Genome-wide Comparison of African-Ancestry Populations from CARe and Other Cohorts Reveals Signals of Natural Selection by Bhatia, G, Patterson, N, Pasaniuc, B, Zaitlen, N, Genovese, G, Pollack, S, Mallick, S, Myers, S, Tandon, A, Spencer, C, Palmer, C, Adeyemo, A, Akylbekova, E, Cupples, L, Divers, J, Fornage, M, Kao, W, Lange, L, Li, M, Musani, S, Mychaleckyj, J, Ogunniyi, A, Papanicolaou, G, Rotimi, C, Rotter, J

Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration by Ahmad, S, Imtiaz, MA, Mishra, A, Wang, R, Herrera-Rivero, M, Bis, JC, Fornage, M, Roshchupkin, G, Hofer, E, Logue, M, Longstreth, WT, Xia, R, Bouteloup, V, Mosley, T, Launer, LJ, Khalil, M, Kuhle, J, Rissman, RA, Chene, G, Dufouil, C, Djoussé, L, Lyons, MJ, Mukamal, KJ, Kremen, WS

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. by Traylor, M, Farrall, M, Holliday, E, Sudlow, C, Hopewell, J, Cheng, Y, Fornage, M, Ikram, M, Malik, R, Bevan, S, Thorsteinsdottir, U, Nalls, M, Longstreth, W, Wiggins, K, Yadav, S, Parati, E, Destefano, A, Worrall, B, Kittner, S, Khan, MS, Reiner, A, Helgadottir, A, Achterberg, S, Fernandez-Cadenas, I, Abboud, S

Common variants at 6q22 and 17q21 are associated with intracranial volume by Ikram, M, Fornage, M, Smith, A, Seshadri, S, Schmidt, R, Debette, S, Vrooman, H, Sigurdsson, S, Ropele, S, Taal, H, Mook-Kanamori, DO, Coker, L, Longstreth, W, Niessen, W, Destefano, A, Beiser, A, Zijdenbos, A, Struchalin, M, Jack, C, Rivadeneira, F, Uitterlinden, A, Knopman, D, Hartikainen, A, Pennell, C, Thiering, E

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. by Bhatia, G, Patterson, N, Pasaniuc, B, Zaitlen, N, Genovese, G, Pollack, S, Mallick, S, Myers, S, Tandon, A, Spencer, C, Palmer, C, Adeyemo, A, Akylbekova, E, Cupples, L, Divers, J, Fornage, M, Kao, W, Lange, L, Li, M, Musani, S, Mychaleckyj, J, Ogunniyi, A, Papanicolaou, G, Rotimi, C, Rotter, J

Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. by Dichgans, M, Malik, R, König, I, Rosand, J, Clarke, R, Gretarsdottir, S, Thorleifsson, G, Mitchell, B, Assimes, T, Levi, C, O'Donnell, C, Fornage, M, Thorsteinsdottir, U, Psaty, B, Hengstenberg, C, Seshadri, S, Erdmann, J, Bis, J, Peters, A, Boncoraglio, G, März, W, Meschia, J, Kathiresan, S, Ikram, M, McPherson, R

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. by Peloso, G, Auer, P, Bis, J, Voorman, A, Morrison, A, Stitziel, N, Brody, J, Khetarpal, SA, Crosby, JR, Fornage, M, Isaacs, A, Jakobsdottir, J, Feitosa, M, Davies, G, Huffman, J, Manichaikul, A, Davis, B, Lohman, K, Joon, A, Smith, A, Grove, M, Zanoni, P, Redon, V, Demissie, S, Lawson, K

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): A meta-analysis of genome-wide association studies by Traylor, M, Farrall, M, Farrall, M, Holliday, E, Sudlow, C, Hopewell, J, Cheng, Y, Fornage, M, Ikram, M, Ikram, M, Ikram, M, Malik, R, Bevan, S, Thorsteinsdottir, U, Thorsteinsdottir, U, Nalls, M, Longstreth, W, Longstreth, W, Wiggins, K, Yadav, S, Parati, E, DeStefano, A, Worrall, B, Worrall, B, Kittner, S

Common variants at 6q22 and 17q21 are associated with intracranial volume. by Ikram, M, Fornage, M, Smith, A, Seshadri, S, Schmidt, R, Debette, S, Vrooman, H, Sigurdsson, S, Ropele, S, Taal, H, Mook-Kanamori, DO, Coker, L, Longstreth, W, Niessen, W, DeStefano, A, Beiser, A, Zijdenbos, A, Struchalin, M, Jack, C, Rivadeneira, F, Uitterlinden, A, Knopman, D, Hartikainen, A, Pennell, C, Thiering, E

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. by Soler Artigas, M, Loth, D, Wain, L, Gharib, SA, Obeidat, M, Tang, W, Zhai, G, Zhao, J, Smith, A, Huffman, J, Albrecht, E, Jackson, C, Evans, D, Cadby, G, Fornage, M, Manichaikul, A, Lopez, L, Johnson, T, Aldrich, M, Aspelund, T, Barroso, I, Campbell, H, Cassano, P, Couper, D, Eiriksdottir, G

Association of exome sequences with plasma C-reactive protein levels in >9000 participants. by Schick, U, Auer, P, Bis, J, Lin, H, Wei, P, Pankratz, N, Lange, L, Brody, J, Stitziel, N, Kim, D, Carlson, C, Fornage, M, Haessler, J, Hsu, L, Jackson, R, Kooperberg, C, Leal, S, Psaty, B, Boerwinkle, E, Tracy, R, Ardissino, D, Shah, S, Willer, C, Loos, R, Melander, O

Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes. by Meschia, J, Arnett, D, Ay, H, Brown, R, Benavente, O, Cole, J, de Bakker, P, Dichgans, M, Doheny, K, Fornage, M, Grewal, R, Gwinn, K, Jern, C, Conde, J, Johnson, J, Jood, K, Laurie, C, Lee, J, Lindgren, A, Markus, H, McArdle, P, McClure, L, Mitchell, B, Schmidt, R, Rexrode, K

Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations by Hu, Y, Tanaka, T, Zhu, J, Guan, W, Wu, J, Psaty, B, McKnight, B, King, I, Sun, Q, Richard, M, Manichaikul, A, Frazier-Wood, A, Kabagambe, E, Hopkins, P, Ordovas, J, Ferrucci, L, Bandinelli, S, Arnett, D, Chen, Y, Liang, S, Siscovick, D, Tsai, M, Rich, S, Fornage, M, Hu, F, Rimm, E, Jensen, M, Lemaitre, R, Mozaffarian, D, Steffen, L, Morris, A, Li, H, Lin, X

Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects by Mishra, A, Chauhan, G, Violleau, M, Vojinovic, D, Jian, X, Bis, J, Li, S, Saba, Y, Grenier-Boley, B, Yang, Q, Bartz, T, Hofer, E, Soumaré, A, Peng, F, Duperron, M, Foglio, M, Mosley, T, Schmidt, R, Psaty, B, Launer, L, Boerwinkle, E, Zhu, Y, Mazoyer, B, Lathrop, M, Bellenguez, C, Van Duijn, C, Ikram, M, Schmidt, H, Longstreth, W, Fornage, M, Seshadri, S, Joutel, A, Tzourio, C, Debette, S

Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium. by Pasaniuc, B, Zaitlen, N, Lettre, G, Chen, G, Tandon, A, Kao, W, Ruczinski, I, Fornage, M, Siscovick, D, Zhu, X, Larkin, E, Lange, L, Cupples, L, Yang, Q, Akylbekova, E, Musani, S, Divers, J, Mychaleckyj, J, Li, M, Papanicolaou, G, Millikan, R, Ambrosone, C, John, E, Bernstein, L, Zheng, W, Hu, J, Ziegler, R, Nyante, S, Bandera, E, Ingles, SA, Press, M, Chanock, S, Deming, S, Rodriguez-Gil, J, Palmer, C, Buxbaum, S, Ekunwe, L, Hirschhorn, J, Henderson, B, Myers, S, Haiman, C, Reich, D, Patterson, N, Wilson, J, Price, A

Meta-analysis of epigenome-wide association studies of cognitive abilities by Marioni, RE, McRae, AF, Bressler, J, Colicino, E, Hannon, E, Li, S, Prada, D, Smith, JA, Trevisi, L, Tsai, P-C, Vojinovic, D, Simino, J, Levy, D, Liu, C, Mendelson, M, Satizabal, CL, Yang, Q, Jhun, MA, Kardia, SLR, Zhao, W, Bandinelli, S, Ferrucci, L, Hernandez, DG, Singleton, AB, Harris, SE, Starr, JM, Kiel, DP, McLean, RR, Just, AC, Schwartz, J, Spiro, A, Vokonas, P, Amin, N, Ikram, MA, Uitterlinden, AG, Van Meurs, JBJ, Spector, TD, Steves, C, Baccarelli, AA, Bell, JT, Van Duijn, CM, Fornage, M, Hsu, Y-H, Mill, J, Mosley, TH, Seshadri, S, Deary, IJ

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies. by Keating, B, Tischfield, S, Murray, S, Bhangale, T, Price, T, Glessner, J, Galver, L, Barrett, J, Grant, S, Farlow, D, Chandrupatla, H, Hansen, M, Ajmal, S, Papanicolaou, G, Guo, Y, Li, M, Derohannessian, S, de Bakker, P, Bailey, S, Montpetit, A, Edmondson, A, Taylor, K, Gai, X, Wang, S, Fornage, M, Shaikh, T, Groop, L, Boehnke, M, Hall, A, Hattersley, A, Frackelton, E, Patterson, N, Chiang, C, Kim, C, Fabsitz, R, Ouwehand, W, Price, A, Munroe, P, Caulfield, M, Drake, T, Boerwinkle, E, Reich, D, Whitehead, A, Cappola, T, Samani, N, Lusis, A, Schadt, E, Wilson, J, Koenig, W, McCarthy, M, Kathiresan, S, Gabriel, S, Hakonarson, H, Anand, S, Reilly, M, Engert, J, Nickerson, D, Rader, D, Hirschhorn, J, Fitzgerald, G

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults by Hofer, E, Roshchupkin, GV, Adams, HHH, Knol, MJ, Lin, H, Li, S, Zare, H, Ahmad, S, Armstrong, NJ, Satizabal, CL, Bernard, M, Bis, JC, Gillespie, NA, Luciano, M, Mishra, A, Scholz, M, Teumer, A, Xia, R, Jian, X, Mosley, TH, Saba, Y, Pirpamer, L, Seiler, S, Becker, JT, Carmichael, O, Rotter, JI, Psaty, BM, Lopez, OL, Amin, N, van der Lee, SJ, Yang, Q, Himali, JJ, Maillard, P, Beiser, AS, DeCarli, C, Karama, S, Lewis, L, Harris, M, Bastin, ME, Deary, IJ, Veronica Witte, A, Beyer, F, Loeffler, M, Mather, KA, Schofield, PR, Thalamuthu, A, Kwok, JB, Wright, MJ, Ames, D, Trollor, J, van Duijn, CM, Grabe, HJ, Longstreth Jr, WT, Fornage, M, Paus, T, Debette, S, Ikram, MA, Schmidt, H, Schmidt, R, Seshadr, S

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke by Cole, J, Xu, H, Ryan, K, Jaworek, T, Dueker, N, McArdle, P, Gaynor, B, Cheng, Y, O'Connell, J, Bevan, S, Malik, R, Ahmed, N, Amouyel, P, Anjum, S, Bis, J, Crosslin, D, Danesh, J, Engelter, S, Fornage, M, Frossard, P, Gieger, C, Giese, A, Grond-Ginsbach, C, Ho, W, Holliday, E, Hopewell, J, Hussain, M, Iqbal, W, Jabeen, S, Jannes, J, Kamal, A, Kamatani, Y, Kanse, S, Kloss, M, Lathrop, M, Leys, D, Lindgren, A, Longstreth, W, Mahmood, K, Meisinger, C, Metso, T, Mosley, T, Müller-Nurasyid, M, Norrving, B, Parati, E, Peters, A, Pezzini, A, Quereshi, I, Rasheed, A, Rauf, A, Salam, T, Shen, J, Słowik, A, Stanne, T, Strauch, K, Tatlisumak, T, Thijs, V, Tiedt, S, Traylor, M, Waldenberger, M, Walters, M, Zhao, W, Boncoraglio, G, Debette, S, Jern, C, Levi, C, Markus, H, Meschia, J, Rolfs, A, Rothwell, P, Saleheen, D, Seshadri, S, Sharma, P, Sudlow, C, Worrall, B, Metastroke Consortium Of The Isgc, Wtccc-2 Consortium, Stine, O, Kittner, S, Mitchell, B

Common variants at 12q15 and 12q24 are associated with infant head circumference. by Taal, H, St Pourcain, B, Thiering, E, Das, S, Mook-Kanamori, DO, Warrington, N, Kaakinen, M, Kreiner-Møller, E, Bradfield, J, Freathy, R, Geller, F, Guxens, M, Cousminer, D, Kerkhof, M, Timpson, N, Ikram, M, Beilin, L, Bønnelykke, K, Buxton, J, Charoen, P, Chawes, B, Eriksson, J, Evans, D, Hofman, A, Kemp, J, Kim, C, Klopp, N, Lahti, J, Lye, S, McMahon, G, Mentch, F, Müller-Nurasyid, M, O'Reilly, P, Prokopenko, I, Rivadeneira, F, Steegers, E, Sunyer, J, Tiesler, C, Yaghootkar, H, Breteler, M, Decarli, C, Breteler, M, Debette, S, Fornage, M, Gudnason, V, Launer, L, van der Lugt, A, Mosley, T, Seshadri, S, Smith, A, Vernooij, M, Blakemore, A, Chiavacci, R, Feenstra, B, Fernandez-Banet, J, Grant, S, Hartikainen, A, van der Heijden, A, Iñiguez, C, Lathrop, M, McArdle, W, Mølgaard, A, Newnham, J, Palmer, L, Palotie, A, Pouta, A, Ring, S, Sovio, U, Standl, M, Uitterlinden, A, Wichmann, H, Vissing, N, DeCarli, C, van Duijn, C, McCarthy, M, Koppelman, G, Estivill, X, Hattersley, A, Melbye, M, Bisgaard, H, Pennell, C, Widen, E, Hakonarson, H, Smith, G, Heinrich, J, Jarvelin, MR, Jaddoe, V