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Prof Alban-Elouen Baruteau is an expert in Cardiology at Centre Hospitalier Universitaire de Nantes (France). As of October 2026, ScienceLeadR ranks Alban-Elouen Baruteau in the top 1% of experts worldwide for Cardiovascular Abnormalities, Congenital Abnormalities and Heart Defects, Congenital. Alban-Elouen Baruteau has authored 218 publications, the most recent in 2026, and is an investigator in 13 clinical trials, 6 of them ongoing. SLR score: 912 (community average: 125). How the SLR is computed.

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Prof Alban-Elouen Baruteau Centre Hospitalier Universitaire de Nantes France
912 ScienceLeadR Reputation 912

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Cardiology

Subspecialties: Pediatrics - Public Health

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Expert Rankings

Top experts on the MeSH terms this expert works on

Organizations

Career arc: 2008 - 2026
Source: PubMed

Institut du Thorax

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 218

Citations

Citations: 4 624 1st author: 52 Last author: 46 Unique author: 4

Main journals

Archives of cardiovascular diseases. Supplements 15
Arch Cardiovasc Dis 14
Cardiol Young 13
Archives of Cardiovascular Diseases Supplements 10
Pediatr Cardiol 10

Best Journals

Eur Heart J 2
Circulation 1
N Engl J Med 1

Breakdown by type

Click a legend label to hide or show it in the chart.

Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Sex-Specific Adaptations in Placental Mitochondrial Biogenesis and Function in babies Born with Critical Congenital Heart Disease.
PMID 42885715 — heart defects, congenital, genes, pregnancy, heart diseases, parturition, infant, newborn, biochemistry, heart, organelle biogenesis, sex, placenta, plasma		Clin Sci (Lond)20260
Erosion and embolization after transcatheter atrial septal defect closure: Findings from a multicenter international survey.
PMID 42665055 — incidence, cardiology, heart septal defects, atrial, child		Int J Cardiol20261
Atypical common arterial trunk with neonatal cyanosis caused by truncal valve-related obstruction of a sinus-origin pulmonary trunk.
PMID 42639756 — cyanosis, truncus arteriosus, cardiovascular diseases		Cardiol Young20260
From outflow tract development to ventriculo-arterial discordance - Developmental and genetic mechanisms of d-TGA and ccTGA.
PMID 42528128 — genes, congenitally corrected transposition of the great arteries, biophysics, biochemistry, multifactorial inheritance, arteries, environment		FEBS Lett20260
Parental perspectives on neurodevelopmental risk communication and care coordination in congenital heart disease: a nationwide survey in France.
PMID 42502114 — heart defects, congenital, heart diseases, heart, communication, schools, diagnosis, pediatrics, child, neurodevelopment		Eur J Pediatr20260

Clinical Studies 13

Sources: ClinicalTrials, EU CTIS

Synthesis

Principal Investigator: 3

By phase:

N/A 10
Phase 3 2
Phase 2/Phase 3 1

By status:

Recruiting 6
Completed 5
Terminated 1
Withdrawn 1

By type:

Interventional 8
Observational 5

By Monocentric/Multicentric:

monocentric 5
multicentric2to4 0
multicentric5to9 2
multicentricup10 6

Main Topics

Ongoing Clinical Trials

6 ongoing trials started since 2021, where this expert is an investigator

Source: ClinicalTrials

Study Phase Status Start
Cardiopediatric Home Monitoring Tool
NCT06741189 — heart defects, congenital, thoracotomy, congenital abnormalities, research design, mortality, blood glucose, muscles, blood, eating, cyanosis, cicatrix, heart rate, heart, hyperthermia, cardiology, diet, morbidity, records, sternotomy, blood glucose self-monitoring, child, oxygen saturation		N/ARecruiting2025
Characterization and Support of Neurodevelopmental Disorders Associated With Congenital Cardiac malfoRmations Neonatal
NCT06690151 — heart defects, congenital, congenital abnormalities, pregnancy, prenatal care, life style, heart diseases, mothers, hospitalization, blood, parturition, genetics, heart, stress, physiological, data collection, brain, neurodevelopmental disorders, genome, diet, meconium, metabolomics, echocardiography, self report, edetic acid, lipidomics, blood circulation, placenta, infant, neurodevelopment		N/ARecruiting2025
Characterization and Support for Neurodevelopmental Disorders Associated With Congenital Heart Defects
NCT06442592 — heart defects, congenital, congenital abnormalities, blood, genetics, blood specimen collection, heart, stress, physiological, neurodevelopmental disorders, pediatrics, edetic acid, child, neurodevelopment		N/ARecruiting2024
Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome
NCT06244433 — whole genome sequencing, sudden infant death, genome, biomarkers, infant death, infant		N/ARecruiting2024
OPTImal Treatment of Sinus VENOSUS Defect
NCT05865119 — heart defects, congenital, congenital abnormalities, stents, heart diseases, safety, rare diseases, heart, vena cava, superior, scimitar syndrome, cardiopulmonary bypass, heart septal defects, atrial, printing, printing, three-dimensional, therapeutics, catheterization, atrial septum, heart septal defects		N/ARecruiting2023

LeadR Networks

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Sources: PubMed, OpenAlex, ClinicalTrials, EU CTIS