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	Endovascular aortic repair: Single centre experience of thoracic endovascular aortic repair and endovascular aneurysm repair. J Pak Med Assoc Nihal F, Kareem T, Ehsan O, Ahmed MA, Ali N, Amin Z. PMID: 41418129 [PubMed - indexed for MEDLINE]
	[Anomalous origin of the left anterior descending artery from the right coronary artery: A case report]. Rev Med Inst Mex Seguro Soc González-Aguirre R, García-Barrera L, Carrillo-Tamez MC, Alarcón-Quilantán RDP, Valadez-Montoya FJ. PMID: 41417929 [PubMed - indexed for MEDLINE]
	Impacts of COVID-19 on pediatric patients with congenital heart disease: a small systematic and integrative literature review. Rev Paul Pediatr Oliveira AM, Cartøgenes AD, Berni LC, Amaral LMB, Machado RL, Oliveira RCS. PMID: 41417317 [PubMed - indexed for MEDLINE]
	Joint analysis of de novo mutations from autism spectrum disorder, schizophrenia, congenital heart disease, and other developmental disorders improves detection power and implicates shared molecular pathways and CNS processes. NAR Genom Bioinform Kealhofer M, Brown R, Riley BP, Nguyen TH. PMID: 41415304 [PubMed - indexed for MEDLINE]
	Incidence of bloodstream infection after open-heart surgery with delayed sternal closure among children with congenital heart disease: a single-center retrospective study. BMC Res Notes Jahromi PY, Gharib B, Rajabi MM, Mirzaaghayan MR. PMID: 41413603 [PubMed - indexed for MEDLINE]
	Expanding the literature on CantÃº syndrome: recognising early clinical and phenotypic clues. BMJ Case Rep Corley L, Dunne E, Prendiville T, Donnelly J. PMID: 41412937 [PubMed - indexed for MEDLINE]
	Arytenoid dislocation in a patient with Marfan syndrome after undergoing aortic arch surgery. BMJ Case Rep Thomson AV, Ogunsusi M, Welsby I. PMID: 41412936 [PubMed - indexed for MEDLINE]
	PERADIGM: Phenotype embedding similarity-based rare disease gene mapping. PLoS Genet Zheng W, Xie Y, Gu J, Li H, Somlo S, Besse W, Zhao H. PMID: 41411243 [PubMed - indexed for MEDLINE]
	ECMO to CPB: A single circuit approach. J Extra Corpor Technol Zalfa J, Duncan D, Kerins P. PMID: 41405042 [PubMed - indexed for MEDLINE]
	Aripiprazole for treatment of attenuated psychosis syndrome in an adolescent with 22q11.21 deletion syndrome: A case report. Medicine (Baltimore) Algarzae NK, Alkhawashki SH, Alkhiri AT, Algazlan M, Alhassan MA, Albalawi W, Sarawi WS. PMID: 41398812 [PubMed - indexed for MEDLINE]
	Patients' research priorities and participation in primary ciliary dyskinesia research. BMJ Open Respir Res Lam YT, Behan L, Dexter K, Dixon L, Kuehni CE, Schreck LD, Lucas JS, Goutaki M. PMID: 41397810 [PubMed - indexed for MEDLINE]
	Serial cerebral magnetic resonance imaging before and after birth in patients with complex congenital heart disease - a prospective, multicentre observational study. Swiss Med Wkly Knirsch W, De Silvestro A, Steger C, Rathke V, Weber R, Von Rhein M, Schneider J, Hutter D, Reich B, Held U, Hackenberg A, Tuura O'Gorman R, Kottke R, Jakab A, BrainCHD Study Group. PMID: 41397378 [PubMed - indexed for MEDLINE]
	The Role of Stress Echocardiography in Patients With Anomalous Aortic Origin of Coronary Arteries: Two Tertiary Cardiac Centers' Experience. Echocardiography Danylenko O, Lwin MT, Kasouridis I, Masding A, Klemperer KV, Macrae R, Monteiro RP, Senior R, Li W. PMID: 41395835 [PubMed - indexed for MEDLINE]
	A survey of antimicrobial therapy for culture-negative sepsis in pediatric congenital heart disease patients. Pediatr Int Ogawa E, Okumura T, Ikeyama T, Ito K. PMID: 41395786 [PubMed - indexed for MEDLINE]
	Split Right Coronary Artery With Sinister Intra-Atrial Course of Posterior Trunk. Methodist Debakey Cardiovasc J Singh D, Ojha V, Pandey NN, Agstam S. PMID: 41393087 [PubMed - indexed for MEDLINE]
	Environmental exposure to per- and polyfluoroalkyl substances and childhood congenital heart disease: a mixed analysis. Front Public Health Jiao X, Zhao L, Xu Y, Gao J, Tang W, Wu Y, Yang L, Huang J, Guo Y, Sun K, Chen S. PMID: 41393011 [PubMed - indexed for MEDLINE]
	Phenotypic Analysis of Embryos in a Noonan Syndrome Model Mouse With the Rit1 A57G Mutation. Mol Genet Genomic Med Suzuki D, Abe T, Niihori T, Kikuchi A, Aoki Y. PMID: 41388936 [PubMed - indexed for MEDLINE]
	Ethical dilemmas in continuing pregnancy after a prenatal diagnosis of congenital heart defects: a systematic review and narrative synthesis. BMC Med Ethics Kalhor F, Tagharrobi Z, Ghaderian M, Taghadosi M, Shahzeydi A, Mah-Najafabadi A, Sharifi S. PMID: 41388275 [PubMed - indexed for MEDLINE]
	Evaluation of Data Sources for Critical Congenital Heart Defect Case Ascertainment in North Carolina. Birth Defects Res Atkinson H, Bergman K, Forestieri N. PMID: 41387200 [PubMed - indexed for MEDLINE]
	Functional analysis across model systems implicates ribosomal proteins in growth and proliferation defects associated with hypoplastic left heart syndrome. Elife Nielsen T, Kervadec A, Theis JL, Missinato MA, Marchant J, Romero M, Marchetti K, Lamba A, Zeng XI, Berenguer M, Walls SM, Schroeder A, Birker K, Duester G, Grossfeld P, Nelson TJ, Olson TM, Ocorr K, Bodmer R, Vogler G, Colas AR. PMID: 41379537 [PubMed - indexed for MEDLINE]

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