Anna Benet‐Pagès
Helmholtz Zentrum München(DE)Medical Genetics Center(DE)
Publications by Year
Research Areas
Genomics and Rare Diseases, Cancer Genomics and Diagnostics, Genetic factors in colorectal cancer, Genomics and Phylogenetic Studies, Parathyroid Disorders and Treatments
Most-Cited Works
- → A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease(2011)898 cited
- → The UCSC Genome Browser database: 2023 update(2022)649 cited
- → The UCSC Genome Browser database: 2021 update(2020)624 cited
- → DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis(2006)518 cited
- → An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia(2004)502 cited
- → The UCSC Genome Browser database: 2025 update(2024)499 cited
- → Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23(2001)493 cited
- → Polypeptide GalNAc-transferase T3 and Familial Tumoral Calcinosis(2006)420 cited
- → Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3(2006)368 cited
- → The UCSC Genome Browser database: 2024 update(2023)346 cited