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Guillaume Jondeau is an expert in Cardiology at Hôpital Bichat-Claude-Bernard (France). As of October 2026, ScienceLeadR ranks Guillaume Jondeau in the top 1% of experts worldwide for Cardiovascular Abnormalities, Aortic Diseases and Congenital Abnormalities. Guillaume Jondeau has authored 492 publications, the most recent in 2026, and is an investigator in 21 clinical trials, 3 of them ongoing. SLR score: 1,753 (community average: 125). How the SLR is computed.

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Guillaume Jondeau Hôpital Bichat-Claude-Bernard France
1 753 ScienceLeadR Reputation 1753

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Cardiology

Subspecialties: Genetics - Public Health - Thoracic And Cardiovascular Surgery

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: 1986 - 2026
Source: PubMed

INSERM

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 492

Citations

Citations: 48 087 1st author: 45 Last author: 102 Unique author: 16

Main journals

Eur Heart J 45
Archives of Cardiovascular Diseases Supplements 29
Arch Mal Coeur Vaiss 28
Arch Cardiovasc Dis 23
J Am Coll Cardiol 23

Best Journals

Eur Heart J 15
N Engl J Med 4
Lancet 2

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
Multimodal data-driven clustering analysis of heart failure patients identifies two distinct patterns of heart failure with preserved ejection fraction: Results from the PACIFIC-PRESERVED study.
PMID 42875459 — biological science disciplines, heart failure, heart, heart failure, diastolic, cluster analysis		Nat Commun20260
Loss of function variants in ADAMTS6: a new connective tissue disorder with heart defect, aortic aneurysm and neurodevelopmental features.
PMID 42829835 — cells, aortic aneurysm, heart, connective tissue, aneurysm, fibrillins, tissues, loeys-dietz syndrome, neurodevelopment		Genet Med20260
Crisis readiness for rare disease populations: learnings and recommendations by the European Reference Networks.
PMID 42604059 — rare diseases, emergencies		Lancet Reg Health Eur20260
Management of pregnancy in women with rare multisystemic vascular diseases: a qualitative survey analysis.
PMID 42365315 — pregnancy, rare diseases, vascular diseases, health personnel		Orphanet J Rare Dis20260
European Reference Networks as core health structures where referring genetic newborn screening positive infants: an innovative operational research framework.
PMID 42359128 — operations research, infant, newborn, rare diseases, neonatal screening, public health, diagnosis, research, therapeutics, artificial intelligence, infant		Front Public Health20260

Clinical Studies 21

Sources: ClinicalTrials, EU CTIS

Synthesis

Principal Investigator: 9 Study Director: 1 Sub-Investigator: 1

By phase:

N/A 13
Phase 3 5
Phase 4 2
Phase 2/Phase 3 1

By status:

Completed 14
Recruiting 4
Terminated 2
Active not recruiting 1

By type:

Interventional 14
Observational 7

By Monocentric/Multicentric:

monocentric 12
multicentric2to4 1
multicentric5to9 1
multicentricup10 7

Main Topics

Cohort/Consortium Investigators 5

Ongoing Clinical Trials

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

Source: ClinicalTrials

Study Phase Status Start
Beta blOckers discoNtinuation in patients presenting heart FaIlure with REcovered left ventricular ejection fraction
2023-508798-94-00 — heart failure, heart		Phase 3Recruiting2025
Noise Associated With a Mechanical Heart Valve Prosthesis Does the Memory of Preoperative Information Have an Influence on Postoperative Quality of Life
NCT07304115 — quality of life, heart, interview, psychological, heart valve prosthesis, memory, heart valves		N/ARecruiting2025
Genetic Newborn Screening for Rare Diseases Within the Screen4Care Project
NCT06549218 — digital technology, whole genome sequencing, infant, newborn, rare diseases, neonatal screening, genome, signs and symptoms, diagnosis, genetic diseases, inborn		N/ARecruiting2024

LeadR Networks

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Sources: PubMed, OpenAlex, ClinicalTrials, EU CTIS