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Bradfield, Jonathan P., Taal, H. Rob, Timpson, Nicholas J., Scherag, André, Lecoeur, Cecile, Warrington, Nicole M., Hypponen, Elina, Holst, Claus, Valcarcel, Beatriz, Thiering, Elisabeth, Salem, Rany M., Schumacher, Fredrick R., Cousminer, Diana L., Sleiman, Patrick M. A., Zhao, Jianhua, Berkowitz, Robert I., Vimaleswaran, Karani S., Jarick, Ivonne, Pennell, Craig E., Evans, David M., St Pourcain, Beate, Berry, Diane J., Mook-Kanamori, Dennis O., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, André G., van Duijn, Cornelia M., van der Valk, Ralf J. P., de Jongste, Johan C., Postma, Dirkje S., Boomsma, Dorret I., Gauderman, W. James, Hassanein, Mohamed T., Lindgren, Cecilia M., Mägi, Reedik, Boreham, Colin A. G., Neville, Charlotte E., Moreno, Luis A., Elliott, Paul, Pouta, Anneli, Hartikainen, Anna-Liisa, Li, Mingyao, Raitakari, Olli, Lehtimäki, Terho, Eriksson, Johan G., Palotie, Aarno, Dallongeville, Jean, Das, Shikta, Deloukas, Panos, McMahon, George, Ring, Susan M., Kemp, John P., Buxton, Jessica L., Blakemore, Alexandra I. F., Bustamante, Mariona, Guxens, Mònica, Hirschhorn, Joel N., Gillman, Matthew W., Kreiner-Møller, Eskil, Bisgaard, Hans, Gilliland, Frank D., Heinrich, Joachim, Wheeler, Eleanor, Barroso, Inês, O'Rahilly, Stephen, Meirhaeghe, Aline, Sørensen, Thorkild I. A., Power, Chris, Palmer, Lyle J., Hinney, Anke, Widen, Elisabeth, Farooqi, I. Sadaf, McCarthy, Mark I., Froguel, Philippe, Meyre, David, Hebebrand, Johannes, Jarvelin, Marjo-Riitta, Jaddoe, Vincent W. V., Smith, George Davey, Hakonarson, Hakon and Grant, Struan F. A. (2012) A genome-wide association meta-analysis identifies new childhood obesity loci. Nature Genetics, 44 5: 526-531. doi:10.1038/ng.2247     185 Cited 192 times in Scopus192 50
Byrne, Enda M., Gehrman, Philip R., Medland, Sarah E., Nyholt, Dale R., Heath, Andrew C., Madden, Pamela A. F., Hickie, Ian B., Van Duijn, Cornelia M., Henders, Anjali K., Montgomery, Grant W., Martin, Nicholas G., Wray, Naomi R. and The Chronogen Consortium (2013) A genome-wide association study of sleep habits and insomnia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162 5: 439-451. doi:10.1002/ajmg.b.32168   87 44 Cited 42 times in Scopus42 4
Direk, Nese, Williams, Stephanie, Smith, Jennifer A., Ripke, Stephan, Air, Tracy, Amare, Azmeraw T., Amin, Najaf, Baune, Bernhard T., Bennett, David A., Blackwood, Douglas H. R., Boomsma, Dorret, Breen, Gerome, Buttenschon, Henriette N., Byrne, Enda M., Borglum, Anders D., Castelao, Enrique, Cichon, Sven, Clarke, Toni-Kim, Cornelis, Marilyn C., Dannlowski, Udo, De Jager, Philip L., Demirkan, Ayse, Domenici, Enrico, van Duijn, Cornelia M., Dunn, Erin C., Eriksson, Johan G., Esko, Tonu, Faul, Jessica D., Ferrucci, Luigi, Fornage, Myriam, de Geus, Eco, Gill, Michael, Gordon, Scott D., Grabe, Hans Jörgen, van Grootheest, Gerard, Hamilton, Steven P., Hartman, Catharina A., Heath, Andrew C., Hek, Karin, Hofman, Albert, Homuth, Georg, Horn, Carsten, Jan Hottenga, Jouke, Kardia, Sharon L. R., Kloiber, Stefan, Koenen, Karestan, Kutalik, Zoltán, Ladwig, Karl-Heinz, Lahti, Jari, Levinson, Douglas F., Lewis, Cathryn M., Lewis, Glyn, Li, Qingqin S., Llewellyn, David J., Lucae, Susanne, Lunetta, Kathryn L., MacIntyre, Donald J., Madden, Pamela, Martin, Nicholas G., McIntosh, Andrew M., Metspalu, Andres, Milaneschi, Yuri, Montgomery, Grant W., Mors, Ole, Mosley, Thomas H., Murabito, Joanne M., Muller-Myhsok, Bertram, Nothen, Markus M., Nyholt, Dale R., O'Donovan, Michael C., Penninx, Brenda W., Pergadia, Michele L., Perlis, Roy, Potash, James B., Preisig, Martin, Purcell, Shaun M., Quiroz, Jorge A., Raikkonen, Katri, Rice, John P., Rietschel, Marcella, Rivera, Margarita, Schulze, Thomas G., Shi, Jianxin, Shyn, Stanley, Sinnamon, Grant C., Smit, Johannes H., Smoller, Jordan W., Snieder, Harold, Tanaka, Toshiko, Tansey, Katherine E., Teumer, Alexander, Uher, Rudolf, Umbricht, Daniel, Van der Auwera, Sandra, Ware, Erin B., Weir, David R., Weissman, Myrna M., Willemsen, Gonneke, Yang, Jingyun, Zhao, Wei, Tiemeier, Henning and Sullivan, Patrick F. (2016) An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biological Psychiatry, 82 5: 322-329. doi:10.1016/j.biopsych.2016.11.013     16 Cited 19 times in Scopus19 10
McCarthy, Shane, Das, Sayantan, Kretzschmar, Warren, Delaneau, Olivier, Wood, Andrew R., Teumer, Alexander, Kang, Hyun Min, Fuchsberger, Christian, Danecek, Petr, Sharp, Kevin, Luo, Yang, Sidore, Carlo, Kwong, Alan, Timpson, Nicholas, Koskinen, Seppo, Vrieze, Scott, Scott, Laura J., Zhang, He, Mahajan, Anubha, Veldink, Jan, Peters, Ulrike, Pato, Carlos, Van Duijn, Cornelia M., Gillies, Christopher E., Gandin, Ilaria, Mezzavilla, Massimo, Gilly, Arthur, Cocca, Massimiliano, Traglia, Michela, Angius, Andrea, Barrett, Jeffrey C., Boomsma, Dorrett, Branham, Kari, Breen, Gerome, Brummett, Chad M., Busonero, Fabio, Campbell, Harry, Chan, Andrew, Chen, Sai, Chew, Emily, Collins, Francis S., Corbin, Laura J., Smith, George Davey, Dedoussis, George, Dorr, Marcus, Farmaki, Aliki-Eleni, Ferrucci, Luigi, Forer, Lukas, Fraser, Ross M., Gabriel, Stacey, Levy, Shawn, Groop, Leif, Harrison, Tabitha, Hattersley, Andrew, Holmen, Oddgeir L., Hveem, Kristian, Kretzler, Matthias, Lee, James C., McGue, Matt, Meitinger, Thomas, Melzer, David, Min, Josine L., Mohlke, Karen L., Vincent, John B., Nauck, Matthias, Nickerson, Deborah, Palotie, Aarno, Pato, Michele, Pirastu, Nicola, McInnis, Melvin, Richards, J Brent, Sala, Cinzia, Salomaa, Veikko, Schlessinger, David, Schoenherr, Sebastian, Slagboom, P Eline, Small, Kerrin, Spector, Timothy, Stambolian, Dwight, Tuke, Marcus, Tuomilehto, Jaakko, Van Den Berg, Leonard H., Van Rheenen, Wouter, Volker, Uwe, Wijmenga, Cisca, Toniolo, Daniela, Zeggini, Eleftheria, Gasparini, Paolo, Sampson, Matthew G., Wilson, James F., Frayling, Timothy, De Bakker, Paul I. W., Swertz, Morris A., McCarroll, Steven, Kooperberg, Charles, Dekker, Annelot, Altshuler, David, Willer, Cristen, Iacono, William, Ripatti, Samuli, Soranzo, Nicole, Walter, Klaudia, Swaroop, Anand, Cucca, Francesco, Anderson, Carl A., Myers, Richard M., Boehnke, Michael, McCarthy, Mark I., Durbin, Richard, Abecasis, Gonçalo and Marchini, Jonathan (2016) A reference panel of 64,976 haplotypes for genotype imputation. Nature Genetics, 48 10: 1279-1283. doi:10.1038/ng.3643     224 Cited 242 times in Scopus242 162
Springelkamp, Henriet, Iglesias, Adriana I., Cuellar-Partida, Gabriel, Amin, Najaf, Burdon, Kathryn P., van Leeuwen, Elisabeth M., Gharahkhani, Puya, Mishra, Aniket, van der Lee, Sven J., Hewitt, Alex W., Rivadeneira, Fernando, Viswanathan, Ananth C., Wolfs, Roger C. W., Martin, Nicholas G., Ramdas, Wishal D., van Koolwijk, Leonieke M., Pennell, Craig E., Vingerling, Johannes R., Mountain, Jenny E., Uitterlinden, Andre G., Hofman, Albert, Mitchell, Paul, Lemij, Hans G., Wang, Jie Jin, Klaver, Caroline C. W., Mackey, David A., Craig, Jamie E., van Duijn, Cornelia M. and MacGregor, Stuart (2015) ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure. Human Molecular Genetics, 24 9: 2689-2699. doi:10.1093/hmg/ddv027     27 Cited 28 times in Scopus28 4
Fernández-Rhodes, Lindsay, Demerath, Ellen W., Cousminer, Diana L., Tao, Ran, Dreyfus, Jill G., Esko, Tõnu, Smith, Albert V., Gudnason, Vilmundur, Harris, Tamara B., Launer, Lenore, McArdle, Patrick F., Yerges-Armstrong, Laura M., Elks, Cathy E., Strachan, David P., Kutalik, Zoltán, Vollenweider, Peter, Feenstra, Bjarke, Boyd, Heather A., Metspalu, Andres, Mihailov, Evelin, Broer, Linda, Zillikens, M. Carola, Oostra, Ben, van Duijn, Cornelia M., Lunetta, Kathryn L., Perry, John R. B., Murray, Anna, Koller, Daniel L., Lai, Dongbing, Corre, Tanguy, Toniolo, Daniela, Albrecht, Eva, Stöckl, Doris, Grallert, Harald, Gieger, Christian, Hayward, Caroline, Polasek, Ozren, Rudan, Igor, Wilson, James F., He, Chunyan, Kraft, Peter, Hu, Frank B., Hunter, David J., Hottenga, Jouke-Jan, Willemsen, Gonneke, Boomsma, Dorret I., Byrne, Enda M., Martin, Nicholas G., Montgomery, Grant W., Warrington, Nicole M., Pennell, Craig E., Stolk, Lisette, Visser, Jenny A., Hofman, Albert, Uitterlinden, André G., Rivadeneira, Fernando, Lin, Peng, Fisher, Sherri L., Bierut, Laura J., Crisponi, Laura, Porcu, Eleonora, Mangino, Massimo, Zhai, Guangju, Spector, Tim D., Buring, Julie E., Rose, Lynda M., Ridker, Paul M., Poole, Charles, Hirschhorn, Joel N., Murabito, Joanne M., Chasman, Daniel I., Widen, Elisabeth, North, Kari E., Ong, Ken K. and Franceschini, Nora (2013) Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. American Journal of Epidemiology, 178 3: 451-460. doi:10.1093/aje/kws473     28 Cited 27 times in Scopus27 6
Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., De Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, Van Der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, Van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent, Karjalainen, Juha, Laibson, David, Lichtenstein, Paul, Liewald, David C., Magnusson, Patrik K. E., Martin, Nicholas G., McGue, Matt, McMahon, George, Pedersen, Nancy L., Pinker, Steven, Porteous, David J., Posthuma, Danielle, Rivadeneira, Fernando, Smithk, Blair H., Starr, John M., Tiemeier, Henning, Timpsonm, Nicholas J., Trzaskowskin, Maciej, Uitterlinden, Andre G., Verhulst, Frank C., Ward, Mary E., Wright, Margaret J., Smith, George Davey, Deary, Ian J., Johannesson, Magnus, Plomin, Robert, Visscher, Peter M., Benjamin, Daniel J., Cesarini, David and Koellinger, Philipp D. (2014) Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences of the United States of America, 111 38: 13790-13794. doi:10.1073/pnas.1404623111     84 Cited 90 times in Scopus90 330
Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., de Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, van der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent, Karjalainen, Juha, Laibson, David, Lichtenstein, Paul, Liewald, David C., Magnusson, Patrik K. E., Martin, Nicholas G., McGue, Matt, McMahon, George, Pedersen, Nancy L., Pinker, Steven, Porteous, David J., Posthuma, Danielle, Rivadeneira, Fernando, Smith, Blair H., Starr, John M., Tiemeier, Henning, Timpson, Nicholas J., Trzaskowski, Maciej, Uitterlinden, Andre G., Verhulst, Frank C., Ward, Mary E., Wright, Margaret J., Smith, George Davey, Deary, Ian J., Johannesson, Magnus, Plomin, Robert, Visscher, PeterM., Benjamin, Daniel J., Cesarini, David and Koellinger, Philipp D. (2014) Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014). Proceedings of the National Academy of Sciences of the United States of America, 112 4: E380-E380. doi:10.1073/pnas.1424631112     3 0 0
Xiao, Xiao, Wang, Lu, Wang, Chuang, Yuan, Ti-Fei, Zhou, Dongsheng, Zheng, Fanfan, Li, Lingyi, Grigoroiu-Serbanescu, Maria, Ikeda, Masashi, Iwata, Nakao, Takahashi, Atsushi, Kamatani, Yoichiro, Kubo, Michiaki, Preisig, Martin, Kutalik, Zoltán, Castelao, Enrique, Pistis, Giorgio, Amin, Najaf, Van Duijn, Cornelia M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Schofield, Peter R., Cichon, Sven, Nöthen, Markus M., Chang, Hong, Luo, Xiong-Jian, Fang, Yiru, Yao, Yong-Gang, Zhang, Chen, Rietschel, Marcella, Li, Ming, Advanced Collaborative Study of Mood Disorder (COSMO) Team and MooDS Bipolar Consortium (2017) Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. Translational Psychiatry, 7 12: . doi:10.1038/s41398-017-0019-0     0 Cited 1 times in Scopus1 2
Nyholt, Dale R., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer, Vries, Boukje De, Terwindt, Gisela M., Ikram, M Arfan, Stam, Anine H., Ligthart, Lannie, Freilinger, Tobias, Alexander, Michael, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Aromaa, Arpo, Eriksson, Johan G., Kaprio, Jaakko, Boomsma, Dorret I., Duijn, Cornelia Van, Raitakari, Olli, Järvelin, Marjo-Riitta, Zwart, John-Anker, Quaye, Lydia, Strachan, David P., Kubisch, Christian, Ferrari, Michel D., Van Den Maagdenberg, Arn M. J. M., Dichgans, Martin, Wessman, Maija, Smith, George Davey, Stefansson, Kari, Chasman, Daniel I. and Palotie, Aarno (2015) Concordance of genetic risk across migraine subgroups: impact on current and future genetic association studies. Cephalalgia, 35 6: 489-499. doi:10.1177/0333102414547784     14 Cited 15 times in Scopus15 1
Patsopoulos, Nikolaos A., Barcellos, Lisa F., Hintzen, Rogier Q., Schaefer, Catherine, Van Duijn, Cornelia M., Noble, Janelle A., Raj, Towfique, Gourraud, Pierre-Antoine, Stranger, Barbara E., Oksenberg, Jorge, Olsson, Tomas, Taylor, Bruce V., Sawcer, Stephen, Hafler, David A., Carrington, Mary, De Jager, Philip L., De Bakker, Paul I. W., ANZgene and Brown, Matthew A. (2013) Fine-mapping the genetic association of the major histocompatibility complex in Multiple sclerosis: HLA and non-HLA effects. PLoS Genetics, 9 11: e1003926. doi:10.1371/journal.pgen.1003926     88 Cited 99 times in Scopus99 18
van der Valk, Ralf J. P., Duijts, Liesbeth, Timpson, Nicolas J., Salam, Muhammad T., Standl, Marie, Curtin, John A., Genuneit, Jon, Kerhof, Marjan, Kreiner-Møller, Eskil, Cáceres, Alejandro, Gref, Anna, Liang, Liming L., Taal, H. Rob, Bouzigon, Emmanuelle, Demenais, Florence, Nadif, Rachel, Ober, Carole, Thompson, Emma E., Estrada, Karol, Hofman, Albert, Uitterlinden, André G., van Duijn, Cornélia, Rivadeneira, Fernando, Li, Xia, Eckel, Sandrah P., Berhane, Kiros, Gauderman, W. James, Granell, Raquel, Evans, David M., St Pourcain, Beate, McArdle, Wendy, Kemp, John P., Smith, George Davey, Tiesler, Carla M. T., Flexeder, Claudia, Simpson, Angela, Murray, Clare S., Fuchs, Oliver, Postma, Dirkje S., Bønnelykke, Klaus, Torrent, Maties, Andersson, Martin, Sleiman, Patrick, Hakonarson, Hakon, Cookson, William O., Moffatt, Miriam F., Paternoster, Lavinia, Melén, Erik, Sunyer, Jordi, Bisgaard, Hans, Koppelman, Gerard H., Ege, Markus, Custovic, Adnan, Heinrich, Joachim, Gilliland, Frank D., Henderson, Alexander J., Jaddoe, Vincent W. V. and de Jongste, Johan C. (2013) Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants. Journal of Allergy and Clinical Immunology, 134 1: 46-55. doi:10.1016/j.jaci.2013.08.053   1 21 Cited 20 times in Scopus20 4
Zhao, Huiying, Eising, Else, De Vries, Boukje, Vijfhuizen, Lisanne S., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer, Stam, Anine H., Arfan Ikram, M., Ligthart, Lannie, Freilinger, Tobias, Alexander, Michael, Müller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Aromas, Arpo, Eriksson, Johan G., Boomsma, Dorret I., Van Duijn, Cornelia M., Zwart, John-Anker, Quaye, Lydia, Kubisch, Christian, Dichgans, Martin, Wessman, Maija, Stefansson, Kari, Chasman, Daniel I., Palotie, Aarno, Martin, Nicholas G., Montgomery, Grant W., Ferrari, Michel D., Terwindt, Gisela M., Van Den Maagdenberg, Arn M. J. M. and Nyholt, Dale R. (2016) Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia, 36 7: 648-657. doi:10.1177/0333102415591497     13 Cited 14 times in Scopus14 2
Eising, Else, Huisman, Sjoerd M. H., Mahfouz, Ahmed, Vijfhuizen, Lisanne S., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Ikram, M. Arfan, Freilinger, Tobias, Kaprio, Jaakko, Boomsma, Dorret I., van Duijn, Cornelia M., Järvelin, Marjo-Riitta R., Zwart, John-Anker, Quaye, Lydia, Strachan, David P., Kubisch, Christian, Dichgans, Martin, Davey Smith, George, Stefansson, Kari, Palotie, Aarno, Chasman, Daniel I., Ferrari, Michel D., Terwindt, Gisela M., de Vries, Boukje, Nyholt, Dale R., Lelieveldt, Boudewijn P. F., van den Maagdenberg, Arn M. J. M. and Reinders, Marcel J. T. (2016) Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas. Human Genetics, 135 4: 425-439. doi:10.1007/s00439-016-1638-x     11 Cited 12 times in Scopus12 12
Jacqueline M. Vink1, August B. Smit, Eco J.C. de Geus, Patrick Sullivan, Gonneke Willemsen, Jouke-Jan Hottenga, Johannes H. Smit, Witte J. Hoogendijk, Frans G. Zitman, Leena Peltonen, Jaakko Kaprio, Nancy L. Pedersen, Patrik K. Magnusson, Tim D. Spector, Kirsten Ohm Kyvik, Katherine I. Morley, Andrew C. Heath, Nicholas G. Martin, Rudi G.J. Westendorp, P. Eline Slagboom, Henning Tiemeier, Albert Hofman, Andre G. Uitterlinden, Yurii S. Aulchenko, Najaf Amin, Cornelia van Duijn, Brenda W. Penninx and Dorret I. Boomsma (2009) Genome-wide Association Study of Smoking Initiation and Current Smoking. American Journal of Human Genetics, 84 3: 367-379. doi:10.1016/j.ajhg.2009.02.001     95 Cited 97 times in Scopus97 6
Francioli, Laurent C., Polak, Paz P., Koren, Amnon, Menelaou, Androniki, Chun, Sung, Renkens, Ivo, van Duijn, Cornelia M., Swertz, Morris, Wijmenga, Cisca, van Ommen, Gertjan, Slagboom, P. Eline, Boomsma, Dorret I., Ye, Kai, Guryev, Victor, Arndt, Peter F., Kloosterman, Wigard P., de Bakker, Paul I. W., Sunyaev, Shamil R., Genome of the Netherlands Consortium and Li, Yingrui (2015) Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics, 47 7: 822-826. doi:10.1038/ng.3292     108 Cited 110 times in Scopus110 176
Roshchupkin, Gennady V., Gutman, Boris A., Vernooij, Meike W., Jahanshad, Neda, Martin, Nicholas G., Hofman, Albert, McMahon, Katie L., van der Lee, Sven J., Van Duijn, Cornelia M., de Zubicaray, Greig I., Uitterlinden, Andre´ G., Wright, Margaret J., Niessen, Wiro J., Thompson, Paul M., Ikram, M. Arfan and Adams, Hieab H.H. (2016) Heritability of the shape of subcortical brain structures in the general population. Nature Communications, 7 13738. doi:10.1038/ncomms13738     9 Cited 13 times in Scopus13 12
Lopes, Margarida C., Hysi, Pirro G., Verhoeven, Virginie J. M., Macgregor, Stuart, Hewitt, Alex W., Montgomery, Grant W., Cumberland, Phillippa, Vingerling, Johannes R., Young, Terri L., van Duijn, Cornelia M., Oostra, Ben, Uitterlinden, Andre G., Rahi, Jugnoo S., Mackey, David A., Klaver, Caroline C. W., Andrew, Toby and Hammond, Christopher J. (2013) Identification of a candidate gene for astigmatism. Investigative Ophthalmology and Visual Science, 54 2: 1260-1267. doi:10.1167/iovs.12-10463     20 Cited 21 times in Scopus21 1
Holliday, Elizabeth G., Smith, Albert V., Cornes, Belinda K., Buitendijk, Gabrielle H. S., Jensen, Richard A., Sim, Xueling, Aspelund, Thor, Aung, Tin, Baird, Paul N., Boerwinkle, Eric, Cheng, Ching Yu, van Duijn, Cornelia M., Eiriksdottir, Gudny, Gudnason, Vilmundur, Harris, Tamara, Hewitt, Alex W., Inouye, Michael, Jonasson, Fridbert, Klein, Barbara E. K., Launer, Lenore, Li, Xiaohui, Liew, Gerald, Lumley, Thomas, McElduff, Patrick, McKnight, Barbara, Mitchell, Paul, Psaty, Bruce M., Rochtchina, Elena, Rotter, Jerome I., Scott, Rodney J., Tay, Wanting, Taylor, Kent, Teo, Yik Ying, Uitterlinden, Andre G., Viswanathan, Ananth, Xie, Sophia, Vingerling, Johannes R., Klaver, Caroline C. W., Tai, E. Shyong, Siscovick, David, Klein, Ronald, Cotch, Mary Frances, Wong, Tien Y., Attia, John, Wang, Jie Jin and Wellcome Trust Case Control Consortium 2 (2013) Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis. PLoS One, 8 1: e53830. doi:10.1371/journal.pone.0053830     84 Cited 69 times in Scopus69 1
Luciano, Michelle, Lopez, Lorna M., de Moor, Marleen H. M., Harris, Sarah E., Davies, Gail, Nutile, Teresa, Krueger, Robert F., Esko, Tonu, Schlessinger, David, Toshiko, Tanaka, Derringer, Jaime L., Realo, Anu, Hansell, Narelle K., Pergadia, Michele L., Pesonen, Anu-Katriina, Sanna, Serena, Terracciano, Antonio, Madden, Pamela A. F., Penninx, Brenda, Spinhoven, Philip, Hartman, Catherina A., Oostra, Ben A., Janssens, A. Cecile J. W., Eriksson, Johan G., Starr, John M., Cannas, Alessandra, Ferrucci, Luigi, Metspalu, Andres, Wright, Margeret J., Heath, Andrew C., van Duijn, Cornelia M., Bierut, Laura J., Raikkonen, Katri, Martin, Nicholas G., Ciullo, Marina, Rujescu, Dan, Boomsma, Dorret I. and Deary, Ian J. (2012) Longevity candidate genes and their association with personality traits in the elderly. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159 B 2: 192-200. doi:10.1002/ajmg.b.32013     6 Cited 6 times in Scopus6 4
Ligthart, Lannie, de Vries, Boukje, Smith, Albert V., Ikram, M. Arfan, Amin, Najaf, Hottenga, Jouke-Jan, Koelewijn, Stephany C., Kattenberg, V. Mathijs, de Moor, Marleen H. M., Janssens, A. Cecile J. W., Aulchenko, Yurii S., Oostra, Ben A., de Geus, Eco J. C., Smit, Johannes H., Zitman, Frans G., Uitterlinden, Andre G., Hofman, Albert, Willemsen, Gonneke, Nyholt, Dale R., Montgomery, Grant W., Terwindt, Gisela M., Gudnason, Vilmundur, Penninx, Brenda W. J. H., Breteler, Monique, Ferrari, Michel D., Launer, Lenore J., van Duijn, Cornelia M., van den Maagdenberg, Arn M. J. M. and Boomsma, Dorret I. (2011) Meta-analysis of genome-wide association for migraine in six population-based European cohorts. European Journal of Human Genetics, 19 8: 901-907. doi:10.1038/ejhg.2011.48     55 Cited 60 times in Scopus60 0
de Moor, Marleen H. M., Boomsma, Dorret, I, de Geus, Eco J. C., Willemsen, Gonneke, Hottenga, Jouke-Jan, Distel, Marijn A., Abecasis, Goncalo R., Terracciano, Antonio, McCrae, Robert R., Costa, Paul T., Hartman, Catharina A., Spinhoven, Philip, Penninx, Brenda W., Esko, Tonu, Allik, Jueri, Realo, Anu, Metspalu, Andres, Hansell, Narelle K., Medland, Sarah E., Wray, Naomi R., Wright, Margie J., Martin, Nicholas G., Amin, Najaf, Aulchenko, Yurii S., Janssens, A. Cecile, Oostra, Ben A. and van Duijn, Cornelia M. (2009). Meta-analysis of genome-wide association results in > 10.000 individuals for the big five personality traits. In: 39th Annual Meeting of the Behavior Genetics Association, Mineapolis, MN, United States, (643-643). 17-20 June 2009 .     3
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