Associated Papers
ClinVAP: a reporting strategy from variants to therapeutic options.
Sürün B et al.
Bioinformatics (oxford, England), 2020
31830259 (PubMed )
Supplement: btz924_supplementary_data.zip › btz924-suppl_data › SupplementaryMaterialB_ExampleReport.pdf
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
Patel D et al.
Jama Network Open, 2019
30924900 (PubMed )
Supplement: jamanetwopen-2-e191350-s001.pdf
Aggressive natural killer-cell leukemia mutational landscape and drug profiling highlight JAK-STAT signaling as therapeutic target.
Dufva O et al.
Nature Communications, 2018
29674644 (PubMed )
Supplement: 41467_2018_3987_MOESM6_ESM.xlsx › NKTCL_L14
Identification of DLEC1 D215N Somatic Mutation in Formalin Fixed Paraffin Embedded Melanoma and Melanocytic Nevi Specimens.
Vieira R et al.
Journal of Skin Cancer, 2013
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