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Paper Details

Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome.
medRxiv
1
2023
D76N, Genetic Arrhythmia, LQT5, Long QT syndrome, Mendelian disease, Participants, Type 5 Long QT Syndrome, arrhythmia disorder, chromosomal regions, chromosomal segments, genetic diseases, genomic segments, monogenic disease, rare genetic disease
Author NameAffiliation
Hung-Hsin ChenVanderbilt University Medical Center
David C SamuelsVanderbilt University Medical Center
Chad D HuffUniversity of Texas MD Anderson Cancer Center
Dan M RodenVanderbilt University Medical Center
Jennifer E BelowVanderbilt University Medical Center
Jennifer E BelowVanderbilt University Medical Center
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Release 1.2