Treffer 1 - 20 von 98 für Suche 'Alvi, M Y', Suchdauer: 1,45s Treffer weiter einschränken
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    Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk von Shrine, Nick, Chen, Jing, Packer, Richard, Hall, Robert J., Guyatt, Anna L., Batini, Chiara, Thompson, Rebecca J., Malik, Vidhi, Moll, Matthew, Tal-Singer, Ruth, Bakke, Per, Fawcett, Katherine A., John, Catherine, Piga, Noemi Nicole, Pozarickij, Alfred, Lin, Kuang, Chen, Zhengming, Li, Liming, Lahousse, Lies, Uitterlinden, Andre G., Oelsner, Elizabeth C., Rich, Stephen S., Kerr, Shona M., Vitart, Veronique, Brown, Michael R., Wielscher, Matthias, Imboden, Medea, Bartz, Traci M., Gharib, Sina A., Flexeder, Claudia, Karrasch, Stefan, Peters, Annette, Hu, Xiaowei, Ortega, Victor E., Meyers, Deborah A., Bleecker, Eugene R., Gupta, Namrata, Smith, Albert Vernon, Luan, Jian’an, Zhao, Jing-Hua, Hansen, Ailin F., Langhammer, Arnulf, Willer, Cristen, Bhatta, Laxmi, Porteous, David, Smith, Blair H., Lee, Jiwon, Daviglus, Martha L., Yu, Bing, Lim, Elise, Xu, Hanfei, O’Connor, George T., Thareja, Gaurav, Suhre, Karsten, Granell, Raquel, Faquih, Tariq O., Hiemstra, Pieter S., Hui, Jennie, James, Alan, Beilby, John, Hysi, Pirro, Koskela, Jukka T., Jin, Jianping, Sikdar, Sinjini, May-Wilson, Sebastian, Kentistou, Katherine A., Free, Robert C., Wang, Xueyang, Gilliland, Frank D., Chen, Zhanghua, Foong, Rachel E., Harris, Sarah E., Taylor, Adele, Redmond, Paul, Cook, James P., Lind, Lars, Lehtimäki, Terho, Pietiläinen, Kirsi H., Pennell, Craig E., Hall, Graham L., Gauderman, W. James, Wilson, James F., Laitinen, Tarja, Salomaa, Veikko, Timpson, Nicholas J., Zeggini, Eleftheria, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben, Weiss, Stefan, Homuth, Georg, Probst-Hensch, Nicole, Jarvelin, Marjo-Riitta, Morrison, Alanna C., Sayers, Ian, Rawlins, Emma L., Strachan, David P., Walters, Robin G., Morris, Andrew P., Tobin, Martin D.

    Veröffentlicht in Nature genetics

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    Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy von Abou Jamra, Rami, Accogli, Andrea, Amburgey, Kimberly, Basinger, Alice A., Ceulemans, Sophia, Charles, Perrine, McRae, Jeremy F., Rajan, Diana, Ambridge, Kirsty, Jones, Philip, Jones, Wendy D., Ahmed, Munaza, Anjum, Uruj, Armstrong, Ruth, Barnicoat, Angela, Bennett, Chris, Blair, Edward, Blyth, Moira, Bourdon, Louise, Brady, Angela, Burn, John, Canham, Natalie, Cilliers, Deirdre, Clayton-Smith, Jill, Coates, Andrea, Cooper, Nicola, Dabir, Tabib, Davies, Sally, Dean, John, Devlin, Gemma, Donnai, Dian, Donnelly, Carina, Evans, Karenza, Fendick, Tina, Goodship, Judith, Green, Andrew, Harrison, Lucy, Holden, Simon, Jarvis, Joanna, Johnson, Diana, Jones, Elizabeth, Kumar, V. K. Ajith, Lachlan, Katherine, Langman, Caroline, Maye, Una, McMullan, Dominic J., McWilliam, Catherine, Metcalfe, Kay, Norman, Andrew, Ogilvie, Caroline, Park, Soo-Mi, Phipps, Julie, Prescott, Katrina, Procter, Annie, Purnell, Hellen, Ross, Alison, Sampson, Julian, Shannon, Nora, Skitt, Zara, Stewart, Fiona, Stewart, Helen, Swaminathan, Ganesh Jawahar, Taylor, Cat, Tein, Mark, Treacy, Becky, Vandersteen, Anthony, Wallwark, Sarah, Waters, Jonathon, Weber, Astrid, Whiteford, Margo, Widaa, Sara, Wilcox, Sarah, Wilkinson, Emily, Parker, Michael, FitzPatrick, David R., Demurger, Florence, Eiset, Saga Elise, Ferrarini, Alessandra, Haack, Tobias B., Hashim, Mona, Jonasson, Amy R., Kok, Fernando, Marcelis, Carlo L.M., McWalter, Kirsty, Mercimek-Andrews, Saadet, Person, Richard, Ramelli, Gian Paolo, Rauch, Anita, Sanchez-Valle, Amarilis, Sattar, Shifteh, Saunders, Carol, Steindl, Katharina, Syrbe, Steffen, Taylor, Jenny C., Trauner, Doris A., Vogel, Ida, Widjaja, Elysa, Zak, Jaroslav, Banka, Siddharth, Rodan, Lance H.


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    Intravenous Thrombolysis in Patients With Cervical Artery Dissection: A Secondary Analysis of the STOP-CAD Study von Shu, Liqi, Akpokiere, Favour, Mandel, Daniel M, Field, Thalia S, Leon Guerrero, Christopher R, Henninger, Nils, Muppa, Jayachandra, Affan, Muhammad, Haq Lodhi, Omair U, Heldner, Mirjam R, Antonenko, Kateryna, Seiffge, David J, Arnold, Marcel, Salehi Omran, Setareh, Crandall, Ross, Lester, Evan, López-Mena, Diego, Arauz, Antonio, Nehme, Ahmad, Boulanger, Marion, Touzé, Emmanuel, Sousa, João André, Sargento-Freitas, João, Barata, Vasco, Castro-Chaves, Paulo, Brito, Maria T, Khan, Muhib, Mallick, Dania, Rothstein, Aaron, Khazaal, Ossama, Kaufmann, Josefin E, Engelter, Stefan T, Traenka, Christopher, Aguiar de Sousa, Diana, Soares, Mafalda D, Rosa, Sara B, Zhou, Lily, Gandhi, Preet, Mancini, Steven, Metanis, Issa, Leker, Ronen R, Pan, Kelly, Dantu, Vishnu, Baumgartner, Karl, Burton, Tina M, Von Rennenberg, Regina, Nolte, Christian H, Choi, Richard, MacDonald, Jason, Bavarsad Shahripour, Reza, Guo, Xiaofan, Ghannam, Malik, Almajali, Mohammad, Samaniego, Edgar A, Rioux, Bastien, Zine-Eddine, Faycal, Poppe, Alexandre, Fonseca, Ana C, Baptista, Maria F, Cruz, Diana, Romoli, Michele, De Marco, Giovanna, Longoni, Marco, Keser, Zafer, Griffin, Kim J, Kuohn, Lindsey, Frontera, Jennifer A, Amar, Jordan Y, Giles, James A, Zedde, Marialuisa, Pascarella, Rosario, Grisendi, Ilaria, Nzwalo, Hipolito, Liebeskind, David S, Molaie, Amir, Cavalier, Annie, Kam, Wayneho, Mac Grory, Brian, Al Kasab, Sami, Anadani, Mohammad, Kicielinski, Kimberly P, Eltatawy, Ali, Chervak, Lina, Chulluncuy Rivas, Roberto, Aziz, Yasmin N, Mistry, Eva A, Bakradze, Ekaterina, Tran, Thanh L, Rodrigo-Gisbert, Marc, Requena, Manuel, Saleh Velez, Faddi G, Garcia, Jorge Ortiz, Muddasani, Varsha, de Havenon, Adam, Sanchez, Sebastian, Vishnu, Venugopalan Y, Yaddanapudi, Sridhara, Adams, Latasha, Browngoehl, Abigail, Ranasinghe, Tamra

    Veröffentlicht in Neurology

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    Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk von Shrine, Nick, Chen, Jing, Packer, Richard, Hall, Robert J., Guyatt, Anna L., Batini, Chiara, Thompson, Rebecca J., Malik, Vidhi, Moll, Matthew, Tal-Singer, Ruth, Bakke, Per, Fawcett, Katherine A., John, Catherine, Piga, Noemi Nicole, Pozarickij, Alfred, Lin, Kuang, Chen, Zhengming, Li, Liming, Lahousse, Lies, Uitterlinden, Andre G., Oelsner, Elizabeth C., Rich, Stephen S., Kerr, Shona M., Vitart, Veronique, Brown, Michael R., Wielscher, Matthias, Imboden, Medea, Bartz, Traci M., Gharib, Sina A., Flexeder, Claudia, Karrasch, Stefan, Peters, Annette, Hu, Xiaowei, Ortega, Victor E., Meyers, Deborah A., Bleecker, Eugene R., Gupta, Namrata, Smith, Albert Vernon, Luan, Jian’an, Zhao, Jing-Hua, Hansen, Ailin F., Langhammer, Arnulf, Willer, Cristen, Bhatta, Laxmi, Porteous, David, Smith, Blair H., Lee, Jiwon, Daviglus, Martha L., Yu, Bing, Lim, Elise, Xu, Hanfei, O’Connor, George T., Thareja, Gaurav, Suhre, Karsten, Granell, Raquel, Faquih, Tariq O., Hiemstra, Pieter S., Hui, Jennie, James, Alan, Beilby, John, Hysi, Pirro, Koskela, Jukka T., Jin, Jianping, Sikdar, Sinjini, May-Wilson, Sebastian, Kentistou, Katherine A., Free, Robert C., Wang, Xueyang, Gilliland, Frank D., Chen, Zhanghua, Foong, Rachel E., Harris, Sarah E., Taylor, Adele, Redmond, Paul, Cook, James P., Lind, Lars, Lehtimäki, Terho, Pietiläinen, Kirsi H., Pennell, Craig E., Hall, Graham L., Gauderman, W. James, Wilson, James F., Laitinen, Tarja, Salomaa, Veikko, Timpson, Nicholas J., Zeggini, Eleftheria, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben, Weiss, Stefan, Homuth, Georg, Probst-Hensch, Nicole, Jarvelin, Marjo-Riitta, Morrison, Alanna C., Sayers, Ian, Rawlins, Emma L., Strachan, David P., Walters, Robin G., Morris, Andrew P., Tobin, Martin D.

    Veröffentlicht in NATURE GENETICS

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