Associated Papers
A multiple sclerosis-protective coding variant reveals an essential role for HDAC7 in regulatory T cells.
Axisa PP et al.
Science Translational Medicine, 2022
Monitoring of Leukemia Clones in B-cell Acute Lymphoblastic Leukemia at Diagnosis and During Treatment by Single-cell DNA Amplicon Sequencing.
Meyers S et al.
Hemasphere, 2022
35291210 (PubMed )
Supplement: hs9-6-e700-s004.xlsx › XG118
Genetics and functional genomics of multiple sclerosis.
Kim W et al.
Seminars in Immunopathology, 2022
Molecular profiling of soft-tissue sarcomas with FoundationOne® Heme identifies potential targets for sarcoma therapy: a single-centre experience.
Scheipl S et al.
Therapeutic Advances in Medical Oncology, 2021
34367342 (PubMed )
Supplement: sj-xlsx-1-tam-10.1177_17588359211029125.xlsx › FMI_Archer
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk.
Unknown Author
Cell, 2018
A rare coding allele in IFIH1 is protective for psoriatic arthritis.
Budu-Aggrey A et al.
Annals of the Rheumatic Diseases, 2017
28501801 (PubMed )
Supplement: annrheumdis-2016-210592supp001.pdf
Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathy.
Wells QS et al.
Circulation. Cardiovascular Genetics, 2013
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