Characterization and identification of success factors for the first-year “parcours accès spécifique santé” (PASS) at the University of Bordeaux allowing PASS validation and entry... von Dupin, Isabelle, Barandon, Séverine, Bertrand, Caroline, Bordenave, Laurence, Chassaing, Véronique, Corcuff, Jean-Benoît, Dubus, Pierre, Duclos, Noémie, Guillon, Jean, Mamani-Matsuda, Maria, Müller, Bernard, Pellegrin, Jean-Luc, Alioum, Amadou

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Première année de fonctionnement du parcours accès spécifique santé (PASS) de l’Université de Bordeaux : caractérisation et identification des facteurs de réussite pour la validati... von Dupin, Isabelle, Barandon, Séverine, Bertrand, Caroline, Bordenave, Laurence, Chassaing, Véronique, Corcuff, Jean-Benoît, Dubus, Pierre, DUCLOS, Noémie C., Guillon, Jean, Mamani-Matsuda, Maria, Müller, Bernard, Pellegrin, Jean-Luc, Alioum, Amadou

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Comparative analysis of the duodenojejunal microbiome with the oral and fecal microbiomes reveals its stronger association with obesity and nutrition von Steinbach, Emilie, Belda, Eugeni, Alili, Rohia, Adriouch, Solia, Dauriat, Charlène J. G., Donatelli, Gianfranco, Dumont, Jean-Loup, Pacini, Filippo, Tuszynski, Thierry, Pelloux, Véronique, Jacques, Flavien, Creusot, Laura, Coles, Emavieve, Taillandier, Paul, Vazquez Gomez, Marta, Masi, Davide, Mateo, Véronique, André, Sébastien, Kordahi, Melissa, Rouault, Christine, Zucker, Jean-Daniel, Sokol, Harry, Genser, Laurent, Chassaing, Benoit, Le Roy, Tiphaine, Clément, Karine

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Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye von Chesneau, Bertrand, Ivashchenko, Véronique, Habib, Christophe, Gaston, Véronique, Escudié, Fréderic, Morel, Godelieve, Capri, Yline, Vincent-Delorme, Catherine, Calvas, Patrick, Chassaing, Nicolas, Plaisancié, Julie

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Structural Variant Disrupting the Expression of the Remote FOXC1 Gene in a Patient with Syndromic Complex Microphthalmia von Plaisancié, Julie, Chesneau, Bertrand, Fares-Taie, Lucas, Rozet, Jean-Michel, Pechmeja, Jacmine, Noero, Julien, Gaston, Véronique, Bailleul-Forestier, Isabelle, Calvas, Patrick, Chassaing, Nicolas

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Correction to: Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye von Chesneau, Bertrand, Ivashchenko, Véronique, Habib, Christophe, Gaston, Véronique, Escudié, Fréderic, Morel, Godelieve, Capri, Yline, Vincent-Delorme, Catherine, Calvas, Patrick, Chassaing, Nicolas, Plaisancié, Julie

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Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens von Patat, Olivier, Pagin, Adrien, Siegfried, Aurore, Mitchell, Valérie, Chassaing, Nicolas, Faguer, Stanislas, Monteil, Laetitia, Gaston, Véronique, Bujan, Louis, Courtade-Saïdi, Monique, Marcelli, François, Lalau, Guy, Rigot, Jean-Marc, Mieusset, Roger, Bieth, Eric

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Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network von Chassaing, Nicolas, Davis, Erica E, McKnight, Kelly L, Niederriter, Adrienne R, Causse, Alexandre, David, Véronique, Desmaison, Annaïck, Lamarre, Sophie, Vincent-Delorme, Catherine, Pasquier, Laurent, Coubes, Christine, Lacombe, Didier, Rossi, Massimiliano, Dufier, Jean-Louis, Dollfus, Helene, Kaplan, Josseline, Katsanis, Nicholas, Etchevers, Heather C, Faguer, Stanislas, Calvas, Patrick

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Structural Variant Disrupting the Expression of the Remote IFOXC1/I Gene in a Patient with Syndromic Complex Microphthalmia von Plaisancié, Julie, Chesneau, Bertrand, Fares-Taie, Lucas, Rozet, Jean-Michel, Pechmeja, Jacmine, Noero, Julien, Gaston, Véronique, Bailleul-Forestier, Isabelle, Calvas, Patrick, Chassaing, Nicolas

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Correction: Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia von Kesim, Yesim, Ceroni, Fabiola, Damián, Alejandra, Blanco-Kelly, Fiona, Ayuso, Carmen, Williamson, Kathy, Paquis-Flucklinger, Véronique, Bax, Dorine A, Plaisancié, Julie, Rieubland, Claudine, Chamlal, Mostafa, Cortón, Marta, Chassaing, Nicolas, Calvas, Patrick, Ragge, Nicola K

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Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia von Kesim, Yesim, Ceroni, Fabiola, Damián, Alejandra, Blanco-Kelly, Fiona, Ayuso, Carmen, Williamson, Kathy, Paquis-Flucklinger, Véronique, Bax, Dorine A, Plaisancié, Julie, Rieubland, Claudine, Chamlal, Mostafa, Cortón, Marta, Chassaing, Nicolas, Calvas, Patrick, Ragge, Nicola K

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Characterization of the antiproliferative activity of Xylopia aethiopica von Choumessi, Aphrodite T, Danel, Mathieu, Chassaing, Stefan, Truchet, Isabelle, Penlap, Véronique B, Pieme, Anatole Constant, Asonganyi, Tazoacha, Ducommun, Bernard, Valette, Annie

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Central venous catheter-related infection: does insertion site still matter? A French multicentric cohort study von Cosme, Vincent, Massart, Nicolas, Reizine, Florian, Machut, Anaïs, Vacheron, Charles-Hervé, Savey, Anne, Friggeri, Arnaud, Lepape, Alain

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Relationship between SARS-CoV-2 infection and ICU-acquired candidemia in critically ill medical patients: a multicenter prospective cohort study von Reizine, Florian, Massart, Nicolas, Mansour, Alexandre, Fedun, Yannick, Machut, Anaïs, Vacheron, Charles-Hervé, Savey, Anne, Friggeri, Arnaud, Lepape, Alain

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Confirmation of FZD5 implication in a cohort of 50 patients with ocular coloboma von Aubert-Mucca, Marion, Pernin-Grandjean, Julie, Marchasson, Sébastien, Gaston, Veronique, Habib, Christophe, Meunier, Isabelle, Sigaudy, Sabine, Kaplan, Josseline, Roche, Olivier, Denis, Danièle, Bitoun, Pierre, Haye, Damien, Verloes, Alain, Calvas, Patrick, Chassaing, Nicolas, Plaisancié, Julie

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Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia von Srour, Myriam, Chitayat, David, Caron, Véronique, Chassaing, Nicolas, Bitoun, Pierre, Patry, Lysanne, Cordier, Marie-Pierre, Capo-Chichi, José-Mario, Francannet, Christine, Calvas, Patrick, Ragge, Nicola, Dobrzeniecka, Sylvia, Hamdan, Fadi F., Rouleau, Guy A., Tremblay, André, Michaud, Jacques L.

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Association between selective digestive decontamination and decreased rate of acquired candidemia in mechanically ventilated ICU patients: a multicenter nationwide study von Reizine, Florian, Massart, Nicolas, Joussellin, Vincent, Machut, Anaïs, Vacheron, Charles-Hervé, Savey, Anne, Friggeri, Arnaud, Lepape, Alain

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Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway von Dubourg, Christèle, Carré, Wilfrid, Hamdi-Rozé, Houda, Mouden, Charlotte, Roume, Joëlle, Abdelmajid, Benmansour, Amram, Daniel, Baumann, Clarisse, Chassaing, Nicolas, Coubes, Christine, Faivre-Olivier, Laurence, Ginglinger, Emmanuelle, Gonzales, Marie, Levy-Mozziconacci, Annie, Lynch, Sally-Ann, Naudion, Sophie, Pasquier, Laurent, Poidvin, Amélie, Prieur, Fabienne, Sarda, Pierre, Toutain, Annick, Dupé, Valérie, Akloul, Linda, Odent, Sylvie, de Tayrac, Marie, David, Véronique

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Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta von Caron, Véronique, Chassaing, Nicolas, Ragge, Nicola, Boschann, Felix, Ngu, Angelina My-Hoa, Meloche, Elisabeth, Chorfi, Sarah, Lakhani, Saquib A., Ji, Weizhen, Steiner, Laurie, Marcadier, Julien, Jansen, Philip R., van de Pol, Laura A., van Hagen, Johanna M., Russi, Alvaro Serrano, Le Guyader, Gwenaël, Nordenskjöld, Magnus, Nordgren, Ann, Anderlid, Britt-Marie, Plaisancié, Julie, Stoltenburg, Corinna, Horn, Denise, Drenckhahn, Anne, Hamdan, Fadi F., Lefebvre, Mathilde, Attie-Bitach, Tania, Forey, Peggy, Smirnov, Vasily, Ernould, Françoise, Jacquemont, Marie-Line, Grotto, Sarah, Alcantud, Alberto, Coret, Alicia, Ferrer-Avargues, Rosario, Srivastava, Siddharth, Vincent-Delorme, Catherine, Romoser, Shelby, Safina, Nicole, Saade, Dimah, Lupski, James R., Calame, Daniel G., Geneviève, David, Chatron, Nicolas, Schluth-Bolard, Caroline, Myers, Kenneth A., Dobyns, William B., Calvas, Patrick, Salmon, Caroline, Holt, Richard, Elmslie, Frances, Allaire, Marc, Prigozhin, Daniil M., Tremblay, André, Michaud, Jacques L.

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Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor Impairment von Srour, Myriam, Caron, Véronique, Pearson, Toni, Nielsen, Sarah B., Lévesque, Sébastien, Delrue, Marie-Ange, Becker, Troy A., Hamdan, Fadi F., Kibar, Zoha, Sattler, Shannon G., Schneider, Michael C., Bitoun, Pierre, Chassaing, Nicolas, Rosenfeld, Jill A., Xia, Fan, Desai, Sonal, Roeder, Elizabeth, Kimonis, Virginia, Schneider, Adele, Littlejohn, Rebecca Okashah, Douzgou, Sofia, Tremblay, André, Michaud, Jacques L.

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