Alexandra Liebmann

A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies

K. Kagan, M. Hoopmann, M. Sturm, 2022, Prenatal diagnosis.

Germline findings in patients with advanced malignancies screened with paired blood-tumour testing for personalised treatment approaches.

C. Schroeder, S. Ossowski, T. Haack, 2022, European journal of cancer.

Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients

C. Schroeder, M. Sturm, A. Dufke, 2023, European Journal of Human Genetics.

Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases

K. Stingl, M. Sturm, S. Ossowski, 2023, Journal of Medical Genetics.

UV-radiation and MC1R germline mutations are risk factors for the development of conventional and spitzoid melanomas in children and adolescents

C. Schroeder, M. Sturm, S. Ossowski, 2023, EBioMedicine.

Characterization of PRAME immunohistochemistry reveals lower expression in pediatric melanoma compared to adult melanoma

I. Brecht, Michael Abele, Matthias Hahn, 2024, Pigment cell & melanoma research.