20. Auvergne Registry of Congenital Anomalies (CEMC‐Auvergne), Department of Clinical Genetics, Centre de Référence des Maladies Rares University Hospital of Clermont‐Ferrand, CNRS‐UMR 6602, Institut Pascal, Axe TGI, équipe PEPRADE Clermont‐Ferrand France

21. Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology National Research Council Pisa Italy

22. Fondazione Toscana Gabriele Monasterio Pisa Italy

23. Population Health Sciences Institute, Faculty of Medical Sciences Newcastle University Newcastle upon Tyne United Kingdom

24. Malformation Monitoring Centre Saxony‐Anhalt Medical Faculty Otto‐von‐Guericke‐University Magdeburg Magdeburg Germany

25. Brittany Registry of Congenital Anomalies, CHU Rennes, Univ Rennes, Inserm, EHESP Irset (Institut de recherche en santé, environnement et travail) ‐ UMR_S 1085 Rennes France

26. Health Intelligence Research and Development Health Service Executive Dublin Ireland

27. National Disease Registration Service NHS Digital Leeds United Kingdom

28. Public Health Knowledge and Research, Public Health Wales Singleton Hospital Swansea United Kingdom

29. Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital University Hospital of Southern Denmark Kolding Denmark

Funder

European Commission

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Developmental Biology,Toxicology,Embryology,Pediatrics, Perinatology and Child Health

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3