Association between atopic dermatitis and attention deficit hyperactivity disorder in U.S. children and adults von Strom, M.A., Fishbein, A.B., Paller, A.S., Silverberg, J.I.

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Classic selective sweeps revealed by massive sequencing in cattle von Qanbari, Saber, Pausch, Hubert, Jansen, Sandra, Somel, Mehmet, Strom, Tim M, Fries, Ruedi, Nielsen, Rasmus, Simianer, Henner

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Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia von Zech, Michael, Boesch, Sylvia, Maier, Esther M., Borggraefe, Ingo, Vill, Katharina, Laccone, Franco, Pilshofer, Veronika, Ceballos-Baumann, Andres, Alhaddad, Bader, Berutti, Riccardo, Poewe, Werner, Haack, Tobias B., Haslinger, Bernhard, Strom, Tim M., Winkelmann, Juliane

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Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine von Dichgans, Martin, Freilinger, Tobias, Eckstein, Gertrud, Babini, Elena, Lorenz-Depiereux, Bettina, Biskup, Saskia, Ferrari, Michel D, Herzog, Jürgen, van den Maagdenberg, Arn MJM, Pusch, Michael, Strom, Tim M

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CRIM1 haploinsufficiency causes defects in eye development in human and mouse von Beleggia, F., Li, Y., Fan, J., Elcio lu, N. H., Toker, E., Wieland, T., Maumenee, I. H., Akarsu, N. A., Meitinger, T., Strom, T. M., Lang, R., Wollnik, B.

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Genetic diagnosis of Mendelian disorders via RNA sequencing von Kremer, Laura S., Bader, Daniel M., Mertes, Christian, Kopajtich, Robert, Pichler, Garwin, Iuso, Arcangela, Haack, Tobias B., Graf, Elisabeth, Schwarzmayr, Thomas, Terrile, Caterina, Koňaříková, Eliška, Repp, Birgit, Kastenmüller, Gabi, Adamski, Jerzy, Lichtner, Peter, Leonhardt, Christoph, Funalot, Benoit, Donati, Alice, Tiranti, Valeria, Lombes, Anne, Jardel, Claude, Gläser, Dieter, Taylor, Robert W., Ghezzi, Daniele, Mayr, Johannes A., Rötig, Agnes, Freisinger, Peter, Distelmaier, Felix, Strom, Tim M., Meitinger, Thomas, Gagneur, Julien, Prokisch, Holger

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Association between atopic dermatitis and extracutaneous infections in US adults von Strom, M.A., Silverberg, J.I.

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Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia von Freischmidt, Axel, Wieland, Thomas, Richter, Benjamin, Ruf, Wolfgang, Schaeffer, Veronique, Müller, Kathrin, Marroquin, Nicolai, Nordin, Frida, Hübers, Annemarie, Weydt, Patrick, Pinto, Susana, Press, Rayomond, Millecamps, Stéphanie, Molko, Nicolas, Bernard, Emilien, Desnuelle, Claude, Soriani, Marie-Hélène, Dorst, Johannes, Graf, Elisabeth, Nordström, Ulrika, Feiler, Marisa S., Putz, Stefan, Boeckers, Tobias M., Meyer, Thomas, Winkler, Andrea S., Winkelman, Juliane, de Carvalho, Mamede, Thal, Dietmar R., Otto, Markus, Brännström, Thomas, Volk, Alexander E, Kursula, Petri, Danzer, Karin M., Lichtner, Peter, Dikic, Ivan, Meitinger, Thomas, Ludolph, Albert C., Strom, Tim M., Andersen, Peter M., Weishaupt, Jochen H.

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Time‐ and compartment‐resolved proteome profiling of the extracellular niche in lung injury and repair von Schiller, Herbert B, Fernandez, Isis E, Burgstaller, Gerald, Schaab, Christoph, Scheltema, Richard A, Schwarzmayr, Thomas, Strom, Tim M, Eickelberg, Oliver, Mann, Matthias

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A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism von Fernandes-Rosa, Fabio L., Daniil, Georgios, Orozco, Ian J., Göppner, Corinna, El Zein, Rami, Jain, Vandana, Boulkroun, Sheerazed, Jeunemaitre, Xavier, Amar, Laurence, Lefebvre, Hervé, Schwarzmayr, Thomas, Strom, Tim M., Jentsch, Thomas J., Zennaro, Maria-Christina

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Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia von Oates, Emily C., Rossor, Alexander M., Hafezparast, Majid, Gonzalez, Michael, Speziani, Fiorella, MacArthur, Daniel G., Lek, Monkol, Cottenie, Ellen, Scoto, Mariacristina, Foley, A. Reghan, Hurles, Matthew, Houlden, Henry, Greensmith, Linda, Auer-Grumbach, Michaela, Pieber, Thomas R., Strom, Tim M., Schule, Rebecca, Herrmann, David N., Sowden, Janet E., Acsadi, Gyula, Menezes, Manoj P., Clarke, Nigel F., Züchner, Stephan, Muntoni, Francesco, North, Kathryn N., Reilly, Mary M.

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Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis von Ghezzi, Daniele, Baruffini, Enrico, Haack, Tobias B., Invernizzi, Federica, Melchionda, Laura, Dallabona, Cristina, Strom, Tim M., Parini, Rossella, Burlina, Alberto B., Meitinger, Thomas, Prokisch, Holger, Ferrero, Ileana, Zeviani, Massimo

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Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature von JAMRA, Rami Abou, PHILIPPE, Orianne, MUNNICH, Arnold, STROM, Tim M, REIS, Andre, COLLEAUX, Laurence, RAAS-ROTHSCHILD, Annick, ECK, Sebastian H, GRAF, Elisabeth, BUCHERT, Rebecca, BORCK, Guntram, EKICI, Arif, BROCKSCHMIDT, Felix F, NÖTHEN, Markus M

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Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets von Lorenz-Depiereux, Bettina, Schnabel, Dirk, Tiosano, Dov, Häusler, Gabriele, Strom, Tim M.

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Biallelic mutations of the methionyl-tRNA synthetase (MARS) cause a specific type of pulmonary alveolar proteinosis prevalent on Réunion Island von Hadchouel, Alice, Wieland, Thomas, Griese, Matthias, Baruffini, Enrico, Lorenz-Depiereux, Bettina, Enaud, Laurent, Graf, Elisabeth, Dubus, Jean Christophe, Halioui-Louhaichi, Sonia, Coulomb, Aurore, Delacourt, Christophe, Eckstein, Gertrud, Zarbock, Ralf, Schwarzmayr, Thomas, Cartault, François, Meitinger, Thomas, Lodi, Tiziana, de Blic, Jacques, Strom, Tim M.

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Effect of hypnotherapy and educational intervention on brain response to visceral stimulus in the irritable bowel syndrome von Lowén, M. B. O., Mayer, E. A., Sjöberg, M., Tillisch, K., Naliboff, B., Labus, J., Lundberg, P., Ström, M., Engström, M., Walter, S. A.

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Genetic Spectrum and Clinical Correlates of Somatic Mutations in Aldosterone-Producing Adenoma von Fernandes-Rosa, Fabio Luiz, Williams, Tracy Ann, Riester, Anna, Steichen, Olivier, Beuschlein, Felix, Boulkroun, Sheerazed, Strom, Tim M, Monticone, Silvia, Amar, Laurence, Meatchi, Tchao, Mantero, Franco, Cicala, Maria-Verena, Quinkler, Marcus, Fallo, Francesco, Allolio, Bruno, Bernini, Giampaolo, Maccario, Mauro, Giacchetti, Gilberta, Jeunemaitre, Xavier, Mulatero, Paolo, Reincke, Martin, Zennaro, Maria-Christina

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Estrogen receptor beta exerts tumor suppressive effects in prostate cancer through repression of androgen receptor activity von Chaurasiya, Surendra, Widmann, Scott, Botero, Cindy, Lin, Chin-Yo, Gustafsson, Jan-Ake, Strom, Anders M.

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Constitutive Activation of PKA Catalytic Subunit in Adrenal Cushing's Syndrome von Beuschlein, Felix, Fassnacht, Martin, Assié, Guillaume, Calebiro, Davide, Stratakis, Constantine A, Osswald, Andrea, Ronchi, Cristina L, Wieland, Thomas, Sbiera, Silviu, Faucz, Fabio R, Schaak, Katrin, Schmittfull, Anett, Schwarzmayr, Thomas, Barreau, Olivia, Vezzosi, Delphine, Rizk-Rabin, Marthe, Zabel, Ulrike, Szarek, Eva, Salpea, Paraskevi, Forlino, Antonella, Vetro, Annalisa, Zuffardi, Orsetta, Kisker, Caroline, Diener, Susanne, Meitinger, Thomas, Lohse, Martin J, Reincke, Martin, Bertherat, Jérome, Strom, Tim M, Allolio, Bruno

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Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA von Haack, Tobias B., Hogarth, Penelope, Kruer, Michael C., Gregory, Allison, Wieland, Thomas, Schwarzmayr, Thomas, Graf, Elisabeth, Sanford, Lynn, Meyer, Esther, Kara, Eleanna, Cuno, Stephan M., Harik, Sami I., Dandu, Vasuki H., Nardocci, Nardo, Zorzi, Giovanna, Dunaway, Todd, Tarnopolsky, Mark, Skinner, Steven, Frucht, Steven, Hanspal, Era, Schrander-Stumpel, Connie, Héron, Delphine, Mignot, Cyril, Garavaglia, Barbara, Bhatia, Kailash, Hardy, John, Strom, Tim M., Boddaert, Nathalie, Houlden, Henry H., Kurian, Manju A., Meitinger, Thomas, Prokisch, Holger, Hayflick, Susan J.

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