Thierry Brue

Endocrinology — Hôpitaux universitaires de Marseille, France

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Endocrinology

Subspecialties: Neurology - Oncology - Public Health

Full career Last 3 years

Main Topics

Publications and Clinical Studies

Publications Clinical Studies

Short Biography

Thierry Brue, MD, PhD, is Professor of endocrinology at Aix-Marseille University (AMU, Marseille, France), endocrinologist at the department of Endocrinology of Conception university hospital, and coordinator of the national and European (ENDO-ERN) rare disease reference centre for pituitary disorders (HYPO); former Director (2019-2024) of the Aix-Marseille University Institute for Rare Diseases, MarMaRa.

Prof. Brue’s main clinical interests are in Neuroendocrinology. His research activities include: clinical research in pituitary disorders, especially participation as investigator in international multicentre clinical trials; experimental research as group leader in the Marseille Medical Genetics AMU-INSERM Laboratory; founder and coordinator of a research network on genetically determined pituitary hormone deficiency (GENHYPOPIT). T. Brue co-authored 360+ articles referenced in PubMed (WoS h-index: 64+; total times cited 13000+, Google Scholars 85+); he is a member of the French Endocrine Society (SFE), the European Society of Endocrinology (ESE), the Endocrine Society (USA), past-President (2018-2020) of the European Neuroendocrine Association (ENEA),


Organizations

Source: Pubmed

Hôpitaux universitaires de Marseille

Publications Synthesis

Source: Pubmed

Number : 525

Citations

Citations: 20 120 1st author: 27 Last author: 117 Unique author: 3

Main journals

Ann Endocrinol (Paris) 145
Eur J Endocrinol 58
J Clin Endocrinol Metab 44
Endocrine Abstracts 27
Pituitary 22

Best Journals

Nat Rev Endocrinol 3
Cell 1
Lancet Oncol 1

Breakdown by type

Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
3D volume growth rate may open new perspectives for the classification of aggressive pituitary adenomas.
endocrinology, growth, neoplasms, classification, adenoma
J Clin Endocrinol Metab20260
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohort.
blood, retrospective studies, phenotype, genotype, diagnosis, tissues, mutation
Ann Endocrinol (Paris)20260
Prevalence, risk factors and management of bone complications in Cushing`s syndrome across Europe. Data from the European Registry on Cushing's syndrome (ERCUSYN).
diabetes mellitus, registries, endocrinology, fractures, bone, osteoporosis, prevalence, risk factors, cushing syndrome, spine
Ann Endocrinol (Paris)20260
Unraveling the Genetic Heterogeneity of Isolated Growth Hormone Deficiency: Insights from the GENHYPOPIT cohort.
genes, dwarfism, pituitary, growth, genetic heterogeneity, phenotype, hormones, genotype, growth hormone
Horm Res Paediatr20260
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohort.
blood, retrospective studies, phenotype, genotype, diagnosis, tissues, mutation
Ann Endocrinol (Paris)20260

Clinical Studies 11

Source: ClinicalTrials

Synthesis

By phase:

Phase 3 6
N/A 3
Phase 2 2

By status:

Completed 8
Recruiting 1
Terminated 1
Unknown 1

By type:

Interventional 8
Observational 3

By Monocentric/Multicentric:

monocentric 1
multicentric2to4 1
multicentric5to9 1
multicentricup10 8

Main Topics

Endocrine System Diseases 10
Nervous System Diseases 8
Musculoskeletal Diseases 5

Cohort/Consortium Investigators 4

LeadR Networks

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Source: Pubmed Source: ClinicalTrials