A cross-platform approach identifies genetic regulators of human metabolism and health von Lotta, Luca A., Pietzner, Maik, Stewart, Isobel D., Wittemans, Laura B. L., Li, Chen, Bonelli, Roberto, Raffler, Johannes, Biggs, Emma K., Oliver-Williams, Clare, Auyeung, Victoria P. W., Luan, Jian’an, Wheeler, Eleanor, Paige, Ellie, Surendran, Praveen, Michelotti, Gregory A., Scott, Robert A., Burgess, Stephen, Zuber, Verena, Sanderson, Eleanor, Koulman, Albert, Imamura, Fumiaki, Forouhi, Nita G., Khaw, Kay-Tee, Griffin, Julian L., Wood, Angela M., Kastenmüller, Gabi, Danesh, John, Butterworth, Adam S., Gribble, Fiona M., Reimann, Frank, Bahlo, Melanie, Fauman, Eric, Wareham, Nicholas J., Langenberg, Claudia

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Aberrant O-GlcNAcylation characterizes chronic lymphocytic leukemia von Shi, Y, Tomic, J, Wen, F, Shaha, S, Bahlo, A, Harrison, R, Dennis, J W, Williams, R, Gross, B J, Walker, S, Zuccolo, J, Deans, J P, Hart, G W, Spaner, D E

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A role for oleoylethanolamide in chronic lymphocytic leukemia von Masoodi, M, Lee, E, Eiden, M, Bahlo, A, Shi, Y, Ceddia, R B, Baccei, C, Prasit, P, Spaner, D E

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HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis‐related morbidity von Gurrin, Lyle C., Bertalli, Nadine A., Dalton, Gregory W., Osborne, Nicholas J., Constantine, Clare C., McLaren, Christine E., English, Dallas R., Gertig, Dorota M., Delatycki, Martin B., Nicoll, Amanda J., Southey, Melissa C., Hopper, John L., Giles, Graham G., Anderson, Gregory J., Olynyk, John K., Powell, Lawrie W., Allen, Katrina J.

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The Natural History of Serum Iron Indices for HFE C282Y Homozygosity Associated With Hereditary Hemochromatosis von Gurrin, Lyle C, Osborne, Nicholas J, Constantine, Clare C, McLaren, Christine E, English, Dallas R, Gertig, Dorota M, Delatycki, Martin B, Southey, Melissa C, Hopper, John L, Giles, Graham G, Anderson, Gregory J, Olynyk, John K, Powell, Laurie W, Allen, Katrina J

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Insights into malaria susceptibility using genome-wide data on 17,000 individuals from Africa, Asia and Oceania von Band, Gavin, Le, Quang Si, Clarke, Geraldine M., Kivinen, Katja, Hubbart, Christina, Jeffreys, Anna E., Rowlands, Kate, Leffler, Ellen M., Jallow, Muminatou, Conway, David J., Sisay-Joof, Fatoumatta, Sirugo, Giorgio, d’Alessandro, Umberto, Toure, Ousmane B., Thera, Mahamadou A., Konate, Salimata, Sissoko, Sibiri, Mangano, Valentina D., Bougouma, Edith C., Sirima, Sodiomon B., Amenga-Etego, Lucas N., Ghansah, Anita K., Hodgson, Abraham V. O., Wilson, Michael D., Enimil, Anthony, Ansong, Daniel, Evans, Jennifer, Ademola, Subulade A., Apinjoh, Tobias O., Ndila, Carolyne M., Manjurano, Alphaxard, Drakeley, Chris, Reyburn, Hugh, Phu, Nguyen Hoan, Quyen, Nguyen Thi Ngoc, Thai, Cao Quang, Hien, Tran Tinh, Teo, Yik Ying, Manning, Laurens, Laman, Moses, Michon, Pascal, Karunajeewa, Harin, Siba, Peter, Allen, Steve, Allen, Angela, Bahlo, Melanie, Davis, Timothy M. E., Simpson, Victoria, Shelton, Jennifer, Spencer, Chris C. A., Busby, George B. J., Kerasidou, Angeliki, Drury, Eleanor, Stalker, Jim, Dilthey, Alexander, Mentzer, Alexander J., McVean, Gil, Bojang, Kalifa A., Doumbo, Ogobara, Modiano, David, Koram, Kwadwo A., Agbenyega, Tsiri, Amodu, Olukemi K., Achidi, Eric, Williams, Thomas N., Marsh, Kevin, Riley, Eleanor M., Molyneux, Malcolm, Taylor, Terrie, Dunstan, Sarah J., Farrar, Jeremy, Mueller, Ivo, Rockett, Kirk A., Kwiatkowski, Dominic P.

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Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects von Patsopoulos, Nikolaos A, Barcellos, Lisa F, Hintzen, Rogier Q, Schaefer, Catherine, van Duijn, Cornelia M, Noble, Janelle A, Raj, Towfique, Gourraud, Pierre-Antoine, Stranger, Barbara E, Oksenberg, Jorge, Olsson, Tomas, Taylor, Bruce V, Sawcer, Stephen, Hafler, David A, Carrington, Mary, De Jager, Philip L, de Bakker, Paul I W

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MicroRNAs miR-17 and miR-20a inhibit T cell activation genes and are under-expressed in MS whole blood von Cox, Mathew B, Cairns, Murray J, Gandhi, Kaushal S, Carroll, Adam P, Moscovis, Sophia, Stewart, Graeme J, Broadley, Simon, Scott, Rodney J, Booth, David R, Lechner-Scott, Jeannette

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Natural history of HFE simple heterozygosity for C282Y and H63D: A prospective 12-year study von Zaloumis, Sophie G, Allen, Katrina J, Bertalli, Nadine A, Turkovic, Lidija, Delatycki, Martin B, Nicoll, Amanda J, McLaren, Christine E, English, Dallas R, Hopper, John L, Giles, Graham G, Anderson, Gregory J, Olynyk, John K, Powell, Lawrie W, Gurrin, Lyle C

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Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 von Bahlo, Melanie, Booth, David R, Broadley, Simon A, Brown, Matthew A, Foote, Simon J, Griffiths, Lyn R, Kilpatrick, Trevor J, Lechner-Scott, Jeanette, Moscato, Pablo, Perreau, Victoria M, Rubio, Justin P, Scott, Rodney J, Stankovich, Jim, Stewart, Graeme J, Taylor, Bruce V, Wiley, James, Clarke, Glynnis, Cox, Mathew B, Csurhes, Peter A, Danoy, Patrick, Drysdale, Karen, Field, Judith, Greer, Judith M, Guru, Preethi, Hadler, Johanna, McMorran, Brendan J, Jensen, Cathy J, Johnson, Laura J, McCallum, Ruth, Merriman, Marilyn, Merriman, Tony, Pryce, Karen, Tajouri, Lotfi, Wilkins, Ella J, Browning, Brian L, Browning, Sharon R, Perera, Devindri, Broadley, Simon, 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

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The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis von Gandhi, Kaushal S., McKay, Fiona C., Cox, Mathew, Riveros, Carlos, Armstrong, Nicola, Heard, Robert N., Vucic, Steve, Williams, David W., Stankovich, Jim, Brown, Matthew, Danoy, Patrick, Stewart, Graeme J., Broadley, Simon, Moscato, Pablo, Lechner-Scott, Jeannette, Scott, Rodney J., Booth, David R.

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Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutations von Spencer‐Smith, Megan, Knight, Jacquelyn L, Lacaze, Emmanuelle, Depienne, Christel, Lockhart, Paul J, Richards, Linda J, Heron, Delphine, Leventer, Richard J, Robinson, Gail A, Ceslis, Amelia, Gibson, Emily, Giraudat, Kim, McIlroy, Alissandra, Paul, Lynn K, Siffredi, Vanessa, Bahlo, Melanie, Barker, Megan, Blondiaux, Eleonore, Edwards, Timothy J, Garel, Catherine, Heide, Solveig, Keren, Boris, Mandelstam, Simone A, Marsh, Ashley PL, McGillivray, George, Mignot, Cyril, Moutard, Marie‐Laure, Nava, Caroline, Pope, Kate, Rastetter, Agnès, Stephenson, Sarah EM, Valence, Stéphanie, de Villemeur, Thierry Billette, Wood, Amanda, Anderson, Vicki, Sherr, Elliott H

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A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosis von Riveros, Carlos, Mellor, Drew, Gandhi, Kaushal S, McKay, Fiona C, Cox, Mathew B, Berretta, Regina, Vaezpour, S Yahya, Inostroza-Ponta, Mario, Broadley, Simon A, Heard, Robert N, Vucic, Stephen, Stewart, Graeme J, Williams, David W, Scott, Rodney J, Lechner-Scott, Jeanette, Booth, David R, Moscato, Pablo

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Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility von Ma, Gerry Z M, Stankovich, Jim, Kilpatrick, Trevor J, Binder, Michele D, Field, Judith

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Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients von Jensen, Cathy J, Stankovich, Jim, Van der Walt, Anneke, Bahlo, Melanie, Taylor, Bruce V, van der Mei, Ingrid A F, Foote, Simon J, Kilpatrick, Trevor J, Johnson, Laura J, Wilkins, Ella, Field, Judith, Danoy, Patrick, Brown, Matthew A, Rubio, Justin P, Butzkueven, Helmut

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A comparison of self-reported and record-linked blood donation history in an Australian cohort von Bertalli, Nadine A., Allen, Katrina J., McLaren, Christine E., Turkovic, Lidija, Osborne, Nicholas J., Constantine, Clare C., Delatycki, Martin B., English, Dallas R., Giles, Graham G., Hopper, John L., Anderson, Gregory J., Olynyk, John K., Powell, Lawrie W., Gurrin, Lyle C.

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No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis von Goris, An, van Setten, Jessica, Diekstra, Frank, Ripke, Stephan, Patsopoulos, Nikolaos A, Sawcer, Stephen J, van Es, Michael, Andersen, Peter M, Melki, Judith, Meininger, Vincent, Hardiman, Orla, Landers, John E, Brown, Jr, Robert H, Shatunov, Aleksey, Leigh, Nigel, Al-Chalabi, Ammar, Shaw, Christopher E, Traynor, Bryan J, Chiò, Adriano, Restagno, Gabriella, Mora, Gabriele, Ophoff, Roel A, Oksenberg, Jorge R, Van Damme, Philip, Compston, Alastair, Robberecht, Wim, Dubois, Bénédicte, van den Berg, Leonard H, De Jager, Philip L, Veldink, Jan H, de Bakker, Paul I W

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Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis von Lin, Rui, Charlesworth, Jac, Stankovich, Jim, Perreau, Victoria M, Brown, Matthew A, Taylor, Bruce V

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Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips von Ritchie, Matthew E, Liu, Ruijie, Carvalho, Benilton S, Irizarry, Rafael A

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Familial recurrence risks for multiple sclerosis in Australia von O'Gorman, C, Freeman, S, Taylor, B V, Butzkueven, H, Broadley, S A

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