Heart Defects, Congenital
"Heart Defects, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life.
Descriptor ID |
D006330
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MeSH Number(s) |
C14.240.400 C14.280.400 C16.131.240.400
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Concept/Terms |
Heart Defects, Congenital- Heart Defects, Congenital
- Congenital Heart Defect
- Defect, Congenital Heart
- Heart, Malformation Of
- Defects, Congenital Heart
- Heart Abnormalities
- Heart Defect, Congenital
- Abnormality, Heart
- Abnormalities, Heart
- Heart Abnormality
- Congenital Heart Defects
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Below are MeSH descriptors whose meaning is more general than "Heart Defects, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Heart Defects, Congenital".
This graph shows the total number of publications written about "Heart Defects, Congenital" by people in this website by year, and whether "Heart Defects, Congenital" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1995 | 5 | 1 | 6 | 1996 | 2 | 3 | 5 | 1997 | 2 | 1 | 3 | 1998 | 5 | 4 | 9 | 1999 | 4 | 1 | 5 | 2000 | 7 | 4 | 11 | 2001 | 3 | 4 | 7 | 2002 | 2 | 2 | 4 | 2003 | 2 | 1 | 3 | 2004 | 4 | 0 | 4 | 2005 | 2 | 3 | 5 | 2006 | 3 | 2 | 5 | 2007 | 4 | 1 | 5 | 2008 | 17 | 0 | 17 | 2009 | 8 | 1 | 9 | 2010 | 19 | 4 | 23 | 2011 | 18 | 1 | 19 | 2012 | 11 | 4 | 15 | 2013 | 23 | 3 | 26 | 2014 | 20 | 6 | 26 | 2015 | 10 | 3 | 13 | 2016 | 17 | 6 | 23 | 2017 | 20 | 4 | 24 | 2018 | 26 | 6 | 32 | 2019 | 19 | 5 | 24 | 2020 | 30 | 1 | 31 | 2021 | 28 | 1 | 29 | 2022 | 21 | 2 | 23 | 2023 | 21 | 0 | 21 | 2024 | 21 | 10 | 31 | 2025 | 6 | 1 | 7 |
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Below are the most recent publications written about "Heart Defects, Congenital" by people in Profiles.
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Feldman ER, Li Y, Cutler DJ, Rosser TC, Wechsler SB, Sanclemente L, Rachubinski AL, Elliott N, Vyas P, Roberts I, Rabin KR, Wagner M, Gelb BD, Espinosa JM, Lupo PJ, de Smith AJ, Sherman SL, Leslie-Clarkson EJ. Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DS. Genet Epidemiol. 2025 Jun; 49(4):e70010.
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Hamlington KL, Cooper EH, Wolter-Warmerdam K, Vielkind ML, Brinton JT, Keck A, Bresselsmith RJ, Maybee J, Jackson A, Hickey F, DeBoer EM. Oscillometry Phenotypes in Children With Down Syndrome. Pediatr Pulmonol. 2025 Apr; 60(4):e71069.
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Gorga SM, Beck T, Chaudhry P, DeFreitas MJ, Fuhrman DY, Joseph C, Krawczeski CD, Kwiatkowski DM, Starr MC, Harer MW, Charlton JR, Askenazi DJ, Selewski DT, Gist KM. Framework for Kidney Health Follow-Up Among Neonates With Critical Cardiac Disease: A Report From the Neonatal Kidney Health Consensus Workshop. J Am Heart Assoc. 2025 Mar 18; 14(6):e040630.
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Jones MB, Caprarola SD, Schlatterer S, O'Donnell M, Pleau C, Staso K, Jonas RA, D'Udekem D'Acoz Y, Munoz R, Carpenter JL, Limperopolous C, Wernovsky G. Building a sustainable neurocardiac critical care program in a paediatric cardiac ICU: insights and lessons learned. Cardiol Young. 2025 Apr; 35(4):738-744.
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Guillouet C, Agostini V, Baujat G, Cocciadiferro D, Pippucci T, Lesieur-Sebellin M, Georget M, Schatz U, Fauth C, Louie RJ, Rogers C, Davis JM, Konstantopoulou V, Mayr JA, Bouman A, Wilke M, VanNoy GE, England EM, Park KL, Brown K, Saenz M, Novelli A, Digilio MC, Mastromoro G, Rongioletti MCA, Piacentini G, Kaiyrzhanov R, Guliyeva S, Hasanova L, Shears D, Bhatnagar I, Stals K, Klaas O, Horvath J, Bouvagnet P, Witmer PD, MacCarrick G, Cisarova K, Good JM, Gorokhova S, Boute O, Smol T, Bruel AL, Patat O, Broadbent JR, Tan TY, Tan NB, Lyonnet S, Busa T, Graziano C, Amiel J, Gordon CT. Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformations. Am J Hum Genet. 2025 Apr 03; 112(4):829-845.
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Edelson JB, Raskin A, Absi M, Adachi I, Aljohani O, Alzubi A, Amdani S, Asante-Korang A, Auerbach S, Bansal N, Bearl D, Boucek K, Butto A, Butts R, Byrnes J, Castleberry C, Conway J, Do N, Dykes J, Friedland-Little J, Greiten L, Henderson H, Hsu D, Jeewa A, Joong A, Khan S, Knoll C, Lantz J, Law S, Lorts A, Maeda K, Martinez H, May L, Mehegan M, Mokshagundam D, Montgomery C, O'Connor M, Parent JJ, Peng DM, Rosenthal DN, Sheybani A, Shezad M, Shugh L, Shwaish N, Spinner J, Su J, Sutcliffe D, Tunuguntla H, VanderPluym C, Vaughn G, Wallis G, Wilkens S, Zinn M, Niebler R. The ACTION VAD registry: A collective five-year experience. J Heart Lung Transplant. 2025 Apr; 44(4):530-540.
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Wolfe KR, Broach R, Clark C, Gerk A, Kelly SL, Maloney EH, Neutts A, Patteson H, Payan M, Riessen S, Watson S, Caprarola SD, Davidson JA. Cognitive Outcomes and Delirium After Cardiac Neurodevelopmental Program Implementation for Children With Congenital Heart Disease. JAMA Netw Open. 2025 Jan 02; 8(1):e2456324.
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Kwiatkowski DM, Auerbach S, Niebler RA. Adjudicating Registry Data: Benefits and Pitfalls-The ACTION Experience. World J Pediatr Congenit Heart Surg. 2025 May; 16(3):309-312.
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Hunter JG, Bera K, Ciancibello L, Bukhari SMA, Sposato J, Gilani KA, Gilkeson R, Gupta A. Real-world impact of high-pitch helical CT on radiation exposure and image quality in infants being evaluated for cardiothoracic pathologies. Pediatr Radiol. 2025 Jan; 55(1):151-158.
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Romanowicz J, Niemiec S, Khailova L, Lehmann T, Mancuso CA, Mitchell MB, Morgan GJ, Twite M, DiMaria MV, Klawitter J, Davidson JA, Frank BS. Perturbations of tryptophan catabolism via the kynurenine pathway are associated with stage 2 postoperative outcomes in single ventricle heart disease. Physiol Rep. 2024 Nov; 12(22):e70133.
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