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  1. Berghaus, Günter [Contributor]; Berghaus, Günter [Editor]; Biasiolo, Monica [Contributor]; Biryukov, Sergey [Contributor]; Blejer, Daniella [Contributor]; Braga, Duarte Drumond [Contributor]; Bury, Stephen J. [Contributor]; Carli, Maddalena [Contributor]; Chirico, Mariateresa [Contributor]; Cioli, Monica [Contributor]; Coronelli, Giacomo [Contributor]; Dorotinsky, Deborah [Contributor]; Eder, Rita [Contributor]; Hunkeler, Thomas [Contributor]; Lazareva, Ekaterina [Contributor]; Mancebo Roca, Juan Agustín [Contributor]; Müller, Larissa Maria [Contributor]; Ostashevsky, Eugene [Contributor]; O’Grady, Deirdre [Contributor]; Pfeifer, Kasper [Contributor]; Rossomakhin, Andrey [Contributor]; Silverman, Renée M. [Contributor]; Subotić, Irina [Contributor]; Van Dijck, Cedric [Contributor]; [...]

    International Yearbook of Futurism Studies : Volume 12, 2022 - [mit 43 sw-Abb]

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    Berlin; Boston: De Gruyter, 2022

    Published in: International Yearbook of Futurism Studies ; Volume 12

  4. Apollinaire, Guillaume; Van Dijck, Cedric

    Curiosities from the Front

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    Modern Language Association (MLA), 2019

    Published in: Publications of the Modern Language Association of America, 134 (2019) 3, Seite 555-561

  8. Theys, Claudia; Vanderhaeghen, Tineke; Van Dijck, Evelien; Peleman, Cedric; Scheepers, Anne; Ibrahim, Joe; Mateiu, Ligia; Timmermans, Steven; Vanden Berghe, Tom; Francque, Sven M.; Van Hul, Wim; Libert, Claude; Vanden Berghe, Wim

    Loss of PPARα function promotes epigenetic dysregulation of lipid homeostasis driving ferroptosis and pyroptosis lipotoxicity in metabolic dysfunction associated Steatotic liver disease (MASLD)

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    Frontiers Media SA, 2024

    Published in: Frontiers in Molecular Medicine, 3 (2024)

  9. Jønch, Aia Elise; Douard, Elise; Moreau, Clara; Van Dijck, Anke; Passeggeri, Marzia; Kooy, Frank; Puechberty, Jacques; Campbell, Carolyn; Sanlaville, Damien; Lefroy, Henrietta; Richetin, Sonia; Pain, Aurelie; Geneviève, David; Kini, Usha; Le Caignec, Cédric; Lespinasse, James; Skytte, Anne-Bine; Isidor, Bertrand; Zweier, Christiane; Caberg, Jean-Hubert; Delrue, Marie-Ange; Møller, Rikke Steensbjerre; Bojesen, Anders; Hjalgrim, Helle; [...]

    Estimating the effect size of the 15Q11.2 BP1–BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice

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    BMJ, 2019

    Published in: Journal of Medical Genetics, 56 (2019) 10, Seite 701-710

  10. Pizzo, Lucilla; Jensen, Matthew; Polyak, Andrew; Rosenfeld, Jill A.; Mannik, Katrin; Krishnan, Arjun; McCready, Elizabeth; Pichon, Olivier; Le Caignec, Cedric; Van Dijck, Anke; Pope, Kate; Voorhoeve, Els; Yoon, Jieun; Stankiewicz, Paweł; Cheung, Sau Wai; Pazuchanics, Damian; Huber, Emily; Kumar, Vijay; Kember, Rachel L.; Mari, Francesca; Curró, Aurora; Castiglia, Lucia; Galesi, Ornella; Avola, Emanuela; [...]

    Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

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    Elsevier BV, 2019

    Published in: Genetics in Medicine, 21 (2019) 4, Seite 816-825