Mette Nyegaard, PhD is an expert in Genetics at Aalborg University Hospital (Denmark). Mette Nyegaard has authored 275 publications, the most recent in 2026, and is an investigator in 4 clinical trials. SLR score: 731 (community average: 125). How the SLR is computed.

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Mette Nyegaard, PhD Aalborg University Hospital Denmark
731 ScienceLeadR Reputation 731
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Genetics

Subspecialties: Cardiology - Public Health

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 2012 - 2028

Source: PubMed

Statens Serum Institut

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 275

Citations

Citations: 14 957 1st author: 8 Last author: 18 Unique author: 0


Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Translational Perspectives on Cardiac Diseases Disproportionately Affecting Women.
PMID 42786602 — heart diseases, heart failure, heart, translational research, biomedical, cardiovascular diseases, arteries, heart failure, systolic, sex characteristics, sex, research, therapeutics, cardiomyopathies, sex differences
J Am Heart Assoc20260
Genetic architecture of cytokine autoantibodies and associated risk of common diseases.
PMID 42768006 — cytokines, autoantibodies, genome
Nat Commun20260
Genetic architecture of endometriosis: risk factors, comorbidities and clinical implications.
PMID 42695929 — endometriosis, cells, genes, comorbidity, reproduction, genetics, pharmaceutical preparations, multiple chronic conditions, embryology, risk factors, therapeutics
Hum Reprod Update20260
Features and Legal Practice of Dried Blood Spot Card Biobanking in Europe: Balancing Research Potential with Parental and Children's Rights.
PMID 42647251 — blood, informed consent, research, child
Int J Neonatal Screen20260
Position effect at the SOX3 locus by an interchromosomal insertion causes hereditary spastic paraplegia.
PMID 42497869 — neurons, genetics, pluripotent stem cells, paraplegia, enhancer elements, genetic, spastic paraplegia, hereditary
Am J Hum Genet20261

Clinical Studies 4

Sources: ClinicalTrials, EU CTIS

Synthesis

By phase:

N/A 4

By status:

Completed 2
Unknown 2

By type:

Interventional 2
Observational 2

By Monocentric/Multicentric:

monocentric 1
multicentric2to4 2
multicentric5to9 1
multicentricup10 0

Main Topics

Cohort/Consortium Investigators 5

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