Characterisation of Chinook salmon (Oncorhynchus tshawytscha) blood and validation of flow cytometry cell count and viability assay kit von Lulijwa, Ronald, Alfaro, Andrea C., Merien, Fabrice, Burdass, Mark, Young, Tim, Meyer, Jill, Nguyen, Thao V., Trembath, Caroline

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Accommodating the cost of growth and swimming in fish-the applicability of exercise-induced growth to juvenile hapuku (Polyprion oxygeneios) von Khan, Javed R, Trembath, Caroline, Pether, Steve, Bruce, Michael, Walker, Seumas P, Herbert, Neill A

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Accommodating the cost of growth and swimming in fish—the applicability of exercise-induced growth to juvenile hapuku (Polyprion oxygeneios) von Khan, Javed R., Trembath, Caroline, Pether, Steve, Bruce, Michael, Walker, Seumas P., Herbert, Neill A.

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Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss von Simpson, Michael A, Irving, Melita D, Asilmaz, Esra, Gray, Mary J, Dafou, Dimitra, Elmslie, Frances V, Mansour, Sahar, Holder, Sue E, Brain, Caroline E, Burton, Barbara K, Kim, Katherine H, Pauli, Richard M, Aftimos, Salim, Stewart, Helen, Kim, Chong Ae, Holder-Espinasse, Muriel, Robertson, Stephen P, Drake, William M, Trembath, Richard C

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Genetic architecture of routinely acquired blood tests in a British South Asian cohort von Jacobs, Benjamin M., Stow, Daniel, Hodgson, Sam, Zöllner, Julia, Samuel, Miriam, Kanoni, Stavroula, Bidi, Saeed, Walter, Klaudia, Langenberg, Claudia, Dobson, Ruth, Finer, Sarah, Morton, Caroline, Siddiqui, Moneeza K., Martin, Hilary C., Pietzner, Maik, Mathur, Rohini, van Heel, David A.

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The transmembrane protein meckelin ( MKS3 ) is mutated in Meckel-Gruber syndrome and the wpk rat von Bennett, Christopher P, Attie-Bitach, Tania, Lilliquist, Stacie, Pasha, Shanaz, Harris, Peter C, Morgan, Neil V, Malik Sharif, Saghira, Maher, Eamonn R, Johnson, Colin A, Tee, Louise J, Maina, Esther N, Bucourt, Martine, Miller, Caroline A, Ward, Christopher J, Goranson, Erin, Trembath, Richard C, McKee, Brandy M, McKeown, Carole, Consugar, Mark, Torres, Vicente E, Cox, Phillip, Smith, Ursula M, Gattone, Vincent H, Whelan, Shelly, Aligianis, Irene A, Batman, Philip A, Woods, C Geoffrey, AlGazali, Lihadh, Punyashthiti, Rachaneekorn, Gissen, Paul, Kelly, Deirdre A

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Rare variant contribution to cholestatic liver disease in a South Asian population in the United Kingdom von Zöllner, Julia, Finer, Sarah, Linton, Kenneth J., van Heel, David A., Williamson, Catherine, Dixon, Peter H.

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Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis von Holliday, Elizabeth G, Smith, Albert V, Cornes, Belinda K, Buitendijk, Gabriëlle H S, Jensen, Richard A, Sim, Xueling, Aspelund, Thor, Aung, Tin, Baird, Paul N, Boerwinkle, Eric, Cheng, Ching Yu, van Duijn, Cornelia M, Eiriksdottir, Gudny, Gudnason, Vilmundur, Harris, Tamara, Hewitt, Alex W, Inouye, Michael, Jonasson, Fridbert, Klein, Barbara E K, Launer, Lenore, Li, Xiaohui, Liew, Gerald, Lumley, Thomas, McElduff, Patrick, McKnight, Barbara, Mitchell, Paul, Psaty, Bruce M, Rochtchina, Elena, Rotter, Jerome I, Scott, Rodney J, Tay, Wanting, Taylor, Kent, Teo, Yik Ying, Uitterlinden, André G, Viswanathan, Ananth, Xie, Sophia, Vingerling, Johannes R, Klaver, Caroline C W, Tai, E Shyong, Siscovick, David, Klein, Ronald, Cotch, Mary Frances, Wong, Tien Y, Attia, John, Wang, Jie Jin

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Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke von Bellenguez, Céline, Bevan, Steve, Gschwendtner, Andreas, Spencer, Chris C A, Burgess, Annette I, Pirinen, Matti, Jackson, Caroline A, Traylor, Matthew, Strange, Amy, Su, Zhan, Band, Gavin, Syme, Paul D, Malik, Rainer, Pera, Joanna, Norrving, Bo, Lemmens, Robin, Freeman, Colin, Schanz, Renata, James, Tom, Poole, Deborah, Murphy, Lee, Segal, Helen, Cortellini, Lynelle, Cheng, Yu-Ching, Woo, Daniel, Nalls, Michael A, Müller-Myhsok, Bertram, Meisinger, Christa, Seedorf, Udo, Ross-Adams, Helen, Boonen, Steven, Wloch-Kopec, Dorota, Valant, Valerie, Slark, Julia, Furie, Karen, Delavaran, Hossein, Langford, Cordelia, Deloukas, Panos, Edkins, Sarah, Hunt, Sarah, Gray, Emma, Dronov, Serge, Peltonen, Leena, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Stefansson, Kari, Boncoraglio, Giorgio B, Parati, Eugenio A, Attia, John, Holliday, Elizabeth, Levi, Chris, Franzosi, Maria-Grazia, Goel, Anuj, Helgadottir, Anna, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Worrall, Bradford B, Kittner, Steven J, Mitchell, Braxton D, Kissela, Brett, Meschia, James F, Thijs, Vincent, Lindgren, Arne, Macleod, Mary Joan, Slowik, Agnieszka, Walters, Matthew, Rosand, Jonathan, Sharma, Pankaj, Farrall, Martin, Sudlow, Cathie L M, Rothwell, Peter M, Dichgans, Martin, Donnelly, Peter, Markus, Hugh S

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Genome‐Wide Association Study Identifies Risk Loci for Cluster Headache von O'Connor, Emer, Fourier, Carmen, Ran, Caroline, Sivakumar, Prasanth, Liesecke, Franziska, Southgate, Laura, Harder, Aster V. E., Vijfhuizen, Lisanne S., Yip, Janice, Giffin, Nicola, Silver, Nicholas, Ahmed, Fayyaz, Hostettler, Isabel C., Davies, Brendan, Cader, M. Zameel, Simpson, Benjamin S., Sullivan, Roisin, Efthymiou, Stephanie, Adebimpe, Joycee, Quinn, Olivia, Campbell, Ciaran, Cavalleri, Gianpiero L., Vikelis, Michail, Kelderman, Tim, Paemeleire, Koen, Kilbride, Emer, Grangeon, Lou, Lagrata, Susie, Danno, Daisuke, Trembath, Richard, Wood, Nicholas W., Kockum, Ingrid, Winsvold, Bendik S., Steinberg, Anna, Sjöstrand, Christina, Waldenlind, Elisabet, Vandrovcova, Jana, Houlden, Henry, Matharu, Manjit, Belin, Andrea Carmine

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Genetic basis of early onset and progression of type 2 diabetes in South Asians von Hodgson, Sam, Williamson, Alice, Bigossi, Margherita, Stow, Daniel, Jacobs, Benjamin M, Samuel, Miriam, Gafton, Joseph, Zöllner, Julia, Spreckley, Marie, Langenberg, Claudia, van Heel, David A, Mathur, Rohini, Siddiqui, Moneeza K, Finer, Sarah

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Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process von Springelkamp, Henriët., Höhn, René, Mishra, Aniket, Hysi, Pirro G., Khor, Chiea-Chuen, Loomis, Stephanie J., Bailey, Jessica N. Cooke, Gibson, Jane, Thorleifsson, Gudmar, Janssen, Sarah F., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Nongpiur, Monisha E., Montgomery, Grant W., Xu, Liang, Mountain, Jenny E., Gharahkhani, Puya, Lu, Yi, Amin, Najaf, Karssen, Lennart C., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Iglesias, Adriana I., Verhoeven, Virginie J. M., Hauser, Michael A., Loon, Seng-Chee, Despriet, Dominiek D. G., Nag, Abhishek, Venturini, Cristina, Sanfilippo, Paul G., Schillert, Arne, Kang, Jae H., Landers, John, Jonasson, Fridbert, Cree, Angela J., van Koolwijk, Leonieke M. E., Rivadeneira, Fernando, Souzeau, Emmanuelle, Jonsson, Vesteinn, Menon, Geeta, Weinreb, Robert N., de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Ennis, Sarah, Thorsteinsdottir, Unnur, Burdon, Kathryn P., Spector, Timothy D., Mirshahi, Alireza, Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Haines, Jonathan L., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Jansonius, Nomdo M., Jonas, Jost B., Cheng, Ching-Yu, Aung, Tin, Viswanathan, Ananth C., Klaver, Caroline C. W., Craig, Jamie E., Macgregor, Stuart, Mackey, David A., Lotery, Andrew J., Stefansson, Kari, Bergen, Arthur A. B., Young, Terri L., Wiggs, Janey L., Pfeiffer, Norbert, Wong, Tien-Yin, Pasquale, Louis R., Hewitt, Alex W., van Duijn, Cornelia M., Hammond, Christopher J.

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Prevalent and Low-Frequency Null Mutations in the Filaggrin Gene Are Associated with Early-Onset and Persistent Atopic Eczema von Brown, Sara J., Sandilands, Aileen, Zhao, Yiwei, Liao, Haihui, Relton, Caroline L., Meggitt, Simon J., Trembath, Richard C., Barker, Jonathan N.W.N., Reynolds, Nick J., Cordell, Heather J., Irwin McLean, W.H.

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Common genetic determinants of intraocular pressure and primary open-angle glaucoma von van Koolwijk, Leonieke M E, Ramdas, Wishal D, Ikram, M Kamran, Jansonius, Nomdo M, Pasutto, Francesca, Hysi, Pirro G, Macgregor, Stuart, Janssen, Sarah F, Hewitt, Alex W, Viswanathan, Ananth C, ten Brink, Jacoline B, Hosseini, S Mohsen, Amin, Najaf, Despriet, Dominiek D G, Willemse-Assink, Jacqueline J M, Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S, Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y, Gramer, Eugen, Welge-Lüssen, Ulrich, Montgomery, Grant W, Carbonaro, Francis, Young, Terri L, Bellenguez, Céline, McGuffin, Peter, Foster, Paul J, Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y, Czudowska, Monika A, Hofman, Albert, Uitterlinden, Andre G, Wolfs, Roger C W, de Jong, Paulus T V M, Oostra, Ben A, Paterson, Andrew D, Mackey, David A, Bergen, Arthur A B, Reis, André, Hammond, Christopher J, Vingerling, Johannes R, Lemij, Hans G, Klaver, Caroline C W, van Duijn, Cornelia M

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Meta-analysis fine-mapping is often miscalibrated at single-variant resolution von Zhou, Wei, Zhou, Wei, Wu, Kuan-Han H., Hirbo, Jibril B., Lopera-Maya, Esteban A., Läll, Kristi, Karjalainen, Juha, Kurki, Mitja, Maasha, Mutaamba, Brumpton, Ben M., Chavan, Sameer, Chen, Tzu-Ting, Ding, Yi, Guare, Lindsay A., Hornsby, Whitney E., Ingold, Nathan, Johnson, Ruth, Laisk, Triin, Lv, Jun, Millwood, Iona Y., Palta, Priit, Uzunovic, Jasmina, Verma, Anurag, Zawistowski, Matthew, Zhong, Xue, Al-Dabhani, Kawthar M., Campbell, Archie, Damrauer, Scott M., Douville, Nicholas J., Finer, Sarah, Fritsche, Lars G., Fthenou, Eleni, Gonzalez-Arroyo, Gilberto, Hunt, Karen A., Ioannidis, Alexander, Jansonius, Nomdo M., Michael Lee, Ming Ta, Lopez-Pineda, Arturo, Marioni, Riccardo E., Moatamed, Babak, Numakura, Kensuke, Rafaels, Nicholas, Richmond, Anne, Rojas-Muñoz, Agustin, Straub, Peter, Vanderwerff, Brett, Vernekar, Manvi, Barnes, Kathleen C., Boezen, Marike, Chen, Zhengming, Chen, Chia-Yen, Cho, Judy, Finucane, Hilary K., Franke, Lude, Ganna, Andrea, Gaunt, Tom R., Huang, Hailiang, Koskela, Jukka T., Lajonchere, Clara, Loos, Ruth J.F., MacGregor, Stuart, Matsuda, Koichi, Olsen, Catherine M., Porteous, David J., Shavit, Jordan A., Takano, Tomohiro, Vonk, Judith M., Whiteman, David C., Wright, John, Boehnke, Michael, Bustamante, Carlos D., Cox, Nancy J., Fatumo, Segun, Geschwind, Daniel H., Hayward, Caroline, Mägi, Reedik, Martin, Hilary C., Medland, Sarah E., Okada, Yukinori, Palotie, Aarno V., Pasaniuc, Bogdan, Sanna, Serena, Stefansson, Kari, Zöllner, Sebastian, BioMe, BioVU, CanPath - Ontario Health Study, China Kadoorie Biobank Collaborative Group, Colorado Center for Personalized Medicine, deCODE Genetics, Estonian Biobank, FinnGen, Generation Scotland, National Biobank of Korea, Taiwan Biobank, The Hunt Study, Ucla Atlas Community Health Initiative, Uganda Genome Resource, Uk Biobank, Martin, Alicia R., Daly, Mark J.

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Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus von Strange, Amy, Bellenguez, Céline, Sim, Xueling, Luben, Robert, Hysi, Pirro G., Ramdas, Wishal D., van Koolwijk, Leonieke M.E., Freeman, Colin, Pirinen, Matti, Su, Zhan, Band, Gavin, Pearson, Richard, Vukcevic, Damjan, Langford, Cordelia, Deloukas, Panos, Hunt, Sarah, Gray, Emma, Dronov, Serge, Potter, Simon C., Tashakkori-Ghanbaria, Avazeh, Edkins, Sarah, Bumpstead, Suzannah J., Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz A.Z., Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N.A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Wood, Nicholas W., Barroso, Ines, Peltonen, Leena, Healey, Paul, McGuffin, Peter, Topouzis, Fotis, Klaver, Caroline C.W., van Duijn, Cornelia M., Mackey, David A., Young, Terri L., Hammond, Christopher J., Khaw, Kay-Tee, Wareham, Nick, Wang, Jie Jin, Wong, Tien Y., Foster, Paul J., Mitchell, Paul, Spencer, Chris C.A., Donnelly, Peter, Viswanathan, Ananth C.

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Genome-wide association study identifies risk loci for cluster headache von O'Connor, Emer, Fourier, Carmen, Ran, Caroline, Sivakumar, Prasanth, Liesecke, Franziska, Southgate, Laura, Harder, Aster V. E, Vijfhuizen, Lisanne S, Yip, Janice, Giffin, Nicola, Silver, Nicholas, Ahmed, Fayyaz, Hostettler, Isabel C, Davies, Brendan, Cader, M. Zameel, Simpson, Benjamin S, Sullivan, Roisin, Efthymiou, Stephanie, Adebimpe, Joycee, Quinn, Olivia, Campbell, Ciaran, Cavalleri, Gianpiero L, Vikelis, Michail, Kelderman, Tim, Paemeleire, Koen, Kilbride, Emer, Grangeon, Lou, Lagrata, Susie, Danno, Daisuke, Trembath, Richard, Wood, Nicholas W, Kockum, Ingrid, Winsvold, Bendik S, Steinberg, Anna, Sjostrand, Christina, Waldenlind, Elisabet, Vandrovcova, Jana, Houlden, Henry, Matharu, Manjit, Belin, Andrea Carmine

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Altered IL-6 signalling and risk of tuberculosis: a multi-ancestry mendelian randomisation study von Hamilton, Fergus, Schurz, Haiko, Yates, Tom A, Gilchrist, James J, Möller, Marlo, Naranbhai, Vivek, Ghazal, Peter, Timpson, Nicholas J, Akhtar, Shaheen, Anwar, Mohammad, Asgar, Omar, Ashraf, Samina, Bidi, Saeed, Breen, Gerome, Chung, Raymond, Collier, David, Curtis, Charles J, Chaudhary, Shabana, Colligan, Grainne, Deloukas, Panos, Durham, Ceri, Durrani, Faiza, Eto, Fabiola, Finer, Sarah, Gafton, Joseph, Angel, Ana, Griffiths, Chris, Harvey, Joanne, Heng, Teng, Huang, Qin Qin, Hurles, Matt, Hunt, Karen A, Hussain, Shapna, Islam, Kamrul, Iyer, Vivek, Jacobs, Benjamin M, Kalantzis, Georgios, Khan, Ahsan, Lavery, Cath, Lee, Sang Hyuck, MacArthur, Daniel, Malik, Sidra, Malawsky, Daniel, Martin, Hilary, Mason, Dan, Mazid, Mohammed Bodrul, McDermott, John, Morton, Caroline, Newman, Bill, Owor, Elizabeth, Qureshi, Asma, Ramachandrappa, Shwetha, Raza, Mehru, Russell, Jessry, Safa, Nishat, Samuel, Miriam, Siddiqui, Moneeza, Simpson, Michael, Spreckley, Marie, Stow, Daniel, Taylor, Michael, Trembath, Richard C, Tricker, Karen, van Heel, David A, Walter, Klaudia, Winckley, Caroline, Wood, Suzanne, Wright, John, Zengeya, Ishevanhu, Zöllner, Julia, Schurz, Haiko, Naranbhai, Vivek, Yates, Tom A, Gilchrist, James J, Parks, Tom, Möller, Marlo, Hoal, Eileen G, Morris, Andrew P, Hill, Adrian V S, van Crevel, Reinout, van Laarhoven, Arjan, Ottenhoff, Tom H M, Metspalu, Andres, Ellis, Magda, Thye, Thorsten, Mahasirimongkol, Surakameth, Pasomsub, Ekawat, Tokunaga, Katsushi, Omae, Yosuke, Yanai, Hideki, Mushiroda, Taisei, Kubo, Michiaki, Takahashi, Atsushi, Kamatani, Yoichiro, Alisjahbana, Bachti, Liu, Wei, Sheng, A-dong, Yang, Yurong, Parks, Tom, Pollara, Gabriele

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Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases von Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Souzeau, Emmanuelle, Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Uitterlinden, André G., Vithana, Eranga N., Foster, Paul J., Hysi, Pirro G., Hewitt, Alex W., Khor, Chiea Chuen, Pasquale, Louis R., Montgomery, Grant W., Klaver, Caroline C. W., Aung, Tin, Pfeiffer, Norbert, Mackey, David A., Hammond, Christopher J., Cheng, Ching-Yu, Craig, Jamie E., Rabinowitz, Yaron S., Wiggs, Janey L., Burdon, Kathryn P., van Duijn, Cornelia M., MacGregor, Stuart

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Polygenic risk score prediction of multiple sclerosis in individuals of South Asian ancestry von Breedon, Joshua R, Marshall, Charles R, Giovannoni, Gavin, van Heel, David A, Dobson, Ruth, Jacobs, Benjamin M

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