Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy
van Waning, Jaap I., Caliskan, Kadir, Hoedemaekers, Yvonne M., van Spaendonck-Zwarts, Karin Y., Baas, Annette F., Boekholdt, S. Matthijs, van Melle, Joost P., Teske, Arco J., Asselbergs, Folkert W., Backx, Ad P.C.M., du Marchie Sarvaas, Gideon J., Dalinghaus, Michiel, Breur, Johannes M.P.J., Linschoten, Marijke P.M., Verlooij, Laura A., Kardys, Isabella, Dooijes, Dennis, Lekanne Deprez, Ronald H., IJpma, Arne S., van den Berg, Maarten P., Hofstra, Robert M.W., van Slegtenhorst, Marjon A., Jongbloed, Jan D.H., Majoor-Krakauer, Danielle
Published in Journal of the American College of Cardiology (20.02.2018)
Published in Journal of the American College of Cardiology (20.02.2018)
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Moderate–severe beta‐thalassemia intermedia phenotype caused by sextuplicated alpha‐globin gene allele in two beta‐thalassemia carriers
Achour, Ahlem, Knijnenburg, Jeroen, Koopmann, Tamara, Raz, Amir, Tischkowitz, Marc, Coates, Thomas D., Baas, F., Harteveld, C. L.
Published in American journal of hematology (01.08.2024)
Published in American journal of hematology (01.08.2024)
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Long-Term Outcome of Open or Endovascular Repair of Abdominal Aortic Aneurysm
De Bruin, Jorg L, Baas, Annette F, Buth, Jaap, Prinssen, Monique, Verhoeven, Eric L.G, Cuypers, Philippe W.M, van Sambeek, Marc R.H.M, Balm, Ron, Grobbee, Diederick E, Blankensteijn, Jan D
Published in The New England journal of medicine (20.05.2010)
Published in The New England journal of medicine (20.05.2010)
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Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring
de Pagter, Mirjam S., van Roosmalen, Markus J., Baas, Annette F., Renkens, Ivo, Duran, Karen J., van Binsbergen, Ellen, Tavakoli-Yaraki, Masoumeh, Hochstenbach, Ron, van der Veken, Lars T., Cuppen, Edwin, Kloosterman, Wigard P.
Published in American journal of human genetics (02.04.2015)
Published in American journal of human genetics (02.04.2015)
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Complete Polarization of Single Intestinal Epithelial Cells upon Activation of LKB1 by STRAD
Baas, Annette F, Kuipers, Jeroen, van der Wel, Nicole N, Batlle, Eduard, Koerten, Henk K, Peters, Peter J, Clevers, Hans C
Published in Cell (06.02.2004)
Published in Cell (06.02.2004)
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CACNA1B mutation is linked to unique myoclonus-dystonia syndrome
Groen, Justus L, Andrade, Arturo, Ritz, Katja, Jalalzadeh, Hamid, Haagmans, Martin, Bradley, Ted E J, Jongejan, Aldo, Verbeek, Dineke S, Nürnberg, Peter, Denome, Sylvia, Hennekam, Raoul C M, Lipscombe, Diane, Baas, Frank, Tijssen, Marina A J
Published in Human molecular genetics (15.02.2015)
Published in Human molecular genetics (15.02.2015)
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Innate and adaptive immunity in amyotrophic lateral sclerosis: Evidence of complement activation
Sta, M, Sylva-Steenland, R.M.R, Casula, M, de Jong, J.M.B.V, Troost, D, Aronica, E, Baas, F
Published in Neurobiology of disease (01.06.2011)
Published in Neurobiology of disease (01.06.2011)
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Deep sequencing of antiviral T-cell responses to HCMV and EBV in humans reveals a stable repertoire that is maintained for many years
Klarenbeek, P L, Remmerswaal, E B M, ten Berge, I J M, Doorenspleet, M E, van Schaik, B D C, Esveldt, R E E, Koch, S D, ten Brinke, A, van Kampen, A H C, Bemelman, F J, Tak, P P, Baas, F, de Vries, N, van Lier, R A W
Published in PLoS pathogens (01.09.2012)
Published in PLoS pathogens (01.09.2012)
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Rheumatoid arthritis synovial tissue harbours dominant B-cell and plasma-cell clones associated with autoreactivity
Doorenspleet, M E, Klarenbeek, P L, de Hair, M J H, van Schaik, B D C, Esveldt, R E E, van Kampen, A H C, Gerlag, D M, Musters, A, Baas, F, Tak, P P, de Vries, N
Published in Annals of the rheumatic diseases (01.04.2014)
Published in Annals of the rheumatic diseases (01.04.2014)
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Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas
Christiaans, I, Kenter, S B, Brink, H C, van Os, T A M, Baas, F, van den Munckhof, P, Kidd, A M J, Hulsebos, T J M
Published in Journal of medical genetics (01.02.2011)
Published in Journal of medical genetics (01.02.2011)
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The unfolded protein response is activated in Alzheimer's disease
Hoozemans, J J M, Veerhuis, R, Van Haastert, E S, Rozemuller, J M, Baas, F, Eikelenboom, P, Scheper, W
Published in Acta neuropathologica (01.08.2005)
Published in Acta neuropathologica (01.08.2005)
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Minocycline for sporadic and hereditary cerebral amyloid angiopathy (BATMAN): study protocol for a placebo-controlled randomized double-blind trial
Voigt, S, Koemans, E A, Rasing, I, van Etten, E S, Terwindt, G M, Baas, F, Kaushik, K, van Es, A C G M, van Buchem, M A, van Osch, M J P, van Walderveen, M A A, Klijn, C J M, Verbeek, M M, van der Weerd, L, Wermer, M J H
Published in Current controlled trials in cardiovascular medicine (05.06.2023)
Published in Current controlled trials in cardiovascular medicine (05.06.2023)
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Statin therapy is associated with improved survival after endovascular and open aneurysm repair
de Bruin, Jorg L., MD, Baas, Annette F., MD, PhD, Heymans, Martijn W., PhD, Buimer, Mathijs G., MD, Prinssen, Monique, MD, PhD, Grobbee, Diederick E., MD, PhD, Blankensteijn, Jan D., MD, PhD
Published in Journal of vascular surgery (2014)
Published in Journal of vascular surgery (2014)
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Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome
Kievit, Anneke, Tessadori, Federico, Douben, Hannie, Jordens, Ingrid, Maurice, Madelon, Hoogeboom, Jeannette, Hennekam, Raoul, Nampoothiri, Sheela, Kayserili, Hülya, Castori, Marco, Whiteford, Margo, Motter, Connie, Melver, Catherine, Cunningham, Michael, Hing, Anne, Kokitsu-Nakata, Nancy M, Vendramini-Pittoli, Siulan, Richieri-Costa, Antonio, Baas, Annette F, Breugem, Corstiaan C, Duran, Karen, Massink, Maarten, Derksen, Patrick W B, van IJcken, Wilfred F J, van Unen, Leontine, Santos-Simarro, Fernando, Lapunzina, Pablo, Gil-da Silva Lopes, Vera L, Lustosa-Mendes, Elaine, Krall, Max, Slavotinek, Anne, Martinez-Glez, Victor, Bakkers, Jeroen, van Gassen, Koen L I, de Klein, Annelies, van den Boogaard, Marie-José H, van Haaften, Gijs
Published in European journal of human genetics : EJHG (01.02.2018)
Published in European journal of human genetics : EJHG (01.02.2018)
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Inflamed target tissue provides a specific niche for highly expanded T-cell clones in early human autoimmune disease
Klarenbeek, P L, de Hair, M J H, Doorenspleet, M E, van Schaik, B D C, Esveldt, R E E, van de Sande, M G H, Cantaert, T, Gerlag, D M, Baeten, D, van Kampen, A H C, Baas, F, Tak, P P, de Vries, N
Published in Annals of the rheumatic diseases (01.06.2012)
Published in Annals of the rheumatic diseases (01.06.2012)
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Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants
Jansen, Mark, Schuldt, Maike, van Driel, Beau O, Schmidt, Amand F, Christiaans, Imke, van der Crabben, Saskia N, Hoedemaekers, Yvonne M, Dooijes, Dennis, Jongbloed, Jan D H, Boven, Ludolf G, Deprez, Ronald H Lekanne, Wilde, Arthur A M, Jans, Judith J M, van der Velden, Jolanda, de Boer, Rudolf A, van Tintelen, J Peter, Asselbergs, Folkert W, Baas, Annette F
Published in International journal of molecular sciences (17.02.2023)
Published in International journal of molecular sciences (17.02.2023)
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CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene
Jongmans, M C J, Admiraal, R J, van der Donk, K P, Vissers, L E L M, Baas, A F, Kapusta, L, van Hagen, J M, Donnai, D, de Ravel, T J, Veltman, J A, Geurts van Kessel, A, De Vries, B B A, Brunner, H G, Hoefsloot, L H, van Ravenswaaij, C M A
Published in Journal of medical genetics (01.04.2006)
Published in Journal of medical genetics (01.04.2006)
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Complement activation in leprosy: a retrospective study shows elevated circulating terminal complement complex in reactional leprosy
Bahia El Idrissi, N., Hakobyan, S., Ramaglia, V., Geluk, A., Morgan, B. Paul, Das, P. Kumar, Baas, F.
Published in Clinical and experimental immunology (01.06.2016)
Published in Clinical and experimental immunology (01.06.2016)
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Endoplasmic reticulum stress activates autophagy but not the proteasome in neuronal cells: implications for Alzheimer's disease
Nijholt, D A T, de Graaf, T R, van Haastert, E S, Oliveira, A Osório, Berkers, C R, Zwart, R, Ovaa, H, Baas, F, Hoozemans, J J M, Scheper, W
Published in Cell death and differentiation (01.06.2011)
Published in Cell death and differentiation (01.06.2011)
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