Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

- Schmidt, Amand F., Holmes, Michael V., Preiss, David, Swerdlow, Daniel I., Denaxas, Spiros, Fatemifar, Ghazaleh, Faraway, Rupert, Finan, Chris, Valentine, Dennis, Fairhurst-Hunter, Zammy, Hartwig, Fernando Pires, Horta, Bernardo Lessa, Hypponen, Elina, Power, Christine, Moldovan, Max, van Iperen, Erik, Hovingh, Kees, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Hancock, Stephen, Attia, John, Holliday, Elizabeth, Scott, Rodney, Teumer, A, Baumeister, S, Doerr, M, Lerch, MM, Voelker, U, Voelzke, H, Ward, J, Pell, JP, Meade, T, Christophersen, IE, Maitland-van der Zee, AH, Baranova, EV, Young, R, Ford, I, Campbell, A, Padmanabhan, S, Bots, ML, Grobbee, DE, Froguel, P, Thuillier, D, Roussel, R, Bonnefond, A, Cariou, B, Smart, M, Bao, Y, Kumari, M, Mahajan, A, Hopewell, JC, Seshadri, S, Dale, C, Costa, RPE, Ridker, PM, Chasman, DI, Reiner, AP, Ritchie, MD, Lange, LA, Cornish, AJ, Dobbins, SE, Hemminki, K, Kinnersley, B, Sanson, M, Labreche, K, Simon, M, Bondy, M, Law, P, Speedy, H, Allan, J, Li, N, Went, M, Weinhold, N, Morgan, G, Sonneveld, P, Nilsson, B, Goldschmidt, H, Sud, A, Engert, A, Hansson, M, Hemingway, H, Asselbergs, FW, Patel, RS, Keating, BJ, Sattar, N, Houlston, R, Casas, JP, Hingorani, AD, Demuth, Juri, Bertram, L, Lill, CM, Coassin, S, Willeit, J, Kiechl, S, Willeit, K, Mason, D, Wright, J, Morris, R, Wanamethee, G, Whincup, P, Ben-Shlomo, Y, McLachlan, S, Price, JF, Kivimaki, M, Welch, C, Sanchez-Galvez, A, Marques-Vidal, P, Nicolaides, A, Panayiotou, AG, Onland-Moret, NC, van der Schouw, YT, Matullo, G, Fiorito, G, Guarrera, S, Sacerdote, C, Wareham, NJ, Langenberg, C, Scott, RA, Luan, J, Bobak, M, Malyutina, S, Pajak, A, Kubinova, R, Tamosiunas, A, Pikhart, H, Grarup, N, Pedersen, O, Hansen, T, Linneberg, A, Jess, T, Cooper, J, Humphries, SE, Brilliant, M, Kitchner, T, Hakonarson, H, Carrell, DS, McCarty, CA, Lester, KH, Larson, EB, Crosslin, DR, de Andrade, M, Roden, DM, Denny, JC, Carty, C, Schofield, P, O'Donnell, M, Yusuf, S, Chong, M, Pare, G, van der Harst, P, Said, MA, Eppinga, RN, Verweij, N, Snieder, H, Christen, T, Mook-Kanamori, DO, Gustafsson, S, Lind, L, Ingelsson, E, Pazoki, R, Franco, O, Hofman, A, Uitterlinden, A, Dehghan, A

Genetic associations with white matter hyperintensities confer risk of lacunar stroke

- Traylor, Matthew, Rutten-Jacobs, Loes C. A., Dichgans, Martin, Markus, Hugh S., Thijs, Vincent, Holliday, Elizabeth G., Levi, Chris, Bevan, Steve, Malik, Rainer, Boncoraglio, Giorgio, Sudlow, Cathie, Rothwell, Peter M.

Common NOTCH3 variants and cerebral small-vessel disease

- Rutten-Jacobs, Loes C. A., Traylor, Matthew, Levi, Christopher, Rost, Natalia S., Rosand, Jonathan, Hassan, Ahamad, Markus, Hugh S., Adib-Samii, Poneh, Thijs, Vincent, Sudlow, Cathie, Rothwell, Peter M., Boncoraglio, Giorgio, Dichgans, Martin, Bevan, Steve, Meschia, James

Effect of genetic variants associated with plasma homocysteine levels on stroke risk

- Cotlarciuc, Iona, Malik, Rainer, Markus, Hugh S., Rosand, Jonathan, Mitchell, Braxton D., Kittner, Steven J., Meschia, James F., van Meurs, Joyce B. J., Uitterlinden, Andre G., Worrall, Bradford B., Dichgans, Martin, Sharma, Pankaj, Holliday, Elizabeth G., Ahmadi, Kourosh R., Paré, Guillaume, Psaty, Bruce M., Fornage, Myriam, Hasan, Nazeeha, Rinne, Paul E., Ikram, M. Arfan

The association between complement component 2/complement factor B polymorphisms and age-related macular degeneration: A HuGE review and meta-analysis

- Thakkinstian, Ammarin, McEvoy, Mark, Akahori, Masakazu, Arning, Astrid, Edwards, Albert O., Seddon, Johanna M., Attia, John, Chakravarthy, Usha, Chakrabarti, Subhabrata, McKay, Gareth J., Ryu, Euijung, Silvestri, Giuliana, Kaur, Inderjeet, Francis, Peter, Iwata, Takeshi

Systematic review and meta-analysis of the association between complement component 3 and age-related macular degeneration: a HuGE review and meta-analysis

- Thakkinstian, Ammarin, McKay, Gareth J., McEvoy, Mark, Chakravarthy, Usha, Chakrabarti, Subhabrata, Silvestri, Guiliana, Kaur, Inderjeet, Li, Xiaoxin, Attia, John

A systematic review and meta-analysis of tumor necrosis factor α-308 polymorphism and Kawasaki disease

- Arj-Ong, Sakda, Thakkinstian, Ammarin, McEvoy, Mark, Attia, John

Combining information from related meta-analyses of genetic association studies

- Thompson, J. R., Minelli, C., Abrams, K. R., Thakkinstian, A., Attia, J.

How should we use information about HWE in the meta-analyses of genetic association studies?

- Minelli, Cosetta, Thompson, John R., Abrams, Keith R., Thakkinstian, Ammarin, Attia, John