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European Journal of Human Genetics : EJHG|January 27, 2025
RNA-sequencing unveils FLT4 splice site variants in variable congenital heart diseaseMaxim Verlee, Erika D'haenens, Laurenz De Cock, et al.
Medrxiv : the Preprint Server for Health Sciences|November 1, 2024
Deep Learning-Based Detection of Carotid Plaques Informs Cardiovascular Risk Prediction and Reveals Genetic Drivers of AtherosclerosisMurad Omarov, Lanyue Zhang, Saman Doroodgar Jorshery, et al.
ACS Medicinal Chemistry Letters|May 17, 2023
Selective Wee1 Inhibitors Led to Antitumor Activity In Vitro and Correlated with MyelosuppressionSatenig Guler, Maria C DiPoto, Alejandro Crespo, et al.
International Journal of Cancer|November 2, 2007
Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomicsJo Vandesompele, Evi Michels, Katleen De Preter, et al.
Medical Image Analysis|November 17, 2022
Learn-Morph-Infer: A new way of solving the inverse problem for brain tumor modelingIvan Ezhov, Kevin Scibilia, Katharina Franitza, et al.
Nature Structural & Molecular Biology|May 20, 2026
Rap1-mediated steric hindrance protects telomeres from MRX sensingStefano Mattarocci, Giordano Reginato, Elda Cannavo, et al.
Haematologica|November 9, 2014
In vitro human embryonic stem cell hematopoiesis mimics MYB-independent yolk sac hematopoiesisStijn Vanhee, Katrien De Mulder, Yasmine Van Caeneghem, et al.
BMC Medicine|December 31, 2024
Assessment of the efficacy of palliative sedation in advanced cancer patients by evaluating discomfort levels: a prospective, international, multicenter observational studyMaaike Rijpstra, Kris Vissers, Alazne Belar, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 25, 2021
Myxoid pleomorphic liposarcoma-a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcomaDavid Creytens, Andrew L Folpe, Christian Koelsche, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinationsSarah Vergult, Andrew Dauber, Barbara Delle Chiaie, et al.
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