Exome arrays capture polygenic rare variant contributions to schizophrenia

por Richards, A. L., Leonenko, G., Walters, J. T., Kavanagh, D. H., Rees, E. G., Evans, A., Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M., McCarroll, S. A., Pocklington, A. J., Holmans, P. A., Owen, M. J., O'Donovan, M. C.
Publicado 2016

Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer

por Stacey, Simon N., Kehr, Birte, Gudmundsson, Julius, Zink, Florian, Jonasdottir, Aslaug, Gudjonsson, Sigurjon A., Sigurdsson, Asgeir, Halldorsson, Bjarni V., Agnarsson, Bjarni A., Benediktsdottir, Kristrun R., Aben, Katja K.H., Vermeulen, Sita H., Cremers, Ruben G., Panadero, Angeles, Helfand, Brian T., Cooper, Phillip R., Donovan, Jenny L., Hamdy, Freddie C., Jinga, Viorel, Okamoto, Ichiro, Jonasson, Jon G., Tryggvadottir, Laufey, Johannsdottir, Hrefna, Kristinsdottir, Anna M., Masson, Gisli, Magnusson, Olafur T., Iordache, Paul D., Helgason, Agnar, Helgason, Hannes, Sulem, Patrick, Gudbjartsson, Daniel F., Kong, Augustine, Jonsson, Eirikur, Barkardottir, Rosa B., Einarsson, Gudmundur V., Rafnar, Thorunn, Thorsteinsdottir, Unnur, Mates, Ioan N., Neal, David E., Catalona, William J., Mayordomo, José I., Kiemeney, Lambertus A., Thorleifsson, Gudmar, Stefansson, Kari
Publicado 2016

Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck

por Wilson, Ian J., Carling, Phillipa J., Alston, Charlotte L., Floros, Vasileios I., Pyle, Angela, Hudson, Gavin, Sallevelt, Suzanne C.E.H., Lamperti, Costanza, Carelli, Valerio, Bindoff, Laurence A., Samuels, David C., Wonnapinij, Passorn, Zeviani, Massimo, Taylor, Robert W., Smeets, Hubert J.M., Horvath, Rita, Chinnery, Patrick F
Publicado 2016

Exploring the complete mutational space of the LDL receptor LA5 domain using molecular dynamics: linking SNPs with disease phenotypes in familial hypercholesterolemia

por Angarica, Vladimir Espinosa, Orozco, Modesto, Sancho, Javier
Publicado 2016

Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms

por Horikoshi, Momoko, Pasquali, Lorenzo, Wiltshire, Steven, Huyghe, Jeroen R., Mahajan, Anubha, Asimit, Jennifer L., Ferreira, Teresa, Locke, Adam E., Robertson, Neil R., Wang, Xu, Sim, Xueling, Fujita, Hayato, Hara, Kazuo, Young, Robin, Zhang, Weihua, Choi, Sungkyoung, Chen, Han, Kaur, Ismeet, Takeuchi, Fumihiko, Fontanillas, Pierre, Thuillier, Dorothée, Yengo, Loic, Below, Jennifer E., Tam, Claudia H.T., Wu, Ying, Abecasis, Gonçalo, Altshuler, David, Bell, Graeme I., Blangero, John, Burtt, Noél P., Duggirala, Ravindranath, Florez, Jose C., Hanis, Craig L., Seielstad, Mark, Atzmon, Gil, Chan, Juliana C.N., Ma, Ronald C.W., Froguel, Philippe, Wilson, James G., Bharadwaj, Dwaipayan, Dupuis, Josee, Meigs, James B., Cho, Yoon Shin, Park, Taesung, Kooner, Jaspal S., Chambers, John C., Saleheen, Danish, Kadowaki, Takashi, Tai, E. Shyong, Mohlke, Karen L., Cox, Nancy J., Ferrer, Jorge, Zeggini, Eleftheria, Kato, Norihiro, Teo, Yik Ying, Boehnke, Michael, McCarthy, Mark I., Morris, Andrew P.
Publicado 2016

Testing the role of predicted gene knockouts in human anthropometric trait variation

por Lessard, Samuel, Manning, Alisa K., Low-Kam, Cécile, Auer, Paul L., Giri, Ayush, Graff, Mariaelisa, Schurmann, Claudia, Yaghootkar, Hanieh, Luan, Jian'an, Esko, Tonu, Karaderi, Tugce, Bottinger, Erwin P., Lu, Yingchang, Carlson, Chris, Caulfield, Mark, Dubé, Marie-Pierre, Jackson, Rebecca D., Kooperberg, Charles, McKnight, Barbara, Mongrain, Ian, Peters, Ulrike, Reiner, Alex P., Rhainds, David, Sotoodehnia, Nona, Hirschhorn, Joel N., Scott, Robert A., Munroe, Patricia B., Frayling, Timothy M., Loos, Ruth J.F., North, Kari E., Edwards, Todd L., Tardif, Jean-Claude, Lindgren, Cecilia M., Lettre, Guillaume
Publicado 2016

Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram

por Verweij, Niek, Mateo Leach, Irene, Isaacs, Aaron, Arking, Dan E., Bis, Joshua C., Pers, Tune H., Van Den Berg, Marten E., Lyytikäinen, Leo-Pekka, Barnett, Phil, Wang, Xinchen, Soliman, Elsayed Z., Van Duijn, Cornelia M., Kähönen, Mika, Van Veldhuisen, Dirk J., Kors, Jan A., Raitakari, Olli T., Silva, Claudia T., Lehtimäki, Terho, Hillege, Hans L., Hirschhorn, Joel N., Boyer, Laurie A., Van Gilst, Wiek H., Alonso, Alvaro, Sotoodehnia, Nona, Eijgelsheim, Mark, De Boer, Rudolf A., De Bakker, Paul I. W., Franke, Lude, Van Der Harst, Pim
Publicado 2016

Integrated analyses of gene expression and genetic association studies in a founder population

por Cusanovich, Darren A., Caliskan, Minal, Billstrand, Christine, Michelini, Katelyn, Chavarria, Claudia, De Leon, Sherryl, Mitrano, Amy, Lewellyn, Noah, Elias, Jack A., Chupp, Geoffrey L., Lang, Roberto M., Shah, Sanjiv J., Decara, Jeanne M., Gilad, Yoav, Ober, Carole
Publicado 2016

Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease

por Offenbacher, Steven, Divaris, Kimon, Barros, Silvana P., Moss, Kevin L., Marchesan, Julie T., Morelli, Thiago, Zhang, Shaoping, Kim, Steven, Sun, Lu, Beck, James D., Laudes, Matthias, Munz, Matthias, Schaefer, Arne S., North, Kari E.
Publicado 2016

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease

por Orlando, Giulia, Law, Philip J., Palin, Kimmo, Tuupanen, Sari, Gylfe, Alexandra, Hänninen, Ulrika A., Cajuso, Tatiana, Tanskanen, Tomas, Kondelin, Johanna, Kaasinen, Eevi, Sarin, Antti-Pekka, Kaprio, Jaakko, Eriksson, Johan G., Rissanen, Harri, Knekt, Paul, Pukkala, Eero, Jousilahti, Pekka, Salomaa, Veikko, Ripatti, Samuli, Palotie, Aarno, Järvinen, Heikki, Renkonen-Sinisalo, Laura, Lepistö, Anna, Böhm, Jan, Mecklin, Jukka-Pekka, Al-Tassan, Nada A., Palles, Claire, Martin, Lynn, Barclay, Ella, Tenesa, Albert, Farrington, Susan, Timofeeva, Maria N., Meyer, Brian F., Wakil, Salma M., Campbell, Harry, Smith, Christopher G., Idziaszczyk, Shelley, Maughan, Timothy S., Kaplan, Richard, Kerr, Rachel, Kerr, David, Buchanan, Daniel D., Ko Win, Aung, Hopper, John, Jenkins, Mark, Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steve, Conti, David, Schumacher, Fred, Casey, Graham, Taipale, Jussi, Cheadle, Jeremy P., Dunlop, Malcolm G., Tomlinson, Ian P., Aaltonen, Lauri A., Houlston, Richard S.
Publicado 2016

Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation

por Gilly, Arthur, Ritchie, Graham Rs, Southam, Lorraine, Farmaki, Aliki-Eleni, Tsafantakis, Emmanouil, Dedoussis, George, Zeggini, Eleftheria
Publicado 2016

A genome-wide association meta-analysis on apolipoprotein A-IV concentrations

por Lamina, Claudia, Friedel, Salome, Coassin, Stefan, Rueedi, Rico, Yousri, Noha A., Seppälä, Ilkka, Gieger, Christian, Schönherr, Sebastian, Forer, Lukas, Erhart, Gertraud, Kollerits, Barbara, Marques-Vidal, Pedro, Ried, Janina, Waeber, Gerard, Bergmann, Sven, Dähnhardt, Doreen, Stöckl, Andrea, Kiechl, Stefan, Raitakari, Olli T., Kähönen, Mika, Willeit, Johann, Kedenko, Ludmilla, Paulweber, Bernhard, Peters, Annette, Meitinger, Thomas, Strauch, Konstantin, Study Group, KORA, Lehtimäki, Terho, Hunt, Steven C., Vollenweider, Peter, Kronenberg, Florian
Publicado 2016

SUGP1 is a novel regulator of cholesterol metabolism

por Kim, Mee J., Yu, Chi-Yi, Theusch, Elizabeth, Naidoo, Devesh, Stevens, Kristen, Kuang, Yu-Lin, Schuetz, Erin, Chaudhry, Amarjit S., Medina, Marisa W.
Publicado 2016

The heritability and patterns of DNA methylation in normal human colorectum

por Rowlatt, Amy, Hernández-Suárez, Gustavo, Sanabria-Salas, María Carolina, Serrano-López, Martha, Rawlik, Konrad, Hernandez-Illan, Eva, Alenda, Cristina, Castillejo, Adela, Soto, Jose Luis, Haley, Chris S., Tenesa, Albert
Publicado 2016

Address in Surgery

Publicado 1903

Address in Medicine

Publicado 1903

President's Address

Publicado 1903

Meeting at St. Bartholomew's Hospital

Publicado 1913

Conference at Birmingham

Publicado 1912

Identification of genetic modifiers of age-at-onset for familial Parkinson’s disease

por Hill-Burns, Erin M., Ross, Owen A., Wissemann, William T., Soto-Ortolaza, Alexandra I., Zareparsi, Sepideh, Siuda, Joanna, Lynch, Timothy, Wszolek, Zbigniew K., Silburn, Peter A., Mellick, George D., Ritz, Beate, Scherzer, Clemens R., Zabetian, Cyrus P., Factor, Stewart A., Breheny, Patrick J., Payami, Haydeh
Publicado 2016