Associated Papers
MAGIS syndrome: phenotypes, pathogenesis, and treatment.
Lamborn IT et al.
Journal of Human Immunity, 2025
Clonal hematopoiesis is associated with distinct rheumatoid arthritis phenotypes.
Hiitola E et al.
Science Advances, 2025
40305610 (PubMed )
Supplement: sciadv.adt9846_tables_s1_to_s13.zip › adt9846_tables_s1_to_s13.xlsx › S3
Testicular large B-cell lymphoma is genetically similar to PCNSL and distinct from nodal DLBCL.
Rivas-Delgado A et al.
Hemasphere, 2024
39380845 (PubMed )
Supplement: HEM3-8-e70024-s001.xlsx › ST7
Germline mutations in a G protein identify signaling cross-talk in T cells.
Ham H et al.
Science (new York, N.y.), 2024
Active Gαi/o mutants accelerate breast tumor metastasis via the c-Src pathway.
Lyu C et al.
Biorxiv : the Preprint Server for Biology, 2023
Monomorphic epitheliotropic intestinal T-cell lymphoma comprises morphologic and genomic heterogeneity impacting outcome.
Veloza L et al.
Haematologica, 2023
35708139 (PubMed )
Supplement: 2022_281226_VELOZA_SUPPL.pdf
Distinct genomic landscape of Chinese pediatric acute myeloid leukemia impacts clinical risk classification.
Liu T et al.
Nature Communications, 2022
35347147 (PubMed )
Supplement: 41467_2022_29336_MOESM8_ESM.xlsx › Sheet1
Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypes.
Ferraro F et al.
Proceedings of the National Academy of Sciences of the United States of America, 2021
34845035 (PubMed )
Supplement: pnas.2116427118.sd02.xlsx › mutations.2021.02.24
Genomic profiling of primary histiocytic sarcoma reveals two molecular subgroups.
Egan C et al.
Haematologica, 2020
Variant recurrence in neurodevelopmental disorders: the use of publicly available genomic data identifies clinically relevant pathogenic missense variants.
Lecoquierre F et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma.
López C et al.
Nature Communications, 2019
30926794 (PubMed )
Supplement: 41467_2019_8578_MOESM9_ESM.xlsx › Tabelle3__3_
JAK-STAT and G-protein-coupled receptor signaling pathways are frequently altered in epitheliotropic intestinal T-cell lymphoma.
Nairismägi ML et al.
Leukemia, 2016
26854024 (PubMed )
Supplement: leu201613x3.xls › ST8
The emerging mutational landscape of G proteins and G-protein-coupled receptors in cancer.
O'Hayre M et al.
Nature Reviews. Cancer, 2013
Absence of GNAI2 codon 179 oncogene mutations in inflammatory bowel disease.
Zhang WJ et al.
Inflammatory Bowel Diseases, 2000
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