A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study

por Silva, Claudia T., Zorkoltseva, Irina V., Amin, Najaf, Demirkan, Ayşe, van Leeuwen, Elisabeth M., Kors, Jan A., van den Berg, Marten, Stricker, Bruno H., Uitterlinden, André G., Kirichenko, Anatoly V., Witteman, Jacqueline C. M., Willemsen, Rob, Oostra, Ben A., Axenovich, Tatiana I., van Duijn, Cornelia M., Isaacs, Aaron
Publicado no Front Genet (2016)

Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands'

por Deelen, Patrick, Menelaou, Androniki, van Leeuwen, Elisabeth M, Kanterakis, Alexandros, van Dijk, Freerk, Medina-Gomez, Carolina, Francioli, Laurent C, Hottenga, Jouke Jan, Karssen, Lennart C, Estrada, Karol, Kreiner-Møller, Eskil, Rivadeneira, Fernando, van Setten, Jessica, Gutierrez-Achury, Javier, Westra, Harm-Jan, Franke, Lude, van Enckevort, David, Dijkstra, Martijn, Byelas, Heorhiy, van Duijn, Cornelia M, de Bakker, Paul I W, Wijmenga, Cisca, Swertz, Morris A
Publicado em 2014

The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels

por van Leeuwen, Elisabeth M., Smouter, Françoise A. S., Kam-Thong, Tony, Karbalai, Nazanin, Smith, Albert V., Harris, Tamara B., Launer, Lenore J., Sitlani, Colleen M., Li, Guo, Brody, Jennifer A., Bis, Joshua C., White, Charles C., Jaiswal, Alok, Oostra, Ben A., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G., Boerwinkle, Eric, Ballantyne, Christie M., Gudnason, Vilmundur, Psaty, Bruce M., Cupples, L. Adrienne, Järvelin, Marjo-Riitta, Ripatti, Samuli, Isaacs, Aaron, Müller-Myhsok, Bertram, Karssen, Lennart C., van Duijn, Cornelia M.
Publicado em 2014

Diagnostic Yield of Sequencing Familial Hypercholesterolemia Genes in Severe Hypercholesterolemia

por Khera, Amit V., Won, Hong-Hee, Peloso, Gina M., Lawson, Kim S., Bartz, Traci M., Deng, Xuan, van Leeuwen, Elisabeth M., Natarajan, Pradeep, Emdin, Connor A., Bick, Alexander G., Morrison, Alanna C., Brody, Jennifer A., Gupta, Namrata, Nomura, Akihiro, Kessler, Thorsten, Duga, Stefano, Bis, Joshua C., van Duijn, Cornelia M., Cupples, L. Adrienne, Psaty, Bruce, Rader, Daniel J., Danesh, John, Schunkert, Heribert, McPherson, Ruth, Farrall, Martin, Watkins, Hugh, Lander, Eric, Wilson, James G., Correa, Adolfo, Boerwinkle, Eric, Merlini, Piera Angelica, Ardissino, Diego, Saleheen, Danish, Gabriel, Stacey, Kathiresan, Sekar
Publicado no J Am Coll Cardiol (2016)

Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA

por Kettunen, Johannes, Demirkan, Ayşe, Würtz, Peter, Draisma, Harmen H.M., Haller, Toomas, Rawal, Rajesh, Vaarhorst, Anika, Kangas, Antti J., Lyytikäinen, Leo-Pekka, Pirinen, Matti, Pool, René, Sarin, Antti-Pekka, Soininen, Pasi, Tukiainen, Taru, Wang, Qin, Tiainen, Mika, Tynkkynen, Tuulia, Amin, Najaf, Zeller, Tanja, Beekman, Marian, Deelen, Joris, van Dijk, Ko Willems, Esko, Tõnu, Hottenga, Jouke-Jan, van Leeuwen, Elisabeth M, Lehtimäki, Terho, Mihailov, Evelin, Rose, Richard J., de Craen, Anton J.M., Gieger, Christian, Kähönen, Mika, Perola, Markus, Blankenberg, Stefan, Savolainen, Markku J., Verhoeven, Aswin, Viikari, Jorma, Willemsen, Gonneke, Boomsma, Dorret I., van Duijn, Cornelia M., Eriksson, Johan, Jula, Antti, Järvelin, Marjo-Riitta, Kaprio, Jaakko, Metspalu, Andres, Raitakari, Olli, Salomaa, Veikko, Slagboom, P. Eline, Waldenberger, Melanie, Ripatti, Samuli, Ala-Korpela, Mika
Publicado no Nat Commun (2016)

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels

por Draisma, Harmen H.M., Pool, René, Kobl, Michael, Jansen, Rick, Petersen, Ann-Kristin, Vaarhorst, Anika A.M., Yet, Idil, Haller, Toomas, Demirkan, Ayşe, Esko, Tõnu, Zhu, Gu, Böhringer, Stefan, Beekman, Marian, van Klinken, Jan Bert, Römisch-Margl, Werner, Prehn, Cornelia, Adamski, Jerzy, de Craen, Anton J.M., van Leeuwen, Elisabeth M., Amin, Najaf, Dharuri, Harish, Westra, Harm-Jan, Franke, Lude, de Geus, Eco J.C., Hottenga, Jouke Jan, Willemsen, Gonneke, Henders, Anjali K., Montgomery, Grant W., Nyholt, Dale R., Whitfield, John B., Penninx, Brenda W., Spector, Tim D., Metspalu, Andres, Slagboom, P. Eline, van Dijk, Ko Willems, ‘t Hoen, Peter A.C., Strauch, Konstantin, Martin, Nicholas G., van Ommen, Gert-Jan B., Illig, Thomas, Bell, Jordana T., Mangino, Massimo, Suhre, Karsten, McCarthy, Mark I., Gieger, Christian, Isaacs, Aaron, van Duijn, Cornelia M., Boomsma, Dorret I.
Publicado no Nat Commun (2015)

The Genome of the Netherlands: design, and project goals

por Boomsma, Dorret I, Wijmenga, Cisca, Slagboom, Eline P, Swertz, Morris A, Karssen, Lennart C, Abdellaoui, Abdel, Ye, Kai, Guryev, Victor, Vermaat, Martijn, van Dijk, Freerk, Francioli, Laurent C, Hottenga, Jouke Jan, Laros, Jeroen F J, Li, Qibin, Li, Yingrui, Cao, Hongzhi, Chen, Ruoyan, Du, Yuanping, Li, Ning, Cao, Sujie, van Setten, Jessica, Menelaou, Androniki, Pulit, Sara L, Hehir-Kwa, Jayne Y, Beekman, Marian, Elbers, Clara C, Byelas, Heorhiy, de Craen, Anton J M, Deelen, Patrick, Dijkstra, Martijn, den Dunnen, Johan T, de Knijff, Peter, Houwing-Duistermaat, Jeanine, Koval, Vyacheslav, Estrada, Karol, Hofman, Albert, Kanterakis, Alexandros, Enckevort, David van, Mai, Hailiang, Kattenberg, Mathijs, van Leeuwen, Elisabeth M, Neerincx, Pieter B T, Oostra, Ben, Rivadeneira, Fernanodo, Suchiman, Eka H D, Uitterlinden, Andre G, Willemsen, Gonneke, Wolffenbuttel, Bruce H, Wang, Jun, de Bakker, Paul I W, van Ommen, Gert-Jan, van Duijn, Cornelia M
Publicado em 2014

Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

por Springelkamp, Henriët, Mishra, Aniket, Hysi, Pirro G., Gharahkhani, Puya, Höhn, René, Khor, Chiea-Chuen, Cooke Bailey, Jessica N., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Koh, Victor, Yazar, Seyhan, Xu, Liang, Forward, Hannah, Kearns, Lisa S., Amin, Najaf, Iglesias, Adriana I., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Demirkan, Ayse, van der Lee, Sven, Loon, Seng-Chee, Rivadeneira, Fernando, Nag, Abhishek, Sanfilippo, Paul G., Schillert, Arne, de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Zhou, Tiger, Burdon, Kathryn P., Spector, Timothy D., Lackner, Karl J., Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Pasquale, Louis R., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Jonas, Jost B., Cheng, Ching-Yu, Aung, Tin, Jansonius, Nomdo M., Klaver, Caroline C. W., Craig, Jamie E., Young, Terri L., Haines, Jonathan L., MacGregor, Stuart, Mackey, David A., Pfeiffer, Norbert, Wong, Tien-Yin, Wiggs, Janey L., Hewitt, Alex W., van Duijn, Cornelia M., Hammond, Christopher J.
Publicado no Genet Epidemiol (2015)

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

por Iotchkova, Valentina, Huang, Jie, Morris, John A., Jain, Deepti, Barbieri, Caterina, Walter, Klaudia, Min, Josine L., Chen, Lu, Astle, William, Cocca, Massimilian, Deelen, Patrick, Elding, Heather, Farmaki, Aliki-Eleni, Franklin, Christopher S., Franberg, Mattias, Gaunt, Tom R., Hofman, Albert, Jiang, Tao, Kleber, Marcus E., Lachance, Genevieve, Luan, Jian'an, Malerba, Giovanni, Matchan, Angela, Mead, Daniel, Memari, Yasin, Ntalla, Ioanna, Panoutsopoulou, Kalliope, Pazoki, Raha, Perry, John R.B., Rivadeneira, Fernando, Sabater-Lleal, Maria, Sennblad, Bengt, Shin, So-Youn, Southam, Lorraine, Traglia, Michela, van Dijk, Freerk, van Leeuwen, Elisabeth M., Zaza, Gianluigi, Zhang, Weihua, Amin, Najaf, Butterworth, Adam, Chambers, John C., Dedoussis, George, Dehghan, Abbas, Franco, Oscar H., Franke, Lude, Frontini, Mattia, Gambaro, Giovanni, Gasparini, Paolo, Hamsten, Anders, Issacs, Aaron, Kooner, Jaspal S., Kooperberg, Charles, Langenberg, Claudia, Marz, Winfried, Scott, Robert A., Swertz, Morris A., Toniolo, Daniela, Uitterlinden, Andre G., van Duijn, Cornelia M., Watkins, Hugh, Zeggini, Eleftheria, Maurano, Mathew T., Timpson, Nicholas J., Reiner, Alexander P., Auer, Paul L., Soranzo, Nicole
Publicado no Nat Genet (2016)

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)

Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

por van Leeuwen, Elisabeth M., Karssen, Lennart C., Deelen, Joris, Isaacs, Aaron, Medina-Gomez, Carolina, Mbarek, Hamdi, Kanterakis, Alexandros, Trompet, Stella, Postmus, Iris, Verweij, Niek, van Enckevort, David J., Huffman, Jennifer E., White, Charles C., Feitosa, Mary F., Bartz, Traci M., Manichaikul, Ani, Joshi, Peter K., Peloso, Gina M., Deelen, Patrick, van Dijk, Freerk, Willemsen, Gonneke, de Geus, Eco J., Milaneschi, Yuri, Penninx, Brenda W.J.H., Francioli, Laurent C., Menelaou, Androniki, Pulit, Sara L., Rivadeneira, Fernando, Hofman, Albert, Oostra, Ben A., Franco, Oscar H., Leach, Irene Mateo, Beekman, Marian, de Craen, Anton J.M., Uh, Hae-Won, Trochet, Holly, Hocking, Lynne J., Porteous, David J., Sattar, Naveed, Packard, Chris J., Buckley, Brendan M., Brody, Jennifer A., Bis, Joshua C., Rotter, Jerome I., Mychaleckyj, Josyf C., Campbell, Harry, Duan, Qing, Lange, Leslie A., Wilson, James F., Hayward, Caroline, Polasek, Ozren, Vitart, Veronique, Rudan, Igor, Wright, Alan F., Rich, Stephen S., Psaty, Bruce M., Borecki, Ingrid B., Kearney, Patricia M., Stott, David J., Adrienne Cupples, L., Jukema, J. Wouter, van der Harst, Pim, Sijbrands, Eric J., Hottenga, Jouke-Jan, Uitterlinden, Andre G., Swertz, Morris A., van Ommen, Gert-Jan B., de Bakker, Paul I.W., Eline Slagboom, P., Boomsma, Dorret I., Wijmenga, Cisca, van Duijn, Cornelia M.
Publicado no Nat Commun (2015)

Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation

por Horikoshi, Momoko, Mӓgi, Reedik, van de Bunt, Martijn, Surakka, Ida, Sarin, Antti-Pekka, Mahajan, Anubha, Marullo, Letizia, Thorleifsson, Gudmar, Hӓgg, Sara, Hottenga, Jouke-Jan, Ladenvall, Claes, Ried, Janina S., Winkler, Thomas W., Willems, Sara M., Pervjakova, Natalia, Esko, Tõnu, Beekman, Marian, Nelson, Christopher P., Willenborg, Christina, Wiltshire, Steven, Ferreira, Teresa, Fernandez, Juan, Gaulton, Kyle J., Steinthorsdottir, Valgerdur, Hamsten, Anders, Magnusson, Patrik K. E., Willemsen, Gonneke, Milaneschi, Yuri, Robertson, Neil R., Groves, Christopher J., Bennett, Amanda J., Lehtimӓki, Terho, Viikari, Jorma S., Rung, Johan, Lyssenko, Valeriya, Perola, Markus, Heid, Iris M., Herder, Christian, Grallert, Harald, Müller-Nurasyid, Martina, Roden, Michael, Hypponen, Elina, Isaacs, Aaron, van Leeuwen, Elisabeth M., Karssen, Lennart C., Mihailov, Evelin, Houwing-Duistermaat, Jeanine J., de Craen, Anton J. M., Deelen, Joris, Havulinna, Aki S., Blades, Matthew, Hengstenberg, Christian, Erdmann, Jeanette, Schunkert, Heribert, Kaprio, Jaakko, Tobin, Martin D., Samani, Nilesh J., Lind, Lars, Salomaa, Veikko, Lindgren, Cecilia M., Slagboom, P. Eline, Metspalu, Andres, van Duijn, Cornelia M., Eriksson, Johan G., Peters, Annette, Gieger, Christian, Jula, Antti, Groop, Leif, Raitakari, Olli T., Power, Chris, Penninx, Brenda W. J. H., de Geus, Eco, Smit, Johannes H., Boomsma, Dorret I., Pedersen, Nancy L., Ingelsson, Erik, Thorsteinsdottir, Unnur, Stefansson, Kari, Ripatti, Samuli, Prokopenko, Inga, McCarthy, Mark I., Morris, Andrew P.
Publicado no PLoS Genet (2015)

The impact of low-frequency and rare variants on lipid levels

por Surakka, Ida, Horikoshi, Momoko, Mägi, Reedik, Sarin, Antti-Pekka, Mahajan, Anubha, Lagou, Vasiliki, Marullo, Letizia, Ferreira, Teresa, Miraglio, Benjamin, Timonen, Sanna, Kettunen, Johannes, Pirinen, Matti, Karjalainen, Juha, Thorleifsson, Gudmar, Hägg, Sara, Hottenga, Jouke-Jan, Isaacs, Aaron, Ladenvall, Claes, Beekman, Marian, Esko, Tõnu, Ried, Janina S, Nelson, Christopher P, Willenborg, Christina, Gustafsson, Stefan, Westra, Harm-Jan, Blades, Matthew, de Craen, Anton JM, de Geus, Eco J, Deelen, Joris, Grallert, Harald, Hamsten, Anders, Havulinna, Aki S., Hengstenberg, Christian, Houwing-Duistermaat, Jeanine J, Hyppönen, Elina, Karssen, Lennart C, Lehtimäki, Terho, Lyssenko, Valeriya, Magnusson, Patrik KE, Mihailov, Evelin, Müller-Nurasyid, Martina, Mpindi, John-Patrick, Pedersen, Nancy L, Penninx, Brenda WJH, Perola, Markus, Pers, Tune H, Peters, Annette, Rung, Johan, Smit, Johannes H, Steinthorsdottir, Valgerdur, Tobin, Martin D, Tsernikova, Natalia, van Leeuwen, Elisabeth M, Viikari, Jorma S, Willems, Sara M, Willemsen, Gonneke, Schunkert, Heribert, Erdmann, Jeanette, Samani, Nilesh J, Kaprio, Jaakko, Lind, Lars, Gieger, Christian, Metspalu, Andres, Slagboom, P Eline, Groop, Leif, van Duijn, Cornelia M, Eriksson, Johan G, Jula, Antti, Salomaa, Veikko, Boomsma, Dorret I, Power, Christine, Raitakari, Olli T, Ingelsson, Erik, Järvelin, Marjo-Riitta, Stefansson, Kari, Franke, Lude, Ikonen, Elina, Kallioniemi, Olli, Pietiäinen, Vilja, Lindgren, Cecilia M, Thorsteinsdottir, Unnur, Palotie, Aarno, McCarthy, Mark I, Morris, Andrew P, Prokopenko, Inga, Ripatti, Samuli
Publicado no Nat Genet (2015)

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

por Springelkamp, Henriët., Höhn, René, Mishra, Aniket, Hysi, Pirro G., Khor, Chiea-Chuen, Loomis, Stephanie J., Bailey, Jessica N. Cooke, Gibson, Jane, Thorleifsson, Gudmar, Janssen, Sarah F., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Nongpiur, Monisha E., Montgomery, Grant W., Xu, Liang, Mountain, Jenny E., Gharahkhani, Puya, Lu, Yi, Amin, Najaf, Karssen, Lennart C., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Iglesias, Adriana I., Verhoeven, Virginie J. M., Hauser, Michael A., Loon, Seng-Chee, Despriet, Dominiek D. G., Nag, Abhishek, Venturini, Cristina, Sanfilippo, Paul G., Schillert, Arne, Kang, Jae H., Landers, John, Jonasson, Fridbert, Cree, Angela J., van Koolwijk, Leonieke M. E., Rivadeneira, Fernando, Souzeau, Emmanuelle, Jonsson, Vesteinn, Menon, Geeta, Weinreb, Robert N., de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Ennis, Sarah, Thorsteinsdottir, Unnur, Burdon, Kathryn P., Spector, Timothy D., Mirshahi, Alireza, Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Haines, Jonathan L., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Jansonius, Nomdo M., Jonas, Jost B., Cheng, Ching-Yu, Aung, Tin, Viswanathan, Ananth C., Klaver, Caroline C. W., Craig, Jamie E., Macgregor, Stuart, Mackey, David A., Lotery, Andrew J., Stefansson, Kari, Bergen, Arthur A. B., Young, Terri L., Wiggs, Janey L., Pfeiffer, Norbert, Wong, Tien-Yin, Pasquale, Louis R., Hewitt, Alex W., van Duijn, Cornelia M., Hammond, Christopher J.
Publicado em 2014

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics

por Springelkamp, Henriët, Iglesias, Adriana I., Mishra, Aniket, Höhn, René, Wojciechowski, Robert, Khawaja, Anthony P., Nag, Abhishek, Wang, Ya Xing, Wang, Jie Jin, Cuellar-Partida, Gabriel, Gibson, Jane, Bailey, Jessica N. Cooke, Vithana, Eranga N., Gharahkhani, Puya, Boutin, Thibaud, Ramdas, Wishal D., Zeller, Tanja, Luben, Robert N., Yonova-Doing, Ekaterina, Viswanathan, Ananth C., Yazar, Seyhan, Cree, Angela J., Haines, Jonathan L., Koh, Jia Yu, Souzeau, Emmanuelle, Wilson, James F., Amin, Najaf, Müller, Christian, Venturini, Cristina, Kearns, Lisa S., Kang, Jae Hee, Tham, Yih Chung, Zhou, Tiger, van Leeuwen, Elisabeth M., Nickels, Stefan, Sanfilippo, Paul, Liao, Jiemin, van der Linde, Herma, Zhao, Wanting, van Koolwijk, Leonieke M.E., Zheng, Li, Rivadeneira, Fernando, Baskaran, Mani, van der Lee, Sven J., Perera, Shamira, de Jong, Paulus T.V.M., Oostra, Ben A., Uitterlinden, André G., Fan, Qiao, Hofman, Albert, Tai, E-Shyong, Vingerling, Johannes R., Sim, Xueling, Wolfs, Roger C.W., Teo, Yik Ying, Lemij, Hans G., Khor, Chiea Chuen, Willemsen, Rob, Lackner, Karl J., Aung, Tin, Jansonius, Nomdo M., Montgomery, Grant, Wild, Philipp S., Young, Terri L., Burdon, Kathryn P., Hysi, Pirro G., Pasquale, Louis R., Wong, Tien Yin, Klaver, Caroline C.W., Hewitt, Alex W., Jonas, Jost B., Mitchell, Paul, Lotery, Andrew J., Foster, Paul J., Vitart, Veronique, Pfeiffer, Norbert, Craig, Jamie E., Mackey, David A., Hammond, Christopher J., Wiggs, Janey L., Cheng, Ching-Yu, van Duijn, Cornelia M., MacGregor, Stuart
Publicado no Hum Mol Genet (2017)

Genome-wide analysis of multiethnic cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

por Hysi, Pirro G, Cheng, Ching-Yu, Springelkamp, Henriët, Macgregor, Stuart, Bailey, Jessica N Cooke, Wojciechowski, Robert, Vitart, Veronique, Nag, Abhishek, Hewitt, Alex W, Höhn, René, Venturini, Cristina, Mirshahi, Alireza, Ramdas, Wishal D., Thorleifsson, Gudmar, Vithana, Eranga, Khor, Chiea-Chuen, Stefansson, Arni B, Liao, Jiemin, Haines, Jonathan L, Amin, Najaf, Wang, Ya Xing, Wild, Philipp S, Ozel, Ayse B, Li, Jun Z, Fleck, Brian W, Zeller, Tanja, Staffieri, Sandra E, Teo, Yik-Ying, Cuellar-Partida, Gabriel, Luo, Xiaoyan, Allingham, R Rand, Richards, Julia E, Senft, Andrea, Karssen, Lennart C, Zheng, Yingfeng, Bellenguez, Céline, Xu, Liang, Iglesias, Adriana I, Wilson, James F, Kang, Jae H, van Leeuwen, Elisabeth M, Jonsson, Vesteinn, Thorsteinsdottir, Unnur, Despriet, Dominiek D.G., Ennis, Sarah, Moroi, Sayoko E, Martin, Nicholas G, Jansonius, Nomdo M, Yazar, Seyhan, Tai, E-Shyong, Amouyel, Philippe, Kirwan, James, van Koolwijk, Leonieke M.E., Hauser, Michael A, Jonasson, Fridbert, Leo, Paul, Loomis, Stephanie J, Fogarty, Rhys, Rivadeneira, Fernando, Kearns, Lisa, Lackner, Karl J, de Jong, Paulus T.V.M., Simpson, Claire L, Pennell, Craig E, Oostra, Ben A, Uitterlinden, André G, Saw, Seang-Mei, Lotery, Andrew J, Bailey-Wilson, Joan E, Hofman, Albert, Vingerling, Johannes R, Maubaret, Cécilia, Pfeiffer, Norbert, Wolfs, Roger C.W., Lemij, Hans G, Young, Terri L, Pasquale, Louis R, Delcourt, Cécile, Spector, Timothy D, Klaver, Caroline C.W., Small, Kerrin S, Burdon, Kathryn P, Stefansson, Kari, Wong, Tien-Yin, Viswanathan, Ananth, Mackey, David A, Craig, Jamie E, Wiggs, Janey L, van Duijn, Cornelia M, Hammond, Christopher J, Aung, Tin
Publicado em 2014

Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C

por van Leeuwen, Elisabeth M, Huffman, Jennifer E, Bis, Joshua C, Isaacs, Aaron, Mulder, Monique, Sabo, Aniko, Smith, Albert V, Demissie, Serkalem, Manichaikul, Ani, Brody, Jennifer A, Feitosa, Mary F, Duan, Qing, Schraut, Katharina E, Navarro, Pau, van Vliet-Ostaptchouk, Jana V, Zhu, Gu, Mbarek, Hamdi, Trompet, Stella, Verweij, Niek, Lyytikäinen, Leo-Pekka, Deelen, Joris, Nolte, Ilja M, van der Laan, Sander W, Davies, Gail, Vermeij-Verdoold, Andrea JM, van Oosterhout, Andy ALJ, Vergeer-Drop, Jeannette M, Arking, Dan E, Trochet, Holly, Medina-Gomez, Carolina, Rivadeneira, Fernando, Uitterlinden, Andre G, Dehghan, Abbas, Franco, Oscar H, Sijbrands, Eric J, Hofman, Albert, White, Charles C, Mychaleckyj, Josyf C, Peloso, Gina M, Swertz, Morris A, Willemsen, Gonneke, de Geus, Eco J, Milaneschi, Yuri, Penninx, Brenda WJH, Ford, Ian, Buckley, Brendan M, de Craen, Anton JM, Starr, John M, Deary, Ian J, Pasterkamp, Gerard, Oldehinkel, Albertine J, Snieder, Harold, Slagboom, P Eline, Nikus, Kjell, Kähönen, Mika, Lehtimäki, Terho, Viikari, Jorma S, Raitakari, Olli T, van der Harst, Pim, Jukema, J Wouter, Hottenga, Jouke-Jan, Boomsma, Dorret I, Whitfield, John B, Montgomery, Grant, Martin, Nicholas G, Polasek, Ozren, Vitart, Veronique, Hayward, Caroline, Kolcic, Ivana, Wright, Alan F, Rudan, Igor, Joshi, Peter K, Wilson, James F, Lange, Leslie A, Wilson, James G, Gudnason, Vilmundur, Harris, Tamar B, Morrison, Alanna C, Borecki, Ingrid B, Rich, Stephen S, Padmanabhan, Sandosh, Psaty, Bruce M, Rotter, Jerome I, Smith, Blair H, Boerwinkle, Eric, Cupples, L Adrienne, van Duijn, Cornelia
Publicado no NPJ Aging Mech Dis (2015)

Identification of seven loci affecting mean telomere length and their association with disease

por Codd, Veryan, Nelson, Christopher P., Albrecht, Eva, Mangino, Massimo, Deelen, Joris, Buxton, Jessica L., Jan Hottenga, Jouke, Fischer, Krista, Esko, Tõnu, Surakka, Ida, Broer, Linda, Nyholt, Dale R., Mateo Leach, Irene, Salo, Perttu, Hägg, Sara, Matthews, Mary K., Palmen, Jutta, Norata, Giuseppe D., O’Reilly, Paul F., Saleheen, Danish, Amin, Najaf, Balmforth, Anthony J., Beekman, Marian, de Boer, Rudolf A., Böhringer, Stefan, Braund, Peter S., Burton, Paul R., de Craen, Anton J. M., Denniff, Matthew, Dong, Yanbin, Douroudis, Konstantinos, Dubinina, Elena, Eriksson, Johan G., Garlaschelli, Katia, Guo, Dehuang, Hartikainen, Anna-Liisa, Henders, Anjali K., Houwing-Duistermaat, Jeanine J., Kananen, Laura, Karssen, Lennart C., Kettunen, Johannes, Klopp, Norman, Lagou, Vasiliki, van Leeuwen, Elisabeth M., Madden, Pamela A., Mägi, Reedik, Magnusson, Patrik K.E., Männistö, Satu, McCarthy, Mark I., Medland, Sarah E., Mihailov, Evelin, Montgomery, Grant W., Oostra, Ben A., Palotie, Aarno, Peters, Annette, Pollard, Helen, Pouta, Anneli, Prokopenko, Inga, Ripatti, Samuli, Salomaa, Veikko, Suchiman, H. Eka D., Valdes, Ana M., Verweij, Niek, Viñuela, Ana, Wang, Xiaoling, Wichmann, H.-Erich, Widen, Elisabeth, Willemsen, Gonneke, Wright, Margaret J., Xia, Kai, Xiao, Xiangjun, van Veldhuisen, Dirk J., Catapano, Alberico L., Tobin, Martin D., Hall, Alistair S., Blakemore, Alexandra I.F., van Gilst, Wiek H., Zhu, Haidong, Erdmann, Jeanette, Reilly, Muredach P., Kathiresan, Sekar, Schunkert, Heribert, Talmud, Philippa J., Pedersen, Nancy L., Perola, Markus, Ouwehand, Willem, Kaprio, Jaakko, Martin, Nicholas G., van Duijn, Cornelia M., Hovatta, Iiris, Gieger, Christian, Metspalu, Andres, Boomsma, Dorret I., Jarvelin, Marjo-Riitta, Slagboom, P. Eline, Thompson, John R., Spector, Tim D., van der Harst, Pim, Samani, Nilesh J.
Publicado em 2013

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

por van Leeuwen, Elisabeth M, Sabo, Aniko, Bis, Joshua C, Huffman, Jennifer E, Manichaikul, Ani, Smith, Albert V, Feitosa, Mary F, Demissie, Serkalem, Joshi, Peter K, Duan, Qing, Marten, Jonathan, van Klinken, Jan B, Surakka, Ida, Nolte, Ilja M, Zhang, Weihua, Mbarek, Hamdi, Li-Gao, Ruifang, Trompet, Stella, Verweij, Niek, Evangelou, Evangelos, Lyytikäinen, Leo-Pekka, Tayo, Bamidele O, Deelen, Joris, van der Most, Peter J, van der Laan, Sander W, Arking, Dan E, Morrison, Alanna, Dehghan, Abbas, Franco, Oscar H, Hofman, Albert, Rivadeneira, Fernando, Sijbrands, Eric J, Uitterlinden, Andre G, Mychaleckyj, Josyf C, Campbell, Archie, Hocking, Lynne J, Padmanabhan, Sandosh, Brody, Jennifer A, Rice, Kenneth M, White, Charles C, Harris, Tamara, Isaacs, Aaron, Campbell, Harry, Lange, Leslie A, Rudan, Igor, Kolcic, Ivana, Navarro, Pau, Zemunik, Tatijana, Salomaa, Veikko, Kooner, Angad S, Kooner, Jaspal S, Lehne, Benjamin, Scott, William R, Tan, Sian-Tsung, de Geus, Eco J, Milaneschi, Yuri, Penninx, Brenda W J H, Willemsen, Gonneke, de Mutsert, Renée, Ford, Ian, Gansevoort, Ron T, Segura-Lepe, Marcelo P, Raitakari, Olli T, Viikari, Jorma S, Nikus, Kjell, Forrester, Terrence, McKenzie, Colin A, de Craen, Anton J M, de Ruijter, Hester M, Pasterkamp, Gerard, Snieder, Harold, Oldehinkel, Albertine J, Slagboom, P Eline, Cooper, Richard S, Kähönen, Mika, Lehtimäki, Terho, Elliott, Paul, van der Harst, Pim, Jukema, J Wouter, Mook-Kanamori, Dennis O, Boomsma, Dorret I, Chambers, John C, Swertz, Morris, Ripatti, Samuli, Willems van Dijk, Ko, Vitart, Veronique, Polasek, Ozren, Hayward, Caroline, Wilson, James G, Wilson, James F, Gudnason, Vilmundur, Rich, Stephen S, Psaty, Bruce M, Borecki, Ingrid B, Boerwinkle, Eric, Rotter, Jerome I, Cupples, L Adrienne, van Duijn, Cornelia M
Publicado no J Med Genet (2016)