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Publications by Cécile Leyronnas
Exome Sequencing Identifies Germline Variants in DIS3 in Familial Multiple Myeloma
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
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Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease
Arthritis and Rheumatology
Rheumatology
Allergy
Immunology
Exome Sequencing Identifies MPL as a Causative Gene in Familial Aplastic Anemia
Haematologica
Hematology
Whole Exome Sequencing Identifies a Troponin T Mutation Hot Spot in Familial Dilated Cardiomyopathy
PLoS ONE
Multidisciplinary
African American Exome Sequencing Identifies Potential Risk Variants at Alzheimer Disease Loci
Neurology: Genetics
Neurology
Genetics
Exome Sequencing Identifies Recurrent Somatic RAC1 Mutations in Melanoma
Nature Genetics
Genetics
Whole‑exome Sequencing Identifies a Novel Mutation (R367G) in SCN5A to Be Associated With Familial Cardiac Conduction Disease
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
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
Defining Clonal Plasticity Using Whole Exome Sequencing in Single Cells in an Index Case of Amp1q21 Multiple Myeloma
Clinical Lymphoma, Myeloma and Leukemia
Cancer Research
Oncology
Hematology
Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype
Ophthalmology
Ophthalmology