Four novel loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

- Ikram, M. Kamran, Xueling, Sim, Jensen, Richard A., Cotch, Mary Frances, Hewitt, Alex W., Attia, John, Holliday, Elizabeth G., Scott, Rodney J., Ikram, M. Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E. K., Breteler, Monique M. B.

Sifting the wheat from the chaff: prioritizing GWAS results by identifying consistency across analytical methods

- Oldmeadow, Christopher, Riveros, Carlos, Klein, Ronald, Attia, John, Holliday, Elizabeth G., Scott, Rodney, Moscato, Pablo, Wang, Jie Jin, Mitchell, Paul, Buitendijk, Gabrielle H. S., Vingerling, Johannes R., Klaver, Caroline C. W.

Are myocardial infarction-associated single-nucleotide polymorphisms associated with ischemic stroke?

- Cheng, Yu-Ching, Anderson, Christopher D., Barlera, Simona, Biffi, Alessandro, Bookman, Ebony, Brott, Thomas G., Brown, Robert D., Chen, Fang, Chen, Wei-Min, Ciusani, Emilio, Cole, John W., Cortellini, Lynelle, Bione, Silvia, Danesh, John, Doheny, Kimberley, Ferrucci, Luigi, Franzosi, Maria Grazia, Frossard, Philippe, Furie, Karen L., Golledge, Jonathan, Hankey, Graeme J., Hernandez, Dena, Holliday, Elizabeth G., Keene, Keith, Hsu, Fang-Chi, Jannes, Jim, Kamal, Ayeesha, Khan, Muhammad Saleem, Kittner, Steven J., Koblar, Simon A., Lewis, Martin, Lincz, Lisa, Lisa, Antonella, Matarin, Mar, Maguire, Jane M., Moscato, Pablo, Mychaleckyj, Josyf C., Parati, Eugenio A., Parolo, Silvia, Pugh, Elizabeth, Rost, Natalia S., Schallert, Michael, Schmidt, Helena, Scott, Rodney J., Sturm, Jonathan W., Nalls, Michael, Yadav, Sunaina, Zaidi, Moazzam, Boncoraglio, Giorgio B., Levi, Christopher Royce, Meschia, James F., Rosand, Jonathan, Sale, Michele, Saleheen, Danish, Schmidt, Reinhold, Sharma, Pankaj, Rasheed, Asif, Worrall, Bradford, Mitchell, Branxton D., Zeginigg, Marion, Attia, John, Baker, Ross

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

- Holliday, Elizabeth G., Maguire, Jane M., Malik, Rainer, McEvoy, Mark, Biros, Erik, Lewis, Martin D., Lincz, Lisa F., Peel, Roseanne, Oldmeadow, Christopher, Smith, Wayne, Moscato, Pablo, Barlera, Simona, Evans, Tiffany-Jane, Bevan, Steve, Bis, Joshua C., Boerwinkle, Eric, Boncoraglio, Giorgio B., Brott, Thomas G., Scott, Rodney J., Levi, Christopher, Attia, John, Koblar, Simon A., Jannes, Jim, Sturm, Jonathan W., Hankey, Graeme J., Baker, Ross, Golledge, Jonathan, Parsons, Mark W.

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

- Traylor, Matthew, Farrall, Martin, Thorsteinsdottir, Unnur, Nalls, Mike A., Longstreth, W. T., Wiggins, Kerri L., Yadav, Sunaina, Parati, Eugenio A., Destefano, Anita L., Worrall, Bradford B., Kittner, Steven J., Khan, Muhammad Saleem, Holliday, Elizabeth G., Reiner, Alex P., Helgadottir, Anna, Achterberg, Sefanja, Fernandez-Cadenas, Israel, Abboud, Sherine, Schmidt, Reinhold, Walters, Matthew, Chen, Wei-Min, Ringelstein, E. Bernd, O'Donnell, Martin, Sudlow, Cathie, Ho, Weang Kee, Pera, Joanna, Lemmens, Robin, Norrving, Bo, Higgins, Peter, Benn, Marianne, Sale, Michele, Kuhlenbaumer, Gregor, Doney, Alexander S. F., Vicente, Astrid M., Hopewell, Jemma C., Delavaran, Hossein, Algra, Ale, Davies, Gail, Oliveira, Sophia A., Palmer, Colin N. A., Deary, Ian, Schmidt, Helena, Pandolfo, Massimo, Montaner, Joan, Carty, Cara, Cheng, Yu-Ching, De Bakker, Paul I. W., Kostulas, Konstantinos, Ferro, Jose M., Van Zuydam, Natalie R., Valdimarsson, Einar, Nordestgaard, Berge G., Lindgren, Anne, Thijs, Vincent, Slowik, Agnieszka, Saleheen, Danish, Fornage, Myriam, Paré, Guillaume, Berger, Klaus, Thorleifsson, Gudmar, Astc, W., Hofman, Albert, Mosley, Thomas H., Mitchell, Branxton D., Furie, Karen, Clarke, Robert, Levi, Christopher, Arfan Ikram, M,, Seshadri, Sudha, Gschwendtner, Andreas, Boncoraglio, Giorgio B., Sharma, Pankaj, Bis, Joshua C., Gretarsdottir, Solveig, Psaty, Bruce M., Rothwell, Peter M., Rosand, Jonathan, Meschia, James F., Malik, Rainer, Stefansson, Kari, Dichgans, Martin, Markus, Hugh S., Bevan, Steve

Genome-wide association and functional follow-up reveals new loci for kidney function

- Pattaro, Cristian, Kottgen, Anna, Li, Man, Uitterlinden, Andre G., Rivadeneira, Fernando, Aulchenko, Yurii S., Polasek, Ozren, Hastie, Nick, Vitart, Veronique, Helmer, Catherine, Wang, Jie Jin, Ruggiero, Daniela, Bergmann, Sven, Gao, Xiaoyi, Kahonen, Mika, Viikari, Jorma, Nikopensius, Tiit, Province, Michael, Ketkar, Shamika, Colhoun, Helen, Doney, Alex, Robino, Antonietta, Giulianini, Franco, Kramer, Bernhard K., Gorski, Mathias, Portas, Laura, Ford, Ian, Buckley, Brendan M., Adam, Martin, Thun, Gian-Andri, Paulweber, Bernhard, Haun, Margot, Sala, Cinzia, Metzger, Marie, Mitchell, Paul, Yang, Qiong, Ciullo, Marina, King, Stuart K., Vollenweider, Peter, Raitakari, Olli, Metspalu, Andres, Palmer, Colin, Gasparini, Paolo, Pirastu, Mario, Jukema, J. Wouter, Probst-Hensch, Nicole M., Hundertmark, Claudia, Kronenberg, Florian, Toniolo, Daniela, Gudnason, Vilmundur, Shuldiner, Alan R., Coresh, Josef, Schmidt, Reinhold, Ferrucci, Luigi, Siscovick, David S., van Duijn, Cornelia M., Borecki, Ingrid, Foster, Meredith C., Kardia, Sharon L. R., Liu, Yongmei, Curhan, Gary C., Rudan, Igor, Gyllensten, Ulf, Wilson, James F., Franke, Andre, Pramstaller, Peter P., Retting, Rainer, Prokopenko, Inga, O'Seaghdha, Conall M., Witteman, Jacqueline C. M., Hayward, Caroline, Ridker, Paul, Parsa, Afshin, Bochud, Murielle, Heid, Iris M., Goessling, Wolfram, Chasman, Daniel I., Kao, W. H. Linda, Fox, Caroline S., Glazer, Nicole, Isaacs, Aaron, Liu, Ching-Ti, Teumer, Alexander, Smith, Albert V., O'Connell, Jeffrey R., Struchalin, Maksim, Tanaka, Toshiko, Li, Guo, Johnson, Andrew D., Gierman, Hinco J., Feitosa, Mary, Hwang, Shih-Jen, Atkinson, Elizabeth J., Garnaas, Maija, Lohman, Kurt, Cornelis, Marilyn C., Johansson, Asa, Tonjes, Anke, Dehghan, Abbas, Chouraki, Vincent, Holliday, Elizabeth G., Sorice, Rossella, Kutalik, Zoltan, Lehtimaki, Terho, Boger, Carsten A., Esko, Tonu, Deshmukh, Harshal, Ulivi, Sheila, Chu, Audrey Y., Murgia, Federico, Trompet, Stella, Imboden, Medea, Kollerits, Barbara, Pistis, Giorgio, CARDIoGRAM Consortium, Fuchsberger, Christian, ICBP Consortium, CARe Consortium, Wellcome Trust Case Control Consortium 2 (WTCCC2), Harris, Tamara B., Launer, Lenore J., Aspelund, Thor, Eiriksdottir, Gudny, Mitchell, Braxton D., Boerwinkle, Eric, Schmidt, Helena, Olden, Matthias, Cavalieri, Margherita, Rao, Madhumathi, Hu, Frank B., Demirkan, Ayse, Oostra, Ben A., de Andrade, Mariza, Turner, Stephen T., Ding, Jingzhong, Andrews, Jeanette S., Freedma, Barry I., Chen, Ming-Huei, Koenig, Wolfgang, Illig, Thomas, Doring, Angela, Wichmann, H.-Erich, Kolcic, Ivana, Zemunik, Tatijana, Boban, Mladen, Minelli, Cosetta, Wheeler, Heather E., Igl, Wilmar, Tin, Adrienne, Zaboli, Ghazal, Wild, Sarah H., Wright, Alan F., Campbell, Harry, Ellinghaus, David, Nothlings, Ute, Jacobs, Gunnar, Biffar, Reiner, Endlich, Karlhans, Ernst, Florian, Taliun, Daniel, Homuth, Georg, Kroemer, Heyo K., Nauck, Matthias, Stracke, Sylvia, Volker, Uwe, Volzke, Henry, Kovacs, Peter, Stumvoll, Michael, Magi, Reedik, Hofman, Albert

Genome-wide association meta-analysis identifies new endometriosis risk loci

- Nyholt, Dale R., Low, Siew-Kee, Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Knichi, Nakamura, Yusuke, Anderson, Carl A., Zondervan, Krina T., Zembutsu, Hitoshi, Montgomery, Grant W., Painter Jodie N., Yun-Chul, Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G.

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

- Chasman, Daniel I., Fuchsberger, Christian, Li, Man, Gao, Xiaoyi, Gorski, Mathias, Yang, Qiong, Hundertmark, Claudia, Foster, Meredith C., O'Seaghdha, Conall M., Glazer, Nicole, Isaacs, Aaron, Liu, Ching-Ti, Pattaro, Cristian, Holliday, Elizabeth G., Teumer, Alexander, Böger, Carsten A., Endlich, Karlhans, Olden, Matthias, Chen, Ming-Huei, Tin, Aadrienne, Taliun, Daniel

17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status

- Adib-Samii, Poneh, Rost, Natalia, Gschwendtner, Andreas, Malik, Rainer, Richie, Alexa, Gamble, Dale, Segal, Helen, Parati, Eugenio A., Ciusani, Emilio, Holliday, Elizabeth G., Maguire, Jane, Wardlaw, Joanna, Traylor, Matthew, Worrall, Bradford, Bis, Joshua, Wiggins, Kerri L., Longstreth, Will, Kittner, Steve J., Cheng, Yu-Ching, Mosley, Thomas, Falcone, Guido J., Furie, Karen L., Leiva-Salinas, Carlos, Devan, William, Lau, Benison C., Saleem Khan, Muhammed, Australian Stroke Genetics Collaborative, Wellcome Trust Case-Control Consortium-2, METASTROKE, Sharma, Pankaj, Fornage, Miriam, Mitchell, Braxton D., Psaty, Bruce M., Sudlow, Cathie, Biffi, Alessandro, Levi, Christopher, Boncoraglio, Giorgio B., Rothwell, Peter M., Meschia, James, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S., Lanfranconi, Silvia, Fitzpatrick, Kaitlin, Bevan, Steve, Kanakis, Allison, Valant, Valerie

Candidate gene association studies in stroke

- Holliday, Elizabeth G., Oldmeadow, Christopher J., Maguire, Jane M., Attia, John

Common variants in mendelian kidney disease genes and their association with renal function

- Parsa, Afshin, Fuchsberger, Christian, Chen, Ming-Huei, Tin, Adrienne, Kim, Young J., Taliun, Daniel, Li, Man, Pramstaller, PP, Feotosa, Mary, Gorski, Mathias, Yang, Qiong, Hundertmark, Claudia, Köttgen, Anna, Holliday, Elizabeth G., O'Seaghdha, Conall M., Pattaro, Cristian, de Andrade, Mariza, Chasman, Daniel I., Teumer, Alexander, Endlich, Karlhans, Olden , Matthias

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

- Talseth-Palmer, Bente A., Holliday, Elizabeth G., Evans, Tiffany-Jane, McEvoy, Mark, Attia, John, Grice, Desma M., Masson, Amy L., Meldrum, Cliff, Spigelman, Allan, Scott, Rodney J.

Genetic association of refractive error and axial length with 15q14 but not 15q25 in the Blue Mountains Eye Study Cohort

- Schache, Maria, Richardson, Andrea J., Sim, Xueling, Holliday, Elizabeth G., Attia, John, Scott, Rodney J., Baird, Paul N., Mitchell, Paul, Wang, Jie Jin, Rochtchina, Elena, Viswanathan, Anath C., Wong, Tien Y., Saw, Seang Mei, Topouzis, Fotis, Xie, Jing

Genetic loci for retinal arteriolar microcirculation

- Sim, Xueling, Jensen, Richard A., Klein, Ronald, Klein, Barbara E. K., Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., de Jong, Paulus T. V. M., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G., Ikram, M. Kamran, van Duijn, Cornelia M., Aspelund, Thor, Eiriksdottir, Gudny, Harris, Tamara B., Jonasson, Fridbert, Launer, Lenore J., The Wellcome Trust Case Control Consortium, Attia, John, Baird, Paul N., Harrap, Stephen, Cotch, Mary Frances, Holliday, Elizabeth G., Inouye, Michael, Rochtchina, Elena, Scott, Rodney J., Viswanathan, Ananth, Global BPGen Consortium, Li, Guo, Smith, Nicholas L., Wiggins, Kerri L., Kuo, Jane Z., Li, Xiaohui, Taylor, Kent D., Hewitt, Alex W., Martin, Nicholas G., Montgomery, Grant W., Sun, Cong, Young, Terri L., Mackey, David A., van Zuydam, Natalie R., Doney, Alex S. F., Palmer, Colin N. A., MacGregor, Stuart, Morris, Andrew D., Rotter, Jerome I., Tai, E. Shyong, Gudnason, Vilmundur, Vingerling, Johannes R., Siscovick, David S., Wang, Jie Jin, Wong, Tien Y., Xie, Jing, Smith, Albert Vernon, Boerwinkle, Eric, Mitchell, Paul

Genome-wide analysis of blood pressure variability and ischemic stroke

- Yadav, Sunaina, Cotlarciuc, Ioana, Holliday, Elizabeth G., Speed, Douglas, Hasan, Nazeeha, Pucek, Mateusz, Rinne, Paul E., Sever, Peter, Stanton, Alice, Shields, Denis C., Maguire, Jane M., McEvoy, Mark, Munroe, Patricia B., Scott, Rodney J., Ferrucci, Luigi, Macleod, Mary J., Attia, John, Markus, Hugh S., Sale, Michele M., Worrall, Bradford B., Mitchell, Braxton D., Dichgans, Martin, Sudlow, Cathy, Khan, Muhammad S., Meschia, James F., Rothwell, Peter M., Caulfield, Mark, Sharma, Pankaj, International Stroke Genetics Consortium,, Nalls, Michael A., Bevan, Steve, Cheng, Yu-Ching, Chen, Wei-Min, Malik, Rainer, McCarthy, Nina S.

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

- Köttgen, Anna, Albrecht, Eva, Yang, Qiong, Tanaka, Toshiko, Johnson, Andrew D., Kutalik, Zoltán, Smith, Albert V., Shi, Julia, Struchalin, Maksim, Middelberg, Rita P. S., Brown, Morris J., Gaffo, Angelo L., Teumer, Alexander, Oldmeadow, Christopher, Scott, Rodney J., Holliday, Elizabeth G., Attia, John, Vitart, Veronique, Krumsiek, Jan, Hundertmark, Claudia, Pistis, Giorgio, Ruggiero, Daniela, O'Seaghdha, Conall M., Haller, Toomas

Genome-wide association study of retinopathy in individuals without diabetes

- Jensen, Richard A., Sim, Xueling, Launer, Lenore J., Smith, Albert Vernon, Boerwinkle, Eric, Cheung, Ning, Hewitt, Alex W., Liew, Gerald, Mitchell, Paul, Wang, Jie Jin, Attia, John, Scott, Rodney, Li, Xiaohui, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Taylor, Kent, Hofman, Albert, de Jong, Paulus T. V. M., Rivadeneira, Fernando, Uitterlinden, Andre G., Tay, Wan-Ting, Cotch, Mary Frances, Teo, Yik Ying, Seielstad, Mark, Liu, Jianjun, Cheng, Ching-Yu, Saw, Seang-Mei, Aung, Tin, Ganesh, Santhi K., O'Donnell, Christopher J., Nalls, Mike A., Wiggins, Kerri L., Ikram, M. Kamran, Kuo, Jane Z., The Blue Mountains Eye Study GWAS Team, CKDGen Consortium, Klein, Cornelia M., van Duijn, Cornelia M., Gudnason, Vilmundur, Klein, Ronald, Siscovick, David S., Rotter, Jerome I., Tai, E. Shong, Holliday, Elizabeth G., Vingerling, Johannes, Wong, Tien Y., Eiriksdottir, Gudny, Harris, Tamara B., Jonasson, Fridbert, Klein, Barbara E. K.

Hints of unique genetic effects for type 2 diabetes in India

- Holliday, Elizabeth G.

Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis

- Holliday, Elizabeth G., Smith, Albert V., 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, Cornes, Belinda K., Li, Xiaohui, Liew, Gerald, Lumley, Thomas, McElduff, Patrick, McKnight, Barbara, Mitchell, Paul, Psaty, Bruce M., Rochtchina, Elena, Rotter, Jerome I., Scott, Rodney J., Buitendijk, Gabrielle H. S., Tay, Wanting, Taylor, Kent, Teo, Yik Ying, Uitterlinden, Andre G., Viswanathan, Ananth, Xie, Sophia, Wellcome Trust Case Control Consortium, Vingerling, Johannes R., Klaver, Caroline C. W., Tai, E. Shyong, Jensen, Richard A., Siscovick, David, Klein, Ronald, Cotch, Mary Frances, Wong, Tien Y., Attia, John, Wang, Jie Jin, Sim, Xueling, Aspelund, Thor, Aung, Tin, Baird, Paul N., Boerwinkle, Eric

Investigation of the relationship between sleep duration, all-cause mortality, and preexisting disease

- Magee, Christoper A., Holliday, Elizabeth G., Attia, John, Kritharides, Leonard, Banks, Emily