Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis von Hager, Jörg, Kamatani, Yoichiro, Cazier, Jean-Baptiste, Youhanna, Sonia, Ghassibe-Sabbagh, Michella, Platt, Daniel E, Abchee, Antoine B, Romanos, Jihane, Khazen, Georges, Othman, Raed, Badro, Danielle A, Haber, Marc, Salloum, Angelique K, Douaihy, Bouchra, Shasha, Nabil, Kabbani, Samer, Sbeite, Hana, Chammas, Elie, el Bayeh, Hamid, Rousseau, Francis, Zelenika, Diana, Gut, Ivo, Lathrop, Mark, Farrall, Martin, Gauguier, Dominique, Zalloua, Pierre A

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TFAP2B influences the effect of dietary fat on weight loss under energy restriction von Stocks, Tanja, Angquist, Lars, Banasik, Karina, Harder, Marie N, Taylor, Moira A, Hager, Jörg, Arner, Peter, Oppert, Jean-Michel, Martinez, J Alfredo, Polak, Jan, Rousseau, Francis, Langin, Dominique, Rössner, Stephan, Holst, Claus, MacDonald, Ian A, Kamatani, Yoichiro, Pfeiffer, Andreas F H, Kunesova, Marie, Saris, Wim H M, Hansen, Torben, Pedersen, Oluf, Astrup, Arne, Sørensen, Thorkild I A

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Technical Validation of a Reverse-Transcription Quantitative Polymerase Chain Reaction In Vitro Diagnostic Test for the Determination of MiR-31-3p Expression Levels in Formalin-Fix... von Ramon, Lucas, David, Catherine, Fontaine, Karine, Lallet, Elodie, Marcaillou, Charles, Martin-Lannerée, Séverine, Decaulne, Virginie, Vazart, Céline, Gélibert, Anne-Héloise, Abdelali, Raouf Ben, Costa, Jean-Marc, Rousseau, Francis, Thiébaut, Raphaële, Yost, Larry, Gaston-Mathé, Yann

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Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia von Rousseau, Francis, Bonaventure, Jacky, Legeai-Mallet, Laurence, Pelet, Anna, Rozet, Jean-Michel, Maroteaux, Pierre, Merrer, Martine Le, Munnich, Arnold

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Dietary factors impact on the association between CTSS variants and obesity related traits von Hooton, Henri, Angquist, Lars, Holst, Claus, Hager, Jorg, Rousseau, Francis, Hansen, Rikke D, Tjønneland, Anne, Roswall, Nina, van der A, Daphne L, Overvad, Kim, Jakobsen, Marianne Uhre, Boeing, Heiner, Meidtner, Karina, Palli, Domenico, Masala, Giovanna, Bouatia-Naji, Nabila, Saris, Wim H M, Feskens, Edith J M, Wareham, Nicolas J, Vimaleswaran, Karani S, Langin, Dominique, Loos, Ruth J F, Sørensen, Thorkild I A, Clément, Karine

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Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1 von Sacco, Roberto, Papaleo, Veruska, Hager, Jorg, Rousseau, Francis, Moessner, Rainald, Militerni, Roberto, Bravaccio, Carmela, Trillo, Simona, Schneider, Cindy, Melmed, Raun, Elia, Maurizio, Curatolo, Paolo, Manzi, Barbara, Pascucci, Tiziana, Puglisi-Allegra, Stefano, Reichelt, Karl-Ludvig, Persico, Antonio M

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Autism risk assessment in siblings of affected children using sex-specific genetic scores von Carayol, Jerome, Schellenberg, Gerard D, Dombroski, Beth, Genin, Emmanuelle, Rousseau, Francis, Dawson, Geraldine

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A Hepatocellular Carcinoma 5-Gene Score Associated With Survival of Patients After Liver Resection von Nault, Jean–Charles, De Reyniès, Aurélien, Villanueva, Augusto, Calderaro, Julien, Rebouissou, Sandra, Couchy, Gabrielle, Decaens, Thomas, Franco, Dominique, Imbeaud, Sandrine, Rousseau, Francis, Azoulay, Daniel, Saric, Jean, Blanc, Jean–Frédéric, Balabaud, Charles, Bioulac–Sage, Paulette, Laurent, Alexis, Laurent–Puig, Pierre, Llovet, Josep M, Zucman–Rossi, Jessica

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Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis von Philippi, Anne, Tores, Frédéric, Carayol, Jérome, Rousseau, Francis, Letexier, Mélanie, Roschmann, Elke, Lindenbaum, Pierre, Benajjou, Abdel, Fontaine, Karine, Vazart, Céline, Gesnouin, Philippe, Brooks, Peter, Hager, Jörg

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Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA von Edery, Patrick, Marcaillou, Charles, Sahbatou, Mourad, Labalme, Audrey, Chastang, Joelle, Touraine, Renaud, Tubacher, Emmanuel, Senni, Faiza, Bober, Michael B., Nampoothiri, Sheela, Jouk, Pierre-Simon, Steichen, Elisabeth, Berland, Siren, Toutain, Annick, Wise, Carol A., Sanlaville, Damien, Rousseau, Francis, Clerget-Darpoux, Françoise, Leutenegger, Anne-Louise

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Stop codon FGFR3 mutations in thanatophoric dwarfism type 1 von Munnich, Arnold, Sanak, Marek, Rousseau, Francis, Bonaventure, Jacky, Merrer, Martine Le, Maroteaux, Pierre, Delezoide, Anne-Lise, Narcy, Françoise, Saugier, Pascale

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Association between miR-31-3p expression and cetuximab efficacy in patients with KRAS wild-type metastatic colorectal cancer: a post-hoc analysis of the New EPOC trial von Pugh, Siân, Thiébaut, Raphaële, Bridgewater, John, Grisoni, Marie-Lise, Moutasim, Karwan, Rousseau, Francis, Thomas, Gareth J, Griffiths, Gareth, Liebaert, François, Primrose, John, Laurent-Puig, Pierre

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Hsa-miR-31-3p Expression Is Linked to Progression-free Survival in Patients with KRAS Wild-type Metastatic Colorectal Cancer Treated with Anti-EGFR Therapy von MANCEAU, Gilles, IMBEAUD, Sandrine, BACHET, Jean-Baptiste, CHIBAUDEL, Benoist, BOUCHE, Olivier, LANDI, Bruno, BIBEAU, Frédéric, LEROY, Karen, PENAULT-LIORCA, Frédérique, VAN LAETHEM, Jean-Luc, DEMETTER, Pieter, TEJPAR, Sabine, THIEBAUT, Raphaële, ROSSI, Simona, MOSAKHANI, Neda, ÖSTERLUND, Pia, RISTAMÄKI, Raija, SARHADI, Virinder, KNUUTILA, Sakari, BOIGE, Valérie, ANDRE, Thierry, LAURENT-PUIG, Pierre, LIEBAERT, François, FONTAINE, Karine, ROUSSEAU, Francis, GENIN, Bérengère, LE CORRE, Delphine, DIDELOT, Audrey, VINCENT, Marc

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Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta von Brooks, Peter, Marcaillou, Charles, Vanpeene, Maud, Saraiva, Jean-Paul, Stockholm, Daniel, Francke, Stephan, Favis, Reyna, Cohen, Nadine, Rousseau, Francis, Tores, Frédéric, Lindenbaum, Pierre, Hager, Jörg, Philippi, Anne

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Converging Evidence for an Association of ATP2B2 Allelic Variants with Autism in Male Subjects von Carayol, Jérôme, Sacco, Roberto, Tores, Frédéric, Rousseau, Francis, Lewin, Patricia, Hager, Jorg, Persico, Antonio M

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The GLO1 C332 (Ala111) allele confers autism vulnerability: Family-based genetic association and functional correlates von Gabriele, Stefano, Lombardi, Federica, Sacco, Roberto, Napolioni, Valerio, Altieri, Laura, Tirindelli, Maria Cristina, Gregorj, Chiara, Bravaccio, Carmela, Rousseau, Francis, Persico, Antonio M

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A gene for achondroplasia-hypochondroplasia maps to chromosome 4p von Munnich, Arnold, Sanak, Marek, Rousseau, Francis, Bonaventure, Jacky, Merrer, Martine Le, Maroteaux, Pierre, Weissenbach, Jean, Landais, Jean-Christophe, Stoll, Claude, Pelet, Anna, Legeai-Mallet, Laurence

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MiR 31 3p as a predictive biomarker of cetuximab efficacy effect in metastatic colorectal cancer (mCRC) patients enrolled in FIRE-3 study von Laurent-Puig, Pierre, Grisoni, Marie-Lise, Heinemann, Volker, Bonnetain, Franck, Fontaine, Karine, Vazart, Celine, Decaulne, Virginie, Rousseau, Francis, Courtieu, Bernard, Liebaert, Francois, Jung, Andreas, Neureiter, Daniel, Thiébaut, Raphaële, Stintzing, Sebastian

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A gender-specific genetic score to predict the risk of autism in siblings von Carayol, Jerome, Rousseau, Francis, Lewin⁎, Patricia

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Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism von Maussion, Gilles, Carayol, Jérôme, Lepagnol-Bestel, Aude-Marie, Tores, Frédéric, Loe-Mie, Yann, Milbreta, Ulla, Rousseau, Francis, Fontaine, Karine, Renaud, Julie, Moalic, Jean-Marie, Philippi, Anne, Chedotal, Alain, Gorwood, Philip, Ramoz, Nicolas, Hager, Jörg, Simonneau, Michel

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