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Clinical and genetic characteristics in lymphoma patients with a second solid malignancy.
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Comparison of BRCA versus non-BRCA germline mutations and associated somatic mutation profiles in patients with unselected breast cancer.
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Aging, 2020
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TAPES: A tool for assessment and prioritisation in exome studies.
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Plos Computational Biology, 2019
31613886 (PubMed )
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CharGer: clinical Characterization of Germline variants.
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Bioinformatics (oxford, England), 2019
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Identification of TNFSF13, SPATC1L, SLC22A25 and SALL4 as novel susceptibility loci for atrial fibrillation by an exome‑wide association study.
Yamada Y et al.
Molecular Medicine Reports, 2017
Molecular defects identified by whole exome sequencing in a child with Fanconi anemia.
Zheng Z et al.
Gene, 2013
Mutations in Fanconi anemia genes and the risk of esophageal cancer.
Akbari MR et al.
Human Genetics, 2011
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