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    Hundreds of variants clustered in genomic loci and biological pathways affect human height by Hui, Jennie, Lokki, Marja-Liisa, Cusi, Daniele, Koskinen, Seppo, Beilby, John P, Salomaa, Veikko, Aben, Katja K, Kovacs, Peter, Soranzo, Nicole, Suh Ngwa, Julius, Glazer, Nicole L, Boucher, Gabrielle, Fox, Caroline S, Penninx, Brenda W, Salvi, Erika, Iribarren, Carlos, Altmaier, Elizabeth L, Gudnason, Vilmundur, Bragi Walters, G, Musk, Arthur W, Montgomery, Grant W, Nyholt, Dale R, Kiemeney, Lambertus, Ohlsson, Claes, Launer, Lenore J, Vandenput, Liesbeth, Campbell, Harry, Schlessinger, David, Vitart, Veronique, Erdmann, Jeanette, Kathiresan, Sekar, Parker, Alex N, Hu, Frank B, Kajantie, Eero, Hao, Ke, Ziegler, Andreas, Liang, Liming, Rissanen, Aila, Hamsten, Anders, Visscher, Peter M, Bergman, Richard N, Amin, Najaf, Gyllensten, Ulf, Segrè, Ayellet V, Voight, Benjamin F, Weyant, Robert J, Schreiber, Stefan, Tyrer, Jonathan P, Luan, Jian'an, Stringham, Heather M, Martin, Nicholas G, Grönberg, Henrik, Boomsma, Dorret I, Hicks, Andrew A, Pastinen, Tomi, Perola, Markus, Schunkert, Heribert, Rudan, Igor, Ripatti, Samuli, Eiriksdottir, Gudny, Citterio, Lorena, Kayser, Manfred, Hua Zhao, Jing, Kolcic, Ivana, Alavere, Helene, Assimes, Themistocles L, Rioux, John D, Oliver Schmidt, Carsten, Hunter, David J, Samani, Nilesh J, Huikuri, Heikki V, Steinthorsdottir, Valgerdur, Beckmann, Jacques S, Pouta, Anneli, Hattersley, Andrew T, Weedon, Michael N, Barroso, Inês, McCarthy, Mark I, Salem, Rany M, Bergmann, Sven, Perry, John R. B, Levinson, Douglas F, van Meurs, Joyce B. J, Lehtimäki, Terho, Thompson, John R, Elosua, Roberto, Mulas, Antonella, Vedantam, Sailaja, Pietiläinen, Kirsi H, Farrall, Martin, Peters, Marjolein J, Kaprio, Jaakko, Aulchenko, Yurii S, Province, Michael A, Ouwehand, Willem H, Lango Allen, Hana, Mark Lathrop, G, Chanock, Stephen J, Hall, Alistair S, Carola Zillikens, M

    Published in Nature (London)
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    Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls by Craddock, Nick, Hurles, Matthew E, Cardin, Niall, Pearson, Richard D, Plagnol, Vincent, Robson, Samuel, Vukcevic, Damjan, Barnes, Chris, Conrad, Donald F, Giannoulatou, Eleni, Holmes, Chris, Marchini, Jonathan L, Stirrups, Kathy, Tobin, Martin D, Wain, Louise V, Yau, Chris, Aerts, Jan, Ahmad, Tariq, Andrews, T Daniel, Arbury, Hazel, Attwood, Anthony, Auton, Adam, Ball, Stephen G, Balmforth, Anthony J, Barrett, Jeffrey C, Barroso, Inês, Barton, Anne, Bennett, Amanda J, Bhaskar, Sanjeev, Blaszczyk, Katarzyna, Bowes, John, Brand, Oliver J, Braund, Peter S, Bredin, Francesca, Breen, Gerome, Brown, Morris J, Bruce, Ian N, Bull, Jaswinder, Burren, Oliver S, Burton, John, Byrnes, Jake, Caesar, Sian, Clee, Chris M, Coffey, Alison J, Connell, John M C, Cooper, Jason D, Dominiczak, Anna F, Downes, Kate, Drummond, Hazel E, Dudakia, Darshna, Dunham, Andrew, Ebbs, Bernadette, Eccles, Diana, Edkins, Sarah, Edwards, Cathryn, Elliot, Anna, Emery, Paul, Evans, David M, Evans, Gareth, Eyre, Steve, Farmer, Anne, Ferrier, I Nicol, Feuk, Lars, Fitzgerald, Tomas, Flynn, Edward, Forbes, Alistair, Forty, Liz, Franklyn, Jayne A, Freathy, Rachel M, Gibbs, Polly, Gilbert, Paul, Gokumen, Omer, Gordon-Smith, Katherine, Gray, Emma, Green, Elaine, Groves, Chris J, Grozeva, Detelina, Gwilliam, Rhian, Hall, Anita, Hammond, Naomi, Hardy, Matt, Harrison, Pile, Hassanali, Neelam, Hebaishi, Husam, Hines, Sarah, Hinks, Anne, Hitman, Graham A, Hocking, Lynne, Howard, Eleanor, Howard, Philip, Howson, Joanna M M, Hughes, Debbie, Hunt, Sarah, Isaacs, John D, Jain, Mahim, Jewell, Derek P, Johnson, Toby, Jolley, Jennifer D, Jones, Ian R, Jones, Lisa A

    Published in Nature (London)
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    Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation by Bis, Joshua C., Jian, Xueqiu, Kunkle, Brian W., Chen, Yuning, Hamilton-Nelson, Kara L., Bush, William S., Salerno, William J., Lancour, Daniel, Ma, Yiyi, Renton, Alan E., Marcora, Edoardo, Farrell, John J., Zhao, Yi, Qu, Liming, Ahmad, Shahzad, Amin, Najaf, Amouyel, Philippe, Beecham, Gary W., Below, Jennifer E., Campion, Dominique, Cantwell, Laura, Charbonnier, Camille, Chung, Jaeyoon, Crane, Paul K., Cruchaga, Carlos, Cupples, L. Adrienne, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Fulton, Lucinda, Gabriel, Stacey B., Genin, Emmanuelle, Gibbs, Richard A., Goate, Alison, Grenier-Boley, Benjamin, Gupta, Namrata, Haines, Jonathan L., Havulinna, Aki S., Helisalmi, Seppo, Hiltunen, Mikko, Howrigan, Daniel P., Ikram, M. Arfan, Kaprio, Jaakko, Konrad, Jan, Kuzma, Amanda, Lander, Eric S., Lathrop, Mark, Lehtimäki, Terho, Lin, Honghuang, Mattila, Kari, Mayeux, Richard, Muzny, Donna M., Nasser, Waleed, Neale, Benjamin, Nho, Kwangsik, Nicolas, Gaël, Patel, Devanshi, Pericak-Vance, Margaret A., Perola, Markus, Psaty, Bruce M., Quenez, Olivier, Rajabli, Farid, Redon, Richard, Reitz, Christiane, Remes, Anne M., Salomaa, Veikko, Sarnowski, Chloe, Schmidt, Helena, Schmidt, Michael, Schmidt, Reinhold, Soininen, Hilkka, Thornton, Timothy A., Tosto, Giuseppe, Tzourio, Christophe, van der Lee, Sven J., van Duijn, Cornelia M., Valladares, Otto, Vardarajan, Badri, Wang, Li-San, Wang, Weixin, Wijsman, Ellen, Wilson, Richard K., Witten, Daniela, Worley, Kim C., Zhang, Xiaoling, Bellenguez, Celine, Lambert, Jean-Charles, Kurki, Mitja I., Palotie, Aarno, Daly, Mark, Boerwinkle, Eric, Lunetta, Kathryn L., Destefano, Anita L., Dupuis, Josée, Martin, Eden R., Schellenberg, Gerard D., Seshadri, Sudha, Naj, Adam C., Fornage, Myriam, Farrer, Lindsay A.

    Published in Molecular psychiatry
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    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk by Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

    Published in Cell
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