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Publications by Thomas Meitinger
Multi-Ancestry Genome-Wide Gene–smoking Interaction Study of 387,272 Individuals Identifies New Loci Associated With Serum Lipids
Nature Genetics
Genetics
Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis
American Journal of Human Genetics
Genetics
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , Which Encode Subcomponents C1r and C1s of Complement
American Journal of Human Genetics
Genetics
CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
American Journal of Human Genetics
Genetics
Bi-Allelic ADPRHL2 Mutations Cause Neurodegeneration With Developmental Delay, Ataxia, and Axonal Neuropathy
American Journal of Human Genetics
Genetics
Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome
American Journal of Human Genetics
Genetics
Common Genetic Variants Associate With Serum Phosphorus Concentration
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology
Genome-Wide Genotyping Demonstrates a Polygenic Risk Score Associated With White Matter Hyperintensity Volume in CADASIL
Stroke
Cardiology
Neurology
Cardiovascular Medicine
Advanced
Medicine
Neuroscience
Specialized Nursing
DeepWAS: Multivariate Genotype-Phenotype Associations by Directly Integrating Regulatory Information Using Deep Learning
PLoS Computational Biology
Molecular Neuroscience
Evolution
Ecology
Genetics
Behavior
Molecular Biology
Systematics
Simulation
Cellular
Computational Theory
Mathematics
Modeling
Large Scale International Replication and Meta-Analysis Study Confirms Association of the 15q14 Locus With Myopia. The CREAM Consortium
Human Genetics
Genetics
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