Showing the latest 455 publications
Publications 91-100 of 455
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Non-Mendelian inheritance patterns and extreme deviation rates of CGG repeats in autism
Annear, D., Vandeweyer, G., Sanchis-Juan, A., Raymond, F., Kooy, R.
Genome Research
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Hospitalisation for COVID-19 predicts long lasting cerebrovascular impairment: A prospective observational cohort study
Tsvetanov, K., Spindler, L., Stamatakis, E., Newcombe, V., Lupson, V., Chatfield, D., et al.
NeuroImage. Clinical
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Demographic, behavioural and occupational risk factors associated with SARS-CoV-2 infection in UK healthcare workers: a retrospective observational study
Cooper, D., Lear, S., Sithole, N., Shaw, A., Stark, H., Ferris, M., et al.
BMJ open
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A Case of Thrombotic Microangiopathy and Acute Sarcoidosis
Martinelli, A., Dunn, W., McClure, M., Walker, I., Stewart, A., Karia, S., et al.
Chest
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Distinction of early complement classical and lectin pathway activation via quantification of C1s/C1-INH and MASP-1/C1-INH complexes using novel ELISAs
Hurler, L., Toonen, E., Kajdácsi, E., van Bree, B., Brandwijk, R., de Bruin, W., et al.
Frontiers in Immunology
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CO-CONNECT: A hybrid architecture to facilitate rapid discovery and access to UK wide data in the response to the COVID-19 pandemic
Jefferson, E., Cole, C., Mumtaz, S., Cox, S., Giles, T., Adejumo, S., et al.
Journal of Medical Internet Research
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Risk and protective factors for new-onset binge eating, low weight, and self-harm symptoms in >35,000 individuals in the UK during the COVID-19 pandemic
Davies, H., Hübel, C., Herle, M., Kakar, S., Mundy, J., Peel, A., et al.
The International Journal of Eating Disorders
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Improvement of large copy number variant detection by whole genome nanopore sequencing
Cuenca-Guardiola, J., de la Morena-Barrio, B., García, J., Sanchis-Juan, A., Corral, J., Fernández-Breis, J.
Journal of Advanced Research
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The compound effect of irradiation and familial pseudohyperkalemia on potassium leak from red blood cells
Meli, A., Linger, R., Stevens-Hernandez, C., Gyongyver, G., Marks, D., Aung, H., et al.
Transfusion
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Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype
Jurkute, N., Cancellieri, F., Pohl, L., Li, C., Heaton, R., Reurink, J., et al.
NPJ genomic medicine