Nadina O. Bruchle
Aachen, NW 52074, Germany
Last Updated: 09/26/2026
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Found 8 publications
Benchmarking whole exome sequencing in the German network for personalized medicine.
Journal: European journal of cancer (Oxford, England : 1990)
Published: June 20, 2024
Direct prediction of Homologous Recombination Deficiency from routine histology in ten different tumor types with attention-based Multiple Instance Learning: a development and validation study.
Journal: medRxiv : the preprint server for health sciences
Published: March 22, 2023
Liquid biopsy in colon cancer: comparison of different circulating DNA extraction systems following absolute quantification of KRAS mutations using Intplex allele-specific PCR.
Journal: Oncotarget
Published: November 30, 2016
Prenatal ultrasound, genotype, and outcome in a large cohort of prenatally affected patients with autosomal-recessive polycystic kidney disease and other hereditary cystic kidney diseases.
Journal: Archives of gynecology and obstetrics
Published: August 24, 2016
NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS features.
Journal: Clinical genetics
Published: January 31, 2016
DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling.
Journal: American journal of human genetics
Published: September 30, 2014
Gain-of-Function Mutation in STIM1 (P.R304W) Is Associated with Stormorken Syndrome.
Journal: Human mutation
Published: February 14, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026