Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity von Kyrousi, Christina, O’Neill, Adam C., Brazovskaja, Agnieska, He, Zhisong, Kielkowski, Pavel, Coquand, Laure, Di Giaimo, Rossella, D’ Andrea, Pierpaolo, Belka, Alexander, Forero Echeverry, Andrea, Mei, Davide, Lenge, Matteo, Cruceanu, Cristiana, Buchsbaum, Isabel Y., Khattak, Shahryar, Fabien, Guimiot, Binder, Elisabeth, Elmslie, Frances, Guerrini, Renzo, Baffet, Alexandre D., Sieber, Stephan A., Treutlein, Barbara, Robertson, Stephen P., Cappello, Silvia

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Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum von Haldipur, Parthiv, Aldinger, Kimberly A, Bernardo, Silvia, Deng, Mei, Timms, Andrew E, Overman, Lynne M, Winter, Conrad, Lisgo, Steven N, Razavi, Ferechte, Silvestri, Evelina, Manganaro, Lucia, Adle-Biassette, Homa, Guimiot, Fabien, Russo, Rosa, Kidron, Debora, Hof, Patrick R, Gerrelli, Dianne, Lindsay, Susan J, Dobyns, William B, Glass, Ian A, Alexandre, Paula, Millen, Kathleen J

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Evidence of disrupted rhombic lip development in the pathogenesis of Dandy–Walker malformation von Haldipur, Parthiv, Bernardo, Silvia, Aldinger, Kimberly A., Sivakumar, Tarika, Millman, Jake, Sjoboen, Alexandria H., Dang, Derek, Dubocanin, Danilo, Deng, Mei, Timms, Andrew E., Davis, Brian D., Plummer, Jasmine T., Mankad, Kshitij, Oztekin, Ozgur, Manganaro, Lucia, Guimiot, Fabien, Adle-Biassette, Homa, Russo, Rosa, Siebert, Joseph R., Kidron, Debora, Petrilli, Giulia, Roux, Nathalie, Razavi, Ferechte, Glass, Ian A., Di Gioia, Cira, Silvestri, Evelina, Millen, Kathleen J.

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CAMSAPs organize an acentrosomal microtubule network from basal varicosities in radial glial cells von Coquand, Laure, Victoria, Guiliana Soraya, Tata, Alice, Carpentieri, Jacopo Amerigo, Brault, Jean-Baptiste, Guimiot, Fabien, Fraisier, Vincent, Baffet, Alexandre D

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Tonate Virus and Fetal Abnormalities, French Guiana, 2019 von Lambert, Veronique, Enfissi, Antoine, Lefebvre, Mathilde, Pomar, Leo, Kedous, Sobhi, Guimiot, Fabien, Carles, Gabriel, Lavergne, Anne, Rousset, Dominique, Hcini, Najeh

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Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms von Haldipur, Parthiv, Dang, Derek, Aldinger, Kimberly A, Janson, Olivia K, Guimiot, Fabien, Adle-Biasette, Homa, Dobyns, William B, Siebert, Joseph R, Russo, Rosa, Millen, Kathleen J

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Decision-making based on sFlt-1/PlGF ratios: are immunoassay results interchangeable for diagnosis or prognosis of preeclampsia? von Lefèvre, Guillaume, Hertig, Alexandre, Guibourdenche, Jean, Lévy, Pacifique, Bailleul, Sophie, Drouin, Dominique, Batusanski, Florence, Guimiot, Fabien, Boulanger, Henri

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Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly von Vuillaumier-Barrot, Sandrine, Bouchet-Séraphin, Céline, Chelbi, Malika, Devisme, Louise, Quentin, Samuel, Gazal, Steven, Laquerrière, Annie, Fallet-Bianco, Catherine, Loget, Philippe, Odent, Sylvie, Carles, Dominique, Bazin, Anne, Aziza, Jacqueline, Clemenson, Alix, Guimiot, Fabien, Bonnière, Maryse, Monnot, Sophie, Bole-Feysot, Christine, Bernard, Jean-Pierre, Loeuillet, Laurence, Gonzales, Marie, Socha, Koryna, Grandchamp, Bernard, Attié-Bitach, Tania, Encha-Razavi, Férechté, Seta, Nathalie

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Distinct subsets of multi-lymphoid progenitors support ontogeny-related changes in human lymphopoiesis von Keita, Seydou, Diop, Samuel, Lekiashvili, Shalva, Chabaane, Emna, Nelson, Elisabeth, Strullu, Marion, Arfeuille, Chloé, Guimiot, Fabien, Domet, Thomas, Duchez, Sophie, Evrard, Bertrand, Darde, Thomas, Larghero, Jerome, Verhoeyen, Els, Cumano, Ana, Macintyre, Elizabeth A., Kasraian, Zeinab, Jouen, François, Goodhardt, Michele, Garrick, David, Chalmel, Frederic, Alhaj Hussen, Kutaiba, Canque, Bruno

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Dynamic Expression Patterns of Progenitor and Pyramidal Neuron Layer Markers in the Developing Human Hippocampus von Cipriani, Sara, Nardelli, Jeannette, Verney, Catherine, Delezoide, Anne-Lise, Guimiot, Fabien, Gressens, Pierre, Adle-Biassette, Homa

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CD4 + CD8 + T-Lymphocytes in Xenogeneic and Human Graft-versus-Host Disease von Alhaj Hussen, Kutaiba, Michonneau, David, Biajoux, Vincent, Keita, Seydou, Dubouchet, Laetitia, Nelson, Elisabeth, Setterblad, Niclas, Le Buanec, Helene, Bouaziz, Jean-David, Guimiot, Fabien, Socié, Gérard, Canque, Bruno

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Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions von Teixeira, Luis, Guimiot, Fabien, Dodé, Catherine, Fallet-Bianco, Catherine, Millar, Robert P, Delezoide, Anne-Lise, Hardelin, Jean-Pierre

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CD117hi expression identifies a human fetal hematopoietic stem cell population with high proliferation and self-renewal potential von Maillard, Loïc, Sanfilippo, Sandra, Domenech, Carine, Kasmi, Nassima, Petit, Laurence, Jacques, Sébastien, Delezoide, Anne-Lise, Guimiot, Fabien, Eladak, Soria, Moison, Delphine, Nicolas, Nour, Rouiller-Fabre, Virginie, Pozzi-Godin, Stéphanie, Mennesson, Benoit, Brival, Marie-Laure, Letourneur, Franck, Jaffredo, Thierry, Chomienne, Christine, Souyri, Michèle

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Studies in an Early Development Window Unveils a Severe HSC Defect in both Murine and Human Fanconi Anemia von Domenech, Carine, Maillard, Loïc, Rousseau, Alix, Guidez, Fabien, Petit, Laurence, Pla, Marika, Clay, Denis, Guimiot, Fabien, Sanfilippo, Sandra, Jacques, Sebastien, de la Grange, Pierre, Robil, Noémie, Soulier, Jean, Souyri, Michèle

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Sostdc1 is expressed in all major compartments of developing and adult mammalian eyes von Valensi, Maud, Goldman, Gabrielle, Marchant, Dominique, Van Den Berghe, Loïc, Jonet, Laurent, Daruich, Alejandra, Robert, Matthieu P., Krejci, Eric, Klein, Christophe, Mascarelli, Frédéric, Versaux-Botteri, Claudine, Moulin, Alexandre, Putterman, Marc, Guimiot, Fabien, Molina, Thierry, Terris, Benoît, Brémond-Gignac, Dominique, Behar-Cohen, Francine, Abitbol, Marc M.

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Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome von Lévy, Jonathan, Coussement, Aurélie, Dupont, Céline, Guimiot, Fabien, Baumann, Clarisse, Viot, Géraldine, Passemard, Sandrine, Capri, Yline, Drunat, Séverine, Verloes, Alain, Pipiras, Eva, Benzacken, Brigitte, Dupont, Jean‐Michel, Tabet, Anne‐Claude

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Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases von Tessier, Aude, Sarreau, Mélie, Pelluard, Fanny, André, Gwenaelle, Blesson, Sophie, Bucourt, Martine, Dechelotte, Pierre, Faivre, Laurence, Frébourg, Thierry, Goldenberg, Alice, Goua, Valérie, Jeanne-Pasquier, Corinne, Guimiot, Fabien, Laquerriere, Annie, Laurent, Nicole, Lefebvre, Mathilde, Loget, Philippe, Maréchaud, Martine, Mechler, Charlotte, Perez, Marie-Josée, Sabourin, Jean Christophe, Verloes, Alain, Patrier, Sophie, Guerrot, Anne-Marie

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Case report: Antenatal diagnostic of a polymalformative syndrome due to biallelic BRCA2 mutations von Anquetil, Aude, Khung Savatovsky, Suonavy, Gavard, Laurent, Bazin, Anne, Guimiot, Fabien, Dubourg, Christele, Mandelbrot, Laurent, Picone, Olivier

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Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene von Saugier-Veber, Pascale, Marguet, Florent, Lecoquierre, François, Adle-Biassette, Homa, Guimiot, Fabien, Cipriani, Sara, Patrier, Sophie, Brasseur-Daudruy, Marie, Goldenberg, Alice, Layet, Valérie, Capri, Yline, Gérard, Marion, Frébourg, Thierry, Laquerrière, Annie

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Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1 von El Khattabi, Laïla, Guimiot, Fabien, Pipiras, Eva, Andrieux, Joris, Baumann, Clarisse, Bouquillon, Sonia, Delezoide, Anne-Lise, Delobel, Bruno, Demurger, Florence, Dessuant, Hélène, Drunat, Séverine, Dubourg, Christelle, Dupont, Céline, Faivre, Laurence, Holder-Espinasse, Muriel, Jaillard, Sylvie, Journel, Hubert, Lyonnet, Stanislas, Malan, Valérie, Masurel, Alice, Marle, Nathalie, Missirian, Chantal, Moerman, Alexandre, Moncla, Anne, Odent, Sylvie, Palumbo, Orazio, Palumbo, Pietro, Ravel, Aimé, Romana, Serge, Tabet, Anne-Claude, Valduga, Mylène, Vermelle, Marie, Carella, Massimo, Dupont, Jean-Michel, Verloes, Alain, Benzacken, Brigitte, Delahaye, Andrée

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