Publications by authors named "Tim Bender"

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Cracking the code: a head-to-head comparison of expert clinicians and artificial intelligence in diagnosing rare diseases.
Georg Wolfgang Sendtner, Martin Muecke, Lorenz Grigull, Tim Bender, Charlotte Behning

Orphanet J Rare Dis· November 2025

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Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer, Tim Bender

Nat Genet· July 2025

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Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer, Tim Bender

Nat Genet· August 2024

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[Diverticulitis? Pleurisy? No! Familial Mediterranean fever? Yes!].
Felix Weckbecker, Tim Theodor Albert Bender

MMW Fortschr Med· February 2024

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A diagnostic support system based on pain drawings: binary and k-disease classification of EDS, GBS, FSHD, PROMM, and a control group with Pain2D.
D Emmert, N Szczypien, Tim T A Bender, L Grigull, A Gass

Orphanet J Rare Dis· March 2023

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Next-generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen-de Vries syndrome.
Fabian Brand, Aswinkumar Vijayananth, Tzung-Chien Hsieh, Axel Schmidt, Sophia Peters, Tim Bender

Hum Mutat· November 2022

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GestaltMatcher facilitates rare disease matching using facial phenotype descriptors.
Tzung-Chien Hsieh, Aviram Bar-Haim, Shahida Moosa, Nadja Ehmke, Karen W Gripp, Tim Bender

Nat Genet· March 2022

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The combined prevalence of classified rare rheumatic diseases is almost double that of ankylosing spondylitis.
Judith Leyens, Tim Th A Bender, Martin Mücke, Christiane Stieber, Dmitrij Kravchenko

Orphanet J Rare Dis· July 2021

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Pain drawings as a diagnostic tool for the differentiation between two pain-associated rare diseases (Ehlers-Danlos-Syndrome, Guillain-Barré-Syndrome).
Larissa Wester, Martin Mücke, Tim Theodor Albert Bender, Julia Sellin, Frank Klawonn

Orphanet J Rare Dis· November 2020

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Therapeutic options for patients with rare rheumatic diseases: a systematic review and meta-analysis.
Tim T A Bender, Judith Leyens, Julia Sellin, Dmitrij Kravchenko, Rupert Conrad

Orphanet J Rare Dis· October 2020

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[Osteoarthritis in elderly patients: Are there effective therapies?].
Tim Theodor Albert Bender, Detmar Jobst, Martin Mücke

MMW Fortschr Med· August 2016

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