Fabian Beier

Late-onset telomere biology disorders in adults: clinical insights and treatment outcomes from a retrospective registry cohort

Virus-reactive T cells expanded in aplastic anemia eliminate hematopoietic progenitor cells by molecular mimicry

Liver disease and transplantation in telomere biology disorders: An international multicenter cohort

Engineering an inducible leukemia-associated fusion protein enables large-scale ex vivo production of functional human phagocytes

Harnessing CD3 diversity to optimize CAR T cells

The Clinical Picture of the ERCC6L2 Disease - from Bone Marrow Failure to Acute Leukemia

Clinical manifestations of telomere biology disorders in adults

Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age-modified Criteria

Telomere biology disorders may manifest as common variable immunodeficiency (CVID)

Interstitial lung diseases associated with mutations of poly(A)‐specific ribonuclease: A multicentre retrospective study

Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue

Determinants of survival after lung transplantation in telomerase-related gene mutation carriers: A retrospective cohort

Telomerase and Pluripotency Factors Jointly Regulate Stemness in Pancreatic Cancer Stem Cells

Converting a leukemic transcription factor into a powerful tool for large-scale ex vivo production of human phagocytes

Clinical Presentation of Patients with Adult Late-Onset Telomere Biology Disorders - Results from the Aachen Telomeropathy Registry

Late-onset and long-lasting autoimmune neutropenia: an analysis from the Italian Neutropenia Registry

Alternative lengthening of telomeres is the major telomere maintenance mechanism in astrocytoma with isocitrate dehydrogenase 1 mutation

RPA1 Gain of Function Causes Human Short Telomere Syndrome with Revertant Somatic Mosaicism

Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL

Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita

The Atypical Kinase RIOK1 Promotes Tumor Growth and Invasive Behavior

Rps14 haploinsufficiency causes a block in erythroid differentiation mediated by S100A8 and S100A9

A novel autosomal recessive TERT T1129P mutation in a dyskeratosis congenita family leads to cellular senescence and loss of CD34+ hematopoietic stem cells not reversible by mTOR-inhibition

Genetic characterization of acquired aplastic anemia by targeted sequencing

Regression of eosinophil counts after diagnosis of chronic graft-versus-host disease as a potential marker for improved clinical outcome

Enterocytes Of Patients With Uncontrolled Acute Graft Versus Host Disease Of The Gut Undergo Massive Telomere Shortening Compared To Unaffected Controls