Johanna C Herkert
11PUBLICATIONS
103CO-AUTHORS
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Publications (11)
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|Sep 27, 2024
Novel variants in the SOX11 gene: clinical description of seven new patients.Beatriz Schincariol-Manhe, Érica Campagnolo, Samira Spineli-Silva
|Jul 03, 2023
Loss-of-function variants in CUL3 cause a syndromic neurodevelopmental disorder.Patrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh
|Sep 30, 2022
Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification.Marijke H van der Meulen, Johanna C Herkert, Susanna L den Boer
|Jul 06, 2022
Expanding the clinical spectrum of primary coenzyme Q10 deficiency type 6: The first case with cardiomyopathy.Lisette Leeuwen, Charlotte M A Lubout, Hessel P Nijenhuis
|Aug 11, 2021
Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility.Irene V van Blokland, Pauline Lanting, Anil P S Ori
|Mar 19, 2021
Lifelines COVID-19 cohort: investigating COVID-19 infection and its health and societal impacts in a Dutch population-based cohort.Katherine Mc Intyre, Pauline Lanting, Patrick Deelen
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Frequent Collaborators
3 joint publications
Patrick Deelen
2 joint publications
Jan D H Jongbloed
2 joint publications
Irene van Blokland
2 joint publications
Judith M Vonk
2 joint publications
Morris A Swertz
2 joint publications
Lude Franke
2 joint publications
Annique Claringbould
2 joint publications
Pauline Lanting
2 joint publications
Thomas Smol
1 joint publications
Kristin M Abbott
