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Träfflista för sökning "WFRF:(Kelly J A) srt2:(2020-2024)"

Search: WFRF:(Kelly J A) > (2020-2024)

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1.
  • 2021
  • swepub:Mat__t
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  • 2021
  • swepub:Mat__t
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  • Kanai, M, et al. (author)
  • 2023
  • swepub:Mat__t
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  • Glasbey, JC, et al. (author)
  • 2021
  • swepub:Mat__t
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  • Niemi, MEK, et al. (author)
  • 2021
  • swepub:Mat__t
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  • Murari, A., et al. (author)
  • A control oriented strategy of disruption prediction to avoid the configuration collapse of tokamak reactors
  • 2024
  • In: Nature Communications. - 2041-1723 .- 2041-1723. ; 15:1
  • Journal article (peer-reviewed)abstract
    • The objective of thermonuclear fusion consists of producing electricity from the coalescence of light nuclei in high temperature plasmas. The most promising route to fusion envisages the confinement of such plasmas with magnetic fields, whose most studied configuration is the tokamak. Disruptions are catastrophic collapses affecting all tokamak devices and one of the main potential showstoppers on the route to a commercial reactor. In this work we report how, deploying innovative analysis methods on thousands of JET experiments covering the isotopic compositions from hydrogen to full tritium and including the major D-T campaign, the nature of the various forms of collapse is investigated in all phases of the discharges. An original approach to proximity detection has been developed, which allows determining both the probability of and the time interval remaining before an incoming disruption, with adaptive, from scratch, real time compatible techniques. The results indicate that physics based prediction and control tools can be developed, to deploy realistic strategies of disruption avoidance and prevention, meeting the requirements of the next generation of devices.
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10.
  • Blokland, G. A. M., et al. (author)
  • Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
  • 2022
  • In: Biological Psychiatry. - : Elsevier BV. - 0006-3223 .- 1873-2402. ; 91:1, s. 102-117
  • Journal article (peer-reviewed)abstract
    • Background: Sex differences in incidence and/or presentation of schizophrenia (SCZ), major depressive disorder (MDD), and bipolar disorder (BIP) are pervasive. Previous evidence for shared genetic risk and sex differences in brain abnormalities across disorders suggest possible shared sex-dependent genetic risk. Methods: We conducted the largest to date genome-wide genotype-by-sex (G×S) interaction of risk for these disorders using 85,735 cases (33,403 SCZ, 19,924 BIP, and 32,408 MDD) and 109,946 controls from the PGC (Psychiatric Genomics Consortium) and iPSYCH. Results: Across disorders, genome-wide significant single nucleotide polymorphism–by-sex interaction was detected for a locus encompassing NKAIN2 (rs117780815, p = 3.2 × 10−8), which interacts with sodium/potassium-transporting ATPase (adenosine triphosphatase) enzymes, implicating neuronal excitability. Three additional loci showed evidence (p < 1 × 10−6) for cross-disorder G×S interaction (rs7302529, p = 1.6 × 10−7; rs73033497, p = 8.8 × 10−7; rs7914279, p = 6.4 × 10−7), implicating various functions. Gene-based analyses identified G×S interaction across disorders (p = 8.97 × 10−7) with transcriptional inhibitor SLTM. Most significant in SCZ was a MOCOS gene locus (rs11665282, p = 1.5 × 10−7), implicating vascular endothelial cells. Secondary analysis of the PGC-SCZ dataset detected an interaction (rs13265509, p = 1.1 × 10−7) in a locus containing IDO2, a kynurenine pathway enzyme with immunoregulatory functions implicated in SCZ, BIP, and MDD. Pathway enrichment analysis detected significant G×S interaction of genes regulating vascular endothelial growth factor receptor signaling in MDD (false discovery rate-corrected p < .05). Conclusions: In the largest genome-wide G×S analysis of mood and psychotic disorders to date, there was substantial genetic overlap between the sexes. However, significant sex-dependent effects were enriched for genes related to neuronal development and immune and vascular functions across and within SCZ, BIP, and MDD at the variant, gene, and pathway levels. © 2021 Society of Biological Psychiatry
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  • Result 1-10 of 230
Type of publication
journal article (199)
conference paper (13)
research review (12)
other publication (1)
Type of content
peer-reviewed (201)
other academic/artistic (24)
Author/Editor
Fischler, B (17)
Sokal, E (17)
Lacaille, F (16)
Debray, D (16)
Nebbia, G. (15)
Arnell, H (15)
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Kelly, D (15)
Wang, JS (15)
Nicastro, E (15)
Jankowska, I (15)
Kelly, M. (14)
Alam, S (13)
Dezsofi, A (13)
Verkade, HJ (13)
Davies, A (12)
Thompson, RJ (12)
Hompes, R (11)
Tsarkov, P (11)
Kelly, J (11)
Bernabeu, JQ (11)
Martin, J. (10)
Burgess, A (10)
Golda, T (10)
Kumar, S (10)
Garcia, J. (10)
Negoi, I (10)
Kim, KM (10)
Sammour, T (10)
Gonzales, E (10)
Davies, M. (9)
Wang, H. (9)
Campain, N (9)
Davies, RJ (9)
Domingo, S (9)
Kanemitsu, Y (9)
Lakkis, Z (9)
Proud, D (9)
Wilson, M (9)
Smart, NJ (9)
Patel, A (9)
Sayyed, R (9)
Saklani, A (9)
Pellino, G (9)
Price, C (9)
Lyons, A (9)
Kelly, S. (9)
Squires, JE (9)
Gonçalves, C (9)
D'Antiga, L (9)
Wolthuis, A (9)
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University
Karolinska Institutet (123)
University of Gothenburg (38)
Uppsala University (38)
Lund University (34)
Stockholm University (21)
Umeå University (18)
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Linköping University (10)
Chalmers University of Technology (7)
Örebro University (6)
Royal Institute of Technology (5)
Högskolan Dalarna (3)
Swedish University of Agricultural Sciences (3)
Halmstad University (1)
Malmö University (1)
Linnaeus University (1)
Karlstad University (1)
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Language
English (230)
Research subject (UKÄ/SCB)
Medical and Health Sciences (79)
Natural sciences (66)
Engineering and Technology (5)
Social Sciences (5)
Humanities (2)

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