First-trimester bleeding characteristics associate with increased risk of preterm birth: data from a prospective pregnancy cohort von Velez Edwards, D.R., Baird, D.D., Hasan, R., Savitz, D.A., Hartmann, K.E.

Volltext

Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and Caucasians von VELEZ, D. R, HULME, W. F, MYERS, J. L, STRYJEWSKI, M. E, ABBATE, E, ESTEVAN, R, PATILLO, S. G, GILBERT, J. R, HAMILTON, C. D, SCOTT, W. K

Volltext

A piecewise thickness-function to the interferometric measurement of the optically transparent thin films von Gasca-Figueroa, D., García-Rodríguez, F. J., Castro-Beltrán, R., Pérez-Pinal, F. J., Vélez-García, R. D., Gutiérrez-Juárez, G.

Volltext

Parkinson disease loci in the mid-western Amish von Davis, M. F., Cummings, A. C., D’Aoust, L. N., Jiang, L., Velez Edwards, D. R., Laux, R., Reinhart-Mercer, L., Fuzzell, D., Scott, W. K., Pericak-Vance, M. A., Lee, S. L., Haines, J. L.

Volltext

Ethnic differences in interleukin 6 (IL‐6) and IL6 receptor genes in spontaneous preterm birth and effects on amniotic fluid protein levels von Velez, D. R., Menon, R., Thorsen, P., Jiang, L., Simhan, H., Morgan, N., Fortunato, S. J., Williams, S. M.

Volltext

Synopsis of Preterm Birth Genetic Association Studies: The Preterm Birth Genetics Knowledge Base (PTBGene) von Dolan, S.M., Hollegaard, M.V., Merialdi, M., Betran, A.P., Allen, T., Abelow, C., Nace, J., Lin, B.K., Khoury, M.J., Ioannidis, J.P.A., Bagade, S., Zheng, X., Dubin, R.A., Bertram, L., Edwards, D.R. Velez, Menon, R.

Volltext

DC-SIGN (CD209), pentraxin 3 and vitamin D receptor gene variants associate with pulmonary tuberculosis risk in West Africans von Olesen, R, Wejse, C, Velez, D R, Bisseye, C, Sodemann, M, Aaby, P, Rabna, P, Worwui, A, Chapman, H, Diatta, M, Adegbola, R A, Hill, P C, Østergaard, L, Williams, S M, Sirugo, G

Volltext

Risk of Miscarriage Among Black Women and White Women in a US Prospective Cohort Study von MUKHERJEE, Sudeshna, VELEZ EDWARDS, Digna R, BAIRD, Donna D, SAVITZ, David A, HARTMANN, Katherine E

Volltext

Epiregulin (EREG) and human V-ATPase (TCIRG1): genetic variation, ethnicity and pulmonary tuberculosis susceptibility in Guinea-Bissau and The Gambia von White, M J, Tacconelli, A, Chen, J S, Wejse, C, Hill, P C, Gomes, V F, Velez-Edwards, D R, Østergaard, L J, Hu, T, Moore, J H, Novelli, G, Scott, W K, Williams, S M, Sirugo, G

Volltext

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

Volltext

Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism von Sapkota, Yadav, Steinthorsdottir, Valgerdur, Morris, Andrew P., Fassbender, Amelie, Rahmioglu, Nilufer, De Vivo, Immaculata, Buring, Julie E., Zhang, Futao, Edwards, Todd L., Jones, Sarah, O, Dorien, Peterse, Daniëlle, Rexrode, Kathryn M., Ridker, Paul M., Schork, Andrew J., MacGregor, Stuart, Martin, Nicholas G., Becker, Christian M., Adachi, Sosuke, Yoshihara, Kosuke, Enomoto, Takayuki, Takahashi, Atsushi, Kamatani, Yoichiro, Matsuda, Koichi, Kubo, Michiaki, Thorleifsson, Gudmar, Geirsson, Reynir T., Thorsteinsdottir, Unnur, Wallace, Leanne M., Yang, Jian, Velez Edwards, Digna R., Nyegaard, Mette, Low, Siew-Kee, Zondervan, Krina T., Missmer, Stacey A., D'Hooghe, Thomas, Montgomery, Grant W., Chasman, Daniel I., Stefansson, Kari, Tung, Joyce Y., Nyholt, Dale R.

Volltext

Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

Volltext

A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies von Joo, Yoonjung Yoonie, Actkins, Ky’Era, Pacheco, Jennifer A, Basile, Anna O, Carroll, Robert, Crosslin, David R, Day, Felix, Denny, Joshua C, Velez Edwards, Digna R, Hakonarson, Hakon, Harley, John B, Hebbring, Scott J, Ho, Kevin, Jarvik, Gail P, Jones, Michelle, Karaderi, Tugce, Mentch, Frank D, Meun, Cindy, Namjou, Bahram, Pendergrass, Sarah, Ritchie, Marylyn D, Stanaway, Ian B, Urbanek, Margrit, Walunas, Theresa L, Smith, Maureen, Chisholm, Rex L, Kho, Abel N, Davis, Lea, Hayes, M Geoffrey

Volltext

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits: Nat Genet von Evangelou, E., Warren, H. R., Mosen-Ansorena, D., Mifsud, B., Pazoki, R., Gao, H., Ntritsos, G., Dimou, N., Cabrera, C. P., Karaman, I., Ng, F. L., Evangelou, M., Witkowska, K., Tzanis, E., Hellwege, J. N., Giri, A., Velez Edwards, D. R., Sun, Y. V., Cho, K., Gaziano, J. M., Wilson, P. W. F., Tsao, P. S., Kovesdy, C. P., Esko, T., Magi, R., Milani, L., Almgren, P., Boutin, T., Debette, Stéphanie, Ding, J., Giulianini, F., Holliday, E. G., Jackson, A. U., Li-Gao, R., Lin, W. Y., Luan, J., Mangino, M., Oldmeadow, C., Prins, B. P., Qian, Y., Sargurupremraj, Muralidharan, Shah, N., Surendran, P., Theriault, S., Verweij, N., Willems, S. M., Zhao, J. H., Amouyel, P., Connell, J., de Mutsert, R., Doney, A. S. F., Farrall, M., Menni, C., Noordam, R., Pare, G., Poulter, N. R., Shields, D. C., Stanton, A., Thom, S., Abecasis, G., Amin, N., Arking, D. E., Ayers, K. L., Barbieri, C. M., Batini, C., Bis, J. C., Blake, T., Bochud, M., Boehnke, M., Boerwinkle, E., Boomsma, D. I., Bottinger, E. P., Braund, P. S., Brumat, M., Campbell, A., Campbell, H., Chakravarti, A., Chambers, J. C., Chauhan, Ganesh, Ciullo, M., Cocca, M., Collins, F., Cordell, H. J., Davies, G., Borst, M. H., Geus, E. J., Deary, I. J., Deelen, J., del Greco, M. F., Demirkale, C. Y., Dorr, M., Ehret, G. B., Elosua, R., Enroth, S., Erzurumluoglu, A. M., Ferreira, T., Franberg, M., Franco, O. H., Gandin, I., Gasparini, P.

Volltext

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits: Nat Genet von Evangelou, E., Warren, H. R., Mosen-Ansorena, D., Mifsud, B., Pazoki, R., Gao, H., Ntritsos, G., Dimou, N., Cabrera, C. P., Karaman, I., Ng, F. L., Evangelou, M., Witkowska, K., Tzanis, E., Hellwege, J. N., Giri, A., Velez Edwards, D. R., Sun, Y. V., Cho, K., Gaziano, J. M., Wilson, P. W. F., Tsao, P. S., Kovesdy, C. P., Esko, T., Magi, R., Milani, L., Almgren, P., Boutin, T., Debette, Stéphanie, Ding, J., Giulianini, F., Holliday, E. G., Jackson, A. U., Li-Gao, R., Lin, W. Y., Luan, J., Mangino, M., Oldmeadow, C., Prins, B. P., Qian, Y., Sargurupremraj, Muralidharan, Shah, N., Surendran, P., Theriault, S., Verweij, N., Willems, S. M., Zhao, J. H., Amouyel, P., Connell, J., de Mutsert, R., Doney, A. S. F., Farrall, M., Menni, C., Noordam, R., Pare, G., Poulter, N. R., Shields, D. C., Stanton, A., Thom, S., Abecasis, G., Amin, N., Arking, D. E., Ayers, K. L., Barbieri, C. M., Batini, C., Bis, J. C., Blake, T., Bochud, M., Boehnke, M., Boerwinkle, E., Boomsma, D. I., Bottinger, E. P., Braund, P. S., Brumat, M., Campbell, A., Campbell, H., Chakravarti, A., Chambers, J. C., Chauhan, Ganesh, Ciullo, M., Cocca, M., Collins, F., Cordell, H. J., Davies, G., de Borst, M. H., de Geus, E. J., Deary, I. J., Deelen, J., del Greco, M. F., Demirkale, C. Y., Dorr, M., Ehret, G. B., Elosua, R., Enroth, S., Erzurumluoglu, A. M., Ferreira, T., Franberg, M., Franco, O. H., Gandin, I., Gasparini, P.

Volltext

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, CS, Makinen, N, Harris, HR, Rahmioglu, N, Uimari, O, Cook, JP, Shigesi, N, Ferreira, T, Velez-Edwards, DR, Edwards, TL, Mortlock, S, Ruhioglu, Z, Day, F, Becker, CM, Karhunen, V, Martikainen, H, Jarvelin, M-R, Cantor, RM, Ridker, PM, Terry, KL, Buring, JE, Gordon, SD, Medland, SE, Montgomery, GW, Nyholt, DR, Hinds, DA, Tung, JY, Perry, JRB, Lind, PA, Painter, JN, Martin, NG, Morris, AP, Chasman, DI, Missmer, SA, Zondervan, KT, Morton, CC, Agee, M, Alipanahi, B, Auton, A, Bell, RK, Bryc, K, Elson, SL, Fontanillas, P, Furlotte, NA, Huber, KE, Kleinman, A, Litterman, NK, McIntyre, MH, Mountain, JL, Noblin, ES, Northover, CAM, Pitts, SJ, Sathirapongsasuti, JF, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Vacic, V, Wilson, CH

Volltext

A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough von Mosley, J D, Shaffer, C M, Van Driest, S L, Weeke, P E, Wells, Q S, Karnes, J H, Velez Edwards, D R, Wei, W-Q, Teixeira, P L, Bastarache, L, Crawford, D C, Li, R, Manolio, T A, Bottinger, E P, McCarty, C A, Linneman, J G, Brilliant, M H, Pacheco, J A, Thompson, W, Chisholm, R L, Jarvik, G P, Crosslin, D R, Carrell, D S, Baldwin, E, Ralston, J, Larson, E B, Grafton, J, Scrol, A, Jouni, H, Kullo, I J, Tromp, G, Borthwick, K M, Kuivaniemi, H, Carey, D J, Ritchie, M D, Bradford, Y, Verma, S S, Chute, C G, Veluchamy, A, Siddiqui, M K, Palmer, C N A, Doney, A, Mahmoud Pour, Seyed Hamidreza, Maitland-van der Zee, A H, Morris, A D, Denny, J C, Roden, D M

Volltext

Large-scale exome-wide association analysis identifies loci for white blood cell traits and pleiotropy with immune-mediated diseases von Tajuddin, SM, Schick, UM, Eicher, JD, Chami, N, Giri, A, Brody, JA, Hill, WD, Kacprowski, T, Li, J, Lyytikäinen, LP, Manichaikul, A, Mihailov, E, O'Donoghue, ML, Pankratz, N, Pazoki, R, Polfus, LM, Smith, AV, Schurmann, C, Vacchi-Suzzi, C, Waterworth, DM, Evangelou, E, Yanek, LR, Burt, A, Chen, MH, Van Rooij, FJ, Floyd, JS, Greinacher, A, Harris, TB, Highland, HM, Lange, LA, Liu, Y, Mägi, R, Nalls, MA, Mathias, RA, Nickerson, DA, Nikus, K, Starr, JM, Tardif, JC, Tzoulaki, I, Velez Edwards, DR, Wallentin, L, Bartz, TM, Becker, LC, Denny, JC, Raffield, LM, Rioux, JD, Friedrich, N, Fornage, M, Gao, H, Hirschhorn, JN, Liewald, DC, Rich, SS, Uitterlinden, A, Bastarache, L, Becker, DM, Boerwinkle, E, De Denus, S, Bottinger, EP, Hayward, C, Hofman, A, Homuth, G, Lange, E, Launer, LJ, Lehtimäki, T, Lu, Y, Metspalu, A, O'Donnell, CJ, Quarells, RC, Richard, M, Torstenson, ES, Taylor, KD, Vergnaud, AC, Zonderman, AB, Crosslin, DR, Deary, IJ, Dörr, M, Elliott, P, Evans, MK, Gudnason, V, Kähönen, M, Psaty, BM, Rotter, JI, Slater, AJ, Dehghan, A, White, HD, Ganesh, SK, Loos, RJ, Esko, T, Faraday, N, Wilson, JG, Cushman, M, Johnson, AD, Edwards, TL, Zakai, NA, Lettre, G, Reiner, AP, Auer, PL

Volltext

Exome genotyping identifies pleiotropic variants associated with red blood cell traits von Chami, N, Chen, MH, Eicher, JD, Evangelou, E, Tajuddin, SM, Love-Gregory, L, Schick, UM, Nomura, A, Giri, A, Kathiresan, S, Grarup, N, Esko, T, Lange, LA, Faraday, N, Abumrad, NA, Edwards, TL, Ganesh, SK, Auer, PL, Johnson, AD, Reiner, AP, Brody, JA, Schurmann, C, Pankratz, N, Yanek, LR, Manichaikul, A, Pazoki, R, Mihailov, E, Hill, WD, Raffield, LM, Burt, A, Becker, DM, Becker, LC, Boerwinkle, E, Bork-Jensen, J, Bottinger, EP, O'Donoghue, ML, Crosslin, DR, Dubé, MP, Elliott, P, Engström, G, Evans, MK, Floyd, JS, Gudnason, V, Hansen, T, Harris, TB, Hayward, C, Hernesniemi, J, Highland, HM, Hirschhorn, JN, Hofman, A, Irvin, MR, Kähönen, M, Launer, LJ, Lehtimäki, T, Li, J, Liewald, DC, Linneberg, A, Liu, Y, Lu, Y, Lyytikäinen, LP, Mägi, R, Mathias, RA, Melander, O, Metspalu, A, Mononen, N, Nalls, MA, Nickerson, DA, Nikus, K, Orho-Melander, M, Pedersen, O, Petersmann, A, Polfus, L, Psaty, BM, Raitakari, OT, Raitoharju, E, Rice, KM, Rivadeneira, F, Rotter, JI, Schmidt, F, Smith, AV, Starr, JM, Taylor, KD, Teumer, A, Thuesen, BH, Torstenson, ES, Tracy, RP, Tzoulaki, I, Zakai, NA, Vacchi-Suzzi, C, Van Duijn, CM, Van Rooij, FJ, Cushman, M, Deary, IJ, Velez Edwards, DR, Vergnaud, AC, Wallentin, L, Waterworth, DM, White, HD, Wilson, JG, Zonderman, AB

Volltext

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals von Eicher, JD, Chami, N, Kacprowski, T, Nomura, A, Chen, MH, Tajuddin, SM, Schick, UM, Slater, AJ, Pankratz, N, Polfus, L, Evans, MK, Engström, G, Orho-Melander, M, Melander, O, O'Donoghue, ML, Waterworth, DM, Wallentin, L, White, HD, Floyd, JS, Bartz, TM, Greinacher, A, Rice, KM, Liewald, DC, Hayward, C, Deary, IJ, Völker, U, Thiele, T, Van Rooij, FJ, Uitterlinden, AG, Franco, OH, Dehghan, A, Edwards, TL, Ganesh, SK, Faraday, N, Auer, PL, Reiner, AP, Lettre, G, Johnson, AD, Giri, A, Brody, JA, Lange, LA, Manichaikul, A, Hill, WD, Evangelou, E, Tzoulaki, I, Vergnaud, AC, Mathias, RA, Becker, DM, Becker, LC, Burt, A, Crosslin, DR, Lyytikäinen, LP, Nikus, K, Hernesniemi, J, Kähönen, M, Raitoharju, E, Mononen, N, Raitakari, OT, Lehtimäki, T, Zakai, NA, Nickerson, DA, Raffield, LM, Quarells, R, Willer, CJ, Peloso, GM, Liu, DJ, Global Lipids Genetics Consortium, Deloukas, P, Samani, NJ, Schunkert, H, Erdmann, J, CARDIoGRAM Exome Consortium, Fornage, M, Richard, M, Tardif, JC, Rioux, JD, Dube, MP, De Denus, S, Bottinger, EP, Loos, RJ, Smith, AV, Harris, TB, Launer, LJ, Torstenson, ES, Liu, Y, Tracy, RP, Rotter, JI, Rich, SS, Highland, HM, Boerwinkle, E, Li, J, Lange, E, Wilson, JG, Mihailov, E, Mägi, R, Hirschhorn, J, Metspalu, A, Esko, T, Nalls, MA, Zonderman, AB

Volltext