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Cell Death & Disease|March 1, 2026
Evaluation of non-canonical p53 functions in DNA replication and recombination for variant classificationRebecca Jansche, Benedikt Heitmeir, Ulrike Faust, et al.
Journal of Genetic Counseling|February 14, 2024
Implementing mainstream genetic counseling within the area-wide network of the German Consortium Hereditary Breast and Ovarian Cancer (GC-HBOC): Satisfaction of primary care providers with the provided state-of-the-art training by the Cologne CenterNatalie Herold, Kathrin Bredow, Corinna Ernst, et al.
Pediatric Nephrology (Berlin, Germany)|January 14, 2017
Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalitiesAgnes Hackl, Katrin Mehler, Ingo Gottschalk, et al.
Geburtshilfe Und Frauenheilkunde|April 24, 2020
Criteria of the German Consortium for Hereditary Breast and Ovarian Cancer for the Classification of Germline Sequence Variants in Risk Genes for Hereditary Breast and Ovarian CancerBarbara Wappenschmidt, Jan Hauke, Ulrike Faust, et al.
Plos One|December 15, 2012
Analysis of 30 putative BRCA1 splicing mutations in hereditary breast and ovarian cancer families identifies exonic splice site mutations that escape in silico predictionBarbara Wappenschmidt, Alexandra A Becker, Jan Hauke, et al.
European Urology Focus|June 14, 2025
Evaluation of Different National Comprehensive Cancer Network Clinical Practice Guidelines in Prostate Cancer for Germline Genetic Testing in Localized and Locally Recurrent Prostate CancerMykyta Kachanov, Alexander E Volk, Fabian Falkenbach, et al.
Acta Neuropathologica|September 6, 2013
Deep sequencing reveals increased DNA methylation in chronic rat epilepsyKatja Kobow, Antony Kaspi, K N Harikrishnan, et al.
Breast Cancer Research : BCR|December 24, 2013
RAD51C deletion screening identifies a recurrent gross deletion in breast cancer and ovarian cancer familiesGioia Schnurbein, Jan Hauke, Barbara Wappenschmidt, et al.
Cancers|January 6, 2021
Performance of In Silico Prediction Tools for the Detection of Germline Copy Number Variations in Cancer Predisposition Genes in 4208 Female Index Patients with Familial Breast and Ovarian CancerLouisa Lepkes, Mohamad Kayali, Britta Blümcke, et al.
Plos One|October 15, 2013
A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotypeJan Hauke, Andrea Schild, Antje Neugebauer, et al.
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