Extensive Association of Common Disease Variants with Regulatory Sequence

od Mokry, Michal, Harakalova, Magdalena, Asselbergs, Folkert W., de Bakker, Paul I. W., Nieuwenhuis, Edward E. S.
Wydane w PLoS One (2016)

Genomic DNA Pooling Strategy for Next-Generation Sequencing-Based Rare Variant Discovery in Abdominal Aortic Aneurysm Regions of Interest—Challenges and Limitations

od Harakalova, Magdalena, Nijman, Isaäc J., Medic, Jelena, Mokry, Michal, Renkens, Ivo, Blankensteijn, Jan D., Kloosterman, Wigard, Baas, Annette F., Cuppen, Edwin
Wydane 2011

Indoxyl Sulfate Stimulates Angiogenesis by Regulating Reactive Oxygen Species Production via CYP1B1

od Pei, Jiayi, Juni, Rio, Harakalova, Magdalena, Duncker, Dirk J., Asselbergs, Folkert W., Koolwijk, Pieter, van Hinsbergh, Victor, Verhaar, Marianne C., Mokry, Michal, Cheng, Caroline
Wydane w Toxins (Basel) (2019)

Genotype‐specific pathogenic effects in human dilated cardiomyopathy

od Bollen, Ilse A. E., Schuldt, Maike, Harakalova, Magdalena, Vink, Aryan, Asselbergs, Folkert W., Pinto, Jose R., Krüger, Martina, Kuster, Diederik W. D., van der Velden, Jolanda
Wydane w J Physiol (2017)

A comparison of two workflows for regulome and transcriptome-based prioritization of genetic variants associated with myocardial mass

od Manduchi, Elisabetta, Hemerich, Daiane, van Setten, Jessica, Tragante, Vinicius, Harakalova, Magdalena, Pei, Jiayi, Williams, Scott M., van der Harst, Pim, Asselbergs, Folkert W., Moore, Jason H.
Wydane w Genet Epidemiol (2019)

Metabolomics in Severe Aortic Stenosis Reveals Intermediates of Nitric Oxide Synthesis as Most Distinctive Markers

od van Driel, Beau Olivier, Schuldt, Maike, Algül, Sila, Levin, Evgeni, Güclü, Ahmet, Germans, Tjeerd, van Rossum, Albert C., Pei, Jiayi, Harakalova, Magdalena, Baas, Annette, Jans, Judith J. M., van der Velden, Jolanda
Wydane w Int J Mol Sci (2021)

Systematic analysis of chromatin interactions at disease associated loci links novel candidate genes to inflammatory bowel disease

od Meddens, Claartje A., Harakalova, Magdalena, van den Dungen, Noortje A. M., Foroughi Asl, Hassan, Hijma, Hemme J., Cuppen, Edwin P. J. G., Björkegren, Johan L. M., Asselbergs, Folkert W., Nieuwenhuis, Edward E. S., Mokry, Michal
Wydane w Genome Biol (2016)

P62‐positive aggregates are homogenously distributed in the myocardium and associated with the type of mutation in genetic cardiomyopathy

od van der Klooster, Zoë Joy, Sepehrkhouy, Shahrzad, Dooijes, Dennis, te Rijdt, Wouter P., Schuiringa, Frederique S. A. M., Lingeman, Jolanthe, van Tintelen, Johannes Peter, Harakalova, Magdalena, Goldschmeding, Roel, Suurmeijer, Albert J. H., Asselbergs, Folkert W., Vink, Aryan
Wydane w J Cell Mol Med (2021)

Joubert syndrome: genotyping a Northern European patient cohort

od Kroes, Hester Y, Monroe, Glen R, van der Zwaag, Bert, Duran, Karen J, de Kovel, Carolien G, van Roosmalen, Mark J, Harakalova, Magdalena, Nijman, Ies J, Kloosterman, Wigard P, Giles, Rachel H, Knoers, Nine VAM, van Haaften, Gijs
Wydane w Eur J Hum Genet (2016)

High Resolution Systematic Digital Histological Quantification of Cardiac Fibrosis and Adipose Tissue in Phospholamban p.Arg14del Mutation Associated Cardiomyopathy

od Gho, Johannes M. I. H., van Es, René, Stathonikos, Nikolas, Harakalova, Magdalena, te Rijdt, Wouter P., Suurmeijer, Albert J. H., van der Heijden, Jeroen F., de Jonge, Nicolaas, Chamuleau, Steven A. J., de Weger, Roel A., Asselbergs, Folkert W., Vink, Aryan
Wydane 2014

Integrative Functional Annotation of 52 Genetic Loci Influencing Myocardial Mass Identifies Candidate Regulatory Variants and Target Genes

od Hemerich, Daiane, Pei, Jiayi, Harakalova, Magdalena, van Setten, Jessica, Boymans, Sander, Boukens, Bas J., Efimov, Igor R., Michels, Michelle, van der Velden, Jolanda, Vink, Aryan, Cheng, Caroline, van der Harst, Pim, Moore, Jason H., Mokry, Michal, Tragante, Vinicius, Asselbergs, Folkert W.
Wydane w Circ Genom Precis Med (2019)

Gene expression profiling of hypertrophic cardiomyocytes identifies new players in pathological remodelling

od Vigil-Garcia, Marta, Demkes, Charlotte J, Eding, Joep E C, Versteeg, Danielle, de Ruiter, Hesther, Perini, Ilaria, Kooijman, Lieneke, Gladka, Monika M, Asselbergs, Folkert W, Vink, Aryan, Harakalova, Magdalena, Bossu, Alexander, van Veen, Toon A B, Boogerd, Cornelis J, van Rooij, Eva
Wydane w Cardiovasc Res (2020)

Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation

od Gregory, Louise C., Ferreira, Carolina B., Young-Baird, Sara K., Williams, Hywel J., Harakalova, Magdalena, van Haaften, Gijs, Rahman, Sofia A., Gaston-Massuet, Carles, Kelberman, Daniel, GOSgene, Qasim, Waseem, Camper, Sally A., Dever, Thomas E., Shah, Pratik, Robinson, Iain C.A.F., Dattani, Mehul T.
Wydane w EBioMedicine (2019)

Massive expansion and cryopreservation of functional human induced pluripotent stem cell-derived cardiomyocytes

od Maas, Renee G.C., Lee, Soah, Harakalova, Magdalena, Snijders Blok, Christian J.B., Goodyer, William R., Hjortnaes, Jesper, Doevendans, Pieter A.F.M., Van Laake, Linda W., van der Velden, Jolanda, Asselbergs, Folkert W., Wu, Joseph C., Sluijter, Joost P.G., Wu, Sean M., Buikema, Jan W.
Wydane w STAR Protoc (2021)

Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus

od Harakalova, Magdalena, van der Smagt, Jasper, de Kovel, Carolien G F, van't Slot, Ruben, Poot, Martin, Nijman, Isaac J, Medic, Jelena, Joziasse, Irene, Deckers, Jaap, Roos-Hesselink, Jolien W, Wessels, Marja W, Baars, Hubert F, Weiss, Marjan M, Pals, Gerard, Golmard, Lisa, Jeunemaitre, Xavier, Lindhout, Dick, Cuppen, Edwin, Baas, Annette F
Wydane 2013

Proteomic and Functional Studies Reveal Detyrosinated Tubulin as Treatment Target in Sarcomere Mutation-Induced Hypertrophic Cardiomyopathy

od Schuldt, Maike, Pei, Jiayi, Harakalova, Magdalena, Dorsch, Larissa M., Schlossarek, Saskia, Mokry, Michal, Knol, Jaco C., Pham, Thang V., Schelfhorst, Tim, Piersma, Sander R., dos Remedios, Cris, Dalinghaus, Michiel, Michels, Michelle, Asselbergs, Folkert W., Moutin, Marie-Jo, Carrier, Lucie, Jimenez, Connie R., van der Velden, Jolanda, Kuster, Diederik W.D.
Wydane w Circ Heart Fail (2021)

Ankyrin repeat and zinc-finger domain-containing 1 mutations are associated with infantile-onset inflammatory bowel disease

od van Haaften-Visser, Désirée Y., Harakalova, Magdalena, Mocholi, Enric, van Montfrans, Joris M., Elkadri, Abdul, Rieter, Ester, Fiedler, Karoline, van Hasselt, Peter M., Triffaux, Emily M. M., van Haelst, Mieke M., Nijman, Isaac J., Kloosterman, Wigard P., Nieuwenhuis, Edward E. S., Muise, Aleixo M., Cuppen, Edwin, Houwen, Roderick H. J., Coffer, Paul J.
Wydane w J Biol Chem (2017)

H3K27ac acetylome signatures reveal the epigenomic reorganization in remodeled non-failing human hearts

od Pei, Jiayi, Harakalova, Magdalena, Treibel, Thomas A., Lumbers, R Thomas, Boukens, Bastiaan J., Efimov, Igor R., van Dinter, Jip T., González, Arantxa, López, Begoña, El Azzouzi, Hamid, van den Dungen, Noortje, van Dijk, Christian G. M., Krebber, Merle M., den Ruijter, Hester M., Pasterkamp, Gerard, Duncker, Dirk J., Nieuwenhuis, Edward E. S., de Weger, Roel, Huibers, Manon M., Vink, Aryan, Moore, Jason H., Moon, James C., Verhaar, Marianne C., Kararigas, Georgios, Mokry, Michal, Asselbergs, Folkert W., Cheng, Caroline
Wydane w Clin Epigenetics (2020)

Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung disease

od van der Crabben, Saskia N., Hennus, Marije P., McGregor, Grant A., Ritter, Deborah I., Nagamani, Sandesh C.S., Wells, Owen S., Harakalova, Magdalena, Chinn, Ivan K., Alt, Aaron, Vondrova, Lucie, Hochstenbach, Ron, van Montfrans, Joris M., Terheggen-Lagro, Suzanne W., van Lieshout, Stef, van Roosmalen, Markus J., Renkens, Ivo, Duran, Karen, Nijman, Isaac J., Kloosterman, Wigard P., Hennekam, Eric, Orange, Jordan S., van Hasselt, Peter M., Wheeler, David A., Palecek, Jan J., Lehmann, Alan R., Oliver, Antony W., Pearl, Laurence H., Plon, Sharon E., Murray, Johanne M., van Haaften, Gijs
Wydane w J Clin Invest (2016)

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

od Garnier, Sophie, Harakalova, Magdalena, Weiss, Stefan, Mokry, Michal, Regitz-Zagrosek, Vera, Hengstenberg, Christian, Cappola, Thomas P, Isnard, Richard, Arbustini, Eloisa, Cook, Stuart A, van Setten, Jessica, Calis, Jorg J A, Hakonarson, Hakon, Morley, Michael P, Stark, Klaus, Prasad, Sanjay K, Li, Jin, O'Regan, Declan P, Grasso, Maurizia, Müller-Nurasyid, Martina, Meitinger, Thomas, Empana, Jean-Philippe, Strauch, Konstantin, Waldenberger, Melanie, Marguiles, Kenneth B, Seidman, Christine E, Kararigas, Georgios, Meder, Benjamin, Haas, Jan, Boutouyrie, Pierre, Lacolley, Patrick, Jouven, Xavier, Erdmann, Jeanette, Blankenberg, Stefan, Wichter, Thomas, Ruppert, Volker, Tavazzi, Luigi, Dubourg, Olivier, Roizes, Gérard, Dorent, Richard, de Groote, Pascal, Fauchier, Laurent, Trochu, Jean-Noël, Aupetit, Jean-François, Bilinska, Zofia T, Germain, Marine, Völker, Uwe, Hemerich, Daiane, Raji, Ibticem, Bacq-Daian, Delphine, Proust, Carole, Remior, Paloma, Gomez-Bueno, Manuel, Lehnert, Kristin, Maas, Renee, Olaso, Robert, Saripella, Ganapathi Varma, Felix, Stephan B, McGinn, Steven, Duboscq-Bidot, Laëtitia, van Mil, Alain, Besse, Céline, Fontaine, Vincent, Blanché, Hélène, Ader, Flavie, Keating, Brendan, Curjol, Angélique, Boland, Anne, Komajda, Michel, Cambien, François, Deleuze, Jean-François, Dörr, Marcus, Asselbergs, Folkert W, Villard, Eric, Trégouët, David-Alexandre, Charron, Philippe
Wydane w Eur Heart J (2021)