Associated Papers
The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe.
Fernandez-Falgueras A et al.
Plos One, 2024
38691546 (PubMed )
Supplement: pone.0297914.s001.xlsx › Hoja1
Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia.
Mojarad BA et al.
Translational Psychiatry, 2021
33526774 (PubMed )
Supplement: 41398_2021_1211_MOESM1_ESM.xlsx › Table_S9
Whole-exome sequencing identifies rare genetic variations in German families with pulmonary sarcoidosis.
Kishore A et al.
Human Genetics, 2018
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