Altered auto-phosphorylation of novel TNNI3K variants associated with AV-nodal re-entry tachycardia and conduction disease von Pham, C, Munoz-Martin, N, Podliesna, S, Milano, A, Beekman, L, Vermeer, A, Frantzen, C, Jansen, S, Van De Laar, I, Nieuwhof, K, Christiaans, I, Bezzina, C.R, Lodder, E.M

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GENOME-WIDE ASSOCIATION STUDY AND META-ANALYSIS IDENTIFY DISEASE SUSCEPTIBILITY LOCI ASSOCIATED WITH TRANSPOSITION OF THE GREAT ARTERIES von Tadros, R., Milosavljevic, D., Lahrouchi, N., Tjong, F.V., Beekman, L., Veldink, J.H., Lodder, E.M., Goodship, J.A., Cordell, H.J., Tanck, M.W., Keavney, B.D., Mulder, B.J., Postma, A.V., Bezzina, C.R.

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Deletion of 1 amino acid in Indian hedgehog leads to brachydactylyA1 von Lodder, E.M., Hoogeboom, A.J.M., Coert, J.H., de Graaff, E.

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GENOME-WIDE ASSOCIATION STUDY AND META-ANALYSIS IDENTIFY DISEASE SUSCEPTIBILITY LOCI ASSOCIATED WITH TRANSPOSITION OF THE GREAT ARTERIES von Tadros, R, Milosavljevic, D, Lahrouchi, N, Tjong, F.V, Beekman, L, Veldink, J.H, Lodder, E.M, Goodship, J.A, Cordell, H.J, Tanck, M.W, Keavney, B.D, Mulder, B.J, Postma, A.V, Bezzina, C.R

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Reclassification of a likely pathogenic Dutch founder variant in KCNH2: implications of reduced penetrance von Copier, J.S., Bootsma, M., Ng, C.A., Wilde, A.A.M., Bertels, R.A., Bikker, H., Christiaans, I., Crabben, S.N. van der, Hol, J.A., Koopmann, T.T., Knijnenburg, J., Lommerse, A.A.J., Smagt, J.J. van der, Bezzina, C.R., Vandenberg, J.I., Verkerk, A.O., Barge-Schaapveld, D.Q.C.M., Lodder, E.M.

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Genetic burden of TNNI3K in diagnostic testing of patients with dilated cardiomyopathy and supraventricular arrhythmias von Pham, C., Andrzejczyk, K., Jurgens, S.J., Deprez, R.L., Palm, K.C.A., Vermeer, A.M.C., Nijman, J., Christiaans, I., Barge-Schaapveld, D.Q.C.M., Dessel, P.F.H.M. van, Beekman, L., Choi, S.H., Lubitz, S.A., Skoric-Milosavljevic, D., Bersselaar, L. van den, Jansen, P.R., Copier, J.S., Ellinor, P.T., Wilde, A.A.M., Bezzina, C.R., Lodder, E.M.

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Low human dystrophin levels prevent cardiac electrophysiological and structural remodelling in a Duchenne mouse model von Marchal, G.A., Putten, M. van, Verkerk, A.O., Casini, S., Putker, K., Amersfoorth, S.C.M. van, Aartsma-Rus, A., Lodder, E.M., Remme, C.A.

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Discovery of predictors of sudden cardiac arrest in diabetes: rationale and outline of the RESCUED (REcognition of Sudden Cardiac arrest vUlnErability in Diabetes) project von Dongen, L.H. van, Harms, P.P., Hoogendoorn, M., Zimmerman, D.S., Lodder, E.M., Hart, L.M. 't, Herings, R., Weert, H.C.P.M. van, Nijpels, G., Swart, K.M.A., Heijden, A.A. van der, Blom, M.T., Elders, P.J., Tan, H.L.

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Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot von Skoric-Milosavljevic, D., Lahrouchi, N., Bosada, F.M., Dombrowsky, G., Williams, S.G., Lesurf, R., Tjong, F.V.Y., Walsh, R., Bouchikhi, I. el, Breckpot, J., Audain, E., Ilgun, A., Beekman, L., Ratbi, I., Strong, A., Muenke, M., Heide, S., Muir, A.M., Hababa, M., Cross, L., Zhou, D.H., Pastinen, T., Zackai, E., Atmani, S., Ouldim, K., Adadi, N., Steindl, K., Rauch, A., Brook, D., Wilsdon, A., Kuipers, I., Blom, N.A., Mulder, B.J., Mefford, H.C., Keren, B., Joset, P., Kruszka, P., Thiffault, I., Sheppard, S.E., Roberts, A., Lodder, E.M., Keavney, B.D., Clur, S.A.B., Mital, S., Hitz, M.P., Christoffels, V.M., Postma, A.V., Bezzina, C.R.

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Common genetic variants contribute to risk of transposition of the great arteries von Skoric-Milosavljevic, D., Tadros, R., Bosada, F.M., Tessadori, F., Weerd, J.H. van, Woudstra, O.I., Tjong, F.V.Y., Lahrouchi, N., Bajolle, F., Cordell, H.J., Agopian, A.J., Blue, G.M., Barge-Schaapveld, D.Q.C.M., Gewillig, M., Preuss, C., Lodder, E.M., Barnett, P., Ilgun, A., Beekman, L., Duijvenboden, K. van, Bokenkamp, R., Muller-Nurasyid, M., Vliegen, H.W., Konings, T.C., Melle, J.P. van, Dijk, A.P.J. van, Kimmenade, R.R.J. van, Roos-Hesselink, J.W., Sieswerda, G., Meijboom, F., Abdul-Khaliq, H., Berger, F., Dittrich, S., Hitz, M.P., Moosmann, J., Riede, F.T., Schubert, S., Galan, P., Lathrop, M., Munter, H.M., Al-Chalabi, A., Shaw, C.E., Shaw, P.J., Morrison, K.E., Veldink, J.H., Berg, L.H. van den, Evans, S., Nobrega, M.A., Aneas, I., Radivojkov-Blagojevic, M., Meitinger, T., Oechslin, E., Mondal, T., Bergin, M.L., Smythe, J.F., Altamirano-Diaz, L., Lougheed, J., Bouma, B.J., Chaix, M.A., Kline, J., Bassett, A.S., Andelfinger, G., Palen, R.L.F. van der, Bouvagnet, P., Clur, S.A.B., Breckpot, J., Kerstjens-Frederikse, W.S., Winlaw, D.S., Bauer, U.M.M., Mital, S., Goldmuntz, E., Keavney, B., Bonnet, D., Mulder, B.J., Tanck, M.W.T., Bakkers, J., Christoffels, V.M., Boogerd, C.J., Postma, A.V., Bezzina, C.R.

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Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy von Lahrouchi, N., Postma, A.V., Salazar, C.M., Laughter, D.M. de, Tjong, F., Piherova, L., Bowling, F.Z., Zimmerman, D., Lodder, E.M., Ta-Shma, A., Perles, Z., Beekman, L., Ilgun, A., Gunst, Q., Hababa, M., Skoric-Milosavljevic, D., Stranecky, V., Tomek, V., Knijff, P. de, Leeuw, R. de, Robinson, J.Y., Burn, S.C., Mustafa, H., Ambrose, M., Moss, T., Jacober, J., Niyazov, D.M., Wolf, B., Kim, K.H., Cherny, S., Rousounides, A., Aristidou-Kallika, A., Tanteles, G., Ange-Line, B., Denomme-Pichon, A.S., Francannet, C., Ortiz, D., Haak, M.C., Harkel, A.D.J. ten, Manten, G.T.R., Dutman, A.C., Bouman, K., Magliozzi, M., Radio, F.C., Santen, G.W.E., Herkert, J.C., Brown, H.A., Elpeleg, O., Hoff, M.J.B. van den, Mulder, B., Airola, M.V., Kmoch, S., Barnett, J.V., Clur, S.A., Frohman, M.A., Bezzina, C.R.

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Deletion of 1 amino acid in Indian hedgehog leads to brachydactylyA1 von Lodder, E.M., Hoogeboom, A.J.M., Coert, J.H., de Graaff, E.

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Rapid SARS-CoV-2 whole-genome sequencing and analysis for informed public health decision-making in the Netherlands von Oude Munnink, Bas B., Nieuwenhuijse, David F., Stein, Mart, O’Toole, Áine, Haverkate, Manon, Mollers, Madelief, Kamga, Sandra K., Schapendonk, Claudia, Pronk, Mark, Lexmond, Pascal, van der Linden, Anne, Bestebroer, Theo, Chestakova, Irina, Overmars, Ronald J., van Nieuwkoop, Stefan, Molenkamp, Richard, van der Eijk, Annemiek A., GeurtsvanKessel, Corine, Vennema, Harry, Meijer, Adam, Rambaut, Andrew, van Dissel, Jaap, Sikkema, Reina S., Timen, Aura, Koopmans, Marion

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Mice with megalencephalic leukoencephalopathy with cysts: A developmental angle von Dubey, Mohit, Bugiani, Marianna, Ridder, Margreet C., Postma, Nienke L., Brouwers, Eelke, Polder, Emiel, Jacobs, J. Gerbren, Baayen, Johannes C., Klooster, Jan, Kamermans, Maarten, Aardse, Romy, de Kock, Christiaan P. J., Dekker, Marien P., van Weering, Jan R. T., Heine, Vivi M., Abbink, Truus E. M., Scheper, Gert C., Boor, Ilja, Lodder, Johannes C., Mansvelder, Huibert D., van der Knaap, Marjo S.

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A Comparison of Health Status and Quality of Life in Patients with Intermittent Claudication von Roijers, J.P., van den Houten, M.M.L., Hopmans, C.J., Vriens, P.W.H.E., Willigendael, E.M., Lodder, P., de Vries, J., Teijink, J.A.W., van der Laan, L.

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Predictive value of Type D personality for impaired endothelial function in coronary artery disease - The SAINTEX-CAD Study von Denollet, J, van Felius, R, Lodder, P, Mommersteeg, P.M.C, Goovaerts, I, Possemiers, N, Vanhees, Luc, Beckers, P, Pattyn, Nele, Van Craenenbroeck, E.M

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Obsessive-compulsive personality disorder symptoms as a risk factor for postpartum depressive symptoms von van Broekhoven, Kiki E. M., Karreman, Annemiek, Hartman, Esther E., Lodder, Paul, Endendijk, Joyce J., Bergink, Veerle, Pop, Victor J. M.

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Optimisation of obliquely sputter deposited media von Bijker, M.D., Visser, E.M., Lodder, J.C., Popma, Th.J.A.

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Oblique metal deposited thin films for magnetic recording von Bijker, M.D., Visser, E.M., Lodder, J.C.

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Oblique sputtered Co and Co80Ni20 thin films von BIJKER, M.D., VISSER, E.M., LODDER, J.C., POPMA, TH.J.A.

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