Diagnosis and Risk Prediction of Dilated Cardiomyopathy in the Era of Big Data and Genomics

por Sammani, Arjan, Baas, Annette F., Asselbergs, Folkert W., te Riele, Anneline S. J. M.
Publicado 2021

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

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

A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trial

por van den Heuvel, Lieke M, Hoedemaekers, Yvonne M, Baas, Annette F, van Tintelen, J Peter, Smets, Ellen M A, Christiaans, Imke
Publicado 2019

Automatic multilabel detection of ICD10 codes in Dutch cardiology discharge letters using neural networks

por Sammani, Arjan, Bagheri, Ayoub, van der Heijden, Peter G. M., te Riele, Anneline S. J. M., Baas, Annette F., Oosters, C. A. J., Oberski, Daniel, Asselbergs, Folkert W.
Publicado 2021

Automatic Identification of Patients With Unexplained Left Ventricular Hypertrophy in Electronic Health Record Data to Improve Targeted Treatment and Family Screening

por Sammani, Arjan, Jansen, Mark, de Vries, Nynke M., de Jonge, Nicolaas, Baas, Annette F., te Riele, Anneline S. J. M., Asselbergs, Folkert W., Oerlemans, Marish I. F. J.
Publicado 2022

Blood‐based biomarkers for the prediction of hypertrophic cardiomyopathy prognosis: a systematic review and meta‐analysis

por Jansen, Mark, Algül, Sila, Bosman, Laurens P., Michels, Michelle, van der Velden, Jolanda, de Boer, Rudolf A., van Tintelen, J. Peter, Asselbergs, Folkert W., Baas, Annette F.
Publicado 2022

Evaluation of the cardiac amyloidosis clinical pathway implementation: a real-world experience

por Brons, Maaike, Muller, Steven A, Rutten, Frans H, van der Meer, Manon G, Vrancken, Alexander F J E, Minnema, Monique C, Baas, Annette F, Asselbergs, Folkert W, Oerlemans, Marish I F J
Publicado 2022

STRAD pseudokinases regulate axogenesis and LKB1 stability

por Veleva-Rotse, Biliana O, Smart, James L, Baas, Annette F, Edmonds, Benjamin, Zhao, Zi-ming, Brown, Allyson, Klug, Lillian R, Hansen, Kelly, Reilly, Gabrielle, Gardner, Alexandria P, Subbiah, Krishnaveni, Gaucher, Eric A, Clevers, Hans, Barnes, Anthony P
Publicado 2014

Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population

por Bourfiss, Mimount, van Vugt, Marion, Alasiri, Abdulrahman I., Ruijsink, Bram, van Setten, Jessica, Schmidt, A. Floriaan, Dooijes, Dennis, Puyol-Antón, Esther, Velthuis, Birgitta K., van Tintelen, J. Peter, te Riele, Anneline S.J.M., Baas, Annette F., Asselbergs, Folkert W.
Publicado 2022

Distinct Metabolomic Signatures in Preclinical and Obstructive Hypertrophic Cardiomyopathy

por Schuldt, Maike, van Driel, Beau, Algül, Sila, Parbhudayal, Rahana Y., Barge-Schaapveld, Daniela Q. C. M., Güçlü, Ahmet, Jansen, Mark, Michels, Michelle, Baas, Annette F., van de Wiel, Mark A., Nieuwdorp, Max, Levin, Evgeni, Germans, Tjeerd, Jans, Judith J. M., van der Velden, Jolanda
Publicado 2021

Results of next‐generation sequencing gene panel diagnostics including copy‐number variation analysis in 810 patients suspected of heritable thoracic aortic disorders

por Overwater, Eline, Marsili, Luisa, Baars, Marieke J.H., Baas, Annette F., van de Beek, Irma, Dulfer, Eelco, van Hagen, Johanna M., Hilhorst‐Hofstee, Yvonne, Kempers, Marlies, Krapels, Ingrid P., Menke, Leonie A., Verhagen, Judith M.A., Yeung, Kak K., Zwijnenburg, Petra J.G., Groenink, Maarten, van Rijn, Peter, Weiss, Marjan M., Voorhoeve, Els, van Tintelen, J. Peter, Houweling, Arjan C., Maugeri, Alessandra
Publicado 2018

Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants

por 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.
Publicado 2023

The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview

por Verheul, Lisa M, van der Ree, Martijn H, Groeneveld, Sanne A, Mulder, Bart A, Christiaans, Imke, Kapel, Gijs F L, Alings, Marco, Bootsma, Marianne, Barge-Schaapveld, Daniela Q C M, Balt, Jippe C, Yap, Sing-Chien, Krapels, Ingrid P C, Ter Bekke, Rachel M A, Volders, Paul G A, van der Crabben, Saskia N, Postema, Pieter G, Wilde, Arthur A M, Dooijes, Dennis, Baas, Annette F, Hassink, Rutger J
Publicado 2023

Genetic Association of Lipids and Lipid Drug Targets With Abdominal Aortic Aneurysm: A Meta-analysis

por Harrison, Seamus C., Holmes, Michael V., Burgess, Stephen, Asselbergs, Folkert W., Jones, Gregory T., Baas, Annette F., van ’t Hof, F. N., de Bakker, Paul I. W., Blankensteijn, Jan D., Powell, Janet T., Saratzis, Athanasios, de Borst, Gert J., Swerdlow, Daniel I., van der Graaf, Yolanda, van Rij, Andre M., Carey, David J., Elmore, James R., Tromp, Gerard, Kuivaniemi, Helena, Sayers, Robert D., Samani, Nilesh J., Bown, Matthew J., Humphries, Steve E.
Publicado 2017

Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification

por van der Meulen, Marijke H., Herkert, Johanna C., den Boer, Susanna L., du Marchie Sarvaas, Gideon J., Blom, Nico A., ten Harkel, Arend D.J., Breur, Hans M.P.J., Rammeloo, Lukas A.J., Tanke, Ronald B., Marcelis, Carlo, van de Laar, Ingrid M.B.H., Verhagen, Judith M.A., Lekanne dit Deprez, Ronald H., Barge-Schaapveld, Daniela Q.C.M., Baas, Annette F., Sammani, Arjan, Christiaans, Imke, van Tintelen, J. Peter, Dalinghaus, Michiel
Publicado 2022

Interleukin-6 receptor pathways in abdominal aortic aneurysm

por Harrison, Seamus C., Smith, Andrew J.P., Jones, Gregory T., Swerdlow, Daniel I., Rampuri, Riaz, Bown, Matthew J., Folkersen, Lasse, Baas, Annette F., de Borst, Gert Jan, Blankensteijn, Jan D., Price, Jacqueline F., van der Graaf, Yolanda, McLachlan, Stela, Agu, Obi, Hofman, Albert, Uitterlinden, Andre G., Franco-Cereceda, Anders, Ruigrok, Ynte M., van't Hof, F.N., Powell, Janet T., van Rij, Andre M., Casas, Juan P., Eriksson, Per, Holmes, Michael V., Asselbergs, Folkert W., Hingorani, Aroon D., Humphries, Steve E.
Publicado 2013

Biallelic Variants in ASNA1, Encoding a Cytosolic Targeting Factor of Tail-Anchored Proteins, Cause Rapidly Progressive Pediatric Cardiomyopathy

por Verhagen, Judith M.A., van den Born, Myrthe, van der Linde, Herma C., G.J. Nikkels, Peter, Verdijk, Rob M., Kivlen, Maryann H., van Unen, Leontine M.A., Baas, Annette F., ter Heide, Henriette, van Osch-Gevers, Lennie, Hoogeveen-Westerveld, Marianne, Herkert, Johanna C., Bertoli-Avella, Aida M., van Slegtenhorst, Marjon A., Wessels, Marja W., Verheijen, Frans W., Hassel, David, Hofstra, Robert M.W., Hegde, Ramanujan S., van Hasselt, Peter M., van Ham, Tjakko J., van de Laar, Ingrid M.B.H.
Publicado 2019

A mutation update for the FLNC gene in myopathies and cardiomyopathies

por Verdonschot, Job A. J., Vanhoutte, Els K., Claes, Godelieve R. F., Helderman‐van den Enden, Apollonia T. J. M., Hoeijmakers, Janneke G. J., Hellebrekers, Debby M. E. I., de Haan, Amber, Christiaans, Imke, Lekanne Deprez, Ronald H., Boen, Hanne M., van Craenenbroeck, Emeline M., Loeys, Bart L., Hoedemaekers, Yvonne M., Marcelis, Carlo, Kempers, Marlies, Brusse, Esther, van Waning, Jaap I., Baas, Annette F., Dooijes, Dennis, Asselbergs, Folkert W., Barge‐Schaapveld, Daniela Q. C. M., Koopman, Pieter, van den Wijngaard, Arthur, Heymans, Stephane R. B., Krapels, Ingrid P. C., Brunner, Han G.
Publicado 2020

A gene-centric study of common carotid artery remodelling

por Harrison, Seamus C., Zabaneh, Delilah, Asselbergs, Folkert W., Drenos, Fotios, Jones, Gregory T., Shah, Sonia, Gertow, Karl, Sennblad, Bengt, Strawbridge, Rona J., Gigante, Bruna, Holewijn, Suzanne, De Graaf, Jacqueline, Vermeulen, Sita, Folkersen, Lasse, van Rij, Andre M., Baldassarre, Damiano, Veglia, Fabrizio, Talmud, Philippa J., Deanfield, John E., Agu, Obi, Kivimaki, Mika, Kumari, Meena, Bown, Matthew J., Nyyssönen, Kristiina, Rauramaa, Rainer, Smit, Andries J., Franco-Cereceda, Anders, Giral, Philippe, Mannarino, Elmo, Silveira, Angela, Syvänen, Ann-Christine, de Borst, Gert J., van der Graaf, Yolanda, de Faire, Ulf, Baas, Annette F., Blankensteijn, Jan D., Wareham, Nicholas J., Fowkes, Gerry, Tzoulaki, Ionna, Price, Jacqueline F., Tremoli, Elena, Hingorani, Aroon D., Eriksson, Per, Hamsten, Anders, Humphries, Steve E.
Publicado 2013

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

por van ’t Hof, Femke N. G., Ruigrok, Ynte M., Lee, Cue Hyunkyu, Ripke, Stephan, Anderson, Graig, de Andrade, Mariza, Baas, Annette F., Blankensteijn, Jan D., Böttinger, Erwin P., Bown, Matthew J., Broderick, Joseph, Bijlenga, Philippe, Carrell, David S., Crawford, Dana C., Crosslin, David R., Ebeling, Christian, Eriksson, Johan G., Fornage, Myriam, Foroud, Tatiana, von und zu Fraunberg, Mikael, Friedrich, Christoph M., Gaál, Emília I., Gottesman, Omri, Guo, Dong‐Chuan, Harrison, Seamus C., Hernesniemi, Juha, Hofman, Albert, Inoue, Ituro, Jääskeläinen, Juha E., Jones, Gregory T., Kiemeney, Lambertus A. L. M., Kivisaari, Riku, Ko, Nerissa, Koskinen, Seppo, Kubo, Michiaki, Kullo, Iftikhar J., Kuivaniemi, Helena, Kurki, Mitja I., Laakso, Aki, Lai, Dongbing, Leal, Suzanne M., Lehto, Hanna, LeMaire, Scott A., Low, Siew‐Kee, Malinowski, Jennifer, McCarty, Catherine A., Milewicz, Dianna M., Mosley, Thomas H., Nakamura, Yusuke, Nakaoka, Hirofumi, Niemelä, Mika, Pacheco, Jennifer, Peissig, Peggy L., Pera, Joanna, Rasmussen‐Torvik, Laura, Ritchie, Marylyn D., Rivadeneira, Fernando, van Rij, Andre M., Santos‐Cortez, Regie Lyn P., Saratzis, Athanasios, Slowik, Agnieszka, Takahashi, Atsushi, Tromp, Gerard, Uitterlinden, André G., Verma, Shefali S., Vermeulen, Sita H., Wang, Gao T., Han, Buhm, Rinkel, Gabriël J. E., de Bakker, Paul I. W., Bown, Matthew J., Harrison, Seamus C., Saratzis, Athanasios, Verissimo, Ana, Wright, Benjamin J., Bumpstead, Suzannah, Baas, Annette F., Gretarsdottir, Solveig, Badger, Stephen A., Child, Anne H., Clough, Rachel E., Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A., Futers, Simon, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew M., van Bockxmeer, Frank M., Matthiasson, Stefan E., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D., Teijink, Joep A. W., Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A., Palmen, Jutta, Smith, Andrew J., Lindholt, Jes S., Bradley, Declan T., Waltham, Matthew, Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E., Potter, Simon, Golledge, Jonathan, Eriksson, Per, Norman, Paul E., Powell, Janet T., Stefansson, Kari, Thompson, John R., Humphries, Steve E., Sayers, Robert D., Deloukas, Panos, Samani, Nilesh J., Jones, Gregory T., Phillip, L. Victoria, van Rij, Andre M., Hill, Geraldine B., Williams, Michael J. A., Thomson, Ian A., Krysa, Jo, Wilkins, Gerard T., Merriman, Tony R., Vasudevan, Thodor M., Lewis, David R., Blair, Ross D., Hill, Andrew A.
Publicado 2016