Back

dr. M. (Magdaléna) Harakalová

dr. M. (Magdaléna) Harakalová

Assistant Professor

Show full profile

Research Output (73)

Genotype-specific pathogenic effects in human dilated cardiomyopathy

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 24 Apr 2017, In: Journal of Physiology (London). 595 , p. 4677-4693 17 p.

Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization

Haitjema Saskia, Meddens Claartje A., Van Der Laan Sander W., Kofink Daniel, Harakalova Magdalena, Tragante Vinicius, Foroughi Asl Hassan, Van Setten Jessica, Brandt Maarten M., Bis Joshua C., O'Donnell Christopher, Cheng Caroline, Hoefer Imo E., Waltenberger Johannes, Biessen Erik A L, Jukema J. Wouter, Doevendans Pieter A.F.M., Nieuwenhuis Edward E.S., Erdmann Jeanette, Björkegren Johan L M, Pasterkamp Gerard, Asselbergs Folkert W., Den Ruijter Hester M., Mokry Michal 1 Apr 2017, In: Circulation-Cardiovascular genetics. 10

Cardiorenal disease connection during post-menopause:The protective role of estrogen in uremic toxins induced microvascular dysfunction

Pei Jiayi, Harakalova Magdalena, den Ruijter Hester, Pasterkamp Gerard, Duncker Dirk J., Verhaar Marianne C., Asselbergs Folkert W., Cheng Caroline 2017, In: International Journal of Cardiology. 238 , p. 22-30 9 p.

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

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 30 Nov 2016, In: Genome Biology. 17

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

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 Isaäc 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 Aug 2016, In: Journal of Clinical Investigation. 126 , p. 2881-2892

Characteristic adaptations of the extracellular matrix in dilated cardiomyopathy

Louzao-Martinez Laura, Vink Aryan, Harakalova Magdalena, Asselbergs Folkert W, Verhaar Marianne C, Cheng Caroline 27 Jun 2016, In: International Journal of Cardiology. 220 , p. 634-646 13 p.

Heterozygous KIDINS220/ARMS nonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity

Josifova Dragana J, Monroe Glen R, Tessadori Federico, de Graaff Esther, van der Zwaag Bert, Mehta Sarju G, Harakalova Magdalena, Duran Karen J, Savelberg Sanne M C, Nijman Isaäc J, Jungbluth Heinz, Hoogenraad Casper C, Bakkers Jeroen, Knoers Nine V, Firth Helen V, Beales Philip L, van Haaften Gijs, van Haelst Mieke M, Mar 2016, In: Human Molecular Genetics. 25 , p. 2158-2167

Joubert syndrome:Genotyping a Northern European patient cohort

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 V A M, van Haaften Gijs 1 Feb 2016, In: European Journal of Human Genetics. 24 , p. 214-220 7 p.

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

Surendran Praveen, Drenos Fotios, Young Robin, Warren Helen, Cook James P, Manning Alisa K, Grarup Niels, Sim Xueling, Barnes Daniel R, Witkowska Kate, Staley James R, Tragante Vinicius, Tukiainen Taru, Yaghootkar Hanieh, Masca Nicholas, Freitag Daniel F, Ferreira Teresa, Giannakopoulou Olga, Tinker Andrew, Harakalova Magdalena, Mihailov Evelin, Liu Chunyu, Kraja Aldi T, Nielsen Sune Fallgaard, Rasheed Asif, Samuel Maria, Zhao Wei, Bonnycastle Lori L, Jackson Anne U, Narisu Narisu, Swift Amy J, Southam Lorraine, Marten Jonathan, Huyghe Jeroen R, Stančáková Alena, Fava Cristiano, Ohlsson Therese, Matchan Angela, Stirrups Kathleen E, Bork-Jensen Jette, Gjesing Anette P, Kontto Jukka, Perola Markus, Shaw-Hawkins Susan, Havulinna Aki S, Zhang He, Donnelly Louise A, de Bakker Paul I W, Numans Mattijs E, Asselbergs Folkert W, 2016, In: Nature Genetics. 48 , p. 1151-1161 11 p.

Extensive Association of Common Disease Variants with Regulatory Sequence

Mokry Michal, Harakalova Magdalena, Asselbergs Folkert W, de Bakker Paul I W, Nieuwenhuis Edward E S 2016, In: PLoS ONE [E]. 11

Thank you for your review!

Has this information helped you?

Please tell us why, so that we can improve our website.

Working at UMC Utrecht

Contact

Emergency?

Directions

Appointments

Practical

umcutrecht.nl uses cookies

This website uses cookies This website displays videos from, among others, YouTube. Such parties place cookies (third-party cookies). If you do not want these cookies, you can indicate that here. We also place cookies ourselves to improve our site.

Read more about the cookie policy

Agree No, rather not