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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2003 1
2004 4
2005 2
2006 1
2007 3
2008 6
2009 7
2010 11
2011 11
2012 9
2013 5
2014 15
2015 17
2016 16
2017 5
2018 13
2019 4
2020 2
2021 10
2022 13
2023 21
2024 7

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163 results

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Page 1
The prevalence of congenital anomalies in Europe.
Dolk H, Loane M, Garne E. Dolk H, et al. Among authors: garne e. Adv Exp Med Biol. 2010;686:349-64. doi: 10.1007/978-90-481-9485-8_20. Adv Exp Med Biol. 2010. PMID: 20824455 Review.
Reply.
Hansen AV, Morris J, Dolk H, Garne E. Hansen AV, et al. Among authors: garne e. J Allergy Clin Immunol. 2016 May;137(5):1624-5. doi: 10.1016/j.jaci.2015.11.048. Epub 2016 Mar 21. J Allergy Clin Immunol. 2016. PMID: 27012639 No abstract available.
Paper 1: The EUROCAT network--organization and processes.
Boyd PA, Haeusler M, Barisic I, Loane M, Garne E, Dolk H. Boyd PA, et al. Among authors: garne e. Birth Defects Res A Clin Mol Teratol. 2011 Mar;91 Suppl 1:S2-15. doi: 10.1002/bdra.20780. Epub 2011 Mar 7. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21384531 Review.
Cerebral palsy and congenital malformations.
Garne E, Dolk H, Krägeloh-Mann I, Holst Ravn S, Cans C; SCPE Collaborative Group. Garne E, et al. Eur J Paediatr Neurol. 2008 Mar;12(2):82-8. doi: 10.1016/j.ejpn.2007.07.001. Epub 2007 Sep 19. Eur J Paediatr Neurol. 2008. PMID: 17881257 Review.
Severe Congenital Heart Defects and Cerebral Palsy.
Garne E, Goldsmith S, Barisic I, Braz P, Dakovic I, Gibson C, Hansen M, Hoei-Hansen CE, Hollung SJ, Klungsøyr K, Smithers-Sheedy H, Virella D, Badawi N, Watson L, McIntyre S. Garne E, et al. J Pediatr. 2023 Nov;262:113617. doi: 10.1016/j.jpeds.2023.113617. Epub 2023 Jul 18. J Pediatr. 2023. PMID: 37473991 Free article.
Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study.
Glinianaia SV, Rankin J, Tan J, Loane M, Garne E, Cavero-Carbonell C, de Walle HEK, Gatt M, Gissler M, Klungsøyr K, Lelong N, Neville A, Pierini A, Tucker DF, Urhoj SK, Wellesley DG, Morris JK. Glinianaia SV, et al. Among authors: garne e. Arch Dis Child. 2023 Jun;108(6):461-467. doi: 10.1136/archdischild-2022-325068. Epub 2023 Mar 7. Arch Dis Child. 2023. PMID: 36882305
Surveillance of multiple congenital anomalies; searching for new associations.
Morris JK, Bergman JEH, Barisic I, Wellesley D, Tucker D, Limb E, Addor MC, Cavero-Carbonell C, Matias Dias C, Draper ES, Echevarría-González-de-Garibay LJ, Gatt M, Klungsøyr K, Lelong N, Luyt K, Materna-Kiryluk A, Nelen V, Neville A, Perthus I, Pierini A, Randrianaivo-Ranjatoelina H, Rankin J, Rissmann A, Rouget F, Sayers G, Wertelecki W, Kinsner-Ovaskainen A, Garne E. Morris JK, et al. Among authors: garne e. Eur J Hum Genet. 2024 Apr;32(4):407-412. doi: 10.1038/s41431-023-01502-w. Epub 2023 Dec 5. Eur J Hum Genet. 2024. PMID: 38052905 Free PMC article. Review.
Gastrostomy and congenital anomalies: a European population-based study.
Garne E, Tan J, Loane M, Baldacci S, Ballardini E, Brigden J, Cavero-Carbonell C, García-Villodre L, Gissler M, Given J, Heino A, Jordan S, Limb E, Neville AJ, Rissmann A, Santoro M, Scanlon L, Urhoj SK, Wellesley DG, Morris J. Garne E, et al. BMJ Paediatr Open. 2022 Jun;6(1):e001526. doi: 10.1136/bmjpo-2022-001526. BMJ Paediatr Open. 2022. PMID: 36053618 Free PMC article.
Crisponi/CISS1 syndrome: A case series.
Alhashem AM, Majeed-Saidan MA, Ammari AN, Alrakaf MS, Nojoom M, Maddirevula S, Faqeih E, Alkuraya FS, Garne E, Kurdi AM. Alhashem AM, et al. Among authors: garne e. Am J Med Genet A. 2016 May;170A(5):1236-41. doi: 10.1002/ajmg.a.37569. Epub 2016 Jan 24. Am J Med Genet A. 2016. PMID: 26804344
163 results