Alexandra Liebmann

Tuebingen, BW, Germany

Last Updated: 09/26/2026

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Found 11 publications

Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.

Prenatal Phenotypic Features of Five Fetal Cases With RNU4ATAC-Associated Microcephalic Osteodysplastic Primordial Dwarfism Type I.

Journal: Prenatal diagnosis

Published: May 07, 2026

Distinct genomic profile of pediatric lung carcinoma: High frequency of ALK fusions and TP53 mutations compared to adults.

Distinct genomic profile of pediatric lung carcinoma: High frequency of ALK fusions and TP53 mutations compared to adults.

Journal: Lung cancer (Amsterdam, Netherlands)

Published: July 23, 2025

Colorectal Carcinoma in Childhood and Adolescence: Microsatellite Instability Correlates With a Favorable Prognosis.

Colorectal Carcinoma in Childhood and Adolescence: Microsatellite Instability Correlates With a Favorable Prognosis.

Journal: Pediatric blood & cancer

Published: February 03, 2025

Expression of the tumor antigens NY-ESO-1, tyrosinase, MAGE-A3, and TPTE in pediatric and adult melanoma: a retrospective case control study.

Expression of the tumor antigens NY-ESO-1, tyrosinase, MAGE-A3, and TPTE in pediatric and adult melanoma: a retrospective case control study.

Journal: Virchows Archiv : an international journal of pathology

Published: April 22, 2024

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

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

Journal: Pigment cell & melanoma research

Published: January 15, 2024

Genomes in clinical care.

Genomes in clinical care.

Journal: NPJ genomic medicine

Published: September 01, 2023

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

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

Journal: Journal of medical genetics

Published: June 20, 2023

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

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

Journal: EBioMedicine

Published: May 19, 2023

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

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

Journal: European journal of human genetics : EJHG

Published: January 28, 2023

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

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

Journal: European journal of cancer (Oxford, England : 1990)

Published: July 01, 2022

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

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

Journal: Prenatal diagnosis

Published: January 11, 2022

Showing 1-11 of 11

Last Updated: 09/26/2026