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  5. Calame, Ingrid [Artist]; Fraser, Pamela [Artist]; Gjerdevik, Nils Erik [Artist]; Henning, Anton [Artist]; Herrera, Arturo [Artist]; Majerus, Michel [Artist]; Morrison, Paul [Artist]; Murakami, Takashi [Artist]; Ostendarp, Carl [Artist]; Prieto, Monique [Artist]; Rae, Fiona [Artist]; Reeves, Jennifer [Artist] ; Christofori, Ralf [Editor]; Steiner, Gerda [Other]; Treder, Klaus-Martin [Other] Württembergischer Kunstverein, Städtische Ausstellungshalle Am Hawerkamp Münster (Westf), Ausstellung Colour Me Blind! 1999 - 2000 Stuttgart; Münster, Westfalen

    Colour me blind! : Malerei in Zeiten von Computergame und Comic ; Ingrid Calame, Pamela Fraser, Nils Erik Gjerdevik, Anton Henning, Arturo Herrera, Michel Majerus, Paul Morrison, Takashi Murakami, Carl Ostendarp, Monique Prieto, Fiona Rae, Jennifer Reeves, Gerda Steiner, Klaus-Martin Treder

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    Köln: König [u.a.], 1999

  6. de Costa, Dominique; Broodman, Ingrid; Calame, Wim; Stingl, Christoph; Dekker, Lennard J. M.; Vernhout, René M.; de Koning, Harry J.; Hoogsteden, Henk C.; Smitt, Peter A. E. Sillevis.; van Klaveren, Rob J.; Luider, Theo M.; VanDuijn, Martijn M.

    Peptides from the Variable Region of Specific Antibodies Are Shared among Lung Cancer Patients

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    Public Library of Science (PLoS), 2014

    Published in: PLoS ONE

  7. Porbahaie, Mojtaba; van den Belt, Maartje; Ulfman, Laurien; Ruijschop, Rianne M. A. J.; Lucas–van de Bos, Elly; Hartog, Anita; Lenz, Stefanie; van Alen-Boerrigter, Ingrid J.; Teodorowicz, Malgorzata; Savelkoul, Huub F. J.; Calame, Wim; van Hoffen, Els; van Neerven, R. J. Joost; Kardinaal, Alwine

    Low doses of diarrhoeagenic E. coli induce enhanced monocyte and mDC responses and prevent development of symptoms after homologous rechallenge

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    Public Library of Science (PLoS), 2023

    Published in: PLOS ONE

  8. Dong, Xiaomin; Tan, Natalie B.; Howell, Katherine B.; Barresi, Sabina; Freeman, Jeremy L.; Vecchio, Davide; Piccione, Maria; Radio, Francesca Clementina; Calame, Daniel; Zong, Shan; Eggers, Stefanie; Scheffer, Ingrid E.; Tan, Tiong Y.; Van Bergen, Nicole J.; Tartaglia, Marco; Christodoulou, John; White, Susan M.

    Bi-allelic LoF NRROS Variants Impairing Active TGF-β1 Delivery Cause a Severe Infantile-Onset Neurodegenerative Condition with Intracranial Calcification

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    Elsevier BV, 2020

    Published in: The American Journal of Human Genetics

  9. Bogaert, Elke; Garde, Aurore; Gautier, Thierry; Rooney, Kathleen; Duffourd, Yannis; LeBlanc, Pontus; van Reempts, Emma; Tran Mau-Them, Frederic; Wentzensen, Ingrid M.; Au, Kit Sing; Richardson, Kate; Northrup, Hope; Gatinois, Vincent; Geneviève, David; Louie, Raymond J.; Lyons, Michael J.; Laulund, Lone Walentin; Brasch-Andersen, Charlotte; Maxel Juul, Trine; El It, Fatima; Marle, Nathalie; Callier, Patrick; Relator, Raissa; Haghshenas, Sadegheh; [...]

    SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability

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    Elsevier BV, 2023

    Published in: The American Journal of Human Genetics

  10. Baxter, Samantha M.; Posey, Jennifer E.; Lake, Nicole J.; Sobreira, Nara; Chong, Jessica X.; Buyske, Steven; Blue, Elizabeth E.; Chadwick, Lisa H.; Coban-Akdemir, Zeynep H.; Doheny, Kimberly F.; Davis, Colleen P.; Lek, Monkol; Wellington, Christopher; Jhangiani, Shalini N.; Gerstein, Mark; Gibbs, Richard A.; Lifton, Richard P.; MacArthur, Daniel G.; Matise, Tara C.; Lupski, James R.; Valle, David; Bamshad, Michael J.; Hamosh, Ada; Mane, Shrikant; [...]

    Centers for Mendelian Genomics: A decade of facilitating gene discovery

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    Elsevier BV, 2022

    Published in: Genetics in Medicine

  11. Mao, Dongxue; Reuter, Chloe M.; Ruzhnikov, Maura R.Z.; Beck, Anita E.; Farrow, Emily G.; Emrick, Lisa T.; Rosenfeld, Jill A.; Mackenzie, Katherine M.; Robak, Laurie; Wheeler, Matthew T.; Burrage, Lindsay C.; Jain, Mahim; Liu, Pengfei; Calame, Daniel; Küry, Sébastien; Sillesen, Martin; Schmitz-Abe, Klaus; Tonduti, Davide; Spaccini, Luigina; Iascone, Maria; Genetti, Casie A.; Koenig, Mary K.; Graf, Madeline; Tran, Alyssa; [...]

    De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

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    Elsevier BV, 2020

    Published in: The American Journal of Human Genetics