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

Year Number of Results
1991 1
1992 1
1993 1
1995 1
1996 2
1997 4
1998 3
1999 6
2000 6
2002 4
2003 4
2004 3
2005 7
2006 7
2007 5
2008 3
2009 3
2010 6
2011 2
2012 2
2013 4
2014 9
2015 11
2016 6
2017 5
2018 5
2019 8
2020 10
2021 6
2022 10
2023 14
2024 2

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147 results

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Page 1
Trisomy 13 and 18-Prevalence and mortality-A multi-registry population based analysis.
Goel N, Morris JK, Tucker D, de Walle HEK, Bakker MK, Kancherla V, Marengo L, Canfield MA, Kallen K, Lelong N, Camelo JL, Stallings EB, Jones AM, Nance A, Huynh MP, Martínez-Fernández ML, Sipek A, Pierini A, Nembhard WN, Goetz D, Rissmann A, Groisman B, Luna-Muñoz L, Szabova E, Lapchenko S, Zarante I, Hurtado-Villa P, Martinez LE, Tagliabue G, Landau D, Gatt M, Dastgiri S, Morgan M. Goel N, et al. Among authors: de walle hek. Am J Med Genet A. 2019 Dec;179(12):2382-2392. doi: 10.1002/ajmg.a.61365. Epub 2019 Sep 30. Am J Med Genet A. 2019. PMID: 31566869 Free PMC article.
Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study.
Bakker MK, Bergman JEH, Krikov S, Amar E, Cocchi G, Cragan J, de Walle HEK, Gatt M, Groisman B, Liu S, Nembhard WN, Pierini A, Rissmann A, Chidambarathanu S, Sipek A Jr, Szabova E, Tagliabue G, Tucker D, Mastroiacovo P, Botto LD. Bakker MK, et al. Among authors: de walle hek. BMJ Open. 2019 Jul 2;9(7):e028139. doi: 10.1136/bmjopen-2018-028139. BMJ Open. 2019. PMID: 31270117 Free PMC article.
Desmin-related myopathy.
van Spaendonck-Zwarts KY, van Hessem L, Jongbloed JD, de Walle HE, Capetanaki Y, van der Kooi AJ, van Langen IM, van den Berg MP, van Tintelen JP. van Spaendonck-Zwarts KY, et al. Among authors: de walle he. Clin Genet. 2011 Oct;80(4):354-66. doi: 10.1111/j.1399-0004.2010.01512.x. Epub 2010 Jul 21. Clin Genet. 2011. PMID: 20718792 Review.
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: de walle hek. 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
Congenital clubfoot in Europe: A population-based study.
Wang H, Barisic I, Loane M, Addor MC, Bailey LM, Gatt M, Klungsoyr K, Mokoroa O, Nelen V, Neville AJ, O'Mahony M, Pierini A, Rissmann A, Verellen-Dumoulin C, de Walle HEK, Wiesel A, Wisniewska K, de Jong-van den Berg LTW, Dolk H, Khoshnood B, Garne E. Wang H, et al. Among authors: de walle hek. Am J Med Genet A. 2019 Apr;179(4):595-601. doi: 10.1002/ajmg.a.61067. Epub 2019 Feb 10. Am J Med Genet A. 2019. PMID: 30740879
Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies.
Claridge H, Tan J, Loane M, Garne E, Barisic I, Cavero-Carbonell C, Dias C, Gatt M, Jordan S, Khoshnood B, Kiuru-Kuhlefelt S, Klungsoyr K, Mokoroa Carollo O, Nelen V, Neville AJ, Pierini A, Randrianaivo H, Rissmann A, Tucker D, de Walle H, Wertelecki W, Morris JK. Claridge H, et al. Among authors: de walle h. BMJ Open. 2023 Jul 27;13(7):e071687. doi: 10.1136/bmjopen-2023-071687. BMJ Open. 2023. PMID: 37500278 Free PMC article. Review.
Acardia: epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and Research.
Botto LD, Feldkamp ML, Amar E, Carey JC, Castilla EE, Clementi M, Cocchi G, de Walle HE, Halliday J, Leoncini E, Li Z, Lowry RB, Marengo LK, Martínez-Frías ML, Merlob P, Morgan M, Muñoz LL, Rissmann A, Ritvanen A, Scarano G, Mastroiacovo P. Botto LD, et al. Among authors: de walle he. Am J Med Genet C Semin Med Genet. 2011 Nov 15;157C(4):262-73. doi: 10.1002/ajmg.c.30318. Epub 2011 Oct 14. Am J Med Genet C Semin Med Genet. 2011. PMID: 22002952 Review.
Ten-Year Survival of Children With Congenital Anomalies: A European Cohort Study.
Glinianaia SV, Rankin J, Pierini A, Coi A, Santoro M, Tan J, Reid A, Garne E, Loane M, Given J, Cavero-Carbonell C, de Walle HEK, Gatt M, Gissler M, Heino A, Khoshnood B, Klungsøyr K, Lelong N, Neville AJ, Thayer DS, Tucker D, Urhøj SK, Wellesley D, Zurriaga O, Morris JK. Glinianaia SV, et al. Among authors: de walle hek. Pediatrics. 2022 Mar 1;149(3):e2021053793. doi: 10.1542/peds.2021-053793. Pediatrics. 2022. PMID: 35146505
Accuracy of congenital anomaly coding in live birth children recorded in European health care databases, a EUROlinkCAT study.
Bakker MK, Loane M, Garne E, Ballardini E, Cavero-Carbonell C, García L, Gissler M, Given J, Heino A, Jamry-Dziurla A, Jordan S, Urhoj SK, Latos-Bieleńska A, Limb E, Lutke R, Neville AJ, Pierini A, Santoro M, Scanlon I, Tan J, Wellesley D, de Walle HEK, Morris JK. Bakker MK, et al. Among authors: de walle hek. Eur J Epidemiol. 2023 Mar;38(3):325-334. doi: 10.1007/s10654-023-00971-z. Epub 2023 Feb 18. Eur J Epidemiol. 2023. PMID: 36807730 Free PMC article.
147 results