Year |
Citation |
Score |
2023 |
Jaouadi H, Jopling C, Bajolle F, Théron A, Faucherre A, Gerard H, Al Dybiat S, Ovaert C, Bonnet D, Avierinos JF, Zaffran S. Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD. Journal of Translational Medicine. 21: 160. PMID 36855159 DOI: 10.1186/s12967-023-03994-y |
0.72 |
|
2022 |
Guimier A, Pontual L, Braddock SR, Torti E, Pérez-Jurado LA, Muñoz-Cabello P, Arumí M, Monaghan KG, Lee H, Wang LK, Pluym ID, Lynch SA, Stals K, Ellard S, Muller C, ... ... Bajolle F, et al. Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans. Human Molecular Genetics. PMID 35396997 DOI: 10.1093/hmg/ddac084 |
0.386 |
|
2022 |
Méot M, Bajolle F, Bonnet D. Submitral aneurysm communicating with coronary sinus in a child. Cardiology in the Young. 32: 1149-1150. PMID 35292123 DOI: 10.1017/S104795112100442X |
0.371 |
|
2021 |
Bajolle F, Malekzadeh-Milani S, Lévy M, Bonnet D. Multifactorial origin of pulmonary hypertension in a child with congenital heart disease, Down syndrome, and mutation. Pulmonary Circulation. 11: 20458940211027433. PMID 34285797 DOI: 10.1177/20458940211027433 |
0.329 |
|
2020 |
Maury P, Thambo JB, Maltret A, Combes N, Hascoet S, Derval N, Ladouceur M, Acar P, Amedro P, Anselme F, Bajolle F, Basquin A, Belli E, Bordachar P, Duthoit G, et al. Position paper concerning the competence, performance and environment required for the practice of ablation in children and in congenital heart disease. Archives of Cardiovascular Diseases. PMID 32461091 DOI: 10.1016/j.acvd.2020.02.002 |
0.31 |
|
2020 |
Moreau J, Lavastre K, Romieu H, Charbonnier F, Guillaumont S, Bredy C, Abassi H, Werner O, De La Villeon G, Requirand A, Auer A, Matecki S, Karsenty C, Guitarte A, Hadeed K, ... ... Bajolle F, et al. Impact of Sophrology on cardiopulmonary fitness in teenagers and young adults with a congenital heart disease: The SOPHROCARE study rationale, design and methods. International Journal of Cardiology. Heart & Vasculature. 27: 100489. PMID 32154361 DOI: 10.1016/j.ijcha.2020.100489 |
0.318 |
|
2018 |
Amedro P, Gavotto A, Legendre A, Lavastre K, Bredy C, De La Villeon G, Matecki S, Vandenberghe D, Ladeveze M, Bajolle F, Bosser G, Bouvaist H, Brosset P, Cohen L, Cohen S, et al. Impact of a centre and home-based cardiac rehabilitation program on the quality of life of teenagers and young adults with congenital heart disease: The QUALI-REHAB study rationale, design and methods. International Journal of Cardiology. PMID 30616811 DOI: 10.1016/j.ijcard.2018.12.050 |
0.351 |
|
2018 |
Pinard A, Eudes N, Mitchell J, Bajolle F, Grelet M, Okoronkwo J, Bonnet D, Collod-Béroud G, Zaffran S. Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect. Molecular Biology Reports. PMID 29923154 DOI: 10.1007/S11033-018-4212-X |
0.613 |
|
2017 |
Odelin G, Faure E, Coulpier F, Di Bonito M, Bajolle F, Studer M, Avierinos JF, Charnay P, Topilko P, Zaffran S. Krox20 defines a subpopulation of cardiac neural crest cells contributing to arterial valves and bicuspid aortic valve. Development (Cambridge, England). PMID 29158447 DOI: 10.1242/Dev.151944 |
0.649 |
|
2016 |
Bensemlali M, Bajolle F, Ladouceur M, Fermont L, Lévy M, Le Bidois J, Salomon LJ, Bonnet D. Associated genetic syndromes and extracardiac malformations strongly influence outcomes of fetuses with congenital heart diseases. Archives of Cardiovascular Diseases. 109: 330-6. PMID 27020512 DOI: 10.1016/j.acvd.2016.01.006 |
0.383 |
|
2015 |
Sanchez-Castro M, Eldjouzi H, Charpentier E, Busson PF, Hauet Q, Lindenbaum P, Delasalle-Guyomarch B, Baudry A, Pichon O, Pascal C, Lefort B, Bajolle F, Pezard P, Schott JJ, Dina C, et al. Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients with Coarctation of the Aorta. Circulation. Cardiovascular Genetics. PMID 26643481 DOI: 10.1161/CIRCGENETICS.115.001213 |
0.502 |
|
2015 |
Laux D, Houyel L, Bajolle F, Raimondi F, Boudjemline Y, Bonnet D. Problems in the diagnosis of discordant atrioventricular with concordant ventriculo-arterial connections: anatomical considerations, surgical management, and long-term outcome. Cardiology in the Young. 26: 127-38. PMID 26365181 DOI: 10.1017/S1047951115000736 |
0.388 |
|
2014 |
Laux D, Bertail C, Bajolle F, Houyel L, Boudjemline Y, Bonnet D. Anomalous left coronary artery connected to the pulmonary artery associated with other cardiac defects: a difficult joint diagnosis. Pediatric Cardiology. 35: 1198-205. PMID 24898291 DOI: 10.1007/s00246-014-0916-4 |
0.484 |
|
2013 |
Laux D, Bessières B, Houyel L, Bonnière M, Magny JF, Bajolle F, Boudjemline Y, Bonnet D. Early neonatal death and congenital left coronary abnormalities: ostial atresia, stenosis and anomalous aortic origin. Archives of Cardiovascular Diseases. 106: 202-8. PMID 23706366 DOI: 10.1016/j.acvd.2013.01.002 |
0.342 |
|
2013 |
Laux D, Malan V, Bajolle F, Boudjemline Y, Amiel J, Bonnet D. FOX gene cluster defects in alveolar capillary dysplasia associated with congenital heart disease. Cardiology in the Young. 23: 697-704. PMID 23331759 DOI: 10.1017/S1047951112001904 |
0.372 |
|
2013 |
Houyel L, Bajolle F, Capderou A, Laux D, Parisot P, Bonnet D. The pattern of the coronary arterial orifices in hearts with congenital malformations of the outflow tracts: a marker of rotation of the outflow tract during cardiac development? Journal of Anatomy. 222: 349-57. PMID 23317176 DOI: 10.1111/joa.12023 |
0.388 |
|
2012 |
Laux D, Houyel L, Bajolle F, Bonnet D. Total anomalous pulmonary venous connection to the unroofed coronary sinus in a neonate. Pediatric Cardiology. 34: 2006-8. PMID 23099664 DOI: 10.1007/s00246-012-0551-x |
0.472 |
|
2010 |
Ryckebüsch L, Bertrand N, Mesbah K, Bajolle F, Niederreither K, Kelly RG, Zaffran S. Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome. Circulation Research. 106: 686-94. PMID 20110535 DOI: 10.1161/Circresaha.109.205732 |
0.725 |
|
2009 |
Bonnet D, Zaffran S, Kelly R, Bajolle F. [Embryological and genetic mechanisms of cardiac great arteries malformations]. Journal De La Societe De Biologie. 203: 161-5. PMID 19527629 DOI: 10.1051/Jbio/2009019 |
0.788 |
|
2009 |
Bajolle F, Zaffran S, Losay J, Ou P, Buckingham M, Bonnet D. Conotruncal defects associated with anomalous pulmonary venous connections. Archives of Cardiovascular Diseases. 102: 105-10. PMID 19303577 DOI: 10.1016/J.Acvd.2008.04.010 |
0.782 |
|
2009 |
Bajolle F, Zaffran S, Bonnet D. Genetics and embryological mechanisms of congenital heart diseases. Archives of Cardiovascular Diseases. 102: 59-63. PMID 19233110 DOI: 10.1016/J.Acvd.2008.06.020 |
0.709 |
|
2008 |
Bajolle F, Zaffran S. [Haemodynamic induces aortic arch asymmetry]. Medecine Sciences : M/S. 24: 354-6. PMID 18405626 DOI: 10.1051/Medsci/2008244354 |
0.515 |
|
2008 |
Bajolle F, Zaffran S, Meilhac SM, Dandonneau M, Chang T, Kelly RG, Buckingham ME. Myocardium at the base of the aorta and pulmonary trunk is prefigured in the outflow tract of the heart and in subdomains of the second heart field. Developmental Biology. 313: 25-34. PMID 18005956 DOI: 10.1016/J.Ydbio.2007.09.023 |
0.712 |
|
2007 |
Prall OW, Menon MK, Solloway MJ, Watanabe Y, Zaffran S, Bajolle F, Biben C, McBride JJ, Robertson BR, Chaulet H, Stennard FA, Wise N, Schaft D, Wolstein O, Furtado MB, et al. An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation. Cell. 128: 947-59. PMID 17350578 DOI: 10.1016/J.Cell.2007.01.042 |
0.771 |
|
2006 |
Marguerie A, Bajolle F, Zaffran S, Brown NA, Dickson C, Buckingham ME, Kelly RG. Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice. Cardiovascular Research. 71: 50-60. PMID 16687131 DOI: 10.1016/J.Cardiores.2006.03.021 |
0.766 |
|
2006 |
Bajolle F, Zaffran S, Kelly RG, Hadchouel J, Bonnet D, Brown NA, Buckingham ME. Rotation of the myocardial wall of the outflow tract is implicated in the normal positioning of the great arteries. Circulation Research. 98: 421-8. PMID 16397144 DOI: 10.1161/01.Res.0000202800.85341.6E |
0.772 |
|
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