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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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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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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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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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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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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Mathematical models for the action of alpha-amylase on amylose von Banks, W., Greenwood, C.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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MOLECULAR PROPERTIES OF THE STARCH COMPONENTS AND THEIR RELATION TO THE STRUCTURE OF THE GRANULE von Banks, W., Greenwood, C. T.

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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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Studies on the biosynthesis of starch granules. 2. The properties of the components of starches from smooth- and wrinkled-seeded peas during growth von GREENWOOD, C T, THOMSON, J

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Comments on “enzymic methods for the microdetermination of glycogen and amylopectin, and their unit chain-lengths” von Banks, W., Greenwood, C.T.

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The structure of hydroxyethyl starch von BANKS, W., GREENWOOD, C. T., MUIR, D. D.

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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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