Ulrike Siebers‐Renelt

Novel<i>FOXF1</i>Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain

Partha Sen, Yaping Yang, C. Navarro et al. · Human Mutation · 2013 · 114 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +15

47 patients with FLNA associated periventricular nodular heterotopia

Max Lange, Burkhard S. Kasper, Axel Bohring et al. · Orphanet Journal of Rare Diseases · 2015 · 105 citations · Full text

Breast cancer risk in <i>BRCA1/2</i> mutation carriers and noncarriers under prospective intensified surveillance

Christoph Engel, Christine Fischer, Silke Zachariae et al. · International Journal of Cancer · 2019 · 55 citations · Full text

Novel Mutations Including Deletions of the Entire<i>OFD1</i>Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability

Izak Johannes Bisschoff, Christine Zeschnigk, Denise Horn et al. · Human Mutation · 2012 · 49 citations · Full text

Ofd1 Gene, Suspected Ofd1, Neurological Disorder +21

SMARCB1 Involvement in the Development of Leiomyoma in a Patient With Schwannomatosis

Theo J.M. Hulsebos, Susan Kenter, Ulrike Siebers‐Renelt et al. · The American Journal of Surgical Pathology · 2014 · 27 citations

Cancer Pathology, Genetics, Pathology +16