Associated Papers
Genetic mutations in lymphocytic variant of hypereosinophilic syndrome: study of five siblings.
Walkenhorst M et al.
Frontiers in Medicine, 2025
41488087 (PubMed )
Supplement: Table_1.xlsx › Data
Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes.
Soukupova J et al.
Plos One, 2018
29649263 (PubMed )
Supplement: pone.0195761.s005.xlsx › S5
Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.
Karageorgos I et al.
Human Genomics, 2015
26092435 (PubMed )
Supplement: 40246_2015_34_MOESM1_ESM.xlsx › FamilyB
Structural and functional characterization of the MERIT40 to understand its role in DNA repair.
Vikrant et al.
Journal of Biomolecular Structure & Dynamics, 2014
Common breast cancer risk variants in the post-COGS era: a comprehensive review.
Maxwell KN et al.
Breast Cancer Research : Bcr, 2013
Germline mutational analysis of the C19orf62 gene in African-American women with breast cancer.
Zheng Y et al.
Breast Cancer Research and Treatment, 2011
Mutation screening of the MERIT40 gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families.
Solyom S et al.
Breast Cancer Research and Treatment, 2010
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