Plasma neurofilament light chain level is not a biomarker of Charcot–Marie–Tooth disease progression: Results of 3‐year follow‐up study von Setlere, Signe, Grosmane, Arta, Kurjane, Natalja, Gailite, Linda, Rots, Dmitrijs, Blennow, Kaj, Zetterberg, Henrik, Kenina, Viktorija

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Whole exome sequencing in young atrial fibrillation patients von Rudaka, I, Vilne, B, Kalejs, O, Rots, D, Trusinskis, K, Gailite, L

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P1392Next generation sequencing in lone atrial fibrillation patients von Rudaka, I, Rots, D, Kalejs, O, Gailite, L

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Cohort Profile: the Etude Epidémiologique sur les Petits Ages Gestationnels-2 (EPIPAGE-2) preterm birth cohort von Lorthe, Elsa, Benhammou, Valérie, Marchand-Martin, Laetitia, Pierrat, Véronique, Lebeaux, Cécile, Durox, Mélanie, Goffinet, François, Kaminski, Monique, Ancel, Pierre-Yves

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Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy von Millere, Elina, Rots, Dmitrijs, Glazere, Ieva, Taurina, Gita, Kurjane, Natalja, Priedite, Viktorija, Gailite, Linda, Blennow, Kaj, Zetterberg, Henrik, Kenina, Viktorija

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Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy von Millere, E, Rots, D, Glazere, I, Taurina, G, Kurjane, N, Priedite, V, Gailite, L, Blennow, K, Zetterberg, H, Kenina, V

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Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein (vol 24, pg 2051, 2022) von Boer, E. de, Ockeloen, C.W., Kampen, R.A., Hampstead, J.E., Dingemans, A.J.M., Rots, D., Lütje, L., Ashraf, T., Baker, R., Barat-Houari, M., Angle, B., Chatron, N., Denommé-Pichon, A.S., Devinsky, O., Dubourg, C., Elmslie, F., Elloumi, H.Z., Faivre, L., Fitzgerald-Butt, S., Geneviéve, D., Goos, J.A.C., Helm, B.M., Kini, U., Lasa-Aranzasti, A., Lesca, G., Lynch, S.A., Mathijssen, I.M.J., McGowan, R., Monaghan, K.G., Odent, S., Pfundt, R., Putoux, A., Reeuwijk, J. van, Santen, G.W.E., Sasaki, E., Sorlin, A., Spek, P.J. van der, Stegmann, A.P.A., Swagemakers, S.M.A., Valenzuela, I., Viora-Dupont, E., Vitobello, A., Ware, S.M., Wéber, M., Gilissen, C., Low, K.J., Fisher, S.E., Vissers, L.E.L.M., Wong, M.M.K., Kleefstra, T.

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Plasma neurofilament light chain as a potential biomarker in Charcot‐Marie‐Tooth disease von Millere, E, Rots, D, Simrén, J, Ashton, NJ, Kupats, E, Micule, I, Priedite, V, Kurjane, N, Blennow, K, Gailite, L, Zetterberg, H, Kenina, V

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The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder von Rots, D., Jakub, T.E., Keung, C., Banka, S., Pfundt, R., Vries, B.B.A. de, Hopman, S.M.J., Binsbergen, E. van, Valenzuela, I., Hempel, M., Bierhals, T., Kortüm, F., Lecoquierre, F., Goldenberg, A., Andersen, C.B., Kibaek, M., Prijoles, E.J., Stevenson, R.E., Everman, D.B., Patterson, W.G., Meng, L.Y., Gijavanekar, C., Dios, K. de, Levy, T., Wagner, M., Wieczorek, D., Benke, P.J., Garcia, M.S.L., Perrier, R., Almeida, P.M., Simoes, M.J., Isidor, B., Deb, W., Schmanski, A.A., Abdul-Rahman, O., Philippe, C., Bruel, A.L., Faivre, L., Vitobello, A., Thauvin, C., Garavelli, L., Caraffi, S.G., Peluso, F., Davis-Keppen, L., Platt, D., Royer, E., Leeuwen, L., Sinnema, M., Bosch, D.S.D.L.G.M., Potgieter, S.T., Joss, S., Splitt, M., Holden, S., Prapa, M., Foulds, N., Douzgou, S., Puura, K., Waltes, R., Chiocchetti, A.G., Freitag, C.M., Satterstrom, F.K., Rubeis, S. de, Gelb, B.D., Branko, A., Kushima, I., Howe, J., Scherer, S.W., Arado, A., Baldo, C., Patat, O., Benedicte, D., Lopergolo, D., Haack, T.B., Bertrand, M., Falb, R.J., Riess, A., Krieg, P., Spranger, S., Iascone, M., Josephi-Taylor, S., Roscioli, T., Buckley, M.F., Liebelt, J., Dagli, A.I., Aten, E., Hurst, A.C.E., Hicks, A., Suri, M., Aliu, E., Naik, S., Coursimault, J., Küpper, H., Petit, F., Ibrahim, V., Top, D., Cara, F. di, Louie, R.J., Stolerman, E., Brunner, H.G., Kleefstra, T.

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Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein von Boer, E. de, Ockeloen, C.W., Kampen, R.A., Hampstead, J.E., Dingemans, A.J.M., Rots, D., Lutje, L., Ashraf, T., Baker, R., Barat-Houari, M., Angle, B., Chatron, N., Denomme-Pichon, A.S., Devinsky, O., Dubourg, C., Elmslie, F., Elloumi, H.Z., Faivre, L., Fitzgerald-Butt, S., Genevieve, D., Goos, J.A.C., Helm, B.M., Kini, U., Lasa-Aranzasti, A., Lesca, G., Lynch, S.A., Mathijssen, I.M.J., McGowan, R., Monaghan, K.G., Odent, S., Pfundt, R., Putoux, A., Reeuwijk, J. van, Santen, G.W.E., Sasaki, E., Sorlin, A., Spek, P.J. van der, Stegmann, A.P.A., Swagemakers, S.M.A., Valenzuela, I., Viora-Dupont, E., Vitobello, A., Ware, S.M., Weber, M., Gilissen, C., Low, K.J., Fisher, S.E., Vissers, L.E.L.M., Wong, M.M.K., Kleefstra, T.

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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature von Rots, D., Chater-Diehl, E., Dingemans, A.J.M., Goodman, S.J., Siu, M.T., Cytrynbaum, C., Choufani, S., Hoang, N., Walker, S., Awamleh, Z., Charkow, J., Meyn, S., Pfundt, R., Rinne, T., Gardeitchik, T., Vries, B.B.A. de, Deden, A.C., Leenders, E., Kwint, M., Stumpel, C.T.R.M., Stevens, S.J.C., Vermeulen, J.R., Harssel, J.V.T. van, Bosch, D.G.M., Gassen, K.L.I. van, Binsbergen, E. van, Geus, C.M. de, Brackel, H., Hempel, M., Lessel, D., Denecke, J., Slavotinek, A., Strober, J., Crunk, A., Folk, L., Wentzensen, I.M., Yang, H., Zou, F.G., Millan, F., Person, R., Xie, Y.L., Liu, S.X., Ousager, L.B., Larsen, M., Schultz-Rogers, L., Morava, E., Klee, E.W., Berry, I.R., Campbell, J., Lindstrom, K., Pruniski, B., Neumeyer, A.M., Radley, J.A., Phornphutkul, C., Schmidt, B., Wilson, W.G., Ounap, K., Reinson, K., Pajusalu, S., Haeringen, A. van, Ruivenkamp, C., Cuperus, R., Santos-Simarro, F., Palomares-Bralo, M., Pacio-Miguez, M., Ritter, A., Bhoj, E., Tonne, E., Tveten, K., Cappuccio, G., Brunetti-Pierri, N., Rowe, L., Bunn, J., Saenz, M., Platzer, K., Mertens, M., Caluseriu, O., Nowaczyk, M.J.M., Cohn, R.D., Kannu, P., Alkhunaizi, E., Chitayat, D., Scherer, S.W., Brunner, H.G., Vissers, L.E.L.M., Kleefstra, T., Koolen, D.A., Weksberg, R.

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Why did hunting weapon design change at Abri Pataud? Lithic use-wear data on armature use and hafting around 24,000-22,000 BP von Taipale, Noora, Chiotti, Laurent, Rots, Veerle

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The Chandra Source Catalog Release 2 Series von Evans, Ian N., Evans, Janet D., Martínez-Galarza, J. Rafael, Miller, Joseph B., Primini, Francis A., Azadi, Mojegan, Burke, Douglas J., Civano, Francesca M., D’Abrusco, Raffaele, Fabbiano, Giuseppina, Graessle, Dale E., Grier, John D., Houck, John C., Lauer, Jennifer, McCollough, Michael L., Nowak, Michael A., Plummer, David A., Rots, Arnold H., Siemiginowska, Aneta, Tibbetts, Michael S.

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Pressure flaking to serrate bifacial points for the hunt during the MIS5 at Sibudu Cave (South Africa) von Rots, Veerle, Lentfer, Carol, Schmid, Viola C, Porraz, Guillaume, Conard, Nicholas J

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Targeted silencing of the oncogenic transcription factor SOX2 in breast cancer von Stolzenburg, Sabine, Rots, Marianne G, Beltran, Adriana S, Rivenbark, Ashley G, Yuan, Xinni, Qian, Haili, Strahl, Brian D, Blancafort, Pilar

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Epigenetics: The neglected key to minimize learning and memory deficits in Down syndrome von DEKKER, Alain D, DE DEYN, Peter P, ROTS, Marianne G

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Epigenetic reprogramming of cancer cells via targeted DNA methylation von Rivenbark, Ashley G., Stolzenburg, Sabine, Beltran, Adriana S., Yuan, Xinni, Rots, Marianne G., Strahl, Brian D., Blancafort, Pilar

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Numerical analysis of a masonry façade subject to tunnelling-induced settlements von Giardina, Giorgia, van de Graaf, Anne V., Hendriks, Max A.N., Rots, Jan G., Marini, Alessandra

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Pneumococcal genetic variability in age-dependent bacterial carriage von Kremer, Philip H C, Ferwerda, Bart, Bootsma, Hester J, Rots, Nienke Y, Wijmenga-Monsuur, Alienke J, Sanders, Elisabeth A M, Trzciński, Krzysztof, Wyllie, Anne L, Turner, Paul, van der Ende, Arie, Brouwer, Matthijs C, Bentley, Stephen D, van de Beek, Diederik, Lees, John A

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Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention von Wang, Zhe, Emmerich, Andrew, Pillon, Nicolas J., Cornelis, Marilyn C., Mazzaferro, Eugenia, Broos, Siacia, Bentley, Amy R., Chong, Mike, Berry, Diane, Feenstra, Bjarke, Feitosa, Mary F., Hall, Leanne M., Huikari, Ville, Karlsson, Robert, Kerr, Kathleen F., Kim, Boram, Monroe, Kristine R., Richmond, Rebecca C., Rivera, Natalia V., Turman, Constance, van Rooij, Frank J. A., Zhao, Jing-Hua, Zhao, Wei, Baumeister, Sebastian E., Brage, Soren, Cole, John W., Collins, Francis S., Cupples, L. Adrienne, Franco, Oscar H., Galesloot, Tessel E., Grarup, Niels, Hui, Jennie, Illig, Thomas, Jago, Russell, James, Alan, Kilpeläinen, Tuomas O., Koh, Woon-Puay, Kolcic, Ivana, Kraft, Peter P., Li, Aihua, Vidal, Pedro Marques, Medland, Sarah E., Milaneschi, Yuri, Pedersen, Nancy L., Peyser, Patricia A., Power, Christine, Raitakari, Olli T., Ridker, Paul M., Rudan, Igor, Sarzynski, Mark A., Scott, Laura J., Scott, Robert A., Siggeirsdottir, Kristin, Teo, Koon K., Thorand, Barbara, Xu, Huichun, Young, Kristin L., Zillikens, M. Carola, Zonderman, Alan B., Ameur, Adam, Bandinelli, Stefania, Bouchard, Claude, Chasman, Daniel I., Deldicque, Louise, Fornage, Myriam, Gudnason, Vilmundur, Gyllensten, Ulf, Hayward, Caroline, Horta, Bernardo L., Hyppönen, Elina, Kardia, Sharon L. R., Kiemeney, Lambertus A., Langenberg, Claudia, Lehtimäki, Terho, Marchand, Loic Le, Magnusson, Patrik K. E., Martin, Nicholas G., Melbye, Mads, Metspalu, Andres, Meyre, David, North, Kari E., Ohlsson, Claes, Pare, Guillaume, Park, Taesung, Pedersen, Oluf, Pers, Tune H., Samani, Nilesh J., Sim, Xueling, Snieder, Harold, Spector, Tim D., van Dam, Rob M., van der Velde, Nathalie, Vollenweider, Peter, Voortman, Trudy, Waeber, Gérard, Wareham, Nicholas J., Wichmann, Heinz-Erich, Krook, Anna, Zierath, Juleen R., Thomis, Martine A. I.

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