Publications by authors named "Insa Halfmeyer"

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Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age-modified Criteria.
Mareike Tometten, Martin Kirschner, Robert Meyer, Matthias Begemann, Insa Halfmeyer

Hemasphere· May 2023

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Approach to Cohort-Wide Re-Analysis of Exome Data in 1000 Individuals with Neurodevelopmental Disorders.
Insa Halfmeyer, Tobias Bartolomaeus, Bernt Popp, Maximilian Radtke, Tobias Helms

Genes (Basel)· December 2022

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Comparison of flow-FISH and MM-qPCR telomere length assessment techniques for the screening of telomeropathies.
Monica S Ventura Ferreira, Martin Kirschner, Insa Halfmeyer, Natalia Estrada, Blanca Xicoy

Ann N Y Acad Sci· April 2020

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Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita.
Martin Kirschner, Angela Maurer, Marcin W Wlodarski, Monica S Ventura Ferreira, Anne-Sophie Bouillon, Insa Halfmeyer

Leukemia· August 2018

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