Ghent University Academic Bibliography

Your filters: cql: author="Kooy, Frank" or (type any "bookEditor issueEditor" and editor="Kooy, Frank")

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- Journal Article
- A1
- open access
Stress and telomere length in leukocytes : investigating the role of GABRA6 gene polymorphism and cortisol

Pablo Martino, Mario Perez-Alarcón, Luna Deconinck, Rudi De Raedt (UGent) , Marie-Anne Vanderhasselt (UGent) , Gosia Kozusznik (UGent) , Frank Kooy, Vanesa Hidalgo, César Venero, Alicia Salvador, et al.

(2025) PSYCHONEUROENDOCRINOLOGY. 173.
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- Conference Paper
- C3
An unexpected high prevalence of Focal Facial Dermal Dysplasia (FFDD) type IV is linked to a founder effect in the Belgian population

Karolien Aelbrecht (UGent) , Aude Beyens (UGent) , Sofie De Meulemeester, Koen Devriendt, Marleen Goeteyn (UGent) , Frank Kooy, Evelyn Meulewaeter, Sofie Symoens (UGent) and Bert Callewaert (UGent)

(2024) 2nd World Congress on Rare Skin Diseases, Abstracts.
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- Journal Article
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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema, Jill Rosenfeld, Pengfei Liu, Hui Guo, Chang N. Kim, Bert B. A. De Vries, Lisenka E. L. M. Vissers, Magnus Nordenskjold, et al.

(2021) GENOME MEDICINE. 13(1).
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Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges

Olivier Vanakker (UGent) , Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener, et al.

(2014) EUROPEAN JOURNAL OF MEDICAL GENETICS. 57(4). p.151-156
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy

Nikhita Ajit Bolar, Arnaud Vanlander (UGent) , Claudia Wilbrecht, Nathalie Van der Aa, Joél Smet (UGent) , Boel De Paepe (UGent) , Geert Vandeweyer, Frank Kooy, François Eyskens, Elien De Latter (UGent) , et al.

(2013) HUMAN MOLECULAR GENETICS. 22(13). p.2590-2602

Academic Bibliography

Stress and telomere length in leukocytes : investigating the role of GABRA6 gene polymorphism and cortisol

An unexpected high prevalence of Focal Facial Dermal Dysplasia (FFDD) type IV is linked to a founder effect in the Belgian population

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges

Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy

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