Publications by authors named "Helena Hinterding"

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Functional characterisation of rare variants in genes encoding the MAPK/ERK signalling pathway identified in long-lived Leiden Longevity Study participants.
Maarouf Baghdadi, Helena Hinterding, Thies Gehrmann, Pasquale Putter, Mara Neuerburg

Geroscience· May 2025

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Recessive TMOD1 mutation causes childhood cardiomyopathy.
Catalina Vasilescu, Mert Colpan, Tiina H Ojala, Tuula Manninen, Aino Mutka, Helena Hinterding

Commun Biol· January 2024

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From mutation to mechanism: deciphering the molecular function of genetic variants linked to human ageing.
Maarouf Baghdadi, Helena M Hinterding, Linda Partridge, Joris Deelen

Brief Funct Genomics· January 2022

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Genetic Basis of Severe Childhood-Onset Cardiomyopathies.
Catalina Vasilescu, Tiina H Ojala, Virginia Brilhante, Simo Ojanen, Helena M Hinterding

J Am Coll Cardiol· November 2018

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