Showing the latest 481 publications
Publications 81-90 of 481
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Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder
Mundy, J., Hübel, C., Adey, B., Davies, H., Davies, M., Coleman, J., et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics: The Official Publication of the International Society of Psychiatric Genetics
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Accelerated waning of the humoral response to COVID-19 vaccines in obesity
van der Klaauw, A., Horner, E., Pereyra-Gerber, P., Agrawal, U., Foster, W., Spencer, S., et al.
Nature Medicine
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Biallelic deleterious germline SH2B3 variants cause a novel syndrome of myeloproliferation and multi-organ autoimmunity
Blombery, P., Pazhakh, V., Albuquerque, A., Maimaris, J., Tu, L., Briones Miranda, B., et al.
EJHaem
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SOX17 Enhancer Variants Disrupt Transcription Factor Binding And Enhancer Inactivity Drives Pulmonary Hypertension
Walters, R., Vasilaki, E., Aman, J., Chen, C., Wu, Y., Liang, O., et al.
Circulation
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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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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