Long-term evolution of transposable elements

Por Le Rouzic, Arnaud, Boutin, Thibaud S., Capy, Pierre
Publicado em 2007

How does selfing affect the dynamics of selfish transposable elements?

Por Boutin, Thibaud S, Le Rouzic, Arnaud, Capy, Pierre
Publicado em 2012

The struggle for life of the genome's selfish architects

Por Hua-Van, Aurélie, Le Rouzic, Arnaud, Boutin, Thibaud S, Filée, Jonathan, Capy, Pierre
Publicado em 2011

Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants

Por Jiang, Xinyi, Dellepiane, Nefeli, Pairo-Castineira, Erola, Boutin, Thibaud, Kumar, Yatendra, Bickmore, Wendy A., Vitart, Veronique
Publicado no Commun Biol (2020)

Insights into the genetic basis of retinal detachment

Por Boutin, Thibaud S, Charteris, David G, Chandra, Aman, Campbell, Susan, Hayward, Caroline, Campbell, Archie, Nandakumar, Priyanka, Hinds, David, Mitry, Danny, Vitart, Veronique
Publicado no Hum Mol Genet (2020)

Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level

Por Matana, Antonela, Brdar, Dubravka, Torlak, Vesela, Boutin, Thibaud, Popović, Marijana, Gunjača, Ivana, Kolčić, Ivana, Boraska Perica, Vesna, Punda, Ante, Polašek, Ozren, Barbalić, Maja, Hayward, Caroline, Zemunik, Tatijana
Publicado no Mol Med (2018)

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

Por Kerr, Shona M., Klaric, Lucija, Halachev, Mihail, Hayward, Caroline, Boutin, Thibaud S., Meynert, Alison M., Semple, Colin A., Tuiskula, Annukka M., Swan, Heikki, Santoyo-Lopez, Javier, Vitart, Veronique, Haley, Chris, Dean, John, Miedzybrodzka, Zosia, Aitman, Timothy J., Wilson, James F.
Publicado no Sci Rep (2019)

Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

Por Bretherick, Andrew D., Canela-Xandri, Oriol, Joshi, Peter K., Clark, David W., Rawlik, Konrad, Boutin, Thibaud S., Zeng, Yanni, Amador, Carmen, Navarro, Pau, Rudan, Igor, Wright, Alan F., Campbell, Harry, Vitart, Veronique, Hayward, Caroline, Wilson, James F., Tenesa, Albert, Ponting, Chris P., Baillie, J. Kenneth, Haley, Chris
Publicado no PLoS Genet (2020)

Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank

Por Hall, Lynsey S., Adams, Mark J., Arnau-Soler, Aleix, Clarke, Toni-Kim, Howard, David M., Zeng, Yanni, Davies, Gail, Hagenaars, Saskia P., Maria Fernandez-Pujals, Ana, Gibson, Jude, Wigmore, Eleanor M., Boutin, Thibaud S., Hayward, Caroline, Scotland, Generation, Porteous, David J., Deary, Ian J., Thomson, Pippa A., Haley, Chris S., McIntosh, Andrew M.
Publicado no Transl Psychiatry (2018)

Characterisation of an inflammation-related epigenetic score and its association with cognitive ability

Por Stevenson, Anna J., McCartney, Daniel L., Hillary, Robert F., Campbell, Archie, Morris, Stewart W., Bermingham, Mairead L., Walker, Rosie M., Evans, Kathryn L., Boutin, Thibaud S., Hayward, Caroline, McRae, Allan F., McColl, Barry W., Spires-Jones, Tara L., McIntosh, Andrew M., Deary, Ian J., Marioni, Riccardo E.
Publicado no Clin Epigenetics (2020)

Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Por Zeng, Yanni, Amador, Carmen, Xia, Charley, Marioni, Riccardo, Sproul, Duncan, Walker, Rosie M., Morris, Stewart W., Bretherick, Andrew, Canela-Xandri, Oriol, Boutin, Thibaud S., Clark, David W., Campbell, Archie, Rawlik, Konrad, Hayward, Caroline, Nagy, Reka, Tenesa, Albert, Porteous, David J., Wilson, James F., Deary, Ian J., Evans, Kathryn L., McIntosh, Andrew M., Navarro, Pau, Haley, Chris S.
Publicado no Nat Commun (2019)

Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation

Por Zeng, Yanni, Amador, Carmen, Xia, Charley, Marioni, Riccardo, Sproul, Duncan, Walker, Rosie M., Morris, Stewart W., Bretherick, Andrew, Canela-Xandri, Oriol, Boutin, Thibaud S., Clark, David W., Campbell, Archie, Rawlik, Konrad, Hayward, Caroline, Nagy, Reka, Tenesa, Albert, Porteous, David J., Wilson, James F., Deary, Ian J., Evans, Kathryn L., McIntosh, Andrew M., Navarro, Pau, Haley, Chris S.
Publicado no Nat Commun (2019)

Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

Por Nagy, Reka, Boutin, Thibaud S., Marten, Jonathan, Huffman, Jennifer E., Kerr, Shona M., Campbell, Archie, Evenden, Louise, Gibson, Jude, Amador, Carmen, Howard, David M., Navarro, Pau, Morris, Andrew, Deary, Ian J., Hocking, Lynne J., Padmanabhan, Sandosh, Smith, Blair H., Joshi, Peter, Wilson, James F., Hastie, Nicholas D., Wright, Alan F., McIntosh, Andrew M., Porteous, David J., Haley, Chris S., Vitart, Veronique, Hayward, Caroline
Publicado no Genome Med (2017)

An epigenome-wide association study of sex-specific chronological ageing

Por McCartney, Daniel L., Zhang, Futao, Hillary, Robert F., Zhang, Qian, Stevenson, Anna J., Walker, Rosie M., Bermingham, Mairead L., Boutin, Thibaud, Morris, Stewart W., Campbell, Archie, Murray, Alison D., Whalley, Heather C., Porteous, David J., Hayward, Caroline, Evans, Kathryn L., Chandra, Tamir, Deary, Ian J., McIntosh, Andrew M., Yang, Jian, Visscher, Peter M., McRae, Allan F., Marioni, Riccardo E.
Publicado no Genome Med (2019)

Multi-trait genome-wide association study identifies new loci associated with optic disc parameters

Por Bonnemaijer, Pieter W. M., Leeuwen, Elisabeth M. van, Iglesias, Adriana I., Gharahkhani, Puya, Vitart, Veronique, Khawaja, Anthony P., Simcoe, Mark, Höhn, René, Cree, Angela J., Igo, Rob P., Gerhold-Ay, Aslihan, Nickels, Stefan, Wilson, James F., Hayward, Caroline, Boutin, Thibaud S., Polašek, Ozren, Aung, Tin, Khor, Chiea Chuen, Amin, Najaf, Lotery, Andrew J., Wiggs, Janey L., Cheng, Ching-Yu, Hysi, Pirro G., Hammond, Christopher J., Thiadens, Alberta A. H. J., MacGregor, Stuart, Klaver, Caroline C. W., Duijn, Cornelia M. van
Publicado no Commun Biol (2019)

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder

Por Zeng, Yanni, Navarro, Pau, Shirali, Masoud, Howard, David M., Adams, Mark J., Hall, Lynsey S., Clarke, Toni-Kim, Thomson, Pippa A., Smith, Blair H., Murray, Alison, Padmanabhan, Sandosh, Hayward, Caroline, Boutin, Thibaud, MacIntyre, Donald J., Lewis, Cathryn M., Wray, Naomi R., Mehta, Divya, Penninx, Brenda W.J.H., Milaneschi, Yuri, Baune, Bernhard T., Air, Tracy, Hottenga, Jouke-Jan, Mbarek, Hamdi, Castelao, Enrique, Pistis, Giorgio, Schulze, Thomas G., Streit, Fabian, Forstner, Andreas J., Byrne, Enda M., Martin, Nicholas G., Breen, Gerome, Müller-Myhsok, Bertram, Lucae, Susanne, Kloiber, Stefan, Domenici, Enrico, Deary, Ian J., Porteous, David J., Haley, Chris S., McIntosh, Andrew M.
Publicado no Biol Psychiatry (2017)

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Por 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
Publicado no Nat Commun (2018)

Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Por 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
Publicado no Nat Commun (2019)

Variants associated with HHIP expression have sex-differential effects on lung function

Por Fawcett, Katherine A., Obeidat, Ma'en, Melbourne, Carl, Shrine, Nick, Guyatt, Anna L., John, Catherine, Luan, Jian'an, Richmond, Anne, Moksnes, Marta R., Granell, Raquel, Weiss, Stefan, Imboden, Medea, May-Wilson, Sebastian, Hysi, Pirro, Boutin, Thibaud S., Portas, Laura, Flexeder, Claudia, Harris, Sarah E., Wang, Carol A., Lyytikäinen, Leo-Pekka, Palviainen, Teemu, Foong, Rachel E., Keidel, Dirk, Minelli, Cosetta, Langenberg, Claudia, Bossé, Yohan, Van den Berge, Maarten, Sin, Don D., Hao, Ke, Campbell, Archie, Porteous, David, Padmanabhan, Sandosh, Smith, Blair H., Evans, David M., Ring, Sue, Langhammer, Arnulf, Hveem, Kristian, Willer, Cristen, Ewert, Ralf, Stubbe, Beate, Pirastu, Nicola, Klaric, Lucija, Joshi, Peter K., Patasova, Karina, Massimo, Mangino, Polasek, Ozren, Starr, John M., Karrasch, Stefan, Strauch, Konstantin, Meitinger, Thomas, Rudan, Igor, Rantanen, Taina, Pietiläinen, Kirsi, Kähönen, Mika, Raitakari, Olli T., Hall, Graham L., Sly, Peter D., Pennell, Craig E., Kaprio, Jaakko, Lehtimäki, Terho, Vitart, Veronique, Deary, Ian J., Jarvis, Debbie, Wilson, James F., Spector, Tim, Probst-Hensch, Nicole, Wareham, Nicholas J., Völzke, Henry, Henderson, John, Strachan, David P., Brumpton, Ben M., Hayward, Caroline, Hall, Ian P., Tobin, Martin D., Wain, Louise V.
Publicado no Wellcome Open Res (2021)

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

Por Folkersen, Lasse, Gustafsson, Stefan, Wang, Qin, Hansen, Daniel Hvidberg, Hedman, Åsa K, Schork, Andrew, Page, Karen, Zhernakova, Daria V, Wu, Yang, Peters, James, Eriksson, Niclas, Bergen, Sarah E, Boutin, Thibaud, Bretherick, Andrew D, Enroth, Stefan, Kalnapenkis, Anette, Gådin, Jesper R, Suur, Bianca, Chen, Yan, Matic, Ljubica, Gale, Jeremy D, Lee, Julie, Zhang, Weidong, Quazi, Amira, Ala-Korpela, Mika, Choi, Seung Hoan, Claringbould, Annique, Danesh, John, Davey-Smith, George, de Masi, Federico, Elmståhl, Sölve, Engström, Gunnar, Fauman, Eric, Fernandez, Celine, Franke, Lude, Franks, Paul, Giedraitis, Vilmantas, Haley, Chris, Hamsten, Anders, Ingason, Andres, Johansson, Åsa, Joshi, Peter K, Lind, Lars, Lindgren, Cecilia M., Lubitz, Steven, Palmer, Tom, Macdonald-Dunlop, Erin, Magnusson, Martin, Melander, Olle, Michaelsson, Karl, Morris, Andrew P., Mägi, Reedik, Nagle, Michael W, Nilsson, Peter M, Nilsson, Jan, Orho-Melander, Marju, Polasek, Ozren, Prins, Bram, Pålsson, Erik, Qi, Ting, Sjögren, Marketa, Sundström, Johan, Surendran, Praveen, Võsa, Urmo, Werge, Thomas, Wernersson, Rasmus, Westra, Harm-Jan, Yang, Jian, Zhernakova, Alexandra, Ärnlöv, Johan, Fu, Jingyuan, Smith, Gustav, Esko, Tonu, Hayward, Caroline, Gyllensten, Ulf, Landen, Mikael, Siegbahn, Agneta, Wilson, Jim F, Wallentin, Lars, Butterworth, Adam S, Holmes, Michael V, Ingelsson, Erik, Mälarstig, Anders
Publicado no Nat Metab (2020)