Resolving the Effects of Maternal and Offspring Genotype on Dyadic Outcomes in Genome Wide Complex Trait Analysis (“M-GCTA”)

di Eaves, Lindon J., Pourcain, Beate St., Smith, George Davey, York, Timothy P., Evans, David M.
Pubblicazione 2014

Prenatal methylmercury exposure and genetic predisposition to cognitive deficit at age 8 years

di Julvez, Jordi, Smith, George Davey, Golding, Jean, Ring, Susan, Pourcain, Beate St., Gonzalez, Juan Ramon, Grandjean, Philippe
Pubblicato in Epidemiology (2013)

Time Outdoors and Physical Activity as Predictors of Incident Myopia in Childhood: A Prospective Cohort Study

di Guggenheim, Jeremy A., Northstone, Kate, McMahon, George, Ness, Andy R., Deere, Kevin, Mattocks, Calum, Pourcain, Beate St, Williams, Cathy
Pubblicazione 2012

Genetic Overlap Between Schizophrenia and Developmental Psychopathology: Longitudinal and Multivariate Polygenic Risk Prediction of Common Psychiatric Traits During Development

di Nivard, Michel G, Gage, Suzanne H, Hottenga, Jouke J, van Beijsterveldt, Catharina E M, Abdellaoui, Abdel, Bartels, Meike, Baselmans, Bart M L, Ligthart, Lannie, Pourcain, Beate St, Boomsma, Dorret I, Munafò, Marcus R, Middeldorp, Christel M
Pubblicato in Schizophr Bull (2017)

Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence

di Pourcain, Beate St, Haworth, C. M. A., Davis, O. S. P., Wang, Kai, Timpson, Nicholas J., Evans, David M., Kemp, John P., Ronald, Angelica, Price, Tom, Meaburn, Emma, Ring, Susan M., Golding, Jean, Hakonarson, Hakon, Plomin, R., Smith, George Davey
Pubblicato in Hum Genet (2016)

Vitamin B-12 Status during Pregnancy and Child’s IQ at Age 8: A Mendelian Randomization Study in the Avon Longitudinal Study of Parents and Children

di Bonilla, Carolina, Lawlor, Debbie A., Taylor, Amy E., Gunnell, David J., Ben–Shlomo, Yoav, Ness, Andrew R., Timpson, Nicholas J., Pourcain, Beate St, Ring, Susan M., Emmett, Pauline M., Smith, A. David, Refsum, Helga, Pennell, Craig E., Brion, Marie-Jo, Smith, George Davey, Lewis, Sarah J.
Pubblicazione 2012

Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate

di Howe, Laurence J, Richardson, Tom G, Arathimos, Ryan, Alvizi, Lucas, Passos-Bueno, Maria R, Stanier, Philip, Nohr, Ellen, Ludwig, Kerstin U, Mangold, Elisabeth, Knapp, Michael, Stergiakouli, Evie, Pourcain, Beate St, Smith, George Davey, Sandy, Jonathan, Relton, Caroline L, Lewis, Sarah J, Hemani, Gibran, Sharp, Gemma C
Pubblicato in Epigenomics (2019)

A genome-wide association study of body mass index across early life and childhood

di Warrington, Nicole M, Howe, Laura D, Paternoster, Lavinia, Kaakinen, Marika, Herrala, Sauli, Huikari, Ville, Wu, Yan Yan, Kemp, John P, Timpson, Nicholas J, Pourcain, Beate St, Davey Smith, George, Tilling, Kate, Jarvelin, Marjo-Riitta, Pennell, Craig E, Evans, David M, Lawlor, Debbie A, Briollais, Laurent, Palmer, Lyle J
Pubblicato in Int J Epidemiol (2015)

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation...

di Zheng, Jie, Erzurumluoglu, A Mesut, Elsworth, Benjamin L, Kemp, John P, Howe, Laurence, Haycock, Philip C, Hemani, Gibran, Tansey, Katherine, Laurin, Charles, Pourcain, Beate St, Warrington, Nicole M, Finucane, Hilary K, Price, Alkes L, Bulik-Sullivan, Brendan K, Anttila, Verneri, Paternoster, Lavinia, Gaunt, Tom R, Evans, David M, Neale, Benjamin M
Pubblicato in Bioinformatics (2017)

Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity

di Gunz, Philipp, Tilot, Amanda K., Wittfeld, Katharina, Teumer, Alexander, Shapland, Chin Yang, van Erp, Theo G.M., Dannemann, Michael, Vernot, Benjamin, Neubauer, Simon, Guadalupe, Tulio, Fernández, Guillén, Brunner, Han G., Enard, Wolfgang, Fallon, James, Hosten, Norbert, Völker, Uwe, Profico, Antonio, Vincenzo, Fabio Di, Manzi, Giorgio, Kelso, Janet, Pourcain, Beate St., Hublin, Jean-Jacques, Franke, Barbara, Pääbo, Svante, Macciardi, Fabio, Grabe, Hans J., Fisher, Simon E.
Pubblicato in Curr Biol (2018)

Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

di Fan, Qiao, Guo, Xiaobo, Tideman, J. Willem L., Williams, Katie M., Yazar, Seyhan, Hosseini, S. Mohsen, Howe, Laura D., Pourcain, Beaté St, Evans, David M., Timpson, Nicholas J., McMahon, George, Hysi, Pirro G., Krapohl, Eva, Wang, Ya Xing, Jonas, Jost B., Baird, Paul Nigel, Wang, Jie Jin, Cheng, Ching-Yu, Teo, Yik-Ying, Wong, Tien-Yin, Ding, Xiaohu, Wojciechowski, Robert, Young, Terri L., Pärssinen, Olavi, Oexle, Konrad, Pfeiffer, Norbert, Bailey-Wilson, Joan E., Paterson, Andrew D., Klaver, Caroline C. W., Plomin, Robert, Hammond, Christopher J., Mackey, David A., He, Mingguang, Saw, Seang-Mei, Williams, Cathy, Guggenheim, Jeremy A.
Pubblicato in Sci Rep (2016)

A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Paediatric Cohorts

di Middeldorp, Christel M., Hammerschlag, Anke R., Ouwens, Klaasjan G., Groen-Blokhuis, Maria M., Pourcain, Beate St., Greven, Corina U., Pappa, Irene, Tiesler, Carla M.T., Ang, Wei, Nolte, Ilja M., Vilor-Tejedor, Natalia, Bacelis, Jonas, Ebejer, Jane L., Zhao, Huiying, Davies, Gareth E., Ehli, Erik A., Evans, David M., Fedko, Iryna O., Guxens, Mònica, Hottenga, Jouke-Jan, Hudziak, James J., Jugessur, Astanand, Kemp, John P., Krapohl, Eva, Martin, Nicholas G., Murcia, Mario, Myhre, Ronny, Ormel, Johan, Ring, Susan M., Standl, Marie, Stergiakouli, Evie, Stoltenberg, Camilla, Thiering, Elisabeth, Timpson, Nicholas J., Trzaskowski, Maciej, van der Most, Peter J., Wang, Carol, Nyholt, Dale R., Medland, Sarah E., Neale, Benjamin, Jacobsson, Bo, Sunyer, Jordi, Hartman, Catharina A., Whitehouse, Andrew J.O., Pennell, Craig E., Heinrich, Joachim, Plomin, Robert, Smith, George Davey, Tiemeier, Henning, Posthuma, Danielle, Boomsma, Dorret I.
Pubblicato in J Am Acad Child Adolesc Psychiatry (2016)

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

di 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
Pubblicazione 2012

Common variants at 12q15 and 12q24 are associated with infant head circumference

di Taal, H Rob, Pourcain, Beate St, Thiering, Elisabeth, Das, Shikta, Mook-Kanamori, Dennis O, Warrington, Nicole M, Kaakinen, Marika, Kreiner-Møller, Eskil, Bradfield, Jonathan P, Freathy, Rachel M, Geller, Frank, Guxens, Mònica, Cousminer, Diana L, Kerkhof, Marjan, Timpson, Nicholas J, Ikram, M Arfan, Beilin, Lawrence J, Bønnelykke, Klaus, Buxton, Jessica L, Charoen, Pimphen, Chawes, Bo Lund Krogsgaard, Eriksson, Johan, Evans, David M, Hofman, Albert, Kemp, John P, Kim, Cecilia E, Klopp, Norman, Lahti, Jari, Lye, Stephen J, McMahon, George, Mentch, Frank D, Müller, Martina, O’Reilly, Paul F, Prokopenko, Inga, Rivadeneira, Fernando, Steegers, Eric A P, Sunyer, Jordi, Tiesler, Carla, Yaghootkar, Hanieh, Breteler, Monique M B, Debette, Stephanie, Fornage, Myriam, Gudnason, Vilmundur, Launer, Lenore J, van der Lugt, Aad, Mosley, Thomas H, Seshadri, Sudha, Smith, Albert V, Vernooij, Meike W, Blakemore, Alexandra IF, Chiavacci, Rosetta M, Feenstra, Bjarke, Fernandez-Benet, Julio, Grant, Struan F A, Hartikainen, Anna-Liisa, van der Heijden, Albert J, Iñiguez, Carmen, Lathrop, Mark, McArdle, Wendy L, Mølgaard, Anne, Newnham, John P, Palmer, Lyle J, Palotie, Aarno, Pouta, Annneli, Ring, Susan M, Sovio, Ulla, Standl, Marie, Uitterlinden, Andre G, Wichmann, H-Erich, Vissing, Nadja Hawwa, DeCarli, Charles, van Duijn, Cornelia M, McCarthy, Mark I, Koppelman, Gerard H., Estivill, Xavier, Hattersley, Andrew T, Melbye, Mads, Bisgaard, Hans, Pennell, Craig E, Widen, Elisabeth, Hakonarson, Hakon, Smith, George Davey, Heinrich, Joachim, Jarvelin, Marjo-Riitta, Jaddoe, Vincent W V
Pubblicazione 2012

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

di Verhoeven, Virginie J. M., Hysi, Pirro G., Saw, Seang-Mei, Vitart, Veronique, Mirshahi, Alireza, Guggenheim, Jeremy A., Cotch, Mary Frances, Yamashiro, Kenji, Baird, Paul N., Mackey, David A., Wojciechowski, Robert, Ikram, M. Kamran, Hewitt, Alex W., Duggal, Priya, Janmahasatian, Sarayut, Khor, Chiea-Chuen, Fan, Qiao, Zhou, Xin, Young, Terri L., Tai, E-Shyong, Goh, Liang-Kee, Li, Yi-Ju, Aung, Tin, Vithana, Eranga, Teo, Yik-Ying, Tay, Wanting, Sim, Xueling, Rudan, Igor, Hayward, Caroline, Wright, Alan F., Polasek, Ozren, Campbell, Harry, Wilson, James F., Fleck, Brian W., Nakata, Isao, Yoshimura, Nagahisa, Yamada, Ryo, Matsuda, Fumihiko, Ohno-Matsui, Kyoko, Nag, Abhishek, McMahon, George, Pourcain, Beate St., Lu, Yi, Rahi, Jugnoo S., Cumberland, Phillippa M., Bhattacharya, Shomi, Simpson, Claire L., Atwood, Larry D., Li, Xiaohui, Raffel, Leslie J., Murgia, Federico, Portas, Laura, Despriet, Dominiek D. G., van Koolwijk, Leonieke M. E., Wolfram, Christian, Lackner, Karl J., Tönjes, Anke, Mägi, Reedik, Lehtimäki, Terho, Kähönen, Mika, Esko, Tõnu, Metspalu, Andres, Rantanen, Taina, Pärssinen, Olavi, Klein, Barbara E., Meitinger, Thomas, Spector, Timothy D., Oostra, Ben A., Smith, Albert V., de Jong, Paulus T. V. M., Hofman, Albert, Amin, Najaf, Karssen, Lennart C., Rivadeneira, Fernando, Vingerling, Johannes R., Eiríksdóttir, Guðný, Gudnason, Vilmundur, Döring, Angela, Bettecken, Thomas, Uitterlinden, André G., Williams, Cathy, Zeller, Tanja, Castagné, Raphaële, Oexle, Konrad, van Duijn, Cornelia M., Iyengar, Sudha K., Mitchell, Paul, Wang, Jie Jin, Höhn, René, Pfeiffer, Norbert, Bailey-Wilson, Joan E., Stambolian, Dwight, Wong, Tien-Yin, Hammond, Christopher J., Klaver, Caroline C. W.
Pubblicazione 2012

META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS

di Paternoster, Lavinia, Standl, Marie, Chen, Chih-Mei, Ramasamy, Adaikalavan, Bønnelykke, Klaus, Duijts, Liesbeth, Ferreira, Manuel A, Alves, Alexessander Couto, Thyssen, Jacob P, Albrecht, Eva, Baurecht, Hansjörg, Feenstra, Bjarke, Sleiman, Patrick MA, Hysi, Pirro, Warrington, Nicole M, Curjuric, Ivan, Myhre, Ronny, Curtin, John A, Groen-Blokhuis, Maria M, Kerkhof, Marjan, Sääf, Annika, Franke, Andre, Ellinghaus, David, Fölster-Holst, Regina, Dermitzakis, Emmanouil, Montgomery, Stephen B, Prokisch, Holger, Heim, Katharina, Hartikainen, Anna-Liisa, Pouta, Anneli, Pekkanen, Juha, Blakemore, Alexandra IF, Buxton, Jessica L, Kaakinen, Marika, Duffy, David L, Madden, Pamela A, Heath, Andrew C, Montgomery, Grant W, Thompson, Philip J, Matheson, Melanie C, Le Souëf, Peter, Pourcain, Beate St, Smith, George Davey, Henderson, John, Kemp, John P, Timpson, Nicholas J, Deloukas, Panos, Ring, Susan M, Wichmann, H-Erich, Müller-Nurasyid, Martina, Novak, Natalija, Klopp, Norman, Rodríguez, Elke, McArdle, Wendy, Linneberg, Allan, Menné, Torkil, Nohr, Ellen A, Hofman, Albert, Uitterlinden, André G, van Duijn, Cornélia M, Rivadeneira, Fernando, de Jongste, Johan C, van der Valk, Ralf JP, Wjst, Matthias, Jogi, Rain, Geller, Frank, Boyd, Heather A, Murray, Jeffrey C, Kim, Cecilia, Mentch, Frank, March, Michael, Mangino, Massimo, Spector, Tim D, Bataille, Veronique, Pennell, Craig E, Holt, Patrick G, Sly, Peter, Tiesler, Carla MT, Thiering, Elisabeth, Illig, Thomas, Imboden, Medea, Nystad, Wenche, Simpson, Angela, Hottenga, Jouke-Jan, Postma, Dirkje, Koppelman, Gerard H, Smit, Henriette A, Söderhäll, Cilla, Chawes, Bo, Kreiner-Møller, Eskil, Bisgaard, Hans, Melén, Erik, Boomsma, Dorret I, Custovic, Adnan, Jacobsson, Bo, Probst-Hensch, Nicole M, Palmer, Lyle J, Glass, Daniel, Hakonarson, Hakon, Melbye, Mads, Jarvis, Deborah L, Jaddoe, Vincent WV, Gieger, Christian, Strachan, David P, Martin, Nicholas G, Jarvelin, Marjo-Riitta, Heinrich, Joachim, Evans, David M, Weidinger, Stephan
Pubblicazione 2011

Genome-wide association study identifies novel locus for neuroticism and shows polygenic association with Major Depressive Disorder

di de Moor, Marleen H.M., van den Berg, Stéphanie M., Verweij, Karin J.H., Krueger, Robert F., Luciano, Michelle, Vasquez, Alejandro Arias, Matteson, Lindsay K., Derringer, Jaime, Esko, Tõnu, Amin, Najaf, Gordon, Scott D., Hansell, Narelle K., Hart, Amy B., Seppälä, Ilkka, Huffman, Jennifer E., Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abecasis, Goncalo R., Adkins, Daniel E., Agrawal, Arpana, Allik, Jüri, Appel, Katja, Bigdeli, Timothy B., Busonero, Fabio, Campbell, Harry, Costa, Paul T., Smith, George Davey, Davies, Gail, de Wit, Harriet, Ding, Jun, Engelhardt, Barbara E., Eriksson, Johan G., Fedko, Iryna O., Ferrucci, Luigi, Franke, Barbara, Giegling, Ina, Grucza, Richard, Hartmann, Annette M., Heath, Andrew C., Heinonen, Kati, Henders, Anjali K., Homuth, Georg, Hottenga, Jouke-Jan, Janzing, Joost, Jokela, Markus, Karlsson, Robert, Kemp, John P., Kirkpatrick, Matthew G., Latvala, Antti, Lehtimäki, Terho, Liewald, David C., Madden, Pamela A.F., Magri, Chiara, Magnusson, Patrik K.E., Marten, Jonathan, Maschio, Andrea, Medland, Sarah E., Mihailov, Evelin, Milaneschi, Yuri, Montgomery, Grant W., Nauck, Matthias, Ouwens, Klaasjan G., Palotie, Aarno, Pettersson, Erik, Polasek, Ozren, Qian, Yong, Pulkki-Råback, Laura, Raitakari, Olli T., Realo, Anu, Rose, Richard J., Ruggiero, Daniela, Schmidt, Carsten O., Slutske, Wendy S., Sorice, Rossella, Starr, John M., Pourcain, Beate St, Sutin, Angelina R., Timpson, Nicholas J., Trochet, Holly, Vermeulen, Sita, Vuoksimaa, Eero, Widen, Elisabeth, Wouda, Jasper, Wright, Margaret J., Zgaga, Lina, Scotland, Generation, Porteous, David, Minelli, Alessandra, Palmer, Abraham A., Rujescu, Dan, Ciullo, Marina, Hayward, Caroline, Rudan, Igor, Metspalu, Andres, Kaprio, Jaakko, Deary, Ian J., Räikkönen, Katri, Wilson, James F., Keltikangas-Järvinen, Liisa, Bierut, Laura J., Hettema, John M., Grabe, Hans J., van Duijn, Cornelia M., Evans, David M., Schlessinger, David, Pedersen, Nancy L., Terracciano, Antonio, McGue, Matt, Penninx, Brenda W.J.H., Martin, Nicholas G., Boomsma, Dorret I.
Pubblicato in JAMA Psychiatry (2015)

Genome-wide association study identifies 48 common genetic variants associated with handedness

di Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., Boyd, Heather A., Breteler, Monique M. B., Campbell, Harry, Chasman, Daniel I., Cherkas, Lynn F., Davies, Gail, de Geus, Eco J. C., Deary, Ian J., Deloukas, Panos, Dick, Danielle M., Duffy, David L., Eriksson, Johan G., Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D., Han, Jiali, Hansen, Thomas F., Hartmann, Annette M., Hayward, Caroline, Heikkilä, Kauko, Hicks, Andrew A., Hirschhorn, Joel N., Hottenga, Jouke-Jan, Huffman, Jennifer E., Hwang, Liang-Dar, Ikram, M. Arfan, Kaprio, Jaakko, Kemp, John P., Khaw, Kay-Tee, Klopp, Norman, Konte, Bettina, Kutalik, Zoltan, Lahti, Jari, Li, Xin, Loos, Ruth J. F., Luciano, Michelle, Magnusson, Sigurdur H., Mangino, Massimo, Marques-Vidal, Pedro, Martin, Nicholas G., McArdle, Wendy L., McCarthy, Mark l., Medina-Gomez, Carolina, Melbye, Mads, Melville, Scott A., Metspalu, Andres, Milani, Lili, Mooser, Vincent, Nelis, Mari, Nyholt, Dale R., O’Connell, Kevin S., Ophoff, Roel A., Palmer, Cameron, Palotie, Aarno, Palviainen, Teemu, Pare, Guillaume, Paternoster, Lavinia, Peltonen, Leena, Penninx, Brenda W. J. H., Polasek, Ozren, Pramstaller, Peter P., Prokopenko, Inga, Raikkonen, Katri, Ripatti, Samuli, Rivadeneira, Fernando, Rudan, Igor, Rujescu, Dan, Smit, Johannes H., Smith, George Davey, Smoller, Jordan W., Soranzo, Nicole, Spector, Tim D., Pourcain, Beate St, Starr, John M., Stefánsson, Hreinn, Steinberg, Stacy, Teder-Laving, Maris, Thorleifsson, Gudmar, Stefánsson, Kári, Timpson, Nicholas J., Uitterlinden, André G., van Duijn, Cornelia M., van Rooij, Frank J. A., Vink, Jaqueline M., Vollenweider, Peter, Vuoksimaa, Eero, Waeber, Gérard, Wareham, Nicholas J., Warrington, Nicole, Waterworth, Dawn, Werge, Thomas, Wichmann, H.-Erich, Widen, Elisabeth, Willemsen, Gonneke, Wright, Alan F., Wright, Margaret J., Xu, Mousheng, Zhao, Jing Hua, Kraft, Peter, Hinds, David A., Lindgren, Cecilia M., Mägi, Reedik, Neale, Benjamin M., Evans, David M., Medland, Sarah E.
Pubblicato in Nat Hum Behav (2021)

Genome-wide association study of circulating interleukin 6 levels identifies novel loci

di Ahluwalia, Tarunveer S, Prins, Bram P, Abdollahi, Mohammadreza, Armstrong, Nicola J, Aslibekyan, Stella, Bain, Lisa, Jefferis, Barbara, Baumert, Jens, Beekman, Marian, Ben-Shlomo, Yoav, Bis, Joshua C, Mitchell, Braxton D, de Geus, Eco, Delgado, Graciela E, Marek, Diana, Eriksson, Joel, Kajantie, Eero, Kanoni, Stavroula, Kemp, John P, Lu, Chen, Marioni, Riccardo E, McLachlan, Stela, Milaneschi, Yuri, Nolte, Ilja M, Petrelis, Alexandros M, Porcu, Eleonora, Sabater-Lleal, Maria, Naderi, Elnaz, Seppälä, Ilkka, Shah, Tina, Singhal, Gaurav, Standl, Marie, Teumer, Alexander, Thalamuthu, Anbupalam, Thiering, Elisabeth, Trompet, Stella, Ballantyne, Christie M, Benjamin, Emelia J, Casas, Juan P, Toben, Catherine, Dedoussis, George, Deelen, Joris, Durda, Peter, Engmann, Jorgen, Feitosa, Mary F, Grallert, Harald, Hammarstedt, Ann, Harris, Sarah E, Homuth, Georg, Hottenga, Jouke-Jan, Jalkanen, Sirpa, Jamshidi, Yalda, Jawahar, Magdalene C, Jess, Tine, Kivimaki, Mika, Kleber, Marcus E, Lahti, Jari, Liu, Yongmei, Marques-Vidal, Pedro, Mellström, Dan, Mooijaart, Simon P, Müller-Nurasyid, Martina, Penninx, Brenda, Revez, Joana A, Rossing, Peter, Räikkönen, Katri, Sattar, Naveed, Scharnagl, Hubert, Sennblad, Bengt, Silveira, Angela, Pourcain, Beate St, Timpson, Nicholas J, Trollor, Julian, van Dongen, Jenny, Van Heemst, Diana, Visvikis-Siest, Sophie, Vollenweider, Peter, Völker, Uwe, Waldenberger, Melanie, Willemsen, Gonneke, Zabaneh, Delilah, Morris, Richard W, Arnett, Donna K, Baune, Bernhard T, Boomsma, Dorret I, Chang, Yen-Pei C, Deary, Ian J, Deloukas, Panos, Eriksson, Johan G, Evans, David M, Ferreira, Manuel A, Gaunt, Tom, Gudnason, Vilmundur, Hamsten, Anders, Heinrich, Joachim, Hingorani, Aroon, Humphries, Steve E, Jukema, J Wouter, Koenig, Wolfgang, Kumari, Meena, Kutalik, Zoltan, Lawlor, Deborah A, Lehtimäki, Terho, März, Winfried, Mather, Karen A, Naitza, Silvia, Nauck, Matthias, Ohlsson, Claes, Price, Jackie F, Raitakari, Olli, Rice, Ken, Sachdev, Perminder S, Slagboom, Eline, Sørensen, Thorkild I A, Spector, Tim, Stacey, David, Stathopoulou, Maria G, Tanaka, Toshiko, Wannamethee, S Goya, Whincup, Peter, Rotter, Jerome I, Dehghan, Abbas, Boerwinkle, Eric, Psaty, Bruce M, Snieder, Harold, Alizadeh, Behrooz Z
Pubblicato in Hum Mol Genet (2021)

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

di Scott, Robert A, Lagou, Vasiliki, Welch, Ryan P, Wheeler, Eleanor, Montasser, May E, Luan, Jian’an, Mägi, Reedik, Strawbridge, Rona J, Rehnberg, Emil, Gustafsson, Stefan, Kanoni, Stavroula, Rasmussen-Torvik, Laura J, Yengo, Loïc, Lecoeur, Cecile, Shungin, Dmitry, Sanna, Serena, Sidore, Carlo, Johnson, Paul C D, Jukema, J Wouter, Johnson, Toby, Mahajan, Anubha, Verweij, Niek, Thorleifsson, Gudmar, Hottenga, Jouke-Jan, Shah, Sonia, Smith, Albert V, Sennblad, Bengt, Gieger, Christian, Salo, Perttu, Perola, Markus, Timpson, Nicholas J, Evans, David M, Pourcain, Beate St, Wu, Ying, Andrews, Jeanette S, Hui, Jennie, Bielak, Lawrence F, Zhao, Wei, Horikoshi, Momoko, Navarro, Pau, Isaacs, Aaron, O’Connell, Jeffrey R, Stirrups, Kathleen, Vitart, Veronique, Hayward, Caroline, Esko, Tönu, Mihailov, Evelin, Fraser, Ross M, Fall, Tove, Voight, Benjamin F, Raychaudhuri, Soumya, Chen, Han, Lindgren, Cecilia M, Morris, Andrew P, Rayner, Nigel W, Robertson, Neil, Rybin, Denis, Liu, Ching-Ti, Beckmann, Jacques S, Willems, Sara M, Chines, Peter S, Jackson, Anne U, Kang, Hyun Min, Stringham, Heather M, Song, Kijoung, Tanaka, Toshiko, Peden, John F, Goel, Anuj, Hicks, Andrew A, An, Ping, Müller-Nurasyid, Martina, Franco-Cereceda, Anders, Folkersen, Lasse, Marullo, Letizia, Jansen, Hanneke, Oldehinkel, Albertine J, Bruinenberg, Marcel, Pankow, James S, North, Kari E, Forouhi, Nita G, Loos, Ruth J F, Edkins, Sarah, Varga, Tibor V, Hallmans, Göran, Oksa, Heikki, Antonella, Mulas, Nagaraja, Ramaiah, Trompet, Stella, Ford, Ian, Bakker, Stephan J L, Kong, Augustine, Kumari, Meena, Gigante, Bruna, Herder, Christian, Munroe, Patricia B, Caulfield, Mark, Antti, Jula, Mangino, Massimo, Small, Kerrin, Miljkovic, Iva, Liu, Yongmei, Atalay, Mustafa, Kiess, Wieland, James, Alan L, Rivadeneira, Fernando, Uitterlinden, Andre G, Palmer, Colin N A, Doney, Alex S F, Willemsen, Gonneke, Smit, Johannes H, Campbell, Susan, Polasek, Ozren, Bonnycastle, Lori L, Hercberg, Serge, Dimitriou, Maria, Bolton, Jennifer L, Fowkes, Gerard R, Kovacs, Peter, Lindström, Jaana, Zemunik, Tatijana, Bandinelli, Stefania, Wild, Sarah H, Basart, Hanneke V, Rathmann, Wolfgang, Grallert, Harald, Maerz, Winfried, Kleber, Marcus E, Boehm, Bernhard O, Peters, Annette, Pramstaller, Peter P, Province, Michael A, Borecki, Ingrid B, Hastie, Nicholas D, Rudan, Igor, Campbell, Harry, Watkins, Hugh, Farrall, Martin, Stumvoll, Michael, Ferrucci, Luigi, Waterworth, Dawn M, Bergman, Richard N, Collins, Francis S, Tuomilehto, Jaakko, Watanabe, Richard M, de Geus, Eco J C, Penninx, Brenda W, Hofman, Albert, Oostra, Ben A, Psaty, Bruce M, Vollenweider, Peter, Wilson, James F, Wright, Alan F, Hovingh, G Kees, Metspalu, Andres, Uusitupa, Matti, Magnusson, Patrik K E, Kyvik, Kirsten O, Kaprio, Jaakko, Price, Jackie F, Dedoussis, George V, Deloukas, Panos, Meneton, Pierre, Lind, Lars, Boehnke, Michael, Shuldiner, Alan R, van Duijn, Cornelia M, Morris, Andrew D, Toenjes, Anke, Peyser, Patricia A, Beilby, John P, Körner, Antje, Kuusisto, Johanna, Laakso, Markku, Bornstein, Stefan R, Schwarz, Peter E H, Lakka, Timo A, Rauramaa, Rainer, Adair, Linda S, Smith, George Davey, Spector, Tim D, Illig, Thomas, de Faire, Ulf, Hamsten, Anders, Gudnason, Vilmundur, Kivimaki, Mika, Hingorani, Aroon, Keinanen-Kiukaanniemi, Sirkka M, Saaristo, Timo E, Boomsma, Dorret I, Stefansson, Kari, van der Harst, Pim, Dupuis, Josée, Pedersen, Nancy L, Sattar, Naveed, Harris, Tamara B, Cucca, Francesco, Ripatti, Samuli, Salomaa, Veikko, Mohlke, Karen L, Balkau, Beverley, Froguel, Philippe, Pouta, Anneli, Jarvelin, Marjo-Riitta, Wareham, Nicholas J, Bouatia-Naji, Nabila, McCarthy, Mark I, Franks, Paul W, Meigs, James B, Teslovich, Tanya M, Florez, Jose C, Langenberg, Claudia, Ingelsson, Erik, Prokopenko, Inga, Barroso, Inês
Pubblicazione 2012