Showing the latest 437 publications
Publications 201-210 of 437
-
Combined Point-of-Care Nucleic Acid and Antibody Testing for SARS-CoV-2 following Emergence of D614G Spike Variant
Mlcochova, P., Collier, D., Ritchie, A., Assennato, S., Hosmillo, M., Goel, N., et al.
Cell Reports. Medicine
-
Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease
Khan, M., Arno, G., Fakin, A., Parfitt, D., Dhooge, P., Albert, S., et al.
Molecular Therapy. Nucleic Acids
-
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Vuckovic, D., Bao, E., Akbari, P., Lareau, C., Mousas, A., Jiang, T., et al.
Cell
-
A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis
Schiff, E., Daich Varela, M., Robson, A., Pierpoint, K., Ba-Abbad, R., Nutan, S., et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
-
Differential IRF8 Transcription Factor Requirement Defines Two Pathways of Dendritic Cell Development in Humans
Cytlak, U., Resteu, A., Pagan, S., Green, K., Milne, P., Maisuria, S., et al.
Immunity
-
Development and validation of a universal blood donor genotyping platform: a multinational prospective study
Gleadall, N., Veldhuisen, B., Gollub, J., Butterworth, A., Ord, J., Penkett, C., et al.
Blood Advances
-
A thermostable, closed SARS-CoV-2 spike protein trimer
Xiong, X., Qu, K., Ciazynska, K., Hosmillo, M., Carter, A., Ebrahimi, S., et al.
Nature Structural & Molecular Biology
-
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans
Wei, W., Pagnamenta, A., Gleadall, N., Sanchis-Juan, A., Stephens, J., Broxholme, J., et al.
Nature Communications
-
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Sims, M., Mayer, L., Collins, J., Bariana, T., Megy, K., Lavenu-Bombled, C., et al.
Blood
-
Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes
Ormondroyd, E., Harper, A., Thomson, K., Mackley, M., Martin, J., Penkett, C., et al.
European journal of human genetics: EJHG