Calpain 3 Is a Rapid-Action, Unidirectional Proteolytic Switch Central to Muscle Remodeling

af de Morrée, Antoine, Lutje Hulsik, David, Impagliazzo, Antonietta, van Haagen, Herman H. H. B. M., de Galan, Paula, van Remoortere, Alexandra, 't Hoen, Peter A. C., van Ommen, GertJan B., Frants, Rune R., van der Maarel, Silvère M.
Udgivet 2010

Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine

af Eising, Else, Shyti, Reinald, ’t Hoen, Peter A. C., Vijfhuizen, Lisanne S., Huisman, Sjoerd M. H., Broos, Ludo A. M., Mahfouz, Ahmed, Reinders, Marcel J. T., Ferrari, Michel D., Tolner, Else A., de Vries, Boukje, van den Maagdenberg, Arn M. J. M.
Udgivet 2016

Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy

af Doorenweerd, Nathalie, Mahfouz, Ahmed, van Putten, Maaike, Kaliyaperumal, Rajaram, t’ Hoen, Peter A. C., Hendriksen, Jos G. M., Aartsma-Rus, Annemieke M., Verschuuren, Jan J. G. M., Niks, Erik H., Reinders, Marcel J. T., Kan, Hermien E., Lelieveldt, Boudewijn P. F.
Udgivet 2017

Author Correction: Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy

af Doorenweerd, Nathalie, Mahfouz, Ahmed, van Putten, Maaike, Kaliyaperumal, Rajaram, t’ Hoen, Peter A. C., Hendriksen, Jos G. M., Aartsma-Rus, Annemieke M., Verschuuren, Jan J. G. M., Niks, Erik H., Reinders, Marcel J. T., Kan, Hermien E., Lelieveldt, Boudewijn P. F.
Udgivet 2018

A SNP panel for identification of DNA and RNA specimens

af Yousefi, Soheil, Abbassi-Daloii, Tooba, Kraaijenbrink, Thirsa, Vermaat, Martijn, Mei, Hailiang, van ‘t Hof, Peter, van Iterson, Maarten, Zhernakova, Daria V., Claringbould, Annique, Franke, Lude, ‘t Hart, Leen M., Slieker, Roderick C., van der Heijden, Amber, de Knijff, Peter, ’t Hoen, Peter A. C.
Udgivet 2018

Optimized Whole Genome Association Scanning for Discovery of HLA Class I-Restricted Minor Histocompatibility Antigens

af Fuchs, Kyra J., Honders, M. Willy, van der Meijden, Edith D., Adriaans, Alwin E., van der Lee, Dyantha I., Pont, Margot J., Monajemi, Ramin, Kielbasa, Szymon M., ’t Hoen, Peter A. C., van Bergen, Cornelis A. M., Falkenburg, J. H. Frederik, Griffioen, Marieke
Udgivet 2020

Towards FAIRification of sensitive and fragmented rare disease patient data: challenges and solutions in European reference network registries

af dos Santos Vieira, Bruna, Bernabé, César H., Zhang, Shuxin, Abaza, Haitham, Benis, Nirupama, Cámara, Alberto, Cornet, Ronald, Le Cornec, Clémence M. A., ’t Hoen, Peter A. C., Schaefer, Franz, van der Velde, K. Joeri, Swertz, Morris A., Wilkinson, Mark D., Jacobsen, Annika, Roos, Marco
Udgivet 2022

Structuring research methods and data with the research object model: genomics workflows as a case study

af Hettne, Kristina M, Dharuri, Harish, Zhao, Jun, Wolstencroft, Katherine, Belhajjame, Khalid, Soiland-Reyes, Stian, Mina, Eleni, Thompson, Mark, Cruickshank, Don, Verdes-Montenegro, Lourdes, Garrido, Julian, de Roure, David, Corcho, Oscar, Klyne, Graham, van Schouwen, Reinout, ‘t Hoen, Peter A C, Bechhofer, Sean, Goble, Carole, Roos, Marco
Udgivet 2014

Skewed X-inactivation is common in the general female population

af Shvetsova, Ekaterina, Sofronova, Alina, Monajemi, Ramin, Gagalova, Kristina, Draisma, Harmen H. M., White, Stefan J., Santen, Gijs W. E., Chuva de Sousa Lopes, Susana M., Heijmans, Bastiaan T., van Meurs, Joyce, Jansen, Rick, Franke, Lude, Kiełbasa, Szymon M., den Dunnen, Johan T., ‘t Hoen, Peter A. C.
Udgivet 2018

Novel Protein-Protein Interactions Inferred from Literature Context

af van Haagen, Herman H. H. B. M., 't Hoen, Peter A. C., Botelho Bovo, Alessandro, de Morrée, Antoine, van Mulligen, Erik M., Chichester, Christine, Kors, Jan A., den Dunnen, Johan T., van Ommen, Gert-Jan B., van der Maarel, Silvère M., Kern, Vinícius Medina, Mons, Barend, Schuemie, Martijn J.
Udgivet 2009

Huntington’s disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer’s disease

af Hensman Moss, Davina J., Flower, Michael D., Lo, Kitty K., Miller, James R. C., van Ommen, Gert-Jan B., ’t Hoen, Peter A. C., Stone, Timothy C., Guinee, Amelia, Langbehn, Douglas R., Jones, Lesley, Plagnol, Vincent, van Roon-Mom, Willeke M. C., Holmans, Peter, Tabrizi, Sarah J.
Udgivet 2017

Transcriptional profiling and biomarker identification reveal tissue specific effects of expanded ataxin-3 in a spinocerebellar ataxia type 3 mouse model

af Toonen, Lodewijk J. A., Overzier, Maurice, Evers, Melvin M., Leon, Leticia G., van der Zeeuw, Sander A. J., Mei, Hailiang, Kielbasa, Szymon M., Goeman, Jelle J., Hettne, Kristina M., Magnusson, Olafur Th., Poirel, Marion, Seyer, Alexandre, ‘t Hoen, Peter A. C., van Roon-Mom, Willeke M. C.
Udgivet 2018

Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference

af Hop, Paul J., Luijk, René, Daxinger, Lucia, van Iterson, Maarten, Dekkers, Koen F., Jansen, Rick, van Meurs, Joyce B. J., ’t Hoen, Peter A. C., Ikram, M. Arfan, van Greevenbroek, Marleen M. J., Boomsma, Dorret I., Slagboom, P. Eline, Veldink, Jan H., van Zwet, Erik W., Heijmans, Bastiaan T.
Udgivet 2020

Annotating Transcriptional Effects of Genetic Variants in Disease‐Relevant Tissue: Transcriptome‐Wide Allelic Imbalance in Osteoarthritic Cartilage

af den Hollander, Wouter, Pulyakhina, Irina, Boer, Cindy, Bomer, Nils, van der Breggen, Ruud, Arindrarto, Wibowo, Couthino de Almeida, Rodrigo, Lakenberg, Nico, Sentner, Thom, Laros, Jeroen F. J., ‘t Hoen, Peter A. C., Slagboom, Eline P. E., Nelissen, Rob G. H. H., van Meurs, Joyce, Ramos, Yolande F. M., Meulenbelt, Ingrid
Udgivet 2019

Tackling the translational challenges of multi-omics research in the realm of European personalised medicine: A workshop report

af Oldoni, Emanuela, Saunders, Gary, Bietrix, Florence, Garcia Bermejo, Maria Laura, Niehues, Anna, ’t Hoen, Peter A. C., Nordlund, Jessica, Hajduch, Marian, Scherer, Andreas, Kivinen, Katja, Pitkänen, Esa, Mäkela, Tomi Pekka, Gut, Ivo, Scollen, Serena, Kozera, Łukasz, Esteller, Manel, Shi, Leming, Ussi, Anton, Andreu, Antonio L., van Gool, Alain J.
Udgivet 2022

Genome-wide identification of directed gene networks using large-scale population genomics data

af Luijk, René, Dekkers, Koen F., van Iterson, Maarten, Arindrarto, Wibowo, Claringbould, Annique, Hop, Paul, Boomsma, Dorret I., van Duijn, Cornelia M., van Greevenbroek, Marleen M. J., Veldink, Jan H., Wijmenga, Cisca, Franke, Lude, ’t Hoen, Peter A. C., Jansen, Rick, van Meurs, Joyce, Mei, Hailiang, Slagboom, P. Eline, Heijmans, Bastiaan T., van Zwet, Erik W.
Udgivet 2018

Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics

af Fest, Jesse, Vijfhuizen, Lisanne S, Goeman, Jelle J, Veth, Olga, Joensuu, Anni, Perola, Markus, Männistö, Satu, Ness-Jensen, Eivind, Hveem, Kristian, Haller, Toomas, Tonisson, Neeme, Mikkel, Kairit, Metspalu, Andres, van Duijn, Cornelia M, Ikram, Arfan, Stricker, Bruno H, Ruiter, Rikje, van Eijck, Casper H J, van Ommen, Gert-Jan B, ʼt Hoen, Peter A C
Udgivet 2019

Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies

af Ayoglu, Burcu, Chaouch, Amina, Lochmüller, Hanns, Politano, Luisa, Bertini, Enrico, Spitali, Pietro, Hiller, Monika, Niks, Eric H, Gualandi, Francesca, Pontén, Fredrik, Bushby, Kate, Aartsma-Rus, Annemieke, Schwartz, Elena, Le Priol, Yannick, Straub, Volker, Uhlén, Mathias, Cirak, Sebahattin, ‘t Hoen, Peter A C, Muntoni, Francesco, Ferlini, Alessandra, Schwenk, Jochen M, Nilsson, Peter, Al-Khalili Szigyarto, Cristina
Udgivet 2014

Brain Transcriptomic Analysis of Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type

af Grand Moursel, Laure, van Roon-Mom, Willeke M. C., Kiełbasa, Szymon M., Mei, Hailiang, Buermans, Henk P. J., van der Graaf, Linda M., Hettne, Kristina M., de Meijer, Emile J., van Duinen, Sjoerd G., Laros, Jeroen F. J., van Buchem, Mark A., ‘t Hoen, Peter A. C., van der Maarel, Silvère M., van der Weerd, Louise
Udgivet 2018

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy

af Spitali, Pietro, Zaharieva, Irina, Bohringer, Stefan, Hiller, Monika, Chaouch, Amina, Roos, Andreas, Scotton, Chiara, Claustres, Mireille, Bello, Luca, McDonald, Craig M., Hoffman, Eric P., Koeks, Zaida, Eka Suchiman, H., Cirak, Sebahattin, Scoto, Mariacristina, Reza, Mojgan, ‘t Hoen, Peter A. C., Niks, Erik H., Tuffery-Giraud, Sylvie, Lochmüller, Hanns, Ferlini, Alessandra, Muntoni, Francesco, Aartsma-Rus, Annemieke
Udgivet 2020