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Number of items: 6.

Jacquemont, S; Reymond, A; Zufferey, F; Harewood, L; Walters, R G; Kutalik, Z; Martinet, D; Shen, Y; Valsesia, A; Beckmann, N D; Thorleifsson, G; Belfiore, M; Bouquillon, S; Campion, D; de Leeuw, N; de Vries, B B A; Esko, T; Fernandez, B A; Fernández-Aranda, F; Fernández-Real, J M; Gratacòs, M; Guilmatre, A; Hoyer, J; Jarvelin, M R; Kooy, R F; Kurg, A; Le Caignec, C; Männik, K; Platt, O S; Sanlaville, D; Van Haelst, M M; Villatoro Gomez, S; Walha, F; Wu, B L; Yu, Y; Abourae, A; Addor, M C; Alembik, Y; Antonarakis, S E; Arveiler, B; Barth, M; Bednarek, N; Béna, F; Bergmann, S; Beri, M; Bernardini, L; Blaumeiser, B; Bonneau, D; Bottani, A; Boute, O; Brunner, H G; Cailley, D; Callier, P; Chiesa, J; Chrast, J; Coin, L; Coutton, C; Cuisset, J M; Cuvellier, J C; David, A; de Freminville, B; Delobel, B; Delrue, M A; Demeer, B; Descamps, D; Didelot, G; Dieterich, K; Disciglio, V; Doco-Fenzy, M; Drunat, S; Duban-Bedu, B; Dubourg, C; El-Sayed Moustafa, J S; Elliott, P; Faas, B H W; Faivre, L; Faudet, A; Fellmann, F; Ferrarini, A; Fisher, R; Flori, E; Forer, L; Gaillard, D; Gerard, M; Gieger, C; Gimelli, S; Gimelli, G; Grabe, H J; Guichet, A; Guillin, O; Hartikainen, A L; Heron, D; Hippolyte, L; Holder, M; Homuth, G; Isidor, B; Jaillard, S; Jaros, Z; Jiménez-Murcia, S; Helas, G J; Jonveaux, P; Kaksonen, S; Keren, B; Kloss-Brandstätter, A; Knoers, N V A M; Koolen, D A; Kroisel, P M; Kronenberg, F; Labalme, A; Landais, E; Lapi, E; Layet, V; Legallic, S; Leheup, B; Leube, B; Lewis, S; Lucas, J; MacDermot, K D; Magnusson, P; Marshall, C; Mathieu-Dramard, M; McCarthy, M I; Meitinger, T; Mencarelli, M A; Merla, G; Moerman, A; Mooser, V; Morice-Picard, F; Mucciolo, M; Nauck, M; Ndiaye, N C; Nordgren, A; Pasquier, L; Petit, F; Pfundt, R; Plessis, G; Rajcan-Separovic, E; Ramelli, G P; Rauch, A; Ravazzolo, R; Reis, A; Renieri, A; Richart, C; Ried, J S; Rieubland, C; Roberts, W; Roetzer, K M; Rooryck, C; Rossi, M; Saemundsen, E; Satre, V; Schurmann, C; Sigurdsson, E; Stavropoulos, D J; Stefansson, H; Tengström, C; Thorsteinsdóttir, U; Tinahones, F J; Touraine, R; Vallée, L; van Binsbergen, E; Van der Aa, N; Vincent-Delorme, C; Visvikis-Siest, S; Vollenweider, P; Völzke, H; Vulto-van Silfhout, A T; Waeber, G; Wallgren-Pettersson, C; Witwicki, R M; Zwolinksi, S; Andrieux, J; Estivill, X; Gusella, J F; Gustafsson, O; Metspalu, A; Scherer, S W; Stefansson, K; Blakemore, A I F; Beckmann, J S; Froguel, P (2011). Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature, 478(7367):97-102.

Grad, I; Hibaoui, Y; Jaconi, M; Chicha, L; Bergström-Tengzelius, R; Sailani, M R; Pelte, M F; Dahoun, S; Mitsiadis, T A; Töhönen, V; Bouillaguet, S; Antonarakis, S E; Kere, J; Zucchelli, M; Hovatta, O; Feki, A (2011). NANOG priming before full reprogramming may generate germ cell tumours. European Cells and Materials, 22:258-274.

Sharp, A J; Migliavacca, E; Dupre, Y; Stathaki, E; Sailani, M R; Baumer, A; Schinzel, A; Mackay, D J; Robinson, D O; Cobellis, G; Cobellis, L; Brunner, H G; Steiner, B; Antonarakis, S E (2010). Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15. Genome Research, 20(9):1271-1278.

Lyle, R; Béna, F; Sarantis, G; Gehrig, C; Lopez, G; Schinzel, A; Lespinasse, J; Bottani, A; Dahoun, S; Taine, L; Doco-Fenzy, M; Cornillet-Lefèbvre, P; Pelet, A; Lyonnet, S; Toutain, A; Colleaux, L; Horst, J; Kennerknecht, I; Wakamatsu, N; Descartes, M; Franklin, J C; Florentin-Arar, L; Kitsiou, S; Yahya-Graison, E A; Costantine, M; Sinet, P M; Delabar, J M; Antonarakis, S E (2009). Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21. European Journal of Human Genetics, 17(4):454-466.

Fellay, J; Ge, D; Shianna, K V; Colombo, S; Ledergerber, B; Cirulli, E T; Urban, T J; Zhang, K; Gumbs, C E; Smith, J P; Castagna, A; Cozzi-Lepri, A; De Luca, A; Easterbrook, P; Günthard, H F; Mallal, S; Mussini, C; Dalmau, J; Martinez-Picado, J; Miro, J M; Obel, N; Wolinsky, S M; Martinson, J J; Detels, R; Margolick, J B; Jacobson, L P; Descombes, P; Antonarakis, S E; Beckmann, J S; O'Brien, S J; Letvin, N L; McMichael, A J; Haynes, B F; Carrington, M; Feng, S; Telenti, A; Goldstein, D B (2009). Common genetic variation and the control of HIV-1 in humans. PLoS Genetics, 5(12):e1000791.

Chrast, R; Scott, H S; Madani, R; Huber, L; Wolfer, D P; Prinz, M; Aguzzi, A; Lipp, H P; Antonarakis, S E (2000). Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome. Human Molecular Genetics, 9(12):1853-1864.

This list was generated on Wed Jul 26 19:49:02 2017 CEST.