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Page 1
Epidemiology of aplasia cutis congenita: A population-based study in Europe.
Coi A, Barisic I, Garne E, Pierini A, Addor MC, Aizpurua Atxega A, Ballardini E, Braz P, Broughan JM, Cavero-Carbonell C, de Walle HEK, Draper ES, Gatt M, Häusler M, Kinsner-Ovaskainen A, Kurinczuk JJ, Lelong N, Luyt K, Mezzasalma L, Mullaney C, Nelen V, Odak L, O'Mahony MT, Perthus I, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wiśniewska K, Yevtushok L, Santoro M. Coi A, et al. Among authors: odak l. J Eur Acad Dermatol Venereol. 2023 Mar;37(3):581-589. doi: 10.1111/jdv.18690. Epub 2022 Nov 11. J Eur Acad Dermatol Venereol. 2023. PMID: 36300660 Free article.
Fraser syndrome: epidemiological study in a European population.
Barisic I, Odak L, Loane M, Garne E, Wellesley D, Calzolari E, Dolk H, Addor MC, Arriola L, Bergman J, Bianca S, Boyd PA, Draper ES, Gatt M, Haeusler M, Khoshnood B, Latos-Bielenska A, McDonnell B, Pierini A, Rankin J, Rissmann A, Queisser-Luft A, Verellen-Dumoulin C, Stone D, Tenconi R. Barisic I, et al. Among authors: odak l. Am J Med Genet A. 2013 May;161A(5):1012-8. doi: 10.1002/ajmg.a.35839. Epub 2013 Mar 26. Am J Med Genet A. 2013. PMID: 23532946
Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe.
Barisic I, Odak L, Loane M, Garne E, Wellesley D, Calzolari E, Dolk H, Addor MC, Arriola L, Bergman J, Bianca S, Doray B, Khoshnood B, Klungsoyr K, McDonnell B, Pierini A, Rankin J, Rissmann A, Rounding C, Queisser-Luft A, Scarano G, Tucker D. Barisic I, et al. Among authors: odak l. Eur J Hum Genet. 2014 Aug;22(8):1026-33. doi: 10.1038/ejhg.2013.287. Epub 2014 Jan 8. Eur J Hum Genet. 2014. PMID: 24398798 Free PMC article.
Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi-registry cohort study.
Santoro M, Coi A, Pierini A, Rankin J, Glinianaia SV, Tan J, Reid A, Garne E, Loane M, Given J, Aizpurua A, Astolfi G, Barisic I, Cavero-Carbonell C, de Walle HEK, Den Hond E, García-Villodre L, Gatt M, Gissler M, Jordan S, Khoshnood B, Kiuru-Kuhlefelt S, Klungsøyr K, Lelong N, Lutke R, Mokoroa O, Nelen V, Neville AJ, Odak L, Rissmann A, Scanlon I, Urhoj SK, Wellesley D, Wertelecki W, Yevtushok L, Morris JK. Santoro M, et al. Among authors: odak l. Paediatr Perinat Epidemiol. 2022 Nov;36(6):792-803. doi: 10.1111/ppe.12884. Epub 2022 Jun 8. Paediatr Perinat Epidemiol. 2022. PMID: 35675091 Free PMC article.
Hospital length of stay among children with and without congenital anomalies across 11 European regions-A population-based data linkage study.
Urhoj SK, Tan J, Morris JK, Given J, Astolfi G, Baldacci S, Barisic I, Brigden J, Cavero-Carbonell C, Evans H, Gissler M, Heino A, Jordan S, Lutke R, Odak L, Puccini A, Santoro M, Scanlon I, de Walle HEK, Wellesley D, Zurriaga Ó, Loane M, Garne E. Urhoj SK, et al. Among authors: odak l. PLoS One. 2022 Jul 22;17(7):e0269874. doi: 10.1371/journal.pone.0269874. eCollection 2022. PLoS One. 2022. PMID: 35867669 Free PMC article.
Information needs of parents of children with congenital anomalies across Europe: a EUROlinkCAT survey.
Marcus E, Latos-Bielenska A, Jamry-Dziurla A, Barišić I, Cavero-Carbonell C, Den Hond E, Garne E, Genard L, Santos AJ, Lutke L, Matias Dias C, Neergaard Pedersen C, Neville AJ, Niemann A, Odak L, Pierini A, Rico J, Rissmann A, Rankin J, Morris JK. Marcus E, et al. Among authors: odak l. BMC Pediatr. 2022 Nov 12;22(1):657. doi: 10.1186/s12887-022-03734-z. BMC Pediatr. 2022. PMID: 36368959 Free PMC article.
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.
Loane M, Given JE, Tan J, Barišić I, Barrachina-Bonet L, Cavero-Carbonell C, Coi A, Densem J, Garne E, Gissler M, Heino A, Jordan S, Lutke R, Neville AJ, Odak L, Puccini A, Santoro M, Scanlon I, Urhoj SK, de Walle HEK, Wellesley D, Morris JK. Loane M, et al. Among authors: odak l. PLoS One. 2023 Aug 30;18(8):e0290711. doi: 10.1371/journal.pone.0290711. eCollection 2023. PLoS One. 2023. PMID: 37647348 Free PMC article.
Dose imbalance of DYRK1A kinase causes systemic progeroid status in Down syndrome by increasing the un-repaired DNA damage and reducing LaminB1 levels.
Murray A, Gough G, Cindrić A, Vučković F, Koschut D, Borelli V, Petrović DJ, Bekavac A, Plećaš A, Hribljan V, Brunmeir R, Jurić J, Pučić-Baković M, Slana A, Deriš H, Frkatović A, Groet J, O'Brien NL, Chen HY, Yeap YJ, Delom F, Havlicek S, Gammon L, Hamburg S, Startin C, D'Souza H, Mitrečić D, Kero M, Odak L, Krušlin B, Krsnik Ž, Kostović I, Foo JN, Loh YH, Dunn NR, de la Luna S, Spector T, Barišić I, Thomas MSC, Strydom A, Franceschi C, Lauc G, Krištić J, Alić I, Nižetić D. Murray A, et al. Among authors: odak l. EBioMedicine. 2023 Aug;94:104692. doi: 10.1016/j.ebiom.2023.104692. Epub 2023 Jul 12. EBioMedicine. 2023. PMID: 37451904 Free PMC article.
16 results