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Morten Duno

9PUBLICATIONS

38CO-AUTHORS

Metabolic medicineGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesPolymerisation mechanismsCardiology (incl. cardiovascular diseases)

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Publications (9)

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|Mar 19, 2026

m.10010T>C Mitochondrial Disease: A Case Report With Hypoparathyroidism and Review of the Literature.

Jacob Mohr, Anja Lisbeth Frederiksen, Morten Duno

|Jan 22, 2026

Genetic diagnosis of CYP21A2-related CAH: adaptive sampling long-read sequencing is an accurate and scalable solution.

Dorte Launholt Lildballe, Morten Reiffenstein Huno, Lukas Ochsner Reynaud Ridder

|Dec 24, 2025

Systematic Review on Genetic Variants in Children With Cerebral Palsy.

Signe V Pedersen, Jesper K Sørensen, Rebecca Fabricius

|Aug 04, 2025

Clinical and Genetic Reassessment in Patients With Clinically Diagnosed Hereditary Polyneuropathy.

Louise Sloth Kodal, Morten Duno, Tina Dysgaard

|Apr 14, 2025

Variants in CAPN3 Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy Combined With Calpain-3 Deficiency.

Thomas Krag, Emily Nasho, Lauren Brady

|Nov 15, 2024

Delineating the Psychiatric Morbidity Spectrum in Congenital Adrenal Hyperplasia: A Population-based Registry Study.

Marie Lind-Holst, Dorte Hansen, Katharina Maria Main

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Frequent Collaborators

2 joint publications

Claus Højbjerg Gravholt

1 joint publications

Rune Holt

1 joint publications

Jens Juul Holst

1 joint publications

Signe Sørensen Torekov

1 joint publications

T H Andreasen

1 joint publications

H G Karstensen

1 joint publications

U Lei

1 joint publications

C Zachariae

1 joint publications

J P Thyssen

1 joint publications

Nicola Hepp

Frequent Collaborators

2 joint publications

Claus Højbjerg Gravholt

1 joint publications

Rune Holt

1 joint publications

Jens Juul Holst

1 joint publications

Signe Sørensen Torekov

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