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Mette Viuff

10PUBLICATIONS

29CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Cancer geneticsDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Obstetrics and gynaecology

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Publications (10)

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|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

|Apr 04, 2024

Endocrine, cardiac and neuropsychological aspects of adult congenital adrenal hyperplasia.

Lukas Ochsner Ridder, Camilla Mains Balle, Anne Skakkebæk

|Jul 03, 2023

The multi-omic landscape of sex chromosome abnormalities: current status and future directions.

Helene Bandsholm Leere Tallaksen, Emma B Johannsen, Jesper Just

|Mar 28, 2023

X chromosome dosage and the genetic impact across human tissues.

Mette Viuff, Anne Skakkebæk, Emma B Johannsen

|Jun 13, 2022

The Changing Face of Turner Syndrome.

Claus H Gravholt, Mette Viuff, Jesper Just

|Mar 18, 2022

Women With Turner Syndrome Are Both Estrogen and Androgen Deficient: The Impact of Hormone Replacement Therapy.

Mette Hansen Viuff, Jesper Just, Sara Brun

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Frequent Collaborators

8 joint publications

Claus Højbjerg Gravholt

4 joint publications

Jesper Just

4 joint publications

Anne Skakkebæk

3 joint publications

Sara Brun

3 joint publications

Niels Holmark Andersen

2 joint publications

Agnethe Berglund

2 joint publications

Lukas Ochsner Ridder

2 joint publications

Emma B Johannsen

1 joint publications

Kirstine Stochholm

1 joint publications

Christian Trolle

Frequent Collaborators

8 joint publications

Claus Højbjerg Gravholt

4 joint publications

Jesper Just

4 joint publications

Anne Skakkebæk

3 joint publications

Sara Brun

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