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Publications by Magali Periquet
Origin of the Mutations in the Parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, Whereas Point Mutations May Result From Founder Effects
American Journal of Human Genetics
Genetics
Related publications
On the Origin of Deletions and Point Mutations in Duchenne Muscular Dystrophy: Most Deletions Arise in Oogenesis and Most Point Mutations Result From Events in Spermatogenesis.
Journal of Medical Genetics
Genetics
Mutations in Exon 2 of GATA1 Are Early Events in Megakaryocytic Malignancies Associated With Trisomy 21
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Structural Effects of Point Mutations in Proteins
Proteins: Structure, Function and Genetics
Biochemistry
Structural Biology
Molecular Biology
The Majority of AML Mutations Are Preexisting Passenger Events
Cancer Discovery
Oncology
Glaucoma-Associated Mutations in the Optineurin Gene Have Limited Impact on Parkin-Dependent Mitophagy
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Founder BRCA1/2 Mutations in the Europe: Implications for Hereditary Breast-Ovarian Cancer Prevention and Control
EPMA Journal
Biochemistry
Health Policy
Drug Discovery
Founder Mutations in the Lipase H Gene in Families With Autosomal Recessive Woolly Hair/Hypotrichosis
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Multicentric Origin of Hemochromatosis Gene (HFE) Mutations
American Journal of Human Genetics
Genetics
IDH1 Mutations Are Early Events in the Development of Astrocytomas and Oligodendrogliomas
American Journal of Pathology
Forensic Medicine
Pathology
