Associated Papers
Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.
Parra-Perez AM et al.
Medcomm, 2025
40989574 (PubMed )
Supplement: MCO2-6-e70394-s001.xlsx › TableS13
Genetic Alterations in Essential Thrombocythemia Progression to Acute Myeloid Leukemia: A Case Series and Review of the Literature.
Ayres-Silva JP et al.
Frontiers in Oncology, 2018
29515972 (PubMed )
Supplement: table_1.xlsx › suppl_table_1
Co-existence of BRAF and NRAS driver mutations in the same melanoma cells results in heterogeneity of targeted therapy resistance.
Raaijmakers MI et al.
Oncotarget, 2016
27791198 (PubMed )
Supplement: oncotarget-07-77163-s002.xlsx › Patient_2_late_met_1
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X.
Schulz E et al.
Nature Communications, 2014
25307848 (PubMed )
Supplement: ncomms6191-s1.pdf
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