Association between sour taste SNP KCNJ2-rs236514, diet quality and mild cognitive impairment in an elderly cohort

- Ferraris, Celeste, Turner, Alexandria, Scarlett, Christopher, Veysey, Martin, Lucock, Mark, Bucher, Tamara, Beckett, Emma L.

DNA variants are an unlikely explanation for the changing quality of spermatozoa within the same individual

- Netherton, Jacob, Ogle, Rachel, Hetherington, Louise, Velkov, Tony, Rose, Ryan, Baker, Mark

NLRP1 variant M1184V decreases inflammasome activation in the context of DPP9 inhibition and asthma severity

- Moecking, Jonas, Laohamonthonkul, Pawat, Huntsman, Scott, Calleja, Dale J., Horvat, Jay C., Hansbro, Phil M., O'Donoghue, Robert J. J., Ting, Jenny P., Burchard, Esteban G., Geyer, Matthias, Gerlic, Motti, Masters, Seth L., Chalker, Katelyn, White, Marquitta J., Harapas, Cassandra R., Yu, Chien-Hasiung, Davidson, Sophia, Hrovat-Schaale, Katja, Hu, Donglei, Eng, Celeste

A de novo mutation in KMT2A (MLL) in monozygotic twins with Wiedemann-Steiner syndrome

- Dunkerton, Sophie, Field, Matthew, Cho, Vicki, Bertram, Edward, Whittle, Belinda, Groves, Alexandra, Goel, Himanshu

Common variants of xeroderma pigmentosum genes and prostate cancer risk

- Mirecka, Aneta, Paszkowska-Szczur, Katarzyna, Gupta, Satish, Gołąb, Adam, Słojewski, Marcin, Sikorski, Andrzej, Lubiński, Jan, Dębniak, Tadeusz, Scott, Rodney J., Górski, Bohdan, van de Wetering, Thierry, Wokołorczyk, Dominika, Gromowski, Tomasz, Serrano-Fernandez, Pablo, Cybulski, Cezary, Kashyap, Aniruddh

Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson s disease a multicenter study

- von Otter, Malin, Bergstrm, Petra, Klein, Christine, Nilsson, Michael, Hammarsten, Ola, Nilsson, Staffan, Zetterberg, Henrik, Quattrone, Aldo, De Marco, Elvira Valeria, Annesi, Grazia, Söderkvist, Peter, Wettinger, Stephanie Bezzina, Drozdzik, Marek, Bialecka, Monika, Nissbrandt, Hans

Importance of different types of prior knowledge in selecting genome-wide findings for follow-up

- Minelli, Cosetta, De Grandi, Alessandro, Fox, Caroline S., Freina, Thomas, Hicks, Andrew A., Marroni, Fabio, Parmigiani, Giovanni, Pastore, Andrea, Pattaro, Cristian, Pfeufer, Arne, Ruggeri, Fabrizio, Schwienbacher, Christine, Weichenberger, Christian X., Taliun, Daniel, Pramstaller, Peter P., Domingues, Francisco S., Thompson, John R., Goegele, Martin, Modenese, Mirko, Attia, John, Barrett, Jennifer H., Boehnke, Michael, Borsani, Guiseppe, Casari, Giorgio

Schizophrenia genetic variants are not associated with intelligence

- Terwisscha van Scheltinga, A. F., Bakker, S. C., Kendler, K. S., Kirov, G. K., Konnerth, H., Konte, B., Krabbendam, L., Krasucki, R., Lasseter, V. K., Laurent, C., Lawrence, J., Lencz, T., Lerer, F. B., Levinson, D. F., Liang, K.-Y., Lichtenstein, P., Lieberman, J. A., Linszen, D. H., Lönnqvist, J., Loughland, C. M., Maclean, A. W., Maher, B. S., Maier, W., Mallet, J., Sklar, P., Malloy, P., Mattheisen, M., Mattingsdal, M., McGhee, K. A., McGrath, J. J., McIntosh, A., McLean, D. E., McQuillin, A., Melle, I., Michie, P. T., Holmans, P. A., Milanova, V., Morris, D. W., Mors, O., Mortensen, P. B., Moskvina, V., Muglia, P., Myin-Germeys, I., Nertney, D. A., Nestadt, G., Nielsen, J., Lin, D.-Y., Nikolov, I., Nordentoft, M., Norton, N., Nöthen, M. M., O'Dushlaine, C. T., Olincy, A., Olsen, L., O'Neill, F. A., Ørntoft, T. F., Owen, M. J., Duan, J., Pantelis, C., Papadimitriou, G., Pato, M. T., Peltonen, L., Petursson, H., Pickard, B., Pimm, J., Pulver, A. E., Puri, V., Quested, D., Andreassen, O. A., Quinn, E. M., Rasmussen, H. B., Réthelyi, J. M., Ribble, R., Rietschel, M., Riley, B. P., Ruggeri, M., Schall, U., Schulze, T. G., Schwab, S. G., Scolnick, E., Scott, R. J., Shi, J., Sigurdsson, E., Silverman, J. M., Spencer, C. C. A., Stefansson, K., Strange, A., Strengman, E., Stroup, T. S., Suvisaari, J., Cichon, S., Terenius, L., Thirumalai, S., Thygesen, J. H., Timm, S., Toncheva, D., Van Den Oord, E., Van Os, J., Van Winkel, R., Veldink, J., Walsh, D., St Clair, D., Wang, A. G., Wiersma, D., Wildenauer, D. B., Williams, H. J., Williams, N. M., Wormley, B., Zammit, S., Sullivan, P. F., O'Donovan, M. C., Daly, M. J., van Haren, N. E. M., Corvin, A., Gejman, P. V., Gurling, H., Werge, T., Rujescu, D., Blackwood, D. H. R., Pato, C. N., Malhotra, A. K., Purcell, S., Dudbridge, F., Neale, B. M., Derks, E. M., Rossin, L., Visscher, P. M., Posthuma, D., Ruderfer, D. M., Fanous, A., Stefansson, H., Steinberg, S., Mowry, B. J., Golimbet, V., De Hert, M., Buizer-Voskamp, J. E., Jönsson, E. G.., Bitter, I., Pietiläinen, O. P. H., Collier, D. A., Tosato, S., Agartz, I., Albus, M., Alexander, M., Amdur, R. L., Amin, F., Cahn, W., Bass, N., Bergen, S. E., Black, D. W., Børglum, A. D., Brown, M. A., Bruggeman, R., Buccola, N. G., Byerley, W. F., Cantor, R. M., Carr, V. J., Ripke, S., Catts, S. V., Choudhury, K., Cloninger, C. R., Cormican, P., Craddock, N., Danoy, P. A., Datta, S., De Haan, L., Demontis, D., Dikeos, D., Ophoff, R. A., Djurovic, S., Donnelly, P., Donohoe, G., Duong, L., Dwyer, S., Fink-Jensen, A., Freedman, R., Freimer, N. B., Friedl, M., Georgieva, L., Kahn, R. S., Giegling, I., Gill, M., Glenthøj, B., Godard, S., Hamshere, M, Hansen, M., Hansen, T., Hartmann, A. M., Henskens, F. A., Hougaard, D. M., Sanders, A. R., Hultman, C. M., Ingason, A., Jablensky, A. V., Jakobsen, K. D., Jay, M., Jürgens, G., Keller, M. C., Kenis, G., Kenny, E., Kim, Y.

SNP prioritization using a Bayesian probability of association

- Thompson, John R., Goegele, Martin, Marroni, Fabio, Pattaro, Cristian, Ruggeri, Fabrizio, Borsani, Giuseppe, Casari, Giorgio, Parmigiani, Giovanni, Pastore, Andrea, Pfeufer, Arne, Schwienbacher, Christine, Taliun, Daniel, Weichenberger, Christian X., Fox, Caroline S., Pramstaller, Peter P., Minelli, Cosetta, Modenese, Mirko, Attia, John, Barrett, Jennifer H., Boehnke, Michael, De Grandi, Alessandro, Domingues, Francisco S., Hicks, Andrew A.

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips

- Ritchie, Matthew E., Ruijie, Liu, Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Moscato, Pablo, Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Carvalho, Benilton S., Booth, David R., Clarke, Glynnis, Cox, Mathew B., Csurhes, Peter A., Danoy, Patrick, Dickinson, Joanne L., Drysdale, Karen, Field, Judith, Greer, Judith M., Griffiths, Lyn R., Irizarry, Rafael A., Guru, Preethi, Hadler, Johanna, Hoban, Ella, McMorran, Brendan J., Jensen, Cathy J., Johnson, Laura J., McCallum, Ruth, Merriman, Marilyn, Merriman, Tony, Polanowski, Andrea, Bahlo, Melanie, Pryce, Karena, Tajouri, Lotfi, Whittock, Lucy, Wilkins, Ella J., Browning, Brian L., Browning, Sharon R., Perera, Devindri, Butzkueven, Helmut, Carroll, William M., Chapman, Caron, Kermode, Allan G., Marriott, Mark, Mason, Deborah, Heard, Robert N., Pender, Michael P., Slee, Mark, Tubridy, Niall, Willoughby, Ernest, Broadley, Simon A., Brown, Matthew A., Foote, Simon J.

Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis

- Dudding, T., Heron, J., Thakkinstian, A., Nurk, E., Golding, J., Pembrey, M., Ring, S. M., Attia, J., Scott, R. J.

Identification and interrogation of highly informative single nucleotide polymorphism sets defined by bacterial multilocus sequence typing databases

- Robertson, Gail A., Thiruvenkataswamy, Venugopal, Shilling, Hayden, Price, Erin P., Huygens, Flavia, Henskens, Frans A., Giffard, Philip M.