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.

Distribution of variants in multiple vitamin D-related loci (DHCR7/NADSYN1, GC, CYP2R1, CYP11A1, CYP24A1, VDR, RXRα and RXRγ) vary between European, East-Asian and Sub-Saharan African-ancestry populations

- Jones, Patrice, Lucock, Mark, Chaplin, George, Jablonski, Nina G., Veysey, Martin, Scarlett, Christopher, Beckett, Emma

Inhibition of vertebrate aldehyde oxidase as a therapeutic treatment for cancer, obesity, aging and amyotrophic lateral sclerosis

- Qiao, Yixue, Maiti, Kaushik, Sultana, Zakia, Fu, Lei, Smith, Roger

Genetic imbalance is associated with functional outcome after Ischemic Stroke

- Pfeiffer, Dorothea, Chen, Bowang, Schlicht, Kristina, Ginsbach, Philip, Abboud, Sherine, Bersano, Anna, Bevan, Steve, Brandt, Tobias, Caso, Valeria, Debette, Stephanie, Erhart, Philipp, Freitag-Wolf, Sandra, Giacalone, Giacomo, Grau, Armin J., Hayani, Eyad, Jern, Christina, Jiménez-Conde, Jordi, Kloss, Manja, Krawczak, Michael, Lee, Jin-Moo, Maguire, Jane M.

Variation within MBP gene predicts disease course in multiple sclerosis

- Zhou, Yuan, Simpson Jr, Steve, Taylor, Bruce V., Charlesworth, Jac C., van der Mei, Ingrid, Lucas, Robyn M., Ponsonby, Anne-Louise, Taylor, Anne-Louise, AUSLONG Investigators Group,, Williams, David, Lechner-Scott, Jeanette

Association between IRF6 and 8q24 polymorphisms and nonsyndromic cleft lip with or without cleft palate: systematic review and meta-analysis

- Wattanawong, Kachin, Rattanasiri, Sasivimol, McEvoy, Mark, Attia, John, Thakkinstian, Ammarin

Converging evolutionary, environmental and clinical ideas on folate metabolism

- Jones, Patrice, Beckett, Emma, Yates, Zoe, Veysey, Martin, Lucock, Mark

Genetic variation in glutamate carboxypeptidase II and interaction with dietary natural vitamin C may predict risk for adenomatous polyp occurrence

- Choi, Jeong-Hwa, Yates, Zoe, Lucock, Mark, Martin, Charlotte, Boyd, Lyndell, Ng, Xiaowei, Skinner, Virginia, Wai, Ron, Kim, Jeongseon, Woo, Hae Dong, Veysey, Martin

Common genetic variants in the plasminogen activation pathway are not associated with multiple sclerosis

- Cox, Mathew B., Bowden, Nikola A., Scott, Rodney J., Lechner-Scott, Jeannette

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

Loss-of-function of the voltage-gated sodium channel Na_V1.5 (channelopathies) in patients with irritable bowel syndrome

- Beyder, Arthur, Mazzone, Amelia, Lindberg, Greger, Karling, Pontus, Ohlsson, Bodil, Gazouli, Maria, Nardone, Gerardo, Cuomo, Rosario, Usai-Satta, Paolo, Galeazzi, Francesca, Neri, Matteo, Portincasa, Piero, Strege, Peter R., Bellini, Massimo, Barbara, Giovanni, Camilleri, Michael, Locke III, G. Richard, Talley, Nicholas J., D'Amato, Mauro, Ackerman, Michael J., Farrugia, Gianrico, Tester, David J., Saito, Yuri A., Bernard, Cheryl E., Enders, Felicty T., Ek, Weronica E., Schmidt, Peter T., Dlugosz, Aldona

Serotonin toxicity from antidepressant overdose and its association with the T102C polymorphism of the 5-HT₂A receptor

- Cooper, J. M., Newby, D. A., Whyte, I. M., Carter, G., Jones, A. L., Isbister, G. K.

Shared genetic susceptibility to ischemic stroke and coronary artery disease : a genome-wide analysis of common variants

- Dichgans, Martin, Malik, Rainer, Ódonnell, Christopher J., Fornage, Myriam, Thorsteinsdottir, Unnur, Psaty, Bruce M., Hengstenberg, Christian, Seshadri, Sudha, Erdmann, Jeanette, Bis, Joshua C., Peters, Annette, Boncoraglio, Giorgio B., König, Inke R., März, Winfred, Meschia, James F., Kathiresan, Sekar, Ikram, M. Arfan, McPherson, Ruth, Stefansson, Kari, Sudlow, Cathie, Reilly, Muredach, Thompson, John R., Sharma, Pankaj, Rosand, Jonathon, Hopewell, Jemma C., Chambers, John C., Watkins, Hugh, Rothwell, Peter M., Roberts, Robert, Markus, Hugh S., Samani, Nilesh J., Farrall, Martin, Schunkert, Heribert, Clarke, Robert, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Mitchell, Branxton D., Assimes, Themistocles L., Levi, Christopher

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.

The association of AGTR2 polymorphisms with preeclampsia and uterine artery bilateral notching is modulated by maternal BMI

- Zhou, A., Dekker, G. A., Lumbers, E. R., Lee, S. Y., Thompson, S. D., McCowan, L. M. E., Roberts, C. T.

Vitamin C-related nutrient-nutrient and nutrient-gene interactions that modify folate status

- Lucock, Mark, Yates, Zoë, Roach, Paul, Veysey, Martin, Boyd, Lyndell, Naylor, Charlotte, Choi, Jeong-Hwa, Ng, Xiaowei, Skinner, Virginia, Wai, Ron, Kho, Jeremy, Tang, Sa

Interleukin-6 gene promoter-572 C allele may play a role in rate of disease progression in multiple sclerosis

- Yan, Jun, Liu, Jia, Mason, Deborah, Griffiths, Lyn, Moscato, Pablo, Slee, Mark, Taylor, Bruce, Wiley, James, Field, Judith, Butzkueven, Helmut, Kilpatrick, Trevor J., Csurhes, Peter A., Lin, Clement Yihao, Pender, Michael P., McCombe, Pamela A., Greer, Judith M., Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZGene),, Scott, Rodney J., Lechner-Scott, Jeannette, Brown, Matthew A., Booth, David R., Stewart, Graeme J., Broadley, Simon

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

- Khor, Chiea Chuen, Davila, Sonia, Wong, Tien Yin, Pang, Junxiong, Mitchell, Paul, Cimaz, Rolando, Dahdah, Nagib, Cheung, Yiu-Fai, Huang, Guo-Ying, Yang, Wanling, Park, In-Sook, Lee, Jong-Keuk, Breunis, Willemijn B., Wu, Jer-Yuarn, Levin, Michael, Burns, Jane C., Burgner, David, Kuijpers, Taco W., Hibberd, Martin L., Attia, John, Scott, Rodney, Holliday, Elizabeth, Lee, Yi-Ching, Shimizu, Chisato, Wright, Victoria J., Yeung, Rae S. M, Tan, Dennis E. K., Sim, Kar Seng, Wang, Jie Jin

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis

- Field, Judith, Browning, Sharon R., Lechner-Scott, Jeanette, Moscato, Pablo, Scott, Rodney J., Stewart, Graeme J., Kilpatrick, Trevor J., Foote, Simon J., Bahlo, Melanie, Butzkueven, Helmut, Wiley, James, Booth, David R., Johnson, Laura J., Taylor, Bruce V., Brown, Matthew A., Rubio, Justin P., Stankovich, Jim, Danoy, Patrick, Varney, Michael D,, Tait, Brian D., Kaushal, S. Gandhi, Charlesworth, Jac C., Heard, Robert N., The Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene)

Association of thymidylate synthase enhancer region polymorphisms with thymidylate synthase activity in vivo

- de Bock, C. E., Garg, M. B., Scott, N., Sakoff, J. A., Scorgie, F. E., Ackland, S. P., Lincz, L. F.