Showing the latest 475 publications
Publications 361-370 of 475
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Human blood Tfr cells are indicators of ongoing humoral activity not fully licensed with suppressive function
Fonseca, V., Agua-Doce, A., Maceiras, A., Pierson, W., Ribeiro, F., Romão, V., et al.
Science Immunology
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Genetic variation at the CD28 locus and its impact on expansion of pro-inflammatory CD28 negative T cells in healthy individuals
Liaskou, E., Jeffery, L., Chanouzas, D., Soskic, B., Seldin, M., Harper, L., et al.
Scientific Reports
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Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locus
Cipriani, V., Silva, R., Arno, G., Pontikos, N., Kalhoro, A., Valeina, S., et al.
Scientific Reports
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The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability
Singh, T., Walters, J., Johnstone, M., Curtis, D., Suvisaari, J., Torniainen, M., et al.
Nature Genetics
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ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients
Carecchio, M., Mencacci, N., Iodice, A., Pons, R., Panteghini, C., Zorzi, G., et al.
Parkinsonism & Related Disorders
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Platelet function is modified by common sequence variation in megakaryocyte super enhancers
Petersen, R., Lambourne, J., Javierre, B., Grassi, L., Kreuzhuber, R., Ruklisa, D., et al.
Nature Communications
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The effect of variation in donor platelet function on transfusion outcome: a semirandomized controlled trial
Kelly, A., Garner, S., Foukaneli, T., Godec, T., Herbert, N., Kahan, B., et al.
Blood
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A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases
Greene, D., Richardson, S., Turro, E.
American Journal of Human Genetics
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HGVA: the Human Genome Variation Archive
Lopez, J., Coll, J., Haimel, M., Kandasamy, S., Tarraga, J., Furio-Tari, P., et al.
Nucleic Acids Research
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CMV immune evasion and manipulation of the immune system with aging
Jackson, S., Redeker, A., Arens, R., van Baarle, D., van den Berg, S., Benedict, C., et al.
GeroScience