Showing the latest 461 publications
Publications 201-210 of 461
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SARS-CoV-2 B.1.1.7 sensitivity to mRNA vaccine-elicited, convalescent and monoclonal antibodies
Collier, D., De Marco, A., Ferreira, I., Meng, B., Datir, R., Walls, A., et al.
medRxiv: The Preprint Server for Health Sciences
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SARS-CoV-2 evolution during treatment of chronic infection
Kemp, S., Collier, D., Datir, R., Ferreira, I., Gayed, S., Jahun, A., et al.
Nature
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A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis
Bell, S., Rigas, A., Magnusson, M., Ferkingstad, E., Allara, E., Bjornsdottir, G., et al.
Communications Biology
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Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
Harper, A., Goel, A., Grace, C., Thomson, K., Petersen, S., Xu, X., et al.
Nature Genetics
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Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease
Annear, D., Vandeweyer, G., Elinck, E., Sanchis-Juan, A., French, C., Raymond, L., et al.
Scientific Reports
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Neutrophil specific granule and NETosis defects in gray platelet syndrome
Aarts, C., Downes, K., Hoogendijk, A., Sprenkeler, E., Gazendam, R., Favier, R., et al.
Blood Advances
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A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant
Morange, P., Peiretti, F., Gourhant, L., Proust, C., Soukarieh, O., Pulcrano-Nicolas, A., et al.
PLoS genetics
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A cross-platform approach identifies genetic regulators of human metabolism and health
Lotta, L., Pietzner, M., Stewart, I., Wittemans, L., Li, C., Bonelli, R., et al.
Nature Genetics
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Bayesian Inference Associates Rare KDR Variants with Specific Phenotypes in Pulmonary Arterial Hypertension
Swietlik, E., Greene, D., Zhu, N., Megy, K., Cogliano, M., Rajaram, S., et al.
Circulation. Genomic and Precision Medicine
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Treatment of COVID-19 with remdesivir in the absence of humoral immunity: a case report
Buckland, M., Galloway, J., Fhogartaigh, C., Meredith, L., Provine, N., Bloor, S., et al.
Nature Communications