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Blood Advances|February 22, 2021
Addition of lenalidomide to intensive treatment in younger and middle-aged adults with newly diagnosed AML: the HOVON-SAKK-132 trialBob Löwenberg, Thomas Pabst, Johan Maertens, et al.
Circulation. Genomic and Precision Medicine|May 13, 2018
Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac ConductionVincenzo Macri, Jennifer A Brody, Dan E Arking, et al.
Leukemia|April 26, 2016
Development and evaluation of a secondary reference panel for BCR-ABL1 quantification on the International ScaleN C P Cross, H E White, T Ernst, et al.
American Journal of Human Genetics|November 27, 2012
Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegiaJanneke H M Schuurs-Hoeijmakers, Michael T Geraghty, Erik-Jan Kamsteeg, et al.
JAMA Neurology|December 16, 2024
Quality Improvement Intervention for Reducing Acute Treatment Times in Ischemic Stroke: A Cluster Randomized Clinical TrialDaniël Hansen, Sanne J den Hartog, Nikki van Leeuwen, et al.
Leukemia|January 31, 2024
Determinants of lenalidomide response with or without erythropoiesis-stimulating agents in myelodysplastic syndromes: the HOVON89 trialA A van de Loosdrecht, E M P Cremers, C Alhan, et al.
Frontiers in Endocrinology|August 28, 2020
Collaboration Around Rare Bone Diseases Leads to the Unique Organizational Incentive of the Amsterdam Bone CenterElisabeth M W Eekhoff, Dimitra Micha, Tymour Forouzanfar, et al.
Cell|November 19, 2016
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex DiseaseWilliam J Astle, Heather Elding, Tao Jiang, et al.
Cell Stem Cell|December 2, 2022
A reference human induced pluripotent stem cell line for large-scale collaborative studiesCaroline B Pantazis, Andrian Yang, Erika Lara, et al.
Human Mutation|May 28, 2019
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classificationMichael T Parsons, Emma Tudini, Hongyan Li, et al.
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