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Publications by Jared M. Evans
Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome
Circulation: Cardiovascular Genetics
Related publications
Exome Sequencing to Identify Novel Genes in Hypertension
Circulation: Cardiovascular Genetics
Novel Characteristics of a Trafficking-Defective G572r-hERG Channel Linked to Hereditary Long QT Syndrome
Canadian Journal of Cardiology
Cardiovascular Medicine
Cardiology
Exome Sequencing to Identify De Novo Mutations in Sporadic ALS Trios
Nature Neuroscience
Neuroscience
Novel Calmodulin Mutations Associated With Congenital Long QT Syndrome Affect Calcium Current in Human Cardiomyocytes
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Long QT Syndrome-Associated F97C and S141R CaV-3 Mutations Exert Pleiotropic Effects on Cardiac L-Type Calcium Channels
Biophysical Journal
Biophysics
Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families
PLoS ONE
Multidisciplinary
Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial M-Aaa Proteases
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Novel Trigenic CACNA1C/DES/MYPN Mutations in a Family of Hypertrophic Cardiomyopathy With Early Repolarization and Short QT Syndrome
Journal of Translational Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
American Journal of Human Genetics
Genetics
