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Publications by Anthony Hinrichs
Identifying Rare Variants From Exome Scans: The GAW17 Experience
BMC Proceedings
Biochemistry
Medicine
Genetics
Molecular Biology
Genetic Studies of Alcoholism and Substance Dependence
American Journal of Human Genetics
Genetics
Related publications
Practicality of Identifying Mitochondria Variants From Exome and RNAseq Data
BMC Bioinformatics
Biochemistry
Applied Mathematics
Computer Science Applications
Structural Biology
Molecular Biology
Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease
Arthritis and Rheumatology
Rheumatology
Allergy
Immunology
Whole-Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
A Probabilistic Method for Identifying Rare Variants Underlying Complex Traits
BMC Genomics
Biotechnology
Genetics
An Improved Burden-Test Pipeline for Identifying Associations From Rare Germline and Somatic Variants
BMC Genomics
Biotechnology
Genetics
Whole Exome Sequencing of Rare Variants in EIF4G1 and VPS35 in Parkinson Disease
Neurology
Neurology
Exome Chip Meta-Analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
Biological Psychiatry
Biological Psychiatry
Using Whole-Exome Sequencing to Identify Variants Inherited From Mosaic Parents
European Journal of Human Genetics
Genetics
Whole Exome Analyses to Examine the Impact of Rare Variants on Left Ventricular Traits in African American Participants From the HyperGEN and GENOA Studies
Journal of Hypertension and Management
