Associated Papers
Large-scale genetic characterization of Parkinson's disease in the African and African admixed populations.
Akçimen F et al.
Brain : a Journal of Neurology, 2025
41058593 (PubMed )
Supplement: awaf379_supplementary_data.zip › brain-2025-00177-File011.xlsx › SupplementaryTable7
A systematic in-silico functional and structural analysis reveals deleterious missense nsSNPs in the human CSF1R gene.
Malhotra P et al.
Molecular Biology Research Communications, 2025
40949796 (PubMed )
Supplement: mbrc-14-291-s001.pdf
Characterization of Philadelphia-like Pre-B Acute Lymphoblastic Leukemia: Experiences in Mexican Pediatric Patients.
Martínez-Anaya D et al.
International Journal of Molecular Sciences, 2022
36076986 (PubMed )
Supplement: ijms-23-09587-s001.zip › ijms-1818043-supplementary.pdf
Phenotypic impacts of CSF1R deficiencies in humans and model organisms.
Hume DA et al.
Journal of Leukocyte Biology, 2020
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