Exploring the Tunable Optical and Mechanical Properties of Multicomponent Low-Molecular-Weight Gelators von Loos, Jeanette N, Boott, Charlotte E, Hayward, Dominic W, Hum, Gabriel, MacLachlan, Mark J

Volltext

Manipulating the Self‐Assembly of Multicomponent Low Molecular Weight Gelators (LMWGs) through Molecular Design von Loos, Jeanette N., D'Acierno, Francesco, Vijay Mody, Urmi, MacLachlan, Mark J.

Volltext

Mouldable multicomponent low molecular weight supergelators von Loos, Jeanette N., Chaudhry, Mohammad T., Li, Zongzhe, MacLachlan, Mark J.

Volltext bestellen

GeMark: Ein bibliometrisches Ranking für Marketing-Zeitschriften von Voeth, Markus, Loos, Jeanette, Herbst, Uta

Volltext

GeMark: Ein bibliometrisches Ranking für Marketing-Zeitschriften von Voeth, Markus, Loos, Jeanette, Herbst, Uta

Volltext

Customer Experience Management bei B2B-Services – Besonderheiten und Erfolgsfaktoren von Voeth, Markus, Loos, Jeanette

Volltext

Die neue Macht der Konsumenten? Einfluss von Verbraucherportalen auf die Verpackungsgestaltung im Lebensmittelbereich von Loos, Jeanette, Braun, Deborah

Volltext

Dasœ Publikationsverhalten deutschsprachiger Marketing-Wissenschaftler :eine empirische Analyse auf Basis bibliometrischer Vergleichsstudien von Loos, Jeanette

Volltext bestellen

Die Wirkung des vertrauensstiftenden Fair Trade-Siegels auf die Kaufentscheidung von Verbrauchern: Erkenntnisse auf Basis einer conjoint-analytischen Untersuchung von Loos, Jeanette, Bertels, Victoria, Müller, Simone

Volltext

Quality control and conduct of genome-wide association meta-analyses von Winkler, Thomas W, Day, Felix R, Croteau-Chonka, Damien C, Wood, Andrew R, Locke, Adam E, Mägi, Reedik, Ferreira, Teresa, Fall, Tove, Graff, Mariaelisa, Justice, Anne E, Luan, Jian'an, Gustafsson, Stefan, Randall, Joshua C, Vedantam, Sailaja, Workalemahu, Tsegaselassie, Kilpeläinen, Tuomas O, Scherag, André, Esko, Tonu, Kutalik, Zoltán, Heid, Iris M, Loos, Ruth J F

Volltext

A structural variation reference for medical and population genetics von Collins, Ryan L., Brand, Harrison, Karczewski, Konrad J., Zhao, Xuefang, Alföldi, Jessica, Francioli, Laurent C., Khera, Amit V., Lowther, Chelsea, Gauthier, Laura D., Wang, Harold, Watts, Nicholas A., Solomonson, Matthew, O’Donnell-Luria, Anne, Baumann, Alexander, Munshi, Ruchi, Walker, Mark, Whelan, Christopher W., Huang, Yongqing, Brookings, Ted, Sharpe, Ted, Stone, Matthew R., Valkanas, Elise, Fu, Jack, Tiao, Grace, Laricchia, Kristen M., Ruano-Rubio, Valentin, Stevens, Christine, Gupta, Namrata, Cusick, Caroline, Margolin, Lauren, Taylor, Kent D., Lin, Henry J., Rich, Stephen S., Post, Wendy S., Chen, Yii-Der Ida, Rotter, Jerome I., Nusbaum, Chad, Philippakis, Anthony, Lander, Eric, Gabriel, Stacey, Neale, Benjamin M., Kathiresan, Sekar, Daly, Mark J., Banks, Eric, MacArthur, Daniel G., Talkowski, Michael E.

Volltext

A genomic mutational constraint map using variation in 76,156 human genomes von Chen, Siwei, Francioli, Laurent C., Goodrich, Julia K., Collins, Ryan L., Kanai, Masahiro, Wang, Qingbo, Alföldi, Jessica, Watts, Nicholas A., Vittal, Christopher, Gauthier, Laura D., Poterba, Timothy, Wilson, Michael W., Tarasova, Yekaterina, Phu, William, Grant, Riley, Yohannes, Mary T., Koenig, Zan, Farjoun, Yossi, Banks, Eric, Donnelly, Stacey, Gabriel, Stacey, Gupta, Namrata, Ferriera, Steven, Tolonen, Charlotte, Novod, Sam, Bergelson, Louis, Roazen, David, Ruano-Rubio, Valentin, Covarrubias, Miguel, Llanwarne, Christopher, Petrillo, Nikelle, Wade, Gordon, Jeandet, Thibault, Munshi, Ruchi, Tibbetts, Kathleen, O’Donnell-Luria, Anne, Solomonson, Matthew, Seed, Cotton, Martin, Alicia R., Talkowski, Michael E., Rehm, Heidi L., Daly, Mark J., Tiao, Grace, Neale, Benjamin M., MacArthur, Daniel G., Karczewski, Konrad J.

Volltext

Association analyses based on false discovery rate implicate new loci for coronary artery disease von Nelson, Christopher P, Goel, Anuj, Butterworth, Adam S, Kanoni, Stavroula, Webb, Tom R, Marouli, Eirini, Zeng, Lingyao, Ntalla, Ioanna, Lai, Florence Y, Hopewell, Jemma C, Giannakopoulou, Olga, Jiang, Tao, Hamby, Stephen E, Di Angelantonio, Emanuele, Assimes, Themistocles L, Bottinger, Erwin P, Chambers, John C, Clarke, Robert, Palmer, Colin N A, Cubbon, Richard M, Ellinor, Patrick, Ermel, Raili, Evangelou, Evangelos, Franks, Paul W, Grace, Christopher, Gu, Dongfeng, Hingorani, Aroon D, Howson, Joanna M M, Ingelsson, Erik, Kastrati, Adnan, Kessler, Thorsten, Kyriakou, Theodosios, Lehtimäki, Terho, Lu, Xiangfeng, Lu, Yingchang, März, Winfried, McPherson, Ruth, Metspalu, Andres, Pujades-Rodriguez, Mar, Ruusalepp, Arno, Schadt, Eric E, Schmidt, Amand F, Sweeting, Michael J, Zalloua, Pierre A, AlGhalayini, Kamal, Keavney, Bernard D, Kooner, Jaspal S, Loos, Ruth J F, Patel, Riyaz S, Rutter, Martin K, Tomaszewski, Maciej, Tzoulaki, Ioanna, Zeggini, Eleftheria, Erdmann, Jeanette, Dedoussis, George, Björkegren, Johan L M, Schunkert, Heribert, Farrall, Martin, Danesh, John, Samani, Nilesh J, Watkins, Hugh, Deloukas, Panos

Volltext

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits von Voight, Benjamin F, Kang, Hyun Min, Ding, Jun, Palmer, Cameron D, Sidore, Carlo, Chines, Peter S, Burtt, Noël P, Fuchsberger, Christian, Li, Yanming, Erdmann, Jeanette, Frayling, Timothy M, Heid, Iris M, Jackson, Anne U, Johnson, Toby, Kilpeläinen, Tuomas O, Lindgren, Cecilia M, Morris, Andrew P, Prokopenko, Inga, Randall, Joshua C, Saxena, Richa, Soranzo, Nicole, Speliotes, Elizabeth K, Teslovich, Tanya M, Wheeler, Eleanor, Maguire, Jared, Parkin, Melissa, Potter, Simon, Rayner, N William, Robertson, Neil, Stirrups, Kathleen, Winckler, Wendy, Sanna, Serena, Mulas, Antonella, Nagaraja, Ramaiah, Cucca, Francesco, Barroso, Inês, Deloukas, Panos, Loos, Ruth J F, Kathiresan, Sekar, Munroe, Patricia B, Newton-Cheh, Christopher, Pfeufer, Arne, Samani, Nilesh J, Schunkert, Heribert, Hirschhorn, Joel N, Altshuler, David, McCarthy, Mark I, Abecasis, Gonçalo R, Boehnke, Michael

Volltext

The mutational constraint spectrum quantified from variation in 141,456 humans von Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, Jessica, Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, Anne H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G.

Volltext

Evaluating drug targets through human loss-of-function genetic variation von Minikel, Eric Vallabh, Karczewski, Konrad J., Martin, Hilary C., Cummings, Beryl B., Whiffin, Nicola, Rhodes, Daniel, Alföldi, Jessica, Trembath, Richard C., van Heel, David A., Daly, Mark J., Schreiber, Stuart L., MacArthur, Daniel G.

Volltext

Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease von Crosby, Jacy, Peloso, Gina M, Auer, Paul L, Crosslin, David R, Stitziel, Nathan O, Lange, Leslie A, Lu, Yingchang, Tang, Zheng-zheng, Zhang, He, Hindy, George, Masca, Nicholas, Stirrups, Kathleen, Kanoni, Stavroula, Do, Ron, Jun, Goo, Hu, Youna, Kang, Hyun Min, Xue, Chenyi, Goel, Anuj, Farrall, Martin, Duga, Stefano, Merlini, Pier Angelica, Asselta, Rosanna, Girelli, Domenico, Olivieri, Oliviero, Martinelli, Nicola, Yin, Wu, Reilly, Dermot, Speliotes, Elizabeth, Fox, Caroline S, Hveem, Kristian, Holmen, Oddgeir L, Nikpay, Majid, Farlow, Deborah N, Assimes, Themistocles L, Franceschini, Nora, Robinson, Jennifer, North, Kari E, Martin, Lisa W, DePristo, Mark, Gupta, Namrata, Escher, Stefan A, Jansson, Jan-Håkan, Van Zuydam, Natalie, Palmer, Colin N A, Wareham, Nicholas, Koch, Werner, Meitinger, Thomas, Peters, Annette, Lieb, Wolfgang, Erbel, Raimund, Konig, Inke R, Kruppa, Jochen, Degenhardt, Franziska, Gottesman, Omri, Bottinger, Erwin P, O'Donnell, Christopher J, Psaty, Bruce M, Ballantyne, Christie M, Abecasis, Goncalo, Ordovas, Jose M, Melander, Olle, Watkins, Hugh, Orho-Melander, Marju, Ardissino, Diego, Loos, Ruth J F, McPherson, Ruth, Willer, Cristen J, Erdmann, Jeanette, Hall, Alistair S, Samani, Nilesh J, Deloukas, Panos, Schunkert, Heribert, Wilson, James G, Kooperberg, Charles, Rich, Stephen S, Tracy, Russell P, Lin, Dan-Yu, Altshuler, David, Gabriel, Stacey, Nickerson, Deborah A, Jarvik, Gail P, Cupples, L Adrienne, Reiner, Alex P, Boerwinkle, Eric, Kathiresan, Sekar

Volltext

Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks von Peloso, Gina M., Auer, Paul L., Bis, Joshua C., Voorman, Arend, Morrison, Alanna C., Stitziel, Nathan O., Brody, Jennifer A., Khetarpal, Sumeet A., Crosby, Jacy R., Fornage, Myriam, Isaacs, Aaron, Jakobsdottir, Johanna, Feitosa, Mary F., Davies, Gail, Huffman, Jennifer E., Manichaikul, Ani, Davis, Brian, Lohman, Kurt, Joon, Aron Y., Smith, Albert V., Grove, Megan L., Zanoni, Paolo, Redon, Valeska, Demissie, Serkalem, Lawson, Kim, Peters, Ulrike, Carlson, Christopher, Jackson, Rebecca D., Ryckman, Kelli K., Mackey, Rachel H., Robinson, Jennifer G., Siscovick, David S., Schreiner, Pamela J., Mychaleckyj, Josyf C., Pankow, James S., Hofman, Albert, Uitterlinden, Andre G., Harris, Tamara B., Taylor, Kent D., Stafford, Jeanette M., Reynolds, Lindsay M., Marioni, Riccardo E., Dehghan, Abbas, Franco, Oscar H., Patel, Aniruddh P., Lu, Yingchang, Hindy, George, Gottesman, Omri, Bottinger, Erwin P., Melander, Olle, Orho-Melander, Marju, Loos, Ruth J.F., Duga, Stefano, Merlini, Piera Angelica, Farrall, Martin, Goel, Anuj, Asselta, Rosanna, Girelli, Domenico, Martinelli, Nicola, Shah, Svati H., Kraus, William E., Li, Mingyao, Rader, Daniel J., Reilly, Muredach P., McPherson, Ruth, Watkins, Hugh, Ardissino, Diego, Zhang, Qunyuan, Wang, Judy, Tsai, Michael Y., Taylor, Herman A., Correa, Adolfo, Griswold, Michael E., Lange, Leslie A., Starr, John M., Rudan, Igor, Eiriksdottir, Gudny, Launer, Lenore J., Ordovas, Jose M., Levy, Daniel, Chen, Y.-D. Ida, Reiner, Alexander P., Hayward, Caroline, Polasek, Ozren, Deary, Ian J., Borecki, Ingrid B., Liu, Yongmei, Gudnason, Vilmundur, Wilson, James G., van Duijn, Cornelia M., Kooperberg, Charles, Rich, Stephen S., Psaty, Bruce M., Rotter, Jerome I., O’Donnell, Christopher J., Rice, Kenneth, Boerwinkle, Eric, Kathiresan, Sekar, Cupples, L. Adrienne

Volltext

A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis von Munz, Matthias, Willenborg, Christina, Richter, Gesa M, Jockel-Schneider, Yvonne, Graetz, Christian, Staufenbiel, Ingmar, Wellmann, Jürgen, Berger, Klaus, Krone, Bastian, Hoffmann, Per, van der Velde, Nathalie, Uitterlinden, André G, de Groot, Lisette C P G M, Sawalha, Amr H, Direskeneli, Haner, Saruhan-Direskeneli, Güher, Guzeldemir-Akcakanat, Esra, Keceli, Gencay, Laudes, Matthias, Noack, Barbara, Teumer, Alexander, Holtfreter, Birte, Kocher, Thomas, Eickholz, Peter, Meyle, Jörg, Doerfer, Christof, Bruckmann, Corinna, Lieb, Wolfgang, Franke, Andre, Schreiber, Stefan, Nohutcu, Rahime M, Erdmann, Jeanette, Loos, Bruno G, Jepsen, Soeren, Dommisch, Henrik, Schaefer, Arne S

Volltext

The effect of LRRK2 loss-of-function variants in humans von Whiffin, Nicola, Armean, Irina M., Kleinman, Aaron, Marshall, Jamie L., Minikel, Eric V., Goodrich, Julia K., Quaife, Nicholas M., Cole, Joanne B., Wang, Qingbo, Karczewski, Konrad J., Cummings, Beryl B., Francioli, Laurent, Laricchia, Kristen, Guan, Anna, Alipanahi, Babak, Morrison, Peter, Baptista, Marco A. S., Merchant, Kalpana M., Ware, James S., Havulinna, Aki S., Iliadou, Bozenna, Lee, Jung-Jin, Nadkarni, Girish N., Whiteman, Cole, Daly, Mark, Esko, Tõnu, Hultman, Christina, Loos, Ruth J. F., Milani, Lili, Palotie, Aarno, Pato, Carlos, Pato, Michele, Saleheen, Danish, Sullivan, Patrick F., Alföldi, Jessica, Cannon, Paul, MacArthur, Daniel G.

Volltext