Associated Papers
Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases.
Bhérer C et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
40791678 (PubMed )
Supplement: media-2.xlsx › Table_S12_ClinVar_PLP_variants
Expanding the Clinical Phenotype with CD79A Mutation and Refractory Helicobacter Bilis Infection.
Sil A et al.
Journal of Clinical Immunology, 2024
Utility of plasma cell-free DNA for de novo detection and quantification of clonal hematopoiesis.
Gutierrez-Rodrigues F et al.
Haematologica, 2022
34587721 (PubMed )
Supplement: 2021_279230_GUTIERREZ-RODRIGUES_SUPPL.pdf
Incidence of the CHEK2 Germline Mutation and Its Impact on Clinicopathological Features, Treatment Responses, and Disease Course in Patients with Papillary Thyroid Carcinoma.
Gąsior-Perczak D et al.
Cancers, 2021
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta.
Lougaris V et al.
Current Allergy and Asthma Reports, 2008
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