Associated Papers
Genomic, transcriptomic and RNA editing analysis of human MM1 and VV2 sporadic Creutzfeldt-Jakob disease.
Tarozzi M et al.
Acta Neuropathologica Communications, 2022
Dementia-related genetic variants in an Italian population of early-onset Alzheimer's disease.
Bartoletti-Stella A et al.
Frontiers in Aging Neuroscience, 2022
36133075 (PubMed )
Supplement: Table_1.XLSX › AD_097_N
Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing.
Varzari A et al.
Frontiers in Genetics, 2022
Whole exome sequencing in thrombophilic pedigrees to identify genetic risk factors for venous thromboembolism.
Cunha MLR et al.
Plos One, 2017
29117201 (PubMed )
Supplement: pone.0187699.s002.xlsx › SNPs_result_filter_strategies
Integrated analysis of germline and somatic variants in ovarian cancer.
Kanchi KL et al.
Nature Communications, 2014
24448499 (PubMed )
Supplement: NIHMS551112-supplement-9.xlsx › S_Data_8
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