De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy von Tran Mau-Them, F., Guibaud, L., Duplomb, L., Keren, B., Lindstrom, K., Marey, I., Mochel, F., van den Boogaard, M. J., Oegema, R., Nava, C., Masurel, A., Jouan, T., Jansen, F. E., Au, M., Chen, Agnes H., Cho, M., Duffourd, Y., Lozier, E., Konovalov, F., Sharkov, A., Korostelev, S., Urteaga, B., Dickson, P., Vera, M., Martínez-Agosto, Julián A., Begemann, A., Zweier, M., Schmitt-Mechelke, T., Rauch, A., Philippe, C., van Gassen, K., Nelson, S., Graham, J. M., Friedman, J., Faivre, L., Lin, H. J., Thauvin-Robinet, C., Vitobello, A.

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The MEF2C-Related and 5q14.3q15 Microdeletion Syndrome von Zweier, M., Rauch, A.

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In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome von Wolff, D., Endele, S., Azzarello-Burri, S., Hoyer, J., Zweier, M., Schanze, I., Schmitt, B., Rauch, A., Reis, A., Zweier, C.

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The Buschke-Ollendorff syndrome: a case report of simultaneous osteo-cutaneous malformations in the hand von Brodbeck, Michael, Yousif, Q, Diener, P A, Zweier, M, Gruenert, J

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Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression von Zweier, M, Rauch, A

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De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy von Tran Mau-Them, F, Guibaud, L, Duplomb, L, Keren, B, Lindstrom, K, Marey, I, Mochel, F, Zweier, M, Schmitt-Mechelke, T

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The MEF2C-related and 5q14.3q15 microdeletion syndrome von Zweier, M, Rauch, A

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The Buschke-Ollendorff syndrome: a case report of simultaneous osteo-cutaneous malformations in the hand von Brodbeck, Michael, Yousif, Q, Diener, P A, Zweier, M, Gruenert, J

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CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila von Zweier, C, de Jong, E K, Zweier, M, Oricco, A, Ousager, L B, Collins, A L, Bijlsma, E K, Oortveld, M A W, Ekici, A B, Reis, A, Schenck, A, Rauch, A

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In-frame deletion and missense mutations of the C-terminal helicase domain of SMARCA2 in three patients with Nicolaides-Baraitser syndrome von Wolff, D, Endele, S, Azzarello-Burri, S, Hoyer, J, Zweier, M, Schanze, I, Schmitt, B, Rauch, A, Reis, A, Zweier, C

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Iron and noncontrast magnetic resonance T2 as a marker of intraplaque iron in human atherosclerosis von Winner, Marshall W., MD, Sharkey-Toppen, Travis, MS, Zhang, Xiaolan, PhD, Pennell, Michael L., PhD, Simonetti, Orlando P., PhD, Zweier, Jay L., MD, Vaccaro, Patrick S., MD, Raman, Subha V., MD

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Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals von Bosch, E, Popp, B, Güse, E, Skinner, C, van der Sluijs, PJ, Maystadt, I, Pinto, AM, Renieri, A, Bruno, LP, Granata, S, Marcelis, C, Baysal, Ö, Hartwich, D, Holthöfer, L, Isidor, B, Cogne, B, Wieczorek, D, Capra, V, Scala, M, De Marco, P, Ognibene, M, Jamra, RA, Platzer, K, Carter, LB, Kuismin, O, van Haeringen, A, Maroofian, R, Valenzuela, I, Cuscó, I, Martinez-Agosto, JA, Rabani, AM, Mefford, HC, Pereira, EM, Close, C, Anyane-Yeboa, K, Wagner, M, Hannibal, MC, Zacher, P, Thiffault, I, Beunders, G, Umair, M, Bhola, PT, McGinnis, E, Millichap, J, van de Kamp, JM, Prijoles, EJ, Dobson, A, Shillington, A, Graham, BH, Garcia, EJ, Galindo, MK, Ropers, FG, Nibbeling, EAR, Hubbard, G, Karimov, C, Goj, G, Bend, R, Rath, J, Morrow, MM, Millan, F, Salpietro, V, Torella, A, Nigro, V, Kurki, M, Stevenson, RE, Santen, GWE, Zweier, M, Campeau, PM, Severino, M, Reis, A, Accogli, A, Vasileiou, G

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Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals von Bosch, E., Popp, B., Güse, E., Skinner, C., Sluijs, P.J. van der, Maystadt, I., Pinto, A.M., Renieri, A., Bruno, L.P., Granata, S., Marcelis, C., Baysal, Ö., Hartwich, D., Holthöfer, L., Isidor, B., Cogne, B., Wieczorek, D., Capra, V., Scala, M., Marco, P. de, Ognibene, M., Abou Jamra, R., Platzer, K., Carter, L.B., Kuismin, O., Haeringen, A. van, Maroofian, R., Valenzuela, I., Cuscó, I., Martinez-Agosto, J.A., Rabani, A.M., Mefford, H.C., Pereira, E.M., Close, C., Anyane-Yeboa, K., Wagner, M., Hannibal, M.C., Zacher, P., Thiffault, I., Beunders, G., Umair, M., Bhola, P.T., Mcginnis, E., Millichap, J., Kamp, J.M. van de, Prijoles, E.J., Dobson, A., Shillington, A., Graham, B.H., Garcia, E.J., Galindo, M.K., Ropers, F.G., Nibbeling, E.A.R., Hubbard, G., Karimov, C., Goj, G., Bend, R., Rath, J., Morrow, M.M., Millan, F., Salpietro, V., Torella, A., Nigro, V., Kurki, M., Stevenson, R.E., Santen, G.W.E., Zweier, M., Campeau, P.M., Severino, M., Reis, A., Accogli, A., Vasileiou, G.

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Ischemic preconditioning preserves mitochondrial membrane potential and limits reactive oxygen species production von Quarrie, Ricardo, MD, Lee, Daniel S., BS, Steinbaugh, Gregory, PhD, Cramer, Brandon, BS, Erdahl, Warren, PhD, Pfeiffer, Douglas R., PhD, Zweier, Jay L., MD, Crestanello, Juan A., MD

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In Vivo Atherosclerotic Plaque Characterization Using Magnetic Susceptibility Distinguishes Symptom-Producing Plaques von Raman, Subha V., MD, MS, FACC, Winner, Marshall W., MD, Tran, Tam, BS, Velayutham, Murugesan, PhD, Simonetti, Orlando P., PhD, Baker, Peter B., MD, Olesik, John, PhD, McCarthy, Beth, RT, Ferketich, Amy K., PhD, Zweier, Jay L., MD, FACC

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The role of oxidants and free radicals in reperfusion injury von ZWEIER, Jay L, HASSAN TALUKDER, M. A

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Cytoglobin regulates blood pressure and vascular tone through nitric oxide metabolism in the vascular wall von Liu, Xiaoping, El-Mahdy, Mohamed A., Boslett, James, Varadharaj, Saradhadevi, Hemann, Craig, Abdelghany, Tamer M., Ismail, Raed S., Little, Sean C., Zhou, Danlei, Thuy, Le Thi Thanh, Kawada, Norifumi, Zweier, Jay L.

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Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability von Hoyer, Juliane, Ekici, Arif B., Endele, Sabine, Popp, Bernt, Zweier, Christiane, Wiesener, Antje, Wohlleber, Eva, Dufke, Andreas, Rossier, Eva, Petsch, Corinna, Zweier, Markus, Göhring, Ina, Zink, Alexander M., Rappold, Gudrun, Schröck, Evelin, Wieczorek, Dagmar, Riess, Olaf, Engels, Hartmut, Rauch, Anita, Reis, André

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A Potent and Specific CD38 Inhibitor Ameliorates Age-Related Metabolic Dysfunction by Reversing Tissue NAD+ Decline von Tarragó, Mariana G., Chini, Claudia C.S., Kanamori, Karina S., Warner, Gina M., Caride, Ariel, de Oliveira, Guilherme C., Rud, Micaela, Samani, Adrienne, Hein, Kyaw Z., Huang, Runqing, Jurk, Diana, Cho, Dong Seong, Boslett, James J., Miller, Jordan D., Zweier, Jay L., Passos, João F., Doles, Jason D., Becherer, David J., Chini, Eduardo N.

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Measurement of Reactive Oxygen Species, Reactive Nitrogen Species, and Redox-Dependent Signaling in the Cardiovascular System: A Scientific Statement From the American Heart Associ... von Griendling, Kathy K, Touyz, Rhian M, Zweier, Jay L, Dikalov, Sergey, Chilian, William, Chen, Yeong-Renn, Harrison, David G, Bhatnagar, Aruni

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