SEMI-AUTOMATED AI BASED ORGAN DELINEATION ON LOW DOSE CT TO FACILITATE PET RADIOTRACER BIODISTRIBUTION MEASUREMENTS by Boellaard, Ronald, de Vries, Bart, van Sluis, Joyce, Pieplenbosch, Simone, Wiegers, Sanne, de Hollander, Marijke, Zijlstra, Josee, Zwezerijnen, Ben

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44 - SEMI-AUTOMATED AI BASED ORGAN DELINEATION ON LOW DOSE CT TO FACILITATE PET RADIOTRACER BIODISTRIBUTION MEASUREMENTS by Boellaard, Ronald, de Vries, Bart, van Sluis, Joyce, Pieplenbosch, Simone, Wiegers, Sanne, de Hollander, Marijke, Zijlstra, Josee, Zwezerijnen, Ben

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Genetically identical twin-pair difference models support the amyloid cascade hypothesis by Coomans, Emma M, Tomassen, Jori, Ossenkoppele, Rik, Tijms, Betty M, Lorenzini, Luigi, ten Kate, Mara, Collij, Lyduine E, Heeman, Fiona, Rikken, Roos M, van der Landen, Sophie M, den Hollander, Marijke E, Golla, Sandeep S V, Yaqub, Maqsood, Windhorst, Albert D, Barkhof, Frederik, Scheltens, Philip, de Geus, Eco J C, Visser, Pieter Jelle, van Berckel, Bart N M, den Braber, Anouk

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Validation of image-derived input function using a long axial field of view PET/CT scanner for two different tracers by Palard-Novello, Xavier, Visser, Denise, Tolboom, Nelleke, Smith, Charlotte L. C., Zwezerijnen, Gerben, van de Giessen, Elsmarieke, den Hollander, Marijke E., Barkhof, Frederik, Windhorst, Albert D., van Berckel, Bart NM, Boellaard, Ronald, Yaqub, Maqsood

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Exome Sequencing and cis-Regulatory Mapping Identify Mutations in MAK, a Gene Encoding a Regulator of Ciliary Length, as a Cause of Retinitis Pigmentosa by Özgül, Rıza Köksal, Siemiatkowska, Anna M., Yücel, Didem, Myers, Connie A., Collin, Rob W.J., Zonneveld, Marijke N., Beryozkin, Avigail, Banin, Eyal, Hoyng, Carel B., van den Born, L. Ingeborgh, Bose, Ron, Shen, Wei, Sharon, Dror, Cremers, Frans P.M., Klevering, B. Jeroen, den Hollander, Anneke I., Corbo, Joseph C.

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Genetically identical twins show comparable tau PET load and spatial distribution by Coomans, Emma M, Tomassen, Jori, Ossenkoppele, Rik, Golla, Sandeep S V, den Hollander, Marijke, Collij, Lyduine E, Weltings, Emma, van der Landen, Sophie, Wolters, Emma E, Windhorst, Albert D, Barkhof, Frederik, de Geus, Eco J C, Scheltens, Philip, Visser, Pieter Jelle, van Berckel, Bart N M, den Braber, Anouk

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Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy by Roosing, Susanne, Lamers, Ideke J.C., de Vrieze, Erik, van den Born, L. Ingeborgh, Lambertus, Stanley, Arts, Heleen H., Boldt, Karsten, de Baere, Elfride, Klaver, Caroline C.W., Coppieters, Frauke, Koolen, David A., Lugtenberg, Dorien, Neveling, Kornelia, van Reeuwijk, Jeroen, Ueffing, Marius, van Beersum, Sylvia E.C., Zonneveld-Vrieling, Marijke N., Peters, Theo A., Hoyng, Carel B., Kremer, Hannie, Hetterschijt, Lisette, Letteboer, Stef J.F., van Wijk, Erwin, Roepman, Ronald, den Hollander, Anneke I., Cremers, Frans P.M.

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Validation and test–retest repeatability performance of parametric methods for [11C]UCB-J PET by Tuncel, Hayel, Boellaard, Ronald, Coomans, Emma M., Hollander-Meeuwsen, Marijke den, de Vries, Erik F. J., Glaudemans, Andor W. J. M., Feltes, Paula Kopschina, García, David Vállez, Verfaillie, Sander C. J., Wolters, Emma E., Sweeney, Steven P., Ryan, J. Michael, Ivarsson, Magnus, Lynch, Berkley A., Schober, Patrick, Scheltens, Philip, Schuit, Robert C., Windhorst, Albert D., De Deyn, Peter P., van Berckel, Bart N. M., Golla, Sandeep S. V.

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High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative of autosomal recessive RP in the Dutch population by Collin, Rob W J, van den Born, L Ingeborgh, Klevering, B Jeroen, de Castro-Miró, Marta, Littink, Karin W, Arimadyo, Kentar, Azam, Maleeha, Yazar, Volkan, Zonneveld, Marijke N, Paun, Codrut C, Siemiatkowska, Anna M, Strom, Tim M, Hehir-Kwa, Jayne Y, Kroes, Hester Y, de Faber, Jan-Tjeerd H N, van Schooneveld, Mary J, Heckenlively, John R, Hoyng, Carel B, den Hollander, Anneke I, Cremers, Frans P M

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A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa by Van Schil, Kristof, Klevering, B Jeroen, Leroy, Bart P, Pott, Jan Willem R, Bandah-Rozenfeld, Dikla, Zonneveld-Vrieling, Marijke N, Sharon, Dror, den Hollander, Anneke I, Cremers, Frans P M, De Baere, Elfride, Collin, Rob W J, van den Born, L Ingeborgh

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Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping by Siemiatkowska, Anna M, Arimadyo, Kentar, Moruz, Luminita M, Astuti, Galuh D N, de Castro-Miro, Marta, Zonneveld, Marijke N, Strom, Tim M, de Wijs, Ilse J, Hoefsloot, Lies H, Faradz, Sultana M H, Cremers, Frans P M, den Hollander, Anneke I, Collin, Rob W J

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Basal Laminar Drusen Caused by Compound Heterozygous Variants in the CFH Gene by Boon, Camiel J.F., Klevering, B. Jeroen, Hoyng, Carel B., Zonneveld-Vrieling, Marijke N., Nabuurs, Sander B., Blokland, Ellen, Cremers, Frans P.M., den Hollander, Anneke I.

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