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Scientific Reports|September 18, 2023
Real world evidence reveals improved survival outcomes in biliary tract cancer through molecular matched targeted treatmentBernhard Doleschal, Hossein Taghizadeh, Gerald Webersinke, et al.
European Journal of Endocrinology|April 15, 2026
Severe Osteogenesis Imperfecta Due to Homozygous Glycine Substitutions in COL1A1 and COL1A2Alexandra Blaschitz, Rodrigo Montero-Lopez, Tamer A El-Sobky, et al.
Nature Communications|June 23, 2016
Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancerPeter Ulz, Jelena Belic, Ricarda Graf, et al.
International Journal of Cancer|July 23, 2015
Recurrent alterations of TNFAIP3 (A20) in T-cell large granular lymphocytic leukemiaPatricia Johansson, Anke Bergmann, Sven Rahmann, et al.
Scientific Reports|February 20, 2026
Oncofetal chondroitin sulfate positive circulating tumor cells as prognostic biomarkers in early-stage melanomaJudith Sunzenauer, Melanie Rammer, Leonhard Stöckl, et al.
Cancers|December 17, 2024
Circulating Tumor DNA (ctDNA) Dynamics Predict Early Response to Treatment in Metastasized Gastroesophageal Cancer (mGEC) After 2 Weeks of Systemic TreatmentStefan Tatalovic, Bernhard Doleschal, Alexander Kupferthaler, et al.
Cancers|December 30, 2025
Rapid Hematological and Molecular Response to Pegylated Interferon in WHO-Defined Pre-Fibrotic MyelofibrosisSigrid Machherndl-Spandl, Marcel Kiehberger, Veronika Sygulla, et al.
Human Molecular Genetics|March 15, 2014
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityMarie Bernkopf, Gerald Webersinke, Chanakan Tongsook, et al.
Cancer Immunology, Immunotherapy : CII|October 2, 2024
Exploring the impact of durvalumab on biliary tract cancer: insights from real-world clinical dataPatrick Reimann, Ilektra-Antonia Mavroeidi, Jonathan Burghofer, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 3, 2025
Biochemical phenotype of hypophosphatasia in asymptomatic individuals carrying ALPL variantsRodrigo Montero-Lopez, Mariam R Farman, Florian Högler, et al.
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