Genetic Predisposition for Adult Lactose Intolerance and Relation to Diet, Bone Density, and Bone Fractures by Obermayer‐Pietsch, Barbara M, Bonelli, Christine M, Walter, Daniela E, Kuhn, Regina J, Fahrleitner‐Pammer, Astrid, Berghold, Andrea, Goessler, Walter, Stepan, Vinzenz, Dobnig, Harald, Leb, Georg, Renner, Wilfried

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Community acquired pneumonia CAP by Wenisch, Christoph, Bonelli, Christine M

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Genetic Components of Lactose Intolerance and Community Frequency by Obermayer‐Pietsch, Barbara M, Bonelli, Christine M, Walter, Daniela, Fahrleitner, Astrid, Stepan, Vinzenz, Dobnig, Harald, Leb, Georg, Renner, Wilfried

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Außerhalb des Krankenhauses erworbene Pneumonie (community acquired pneumonia CAP) by Wenisch, Christoph, Bonelli, Christine M.

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Large-Scale Analysis of Association Between LRP5 and LRP6 Variants and Osteoporosis by van Meurs, Joyce B. J, Trikalinos, Thomas A, Ralston, Stuart H, Balcells, Susana, Brandi, Maria Luisa, Brixen, Kim, Kiel, Douglas P, Langdahl, Bente L, Lips, Paul, Ljunggren, Östen, Lorenc, Roman, Obermayer-Pietsch, Barbara, Ohlsson, Claes, Pettersson, Ulrika, Reid, David M, Rousseau, Francois, Scollen, Serena, Van Hul, Wim, Agueda, Lidia, Åkesson, Kristina, Benevolenskaya, Lidia I, Ferrari, Serge L, Hallmans, Göran, Hofman, Albert, Husted, Lise Bjerre, Kruk, Marcin, Kaptoge, Stephen, Karasik, David, Karlsson, Magnus K, Lorentzon, Mattias, Masi, Laura, McGuigan, Fiona E. A, Mellström, Dan, Mosekilde, Leif, Nogues, Xavier, Pols, Huibert A. P, Reeve, Jonathan, Renner, Wilfried, Rivadeneira, Fernando, van Schoor, Natasja M, Weber, Kurt, Ioannidis, John P. A, Uitterlinden, André G, GENOMOS Study, for the

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Suicidal ideation in a European Huntington's disease population by Hubers, Anna A.M, van Duijn, Erik, Roos, Raymund A.C, Craufurd, David, Rickards, Hugh, Bernhard Landwehrmeyer, G, van der Mast, Rose C, Giltay, Erik J

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The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients by Metzger, Silke, Walter, Carolin, Riess, Olaf, Roos, Raymund A C, Nielsen, Jørgen E, Craufurd, David, Nguyen, Huu Phuc

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Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: The GENOMOS study by Langdahl, Bente L, Uitterlinden, André G, Ralston, Stuart H, Trikalinos, Thomas A, Balcells, Susanne, Brandi, Maria Luisa, Scollen, Serena, Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Reid, David M, Armas, Jácome Bruges, Arp, Pascal P, Bassiti, Amelia, Bustamante, Mariona, Husted, Lise Bjerre, Carey, Alison H, Pérez Cano, Ramon, Dobnig, Harald, Dunning, Alison M, Fahrleitner-Pammer, Astrid, Falchetti, Alberto, Karczmarewicz, Elzbieta, Kruk, Marcin, van Leeuwen, Johannes P.T.M, Masi, Laura, van Meurs, Joyce B.J, Mangion, Jon, McGuigan, Fiona E.A, Mellibovsky, Leonardo, Mosekilde, Leif, Nogués, Xavier, Pols, Huibert A.P, Reeve, Jonathan, Renner, Wilfried, Rivadeneira, Fernando, van Schoor, Natasja M, Ioannidis, John P.A

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Discrepancies in reporting the CAG repeat lengths for Huntington's disease by Quarrell, Oliver W, Handley, Olivia, O'Donovan, Kirsty, Dumoulin, Christine, Ramos-Arroyo, Maria, Biunno, Ida, Bauer, Peter, Kline, Margaret, Landwehrmeyer, G Bernhard

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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study by Moss, Davina, Pardiñas, Antonio, Langbehn, Douglas, Lo, Kitty, Leavitt, Blair, Roos, Raymund, Durr, Alexandra, Mead, Simon, Holmans, Peter, Jones, Lesley, Tabrizi, Sarah, Coleman, A, Santos, R Dar, Decolongon, J, Sturrock, A, Bardinet, E, Ret, C Jauff, Justo, D, Lehericy, S, Marelli, C, Nigaud, K, Valabrègue, R, van den Bogaard, Sja, Dumas, E, van der Grond, J, t'Hart, Ep, Jurgens, C, Witjes-Ane, M-N, Arran, N, Callaghan, J, Stopford, C, Frost, C, Jones, R, Hobbs, N, Lahiri, N, Ordidge, R, Owen, G, Pepple, T, Read, J, Say, M, Wild, E, Patel, A, Fox, N, Gibbard, C, Malone, I, Crawford, H, Whitehead, D, Keenan, S, Cash, D, Berna, C, Bechtel, N, Bohlen, S, Man, a Hoff, Kraus, P, Axelson, E, Wang, C, Acharya, T, Lee, S, Monaco, W, Campbell, C, Queller, S, Whitlock, K, Campbell, M, Frajman, E, Milchman, C, O'Regan, A, Labuschagne, I, Stout, J, Landwehrmeyer, B, Craufurd, D, Scahill, R, Hicks, S, Kennard, C, Johnson, H, Tobin, A, Rosas, Hd, Reilmann, R, Borowsky, B, Pourchot, C, Andrews, S, Bachoud-Lévi, Anne-Catherine, Bentivoglio, Anna Rita, Biunno, Ida, Bonelli, Raphael, Burgunder, Jean-Marc, Dunnett, Stephen, Ferreira, Joaquim, Handley, Olivia, Heiberg, Arvid, Illmann, Torsten, Landwehrmeyer, G. Bernhard, Levey, Jamie, Ramos-Arroyo, Maria, Nielsen, Jørgen, Koivisto, Susana Pro, Päivärinta, Markku, Roos, Raymund A.C., Sebastián, a Rojo, Vandenberghe, Wim, Verellen-Dumoulin, Christine

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NMDA receptor gene variations as modifiers in Huntington disease: a replication study by Saft, Carsten, Epplen, Jörg T, Wieczorek, Stefan, Landwehrmeyer, G Bernhard, Roos, Raymund A C, de Yebenes, Justo Garcia, Dose, Matthias, Tabrizi, Sarah J, Craufurd, David, Arning, Larissa

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