Future cooling gap in shared socioeconomic pathways
Andrijevic, Marina, Byers, Edward, Mastrucci, Alessio, Smits, Jeroen, Fuss, Sabine
Published in Environmental research letters (01.09.2021)
Published in Environmental research letters (01.09.2021)
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Journal Article
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients
Smits, Jeroen P.P, Eckardt, Lars, Probst, Vincent, Bezzina, Connie R, Schott, Jean Jacques, Remme, Carol Ann, Haverkamp, Wilhelm, Breithardt, Günter, Escande, Denis, Schulze-Bahr, Eric, LeMarec, Hervé, Wilde, Arthur A.M
Published in Journal of the American College of Cardiology (17.07.2002)
Published in Journal of the American College of Cardiology (17.07.2002)
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Journal Article
Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome
ECKARDT, Lars, PROBST, Vincent, BORGGREFE, Martin, LEMAREC, Herve, BÖCKER, Dirk, WILDE, Arthur A. M, SMITS, Jeroen P. P, BAHR, Eric Schulze, WOLPERT, Christian, SCHIMPF, Rainer, WICHTER, Thomas, BOISSEAU, Pierre, HEINECKE, Achim, BREITHARDT, Günter
Published in Circulation (New York, N.Y.) (25.01.2005)
Published in Circulation (New York, N.Y.) (25.01.2005)
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Journal Article
The Low Dimensionality of Development
Kraemer, Guido, Reichstein, Markus, Camps-Valls, Gustau, Smits, Jeroen, Mahecha, Miguel D
Published in Social indicators research (01.08.2020)
Published in Social indicators research (01.08.2020)
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Journal Article
Cochlear supporting cells require GAS2 for cytoskeletal architecture and hearing
Chen, Tingfang, Rohacek, Alex M., Caporizzo, Matthew, Nankali, Amir, Smits, Jeroen J., Oostrik, Jaap, Lanting, Cornelis P., Kücük, Erdi, Gilissen, Christian, van de Kamp, Jiddeke M., Pennings, Ronald J.E., Rakowiecki, Staci M., Kaestner, Klaus H., Ohlemiller, Kevin K., Oghalai, John S., Kremer, Hannie, Prosser, Benjamin L., Epstein, Douglas J.
Published in Developmental cell (17.05.2021)
Published in Developmental cell (17.05.2021)
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Journal Article
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
Bassani, Sissy, van Beelen, Edward, Rossel, Mireille, Voisin, Norine, Morgan, Anna, Arribat, Yoan, Chatron, Nicolas, Chrast, Jacqueline, Cocca, Massimiliano, Delprat, Benjamin, Faletra, Flavio, Giannuzzi, Giuliana, Guex, Nicolas, Machavoine, Roxane, Pradervand, Sylvain, Smits, Jeroen J, van de Kamp, Jiddeke M, Ziegler, Alban, Amati, Francesca, Marlin, Sandrine, Kremer, Hannie, Locher, Heiko, Maurice, Tangui, Gasparini, Paolo, Girotto, Giorgia, Reymond, Alexandre
Published in Human molecular genetics (15.09.2021)
Published in Human molecular genetics (15.09.2021)
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Journal Article
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder
Rots, Dmitrijs, Jakub, Taryn E., Keung, Crystal, Jackson, Adam, Banka, Siddharth, Pfundt, Rolph, de Vries, Bert B.A., van Jaarsveld, Richard H., Hopman, Saskia M.J., Valenzuela, Irene, Hempel, Maja, Bierhals, Tatjana, Kortüm, Fanny, Lecoquierre, Francois, Goldenberg, Alice, Hertz, Jens Michael, Kibæk, Maria, Prijoles, Eloise J., Stevenson, Roger E., Everman, David B., Patterson, Wesley G., Meng, Linyan, Gijavanekar, Charul, De Dios, Karl, Lakhani, Shenela, Levy, Tess, Wieczorek, Dagmar, Benke, Paul J., Lopez Garcia, María Soledad, Perrier, Renee, Sousa, Sergio B., Almeida, Pedro M., Isidor, Bertrand, Deb, Wallid, Schmanski, Andrew A., Abdul-Rahman, Omar, Philippe, Christophe, Bruel, Ange-Line, Faivre, Laurence, Thauvin, Christel, Smits, Jeroen J., Garavelli, Livia, Caraffi, Stefano G., Peluso, Francesca, Royer, Erin, Leeuwen, Lisette, Stegmann, Alexander P.A., Stumpel, Constance T.R.M., Tiller, George E., Bosch, Daniëlle G.M., Potgieter, Stephanus T., Joss, Shelagh, Splitt, Miranda, Holden, Simon, Prapa, Matina, Foulds, Nicola, Waltes, Regina, Chiocchetti, Andreas G., Freitag, Christine M., De Rubeis, Silvia, Buxbaum, Joseph, Gelb, Bruce D., Branko, Aleksic, Kushima, Itaru, Howe, Jennifer, Scherer, Stephen W., Arado, Alessia, Baldo, Chiara, Patat, Olivier, Bénédicte, Demeer, Lopergolo, Diego, Santorelli, Filippo M., Dufke, Andreas, Falb, Ruth J., Rieß, Angelika, Krieg, Peter, Spranger, Stephanie, Iascone, Maria, Josephi-Taylor, Sarah, Roscioli, Tony, Buckley, Michael F., Liebelt, Jan, Dagli, Aditi I., Aten, Emmelien, Hurst, Anna C.E., Suri, Mohnish, Aliu, Ermal, Naik, Sunil, Coursimault, Juliette, Nicolas, Gaël, Küpper, Hanna, Ibrahim, Veyan, Top, Deniz, Di Cara, Francesca, Louie, Raymond J., Stolerman, Elliot, Brunner, Han G., Vissers, Lisenka E.L.M., Kramer, Jamie M., Kleefstra, Tjitske
Published in American journal of human genetics (01.06.2023)
Published in American journal of human genetics (01.06.2023)
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Journal Article
A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss
de Bruijn, Suzanne E, Smits, Jeroen J, Liu, Chang, Lanting, Cornelis P, Beynon, Andy J, Blankevoort, Joëlle, Oostrik, Jaap, Koole, Wouter, de Vrieze, Erik, Cremers, Cor W R J, Cremers, Frans P M, Roosing, Susanne, Yntema, Helger G, Kunst, Henricus P M, Zhao, Bo, Pennings, Ronald J E, Kremer, Hannie
Published in Journal of medical genetics (01.02.2021)
Published in Journal of medical genetics (01.02.2021)
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Journal Article
Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss
Bueno, André S, Nunes, Kelly, Dias, Alex M M, Alves, Leandro U, Mendes, Beatriz C A, Sampaio-Silva, Juliana, Smits, Jeroen, Yntema, Helger G, Meyer, Diogo, Lezirovitz, Karina, Mingroni-Netto, Regina C
Published in European journal of human genetics : EJHG (01.01.2022)
Published in European journal of human genetics : EJHG (01.01.2022)
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