Peter R. Papenhausen

机构：Moffitt Cancer Center

发表论文 121 篇 · 总被引 3583 次 · h-index 26

代表论文

• The Role of c-MYC in B-Cell Lymphomas: Diagnostic and Molecular Aspects (2017 · Genes · 被引 181)
• DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome (2016 · The American Journal of Human Genetics · 被引 124)
• Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency (2013 · Molecular Genetics and Metabolism · 被引 76)
• Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype (2013 · American Journal of Medical Genetics Part A · 被引 57)
• Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres (2011 · Chromosoma · 被引 52)
• Clinical experience of laboratory follow‐up with noninvasive prenatal testing using cell‐free DNA and positive microdeletion results in 349 cases (2018 · Prenatal Diagnosis · 被引 41)