Associated Papers
Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma.
Villa M et al.
British Journal of Cancer, 2024
39478125 (PubMed )
Supplement: 41416_2024_2881_MOESM1_ESM.pdf
Exome sequencing identifies novel genetic variants associated with varicose veins.
Zhang DD et al.
Plos Genetics, 2024
38980841 (PubMed )
Supplement: pgen.1011339.s009.xlsx › Sheet1
Contribution of rare and common coding variants to haematological malignancies in the UK biobank.
Zöller B et al.
Leukemia Research Reports, 2023
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-AN-A0FW-01A.domain
An extensive analysis of the hereditary hemochromatosis gene HFE and neighboring histone genes: associations with childhood leukemia.
Davis CF et al.
Annals of Hematology, 2010
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