Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Mikhail Ognenovski
Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease
Arthritis and Rheumatology
Rheumatology
Allergy
Immunology
Epigenome Profiling Reveals Significant DNA Demethylation of Interferon Signature Genes in Lupus Neutrophils
Journal of Autoimmunity
Allergy
Immunology
Related publications
Whole-Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
Whole Exome Sequencing of Rare Variants in EIF4G1 and VPS35 in Parkinson Disease
Neurology
Neurology
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
African American Exome Sequencing Identifies Potential Risk Variants at Alzheimer Disease Loci
Neurology: Genetics
Neurology
Genetics
Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases
Genomics and Informatics
Evolution
Ecology
Genetics
Systematics
Health Informatics
Behavior
Exome Sequencing Identifies Germline Variants in DIS3 in Familial Multiple Myeloma
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
Whole-Exome Sequencing Identifies Somatic ATRX Mutations in Pheochromocytomas and Paragangliomas
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype
Ophthalmology
Ophthalmology
Whole Exome Sequencing Identified Sixty-Five Coding Mutations in Four Neuroblastoma Tumors
Scientific Reports
Multidisciplinary