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

Year Number of Results
1982 1
1987 1
1994 2
1996 1
1998 1
1999 2
2001 3
2003 1
2004 1
2005 4
2006 2
2009 1
2010 1
2011 4
2012 4
2013 3
2014 9
2015 3
2016 4
2017 4
2018 7
2019 2
2020 4
2021 3
2022 2
2023 7
2024 2

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68 results

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Page 1
Gene ontology enrichment analysis of congenital diaphragmatic hernia-associated genes.
Dalmer TRA, Clugston RD. Dalmer TRA, et al. Pediatr Res. 2019 Jan;85(1):13-19. doi: 10.1038/s41390-018-0192-8. Epub 2018 Sep 25. Pediatr Res. 2019. PMID: 30287891 Free PMC article. Review.
Congenital diaphragmatic hernia (CDH) is a commonly occurring major congenital anomaly with a profound impact on neonatal mortality. ...
Congenital diaphragmatic hernia (CDH) is a commonly occurring major congenital anomaly with a profound impact on neonat …
Mental Health Conditions Among Children and Adolescents With Congenital Heart Disease: A Danish Population-Based Cohort Study.
Miles KG, Farkas DK, Laugesen K, Sørensen HT, Kasparian NA, Madsen N. Miles KG, et al. Circulation. 2023 Oct 31;148(18):1381-1394. doi: 10.1161/CIRCULATIONAHA.123.064705. Epub 2023 Sep 18. Circulation. 2023. PMID: 37721036 Free PMC article.
RESULTS: The cumulative incidence of mental health conditions by 18 years of age in the CHD cohort was 35.1% (95% CI, 34.0%-36.1%), corresponding to aHRs of 1.64 (95% CI, 1.58-1.71), 1.41 (95% CI, 1.30-1.52), and 1.02 (95% CI, 0.98-1.07) compared with the general population, sibl …
RESULTS: The cumulative incidence of mental health conditions by 18 years of age in the CHD cohort was 35.1% (95% CI, 34.0%-36.1%), correspo …
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. 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
We aimed to assess prevalence, birth outcome, associated anomalies and prenatal diagnosis of congenital clubfoot in Europe using data from the EUROCAT network, and to validate the recording of congenital clubfoot as a major congenital anomaly by EUROCAT regis …
We aimed to assess prevalence, birth outcome, associated anomalies and prenatal diagnosis of congenital clubfoot in Europe using data from t …
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study.
Griffin EL, Nees SN, Morton SU, Wynn J, Patel N, Jobanputra V, Robinson S, Kochav SM, Tao A, Andrews C, Cross N, Geva J, Lanzilotta K, Ritter A, Taillie E, Thompson A, Meyer C, Akers R, King EC, Cnota JF, Kim RW, Porter GA Jr, Brueckner M, Seidman CE, Shen Y, Gelb BD, Goldmuntz E, Newburger JW, Roberts AE, Chung WK. Griffin EL, et al. Circ Genom Precis Med. 2023 Apr;16(2):e003791. doi: 10.1161/CIRCGEN.122.003791. Epub 2023 Feb 21. Circ Genom Precis Med. 2023. PMID: 36803080 Free PMC article.
BACKGROUND: Congenital heart disease (CHD) is the most common major congenital anomaly and causes significant morbidity and mortality. ...
BACKGROUND: Congenital heart disease (CHD) is the most common major congenital anomaly and causes significant morbidity …
A population-based matched cohort study of major congenital anomalies following COVID-19 vaccination and SARS-CoV-2 infection.
Calvert C, Carruthers J, Denny C, Donaghy J, Hopcroft LEM, Hopkins L, Goulding A, Lindsay L, McLaughlin T, Moore E, Taylor B, Loane M, Dolk H, Morris J, Auyeung B, Bhaskaran K, Gibbons CL, Katikireddi SV, O'Leary M, McAllister D, Shi T, Simpson CR, Robertson C, Sheikh A, Stock SJ, Wood R. Calvert C, et al. Nat Commun. 2023 Jan 6;14(1):107. doi: 10.1038/s41467-022-35771-8. Nat Commun. 2023. PMID: 36609574 Free PMC article.
Here we report a national, population-based, matched cohort study using linked electronic health records from Scotland (May 2020-April 2022) to estimate the association between COVID-19 vaccination and, separately, SARS-CoV-2 infection between six weeks pre-conception and 19 week …
Here we report a national, population-based, matched cohort study using linked electronic health records from Scotland (May 2020-April 2022) …
Postlicensure safety surveillance of congenital anomaly and miscarriage among pregnancies exposed to quadrivalent human papillomavirus vaccine.
Sy LS, Meyer KI, Klein NP, Chao C, Velicer C, Cheetham TC, Ackerson BK, Slezak JM, Takhar HS, Hansen J, Deosaransingh K, Liaw KL, Jacobsen SJ. Sy LS, et al. Hum Vaccin Immunother. 2018 Feb 1;14(2):412-419. doi: 10.1080/21645515.2017.1403702. Epub 2017 Dec 14. Hum Vaccin Immunother. 2018. PMID: 29140750 Free PMC article.
The SRC noted no safety signal for congenital anomaly or miscarriage associated with 4vHPV exposure during pregnancy. The rate of major congenital anomaly (3.6%) was in the range of background estimates from the literature. ...
The SRC noted no safety signal for congenital anomaly or miscarriage associated with 4vHPV exposure during pregnancy. The rate of major …
Implication of chromosomal microarray analysis prior to in-utero repair of fetal open neural tube defect.
Zemet R, Krispin E, Johnson RM, Kumar NR, Westerfield LE, Stover S, Mann DG, Castillo J, Castillo HA, Nassr AA, Sanz Cortes M, Donepudi R, Espinoza J, Whitehead WE, Belfort MA, Shamshirsaz AA, Van den Veyver IB. Zemet R, et al. Ultrasound Obstet Gynecol. 2023 Jun;61(6):719-727. doi: 10.1002/uog.26152. Ultrasound Obstet Gynecol. 2023. PMID: 36610024 Review.
While current guidelines recommend genetic testing by chromosomal microarray analysis (CMA) when a major congenital anomaly is detected prenatally, the requirement for an in-utero repair, based on the Management of Myelomeningocele Study (MOMS) criteria, is a …
While current guidelines recommend genetic testing by chromosomal microarray analysis (CMA) when a major congenital anomaly …
Day 5 versus day 3 embryo biopsy for preimplantation genetic testing for monogenic/single gene defects.
Vlajkovic T, Grigore M, van Eekelen R, Puscasiu L. Vlajkovic T, et al. Cochrane Database Syst Rev. 2022 Nov 24;11(11):CD013233. doi: 10.1002/14651858.CD013233.pub2. Cochrane Database Syst Rev. 2022. PMID: 36423200 Free PMC article. Review.
No studies reported on gestational age at birth, birthweight, neonatal mortality and major congenital anomaly. AUTHORS' CONCLUSIONS: We are uncertain if there is a difference in live births and miscarriages, viable intrauterine pregnancies, ectopic pregnancie …
No studies reported on gestational age at birth, birthweight, neonatal mortality and major congenital anomaly. AUTHORS' …
Congenital anomalies in children with cerebral palsy in rural Bangladesh.
Manlongat E, Mcintyre S, Smithers-Sheedy H, Trivedi A, Muhit M, Badawi N, Khandaker G. Manlongat E, et al. Dev Med Child Neurol. 2020 Apr;62(4):463-469. doi: 10.1111/dmcn.14456. Epub 2020 Jan 6. Dev Med Child Neurol. 2020. PMID: 31903557 Free article.
RESULTS: Between January 2015 and December 2016, 726 children with CP were newly registered with the BCPR (277 females, 449 males; mean age [SD] at registration 90mo [54mo], 4mo-18y). Seventy-eight children (11%) had a major congenital anomaly. Neurological ( …
RESULTS: Between January 2015 and December 2016, 726 children with CP were newly registered with the BCPR (277 females, 449 males; mean age …
68 results