Associated Papers
The potential of deep learning on the discovery of new genes implicated in differences of sex development.
von der Decken I et al.
Computational and Structural Biotechnology Journal, 2026
The Influence of a Genetic Variant in CCDC78 on LMNA-Associated Skeletal Muscle Disease.
Mohar NP et al.
International Journal of Molecular Sciences, 2024
Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics Approach.
Bajpai AK et al.
Genes, 2023
Molecular characterization of sub-frontal recurrent medulloblastomas reveals potential clinical relevance.
Chen Z et al.
Frontiers in Neurology, 2023
37181548 (PubMed )
Supplement: Data_Sheet_2.xlsx › Germline_mutation-case_1
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.
Weng LC et al.
Circulation. Genomic and Precision Medicine, 2020
POT1 and Damage Response Malfunction Trigger Acquisition of Somatic Activating Mutations in the VEGF Pathway in Cardiac Angiosarcomas.
Calvete O et al.
Journal of the American Heart Association, 2019
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Wuttke M et al.
Nature Genetics, 2019
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation.
Thorolfsdottir RB et al.
Communications Biology, 2018
30271950 (PubMed )
Supplement: 42003_2018_68_MOESM1_ESM.pdf
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