The nature of nurture: Effects of parental genotypes by Kong, Augustine, Thorleifsson, Gudmar, Frigge, Michael L, Vilhjalmsson, Bjarni J, Young, Alexander I, Thorgeirsson, Thorgeir E, Benonisdottir, Stefania, Oddsson, Asmundur, Halldorsson, Bjarni V, Masson, Gisli, Gudbjartsson, Daniel F, Helgason, Agnar, Bjornsdottir, Gyda, Thorsteinsdottir, Unnur, Stefansson, Kari

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Sequence variants at CYP1A1―CYP1A2 and AHR associate with coffee consumption by SULEM, Patrick, GUDBJARTSSON, Daniel F, MÄGI, Reedik, YANEK, Lisa R, BECKER, Lewis C, BOYD, Heather A, STACEY, Simon N, WALTERS, G. Bragi, JONASDOTTIR, Adalbjorg, THORLEIFSSON, Gudmar, HOLM, Hilma, GUDJONSSON, Sigurjon A, GELLER, Frank, RAFNAR, Thorunn, BJÖRNSDOTTIR, Gyda, BECKER, Diane M, MELBYE, Mads, KONG, Augustine, TÖNJES, Anke, THORGEIRSSON, Thorgeir, THORSTEINSDOTTIR, Unnur, KIEMENEY, Lambertus A, STEFANSSON, Kari, PROKOPENKO, Inga, FEENSTRA, Bjarke, ABEN, Katja K. H, FRANKE, Barbara, DEN HEIJER, Martin, KOVACS, Peter, STUMVOLLL, Michael

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CNVs conferring risk of autism or schizophrenia affect cognition in controls by Stefansson, Hreinn, Meyer-Lindenberg, Andreas, Steinberg, Stacy, Magnusdottir, Brynja, Morgen, Katrin, Arnarsdottir, Sunna, Bjornsdottir, Gyda, Walters, G. Bragi, Jonsdottir, Gudrun A., Doyle, Orla M., Tost, Heike, Grimm, Oliver, Kristjansdottir, Solveig, Snorrason, Heimir, Davidsdottir, Solveig R., Gudmundsson, Larus J., Jonsson, Gudbjorn F., Stefansdottir, Berglind, Helgadottir, Isafold, Haraldsson, Magnus, Jonsdottir, Birna, Thygesen, Johan H., Schwarz, Adam J., Didriksen, Michael, Stensbøl, Tine B., Brammer, Michael, Kapur, Shitij, Halldorsson, Jonas G., Hreidarsson, Stefan, Saemundsen, Evald, Sigurdsson, Engilbert, Stefansson, Kari

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A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline by Jonsson, Thorlakur, Atwal, Jasvinder K., Steinberg, Stacy, Snaedal, Jon, Jonsson, Palmi V., Bjornsson, Sigurbjorn, Stefansson, Hreinn, Sulem, Patrick, Gudbjartsson, Daniel, Maloney, Janice, Hoyte, Kwame, Gustafson, Amy, Liu, Yichin, Lu, Yanmei, Bhangale, Tushar, Graham, Robert R., Huttenlocher, Johanna, Bjornsdottir, Gyda, Andreassen, Ole A., Jönsson, Erik G., Palotie, Aarno, Behrens, Timothy W., Magnusson, Olafur T., Kong, Augustine, Thorsteinsdottir, Unnur, Watts, Ryan J., Stefansson, Kari

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Genetics of gene expression and its effect on disease by Schadt, Eric E, Stefansson, Kari, Emilsson, Valur, Thorleifsson, Gudmar, Zhang, Bin, Leonardson, Amy S, Zink, Florian, Zhu, Jun, Carlson, Sonia, Helgason, Agnar, Walters, G. Bragi, Gunnarsdottir, Steinunn, Mouy, Magali, Steinthorsdottir, Valgerdur, Eiriksdottir, Gudrun H, Bjornsdottir, Gyda, Reynisdottir, Inga, Gudbjartsson, Daniel, Helgadottir, Anna, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Styrkarsdottir, Unnur, Gretarsdottir, Solveig, Magnusson, Kristinn P, Stefansson, Hreinn, Fossdal, Ragnheidur, Kristjansson, Kristleifur, Gislason, Hjortur G, Stefansson, Tryggvi, Leifsson, Bjorn G, Thorsteinsdottir, Unnur, Lamb, John R, Gulcher, Jeffrey R, Reitman, Marc L, Kong, Augustine

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A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome by Skuladottir, Astros Th, Bjornsdottir, Gyda, Ferkingstad, Egil, Einarsson, Gudmundur, Stefansdottir, Lilja, Nawaz, Muhammad Sulaman, Oddsson, Asmundur, Olafsdottir, Thorunn A., Saevarsdottir, Saedis, Walters, G. Bragi, Magnusson, Sigurdur H., Bjornsdottir, Anna, Sveinsson, Olafur A., Vikingsson, Arnor, Hansen, Thomas Folkmann, Jacobsen, Rikke Louise, Erikstrup, Christian, Schwinn, Michael, Brunak, Søren, Banasik, Karina, Ostrowski, Sisse Rye, Troelsen, Anders, Henkel, Cecilie, Pedersen, Ole Birger, Jonsdottir, Ingileif, Gudbjartsson, Daniel F., Sulem, Patrick, Thorgeirsson, Thorgeir E., Stefansson, Hreinn, Stefansson, Kari

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Sequence variants associated with BMI affect disease risk through BMI itself by Einarsson, Gudmundur, Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Zink, Florian, Helgason, Hannes, Olafsdottir, Thorhildur, Rognvaldsson, Solvi, Tragante, Vinicius, Ulfarsson, Magnus O., Sveinbjornsson, Gardar, Snaebjarnarson, Audunn S., Einarsson, Hafsteinn, Aegisdottir, Hildur M., Jonsdottir, Gudrun A., Helgadottir, Anna, Gretarsdottir, Solveig, Styrkarsdottir, Unnur, Arnason, Hannes K., Bjarnason, Ragnar, Sigurdsson, Emil, Arnar, David O., Bjornsson, Einar S., Palsson, Runolfur, Bjornsdottir, Gyda, Stefansson, Hreinn, Thorgeirsson, Thorgeir, Sulem, Patrick, Thorsteinsdottir, Unnur, Holm, Hilma, Gudbjartsson, Daniel F., Stefansson, Kari

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A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy by Skuladottir, Astros Th, Bjornsdottir, Gyda, Thorleifsson, Gudmar, Walters, G. Bragi, Nawaz, Muhammad Sulaman, Moore, Kristjan Helgi Swerford, Olason, Pall I., Thorgeirsson, Thorgeir E., Sigurpalsdottir, Brynja, Sveinbjornsson, Gardar, Eggertsson, Hannes P., Magnusson, Sigurdur H., Oddsson, Asmundur, Bjornsdottir, Anna, Vikingsson, Arnor, Sveinsson, Olafur A., Hrafnsdottir, Maria G., Sigurdardottir, Gudrun R., Halldorsson, Bjarni V., Hansen, Thomas Folkmann, Paarup, Helene, Erikstrup, Christian, Nielsen, Kaspar, Klokker, Mads, Bruun, Mie Topholm, Sorensen, Erik, Banasik, Karina, Burgdorf, Kristoffer S., Pedersen, Ole Birger, Ullum, Henrik, Jonsdottir, Ingileif, Stefansson, Hreinn, Stefansson, Kari

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Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation by Bjornsdottir, Gyda, Benonisdottir, Stefania, Sveinbjornsson, Gardar, Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Walters, G. Bragi, Bjornsson, Aron, Olafsson, Ingvar H., Ulfarsson, Elfar, Vikingsson, Arnor, Hansdottir, Ragnheidur, Karlsson, Karl O., Rafnar, Thorunn, Jonsdottir, Ingileif, Frigge, Michael L., Kong, Augustine, Oddsson, Asmundur, Masson, Gisli, Magnusson, Olafur T., Gudbjartsson, Tomas, Stefansson, Hreinn, Sulem, Patrick, Gudbjartsson, Daniel, Thorsteinsdottir, Unnur, Thorgeirsson, Thorgeir E., Stefansson, Kari

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Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database by Fridriksdottir, Run, Jonsson, Arnar J, Jensson, Brynjar O, Sverrisson, Kristinn O, Arnadottir, Gudny A, Skarphedinsdottir, Sigurbjorg J, Katrinardottir, Hildigunnur, Snaebjornsdottir, Steinunn, Jonsson, Hakon, Eiriksson, Ogmundur, Oskarsson, Gudjon R, Oddsson, Asmundur, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Sigurdsson, Gisli H, Indridason, Einar P, Sigurdsson, Stefan B, Bjornsdottir, Gyda, Saemundsdottir, Jona, Magnusson, Olafur T, Bjornsson, Hans T, Thorsteinsdottir, Unnur, Sigurdsson, Theodor S, Sulem, Patrick, Sigurdsson, Martin I, Stefansson, Kari

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A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy by Bjornsdottir, Gyda, Ivarsdottir, Erna V., Bjarnadottir, Kristbjorg, Benonisdottir, Stefania, Gylfadottir, Sandra Sif, Arnadottir, Gudny A., Benediktsson, Rafn, Halldorsson, Gisli Hreinn, Helgadottir, Anna, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Jonsdottir, Ingileif, Kristinsdottir, Anna Margret, Magnusson, Olafur Th, Masson, Gisli, Melsted, Pall, Rafnar, Thorunn, Sigurdsson, Asgeir, Sigurdsson, Gunnar, Skuladottir, Astros, Steinthorsdottir, Valgerdur, Styrkarsdottir, Unnur, Thorgeirsson, Gudmundur, Thorleifsson, Gudmar, Vikingsson, Arnor, Gudbjartsson, Daniel F., Holm, Hilma, Stefansson, Hreinn, Thorsteinsdottir, Unnur, Norddahl, Gudmundur L., Sulem, Patrick, Thorgeirsson, Thorgeir E., Stefansson, Kari

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Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria by Kristjansson, Ragnar P., Oskarsson, Gudjon R., Skuladottir, Astros, Oddsson, Asmundur, Rognvaldsson, Solvi, Sveinbjornsson, Gardar, Lund, Sigrun H., Jensson, Brynjar O., Styrmisdottir, Edda L., Halldorsson, Gisli H., Ferkingstad, Egil, Eldjarn, Grimur Hjorleifsson, Beyter, Doruk, Kristmundsdottir, Snædis, Juliusson, Kristinn, Fridriksdottir, Run, Arnadottir, Gudny A., Katrinardottir, Hildigunnur, Snorradottir, Margret H., Tragante, Vinicius, Stefansdottir, Lilja, Ivarsdottir, Erna V., Bjornsdottir, Gyda, Halldorsson, Bjarni V., Thorleifsson, Gudmar, Ludviksson, Bjorn R., Onundarson, Pall T., Saevarsdottir, Saedis, Melsted, Pall, Norddahl, Gudmundur L., Bjornsdottir, Unnur S., Olafsdottir, Thorunn, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Sulem, Patrick, Stefansson, Kari

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Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease by Skuladottir, Astros Th, Tragante, Vinicius, Sveinbjornsson, Gardar, Helgason, Hannes, Sturluson, Arni, Bjornsdottir, Anna, Jonsson, Palmi, Palmadottir, Vala, Sveinsson, Olafur A., Jensson, Brynjar O., Gudjonsson, Sigurjon A., Ivarsdottir, Erna V., Gisladottir, Rosa S., Gunnarsson, Arni F., Walters, G. Bragi, Jonsdottir, Gudrun A., Thorgeirsson, Thorgeir E., Bjornsdottir, Gyda, Holm, Hilma, Gudbjartsson, Daniel F., Sulem, Patrick, Stefansson, Hreinn, Stefansson, Kari

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A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo by Skuladottir, Astros Th, Bjornsdottir, Gyda, Nawaz, Muhammad Sulaman, Petersen, Hannes, Rognvaldsson, Solvi, Moore, Kristjan Helgi Swerford, Olafsson, Pall I., Magnusson, Sigurður H., Bjornsdottir, Anna, Sveinsson, Olafur A., Sigurdardottir, Gudrun R., Saevarsdottir, Saedis, Ivarsdottir, Erna V., Stefansdottir, Lilja, Gunnarsson, Bjarni, Muhlestein, Joseph B., Knowlton, Kirk U., Jones, David A., Nadauld, Lincoln D., Hartmann, Annette M., Rujescu, Dan, Strupp, Michael, Walters, G. Bragi, Thorgeirsson, Thorgeir E., Jonsdottir, Ingileif, Holm, Hilma, Thorleifsson, Gudmar, Gudbjartsson, Daniel F., Sulem, Patrick, Stefansson, Hreinn, Stefansson, Kari

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GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis by Skuladottir, Astros Th, Stefansdottir, Lilja, Halldorsson, Gisli H., Stefansson, Olafur A., Bjornsdottir, Anna, Jonsson, Palmi, Palmadottir, Vala, Thorgeirsson, Thorgeir E., Walters, G. Bragi, Gisladottir, Rosa S., Bjornsdottir, Gyda, Jonsdottir, Gudrun A., Sulem, Patrick, Gudbjartsson, Daniel F., Knowlton, Kirk U., Jones, David A., Ottas, Aigar, Pedersen, Ole B., Didriksen, Maria, Brunak, Søren, Banasik, Karina, Hansen, Thomas Folkmann, Erikstrup, Christian, Haavik, Jan, Andreassen, Ole A., Rye, David, Igland, Jannicke, Ostrowski, Sisse Rye, Milani, Lili A., Nadauld, Lincoln D., Stefansson, Hreinn, Stefansson, Kari

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Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles by Hautakangas, Heidi, Winsvold, Bendik K S, Ruotsalainen, Sanni, Bjornsdottir, Gyda, Harder, Aster V. E, Kogelman, Lisette J. A, Thomas, Laurent, Noordam, Raymond, Benner, Christian, Gormley, Padhraig, Artto, Ville, Banasik, Karina, Bjornsdottir, Anna, Boomsma, Dorret I, Brumpton, Ben Michael, Burgdorf, Kristoffer Sølvsten, Buring, Julie E, Chalmer, Mona Ameri, de Boer, Irene, Dichgans, Martin, Erikstrup, Christian, Färkkilä, Markus, Gabrielsen, Maiken Elvestad, Ghanbari, Mohsen, Hagen, Knut, Häppölä, Paavo, Hottenga, Jouke-Jan, Hrafnsdottir, Maria G, Hveem, Kristian, Johnsen, Marianne Bakke, Kähönen, Mika, Kristoffersen, Espen Saxhaug, Kurth, Tobias, Lehtimäki, Terho, Lighart, Lannie, Magnusson, Sigurdur H, Malik, Rainer, Pedersen, Ole Birger, Pelzer, Nadine, Penninx, Brenda W. J. H, Ran, Caroline, Ridker, Paul M, Rosendaal, Frits Richard, Sigurdardottir, Gudrun R, Skogholt, Anne Heidi, Sveinsson, Olafur A, Thorgeirsson, Thorgeir E, Ullum, Henrik, Zwart, John Anker Henrik

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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use by Liu, Ming, Jiang, Yu, Wedow, Robbee, Li, Yue, Brazel, David M, Chen, Fang, Datta, Gargi, Davila-Velderrain, Jose, Mitchell, Amy, Skogholt, Anne Heidi, Sivertsen, Børge, Stordal, Eystein, Morken, Gunnar, Kallestad, Håvard, Heuch, Ingrid, Zwart, John-Anker, Fjukstad, Katrine Kveli, Pedersen, Linda Margareth, Johnsen, Marianne Bakke, Skrove, Marit Synnøve, Indredavik, Marit Sæbø, Drange, Ole Kristian, Bjerkeset, Ottar, Børte, Sigrid, Stensland, Synne, Choquet, Hélène, Docherty, Anna R, Faul, Jessica D, Foerster, Johanna R, Fritsche, Lars, Gabrielsen, Maiken Elvestad, Gordon, Scott D, Haessler, Jeffrey, Hottenga, Jouke-Jan, Huang, Hongyan, Jang, Seon-Kyeong, Jansen, Philip R, Ling, Yueh, Mägi, Reedik, Matoba, Nana, McMahon, George, Mulas, Antonella, Orrú, Valeria, Palviainen, Teemu, Pandit, Anita, Reginsson, Gunnar W, Smith, Jennifer A, Taylor, Amy E, Turman, Constance, Willemsen, Gonneke, Young, Hannah, Young, Kendra A, Zajac, Gregory J.M, Zhao, Wei, Zhou, Wei, Björnsdóttir, Gyda Thora, Boardman, Jason D, Boehnke, Michael, Boomsma, Dorret I, Chen, Chu, Davies, Gareth E, Eaton, Charles B, Winsvold, Bendik K S, Hveem, Kristian, Vrieze, Scott

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Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations by Boer, Cindy G., Hatzikotoulas, Konstantinos, Southam, Lorraine, Zhang, Yanfei, Coutinho de Almeida, Rodrigo, Wu, Tian T., Zheng, Jie, Hartley, April, Teder-Laving, Maris, Terao, Chikashi, Zengini, Eleni, Alexiadis, George, Bjornsdottir, Gyda, Gilly, Arthur, Ingvarsson, Thorvaldur, Luetge, Almut, Lund, Sigrun H., Mangino, Massimo, Takuwa, Hiroshi, Thomas, Laurent F., Loughlin, John, Arden, Nigel, Doherty, Michael, Ollier, William E.R., Spector, Tim D., Wallis, Gillian A., Martinsen, Amy E., Fors, Egil Andreas, Hagen, Knut, Nilsen, Kristian Bernhard, Lie, Marie Udnesseter, Børte, Sigrid, Brumpton, Ben, Fritsche, Lars G., Zhou, Wei, Heuch, Ingrid, Storheim, Kjersti, Tyrpenou, Evangelos, Koukakis, Athanasios, Efstathios, Chronopoulos, Nikolaou, Vasileios S., Malizos, Konstantinos, Anastasopoulou, Lydia, Abecasis, Goncalo, Baras, Aris, Cantor, Michael, Coppola, Giovanni, Lotta, Luca A., Shuldiner, Alan, Karalis, Katia, Siminovitch, Katherine, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Padilla, Maria Sotiropoulos, Widom, Louis, Wolf, Sarah E., Pradhan, Manasi, Manoochehri, Kia, Bai, Xiaodong, Balasubramanian, Suganthi, Boutkov, Boris, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Maxwell, Evan K., Orelus, Max, Panea, Razvan, Polanco, Tommy, Salerno, William, Staples, Jeffrey C., Li, Dadong, Sharma, Deepika, Banerjee, Ilanjana, Locke, Adam, Haas, Mary, Akbari, Parsa, Ferreira, Manuel A.R., Jones, Marcus B., Mitnaul, Lyndon J., Babis, George C., Cheung, Jason Pui Yin, Kang, Jae Hee, Lietman, Steven A., Samartzis, Dino, Stefansson, Kari, Uitterlinden, André G., Davey Smith, George, Valdes, Ana M., Tsezou, Aspasia, Cheah, Kathryn S.E., Hveem, Kristian, Wilkinson, J. Mark, Meulenbelt, Ingrid, Lee, Ming Ta Michael, van Meurs, Joyce B.J., Styrkársdóttir, Unnur, Zeggini, Eleftheria

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Genetic diversity fuels gene discovery for tobacco and alcohol use by Wang, Xingyan, Jang, Seon-Kyeong, Jiang, Yu, Khunsriraksakul, Chachrit, Addison, Clifton, Aliev, Fazil, Arnett, Donna K., Ashley-Koch, Allison E., Barr, R. Graham, Bielak, Lawrence F., Benjamin, Emelia J., Bis, Joshua C., Bjornsdottir, Gyda, Blangero, John, Chavan, Sameer, Chen, Yii-Der Ida, Chen, Zhengming, Cheng, Iona, Choquet, Hélène, Cole, John W., Cucca, Francesco, Dick, Danielle M., Fernandes Silva, Lilian, Fiorillo, Edoardo, Garrett, Melanie E., Glahn, David C., Gordon, Scott D., Gu, Dongfeng, Gudbjartsson, Daniel F., Hall, Michael E., Haller, Toomas, Harris, Kathleen Mullan, He, Jiang, Hewitt, John K., Hickie, Ian, Hidalgo, Bertha, Hokanson, John E., Hottenga, JoukeJan, Hwu, Chii-Min, Jee, Yon Ho, Joo, Yoonjung Y., Kamatani, Yoichiro, Kaplan, Robert C., Kelly, Tanika N., Kraft, Peter, Krauter, Kenneth, Laakso, Markku, Lasky-Su, Jessica, Li, Liming, Lloyd-Jones, Donald M., Mägi, Reedik, Manichaikul, Ani, Mathur, Ravi, Matoba, Nana, McArdle, Patrick F., Metspalu, Andres, Moll, Matthew, Montasser, May E., Nielsen, Jonas B., Oelsner, Elizabeth C., Orrù, Valeria, Palmer, Nicholette D., Park, S. Lani, Peters, Ulrike, Peters, Annette, Polderman, Tinca J. C., Rafaels, Nicholas, Reiner, Alex P., Roan, Carol, Rotter, Jerome I., Runarsdottir, Valgerdur, Saccone, Nancy L., Shadyab, Aladdin H., Shringarpure, Suyash S., Sicinski, Kamil, Smith, Jennifer A., Smith, Nicholas L., Sotoodehnia, Nona, Stallings, Michael C., Stefansson, Hreinn, Syed, Moin, Tal-Singer, Ruth, Telen, Marilyn J., Tiwari, Hemant, Wall, Tamara L., White, Wendy B., Whitfield, John B., Wiggins, Kerri L., Willemsen, Gonneke, Willer, Cristen J., Xu, Huichun, Yanek, Lisa R., Young, Kendra A., Yu, Bing, Zhao, Wei, Zöllner, Sebastian, Bierut, Laura J., Gagliano Taliun, Sarah A., Munafò, Marcus R., Liu, Dajiang J.

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Genome-wide association study identifies 74 loci associated with educational attainment by Turley, Patrick, Chen, Guo-Bo, Emilsson, Valur, Meddens, S. Fleur W., Thom, Kevin, Timshel, Pascal, Bacelis, Jonas, Baumbach, Clemens, Girotto, Giorgia, Gupta, Richa, Hofer, Edith, Horikoshi, Momoko, Lind, Penelope A., Mangino, Massimo, Marten, Jonathan, Pervjakova, Natalia, Peyrot, Wouter J., Qian, Yong, Schmidt, Börge, Schraut, Katharina E., Teumer, Alexander, Westra, Harm-Jan, Alizadeh, Behrooz Z., Bakshi, Andrew, Baumeister, Sebastian E., Bønnelykke, Klaus, Boyle, Patricia A., Davies, Gail, De Neve, Jan-Emmanuel, Demuth, Ilja, Ding, Jun, Eisele, Lewin, Eklund, Niina, Faul, Jessica D., Forstner, Andreas J., Gunnarsson, Bjarni, Halldórsson, Bjarni V., Heath, Andrew C., Hocking, Lynne J., Hottenga, Jouke-Jan, de Jager, Philip L., Joshi, Peter K., Kaakinen, Marika A., Kiemeney, Lambertus A. L. M., Koskinen, Seppo, Kraja, Aldi T., Kroh, Martin, Lichtenstein, Paul, Lichtner, Peter, Liewald, David C. M., Loukola, Anu, Madden, Pamela A., Mäki-Opas, Tomi, Marioni, Riccardo E., Marques-Vidal, Pedro, Meddens, Gerardus A., Meisinger, Christa, Montgomery, Grant W., Nyholt, Dale R., Ollier, William E. R., Pedersen, Nancy L., Robino, Antonietta, Rostapshova, Olga, Sanders, Alan R., Sarin, Antti-Pekka, Terracciano, Antonio, Tobin, Martin D., Ulivi, Sheila, van Rooij, Frank J. A., Venturini, Cristina, Vinkhuyzen, Anna A. E., Vonk, Judith M., Vozzi, Diego, Ware, Erin B., Berger, Klaus, Chabris, Christopher F., Cucca, Francesco, Deary, Ian J., Dedoussis, George V., Groenen, Patrick J. F., Hinds, David A., Kaprio, Jaakko, Magnusson, Patrik K. E., Metspalu, Andres, Perola, Markus, Samani, Nilesh J., Schlessinger, David, Schmidt, Reinhold, Sørensen, Thorkild I. A., Spector, Tim D., Stefansson, Kari, Thorsteinsdottir, Unnur, Tiemeier, Henning, Weir, David R., Krueger, Robert F., Hofman, Albert, Meyer, Michelle N., Visscher, Peter M., Esko, Tõnu, Koellinger, Philipp D.

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