Treffer 1 - 17 von 17 für Suche 'de Jager, Naomi', Suchdauer: 1,02s Treffer weiter einschränken
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    New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis von Lee, S Hong, Byrne, Enda M, Hultman, Christina M, Kähler, Anna, Vinkhuyzen, Anna A E, Ripke, Stephan, Andreassen, Ole A, Frisell, Thomas, Gusev, Alexander, Hu, Xinli, Karlsson, Robert, Mantzioris, Vasilis X, McGrath, John J, Mehta, Divya, Stahl, Eli A, Zhao, Qiongyi, Kendler, Kenneth S, Sullivan, Patrick F, Price, Alkes L, O'Donovan, Michael, Okada, Yukinori, Mowry, Bryan J, Raychaudhuri, Soumya, Wray, Naomi R, Byerley, William, Cahn, Wiepke, Cantor, Rita M, Cichon, Sven, Cormican, Paul, Curtis, David, Djurovic, Srdjan, Escott-Price, Valentina, Gejman, Pablo V, Georgieva, Lyudmila, Giegling, Ina, Hansen, Thomas F, Ingason, Andrés, Kim, Yunjung, Konte, Bettina, Lee, Phil H, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek W, Nöthen, Markus M, O'Dushlaine, Colm, Olincy, Ann, Olsen, Line, Pato, Carlos N, Pato, Michele T, Pickard, Benjamin S, Posthuma, Danielle, Rasmussen, Henrik B, Rietschel, Marcella, Rujescu, Dan, Schulze, Thomas G, Silverman, Jeremy M, Thirumalai, Srinivasa, Werge, Thomas, Agartz, Ingrid, Amin, Farooq, Azevedo, Maria H, Bass, Nicholas, Black, Donald W, Blackwood, Douglas H R, Bruggeman, Richard, Buccola, Nancy G, Choudhury, Khalid, Cloninger, Robert C, Corvin, Aiden, Craddock, Nicholas, Daly, Mark J, Datta, Susmita, Donohoe, Gary J, Duan, Jubao, Dudbridge, Frank, Fanous, Ayman, Freedman, Robert, Freimer, Nelson B, Friedl, Marion, Gill, Michael, Gurling, Hugh, De Haan, Lieuwe, Hamshere, Marian L, Hartmann, Annette M, Holmans, Peter A, Kahn, René S, Keller, Matthew C, Kenny, Elaine, Kirov, George K, Krabbendam, Lydia, Krasucki, Robert, Lawrence, Jacob, Lencz, Todd, Levinson, Douglas F, Lieberman, Jeffrey A, Lin, Dan-Yu, Linszen, Don H, Magnusson, Patrik K E, Maier, Wolfgang, Malhotra, Anil K


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    Stroke genetics informs drug discovery and risk prediction across ancestries von Mishra, Aniket, Malik, Rainer, Hachiya, Tsuyoshi, Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C, Koido, Masaru, Le Grand, Quentin, Krebs, Kristi, Liaw, Yi-Ching, Lin, Kuang, Srinivasasainagendra, Vinodh, Parodi, Livia, Bae, Hee-Joon, Chauhan, Ganesh, Jee, Yon Ho, Abedi, Vida, Nygaard, Marianne, Leonard, Hampton L, Knol, Maria J, Ago, Tetsuro, Armstrong, Nicole D, Bartz, Traci M, Bennett, David A, Bis, Joshua C, Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M, Cho, Kelly, de Cid, Rafael, Endres, Matthias, Gasca, Natalie C, Gudnason, Vilmundur, Hata, Jun, Havulinna, Aki S, Hopewell, Jemma C, Hyacinth, Hyacinth I, Inouye, Michael, Jeon, Christina E, Kamouchi, Masahiro, Kitazono, Takanari, Kittner, Steven J, Lacaze, Paul, Lee, Keon-Joo, Lepik, Kaido, Li, Jiang, Markus, Hugh S, Marston, Nicholas A, Mosley, Thomas H, Ovbiagele, Bruce, Psaty, Bruce M, Rich, Stephen S, Rosand, Jonathan, Sabatine, Marc S, Saleheen, Danish, Sandset, Else Charlotte, Sargurupremraj, Muralidharan, Sun, Yan V, Tatlisumak, Turgut, Tiwari, Hemant K, Trégouët, David-Alexandre, Trompet, Stella, Tuladhar, Anil Man, van Vugt, Marion, Wennberg, Patrik, Woo, Daniel, Yang, Qiong, INVENT Consortium, Dutch Parelsnoer Initiative (PSI) Cerebrovascular Disease Study Group, FinnGen Consortium, NINDS Stroke Genetics Network (SiGN), Biobank Japan, CHARGE Consortium, Millwood, Iona Y, Gieger, Christian, Ninomiya, Toshiharu, Jukema, J Wouter, Rissanen, Ina L, Strbian, Daniel, Kim, Young Jin, Chen, Pei-Hsin, Irvin, Marguerite R, Christensen, Kaare, Rundek, Tatjana, Worrall, Bradford B, Lathrop, G Mark, França, Paulo HC, de Leeuw, Frank-Erik, Liman, Thomas, Haeusler, Karl Georg, Ruigrok, Ynte M, Longstreth, WT, Jung, Keum Ji, Paré, Guillaume, Walters, Robin G, Ruff, Christian T, Milani, Lili, Kamatani, Yoichiro, Dichgans, Martin

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    Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries von Mishra, Aniket, Malik, Rainer, Hachiya, Tsuyoshi, Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C, Koido, Masaru, Le Grand, Quentin, Krebs, Kristi, Liaw, Yi-Ching, Lin, Kuang, Srinivasasainagendra, Vinodh, Parodi, Livia, Bae, Hee-Joon, Chauhan, Ganesh, Jee, Yon Ho, Abedi, Vida, Nygaard, Marianne, Leonard, Hampton L, Knol, Maria J, Ago, Tetsuro, Armstrong, Nicole D, Bartz, Traci M, Bennett, David A, Bis, Joshua C, Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M, Cho, Kelly, de Cid, Rafael, Endres, Matthias, Gasca, Natalie C, Gudnason, Vilmundur, Hata, Jun, Havulinna, Aki S, Hopewell, Jemma C, Hyacinth, Hyacinth I, Inouye, Michael, Jeon, Christina E, Kamouchi, Masahiro, Kitazono, Takanari, Kittner, Steven J, Lacaze, Paul, Lee, Keon-Joo, Lepik, Kaido, Li, Jiang, Markus, Hugh S, Marston, Nicholas A, Mosley, Thomas H, Ovbiagele, Bruce, Psaty, Bruce M, Rich, Stephen S, Rosand, Jonathan, Sabatine, Marc S, Saleheen, Danish, Sandset, Else Charlotte, Sargurupremraj, Muralidharan, Sun, Yan V, Tatlisumak, Turgut, Tiwari, Hemant K, Trégouët, David-Alexandre, Trompet, Stella, Tuladhar, Anil Man, van Vugt, Marion, Wennberg, Patrik, Woo, Daniel, Yang, Qiong, INVENT Consortium, Dutch Parelsnoer Initiative (PSI) Cerebrovascular Disease Study Group, FinnGen Consortium, NINDS Stroke Genetics Network (SiGN), Biobank Japan, CHARGE Consortium, Millwood, Iona Y, Gieger, Christian, Ninomiya, Toshiharu, Jukema, J Wouter, Rissanen, Ina L, Strbian, Daniel, Kim, Young Jin, Chen, Pei-Hsin, Irvin, Marguerite R, Christensen, Kaare, Rundek, Tatjana, Worrall, Bradford B, Lathrop, G Mark, França, Paulo HC, de Leeuw, Frank-Erik, Liman, Thomas, Haeusler, Karl Georg, Ruigrok, Ynte M, Longstreth, WT, Jung, Keum Ji, Paré, Guillaume, Walters, Robin G, Ruff, Christian T, Milani, Lili, Kamatani, Yoichiro, Dichgans, Martin

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    Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries von Mishra, Aniket, Malik, Rainer, Hachiya, Tsuyoshi, Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C, Koido, Masaru, Le Grand, Quentin, Krebs, Kristi, Liaw, Yi-Ching, Lin, Kuang, Srinivasasainagendra, Vinodh, Parodi, Livia, Bae, Hee-Joon, Chauhan, Ganesh, Jee, Yon Ho, Abedi, Vida, Nygaard, Marianne, Leonard, Hampton L, Knol, Maria J, Ago, Tetsuro, Armstrong, Nicole D, Bartz, Traci M, Bennett, David A, Bis, Joshua C, Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M, Cho, Kelly, de Cid, Rafael, Endres, Matthias, Gasca, Natalie C, Gudnason, Vilmundur, Hata, Jun, Havulinna, Aki S, Hopewell, Jemma C, Hyacinth, Hyacinth I, Inouye, Michael, Jeon, Christina E, Kamouchi, Masahiro, Kitazono, Takanari, Kittner, Steven J, Lacaze, Paul, Lee, Keon-Joo, Lepik, Kaido, Li, Jiang, Markus, Hugh S, Marston, Nicholas A, Mosley, Thomas H, Ovbiagele, Bruce, Psaty, Bruce M, Rich, Stephen S, Rosand, Jonathan, Sabatine, Marc S, Saleheen, Danish, Sandset, Else Charlotte, Sargurupremraj, Muralidharan, Sun, Yan V, Tatlisumak, Turgut, Tiwari, Hemant K, Trégouët, David-Alexandre, Trompet, Stella, Tuladhar, Anil Man, van Vugt, Marion, Wennberg, Patrik, Woo, Daniel, Yang, Qiong, INVENT Consortium, Dutch Parelsnoer Initiative (PSI) Cerebrovascular Disease Study Group, FinnGen Consortium, NINDS Stroke Genetics Network (SiGN), Biobank Japan, CHARGE Consortium, Millwood, Iona Y, Gieger, Christian, Ninomiya, Toshiharu, Jukema, J Wouter, Rissanen, Ina L, Strbian, Daniel, Kim, Young Jin, Chen, Pei-Hsin, Irvin, Marguerite R, Christensen, Kaare, Rundek, Tatjana, Worrall, Bradford B, Lathrop, G Mark, França, Paulo HC, de Leeuw, Frank-Erik, Liman, Thomas, Haeusler, Karl Georg, Ruigrok, Ynte M, Longstreth, WT, Jung, Keum Ji, Paré, Guillaume, Walters, Robin G, Ruff, Christian T, Milani, Lili, Kamatani, Yoichiro, Dichgans, Martin

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