Dennis S. Witt
Tuebingen, BW, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefits.
Journal: Breast (Edinburgh, Scotland)
Published: February 16, 2025
Calculating Future 10-Year Breast Cancer Risks in Risk-Adapted Surveillance: A Method Comparison and Application in Clinical Practice.
Journal: Cancer prevention research (Philadelphia, Pa.)
Published: July 19, 2024
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
HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder.
Journal: American journal of human genetics
Published: January 26, 2023
Clustered variants in the 5' coding region of TRA2B cause a distinctive neurodevelopmental syndrome.
Clustered variants in the 5' coding region of TRA2B cause a distinctive neurodevelopmental syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 21, 2022
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome.
Journal: Molecular genetics & genomic medicine
Published: August 30, 2022
A Novel, Apparently Silent Variant in MFSD8 Causes Neuronal Ceroid Lipofuscinosis with Marked Intrafamilial Variability.
Journal: International journal of molecular sciences
Published: January 24, 2022
Magnetic Phases of Sputter Deposited Thin-Film Erbium.
Journal: Scientific reports
Published: June 29, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026