Ulrike A. Faust
Tuebingen, BW, Germany
Last Updated: 09/26/2026
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Found 25 publications
Evaluation of non-canonical p53 functions in DNA replication and recombination for variant classification.
Journal: Cell death & disease
Published: September 22, 2025
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
Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefits.
Journal: Breast (Edinburgh, Scotland)
Published: February 16, 2025
Reclassification of ATM Missense Variants of Uncertain Significance by Integrating Results from Systematic Functional Assays into an ACMG Points-Based Framework.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: November 22, 2024
Post-Abortem Detection of a Pathogenic Somatic PIK3CA-Variant in an Abdominal Lymphangioma That Is Not Present in Cultured Amniotic Fluid Cells.
Journal: Prenatal diagnosis
Published: July 17, 2024
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
ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways-lessons from breast cancer patients.
Journal: Cell death & disease
Published: October 06, 2022
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome.
Journal: Molecular genetics & genomic medicine
Published: August 30, 2022
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
Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants.
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: January 25, 2022
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.
Journal: Communications biology
Published: November 15, 2021
Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data.
Journal: Molecular genetics & genomic medicine
Published: May 17, 2021
Last Updated: 09/26/2026