Association of LY9 in UK and Canadian SLE families von Graham, D S Cunninghame, Vyse, T J, Fortin, P R, Montpetit, A, Cai, Y-c, Lim, S, McKenzie, T, Farwell, L, Rhodes, B, Chad, L, Hudson, T J, Sharpe, A, Terhorst, C, Greenwood, C M T, Wither, J, Rioux, J D

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The Founder Mutation MSH21906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population von Foulkes, W.D., Thiffault, I., Gruber, S.B., Horwitz, M., Hamel, N., Lee, C., Shia, J., Markowitz, A., Figer, A., Friedman, E., Farber, D., Greenwood, C. M.T., Bonner, J.D., Nafa, K., Walsh, T., Marcus, V., Tomsho, L., Gebert, J., Macrae, F.A., Gaff, C.L., Paillerets, B. Bressac-de, Gregersen, P.K., Weitzel, J.N., Gordon, P.H., MacNamara, E., King, M.-C., Hampel, H., de la Chapelle, A., Boyd, J., Offit, K., Rennert, G., Chong, G., Ellis, N.A.

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Stability of the human sperm DNA methylome to folic acid fortification and short-term supplementation von Chan, D., McGraw, S., Klein, K., Wallock, L.M., Konermann, C., Plass, C., Chan, P., Robaire, B., Jacob, R.A., Greenwood, C.M.T., Trasler, J.M.

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Opioid receptor mu 1 gene, fat intake and obesity in adolescence von Haghighi, A, Melka, M G, Bernard, M, Abrahamowicz, M, Leonard, G T, Richer, L, Perron, M, Veillette, S, Xu, C J, Greenwood, C M T, Dias, A, El-Sohemy, A, Gaudet, D, Paus, T, Pausova, Z

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Elevated rates of schizophrenia in a familial sample with mental illness and intellectual disability von Greenwood, C. M. T., Husted, J., Bomba, M. D., Hodgkinson, K. A., Bassett, A. S.

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Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases von Chen, Yiheng, Lu, Tianyuan, Pettersson-Kymmer, Ulrika, Stewart, Isobel D., Butler-Laporte, Guillaume, Nakanishi, Tomoko, Cerani, Agustin, Liang, Kevin Y. H., Yoshiji, Satoshi, Willett, Julian Daniel Sunday, Su, Chen-Yang, Raina, Parminder, Greenwood, Celia M. T., Farjoun, Yossi, Forgetta, Vincenzo, Langenberg, Claudia, Zhou, Sirui, Ohlsson, Claes, Richards, J. Brent

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Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study von Forgetta, Vincenzo, Keller-Baruch, Julyan, Forest, Marie, Durand, Audrey, Bhatnagar, Sahir, Kemp, John P, Nethander, Maria, Evans, Daniel, Morris, John A, Kiel, Douglas P, Rivadeneira, Fernando, Johansson, Helena, Harvey, Nicholas C, Mellström, Dan, Karlsson, Magnus, Cooper, Cyrus, Evans, David M, Clarke, Robert, Kanis, John A, Orwoll, Eric, McCloskey, Eugene V, Ohlsson, Claes, Pineau, Joelle, Leslie, William D, Greenwood, Celia M T, Richards, J Brent

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Variants of the SFTPA1 and SFTPA2 genes and susceptibility to tuberculosis in Ethiopia von MALIK, S, GREENWOOD, C. M. T, EGUALE, T, KIFLE, A, BEYENE, J, HABTE, A, TADESSE, A, GEBREXABHER, H, BRITTON, S, SCHURR, E

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Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis von Manousaki, Despoina, Dudding, Tom, Haworth, Simon, Hsu, Yi-Hsiang, Liu, Ching-Ti, Medina-Gómez, Carolina, Voortman, Trudy, van der Velde, Nathalie, Melhus, Håkan, Robinson-Cohen, Cassianne, Cousminer, Diana L., Nethander, Maria, Vandenput, Liesbeth, Noordam, Raymond, Forgetta, Vincenzo, Greenwood, Celia M.T., Biggs, Mary L., Psaty, Bruce M., Rotter, Jerome I., Zemel, Babette S., Mitchell, Jonathan A., Taylor, Bruce, Lorentzon, Mattias, Karlsson, Magnus, Jaddoe, Vincent V.W., Tiemeier, Henning, Campos-Obando, Natalia, Franco, Oscar H., Utterlinden, Andre G., Broer, Linda, van Schoor, Natasja M., Ham, Annelies C., Ikram, M. Arfan, Karasik, David, de Mutsert, Renée, Rosendaal, Frits R., den Heijer, Martin, Wang, Thomas J., Lind, Lars, Orwoll, Eric S., Mook-Kanamori, Dennis O., Michaëlsson, Karl, Kestenbaum, Bryan, Ohlsson, Claes, Mellström, Dan, de Groot, Lisette C.P.G.M., Grant, Struan F.A., Kiel, Douglas P., Zillikens, M. Carola, Rivadeneira, Fernando, Sawcer, Stephen, Timpson, Nicholas J., Richards, J. Brent

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The HNPCC associated MSH21906G→C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population von Sun, S, Greenwood, C M T, Thiffault, I, Hamel, N, Chong, G, Foulkes, W D

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Heritability of schizophrenia and major affective disorder as a function of age, in the presence of strong cohort effects von Husted, Janice A, Greenwood, Celia M T, Bassett, Anne S

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A tree-based model for allele-sharing-based linkage analysis in human complex diseases von Xu, W., Schulze, T.G., DePaulo, J.R., Bull, S.B., McMahon, F.J., Greenwood, C.M.T.

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HostSeq: a Canadian whole genome sequencing and clinical data resource von Yoo, S, Garg, E, Elliott, L T, Hung, R J, Halevy, A R, Brooks, J D, Bull, S B, Gagnon, F, Greenwood, Cmt, Lawless, J F, Paterson, A D, Sun, L, Zawati, M H, Lerner-Ellis, J, Abraham, Rjs, Birol, I, Bourque, G, Garant, J-M, Gosselin, C, Li, J, Whitney, J, Thiruvahindrapuram, B, Herbrick, J-A, Lorenti, M, Reuter, M S, Adeoye, O O, Liu, S, Allen, U, Bernier, F P, Biggs, C M, Cheung, A M, Cowan, J, Herridge, M, Maslove, D M, Modi, B P, Mooser, V, Morris, S K, Ostrowski, M, Parekh, R S, Pfeffer, G, Suchowersky, O, Taher, J, Upton, J, Warren, R L, Yeung, Rsm, Aziz, N, Turvey, S E, Knoppers, B M, Lathrop, M, Jones, Sjm, Scherer, S W, Strug, L J

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Linkage of Tuberculosis to Chromosome 2q35 Loci, Including NRAMP1, in a Large Aboriginal Canadian Family von Greenwood, Celia M.T., Fujiwara, T. Mary, Boothroyd, Lucy J., Miller, Mark A., Frappier, Danielle, Fanning, E. Anne, Schurr, Erwin, Morgan, Kenneth

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Validation of a predictive model of idiopathic membranous nephropathy: Its clinical and research implications von Cattran, Daniel C., Pei, York, Greenwood, Celia M.T., Ponticelli, Claudio, Passerini, Patrizia, Honkanen, Eero

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A hierarchical clustering method for estimating copy number variation von Xing, Baifang, Greenwood, Celia M. T., Bull, Shelley B.

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Analysis of Affected Sib Pairs, with Covariates—With and Without Constraints von Greenwood, Celia M.T., Bull, Shelley B.

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Efficient p-value estimation in massively parallel testing problems von Kustra, Rafal, Shi, Xiaofei, Murdoch, Duncan J., Greenwood, Celia M. T., Rangrej, Jagadish

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The HNPCC associated MSH21906G arrow right C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population von Sun, S, Greenwood, C M T, Thiffault, I, Hamel, N, Chong, G, Foulkes, W D

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Patients with systemic autoimmune diseases could not distinguish comorbidities from their index disease von Hudson, Marie, Bernatsky, Sasha, Taillefer, Suzanne, Fortin, Paul R, Wither, Joan, Baron, Murray

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