Placental Growth Factor (PlGF)–Specific Uptake in Tumor Microenvironment of 89 Zr-Labeled PlGF Antibody RO5323441 von Oude Munnink, Thijs H., Tamas, Karin R., Lub-de Hooge, Marjolijn N., Vedelaar, Silke R., Timmer-Bosscha, Hetty, Walenkamp, Annemiek M.E., Weidner, K. Michael, Herting, Frank, Tessier, Jean, de Vries, Elisabeth G.E.

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Placental Growth Factor (PlGF)-Specific Uptake in Tumor Microenvironment of ^sup 89^Zr-Labeled PlGF Antibody RO5323441 von Munnink, Thijs H Oude, Tamas, Karin R, Lub-de Hooge, Marjolijn N, Vedelaar, Silke R, Timmer-Bosscha, Hetty, Walenkamp, Annemiek ME, Weidner, K Michael, Herting, Frank, Tessier, Jean, de Vries, Elisabeth GE

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Placental growth factor (PlGF)-specific uptake in tumor microenvironment of 89Zr-labeled PlGF antibody RO5323441 von Oude Munnink, Thijs H, Tamas, Karin R, Lub-de Hooge, Marjolijn N, Vedelaar, Silke R, Timmer-Bosscha, Hetty, Walenkamp, Annemiek M E, Weidner, K Michael, Herting, Frank, Tessier, Jean, de Vries, Elisabeth G E

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Population genomics of Bronze Age Eurasia von Allentoft, Morten E., Sikora, Martin, Sjögren, Karl-Göran, Rasmussen, Simon, Rasmussen, Morten, Stenderup, Jesper, Damgaard, Peter B., Schroeder, Hannes, Ahlström, Torbjörn, Vinner, Lasse, Malaspinas, Anna-Sapfo, Margaryan, Ashot, Higham, Tom, Chivall, David, Lynnerup, Niels, Harvig, Lise, Baron, Justyna, Casa, Philippe Della, Dąbrowski, Paweł, Duffy, Paul R., Ebel, Alexander V., Epimakhov, Andrey, Frei, Karin, Furmanek, Mirosław, Gralak, Tomasz, Gromov, Andrey, Gronkiewicz, Stanisław, Grupe, Gisela, Hajdu, Tamás, Jarysz, Radosław, Khartanovich, Valeri, Khokhlov, Alexandr, Kiss, Viktória, Kolář, Jan, Kriiska, Aivar, Lasak, Irena, Longhi, Cristina, McGlynn, George, Merkevicius, Algimantas, Merkyte, Inga, Metspalu, Mait, Mkrtchyan, Ruzan, Moiseyev, Vyacheslav, Paja, László, Pálfi, György, Pokutta, Dalia, Pospieszny, Łukasz, Price, T. Douglas, Saag, Lehti, Sablin, Mikhail, Shishlina, Natalia, Smrčka, Václav, Soenov, Vasilii I., Szeverényi, Vajk, Tóth, Gusztáv, Trifanova, Synaru V., Varul, Liivi, Vicze, Magdolna, Yepiskoposyan, Levon, Zhitenev, Vladislav, Orlando, Ludovic, Sicheritz-Pontén, Thomas, Brunak, Søren, Nielsen, Rasmus, Kristiansen, Kristian, Willerslev, Eske

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Gemcitabine Plus Capecitabine Compared With Gemcitabine Alone in Advanced Pancreatic Cancer: A Randomized, Multicenter, Phase III Trial of the Swiss Group for Clinical Cancer Resea... von HERRMANN, Richard, BODOKY, György, KDHNE, Claus-Henning, MINGRONE, Walter, STEMMER, Salomon M, TAMAS, Karin, KORNEK, Gabriela V, KOEBERLE, Dieter, CINA, Susanne, BERNHARD, Jürg, DIETRICH, Daniel, SCHEITHAUER, Werner, RUHSTALLER, Thomas, GLIMELIUS, Bengt, BAJETTA, Emilio, SCHÜLLER, Johannes, SALETTI, Piercarlo, BAUER, Jean, FIGER, Arie, PESTALOZZI, Bernhard

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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease von Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B

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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease von Beilina, Alexandria, Rudenko, Iakov N., Kaganovich, Alice, Civiero, Laura, Chau, Hien, Kalia, Suneil K., Kalia, Lorraine V., Lobbestael, Evy, Chia, Ruth, Ndukwe, Kelechi, Ding, Jinhui, Nalls, Mike A., Olszewski, Maciej, Hauser, David N., Kumaran, Ravindran, Lozano, Andres M., Baekelandt, Veerle, Greene, Lois E., Taymans, Jean-Marc, Greggio, Elisa, Cookson, Mark R.

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Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease von Robak, Laurie A, Jansen, Iris E, van Rooij, Jeroen, Uitterlinden, André G, Kraaij, Robert, Jankovic, Joseph, Heutink, Peter, Shulman, Joshua M

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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy von Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.

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Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption von Cornelis, M C, Byrne, E M, Esko, T, Nalls, M A, Paynter, N, Monda, K L, Amin, N, Renstrom, F, Cavadino, A, Nolte, I M, Teumer, A, Yu, K, Manichaikul, A, Wojczynski, M K, Vink, J M, Zhao, J H, Burlutsky, G, Lahti, J, Lemaitre, R N, Eriksson, J, Musani, S K, Tanaka, T, Luan, J, Hui, J, Ho, W-K, Magnusson, P K E, Pedersen, N L, Couper, D, Oostra, B A, Tiemeier, H W, Uitterlinden, A G, Barroso, I, Xue, L, Kaakinen, M, Milani, L, Power, C, Baumeister, S E, Biffar, R, Kutalik, Z, Jacobs, D R, Lind, L, Jensen, M, Luben, R N, Wang, J J, Männistö, S, Lehtimäki, T, Viikari, J, Mozaffarian, D, Mukamal, K, Döring, A, Montgomery, G W, Dahmen, N, Tucker, K L, Ferrucci, L, Treur, J L, Mellström, D, Hottenga, J J, Tönjes, A, Deloukas, P, Kanoni, S, Lorentzon, M, Houston, D K, Liu, Y, Mason, M A, Zonderman, A B, Franke, L, Kristal, B S, Karjalainen, J, Reed, D R, Westra, H-J, Evans, M K, Dedoussis, G, Stumvoll, M, Bandinelli, S, Ordovas, J M, Chan, A T, Ohlsson, C, Gieger, C, Martin, N G, Siscovick, D S, Raitakari, O, Eriksson, J G, Mitchell, P, Hunter, D J, Rimm, E B, Borecki, I B, Vollenweider, P, Grabe, H J, Neuhouser, M L, Wolffenbuttel, B H R, Hyppönen, E, Cupples, L A, Franks, P W, van Duijn, C M, Heiss, G, Metspalu, A, North, K E, Ingelsson, E, Nettleton, J A, van Dam, R M

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Should formula for infants provide arachidonic acid along with DHA? A position paper of the European Academy of Paediatrics and the Child Health Foundation von Koletzko, Berthold, Bergmann, Karin, Brenna, J Thomas, Calder, Philip C, Campoy, Cristina, Clandinin, M Tom, Colombo, John, Daly, Mandy, Decsi, Tamás, Demmelmair, Hans, Domellöf, Magnus, FidlerMis, Nataša, Gonzalez-Casanova, Ines, van Goudoever, Johannes B, Hadjipanayis, Adamos, Hernell, Olle, Lapillonne, Alexandre, Mader, Silke, Martin, Camilia R, Matthäus, Valerie, Ramakrishan, Usha, Smuts, Cornelius M, Strain, Sean JJ, Tanjung, Conny, Tounian, Patrick, Carlson, Susan E

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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies von Nalls, Michael A, Plagnol, Vincent, Hernandez, Dena G, Sharma, Manu, Sheerin, Una-Marie, Saad, Mohamad, Simón-Sánchez, J, Schulte, Claudia, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Stefánsson, Kári, Martinez, Maria, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B, Wood, Nicholas W

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Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing von Jansen, Iris E, Ye, Hui, Heetveld, Sasja, Lechler, Marie C, Michels, Helen, Seinstra, Renée I, Lubbe, Steven J, Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa, Gibbs, J Raphael, Nalls, Mike A, Ryten, Mina, Botia, Juan A, Vandrovcova, Jana, Simon-Sanchez, Javier, Castillo-Lizardo, Melissa, Rizzu, Patrizia, Blauwendraat, Cornelis, Chouhan, Amit K, Li, Yarong, Yogi, Puja, Amin, Najaf, van Duijn, Cornelia M, Morris, Huw R, Brice, Alexis, Singleton, Andrew B, David, Della C, Nollen, Ellen A, Jain, Shushant, Shulman, Joshua M, Heutink, Peter

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COVID‐19‐related medicine utilization study in pregnancy: The COVI‐PREG cohort von Favre, Guillaume, Maisonneuve, Emeline, Winterfeld, Ursula, Lepigeon, Karine, Bloemenkamp, Kitty W. M., Nordeng, Hedvig, Siiskonen, Satu J., Panchaud, Alice, Goncé, Anna, Poncelet, Christophe, Surita, Fernanda, Dantas‐Silva, Amanda, Luz, Adriana, Quibel, Thibaud, Campelo, Sonia, Hcini, Najeh, Lambert, Veronique, Nieto‐Calvache, Albaro José, Sinisterra‐Díaz, Stiven Ernesto, Maya, Juliana, Pérez, Paola Marsela, Bryon, Adriana Messa, Luca, Carmen, Etchegaray, Adolfo, Moren, Juliana, Qaderi, Shohra, Eggel, Beatrice, Geary, Michael, Donnelly, Jennifer, Kennelly, Maria, Salameh, Fadi‐Tamas, Brugger, Romina Capoccia, Grechukhina, Olga, Fuenzalida, Javiera, Surbek, Daniel, Radan, Anda‐Petronela, Moser, Mirjam, Richter, Jute, Pinto, Pedro Viana, Sichitiu, Johana, Ville, Yves, Stirnemann, Julien, Haratz, Karina Krajden, Malinger, Gustavo, Tallarek, Ann‐Christin, Hecher, Kurt, Schuler‐Faccini, Lavinia, Scherer, Mariana Horn, Wender, Maria Celeste Osorio, Oppermann, Maria Lucia Da Rocha, Bohrer, Betania, Friedrich, Luciana, Papadia, Andrea, Polli, Christian, Nielsen‐Saines, Karin, Fajardo, Viviana, Garabedian, Charles, Ghesquiere, Louise, Grawe, Claudia, Voekt, Cora Alexandra, Böckenhoff, Paul, Strizek, Brigitte, Sentilhes, Loïc, Mattuizzi, Aurélien, Rossier, Marie‐Claude, Eggemann, Caroline, Feuerschuette, Otto Henrique May, Breton, Bénédicte, Toussaint, Arnaud, Sa, Renato Augusto Moreira, Elbahnasawy, Mohamed, Abd‐Elsalam, Sherief, Ducarme, Guillaume, Parco, Cecile, Derouich, Mohamed, Canales, Manuel Guerra, Britschgi, Carina, Prentl, Elke Barbara, Maisel, Jessica, Hoesli, Irene, Monod, Cécile, Vetter, Grit, Blume, Carolin, Kalimeris, Stylianos, Martins, Inês, Camps, Diogo Ayres, Boulvain, Michel, Bütikofer, Kathrin, Bernardes, Lisandra Stein, Santos, Cristina Nunes, Micheletti, Bruna Hipólito, Pereira, Natálya Gonçalves, Sturm, Stefanie, Wardhana, Manggala Pasca, Dajti, Irida, Kharouf, Feras, Yin, Mingzhu, Hernandez, Olivia, Masmejan, Sophie, Lepigeon, Karine

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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease von KELLER, Margaux F, SAAD, Mohamad, SCHULTE, Claudia, MOSKVINA, Valentina, DURR, Alexandra, HOLMANS, Peter, KILARSKI, Laura L, GUERREIRO, Rita, HERNANDEZ, Dena G, BRICE, Alexis, YLIKOTILA, Pauli, STEFANSSON, Hreinn, BRAS, Jose, MAJAMAA, Kari, MORRIS, Huw R, WILLIAMS, Nigel, GASSER, Thomas, HEUTINK, Peter, WOOD, Nicholas W, HARDY, John, MARTINEZ, Maria, SINGLETON, Andrew B, NALLS, Michael A, BETTELLA, Francesco, NICOLAOU, Nayia, SIMON-SANCHEZ, Javier, MITTAG, Florian, BÜCHEL, Finja, SHARMA, Manu, RAPHAEL GIBBS, J

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Clinical Benefit and Quality of Life in Patients With Advanced Pancreatic Cancer Receiving Gemcitabine Plus Capecitabine Versus Gemcitabine Alone: A Randomized Multicenter Phase II... von BERNHARD, Jürg, DIETRICH, Daniel, BAUER, Jean, FIGER, Arie, PESTALOZZI, Bernhard C, KÖHNE, Claus-Henning, MINGRONE, Walter, STEMMER, Salomon M, TAMAS, Karin, KORNEK, Gabriela V, KOEBERLE, Dieter, HERRMANN, Richard, SCHEITHAUER, Werner, GERBER, Daniela, BODOKY, György, RUHSTALLER, Thomas, GLIMELIUS, Bengt, BAJETTA, Emilia, SCHÜLLER, Johannes, SALETTI, Piercarlo

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Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study von Pichler, Irene, Del Greco M, Fabiola, Gögele, Martin, Lill, Christina M, Bertram, Lars, Do, Chuong B, Eriksson, Nicholas, Foroud, Tatiana, Myers, Richard H, Nalls, Michael, Keller, Margaux F, Benyamin, Beben, Whitfield, John B, Pramstaller, Peter P, Hicks, Andrew A, Thompson, John R, Minelli, Cosetta

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A two-stage meta-analysis identifies several new loci for Parkinson's disease

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Harmonization of Human Biomonitoring Studies in Europe: Characteristics of the HBM4EU-Aligned Studies Participants von Gilles, Liese, Govarts, Eva, Rodriguez Martin, Laura, Andersson, Anna-Maria, Appenzeller, Brice M R, Barbone, Fabio, Castaño, Argelia, Coertjens, Dries, Den Hond, Elly, Dzhedzheia, Vazha, Eržen, Ivan, López, Marta Esteban, Fábelová, Lucia, Fillol, Clémence, Franken, Carmen, Frederiksen, Hanne, Gabriel, Catherine, Haug, Line Småstuen, Horvat, Milena, Halldórsson, Thórhallur Ingi, Janasik, Beata, Holcer, Nataša Janev, Kakucs, Réka, Karakitsios, Spyros, Katsonouri, Andromachi, Klánová, Jana, Kold-Jensen, Tina, Kolossa-Gehring, Marike, Konstantinou, Corina, Koponen, Jani, Lignell, Sanna, Lindroos, Anna Karin, Makris, Konstantinos C, Mazej, Darja, Morrens, Bert, Murínová, Ľubica Palkovičová, Namorado, Sónia, Pedraza-Diaz, Susana, Peisker, Jasmin, Probst-Hensch, Nicole, Rambaud, Loïc, Rosolen, Valentina, Rucic, Enrico, Rüther, Maria, Sarigiannis, Dimosthenis, Tratnik, Janja Snoj, Standaert, Arnout, Stewart, Lorraine, Szigeti, Tamás, Thomsen, Cathrine, Tolonen, Hanna, Eiríksdóttir, Ása, Van Nieuwenhuyse, An, Verheyen, Veerle J, Vlaanderen, Jelle, Vogel, Nina, Wasowicz, Wojciech, Weber, Till, Zock, Jan-Paul, Sepai, Ovnair, Schoeters, Greet

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NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases von Nalls, Mike A, Bras, Jose, Hernandez, Dena G, Keller, Margaux F, Majounie, Elisa, Renton, Alan E, Saad, Mohamad, Jansen, Iris, Guerreiro, Rita, Lubbe, Steven, Plagnol, Vincent, Gibbs, J. Raphael, Schulte, Claudia, Pankratz, Nathan, Sutherland, Margaret, Bertram, Lars, Lill, Christina M, DeStefano, Anita L, Faroud, Tatiana, Eriksson, Nicholas, Tung, Joyce Y, Edsall, Connor, Nichols, Noah, Brooks, Janet, Arepalli, Sampath, Pliner, Hannah, Letson, Chris, Heutink, Peter, Martinez, Maria, Gasser, Thomas, Traynor, Bryan J, Wood, Nick, Hardy, John, Singleton, Andrew B

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