MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
IRF2BPL Is Associated with Neurological Phenotypes. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
IRF2BPL Is Associated with Neurological Phenotypes. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Further evidence for the involvement of EFL1 in a Shwachman-Diamond-like syndrome and expansion of the phenotypic features. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
