Suchergebnisse - Meyer, Vincent

Impact of pre- and post-variant filtration strategies on imputation von Charon, Céline, Allodji, Rodrigue, Meyer, Vincent, Deleuze, Jean-François

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Publisher Correction: Impact of pre- and post-variant filtration strategies on imputation von Charon, Céline, Allodji, Rodrigue, Meyer, Vincent, Deleuze, Jean‑François

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Global Overview of Response Rates in Patient and Health Care Professional Surveys in Surgery: A Systematic Review von Meyer, Vincent Maurice, Benjamens, Stan, Moumni, Mostafa El, Lange, Johan F. M., Pol, Robert A.

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Role of Local Excision for Suspected Regrowth in a Watch and Wait Strategy for Rectal Cancer von Geubels, Barbara M., Meyer, Vincent M., van Westreenen, Henderik L., Beets, Geerard L., Grotenhuis, Brechtje A.

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Region-specific expression of young small-scale duplications in the human central nervous system von Brohard-Julien, Solène, Frouin, Vincent, Meyer, Vincent, Chalabi, Smahane, Deleuze, Jean-François, Le Floch, Edith, Battail, Christophe

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A comparison of high-throughput SARS-CoV-2 sequencing methods from nasopharyngeal samples von Gerber, Zuzana, Daviaud, Christian, Delafoy, Damien, Sandron, Florian, Alidjinou, Enagnon Kazali, Mercier, Jonathan, Gerber, Sylvain, Meyer, Vincent, Boland, Anne, Bocket, Laurence, Olaso, Robert, Deleuze, Jean-François

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Haploinsufficiency of Dmxl2, Encoding a Synaptic Protein, Causes Infertility Associated with a Loss of GnRH Neurons in Mouse von Tata, Brooke, Huijbregts, Lukas, Jacquier, Sandrine, Csaba, Zsolt, Genin, Emmanuelle, Meyer, Vincent, Leka, Sofia, Dupont, Joelle, Charles, Perrine, Chevenne, Didier, Carel, Jean-Claude, Léger, Juliane, de Roux, Nicolas

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Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes von Simioni, Milena, Artiguenave, François, Meyer, Vincent, Sgardioli, Ilária C., Viguetti-Campos, Nilma L., Lopes Monlleó, Isabella, Maciel-Guerra, Andréa T., Steiner, Carlos E., Gil-da-Silva-Lopes, Vera L.

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Delayed Surgery after Neoadjuvant Treatment for Rectal Cancer Does Not Lead to Impaired Quality of Life, Worry for Cancer, or Regret von Meyer, Vincent Maurice, Meuzelaar, Richtje R, Schoenaker, Yvonne, de Groot, Jan-Willem, de Boer, Edwin, Reerink, Onno, de Vos tot Nederveen Cappel, Wouter, Beets, Geerard L, van Westreenen, Henderik L

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Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples von Bonnet, Eric, Moutet, Marie-Laure, Baulard, Céline, Bacq-Daian, Delphine, Sandron, Florian, Mesrob, Lilia, Fin, Bertrand, Delépine, Marc, Palomares, Marie-Ange, Jubin, Claire, Blanché, Hélène, Meyer, Vincent, Boland, Anne, Olaso, Robert, Deleuze, Jean-François

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Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesis von Letouzé, Eric, Shinde, Jayendra, Renault, Victor, Couchy, Gabrielle, Blanc, Jean-Frédéric, Tubacher, Emmanuel, Bayard, Quentin, Bacq, Delphine, Meyer, Vincent, Semhoun, Jérémy, Bioulac-Sage, Paulette, Prévôt, Sophie, Azoulay, Daniel, Paradis, Valérie, Imbeaud, Sandrine, Deleuze, Jean-François, Zucman-Rossi, Jessica

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QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction von Deveau, Paul, Colmet Daage, Leo, Oldridge, Derek, Bernard, Virginie, Bellini, Angela, Chicard, Mathieu, Clement, Nathalie, Lapouble, Eve, Combaret, Valerie, Boland, Anne, Meyer, Vincent, Deleuze, Jean-Francois, Janoueix-Lerosey, Isabelle, Barillot, Emmanuel, Delattre, Olivier, Maris, John M, Schleiermacher, Gudrun, Boeva, Valentina

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Association of modifiers and other genetic factors explain Marfan syndrome clinical variability von Aubart, Melodie, Gazal, Steven, Arnaud, Pauline, Benarroch, Louise, Gross, Marie-Sylvie, Buratti, Julien, Boland, Anne, Meyer, Vincent, Zouali, Habib, Hanna, Nadine, Milleron, Olivier, Stheneur, Chantal, Bourgeron, Thomas, Desguerre, Isabelle, Jacob, Marie-Paule, Gouya, Laurent, Génin, Emmanuelle, Deleuze, Jean-François, Jondeau, Guillaume, Boileau, Catherine

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Papua New Guinean Genomes Reveal the Complex Settlement of North Sahul von Brucato, Nicolas, André, Mathilde, Tsang, Roxanne, Saag, Lauri, Kariwiga, Jason, Sesuki, Kylie, Beni, Teppsy, Pomat, William, Muke, John, Meyer, Vincent, Boland, Anne, Deleuze, Jean-François, Sudoyo, Herawati, Mondal, Mayukh, Pagani, Luca, Gallego Romero, Irene, Metspalu, Mait, Cox, Murray P, Leavesley, Matthew, Ricaut, François-Xavier

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The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMD von Gargaun, Elena, Falcone, Sestina, Solé, Guilhem, Durigneux, Julien, Urtizberea, Andoni, Cuisset, Jean Marie, Benkhelifa-Ziyyat, Sofia, Julien, Laura, Boland, Anne, Sandron, Florian, Meyer, Vincent, Deleuze, Jean François, Salgado, David, Desvignes, Jean-Pierre, Béroud, Christophe, Chessel, Anatole, Blesius, Alexia, Krahn, Martin, Levy, Nicolas, Leturcq, France, Pietri-Rouxel, France

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KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations von Klebe, Stephan, Lossos, Alexander, Azzedine, Hamid, Mundwiller, Emeline, Sheffer, Ruth, Gaussen, Marion, Marelli, Cecilia, Nawara, Magdalena, Carpentier, Wassila, Meyer, Vincent, Rastetter, Agnès, Martin, Elodie, Bouteiller, Delphine, Orlando, Laurent, Gyapay, Gabor, El-Hachimi, Khalid H, Zimmerman, Batel, Gamliel, Moriya, Misk, Adel, Lerer, Israela, Brice, Alexis, Durr, Alexandra, Stevanin, Giovanni

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Cyclin A2/E1 activation defines a hepatocellular carcinoma subclass with a rearrangement signature of replication stress von Bayard, Quentin, Meunier, Léa, Peneau, Camille, Renault, Victor, Shinde, Jayendra, Nault, Jean-Charles, Mami, Iadh, Couchy, Gabrielle, Amaddeo, Giuliana, Tubacher, Emmanuel, Bacq, Delphine, Meyer, Vincent, La Bella, Tiziana, Debaillon-Vesque, Audrey, Bioulac-Sage, Paulette, Seror, Olivier, Blanc, Jean-Frédéric, Calderaro, Julien, Deleuze, Jean-François, Imbeaud, Sandrine, Zucman-Rossi, Jessica, Letouzé, Eric

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Report on three additional patients and genotype–phenotype correlation in SLC25A22-related disorders group von Lemattre, Camille, Imbert-Bouteille, Marion, Gatinois, Vincent, Benit, Paule, Sanchez, Elodie, Guignard, Thomas, Tran Mau-Them, Frédéric, Haquet, Emmanuelle, Rivier, François, Carme, Emilie, Roubertie, Agathe, Boland, Anne, Lechner, Doris, Meyer, Vincent, Thevenon, Julien, Duffourd, Yannis, Rivière, Jean-Baptiste, Deleuze, Jean-François, Wells, Constance, Molinari, Florence, Rustin, Pierre, Blanchet, Patricia, Geneviève, David

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SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome von Hanchate, Naresh Kumar, Giacobini, Paolo, Lhuillier, Pierre, Parkash, Jyoti, Espy, Cécile, Fouveaut, Corinne, Leroy, Chrystel, Baron, Stéphanie, Campagne, Céline, Vanacker, Charlotte, Collier, Francis, Cruaud, Corinne, Meyer, Vincent, García-Piñero, Alfons, Dewailly, Didier, Cortet-Rudelli, Christine, Gersak, Ksenija, Metz, Chantal, Chabrier, Gérard, Pugeat, Michel, Young, Jacques, Hardelin, Jean-Pierre, Prevot, Vincent, Dodé, Catherine

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ABCA7 rare variants and Alzheimer disease risk von Le Guennec, Kilan, Nicolas, Gaël, Quenez, Olivier, Charbonnier, Camille, Wallon, David, Bellenguez, Céline, Grenier-Boley, Benjamin, Rousseau, Stéphane, Richard, Anne-Claire, Rovelet-Lecrux, Anne, Bacq, Delphine, Garnier, Jean-Guillaume, Olaso, Robert, Boland, Anne, Meyer, Vincent, Deleuze, Jean-François, Amouyel, Philippe, Munter, Hans Markus, Bourque, Guillaume, Lathrop, Mark, Frebourg, Thierry, Redon, Richard, Letenneur, Luc, Dartigues, Jean-François, Pasquier, Florence, Rollin-Sillaire, Adeline, Génin, Emmanuelle, Lambert, Jean-Charles, Hannequin, Didier, Campion, Dominique

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