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drs. M.K. (Mark) Bakker

drs. M.K. (Mark) Bakker

Researcher/Postdoc
drs. M.K. (Mark) Bakker
  • Neurology & Neurosurgery

Research Output (17)

Author Correction:Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

van Rheenen Wouter, van der Spek Rick A A, Bakker Mark K, van Vugt Joke J F A, Hop Paul J, Zwamborn Ramona A J, de Klein Niek, Westra Harm-Jan, Bakker Olivier B, Deelen Patrick, Shireby Gemma, Hannon Eilis, Moisse Matthieu, Baird Denis, Restuadi Restuadi, Dolzhenko Egor, Dekker Annelot M, Gawor Klara, Westeneng Henk-Jan, Tazelaar Gijs H P, van Eijk Kristel R, Kooyman Maarten, Byrne Ross P, Doherty Mark, Heverin Mark, Al Khleifat Ahmad, Iacoangeli Alfredo, Shatunov Aleksey, Ticozzi Nicola, Cooper-Knock Johnathan, Smith Bradley N, Gromicho Marta, Chandran Siddharthan, Pal Suvankar, Morrison Karen E, Shaw Pamela J, Hardy John, Orrell Richard W, Sendtner Michael, Meyer Thomas, Başak Nazli, van der Kooi Anneke J, Ratti Antonia, Ophoff Roel A, van Es Michael A, Pasterkamp R Jeroen, McLaughlin Russell L, Kenna Kevin P, van den Berg Leonard H, Veldink Jan H, 2022, In: Nature Genetics. 54 , p. 361-361 1 p.

Genome-wide linkage analysis combined with genome sequencing in large families with intracranial aneurysms

Bakker Mark K., Cobyte Suze, Hennekam Frederic A.M., Rinkel Gabriel J.E., Veldink Jan H., Ruigrok Ynte M. 2022, In: European Journal of Human Genetics. 30 , p. 833-840 8 p.

Genome-Wide Association Study of Clinical Outcome After Aneurysmal Subarachnoid Haemorrhage:Protocol

Gaastra Ben, Alexander Sheila, Bakker Mark K., Bhagat Hemant, Bijlenga Philippe, Blackburn Spiros, Collins Malie K., Doré Sylvain, Griessenauer Christoph, Hendrix Philipp, Hong Eun Pyo, Hostettler Isabel C., Houlden Henry, IIhara Koji, Jeon Jin Pyeong, Kim Bong Jun, Kumar Munish, Morel Sandrine, Nyquist Paul, Ren Dianxu, Ruigrok Ynte M., Werring David, Galea Ian, Bulters Diederik, Tapper Will 2022, In: Translational Stroke Research. 13 , p. 565-576 12 p.

Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

Georges Adrien, Yang Min Lee, Berrandou Takiy Eddine, Bakker Mark K., Dikilitas Ozan, Kiando Soto Romuald, Ma Lijiang, Satterfield Benjamin A., Sengupta Sebanti, Yu Mengyao, Deleuze Jean François, Dupré Delia, Hunker Kristina L., Kyryachenko Sergiy, Liu Lu, Sayoud-Sadeg Ines, Amar Laurence, Brummett Chad M., Coleman Dawn M., d'Escamard Valentina, de Leeuw Peter, Fendrikova-Mahlay Natalia, Kadian-Dodov Daniella, Li Jun Z., Lorthioir Aurélien, Pappaccogli Marco, Prejbisz Aleksander, Smigielski Witold, Stanley James C., Zawistowski Matthew, Zhou Xiang, Zöllner Sebastian, Amouyel Philippe, De Buyzere Marc L., Debette Stéphanie, Dobrowolski Piotr, Drygas Wojciech, Gornik Heather L., Olin Jeffrey W., Piwonski Jerzy, Rietzschel Ernst R., Ruigrok Ynte M., Vikkula Miikka, Warchol Celinska Ewa, Januszewicz Andrzej, Kullo Iftikhar J., Azizi Michel, Jeunemaitre Xavier, Persu Alexandre, Kovacic Jason C., , , Dec 2021, In: Nature Communications. 12 , p. 1-16 1 p.

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

van Rheenen Wouter, van der Spek Rick A A, Bakker Mark K, van Vugt Joke J F A, Hop Paul J, Zwamborn Ramona A J, de Klein Niek, Westra Harm-Jan, Bakker Olivier B, Deelen Patrick, Shireby Gemma, Hannon Eilis, Moisse Matthieu, Baird Denis, Restuadi Restuadi, Dolzhenko Egor, Dekker Annelot M, Gawor Klara, Westeneng Henk-Jan, Tazelaar Gijs H P, van Eijk Kristel R, Kooyman Maarten, Byrne Ross P, Doherty Mark, Heverin Mark, Al Khleifat Ahmad, Iacoangeli Alfredo, Shatunov Aleksey, Ticozzi Nicola, Cooper-Knock Johnathan, Smith Bradley N, Gromicho Marta, Chandran Siddharthan, Pal Suvankar, Morrison Karen E, Shaw Pamela J, Hardy John, Orrell Richard W, Sendtner Michael, Meyer Thomas, Başak Nazli, van der Kooi Anneke J, Ratti Antonia, Ophoff Roel A, van Es Michael A, Pasterkamp R Jeroen, McLaughlin Russell L, Kenna Kevin P, van den Berg Leonard H, Veldink Jan H, Dec 2021, In: Nature Genetics. 53 , p. 1636-1648 13 p.

Modifiable risk factors for intracranial aneurysm and aneurysmal subarachnoid hemorrhage:A mendelian randomization study

Karhunen Ville, Bakker Mark K., Ruigrok Ynte M., Gill Dipender, Larsson Susanna C. 16 Nov 2021, In: Journal of the American Heart Association. 10 , p. 1-8 8 p.

Role of Rare Genetic Variants Found in Families with Intracranial Aneurysms in the General Dutch and UK Population

Bakker Mark K., Ettema Roos A., Klostermann Maxime, Rinkel Gabriël J.E., Veldink Jan H., Ruigrok Ynte M. Sep 2021, In: Stroke. 52 , p. E540-E541

Genetics of Intracranial Aneurysms

Bakker Mark K., Ruigrok Ynte M. 2021, In: Stroke. 52 , p. 3004-3012 9 p.

Genetic basis of lacunar stroke:a pooled analysis of individual patient data and genome-wide association studies

Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K., Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J., Griessenauer Christoph J., Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P., Lindgren Arne, Meschia James F., Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D., Kittner Steven J., Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M., Anderson Christopher D., Wardlaw Joanna, Lewis Cathryn M., Markus Hugh S., , , , 2021, In: The Lancet Neurology. 20 , p. 351-361 11 p.

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