Sofia Douzgou Houge

22PUBLICATIONS
168CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Reaction kinetics and dynamicsDevelopmental genetics (incl. sex determination)Gene and molecular therapy
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Publications (22)

|Sep 16, 2026
Caring for Rare Genetic Disease: A Vision for the Future.

|Aug 10, 2026
An episignature informed systematic analysis to ascertain the clinical significance and consequences of CHD8 missense variants.

|Jun 24, 2025
Houge-Janssens syndrome.

Gunnar Douzgos Houge, Sofia Douzgou Houge, Tzung-Chien Hsieh

|Oct 18, 2024
Epigenomic and phenotypic characterization of DEGCAGS syndrome.

Karim Karimi, Denisa Weis, Ingvild Aukrust

|Jul 12, 2024
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Eva Vanbelleghem, Tim Van Damme, Aude Beyens

|Jun 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

Hellen Lesmann, Alexander Hustinx, Shahida Moosa

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Frequent Collaborators

4 joint publications

Bekim Sadikovic

3 joint publications

Siddharth Banka

3 joint publications

Renske Oegema

3 joint publications

Jennifer Kerkhof