Treffer 1 - 20 von 26 für Suche 'Power, Jacob L', Suchdauer: 1,36s Treffer weiter einschränken
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    An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ruiter, Jos P.N., van Lint, Alida E.M., Pras-Raves, Mia, Wever, Eric, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Perlman, Seth, Martin, Nicole, Brault, Jennifer, Gahl, William A., Alejandro, Mercedes E., Dai, Hongzheng, Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Moretti, Paolo M., Murdock, David R., Nicholas, Sarah K., Potocki, Lorraine, Scott, Daryl A., Eng, Christine M., Deardorff, Matthew, Hassey, Kelly, Sullivan, Kathleen, Tan, Queenie K.-G., Beggs, Alan H., Berry, Gerard T., Cooper, Cynthia M., Pallais, J. Carl, Rodan, Lance H., Kelley, Emily G., Morava, Eva, Forghani, Irman, Lam, Byron, Levitt, Roy, Liu, Xue Zhong, McCauley, Jacob, Tekin, Mustafa, Thorson, Willa, Findley, Laurie C., Krasnewich, Donna M., Manolio, Teri A., Goldrich, Madison P., Draper, David D., Nath, Avi, Pusey, Barbara N., Toro, Camilo, Baker, Eva, Gochuico, Bernadette, Mosbrook-Davis, Deborah, Rossignol, Francis, Adam, Margaret, Amendola, Laura, Cunningham, Michael, Jarvik, Gail P., Jarvik, Jeffrey, Lam, Christina, Raskind, Wendy, Sybert, Virginia, Ashley, Euan A., Coakley, Terra R., Hom, Jason, Majcherska, Marta M., Martin, Beth A., Marwaha, Shruti, Ruzhnikov, Maura, Tabor, Holly K., Tucker, Brianna M., Zastrow, Diane B., Byrd, William E., Dell’Angelica, Esteban C., Douine, Emilie D., Mak, Bryan C., Martin, Martin G., Martínez-Agosto, Julian A., McGee, Elisabeth, Nelson, Stanley F., Parker, Neil H., Sinsheimer, Janet S., Wang, Lee-kai, Perry, Katherine Wesseling, Woods, Jeremy D., Pace, Laura, Marth, Gabor, Viskochil, Dave, Bayrak-Toydemir, Pinar, Duncan, Laura, Robertson, Amy K., Solem, Emily, Schedl, Timothy, Shin, Jimann, Solnica-Krezel, Lilianna, Waisfisz, Quinten, Zwijnenburg, Petra J.G., Wanders, Ronald J.A., Vaz, Frédéric M.

    Veröffentlicht in Genetics in medicine

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    Risk prediction for acute kidney injury in acute medical admissions in the UK von Blackburn, Anna, Gunda, Smita, Lopez, Berenice, Edwards, James, Spittle, Nick, Preston, Rob, Baines, Richard, Little, Jane, Falayajo, Akin, Mahmoud, Huda, Selby, Nicholas M, Shaw, Sue, Trowbridge, Stephen, Coutinho, Andrew, Samarasinghe, Yohan, Farmer, Chris, Beeson, Claire, John, Ian, Gisby, Sharon, Forni, Lui, Dachsel, Martin, Fallouh, Bassam, Ward, Emily, Sood, Bhrigu, Ostermann, Marlies, Mohanty, Manab, Robert, Stephanie, MacLaughlin, Helen, Banerjee, Anita, Wright, Kelly, Tomlinson, Laurie, de Wolff, Jacob, Laing, Chris, Prowle, John, DeFreitas, Sarah, Balasubramaniam, Gowrie, McGuiness, Daniel, Murray, Jon, Kanagasundaram, Suren, Harron, Camille, Magee, Brian, Harty, John, Maxwell, Peter, Morgan, Neal, Leaonard, Niall, McCarroll, Frank, Kuan, Ying, Chakraborty, Tapas, Ahmed, Aimun, Ponnusamy, Arvind, Brown, Becky, Ahmed, Shahed, Henney, Bob, Hammersley, Shirley, Obale, Begho, Nipah, Rob, Al-Sayed, Tam, Varia, Ragit, Skinner, Christopher, Young, Innes, Clark, Laura, Bassiouni, Ibrahim, Finlay, Sian, Moonie, Alasdair, Douglas, Alistair, Bell, Samira, Duthie, Fiona, Thetford, David, White, Beth, McQuarrie, Emily, McCallum, Linsay, Campbell, Iona, Millar, James, McCormick, Jenna L, Allen, Ruridh, Jamdar, Ravi, Murray, Eleanor, Hand, Malcolm, Harmouche, Ali, Fattah, Hasan, Farquhar, Fiona, Condy-Young, Helen, Morrison, Jennifer, Power, Bert, Udayaraj, Uday, Murray, Paul, Mulgrew, Chris, Boddana, Preetham, Prescott, Craig, Uniake, Mark, Bonfield, Becky, Edwards, Helena, Armstrong, Kirsty, Whitehead, Duncan, Miller, Alice, Waters, Helen, Carr, Steve, Dickenson, Steve, Subbe, Chris, Phillips, Aled


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    Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals von Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jiang, Yunxuan, Hicks, Barry, Agee, Michelle, Auton, Adam, Bryc, Katarzyna, Fontanillas, Pierre, Furlotte, Nicholas A., Huber, Karen E., McIntyre, Matthew H., Mountain, Joanna L., Northover, Carrie A. M., Sazonova, Olga V., Shelton, Janie F., Tung, Joyce Y., Vacic, Vladimir, Wilson, Catherine H., Fontana, Mark Alan, Meddens, S. Fleur W., de Vlaming, Ronald, Ahluwalia, Tarunveer S., Bacelis, Jonas, Baumbach, Clemens, Gupta, Richa, Hall, Leanne M., Harris, Sarah E., Hofer, Edith, Horikoshi, Momoko, Karlsson, Robert, Lahti, Jari, Lindgren, Karl-Oskar, Liu, Tian, Mihailov, Evelin, Oldmeadow, Christopher, Raitakari, Olli, Shi, Jianxin, Teumer, Alexander, Wellmann, Juergen, Amin, Najaf, Davies, Gail, De Neve, Jan-Emmanuel, Deloukas, Panos, Demuth, Ilja, Eisele, Lewin, Feitosa, Mary F., Gandin, Ilaria, Gunnarsson, Bjarni, Halldórsson, Bjarni V., Harris, Tamara B., Holliday, Elizabeth G., Joshi, Peter K., Jugessur, Astanand, Kanoni, Stavroula, Keltigangas-Järvinen, Liisa, Kiemeney, Lambertus A. L. M., Koskinen, Seppo, Lichtner, Peter, Liewald, David C. M., Nelson, Christopher P., Ollier, William E. R., Palotie, Aarno, Räikkönen, Katri, Robino, Antonietta, Rudan, Igor, Schmidt, Helena, Strauch, Konstantin, Terracciano, Antonio, Tobin, Martin D., Vozzi, Diego, Bisgaard, Hans, Borecki, Ingrid B., Bültmann, Ute, Chabris, Christopher F., Eriksson, Johan G., Franke, Barbara, Grabe, Hans-Jörgen, Gratten, Jacob, Groenen, Patrick J. F., Gudnason, Vilmundur, Kardia, Sharon L. R., Lehrer, Steven F., McGue, Matt, Posthuma, Danielle, Province, Michael A., Samani, Nilesh J., Sørensen, Thorkild I. A., Timpson, Nicholas J., Uitterlinden, André G., Conley, Dalton C., Smith, George Davey, Laibson, David I., Yang, Jian, Watson, Chelsea, Jala, Jonathan, Meyer, Michelle N., Lee, James J., Yengo, Loic, Cesarini, David


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    Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses von Okbay, Aysu, Baselmans, Bart M L, Neve, Jan-Emmanuel De, Turley, Patrick, Nivard, Michel G, Fontana, Mark Alan, Meddens, S Fleur W, Linnér, Richard Karlsson, Rietveld, Cornelius A, Derringer, Jaime, Gratten, Jacob, Lee, James J, Liu, Jimmy Z, de Vlaming, Ronald, Ahluwalia, Tarunveer S, Buchwald, Jadwiga, Cavadino, Alana, Frazier-Wood, Alexis C, Furlotte, Nicholas A, Garfield, Victoria, Geisel, Marie Henrike, Gonzalez, Juan R, Haitjema, Saskia, Karlsson, Robert, van der Laan, Sander W, Ladwig, Karl-Heinz, Lahti, Jari, van der Lee, Sven J, Lind, Penelope A, Liu, Tian, Matteson, Lindsay, Mihailov, Evelin, Miller, Michael B, Minica, Camelia C, Nolte, Ilja M, Mook-Kanamori, Dennis, van der Most, Peter J, Oldmeadow, Christopher, Qian, Yong, Raitakari, Olli, Rawal, Rajesh, Realo, Anu, Rueedi, Rico, Schmidt, Börge, Smith, Albert V, Stergiakouli, Evie, Tanaka, Toshiko, Taylor, Kent, Thorleifsson, Gudmar, Wedenoja, Juho, Wellmann, Juergen, Westra, Harm-Jan, Willems, Sara M, Zhao, Wei, Amin, Najaf, Bakshi, Andrew, Bergmann, Sven, Bjornsdottir, Gyda, Boyle, Patricia A, Cherney, Samantha, Cox, Simon R, Davies, Gail, Davis, Oliver S P, Ding, Jun, Direk, Nese, Eibich, Peter, Emeny, Rebecca T, Fatemifar, Ghazaleh, Faul, Jessica D, Ferrucci, Luigi, Forstner, Andreas J, Gieger, Christian, Gupta, Richa, Harris, Tamara B, Harris, Juliette M, Holliday, Elizabeth G, Hottenga, Jouke-Jan, Jager, Philip L De, Kaakinen, Marika A, Kajantie, Eero, Karhunen, Ville, Kolcic, Ivana, Kumari, Meena, Launer, Lenore J, Franke, Lude, Li-Gao, Ruifang, Liewald, David C, Koini, Marisa, Loukola, Anu, Marques-Vidal, Pedro, Montgomery, Grant W, Mosing, Miriam A, Paternoster, Lavinia, Pattie, Alison, Petrovic, Katja E, Pulkki-Råback, Laura, Quaye, Lydia, Räikkönen, Katri, Rudan, Igor, Scott, Rodney J

    Veröffentlicht in Nature genetics

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    Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses von Okbay, Aysu, Baselmans, Bart M L, De Neve, Jan-Emmanuel, Turley, Patrick, Nivard, Michel G, Fontana, Mark Alan, Meddens, S Fleur W, Linnér, Richard Karlsson, Rietveld, Cornelius A, Derringer, Jaime, Gratten, Jacob, Lee, James J, Liu, Jimmy Z, de Vlaming, Ronald, Ahluwalia, Tarunveer S, Buchwald, Jadwiga, Cavadino, Alana, Frazier-Wood, Alexis C, Furlotte, Nicholas A, Garfield, Victoria, Geisel, Marie Henrike, Gonzalez, Juan R, Haitjema, Saskia, Karlsson, Robert, van der Laan, Sander W, Ladwig, Karl-Heinz, Lahti, Jari, van der Lee, Sven J, Lind, Penelope A, Liu, Tian, Matteson, Lindsay, Mihailov, Evelin, Miller, Michael B, Minica, Camelia C, Nolte, Ilja M, Mook-Kanamori, Dennis, van der Most, Peter J, Oldmeadow, Christopher, Qian, Yong, Raitakari, Olli, Rawal, Rajesh, Realo, Anu, Rueedi, Rico, Schmidt, Börge, Smith, Albert V, Stergiakouli, Evie, Tanaka, Toshiko, Taylor, Kent, Thorleifsson, Gudmar, Wedenoja, Juho, Wellmann, Juergen, Westra, Harm-Jan, Willems, Sara M, Zhao, Wei, Amin, Najaf, Bakshi, Andrew, Bergmann, Sven, Bjornsdottir, Gyda, Boyle, Patricia A, Cherney, Samantha, Cox, Simon R, Davies, Gail, Davis, Oliver S P, Ding, Jun, Direk, Nese, Eibich, Peter, Emeny, Rebecca T, Fatemifar, Ghazaleh, Faul, Jessica D, Ferrucci, Luigi, Forstner, Andreas J, Gieger, Christian, Gupta, Richa, Harris, Tamara B, Harris, Juliette M, Holliday, Elizabeth G, Hottenga, Jouke-Jan, De Jager, Philip L, Kaakinen, Marika A, Kajantie, Eero, Karhunen, Ville, Kolcic, Ivana, Kumari, Meena, Launer, Lenore J, Franke, Lude, Li-Gao, Ruifang, Liewald, David C, Koini, Marisa, Loukola, Anu, Marques-Vidal, Pedro, Montgomery, Grant W, Mosing, Miriam A, Paternoster, Lavinia, Pattie, Alison, Petrovic, Katja E, Pulkki-Råback, Laura, Quaye, Lydia, Räikkönen, Katri, Rudan, Igor, Scott, Rodney J

    Veröffentlicht in Nature genetics

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