Association between the MnSOD Ala-9Val polymorphism and development of schizophrenia and abnormal involuntary movements in the Xhosa population von Hitzeroth, Angelika, Niehaus, Dana J.H., Koen, Liezl, Botes, Willem C., Deleuze, J.F., Warnich, Louise

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The Impact of Genetic Variations in ADORA2A in the Association between Caffeine Consumption and Sleep von Erblang, Mégane, Drogou, Catherine, Gomez-Merino, Danielle, Metlaine, Arnaud, Boland, Anne, Deleuze, Jean François, Thomas, Claire, Sauvet, Fabien, Chennaoui, Mounir

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Hypogonadisme hypogonadotrophique (HH) familial avec syndrome cérébelleux. Découverte par exome de mutations du gène Patatin-like Phospholipase Domain Containing 6 . Relations géno... von Francou, B., Dr, Bouligand, J., Dr, Kaloustian, E., Dr, Kamenicky, P., Dr, Chabrolle, C., Dr, Deleuze, J.F., Dr, Meyer, V., Dr, Brailly-Tabard, S., Dr, Chanson, P., Pr, Guiochon-Mantel, A., Pr, Young, J., Pr

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P.1.a.035 - RNA signature and prediction to treatment response in first episode schizophrenia von Troudet, R., Bel Haj Ali, W., Barau, C., Boland-Auge, A., Deleuze, J.F., Leboyer, M., Jamain, S.

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RNA signature and prediction to treatment response in first episode schizophrenia von Troudet, R., Bel Haj Ali, W., Barau, C., Boland-Auge, A., Deleuze, J.F., Leboyer, M., Jamain, S.

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Novel genes associated with isolated optic nerve hypoplasia in 6 family trios ‐ a clinical and exome study von Bitoun, P., Boland Auge, A., Bacq Daian, D., PIpiras, E., Benzacken, B., Kuzbari, S., Renault, V., Parfait, B., Deleuze, J.F.

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Interactions Gène-Gène associées à la Polyarthrite Rhumatoïde dans la voie des adhérences focales von Veyssiere, M., Chalabi, S., Michou, L., Cornélis, F., Boland, A., Olaso, R., Deleuze, J.F., Petit-Teixeira, E., Chaudru, V.

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RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome von Belbachir, N., Portero, V., Gourraud, J.B., Jesel, L., Guilluy, C., Gaborit, N., Girardeau, A., Bonnaud, S., Pattier, S., Scott, C., Burel, S., Gaignerie, A., Genin, E., Deleuze, J.F., Dina, C., Schott, J.J., Probst, V., Redon, R., Charpentier, F., Le Scouarnec, S.

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La première étude d’association génome entier dans la neurofibromatose de type 1 : vers l’identification des modificateurs génétiques de l’expression clinique de la maladie... von Sabbagh, A., Pacot, L., Parfait, B., Boland-Auge, A., Bacq-Daian, D., Laurendeau, I., Ferkal, S., Briand, A., Allanore, L., Deleuze, J.F., Vidaud, M., Vidaud, D., Pasmant, E., Wolkenstein, P.

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Viva Europa, a Land of Excellence in Research and Innovation for Health and Wellbeing von Auffray, C, Sagner, M, Abdelhak, S, Adcock, I, Agusti, A, Amaral, M, Antonarakis, S, Arena, R, Argoul, F, Balling, R, Barabasi, A.L, Beckmann, J, Bjartell, A, Blomberg, N, Bourgeon, T, Boutron, B, Brahmachari, S, Brechot, C, Brightling, C, Cascante, M, Cesario, A, Charron, D, Chen, S.J, Chen, Z, Chung, F, Clement, K, Conesa, A, Cozzone, A, de Jong, M, Deleuze, J.F, Demotes, J, di Meglio, A, Djukanovic, R, Dogrusoz, U, Epel, E, Fischer, A, Gelemanovic, A, Goble, C, Gojobori, T, Goldman, M, Goossens, H, Gros, F, Guo, Y.K, Hainaut, P, Harrison, D, Hoffmann, H, Hood, L, Hunter, P, Jacob, Y, Kitano, H, Klingmuller, U, Knoppers, B, Kolch, W, Koopmans, M, Lancet, D, Laville, M, Lehn, J.M, Lévi, F, Lisistsa, A, Lotteau, V, Magnan, A, Mayosi, B, Metspalu, A, Moreau, Yves, N'Dow, J, Nicod, L, Noble, D, Nogueira, M.M, Norrby-Teglund, A, Nottale, L, Openshaw, P, Ozturk, M, Palkonen, S, Parodi, S, Pellet, J, Polasek, O, Price, N, Pristipino, C, Radstake, T, Raes, M, Roca, J, Rozman, D, Sabatier, P, Sasson, S, Schmeck, B, Serageldin, I, Simonds, A, Soares, B, Sterk, P, Superti-Furga, G, Supple, D, Tegner, J, Uhlen, M, van der Werf, S, Villoslada, P, Vinciguerra, M, Volpert, V, Webb, S, Wouters, E, Sanz, F

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Association of ABO blood groups with venous thrombosis recurrence in middle-aged patients: insights from a weighted Cox analysis dedicated to ambispective design von Munsch, G., Goumidi, L., Vlieg, A.V., Ibrahim-Kosta, M., Bruzelius, M., Deleuze, J.F., Rosendaal, F.R., Jacqmin-Gadda, H., Morange, P.E., Trégouët, D.A.

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Analysis and annotation of DNA methylation in two nonhuman primate species using the Infinium Human Methylation 450K and EPIC BeadChips von Pichon, F., Shen, Y.M., Busato, F., Jochems, S.P., Jacquelin, B., Grand, R. le, Deleuze, J.F., Muller-Trutwin, M., Tost, J.

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Association Studies in Candidate Genes: Strategies to Select SNPs to Be Tested von Cousin, E., Genin, E., Mace, S., Ricard, S., Chansac, C., del Zompo, M., Deleuze, J.F.

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Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism von Ward, J, Le, Ngoc-Quynh, Suryakant, S, Brody, Jennifer A, Amouyel, Philippe, Boland, A, Bown, R, Cullen, B, Debette, S, Deleuze, J.F, Emmerich, J, Graham, N, Germain, M, Anderson, J.J, Pell, J.P, Lyall, D.M, Lyall, L.M, Smith, D.J, Wiggins, Kerri L, Soria Fernández, José Manuel, Souto, Juan Carlos, Morange, Pierre-Emmanuel, Smith, N.L, Trégouët, David-Alexandre, Sabater-Lleal, Maria, Strawbridge, Rona J, Universitat Autònoma de Barcelona

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Antithrombin, protein C, and protein S: genome and transcriptome-wide association studies identify 7 novel loci regulating plasma levels von Ji, Y.K., Temprano-Sagrera, G., Holle, L.A., Bebo, A., Brody, J.A., , N.Q. le, Kangro, K., Brown, M.R., Martinez-Perez, A., Sitlani, C.M., Suchon, P., Kleber, M.E., Emmert, D.B., Ozel, A.B., Dobson, D.A., Tang, W.H., Llobet, D., Tracy, R.P., Deleuze, J.F., Delgado, G.E., Gögele, M., Wiggins, K.L., Souto, J.C., Pankow, J.S., Taylor, K.D., Trégouët, D.A., Moissl, A.P., Fuchsberger, C., Rosendaal, F.R., Morrison, A.C., Soria, J.M., Cushman, M., Morange, P.E., März, W., Hicks, A.A., Desch, K.C., Johnson, A.D., Vries, P.S. de, Wolberg, A.S., Smith, N.L., Sabater-Lleal, M.

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Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease von Young, W.J., Haessler, J., Benjamins, J.W., Repetto, L., Yao, J., Isaacs, A., Harper, A.R., Ramirez, J., Garnier, S., Duijvenboden, S. van, Baldassari, A.R., Concas, M.P., Duong, T., Foco, L., Isaksen, J.L., Mei, H., Noordam, R., Nursyifa, C., Richmond, A., Santolalla, M.L., Sitlani, C.M., Soroush, N., Thériault, S., Trompet, S., Aeschbacher, S., Ahmadizar, F., Alonso, A., Brody, J.A., Campbell, A., Correa, A., Darbar, D., Luca, A. de, Deleuze, J.F., Ellervik, C., Fuchsberger, C., Goel, A., Grace, C., Guo, X.Q., Hansen, T., Heckbert, S.R., Jackson, R.D., Kors, J.A., Lima-Costa, M.F., Linneberg, A., Macfarlane, P.W., Morrison, A.C., Navarro, P., Porteous, D.J., Pramstaller, P.P., Reiner, A.P., Risch, L., Schotten, U., Shen, X., Sinagra, G., Soliman, E.Z., Stoll, M., Tarazona-Santos, E., Tinker, A., Trajanoska, K., Villard, E., Warren, H.R., Whitsel, E.A., Wiggins, K.L., Arking, D.E., Avery, C.L., Conen, D., Girotto, G., Grarup, N., Hayward, C., Jukema, J.W., Mook-Kanamori, D.O., Olesen, M.S., Padmanabhan, S., Psaty, B.M., Pattaro, C., Ribeiro, A.L.P., Rotter, J.I., Stricker, B.H., Harst, P. van der, Duijn, C.M. van, Verweij, N., Wilson, J.G., Orini, M., Charron, P., Watkins, H., Kooperberg, C., Lin, H.J., Wilson, J.F., Kanters, J.K., Sotoodehnia, N., Mifsud, B., Lambiase, P.D., Tereshchenko, L.G., Munroe, P.B.

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Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation von Goumidi, L., Thibord, F., Wiggins, K.L., Li-Gao, R.F., Brown, M.R., Vlieg, A.V., Souto, J.C., Soria, J.M., Ibrahim-Kosta, M., Saut, N., Daian, D., Olaso, R., Amouyel, P., Debette, S., Boland, A., Bailly, P., Morrison, A.C., Mook-Kanamori, D.O., Deleuze, J.F., Johnson, A., Vries, P.S. de, Sabater-Lleal, M., Chiaroni, J., Smith, N.L., Rosendaal, F.R., Chasman, D.I., Tregouet, D.A., Morange, P.E.

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Cross-ancestry investigation of venousc genomic predictors von Thibord, F., Klarin, D., Brody, J.A., Chen, M.H., Levin, M.G., Chasman, D.I., Goode, E.L., Hveem, K., Teder-Laving, M., Martinez-Perez, A., Aissi, D., Daian-Bacq, D., Ito, K., Natarajan, P., Lutsey, P.L., Nadkarni, G.N., Vries, P.S. de, Cuellar-Partida, G., Wolford, B.N., Pattee, J.W., Kooperberg, C., Braekkan, S.K., Li-Gao, R.F., Saut, N., Sept, C., Germain, M., Judy, R.L., Wiggins, K.L., Ko, D., O'Donnell, C.J., Taylor, K.D., Giulianini, F., Andrade, M. de, Nost, T.H., Boland, A., Empana, J.P., Koyama, S., Gilliland, T., , R. do, Huffman, J.E., Wang, X., Zhou, W., Soria, J.M., Souto, J.C., Pankratz, N., Haessler, J., Hindberg, K., Rosendaal, F.R., Turman, C., Olaso, R., Kember, R.L., Bartz, T.M., Lynch, J.A., Heckbert, S.R., Armasu, S.M., Brumpton, B., Smadja, D.M., Jouven, X., Komuro, I., Clapham, K.R., Loos, R.J.F., Willer, C.J., Sabater-Lleal, M., Pankow, J.S., Reiner, A.P., Morelli, V.M., Ridker, P.M., Vlieg, A.V., Deleuze, J.F., Kraft, P., Rader, D.J., Lee, K.M., Psaty, B.M., Skogholt, A.H., Emmerich, J., Suchon, P., Rich, S.S., Vy, H.T., Tang, W.H., Jackson, R.D., Hansen, J.B., Morange, P.E., Kabrhel, C., Tregouet, D.A., Damrauer, S.M., Johnson, A.D., Smith, N.L.

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Gender specific airway gene expression in COPD sub-phenotypes supports a role of mitochondria and of different types of leukocytes von Esteve-Codina, A., Hofer, T.P., Burggraf, D., Heiss-Neumann, M.S., Gesierich, W., Boland, A., Olaso, R., Bihoreau, M.T., Deleuze, J.F., Moeller, W., Schmid, O., Artigas, M.S., Renner, K., Hohlfeld, J.M., Welte, T., Fuehner, T., Jerrentrup, L., Koczulla, A.R., Greulich, T., Prasse, A., Muller-Quernheim, J., Gupta, S., Brightling, C., Subramanian, D.R., Parr, D.G., Kolsum, U., Gupta, V., Barta, I., Dome, B., Strausz, J., Stendardo, M., Piattella, M., Boschetto, P., Korzybski, D., Gorecka, D., Nowinski, A., Dabad, M., Fernandez-Callejo, M., Endesfelder, D., Castell, W. zu, Hiemstra, P.S., Venge, P., Noessner, E., Griebel, T., Heath, S., Singh, D., Gut, I., Ziegler-Heitbrock, L.

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Construction of a 3.7-Mb Physical Map within Human Chromosome 20p12 Ordering 18 Markers in the Alagille Syndrome Locus von Pollet, Nicolas, Dhorne-Pollet, Sophie, Deleuze, Jean-François, Boccaccio, Claire, Driancourt, Catherine, Raynaud, Nicole, Le Paslier, Denis, Hadchouel, Michelle, Meunier-Rotival, Michèle

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