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Results by year

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

Year Number of Results
1986 1
1988 2
1990 1
1991 2
1992 2
1994 2
1995 1
1996 1
1998 2
1999 1
2000 4
2001 1
2002 1
2003 2
2004 4
2005 3
2006 1
2007 1
2008 5
2009 4
2010 3
2011 5
2012 6
2013 7
2014 14
2015 11
2016 7
2017 5
2018 6
2019 9
2020 6
2021 5
2022 11
2023 0
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Article type
Publication date

Search Results

116 results
Results by year
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Page 1
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Among authors: wellesley dg. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article.
Trends in congenital anomalies in Europe from 1980 to 2012.
Morris JK, Springett AL, Greenlees R, Loane M, Addor MC, Arriola L, Barisic I, Bergman JEH, Csaky-Szunyogh M, Dias C, Draper ES, Garne E, Gatt M, Khoshnood B, Klungsoyr K, Lynch C, McDonnell R, Nelen V, Neville AJ, O'Mahony M, Pierini A, Queisser-Luft A, Randrianaivo H, Rankin J, Rissmann A, Kurinczuk J, Tucker D, Verellen-Dumoulin C, Wellesley D, Dolk H. Morris JK, et al. Among authors: wellesley d. PLoS One. 2018 Apr 5;13(4):e0194986. doi: 10.1371/journal.pone.0194986. eCollection 2018. PLoS One. 2018. PMID: 29621304 Free PMC article.
Prenatal diagnosis of chromosomal imbalances.
Wellesley DG, Lucassen A. Wellesley DG, et al. Arch Dis Child Fetal Neonatal Ed. 2014 Jul;99(4):F338-41. doi: 10.1136/archdischild-2013-304835. Epub 2014 Mar 5. Arch Dis Child Fetal Neonatal Ed. 2014. PMID: 24792776 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. Among authors: wellesley dg. BMJ Paediatr Open. 2022 Jun;6(1):e001526. doi: 10.1136/bmjpo-2022-001526. BMJ Paediatr Open. 2022. PMID: 36053618 Free PMC article.
Fetal renal anomalies and genetic syndromes.
Wellesley D, Howe DT. Wellesley D, et al. Prenat Diagn. 2001 Nov;21(11):992-1003. doi: 10.1002/pd.209. Prenat Diagn. 2001. PMID: 11746154 Review.
Paper 6: EUROCAT member registries: organization and activities.
Greenlees R, Neville A, Addor MC, Amar E, Arriola L, Bakker M, Barisic I, Boyd PA, Calzolari E, Doray B, Draper E, Vollset SE, Garne E, Gatt M, Haeusler M, Kallen K, Khoshnood B, Latos-Bielenska A, Martinez-Frias ML, Materna-Kiryluk A, Dias CM, McDonnell B, Mullaney C, Nelen V, O'Mahony M, Pierini A, Queisser-Luft A, Randrianaivo-Ranjatoélina H, Rankin J, Rissmann A, Ritvanen A, Salvador J, Sipek A, Tucker D, Verellen-Dumoulin C, Wellesley D, Wertelecki W. Greenlees R, et al. Among authors: wellesley d. Birth Defects Res A Clin Mol Teratol. 2011 Mar;91 Suppl 1:S51-S100. doi: 10.1002/bdra.20775. Epub 2011 Mar 4. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21381185 Free article. Review.
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: wellesley d. J Eur Acad Dermatol Venereol. 2022 Oct 27. doi: 10.1111/jdv.18690. Online ahead of print. J Eur Acad Dermatol Venereol. 2022. PMID: 36300660
Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data.
Hardcastle A, Berry AM, Campbell IM, Zhao X, Liu P, Gerard AE, Rosenfeld JA, Sisoudiya SD, Hernandez-Garcia A, Loddo S, Di Tommaso S, Novelli A, Dentici ML, Capolino R, Digilio MC, Graziani L, Rustad CF, Neas K, Ferrero GB, Brusco A, Di Gregorio E, Wellesley D, Beneteau C, Joubert M, Van Den Bogaert K, Boogaerts A, McMullan DJ, Dean J, Giuffrida MG, Bernardini L, Varghese V, Shannon NL, Harrison RE, Lam WWK, McKee S, Turnpenny PD, Cole T, Morton J, Eason J, Jones MC, Hall R, Wright M, Horridge K, Shaw CA, Chung WK, Scott DA. Hardcastle A, et al. Among authors: wellesley d. Am J Med Genet A. 2022 Oct;188(10):2958-2968. doi: 10.1002/ajmg.a.62919. Epub 2022 Jul 29. Am J Med Genet A. 2022. PMID: 35904974
116 results