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Article
Open AccessCopy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma
Esophageal adenocarcinoma (EA) is among the leading causes of cancer mortality, especially in developed countries. A high level of somatic copy number alterations (CNAs) accumulates over the decades in the pro...
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Article
Open AccessErratum To: Genetic variants in the MRPS30region and postmenopausal breast cancer risk
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Article
Open AccessGenetic variants in the MRPS30 region and postmenopausal breast cancer risk
Genome-wide association studies have identified several genomic regions that are associated with breast cancer risk, but these provide an explanation for only a small fraction of familial breast cancer aggrega...