Výsledky vyhledávání - Tachmazidou, Ioanna

Rare Variant Association Testing for Next-Generation Sequencing Data via Hierarchical Clustering Autor Tachmazidou, Ioanna, Morris, Andrew, Zeggini, Eleftheria

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In search of low-frequency and rare variants affecting complex traits Autor Panoutsopoulou, Kalliope, Tachmazidou, Ioanna, Zeggini, Eleftheria

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Genetic Association Mapping via Evolution-Based Clustering of Haplotypes Autor Tachmazidou, Ioanna, Verzilli, Claudio J, Iorio, Maria De

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Bayesian survival analysis in genetic association studies Autor Tachmazidou, Ioanna, Andrew, Toby, Verzilli, Claudio J., Johnson, Michael R., De Iorio, Maria

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Estimating Genome-Wide Significance for Whole-Genome Sequencing Studies Autor Xu, ChangJiang, Tachmazidou, Ioanna, Walter, Klaudia, Ciampi, Antonio, Zeggini, Eleftheria, Greenwood, Celia M T

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Candidate genes for obesity-susceptibility show enriched association within a large genome-wide association study for BMI Autor Vimaleswaran, Karani S., Tachmazidou, Ioanna, Zhao, Jing Hua, Hirschhorn, Joel N., Dudbridge, Frank, Loos, Ruth J.F.

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A novel variant in GLIS3 is associated with osteoarthritis Autor Casalone, Elisabetta, Tachmazidou, Ioanna, Zengini, Eleni, Hatzikotoulas, Konstantinos, Hackinger, Sophie, Suveges, Daniel, Steinberg, Julia, Rayner, Nigel William, Wilkinson, Jeremy Mark, Panoutsopoulou, Kalliope, Zeggini, Eleftheria

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Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits Autor Southam, Lorraine, Gilly, Arthur, Süveges, Dániel, Farmaki, Aliki-Eleni, Schwartzentruber, Jeremy, Tachmazidou, Ioanna, Matchan, Angela, Rayner, Nigel W., Tsafantakis, Emmanouil, Karaleftheri, Maria, Xue, Yali, Dedoussis, George, Zeggini, Eleftheria

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The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA? Autor MacInnes, Scott J., Hatzikotoulas, Konstantinos, Fenstad, Anne Marie, Shah, Karan, Southam, Lorraine, Tachmazidou, Ioanna, Hallan, Geir, Dale, Hårvard, Panoutsopoulou, Kalliope, Furnes, Ove, Zeggini, Eleftheria, Wilkinson, J. Mark

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Erratum to: The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA? Autor MacInnes, Scott J., Hatzikotoulas, Konstantinos, Fenstad, Anne Marie, Shah, Karan, Southam, Lorraine, Tachmazidou, Ioanna, Hallan, Geir, Dale, Hårvard, Panoutsopoulou, Kalliope, Furnes, Ove, Zeggini, Eleftheria, Wilkinson, J. Mark

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Using ancestry-informative markers to identify fine structure across 15 populations of European origin Autor Huckins, Laura M, Boraska, Vesna, Franklin, Christopher S, Floyd, James A B, Southam, Lorraine, Sullivan, Patrick F, Bulik, Cynthia M, Collier, David A, Tyler-Smith, Chris, Zeggini, Eleftheria, Tachmazidou, Ioanna

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Rare variant contribution to human disease in 281,104 UK Biobank exomes Autor Wang, Quanli, Dhindsa, Ryan S., Carss, Keren, Harper, Andrew R., Nag, Abhishek, Tachmazidou, Ioanna, Vitsios, Dimitrios, Deevi, Sri V. V., Mackay, Alex, Muthas, Daniel, Hühn, Michael, Monkley, Susan, Olsson, Henric, Wasilewski, Sebastian, Smith, Katherine R., March, Ruth, Platt, Adam, Haefliger, Carolina, Petrovski, Slavé

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Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank Autor Tachmazidou, Ioanna, Hatzikotoulas, Konstantinos, Southam, Lorraine, Esparza-Gordillo, Jorge, Haberland, Valeriia, Zheng, Jie, Johnson, Toby, Koprulu, Mine, Zengini, Eleni, Steinberg, Julia, Wilkinson, Jeremy M, Bhatnagar, Sahir, Hoffman, Joshua D, Buchan, Natalie, Süveges, Dániel, Yerges-Armstrong, Laura, Smith, George Davey, Gaunt, Tom R, Scott, Robert A, McCarthy, Linda C, Zeggini, Eleftheria

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A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates Autor Tachmazidou, Ioanna, Dedoussis, George, Southam, Lorraine, Farmaki, Aliki-Eleni, Ritchie, Graham R. S., Xifara, Dionysia K., Matchan, Angela, Hatzikotoulas, Konstantinos, Rayner, Nigel W., Chen, Yuan, Pollin, Toni I., O’Connell, Jeffrey R., Yerges-Armstrong, Laura M., Kiagiadaki, Chrysoula, Panoutsopoulou, Kalliope, Schwartzentruber, Jeremy, Moutsianas, Loukas, Tsafantakis, Emmanouil, Tyler-Smith, Chris, McVean, Gil, Xue, Yali, Zeggini, Eleftheria

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Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis Autor Zengini, Eleni, Hatzikotoulas, Konstantinos, Tachmazidou, Ioanna, Steinberg, Julia, Hartwig, Fernando P., Southam, Lorraine, Hackinger, Sophie, Boer, Cindy G., Styrkarsdottir, Unnur, Gilly, Arthur, Suveges, Daniel, Killian, Britt, Ingvarsson, Thorvaldur, Jonsson, Helgi, Babis, George C., McCaskie, Andrew, Uitterlinden, Andre G., van Meurs, Joyce B. J., Thorsteinsdottir, Unnur, Stefansson, Kari, Smith, George Davey, Wilkinson, Jeremy M., Zeggini, Eleftheria

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A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy Autor Speed, Doug, Hoggart, Clive, Petrovski, Slave, Tachmazidou, Ioanna, Coffey, Alison, Jorgensen, Andrea, Eleftherohorinou, Hariklia, De Iorio, Maria, Todaro, Marian, De, Tisham, Smith, David, Smith, Philip E., Jackson, Margaret, Cooper, Paul, Kellett, Mark, Howell, Stephen, Newton, Mark, Yerra, Raju, Tan, Meng, French, Chris, Reuber, Markus, Sills, Graeme E., Chadwick, David, Pirmohamed, Munir, Bentley, David, Scheffer, Ingrid, Berkovic, Samuel, Balding, David, Palotie, Aarno, Marson, Anthony, O'Brien, Terence J., Johnson, Michael R.

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Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants Autor Panoutsopoulou, Kalliope, Hatzikotoulas, Konstantinos, Xifara, Dionysia Kiara, Colonna, Vincenza, Farmaki, Aliki-Eleni, Ritchie, Graham R. S., Southam, Lorraine, Gilly, Arthur, Tachmazidou, Ioanna, Fatumo, Segun, Matchan, Angela, Rayner, Nigel W., Ntalla, Ioanna, Mezzavilla, Massimo, Chen, Yuan, Kiagiadaki, Chrysoula, Zengini, Eleni, Mamakou, Vasiliki, Athanasiadis, Antonis, Giannakopoulou, Margarita, Kariakli, Vassiliki-Eirini, Nsubuga, Rebecca N., Karabarinde, Alex, Sandhu, Manjinder, McVean, Gil, Tyler-Smith, Chris, Tsafantakis, Emmanouil, Karaleftheri, Maria, Xue, Yali, Dedoussis, George, Zeggini, Eleftheria

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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans Autor Timpson, Nicholas J., Walter, Klaudia, Min, Josine L., Tachmazidou, Ioanna, Malerba, Giovanni, Shin, So-Youn, Chen, Lu, Futema, Marta, Southam, Lorraine, Iotchkova, Valentina, Cocca, Massimiliano, Huang, Jie, Memari, Yasin, McCarthy, Shane, Danecek, Petr, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Perry, John R. B., Ring, Susan M., Gaye, Amadou, Dedoussis, George, Farmaki, Aliki-Eleni, Burton, Paul, Talmud, Philippa J., Gambaro, Giovanni, Spector, Tim D., Smith, George Davey, Durbin, Richard, Richards, J Brent, Humphries, Steve E., Zeggini, Eleftheria, Soranzo, Nicole

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Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans Autor Timpson, Nicholas J., Walter, Klaudia, Min, Josine L., Tachmazidou, Ioanna, Malerba, Giovanni, Shin, So-Youn, Chen, Lu, Futema, Marta, Southam, Lorraine, Iotchkova, Valentina, Cocca, Massimiliano, Huang, Jie, Memari, Yasin, McCarthy, Shane, Danecek, Petr, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Perry, John R. B., Ring, Susan M., Gaye, Amadou, Dedoussis, George, Farmaki, Aliki-Eleni, Burton, Paul, Talmud, Philippa J., Gambaro, Giovanni, Spector, Tim D., Smith, George Davey, Durbin, Richard, Richards, J. Brent, Humphries, Steve E., Zeggini, Eleftheria, Soranzo, Nicole

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Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity Autor Hendricks, Audrey E., Bochukova, Elena G., Marenne, Gaëlle, Keogh, Julia M., Atanassova, Neli, Bounds, Rebecca, Wheeler, Eleanor, Mistry, Vanisha, Henning, Elana, Körner, Antje, Muddyman, Dawn, McCarthy, Shane, Hinney, Anke, Hebebrand, Johannes, Scott, Robert A., Langenberg, Claudia, Wareham, Nick J., Surendran, Praveen, Howson, Joanna M., Butterworth, Adam S., Danesh, John, Nordestgaard, Børge G, Nielsen, Sune F, Afzal, Shoaib, Papadia, Sofia, Ashford, Sofie, Garg, Sumedha, Millhauser, Glenn L., Palomino, Rafael I., Kwasniewska, Alexandra, Tachmazidou, Ioanna, O’Rahilly, Stephen, Zeggini, Eleftheria, Barroso, Inês, Farooqi, I. Sadaf

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