Stefanie Engert

Association of Type and Location of<i>BRCA1</i>and<i>BRCA2</i>Mutations With Risk of Breast and Ovarian Cancer

Timothy R. Rebbeck, Nandita Mitra, Fei Wan et al. · JAMA · 2015 · 484 citations · Full text

A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor

Juliane Ramser, Fatima Abidi, Céline Burcklé et al. · Human Molecular Genetics · 2005 · 181 citations

Genetics, Epilepsy Points, Renin Receptor Gene +17

Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker

Ariane Sadr‐Nabavi, Juliane Ramser, J. Naehrig et al. · International Journal of Cancer · 2008 · 86 citations · Full text

Breast Oncology, Medicine, Tumor Growth +14

MLPA screening in the<i>BRCA1</i>gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases

Stefanie Engert, Barbara Wappenschmidt, Beate Betz et al. · Human Mutation · 2008 · 86 citations

Breast Oncology, Engineering, Single Early-onset Cases +15

Analysis of 30 Putative BRCA1 Splicing Mutations in Hereditary Breast and Ovarian Cancer Families Identifies Exonic Splice Site Mutations That Escape In Silico Prediction

Barbara Wappenschmidt, Alexandra Becker, Jan Hauke et al. · PLoS ONE · 2012 · 51 citations · Full text

Engineering, Genetics, Molecular Biology +18