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)

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|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

Peter M Krawitz

Tzung-Chien Hsieh

Hannah Klinkhammer

Behnam Javanmardi

Frederik Braun

Tobias B Haack

Shahida Moosa

Rocio Rius

Nicola Whiffin

Miguel A Ibarra-Arrelano

Frequent Collaborators

Peter M Krawitz

Tzung-Chien Hsieh

Hannah Klinkhammer

Behnam Javanmardi