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Klaus Dieterich is an expert in Genetics at Centre Hospitalier Universitaire de Grenoble (France). As of October 2026, ScienceLeadR ranks Klaus Dieterich in the top 1% of experts worldwide for Arthrogryposis and Congenital Abnormalities. Klaus Dieterich has authored 99 publications, the most recent in 2026, and is an investigator in 9 clinical trials, 2 of them ongoing. SLR score: 489 (community average: 125). How the SLR is computed.

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Klaus Dieterich Centre Hospitalier Universitaire de Grenoble France
489 ScienceLeadR Reputation 489

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Genetics

Subspecialties: Neurology - Pediatrics - Biochemistry

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: 2007 - 2026
Source: PubMed

Centre Hospitalier Universitaire de Grenoble

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 99

Citations

Citations: 2 715 1st author: 5 Last author: 11 Unique author: 2

Main journals

J Med Genet 11
Am J Med Genet A 10
Am J Med Genet C Semin Med Genet 7
Eur J Hum Genet 6
Genet Med 6

Best Journals

Circulation 1
Nature 1

Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Arthrogryposis Multiplex Congenita in Pediatric Age: Correlation Between MUScular MRI and Functional Evaluation (AMUSE), Toward a Biomechanical Model.
PMID 42717532 — muscles, arthrogryposis, genetics, medical		Am J Med Genet C Semin Med Genet20260
The International Consortium for Arthrogryposis: A Collaborative Framework for Early Detection, Care, Research, and Education.
PMID 42362964 — multiple chronic conditions, arthrogryposis, research, physical exertion, education, genetics, medical		Am J Med Genet C Semin Med Genet20260
Decoding splicing variants in high-throughput sequencing: a functional validation approach integrating deep learning tools.
PMID 42362801 — deep learning, learning, enhancer elements, genetic, genetics, medical		Eur J Hum Genet20261
Spinal Involvement in a Pediatric and Adult Cohort of Patients With Arthrogryposis Multiplex Congenita.
PMID 42161899 — scoliosis, arthrogryposis, prevalence, child, spine		Am J Med Genet C Semin Med Genet20260
35 Individuals With HUWE1-Related Neurodevelopmental Disorder and Suggested Clinical Evaluations.
PMID 41975654 — neurodevelopmental disorders, fetal growth retardation, genetics, medical, neurodevelopment		Am J Med Genet A20260

Clinical Studies 9

Sources: ClinicalTrials, EU CTIS

Synthesis

Principal Investigator: 3 Study Director: 2

By phase:

N/A 8
Phase 3 1

By status:

Completed 4
Recruiting 3
Not yet recruiting 1
Unknown 1

By type:

Observational 6
Interventional 3

By Monocentric/Multicentric:

monocentric 5
multicentric2to4 1
multicentric5to9 0
multicentricup10 3

Main Topics

Ongoing Clinical Trials

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

Source: ClinicalTrials

Study Phase Status Start
Piezo2 related Arthrogryposis physiopathOLOgy 3
NCT07360574 — pain, arthrogryposis, therapeutics, mutation		N/ANot yet recruiting2026
Technical Feasibility Study of Ultrasound Muscle Imaging in Antenatal Ultrasound
NCT06130592 — feasibility studies, muscles, arthrogryposis		N/ARecruiting2024

LeadR Networks

Main global connection map

Sources: PubMed, OpenAlex, ClinicalTrials, EU CTIS