Alexander Hustinx

7PUBLICATIONS
138CO-AUTHORS
NeurogeneticsGenetic immunologyGene expression (incl. microarray and other genome-wide approaches)Orthodontics and dentofacial orthopaedics
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Publications (7)

|May 18, 2026
Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

|Apr 08, 2026
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Rocio Rius, Alexander J M Blakes, Yuyang Chen

|Jun 26, 2025
Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene.

Nikolas Pontikos, William A Woof, Siying Lin

|Jan 15, 2025
GestaltGAN: synthetic photorealistic portraits of individuals with rare genetic disorders.

Aron Kirchhoff, Alexander Hustinx, Behnam Javanmardi

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

Hellen Lesmann, Alexander Hustinx, Shahida Moosa

|May 10, 2024
Next-generation phenotyping in Nigerian children with Cornelia de Lange syndrome.

Annabelle Arlt, Alexej Knaus, Tzung-Chien Hsieh

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Frequent Collaborators

5 joint publications

Peter M Krawitz

4 joint publications

Tzung-Chien Hsieh

4 joint publications

Hannah Klinkhammer

4 joint publications

Behnam Javanmardi