Replication of Established Common Genetic Variants for Adult BMI and Childhood Obesity in Greek Adolescents: The TEENAGE Study

por Ntalla, Ioanna, Panoutsopoulou, Kalliope, Vlachou, Panagiota, Southam, Lorraine, William Rayner, Nigel, Zeggini, Eleftheria, Dedoussis, George V
Publicado 2013

Population‐wide copy number variation calling using variant call format files from 6,898 individuals

por Png, Grace, Suveges, Daniel, Park, Young‐Chan, Walter, Klaudia, Kundu, Kousik, Ntalla, Ioanna, Tsafantakis, Emmanouil, Karaleftheri, Maria, Dedoussis, George, Zeggini, Eleftheria, Gilly, Arthur
Publicado 2019

Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system

por Ramírez, Julia, Duijvenboden, Stefan van, Ntalla, Ioanna, Mifsud, Borbala, Warren, Helen R, Tzanis, Evan, Orini, Michele, Tinker, Andrew, Lambiase, Pier D., Munroe, Patricia B.
Publicado 2018

Global real‐world evidence of sofosbuvir/velpatasvir as simple, effective HCV treatment: Analysis of 5552 patients from 12 cohorts

por Mangia, Alessandra, Milligan, Scott, Khalili, Mandana, Fagiuoli, Stefano, Shafran, Stephen D., Carrat, Fabrice, Ouzan, Denis, Papatheodoridis, George, Ramji, Alnoor, Borgia, Sergio M., Wedemeyer, Heiner, Losappio, Ruggero, Pérez‐Hernandez, Francisco, Wick, Nicole, Brown, Robert S., Lampertico, Pietro, Doucette, Karen, Ntalla, Ioanna, Ramroth, Heribert, Mertens, Michael, Vanstraelen, Kim, Turnes, Juan
Publicado 2020

Genome-Wide Association Analysis of Eating Disorder-Related Symptoms, Behaviors, and Personality Traits

por Boraska, Vesna, Davis, Oliver SP, Cherkas, Lynn F, Helder, Sietske G, Harris, Juliette, Krug, Isabel, Pei-Chi Liao, Thomas, Treasure, Janet, Ntalla, Ioanna, Karhunen, Leila, Keski-Rahkonen, Anna, Christakopoulou, Danai, Raevuori, Anu, Shin, So-Youn, Dedoussis, George V, Kaprio, Jaakko, Soranzo, Nicole, Spector, Tim D, Collier, David A, Zeggini, Eleftheria
Publicado 2012

Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

por Gilly, Arthur, Suveges, Daniel, Kuchenbaecker, Karoline, Pollard, Martin, Southam, Lorraine, Hatzikotoulas, Konstantinos, Farmaki, Aliki-Eleni, Bjornland, Thea, Waples, Ryan, Appel, Emil V. R., Casalone, Elisabetta, Melloni, Giorgio, Kilian, Britt, Rayner, Nigel W., Ntalla, Ioanna, Kundu, Kousik, Walter, Klaudia, Danesh, John, Butterworth, Adam, Barroso, Inês, Tsafantakis, Emmanouil, Dedoussis, George, Moltke, Ida, Zeggini, Eleftheria
Publicado 2018

Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

por Gilly, Arthur, Suveges, Daniel, Kuchenbaecker, Karoline, Pollard, Martin, Southam, Lorraine, Hatzikotoulas, Konstantinos, Farmaki, Aliki-Eleni, Bjornland, Thea, Waples, Ryan, Appel, Emil V. R., Casalone, Elisabetta, Melloni, Giorgio, Kilian, Britt, Rayner, Nigel W., Ntalla, Ioanna, Kundu, Kousik, Walter, Klaudia, Danesh, John, Butterworth, Adam, Barroso, Inês, Tsafantakis, Emmanouil, Dedoussis, George, Moltke, Ida, Zeggini, Eleftheria
Publicado 2018

Global Real-World Evidence of Sofosbuvir/Velpatasvir as a Highly Effective Treatment and Elimination Tool in People with Hepatitis C Infection Experiencing Mental Health Disorders

por Wedemeyer, Heiner, Di Marco, Vito, Garcia-Retortillo, Montserrat, Teti, Elisabetta, Fraser, Chris, Morano Amado, Luis Enrique, Rodriguez-Tajes, Sergio, Acosta-López, Silvia, O’Loan, Joss, Milella, Michele, Buti, Maria, Guerra-Veloz, María Fernanda, Ramji, Alnoor, Fenech, Mary, Martins, Alexandra, Borgia, Sergio M., Vanstraelen, Kim, Mertens, Michael, Hernández, Cándido, Ntalla, Ioanna, Ramroth, Heribert, Milligan, Scott
Publicado 2022

Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease

por Grove, Jane I., Lo, Peggy C.K., Shrine, Nick, Barwell, Julian, Wain, Louise V., Tobin, Martin D., Salter, Andrew M., Borkar, Aditi N., Cuevas-Ocaña, Sara, Bennett, Neil, John, Catherine, Ntalla, Ioanna, Jones, Gabriela E., Neal, Christopher P., Thomas, Mervyn G., Kuht, Helen, Gupta, Pankaj, Vemala, Vishwaraj M., Grant, Allister, Adewoye, Adeolu B., Shenoy, Kotacherry T., Balakumaran, Leena K., Hollox, Edward J., Hannan, Nicholas R.F., Aithal, Guruprasad P.
Publicado 2023

Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants

por 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
Publicado 2014

Cohort Profile: Extended Cohort for E-health, Environment and DNA (EXCEED)

por John, Catherine, Reeve, Nicola F, Free, Robert C, Williams, Alexander T, Ntalla, Ioanna, Farmaki, Aliki-Eleni, Bethea, Jane, Barton, Linda M, Shrine, Nick, Batini, Chiara, Packer, Richard, Terry, Sarah, Hargadon, Beverley, Wang, Qingning, Melbourne, Carl A, Adams, Emma L, Bee, Catherine E, Harrington, Kyla, Miola, José, Brunskill, Nigel J, Brightling, Christopher E, Barwell, Julian, Wallace, Susan E, Hsu, Ron, Shepherd, David J, Hollox, Edward J, Wain, Louise V, Tobin, Martin D
Publicado 2019

Corrigendum to: Cohort profile: Extended Cohort for E-health, Environment and DNA (EXCEED)

por John, Catherine, Reeve, Nicola F, Free, Robert C, Williams, Alexander T, Ntalla, Ioanna, Farmaki, Aliki-Eleni, Bethea, Jane, Barton, Linda M, Shrine, Nick, Batini, Chiara, Packer, Richard, Terry, Sarah, Hargadon, Beverley, Wang, Qingning, Melbourne, Carl A, Adams, Emma L, Bee, Catherine E, Harrington, Kyla, Miola, José, Brunskill, Nigel J, Brightling, Christopher E, Barwell, Julian, Wallace, Susan E, Hsu, Ron, Shepherd, David J, Hollox, Edward J, Wain, Louise V, Tobin, Martin D
Publicado 2019

Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease

por Williams, Alexander T., Chen, Jing, Coley, Kayesha, Batini, Chiara, Izquierdo, Abril, Packer, Richard, Abner, Erik, Kanoni, Stavroula, Shepherd, David J., Free, Robert C., Hollox, Edward J., Brunskill, Nigel J., Ntalla, Ioanna, Reeve, Nicola, Brightling, Christopher E., Venn, Laura, Adams, Emma, Bee, Catherine, Wallace, Susan E., Pareek, Manish, Hansell, Anna L., Esko, Tõnu, Stow, Daniel, Jacobs, Benjamin M., van Heel, David A., Hennah, William, Rao, Balasubramanya S., Dudbridge, Frank, Wain, Louise V., Shrine, Nick, Tobin, Martin D., John, Catherine
Publicado 2023

Association of Genetic Loci With Glucose Levels in Childhood and Adolescence: A Meta-Analysis of Over 6,000 Children

por Barker, Adam, Sharp, Stephen J., Timpson, Nicholas J., Bouatia-Naji, Nabila, Warrington, Nicole M., Kanoni, Stavroula, Beilin, Lawrence J., Brage, Soren, Deloukas, Panos, Evans, David M., Grontved, Anders, Hassanali, Neelam, Lawlor, Deborah A., Lecoeur, Cecile, Loos, Ruth J.F., Lye, Stephen J., McCarthy, Mark I., Mori, Trevor A., Ndiaye, Ndeye Coumba, Newnham, John P., Ntalla, Ioanna, Pennell, Craig E., St Pourcain, Beate, Prokopenko, Inga, Ring, Susan M., Sattar, Naveed, Visvikis-Siest, Sophie, Dedoussis, George V., Palmer, Lyle J., Froguel, Philippe, Smith, George Davey, Ekelund, Ulf, Wareham, Nicholas J., Langenberg, Claudia
Publicado 2011

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

por Wain, Louise V, Shrine, Nick, Miller, Suzanne, Jackson, Victoria E, Ntalla, Ioanna, Artigas, María Soler, Billington, Charlotte K, Kheirallah, Abdul Kader, Allen, Richard, Cook, James P, Probert, Kelly, Obeidat, Ma'en, Bossé, Yohan, Hao, Ke, Postma, Dirkje S, Paré, Peter D, Ramasamy, Adaikalavan, Mägi, Reedik, Mihailov, Evelin, Reinmaa, Eva, Melén, Erik, O'Connell, Jared, Frangou, Eleni, Delaneau, Olivier, Freeman, Colin, Petkova, Desislava, McCarthy, Mark, Sayers, Ian, Deloukas, Panos, Hubbard, Richard, Pavord, Ian, Hansell, Anna L, Thomson, Neil C, Zeggini, Eleftheria, Morris, Andrew P, Marchini, Jonathan, Strachan, David P, Tobin, Martin D, Hall, Ian P
Publicado 2015

Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12

por Jackson, Victoria E, Ntalla, Ioanna, Sayers, Ian, Morris, Richard, Whincup, Peter, Casas, Juan-Pablo, Amuzu, Antoinette, Choi, Minkyoung, Dale, Caroline, Kumari, Meena, Engmann, Jorgen, Kalsheker, Noor, Chappell, Sally, Guetta-Baranes, Tamar, McKeever, Tricia M, Palmer, Colin N A, Tavendale, Roger, Holloway, John W, Sayer, Avan A, Dennison, Elaine M, Cooper, Cyrus, Bafadhel, Mona, Barker, Bethan, Brightling, Chris, Bolton, Charlotte E, John, Michelle E, Parker, Stuart G, Moffat, Miriam F, Wardlaw, Andrew J, Connolly, Martin J, Porteous, David J, Smith, Blair H, Padmanabhan, Sandosh, Hocking, Lynne, Stirrups, Kathleen E, Deloukas, Panos, Strachan, David P, Hall, Ian P, Tobin, Martin D, Wain, Louise V
Publicado 2016

Dietary Intake, FTO Genetic Variants, and Adiposity: A Combined Analysis of Over 16,000 Children and Adolescents

por Qi, Qibin, Downer, Mary K., Kilpeläinen, Tuomas O., Taal, H. Rob, Barton, Sheila J., Ntalla, Ioanna, Standl, Marie, Boraska, Vesna, Huikari, Ville, Kiefte-de Jong, Jessica C., Körner, Antje, Lakka, Timo A., Liu, Gaifen, Magnusson, Jessica, Okuda, Masayuki, Raitakari, Olli, Richmond, Rebecca, Scott, Robert A., Bailey, Mark E.S., Scheuermann, Kathrin, Holloway, John W., Inskip, Hazel, Isasi, Carmen R., Mossavar-Rahmani, Yasmin, Jaddoe, Vincent W.V., Laitinen, Jaana, Lindi, Virpi, Melén, Erik, Pitsiladis, Yannis, Pitkänen, Niina, Snieder, Harold, Heinrich, Joachim, Timpson, Nicholas J., Wang, Tao, Yuji, Hinoda, Zeggini, Eleftheria, Dedoussis, George V., Kaplan, Robert C., Wylie-Rosett, Judith, Loos, Ruth J.F., Hu, Frank B., Qi, Lu
Publicado 2015

Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts

por Boraska, Vesna, Day-Williams, Aaron, Franklin, Christopher S., Elliott, Katherine S., Panoutsopoulou, Kalliope, Tachmazidou, Ioanna, Albrecht, Eva, Bandinelli, Stefania, Beilin, Lawrence J., Bochud, Murielle, Cadby, Gemma, Ernst, Florian, Evans, David M., Hayward, Caroline, Hicks, Andrew A., Huffman, Jennifer, Huth, Cornelia, James, Alan L., Klopp, Norman, Kolcic, Ivana, Kutalik, Zoltán, Lawlor, Debbie A., Musk, Arthur W., Pehlic, Marina, Pennell, Craig E., Perry, John R. B., Peters, Annette, Polasek, Ozren, Pourcain, Beate St, Ring, Susan M., Salvi, Erika, Schipf, Sabine, Staessen, Jan A., Teumer, Alexander, Timpson, Nicholas, Vitart, Veronique, Warrington, Nicole M., Yaghootkar, Hanieh, Zemunik, Tatijana, Zgaga, Lina, An, Ping, Anttila, Verneri, Borecki, Ingrid B., Holmen, Jostein, Ntalla, Ioanna, Palotie, Aarno, Pietiläinen, Kirsi H., Wedenoja, Juho, Winsvold, Bendik S., Dedoussis, George V., Kaprio, Jaakko, Province, Michael A., Zwart, John-Anker, Burnier, Michel, Campbell, Harry, Cusi, Daniele, Davey Smith, George, Frayling, Timothy M., Gieger, Christian, Palmer, Lyle J., Pramstaller, Peter P., Rudan, Igor, Völzke, Henry, Wichmann, H. -Erich, Wright, Alan F., Zeggini, Eleftheria
Publicado 2012

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

por Warren, Helen R, Evangelou, Evangelos, Cabrera, Claudia P, Gao, He, Ren, Meixia, Mifsud, Borbala, Ntalla, Ioanna, Surendran, Praveen, Liu, Chunyu, Cook, James P, Kraja, Aldi T, Drenos, Fotios, Loh, Marie, Verweij, Niek, Marten, Jonathan, Karaman, Ibrahim, Segura Lepe, Marcelo P, O’Reilly, Paul F, Knight, Joanne, Snieder, Harold, Kato, Norihiro, He, Jiang, Tai, E Shyong, Said, M Abdullah, Porteous, David, Alver, Maris, Poulter, Neil, Farrall, Martin, Gansevoort, Ron T, Padmanabhan, Sandosh, Mägi, Reedik, Stanton, Alice, Connell, John, Bakker, Stephan J L, Metspalu, Andres, Shields, Denis C, Thom, Simon, Brown, Morris, Sever, Peter, Esko, Tõnu, Hayward, Caroline, van der Harst, Pim, Saleheen, Danish, Chowdhury, Rajiv, Chambers, John C, Chasman, Daniel I, Chakravarti, Aravinda, Newton-Cheh, Christopher, Lindgren, Cecilia M, Levy, Daniel, Kooner, Jaspal S, Keavney, Bernard, Tomaszewski, Maciej, Samani, Nilesh J, Howson, Joanna M M, Tobin, Martin D, Munroe, Patricia B, Ehret, Georg B, Wain, Louise V, Barnes, Michael R, Tzoulaki, Ioanna, Caulfield, Mark J, Elliott, Paul
Publicado 2017

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

por Artigas, María Soler, Wain, Louise V., Miller, Suzanne, Kheirallah, Abdul Kader, Huffman, Jennifer E., Ntalla, Ioanna, Shrine, Nick, Obeidat, Ma'en, Trochet, Holly, McArdle, Wendy L., Alves, Alexessander Couto, Hui, Jennie, Zhao, Jing Hua, Joshi, Peter K., Teumer, Alexander, Albrecht, Eva, Imboden, Medea, Rawal, Rajesh, Lopez, Lorna M., Marten, Jonathan, Enroth, Stefan, Surakka, Ida, Polasek, Ozren, Lyytikäinen, Leo-Pekka, Granell, Raquel, Hysi, Pirro G., Flexeder, Claudia, Mahajan, Anubha, Beilby, John, Bossé, Yohan, Brandsma, Corry-Anke, Campbell, Harry, Gieger, Christian, Gläser, Sven, González, Juan R., Grallert, Harald, Hammond, Chris J., Harris, Sarah E., Hartikainen, Anna-Liisa, Heliövaara, Markku, Henderson, John, Hocking, Lynne, Horikoshi, Momoko, Hutri-Kähönen, Nina, Ingelsson, Erik, Johansson, Åsa, Kemp, John P., Kolcic, Ivana, Kumar, Ashish, Lind, Lars, Melén, Erik, Musk, Arthur W., Navarro, Pau, Nickle, David C., Padmanabhan, Sandosh, Raitakari, Olli T., Ried, Janina S., Ripatti, Samuli, Schulz, Holger, Scott, Robert A., Sin, Don D., Starr, John M., Viñuela, Ana, Völzke, Henry, Wild, Sarah H., Wright, Alan F., Zemunik, Tatijana, Jarvis, Deborah L., Spector, Tim D., Evans, David M., Lehtimäki, Terho, Vitart, Veronique, Kähönen, Mika, Gyllensten, Ulf, Rudan, Igor, Deary, Ian J., Karrasch, Stefan, Probst-Hensch, Nicole M., Heinrich, Joachim, Stubbe, Beate, Wilson, James F., Wareham, Nicholas J., James, Alan L., Morris, Andrew P., Jarvelin, Marjo-Riitta, Hayward, Caroline, Sayers, Ian, Strachan, David P., Hall, Ian P., Tobin, Martin D.
Publicado 2015