Showing the latest 543 publications
Publications 141-150 of 543
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Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension
Postma, A., Rapp, C., Knoflach, K., Volk, A., Lemke, J., Ackermann, M., et al.
Genetics in Medicine Open
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Regulation of immune responses in primary biliary cholangitis: a transcriptomic analysis of peripheral immune cells
Mulcahy, V., Liaskou, E., Martin, J., Kotagiri, P., Badrock, J., Jones, R., et al.
Hepatology Communications
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An atlas of genetic scores to predict multi-omic traits
Xu, Y., Ritchie, S., Liang, Y., Timmers, P., Pietzner, M., Lannelongue, L., et al.
Nature
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Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups
Hurler, L., Szilágyi, Á., Mescia, F., Bergamaschi, L., Mező, B., Sinkovits, G., et al.
Frontiers in Immunology
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The Impact of COVID-19 Lockdown on Adults with Major Depressive Disorder from Catalonia: A Decentralized Longitudinal Study
Lavalle, R., Condominas, E., Haro, J., Giné-Vázquez, I., Bailon, R., Laporta, E., et al.
International Journal of Environmental Research and Public Health
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B lymphocyte responses in Parkinson's disease and their possible significance in disease progression
Scott, K., Chong, Y., Park, S., Wijeyekoon, R., Hayat, S., Mathews, R., et al.
Brain Communications
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Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
Sharma, M., Leung, D., Momenilandi, M., Jones, L., Pacillo, L., James, A., et al.
The Journal of Experimental Medicine
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The common IL1A single nucleotide polymorphism rs17561 is a hypomorphic mutation that significantly reduces interleukin-1α release from human blood cells
Wiggins, K., Pyrillou, K., Humphry, M., Butterworth, A., Clarke, M.
Immunology
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Prevalence of CFTR variants in PID patients with bronchiectasis - an important modifying co-factor
Lawless, D., Allen, H., Thaventhiran, J., Goddard, S., Burren, O., Robson, E., et al.
The Journal of Allergy and Clinical Immunology
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Escape from X-inactivation in twins exhibits intra- and inter-individual variability across tissues and is heritable
Zito, A., Roberts, A., Visconti, A., Rossi, N., Andres-Ejarque, R., Nardone, S., et al.
PLoS genetics