Associated Papers
Association Analysis of Rare CNTN5 Variants With Autism Spectrum Disorder in a Japanese Population.
Hadi AF et al.
Neuropsychopharmacology Reports, 2025
EBV+ nodal T/NK-cell lymphoma associated with clonal hematopoiesis and structural variations of the viral genome.
Kato S et al.
Blood Advances, 2024
38429084 (PubMed )
Supplement: BLOODA_ADV-2023-012019-mmc1.pdf
Identification of metastasis driver genes by massive parallel sequencing of successive steps of breast cancer progression.
Krøigård AB et al.
Plos One, 2018
29293529 (PubMed )
Supplement: pone.0189887.s004.xlsx › Ark1
Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors.
Chmielecki J et al.
Nature Genetics, 2013
23313954 (PubMed )
Supplement: NIHMS474988-supplement-1.pdf
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