Definition of a Fundamental Repeating Unit in Streptococcal Glucosyltransferase Glucan-binding Regions and Related Sequences von Giffard, P.M., Jacques, N.A.

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Deletion of competence-induced genes over-expressed in biofilms caused transformation deficiencies in Streptococcus mutans von Eaton, R.E., Jacques, N.A.

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Proteome Analysis of Oral Pathogens von Macarthur, D.J., Jacques, N.A.

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Interventions for prevention of otitis media may be most effective if implemented in the first weeks of life von Smith-Vaughan, Heidi, Byun, Roy, Halpin, Stephen, Nadkarni, Mangala A, Jacques, Nicholas A, Hunter, Neil, Morris, Peter S, Leach, Amanda J

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Enumeration of Oral Streptococci on Media Containing Different Concentrations of Sodium and Potassium Ions von Willcox, M.D.P., Irwin, A.M., Jacques, N.A., Knox, K.W.

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Intricacies of the Molecular Machinery of Catecholamine Biosynthesis and Secretion by Chromaffin Cells of the Normal Adrenal Medulla and in Pheochromocytoma and Paraganglioma von Berends, Annika M A, Eisenhofer, Graeme, Fishbein, Lauren, Horst-Schrivers, Anouk N A V D, Kema, Ido P, Links, Thera P, Lenders, Jacques W M, Kerstens, Michiel N

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Activation of PPARβ/δ Causes a Psoriasis-Like Skin Disease In Vivo von Romanowska, Malgorzata, Reilly, Louise, Palmer, Colin N. A., Gustafsson, Mattias C. U., Foerster, John

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Seismicity of the Baikal rift system from regional network observations von Radziminovich, N.A., Gileva, N.A., Melnikova, V.I., Ochkovskaya, M.G.

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Circulating adrenomedullin and B-type natriuretic peptide do not predict blood pressure fluctuations during pheochromocytoma resection: a cross-sectional study von Berends, Annika M A, Buitenwerf, Edward, Riphagen, Ineke J, Lenders, Jacques W M, Timmers, Henri J L M, Kruijff, Schelto, Links, Thera P, van der Horst-Schrivers, Anouk N A, Stegeman, Coen A, Eekhoff, Elisabeth M W, Feelders, Richard A, Corssmit, Eleonora P M, Groote Veldman, Ronald, Haak, Harm R, Muller Kobold, Anneke C, Kerstens, Michiel N

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ENIGMA-Evidence-based network for the interpretation of germline mutant alleles: An international initiative to evaluate risk and clinical significance associated with sequence var... von Spurdle, Amanda B., Healey, Sue, Devereau, Andrew, Hogervorst, Frans B. L., Monteiro, Alvaro N. A., Nathanson, Katherine L., Radice, Paolo, Stoppa-Lyonnet, Dominique, Tavtigian, Sean, Wappenschmidt, Barbara, Couch, Fergus J., Goldgar, David E.

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Variants in MTNR1B influence fasting glucose levels von Ahmadi, Kourosh, Mooser, Vincent, Wichmann, H-Erich, Sandhu, Manjinder, Saramies, Jouko, Palmer, Colin N A, Isomaa, Bo, Peltonen, Leena, Schlessinger, David, Thorsteinsdottir, Unnur, Hottenga, Jouke-Jan, Jarvelin, Marjo Riitta, McCann, Owen T, Dupuis, Josée, Manning, Alisa K, Cervino, Alessandra, Zeggini, Eleftheria, Boomsma, Dorret I, Soranzo, Nicole, Sijbrands, Eric, Crisponi, Laura, Willemsen, Gonneke, Van Duijn, Cornelia, Stefansson, Kari, Scuteri, Angelo, Watanabe, Richard M, Potter, Simon C, Groop, Leif C, Zhao, Jing Hua, Deloukas, Panos, Freimer, Nelson, Beckmann, Jacques S, Boehnke, Michael, Smit, Jan H, Kong, Augustine, Fox, Caroline S, Bergman, Richard N, Chen, Wei-Min, Cupples, L Adrienne, Florez, Jose C, Erdos, Michael R, Hunt, Sarah, Song, Kijoung, Bochud, Murielle, Kuusisto, Johanna, Dehghan, Abbas, Lindblad, Ulf, Altshuler, David, Sharp, Stephen, Yuan, Xin, Tuomi, Tiinamaija, Vollenweider, Peter, Penninx, Brenda WJH, Aulchenko, Yurii, Saxena, Richa, Voight, Benjamin F, McCarthy, Mark I, Lim, Noha, Lakatta, Edward, Mohlke, Karen L, Uitterlinden, André G, Illig, Thomas, Elliott, Paul, Naitza, Silvia, Randall, Joshua, Krestyaninova, Maria, Morris, Andrew D, Lindgren, Cecilia M, Collins, Francis S, Abecasis, Gonçalo R, Buchanan, Thomas A, Scott, Laura J, Gateva, Vesela, Sanna, Serena, Johnson, Toby, Doney, Alex S F, Spector, Tim D, Waeber, Gerard, Uda, Manuela, Orrù, Marco, Laakso, Markku, Barroso, Inês, Rathmann, Wolfgang, de Geus, Eco J C, Bonnycastle, Lori L, Thorleifsson, Gudmar, Stringham, Heather M, Waterworth, Dawn, Meigs, James B, Wheeler, Eleanor, Witteman, Jacqueline C M, Loos, Ruth J F, Kaakinen, Marika, Lyssenko, Valeriya, Wareham, Nicholas J, Prokopenko, Inga, Cao, Antonio, Scheet, Paul, Hughes, Thomas E, Langenberg, Claudia

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Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth von Beaumont, Robin N., Flatley, Christopher, Vaudel, Marc, Wu, Xiaoping, Chen, Jing, Moen, Gunn-Helen, Skotte, Line, Helgeland, Øyvind, Solé-Navais, Pol, Banasik, Karina, Albiñana, Clara, Ronkainen, Justiina, Fadista, João, Stinson, Sara Elizabeth, Trajanoska, Katerina, Wang, Carol A., Westergaard, David, Srinivasan, Sundararajan, Sánchez-Soriano, Carlos, Bilbao, Jose Ramon, Allard, Catherine, Groleau, Marika, Kuulasmaa, Teemu, Leirer, Daniel J., White, Frédérique, Jacques, Pierre-Étienne, Cheng, Haoxiang, Hao, Ke, Andreassen, Ole A., Åsvold, Bjørn Olav, Atalay, Mustafa, Bhatta, Laxmi, Bouchard, Luigi, Brumpton, Ben Michael, Brunak, Søren, Bybjerg-Grauholm, Jonas, Ebbing, Cathrine, Elliott, Paul, Engelbrechtsen, Line, Erikstrup, Christian, Estarlich, Marisa, Franks, Stephen, Gaillard, Romy, Geller, Frank, Grove, Jakob, Hougaard, David M., Kajantie, Eero, Morgen, Camilla S., Nohr, Ellen A., Nyegaard, Mette, Palmer, Colin N. A., Pedersen, Ole Birger, Rivadeneira, Fernando, Sebert, Sylvain, Shields, Beverley M., Stoltenberg, Camilla, Surakka, Ida, Thørner, Lise Wegner, Ullum, Henrik, Vaarasmaki, Marja, Vilhjalmsson, Bjarni J., Willer, Cristen J., Lakka, Timo A., Gybel-Brask, Dorte, Bustamante, Mariona, Hansen, Torben, Pearson, Ewan R., Reynolds, Rebecca M., Ostrowski, Sisse R., Pennell, Craig E., Jaddoe, Vincent W. V., Felix, Janine F., Hattersley, Andrew T., Melbye, Mads, Lawlor, Deborah A., Hveem, Kristian, Werge, Thomas, Nielsen, Henriette Svarre, Magnus, Per, Evans, David M., Jacobsson, Bo, Järvelin, Marjo-Riitta, Zhang, Ge, Hivert, Marie-France, Johansson, Stefan, Freathy, Rachel M., Feenstra, Bjarke, Njølstad, Pål R.

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Genome-wide association analysis identifies 20 loci that influence adult height von Wallace, Chris, Mooser, Vincent, Johnson, Toby, Bergmann, Sven, Dominiczak, Anna, Weedon, Michael N, Waterworth, Dawn M, Morris, Andrew D, Perry, John R B, Ouwehand, Willem H, Munroe, Patricia B, Lango, Hana, Frayling, Timothy M, Lindgren, Cecilia M, Shields, Beverly, Palmer, Colin N A, Hall, Alistair S, McCarthy, Mark I, Freathy, Rachel M, Beckmann, Jacques S, Stevens, Suzanne, Caulfield, Mark, Prokopenko, Inga, Mangino, Massimo, Vollenweider, Peter, Hattersley, Andrew T, Samani, Nilesh J, Evans, David M, Farrall, Martin

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Developmental fluoxetine exposure differentially alters central and peripheral measures of the HPA system in adolescent male and female offspring von Pawluski, J.L, Rayen, I, Niessen, N.A, Kristensen, S, van Donkelaar, E.L, Balthazart, J, Steinbusch, H.W, Charlier, T.D

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Functional characterization of 84 PALB2 variants of uncertain significance von Wiltshire, Timothy, Ducy, Mandy, Foo, Tzeh Keong, Hu, Chunling, Lee, Kun Y., Belur Nagaraj, Anil, Rodrigue, Amélie, Gomes, Thiago T., Simard, Jacques, Monteiro, Alvaro, Xia, Bing, Carvalho, Marcelo A., Masson, Jean-Yves, Couch, Fergus J.

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Unilateral versus bilateral correction of unicoronal synostosis: An analysis of long-term results von Cornelissen, Martijn J, van der Vlugt, Joris J, Willemsen, Joep C.N, van Adrichem, Leon N.A, Mathijssen, Irene M.J, van der Meulen, Jacques J.N.M

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PALB2 Variants: Protein Domains and Cancer Susceptibility von Nepomuceno, Thales C, Carvalho, Marcelo A, Rodrigue, Amélie, Simard, Jacques, Masson, Jean-Yves, Monteiro, Alvaro N A

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Papilledema in isolated single-suture craniosynostosis: prevalence and predictive factors von Florisson, Joyce M G, van Veelen, Marie-Lise C, Bannink, Natalja, van Adrichem, Léon N A, van der Meulen, Jacques J N M, Bartels, Marjolijn C, Mathijssen, Irene M J

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Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia von Kendler, Kenneth S., Walters, James, Blackwell, Jenefer M., Bramon, Elvira, Markus, Hugh S., Rautanen, Anna, Freeman, Colin, Hopkins, Lucinda, Edkins, Sarah, Bumpstead, Suzannah J., Dronov, Serge, Gillman, Matthew, Gray, Emma, Liddle, Jennifer, Potter, Simon C., Weston, Paul, Ripke, Stephan, Farh, Kai‐How, Holmans, Peter A., Lee, Phil, Huang, Hailiang, Bacanu, Silviu A., Belliveau, Richard A., Bene, Judit, Bigdeli, Tim B., Bruggeman, Richard, Cahn, Wiepke, Carrera, Noa, Cheung, Eric F. C., Cohen, David, Craddock, Nick, Davis, Kenneth L., Dinan, Timothy, Drapeau, Elodie, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Farrell, Martilias S., Franke, Lude, Freimer, Nelson B., Friedman, Joseph I., Fromer, Menachem, Gratten, Jacob, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Hofman, Andrea, Hollegaard, Mads V., Joa, Inge, Keller, Matthew C., Klovins, Janis, Konte, Bettina, Kucinskiene, Zita Ausrele, Laurent, Claudine, Loughland, Carmel M., Mallet, Jacques, Mattheisen, Manuel, McCarley, Robert W., McDonald, Colm, Meier, Sandra, Meijer, Carin J., Metspalu, Andres, Milani, Lili, Milanova, Vihra, Mokrab, Younes, Myin‐Germeys, Inez, Nenadic, Igor, Nikitina‐Zake, Liene, O'Callaghan, Eadbhard, O'Neill, F. Anthony, Paunio, Tiina, Pejovic‐Milovancevic, Milica, Perkins, Diana O., Pietiläinen, Olli, Quested, Digby, Reichenberg, Abraham, Salomaa, Veikko, Scolnick, Edward M., Silagadze, Teimuraz, So, Hon‐Cheong, Spencer, Chris C. A., Suvisaari, Jaana, Szatkiewicz, Jin P., Thirumalai, Srinivas, Tosato, Sarah, Waddington, John, Wang, Qiang, Williams, Nigel M., Witt, Stephanie H., Wormley, Brandon K., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Buxbaum, Joseph D., Jablensky, Assen V., Knight, Jo, Levinson, Douglas F., Malhotra, Anil K., Weinberger, Daniel R., Werge, Thomas

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On the origin of bitemporal hollowing von van der Meulen, Jacques J N M, Willemsen, Joep, van der Vlugt, Joris, Nazir, Patricia R N, Hilling, Denise, Mathijssen, Irene M J, Ongkosuwito, Edwin, van Adrichem, Leon N A, Vaandrager, Michiel J M, Hovius, Steven E R

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