Ferdy S van Geest

7PUBLICATIONS
71CO-AUTHORS
Gene and molecular therapyMicroelectromechanical systems (MEMS)Haematological tumoursGene expression (incl. microarray and other genome-wide approaches)Infant and child health
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Publications (7)

|Oct 29, 2025
Extreme resistance to thyroid hormone caused by a novel mosaic thyroid hormone receptor beta mutation.

Ferdy S van Geest, Wenjun Liao, Paul G Voorhoeve

|May 27, 2025
MCT8 Deficiency in Females.

Stefan Groeneweg, Ferdy S van Geest, Floor van der Most

|May 14, 2025
Molecular mechanism of thyroxine transport by monocarboxylate transporters.

Matteo Tassinari, Giorgia Tanzi, Francesco Maggiore

|Mar 13, 2025
Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration.

Stefan Groeneweg, Ferdy S van Geest, Mariano Martín

|Jul 14, 2023
Parent Perspectives on Complex Needs in Patients With MCT8 Deficiency: An International, Prospective, Registry Study.

Ferdy S van Geest, Stefan Groeneweg, Veronica M Popa

|Oct 22, 2021
Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study.

Ferdy S van Geest, Stefan Groeneweg, Erica L T van den Akker

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Frequent Collaborators

6 joint publications

W Edward Visser

3 joint publications

Stefan Groeneweg

3 joint publications

Enrico Bertini

2 joint publications

Nicola Brunetti-Pierri