Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

26 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
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.
Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.
Wright CF, Campbell P, Eberhardt RY, Aitken S, Perrett D, Brent S, Danecek P, Gardner EJ, Chundru VK, Lindsay SJ, Andrews K, Hampstead J, Kaplanis J, Samocha KE, Middleton A, Foreman J, Hobson RJ, Parker MJ, Martin HC, FitzPatrick DR, Hurles ME, Firth HV; DDD Study. Wright CF, et al. N Engl J Med. 2023 Apr 27;388(17):1559-1571. doi: 10.1056/NEJMoa2209046. Epub 2023 Apr 12. N Engl J Med. 2023. PMID: 37043637 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. PLoS One. 2023 Aug 30;18(8):e0290711. doi: 10.1371/journal.pone.0290711. eCollection 2023. PLoS One. 2023. PMID: 37647348 Free PMC article.
The burden of disease for children born alive with Turner syndrome-A European cohort study.
Andersen AR, Urhoj SK, Tan J, Cavero-Carbonell C, Gatt M, Gissler M, Klungsoyr K, Khoshnood B, Morris J, Neville AJ, Pierini A, Scanlon I, de Walle HEK, Wellesley D, Garne E, Loane M. Andersen AR, et al. Birth Defects Res. 2023 Oct 1;115(16):1459-1468. doi: 10.1002/bdr2.2222. Epub 2023 Jul 26. Birth Defects Res. 2023. PMID: 37493268
Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study.
Santoro M, Garne E, Coi A, Tan J, Loane M, Ballardini E, Cavero-Carbonell C, de Walle HE, Gatt M, Gissler M, Jordan S, Klungsøyr K, Lelong N, Urhoj SK, Wellesley DG, Morris JK. Santoro M, et al. Among authors: wellesley dg. Arch Dis Child. 2023 Jul;108(7):550-555. doi: 10.1136/archdischild-2022-324716. Epub 2023 May 9. Arch Dis Child. 2023. PMID: 37160334 Free PMC article.
European study showed that children with congenital anomalies often underwent multiple surgical procedures at different ages across Europe.
Garne E, Loane M, Tan J, Ballardini E, Brigden J, Cavero-Carbonell C, Coi A, Damkjaer M, Garcia-Villodre L, Gissler M, Given J, Heino A, Jordan S, Limb E, Neville A, Rissmann A, Santoro M, Scanlon I, Urhoj SK, Wellesley D, Morris J. Garne E, et al. Acta Paediatr. 2023 Jun;112(6):1304-1311. doi: 10.1111/apa.16726. Epub 2023 Mar 8. Acta Paediatr. 2023. PMID: 36823678
Higher risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study.
Urhoj SK, Morris J, Loane M, Ballardini E, Barrachina-Bonet L, Cavero-Carbonell C, Coi A, Gissler M, Given J, Heino A, Jordan S, Neville A, Santoro M, Tan J, Tucker D, Wellesley D, Garne E, Damkjaer M. Urhoj SK, et al. Acta Paediatr. 2024 May;113(5):1024-1031. doi: 10.1111/apa.17136. Epub 2024 Feb 7. Acta Paediatr. 2024. PMID: 38324400
Maternal age and the prevalence of congenital heart defects in Europe, 1995-2015: A register-based study.
Mamasoula C, Bigirumurame T, Chadwick T, Addor MC, Cavero-Carbonell C, Dias CM, Echevarría-González-de-Garibay LJ, Gatt M, Khoshnood B, Klungsoyr K, Randall K, Stoianova S, Haeusler M, Nelen V, Neville AJ, Perthus I, Pierini A, Bertaut-Nativel B, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Zymak-Zakutnia N, Barisic I, de Walle HEK, Lanzoni M, Sayers G, Mullaney C, Pennington L, Rankin J. Mamasoula C, et al. Birth Defects Res. 2023 Apr 1;115(6):583-594. doi: 10.1002/bdr2.2152. Epub 2023 Feb 3. Birth Defects Res. 2023. PMID: 36734416
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. 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.
26 results