Shared history von Maier, Em Dzhali, Beardsley, Felicia R.

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Diagnostic Challenges Using a 2-Tier Strategy for Methylmalonic Acidurias: Data from 1.2 Million Dried Blood Spots von Weiss, Katharina J., Röschinger, Wulf, Blessing, Holger, Lotz-Havla, Amelie S., Schiergens, Katharina A., Maier, Esther M.

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Why science? Scientists share their stories von Buckley, Ralf C, Arcos, Denisse Fierro, Clinciu, Daniel L, Scarf, Damian, Trinder, Mark, Santee, Endia J, Kirk, Katherine, Watkins, Tim, Merluzzi, Andrew, Shishmahal, Haider Ali, Morrow, Rebekah, Maier, Em Dzhali, Beardsley, Felicia R, da Silva Lopes, Karen, James, Joshua I, Qasim, Hassnain, Rosenberg, Jessica, Kitsinelis, Spiros, VanWees, Samantha

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188. Visualizing the Impact of a Wedding Leading to COVID-19 Outbreaks in Healthcare Settings, Washington State, July – August 2020 von Brezak, Audrey, Unutzer, Anna, Lewis, James W, Clark, Shauna, Ferro, Jessica, Bliesner, Siri, Loughran, Julie, Kawakami, Vance, Deya, Ruth, Makayoto, Rhodah, Maier, Em, Whitney, Holly, Bevers, Elyse, Templeton, Allison A, Burlingham, Bonnie, Lewis, Larissa, Podczervinski, Sara T

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Genotypic and phenotypic characterization of Noonan syndrome: New data and review of the literature von Jongmans, Marjolijn, Sistermans, Erik A., Rikken, Alwin, Nillesen, Willy M., Tamminga, Rienk, Patton, Michael, Maier, Esther M., Tartaglia, Marco, Noordam, Kees, van der Burgt, Ineke

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Validation of MCADD newborn screening von Maier, EM, Pongratz, J, Muntau, AC, Liebl, B, Nennstiel-Ratzel, U, Busch, U, Fingerhut, R, Olgemöller, B, Roscher, AA, Röschinger, W

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Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation von Maier, Esther M., Kammerer, Stefan, Muntau, Ania C., Wichers, Maria, Braun, Andreas, Roscher, Adelbert A.

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Reduced incidence of severe metabolic crisis or death in children with medium chain acyl-CoA dehydrogenase deficiency homozygous for c.985A > G identified by neonatal screening von Nennstiel-Ratzel, Uta, Arenz, Stephan, Maier, Esther M., Knerr, Ina, Baumkötter, Joachim, Röschinger, Wulf, Liebl, Bernhard, Hadorn, Hans-Beat, Roscher, Adelbert A., von Kries, Rüdiger

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Mutations in the Proenteropeptidase Gene Are the Molecular Cause of Congenital Enteropeptidase Deficiency von Holzinger, Andreas, Maier, Esther M., Bück, Cornelius, Mayerhofer, Peter U., Kappler, Matthias, Haworth, James C., Moroz, Stanley P., Hadorn, Hans-Beat, Sadler, J. Evan, Roscher, Adelbert A.

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Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene von Coenen, Marieke J. H., van den Heuvel, Lambert P., Ugalde, Cristina, ten Brinke, Marike, Nijtmans, Leo G. J., Trijbels, Frans J. M., Beblo, Skadi, Maier, Esther M., Muntau, Ania C., Smeitink, Jan A. M.

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Antitrypsin and the prevalence and severity of asthma von von Ehrenstein, O.S, Maier, E.M, Weiland, S.K, Carr, D, Hirsch, T, Nicolai, T, Roscher, A.A, von Mutius, E

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First-trimester increased nuchal translucency as a prenatal sign of Zellweger syndrome von Strenge, S., Froster, U. G., Wanders, R. J. A., Gartner, J., Maier, E. M., Muntau, A. C., Faber, R.

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Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analyses von Maier, Esther M., Roscher, Adelbert A., Kammerer, Stefan, Mehnert, Karl, Conzelmann, Ernst, Holzinger, Andreas

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Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults: A 2-Sample Mendelian Randomization Study von Choi, Karmel W, Chen, Chia-Yen, Stein, Murray B, Klimentidis, Yann C, Wang, Min-Jung, Koenen, Karestan C, Smoller, Jordan W

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Spinal upregulation of glutamate transporter GLT-1 by ceftriaxone: therapeutic efficacy in a range of experimental nervous system disorders von Ramos, K.M, Lewis, M.T, Morgan, K.N, Crysdale, N.Y, Kroll, J.L, Taylor, F.R, Harrison, J.A, Sloane, E.M, Maier, S.F, Watkins, L.R

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank von Coleman, Jonathan R. I., Peyrot, Wouter J., Purves, Kirstin L., Davis, Katrina A. S., Rayner, Christopher, Choi, Shing Wan, Hübel, Christopher, Gaspar, Héléna A., Kan, Carol, Van der Auwera, Sandra, Adams, Mark James, Lyall, Donald M., Choi, Karmel W., Dunn, Erin C., Vassos, Evangelos, Danese, Andrea, Maughan, Barbara, Grabe, Hans J., Lewis, Cathryn M., O’Reilly, Paul F., McIntosh, Andrew M., Smith, Daniel J., Wray, Naomi R., Hotopf, Matthew, Eley, Thalia C., Breen, Gerome

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression von Ripke, Stephan, Trzaskowski, Maciej, Byrne, Enda M., Adams, Mark J., Andlauer, Till M. F., Bacanu, Silviu-Alin, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bybjerg-Grauholm, Jonas, Castelao, Enrique, Couvy-Duchesne, Baptiste, Craddock, Nick, Deary, Ian J., Finucane, Hilary K., Forstner, Andreas J., Frank, Josef, Gill, Michael, Goes, Fernando S., Grove, Jakob, Hall, Lynsey S., Hannon, Eilis, Hansen, Thomas F., Hickie, Ian B., Hoffmann, Per, Horn, Carsten, Hougaard, David M., Hyde, Craig L., Jorgenson, Eric, Knowles, James A., Kraft, Julia, Krogh, Jesper, Kutalik, Zoltán, Lane, Jacqueline M., Li, Yihan, Li, Yun, Liu, Xiaoxiao, Lu, Leina, MacIntyre, Donald J., MacKinnon, Dean F., Maier, Robert M., Marchini, Jonathan, Mbarek, Hamdi, McGrath, Patrick, Mehta, Divya, Montgomery, Grant W., Nauck, Matthias, Nivard, Michel G., Pedersen, Carsten Bøcker, Posthuma, Danielle, Purcell, Shaun M., Quiroz, Jorge A., Saeed Mirza, Saira, Schoevers, Robert, Schulte, Eva C., Shi, Jianxin, Shyn, Stanley I., Smit, Johannes H., Smith, Daniel J., Stockmeier, Craig A., Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Tian, Chao, Treutlein, Jens, van Hemert, Albert M., Viktorin, Alexander, Visscher, Peter M., Wang, Yunpeng, Weinsheimer, Shantel Marie, Wellmann, Jürgen, Witt, Stephanie H., Wu, Yang, Xi, Hualin S., Yang, Jian, Zhang, Futao, Baune, Bernhard T., Berger, Klaus, de Geus, E. C. J., Domschke, Katharina, Esko, Tõnu, Hinds, David A., Li, Qingqin S., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Müller-Myhsok, Bertram, O’Donovan, Michael C., Paciga, Sara A., Pedersen, Nancy L., Perlis, Roy H., Potash, James B., Schaefer, Catherine, Schulze, Thomas G., Uher, Rudolf, Völzke, Henry, Winslow, Ashley R., Børglum, Anders D.

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Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis optica von Rostásy, K, Mader, S, Hennes, EM, Schanda, K, Gredler, V, Guenther, A, Blaschek, A, Korenke, C, Pritsch, M, Pohl, D, Maier, O, Kuchukhidze, G, Brunner-Krainz, M, Berger, T, Reindl, M

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Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior von Ganna, Andrea, Verweij, Karin J H, Nivard, Michel G, Maier, Robert, Wedow, Robbee, Busch, Alexander S, Abdellaoui, Abdel, Guo, Shengru, Sathirapongsasuti, J Fah, Lichtenstein, Paul, Lundström, Sebastian, Långström, Niklas, Auton, Adam, Harris, Kathleen Mullan, Beecham, Gary W, Martin, Eden R, Sanders, Alan R, Perry, John R B, Neale, Benjamin M, Zietsch, Brendan P

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