Treffer 1 - 20 von 4.478 für Suche 'Wood, Nicholas I', Suchdauer: 1,93s Treffer weiter einschränken
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    Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study von Ibañez, Kristina, Polke, James, Hagelstrom, R Tanner, Dolzhenko, Egor, Pasko, Dorota, Thomas, Ellen Rachel Amy, Smith, Katherine R, McDonagh, Ellen M, Polychronopoulos, Dimitris, Chan, Georgia, Davison, James E, Festenstein, Richard, Fratta, Pietro, Giunti, Paola, Howard, Robin, Venkata, Laxmi, Laurá, Matilde, Morris, Huw, Robinson, Robert, Rosser, Elisabeth, Faravelli, Francesca, Schrag, Anette, Schott, Jonathan M, Wood, Nicholas W, Bourn, David, Eggleton, Kelly, Twiss, Philip, Almheiri, Ghareesa, Sheikh, Isabella, Vandrovcova, Jana, Brittain, Helen, Baple, Emma, Moutsianas, Loukas, Deshpande, Viraj, Perry, Denise L, Ajay, Subramanian S., Rajan, Vani, Oprych, Kathryn, Chinnery, Patrick F, Wilson, Gill, Ellard, Sian, Temple, I Karen, McMullan, Dom, Naresh, Kikkeri, Flinter, Frances A, Taylor, Jenny C, Greenhalgh, Lynn, Newman, William, Brennan, Paul, Sayer, John A, Raymond, F Lucy, Deans, Zandra C, Hill, Sue, Fowler, Tom, Scott, Richard H, Chinnery, Patrick F, Rendon, Augusto, Eberle, Michael A, Taft, Ryan J, Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boissiere, Jeanne M., Devereau, Andrew, Elgar, Greg, Foulger, Rebecca E., Furió-Tarí, Pedro, Hackett, Joanne, Hamblin, Angela, Holman, James, Hubbard, Tim J.P., Jones, Louise J., Kayikci, Melis, Lawson, Kay, Leigh, Sarah E.A., Leong, Ivonne U.S., Maleady-Crowe, Fiona, Mason, Joanne, Mueller, Michael, Murugaesu, Nirupa, Odhams, Chris A., Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Riesgo-Ferreiro, Pablo, Ryten, Mina, Savage, Kevin, Sawant, Kushmita, Sieghart, Alexander, Smedley, Damian, Sosinsky, Alona, Spooner, William, Stevens, Helen E., Stuckey, Alexander, Sultana, Razvan, Tregidgo, Carolyn, Walsh, Emma, Watters, Sarah A., Williams, Eleanor, Zarowiecki, Magdalena

    Veröffentlicht in Lancet neurology

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    Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins von Postmus, Iris, Trompet, Stella, Deshmukh, Harshal A., Barnes, Michael R., Li, Xiaohui, Warren, Helen R., Chasman, Daniel I., Zhou, Kaixin, Arsenault, Benoit J., Donnelly, Louise A., Wiggins, Kerri L., Avery, Christy L., Griffin, Paula, Feng, QiPing, Taylor, Kent D., Li, Guo, Evans, Daniel S., Smith, Albert V., de Keyser, Catherine E., Johnson, Andrew D., de Craen, Anton J. M., Buckley, Brendan M., Ford, Ian, Westendorp, Rudi G. J., Eline Slagboom, P., Sattar, Naveed, Munroe, Patricia B., Sever, Peter, Poulter, Neil, Stanton, Alice, Shields, Denis C., O’Brien, Eoin, Shaw-Hawkins, Sue, Ida Chen, Y.-D., Nickerson, Deborah A., Smith, Joshua D., Pierre Dubé, Marie, Matthijs Boekholdt, S., Kees Hovingh, G., Kastelein, John J. P., McKeigue, Paul M., Betteridge, John, Neil, Andrew, Durrington, Paul N., Doney, Alex, Carr, Fiona, Morris, Andrew, McCarthy, Mark I., Groop, Leif, Ahlqvist, Emma, Bis, Joshua C., Rice, Kenneth, Smith, Nicholas L., Lumley, Thomas, Whitsel, Eric A., Stürmer, Til, Boerwinkle, Eric, Ngwa, Julius S., O’Donnell, Christopher J., Wei, Wei-Qi, Wilke, Russell A., Liu, Ching-Ti, Sun, Fangui, Guo, Xiuqing, Heckbert, Susan R, Post, Wendy, Sotoodehnia, Nona, Arnold, Alice M., Stafford, Jeanette M., Ding, Jingzhong, Herrington, David M., Kritchevsky, Stephen B., Eiriksdottir, Gudny, Launer, Leonore J., Harris, Tamara B., Chu, Audrey Y., Giulianini, Franco, MacFadyen, Jean G., Barratt, Bryan J., Nyberg, Fredrik, Stricker, Bruno H., Uitterlinden, André G., Hofman, Albert, Rivadeneira, Fernando, Emilsson, Valur, Franco, Oscar H., Ridker, Paul M., Gudnason, Vilmundur, Liu, Yongmei, Denny, Joshua C., Ballantyne, Christie M., Adrienne Cupples, L., Psaty, Bruce M., Palmer, Colin N. A., Tardif, Jean-Claude, Colhoun, Helen M., Hitman, Graham, Krauss, Ronald M., Wouter Jukema, J, Caulfield, Mark J.

    Veröffentlicht in Nature communications

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    Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score von Iwaki, Hirotaka, Makarious, Mary B., Bandrés‐Ciga, Sara, Leonard, Hampton L., Gibbs, J. Raphael, Singleton, Andrew B., Middlehurst, Ben, Kia, Demis A, Houlden, Henry, Morris, Huw R, Plun‐Favreau, Helene, Quinn, John, Mok, Kin Y, Kinghorn, Kerri J., Wood, Nicholas W, Lewis, Patrick, Lovering, Ruth, Rizig, Mie, Ryten, Mina, Guelfi, Sebastian, Escott‐Price, Valentina, Chelban, Viorica, Foltynie, Thomas, Williams, Nigel, Morrison, Karen E., Clarke, Carl, Brice, Alexis, Danjou, Fabrice, Lesage, Suzanne, Martinez, Maria, Simón‐Sánchez, Javier, Heutink, Peter, Rizzu, Patrizia, Sharma, Manu, Gasser, Thomas, Bandres‐Ciga, Sara, Blauwendraat, Cornelis, Craig, David W., Billingsley, Kimberley, Narendra, Derek, Raphael Gibbs, J, Shulman, Joshua M., Iwaki, Hirotaka, Leonard, Hampton L., Nalls, Mike A., Finkbeiner, Steven, Lungu, Codrin, Singleton, Andrew B, Gan‐Or, Ziv, Rouleau, Guy A., Krohn, Lynne, Aguilar, Miquel, Alvarez, Ignacio, Alvarez, Victoria, Barrero, Francisco Javier, Yarza, Jesús Alberto Bergareche, Bonilla‐Toribio, Marta, Boungiorno, María Teresa, Buiza‐Rueda, Dolores, Cámara, Ana, Carrillo, Fátima, Carrión‐Claro, Mario, Cerdan, Debora, Diez‐Fairen, Monica, Dols‐Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla‐Sevilla, Francisco, Feliz, Cici, Fernández, Manel, Gonzalez‐Aramburu, Isabel, Pagola, Ana Gorostidi, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Jimenez‐Escrig, Adriano, Kulisevsky, Jaime, Labrador‐Espinosa, Miguel A., Lopez‐Sendon, Jose Luis, Torres, Irene Martínez, Mir, Pablo, Rezola, Elisabet Mondragon, Periñán‐Tocino, Teresa, Ruiz‐Martínez, Javier, Ruz, Clara, Rodriguez, Antonio Sanchez, Tabernero, Cesar, Tartari, Juan Pablo, Tolosa, Eduard, Valldeoriola, Francesc, Vela, Lydia, Vives, Francisco, Zimprich, Alexander, Koks, Sulev, Siitonen, Ari, Kaiyrzhanov, Coordinator ‐ Rauan, Zharkinbekova, Nazira, Aitkulova, Akbota, Kaishybayeva, Gulnaz, Karimova, Altynay

    Veröffentlicht in Movement disorders

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    The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease von Saez‐Atienzar, Sara, Bonet‐Ponce, Luis, Vitale, Dan, Blauwendraat, Cornelis, Pihlstrøm, Lasse, Gan‐Or, Ziv, Noyce, Alastair J, Middlehurst, Ben, Kia, Demis A, Tan, Manuela, Houlden, Henry, Holmans, Peter, Hardy, John, Mok, Kin Y, Kinghorn, Kerri J., Wood, Nicholas W, Lovering, Ruth, RņBibo, Lea, Rizig, Mie, Ryten, Mina, Guelfi, Sebastian, Escott‐Price, Valentina, Chelban, Viorica, Foltynie, Thomas, Williams, Nigel, Morrison, Karen E., Brice, Alexis, Danjou, Fabrice, Corvol, Jean‐Christophe, Brockmann, Kathrin, Rizzu, Patrizia, Gasser, Thomas, Bandres‐Ciga, Sara, Blauwendraat, Cornelis, Craig, David W., Faghri, Faraz, Gibbs, J Raphael, Hernandez, Dena G., Shulman, Joshua M., Iwaki, Hirotaka, Robak, Laurie, Lubbe, Steven, Mencacci, Niccolo E., Lungu, Codrin, Scholz, Sonja W., Reed, Xylena, Alcalay, Roy N., Hilten, Jacobus J, Marinus, Johan, Aguilar, Miquel, Alvarez, Victoria, Barrero, Francisco Javier, Yarza, Jesɐs Alberto Bergareche, Bernal‐Bernal, Inmaculada, Blazquez, Marta, Bonilla‐Toribio, Marta, Buiza‐Rueda, Dolores, CarriɃn‐Claro, Mario, ClarimɃn, Jordi, Compta, Yaroslau, Casa, Beatrȷz, Dols‐Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Ezquerra, Mario, Feliz, Cici, Garcia, Ciara, Garcȷa‐Ruiz, Pedro, Heredia, Maria Jose Gomez, Gonzalez‐Aramburu, Isabel, Pagola, Ana Gorostidi, Infante, Jon, Jimenez‐Escrig, Adriano, Kulisevsky, Jaime, Munain Arregui, Adolfo LɃpez, Macias, Daniel, Torres, Irene Martȷnez, Marȷn, Juan, Marti, Maria Jose, Martȷnez‐Castrillo, Juan Carlos, Mȳndez‐del‐Barrio, Carlota, Mata, Marina, MuɁoz, Esteban, Pagonabarraga, Javier, Pascual‐Sedano, Berta, PeriɁȥn‐Tocino, Teresa, Ruiz‐Martȷnez, Javier, Rodriguez, Antonio Sanchez, Sierra, Marȷa, Tabernero, Cesar, Tartari, Juan Pablo, Tejera‐Parrado, Cristina, Valldeoriola, Francesc, Vargas‐Gonzȥlez, Laura, Vela, Lydia, Vives, Francisco, Zimprich, Alexander, Koks, Sulev, Hassin‐Baer, Sharon, Nalls, Mike A.

    Veröffentlicht in Movement disorders

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    The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight von Ahmed, Sarah, Jesús, Silvia, Méndez‐del‐Barrio, Carlota, Vargas‐González, Laura, Tartari, Juan Pablo, Mondragon, Elisabet, Vinagre‐Aragon, Ana, Dols‐Icardo, Oriol, Pascual‐Sedano, Berta, Ezquerra, Mario, Cámara, Ana, Compta, Yaroslau, Fernández, Manel, Sierra, María, Menéndez‐González, Manuel, García‐Ruiz, Pedro, Vela‐Desojo, Lydia, Barrero, Francisco Javier, Mínguez‐Castellanos, Adolfo, Cerdan, Debora, Gomez Heredia, Maria Jose, Feliz, Cici, Lopez‐Sendon, Jose Luis, Martínez Torres, Irene, Kim, Jonggeol Jeffrey, Botia, Juan A., Morrison, Karen E., Morris, Huw, Edsall, Connor, Vives, Francisco, Duran, Raquel, Hoenicka, Janet, Alvarez, Victoria, Marti, Maria José, Singleton, Andrew, Noyce, Alastair J, Holmans, Peter, Trabzuni, Daniah, Bras, Jose, Wood, Nicholas W, Guerreiro, Rita, Guelfi, Sebastian, Chelban, Viorica, Foltynie, Thomas, Morrison, Karen E., Brockmann, Kathrin, Gasser, Thomas, Cookson, Mark R, Blauwendraat, Cornelis, Craig, David W., Faghri, Faraz, Gibbs, J Raphael, Shulman, Joshua M., Leonard, Hampton L., Nalls, Mike A., Robak, Laurie, Lubbe, Steven, Mencacci, Niccolo E., Alcalay, Roy N., Krohn, Lynne, Aguilar, Miquel, Alvarez, Ignacio, Yarza, Jesús Alberto Bergareche, Blazquez, Marta, Botía, Juan A., Boungiorno, María Teresa, Buiza-Rueda, Dolores, Clarimón, Jordi, Casa, Beatríz, Diez-Fairen, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Fernández, Manel, Heredia, Maria Jose Gomez, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Jimenez-Escrig, Adriano, Arregui, Adolfo López de Munain, Marín, Juan, Mata, Marina, Mínguez, Adolfo, Mir, Pablo, Pascual-Sedano, Berta, Pastor, Pau, Errazquin, Francisco Perez, Ruiz-Martínez, Javier, Rodriguez, Antonio Sanchez, Sierra, María, Suarez-Sanmartin, Esther, Tolosa, Eduard, Valldeoriola, Francesc, Vargas-González, Laura, Zimprich, Alexander, Taba, Pille, Dalgard, Clifton L., Adeleye, Adelani, Soltis, Anthony R., Bacikova, Dagmar, Wilkerson, Matthew D.

    Veröffentlicht in Movement disorders

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    A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome von Aung, Tin, Ozaki, Mineo, Li, Zheng, Uebe, Steffen, Harder, Jeffrey M, Chan, Anita S Y, Lee, Mei Chin, Burdon, Kathryn P, Pakravan, Mohammad, Wang, Ya Xing, Williams, Susan, Huang, Lulin, Foo, Jia Nee, Kumar, Rajesh S, Ueno, Morio, Manabe, Shin-ichi, Hayashi, Ken, Ideta, Ryuichi, Mori, Yosai, Miyata, Kazunori, Sugiyama, Kazuhisa, Higashide, Tomomi, Chihara, Etsuo, Inoue, Kenji, Yoshida, Akitoshi, Yanagi, Masahide, Aihara, Makoto, Ohashi, Tsutomu, Sakurai, Toshiya, Sugimoto, Takako, Chuman, Hideki, Yamashiro, Kenji, Gotoh, Norimoto, Osman, Essam A, Al-Obeidan, Saleh A, Al-Jasim, Leyla, Shahwan, Sami Al, Leo, Paul, Yetkin, Yaz, Oğuz, Çilingir, Kanavi, Mozhgan Rezaei, Yazdani, Shahin, Akopov, Evgeny L, Howell, Gareth R, Goh, Yufen, Meah, Wee Yang, Peh, Su Qin, Lukasik, Urszula, Krumbiegel, Mandy, Vithana, Eranga N, Wong, Tien Yin, Liu, Yutao, Challa, Pratap, Hewitt, Alex W, Mitchell, Paul, Ziskind, Ari, Venkatesh, Rangaraj, Vijayan, Saravanan, Zhao, Peiquan, Guadarrama-Vallejo, Dalia, Perera, Shamira A, Husain, Rahat, Ho, Su-Ling, Welge-Luessen, Ulrich-Christoph, Schloetzer-Schrehardt, Ursula, Herms, Stefan, Nöthen, Markus M, Weisschuh, Nicole, Ghosh, Arkasubhra, Teo, Yik Ying, Brown, Matthew A, Lischinsky, Ignacio, Crowston, Jonathan G, Sang, Jinghong, Zhang, Nihong, You, Qisheng, Founti, Panayiota, Lambropoulos, Alexandros, Anastasopoulos, Eleftherios, Rhee, Douglas J, May-Bolchakova, Inna, Heegaard, Steffen, Alward, Wallace L M, Jonas, Jost B, Xu, Liang, Chowbay, Balram, Schaeffeler, Elke, Lerner, Fabian, Yang, Zhenglin, Frezzotti, Paolo, Kinoshita, Shigeru, Inatani, Masaru, Tashiro, Kei, Reis, André, Edward, Deepak P, Pasquale, Louis R, Wiggs, Janey L, Yoshimura, Nagahisa, Ritch, Robert, Khor, Chiea-Chuen

    Veröffentlicht in Nature genetics

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    Multiethnic Meta-Analysis of Genome-Wide Association Studies in >100 000 Subjects Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Between Ci... von Sabater-Lleal, Maria, Huang, Jie, Chasman, Daniel, Naitza, Silvia, Dehghan, Abbas, Teumer, Alexander, Folkersen, Lasse, Basu, Saonli, Rudnicka, Alicja R., Trompet, Stella, Mälarstig, Anders, Baumert, Jens, Guo, Xiuqing, Hottenga, Jouke J., Shin, So-Youn, Lopez, Lorna M., Lahti, Jari, Oudot-Mellakh, Tiphaine, Wilson, James F., Navarro, Pau, Huffman, Jennifer E., Zemunik, Tatijana, Mehra, Reena, Rudan, Igor, Wright, Alan F., Campbell, Harry, Wallace, Robert, Liu, Simin, Eaton, Charles B., Becker, Diane M., Becker, Lewis C., Räikkönen, Katri, Widen, Elisabeth, Palotie, Aarno, Fornage, Myriam, Green, David, Gross, Myron, Harris, Sarah E., Starr, John M., Williams, Frances M.K., Spector, Timothy D., Strawbridge, Rona J., Silveira, Angela, Sennblad, Bengt, Uitterlinden, Andre G., Franco, Oscar H., Hofman, Albert, van Dongen, Jenny, Yao, Jie, Swords Jenny, Nancy, Haritunians, Talin, Lumley, Thomas, Taylor, Kent D., Peters, Annette, Illig, Thomas, Kocher, Thomas, Franzosi, Maria Grazia, Seedorf, Udo, Clarke, Robert, Schlessinger, David, Stott, David J., Sattar, Naveed, Buckley, Brendan M., Lowe, Gordon D., Chen, Ming-Huei, Tofler, Geoffrey H., Song, Jaejoon, Boerwinkle, Eric, Rose, Lynda M., Franco-Cereceda, Anders, Teichert, Martina, Mosley, Thomas H., Bevan, Steve, Dichgans, Martin, Sudlow, Cathie L.M., Hopewell, Jemma C., Chambers, John C., Saleheen, Danish, Kooner, Jaspal S., Danesh, John, Nelson, Christopher P., Reilly, Muredach P., Kathiresan, Sekar, Schunkert, Heribert, Morange, Pierre-Emmanuel, Ferrucci, Luigi, Eriksson, Johan G., Jacobs, David, Deary, Ian J., Soranzo, Nicole, Tracy, Russell P., Hayward, Caroline, Koenig, Wolfgang, Cucca, Francesco, Samani, Nilesh J., Smith, Nicholas L., Ridker, Paul M, Tang, Weihong, Hamsten, Anders, O’Donnell, Christopher J.

    Veröffentlicht in Circulation (New York, N.Y.)

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    GWAS meta-analysis of 16 790 patients with Barrett’s oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology be... von Speller, Jan, Borisov, Oleg, Hess, Timo, Kreuser, Nicole, Alakus, Hakan, May, Andrea, Schmidt, Thomas, Thieme, Rene, Hillmer, Axel M, Lyros, Orestis, Dietrich, Arne, Lordick, Florian, Stocker, Gertraud, Hohaus, Michael, Reim, Daniel, Kandler, Jennis, Fuchs, Claudia, Lang, Hauke, Grimminger, Peter P, Dakkak, Dani, Görg, Siegfried, Franke, Andre, Galavotti, Sara, Dommermuth, Jens, Rösch, Thomas, Messmann, Helmut, Nöthen, Markus M, Vaughan, Thomas L, Tomlinson, Ian, Jankowski, Janusz, Vieth, Michael, MacGregor, Stuart, Gockel, Ines, Palles, Claire, Schumacher, Johannes, Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin NA, Plomin, Robert, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Pearson, Richard, Strange, Amy, Vukcevic, Damjan, Langford, Cordelia, Hunt, Sarah E, Gwilliam, Rhian, Bumpstead, Suzannah J, Dronov, Serge, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, Paul, Widaa, Sara, Whittaker, Pamela, Beckett, Conrad, Cullen, Sue, Dhar, Ameet, Kejariwal, Deepak, Sargeant, Ian, Winter, Helen, Dixon, Andrew, McMurty, Hugh, Johnson, Matthew, MacDonald, Chris, Haig, Chris, Senapati, Siba, Bhandari, Pradeep, Ang, Yeng, Smith, Mark, Ramadas, Arvind, Panter, Simon, Lovat, Laurence, Patel, Praful, Falk, Stephen, Nwokolo, Chuka, deCaestecker, John, Ramakrishnan, Subramaniam, Kelly, Sean, Prenen, Hans, Corley, Douglas A, Shaheen, Nicholas J, Hardie, Laura J, Risch, Harvey A, Ye, Weimin, Liu, Geoffrey, Whiteman, David C

    Veröffentlicht in Gut

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