T. Bender

Next‐generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen‐de Vries syndrome

Alexej Knaus, Tzung-Chien Hsieh, P. Krawitz, 2022, Human mutation.

GestaltMatcher facilitates rare disease matching using facial phenotype descriptors

D. Horn, S. Mundlos, M. Spielmann, 2022, Nature Genetics.

GestaltMatcher facilitates rare disease matching using facial phenotype descriptors

M. Nöthen, D. Horn, S. Mundlos, 2022, Nature Genetics.

GestaltMatcher: Overcoming the limits of rare disease matching using facial phenotypic descriptors

M. Nöthen, D. Horn, S. Mundlos, 2021, medRxiv.

Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

Heinen, Heiko, Kehrer, 2023, medRxiv.

The combined prevalence of classified rare rheumatic diseases is almost double that of ankylosing spondylitis

M. Seidel, Tim Bender, M. Mücke, 2021, Orphanet Journal of Rare Diseases.

State-of-Charge Estimation of Lithium-ion Battery Based on a Combined Method of Neural Network and Unscented Kalman filter

Giovanni Vagnoni, T. Bender, Seyedmehdi Hosseininasab, 2020, 2020 IEEE Vehicle Power and Propulsion Conference (VPPC).