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Publications by Asier Larrea-Sebal
Mutation Type Classification and Pathogenicity Assignment of Sixteen Missense Variants Located in the EGF-precursor Homology Domain of the LDLR
Scientific Reports
Multidisciplinary
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Predicting Pathogenicity of Missense Variants With Weakly Supervised Regression
Human Mutation
Genetics
Consideration of Cosegregation in the Pathogenicity Classification of Genomic Variants
American Journal of Human Genetics
Genetics
[PROVISIONAL] Determining the Pathogenicity of CFTR Missense Variants: Multiple Comparison of in Silico Predictors and Variant Annotation Databases
Genetics and Molecular Biology
Genetics
Molecular Biology
Single Missense Mutation in the Tyrosine Kinase Catalytic Domain of the RET Protooncogene Is Associated With Multiple Endocrine Neoplasia Type 2B.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Author Correction: Characterization of a Recurrent Missense Mutation in the Forkhead DNA-binding Domain of FOXP1
Scientific Reports
Multidisciplinary
Identification of a Novel Missense Mutation in NIPAL4 Gene: First 3D Model Construction Predicted Its Pathogenicity
Molecular genetics & genomic medicine
Genetics
Molecular Biology
A High-Throughput Functional Complementation Assay for Classification of BRCA1 Missense Variants
Cancer Discovery
Oncology
Novel Amyloid Precursor Protein Gene Missense Mutation (D678N) in Probable Familial Alzheimer's Disease
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Affected Siblings With Alzheimer's Disease Had Missense Mutation of Codon 717 in Amyloid Precursor Protein Gene.
Japanese Journal of Geriatrics
Gerontology
Geriatrics