Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids von Alcala, N., Leblay, N., Gabriel, A. A. G., Mangiante, L., Hervas, D., Giffon, T., Sertier, A. S., Ferrari, A., Derks, J., Ghantous, A., Delhomme, T. M., Chabrier, A., Cuenin, C., Abedi-Ardekani, B., Boland, A., Olaso, R., Meyer, V., Altmuller, J., Le Calvez-Kelm, F., Durand, G., Voegele, C., Boyault, S., Moonen, L., Lemaitre, N., Lorimier, P., Toffart, A. C., Soltermann, A., Clement, J. H., Saenger, J., Field, J. K., Brevet, M., Blanc-Fournier, C., Galateau-Salle, F., Le Stang, N., Russell, P. A., Wright, G., Sozzi, G., Pastorino, U., Lacomme, S., Vignaud, J. M., Hofman, V., Hofman, P., Brustugun, O. T., Lund-Iversen, M., Thomas de Montpreville, V., Muscarella, L. A., Graziano, P., Popper, H., Stojsic, J., Deleuze, J. F., Herceg, Z., Viari, A., Nuernberg, P., Pelosi, G., Dingemans, A. M. C., Milione, M., Roz, L., Brcic, L., Volante, M., Papotti, M. G., Caux, C., Sandoval, J., Hernandez-Vargas, H., Brambilla, E., Speel, E. J. M., Girard, N., Lantuejoul, S., McKay, J. D., Foll, M., Fernandez-Cuesta, L.

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Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells von Stouffer, M.A., Khalaf-Nazzal, R., Cifuentes-Diaz, C., Albertini, G., Bandet, E., Grannec, G., Lavilla, V., Deleuze, J.-F., Olaso, R., Nosten-Bertrand, M., Francis, F.

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Highly efficient and sensitive membrane-based concentration process allows quantification, surveillance, and sequencing of viruses in large volumes of wastewater von El Soufi, G, Di Jorio, L, Gerber, Z, Cluzel, N, Van Assche, J, Delafoy, D, Olaso, R, Daviaud, C, Loustau, T, Schwartz, C, Trebouet, D, Hernalsteens, O, Marechal, V, Raffestin, S, Rousset, D, Van Lint, C, Deleuze, J F, Boni, M, Rohr, O, Villain-Gambier, M, Wallet, C

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17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression von Le Guennec, K, Quenez, O, Nicolas, G, Wallon, D, Rousseau, S, Richard, A-C, Alexander, J, Paschou, P, Charbonnier, C, Bellenguez, C, Grenier-Boley, B, Lechner, D, Bihoreau, M-T, Olaso, R, Boland, A, Meyer, V, Deleuze, J-F, Amouyel, P, Munter, H M, Bourque, G, Lathrop, M, Frebourg, T, Redon, R, Letenneur, L, Dartigues, J-F, Martinaud, O, Kalev, O, Mehrabian, S, Traykov, L, Ströbel, T, Le Ber, I, Caroppo, P, Epelbaum, S, Jonveaux, T, Pasquier, F, Rollin-Sillaire, A, Génin, E, Guyant-Maréchal, L, Kovacs, G G, Lambert, J-C, Hannequin, D, Campion, D, Rovelet-Lecrux, A

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SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease von Nicolas, G, Charbonnier, C, Wallon, D, Quenez, O, Bellenguez, C, Grenier-Boley, B, Rousseau, S, Richard, A-C, Rovelet-Lecrux, A, Le Guennec, K, Bacq, D, Garnier, J-G, Olaso, R, Boland, A, Meyer, V, Deleuze, J-F, Amouyel, P, Munter, H M, Bourque, G, Lathrop, M, Frebourg, T, Redon, R, Letenneur, L, Dartigues, J-F, Génin, E, Lambert, J-C, Hannequin, D, Campion, D

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Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation von Ibrahim-Kosta, M., Suchon, P., Couturaud, F., Smadja, D., Olaso, R., Germain, M., Saut, N., Goumidi, L., Derbois, C., Thibord, F., Debette, S., Amouyel, P., Deleuze, J. F., van Doorn, P., Castoldi, E., Patin, E., Alessi, M. C., Trégouët, D. A., Morange, P. E.

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30 years of intelligence models in management and business: A bibliometric review von López-Robles, J.R., Otegi-Olaso, J.R., Porto Gómez, I., Cobo, M.J.

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Is there still room for additional common susceptibility alleles for venous thromboembolism? von Trégouët, D. A., Delluc, A., Roche, A., Derbois, C., Olaso, R., Germain, M., Andrade, M., Tang, W., Chasman, D. I., Hylckama Vlieg, A., Reitsma, P. H., Kabrhel, C., Smith, N., Morange, P. E.

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AB0004 Characterization of Putative Pre-RA Signatures by Transcriptome Analysis von Petit-Teixeira, E., Derbois, C., Dalmasso, C., Olaso, R., Ambroise, C., Ben Kilani, M.S., Deleuze, J.-F., Gabay, C., Cornelis, F., Finckh, A.

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A transcriptomic analysis of type II autosomal dominant osteopetrosis osteoclasts von Coudert, A.E, Olaso, R, Collet, C, de Vernejoul, M.-C

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Is Aicardi Syndrome truly linked to a mutation on X-Chromosome? von Cavallin, M, Nitschké, P, Petit, J.B, Meyer, V, Olaso, R, Darra, F, Fiorini, E, Lebon, S, Veggiotti, P.A, Vigevano, F, Gataullina, S, Bourgeois, M, Arzimanoglou, A, Epitashvili, N, Desguerre, I, Dulac, O, Dalla Bernardina, B, Bahi-Buisson, N

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Transforming Growth Factor β1 and β2 Reduce the Number of Gonocytes by Increasing Apoptosis von Olaso, R., Pairault, C., Boulogne, B., Durand, P., Habert, R.

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Transforming growth factor beta 1 and beta 2 reduce the number of gonocytes by increasing apoptosis von Olaso, R., Pairault, C., Boulogne, B., Durand, P., Habert, René

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Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells von Stouffer, M.A, Khalaf-Nazzal, R, Cifuentes-Diaz, C, Albertini, G, Bandet, E, Grannec, G, Lavilla, V, Deleuze, J.-F, Olaso, R, Nosten-Bertrand, M, Francis, F

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Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation von Goumidi, Louisa, Thibord, Florian, Wiggins, Kerri L., Li-Gao, Ruifang, Brown, Mickael R., van Hylckama Vlieg, Astrid, Souto, Joan-Carles, Soria, José-Manuel, Ibrahim-Kosta, Manal, Saut, Noémie, Daian, Delphine, Olaso, Robert, Amouyel, Philippe, Debette, Stéphanie, Boland, Anne, Bailly, Pascal, Morrison, Alanna C., Mook-Kanamori, Denis O., Deleuze, Jean-François, Johnson, Andrew, de Vries, Paul S., Sabater-Lleal, Maria, Chiaroni, Jacques, Smith, Nicholas L., Rosendaal, Frits R., Chasman, Daniel I., Trégouët, David-Alexandre, Morange, Pierre-Emmanuel

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An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism von Razzaq, Misbah, Iglesias, Maria Jesus, Ibrahim-Kosta, Manal, Goumidi, Louisa, Soukarieh, Omar, Proust, Carole, Roux, Maguelonne, Suchon, Pierre, Boland, Anne, Daiain, Delphine, Olaso, Robert, Havervall, Sebastian, Thalin, Charlotte, Butler, Lynn, Deleuze, Jean-François, Odeberg, Jacob, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre

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Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors von Thibord, Florian, Klarin, Derek, Brody, Jennifer A., Chen, Ming-Huei, Levin, Michael G., Chasman, Daniel I., Goode, Ellen L., Hveem, Kristian, Teder-Laving, Maris, Martinez-Perez, Angel, Aïssi, Dylan, Daian-Bacq, Delphine, Ito, Kaoru, Natarajan, Pradeep, Lutsey, Pamela L., Nadkarni, Girish N., de Vries, Paul S., Cuellar-Partida, Gabriel, Wolford, Brooke N., Pattee, Jack W., Kooperberg, Charles, Braekkan, Sigrid K., Li-Gao, Ruifang, Saut, Noemie, Sept, Corriene, Germain, Marine, Judy, Renae L., Wiggins, Kerri L., Ko, Darae, O’Donnell, Christopher J., Taylor, Kent D., Giulianini, Franco, De Andrade, Mariza, Nøst, Therese H., Boland, Anne, Empana, Jean-Philippe, Koyama, Satoshi, Gilliland, Thomas, Do, Ron, Huffman, Jennifer E., Wang, Xin, Zhou, Wei, Manuel Soria, Jose, Carlos Souto, Juan, Pankratz, Nathan, Haessler, Jeffery, Hindberg, Kristian, Rosendaal, Frits R., Turman, Constance, Olaso, Robert, Kember, Rachel L., Bartz, Traci M., Lynch, Julie A., Heckbert, Susan R., Armasu, Sebastian M., Brumpton, Ben, Smadja, David M., Jouven, Xavier, Komuro, Issei, Clapham, Katharine R., Loos, Ruth J.F., Willer, Cristen J., Sabater-Lleal, Maria, Pankow, James S., Reiner, Alexander P., Morelli, Vania M., Ridker, Paul M, Vlieg, Astrid van Hylckama, Deleuze, Jean-François, Kraft, Peter, Rader, Daniel J., Min Lee, Kyung, Psaty, Bruce M., Heidi Skogholt, Anne, Emmerich, Joseph, Suchon, Pierre, Rich, Stephen S., Vy, Ha My T., Tang, Weihong, Jackson, Rebecca D., Hansen, John-Bjarne, Morange, Pierre-Emmanuel, Kabrhel, Christopher, Trégouët, David-Alexandre, Damrauer, Scott M., Johnson, Andrew D., Smith, Nicholas L.

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Investigation of candidate gene copy number identifies FCGR3B as a potential biomarker for rheumatoid arthritis von Ben Kilani, Mohamed Sahbi, Cornélis, François, Olaso, Robert, Chaudru, Valerie, Petit-Teixeira, Elisabeth

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Deep intronic NIPBL de novo mutations and differential diagnoses revealed by whole genome and RNA sequencing in Cornelia de Lange syndrome patients von Coursimault, Juliette, Cassinari, Kévin, Lecoquierre, François, Quenez, Olivier, Coutant, Sophie, Derambure, Céline, Vezain, Myriam, Drouot, Nathalie, Vera, Gabriella, Schaefer, Elise, Philippe, Anaïs, Doray, Bérénice, Lambert, Laëtitia, Ghoumid, Jamal, Smol, Thomas, Rama, Mélanie, Legendre, Marine, Lacombe, Didier, Fergelot, Patricia, Olaso, Robert, Boland, Anne, Deleuze, Jean‐François, Goldenberg, Alice, Saugier‐Veber, Pascale, Nicolas, Gaël

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Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers von Sugier, Pierre‐Emmanuel, Lucotte, Elise A., Domenighetti, Cloé, Law, Matthew H., Iles, Mark M., Brown, Kevin, Amos, Christopher, McKay, James D., Hung, Rayjean J., Karimi, Mojgan, Bacq‐Daian, Delphine, Boland‐Augé, Anne, Olaso, Robert, Deleuze, Jean‐françois, Lesueur, Fabienne, Ostroumova, Evgenia, Kesminiene, Ausrele, Vathaire, Florent, Guénel, Pascal, Sreelatha, Ashwin Ashok Kumar, Schulte, Claudia, Grover, Sandeep, May, Patrick, Bobbili, Dheeraj R., Radivojkov‐Blagojevic, Milena, Lichtner, Peter, Singleton, Andrew B., Hernandez, Dena G., Edsall, Connor, Mellick, George D., Zimprich, Alexander, Pirker, Walter, Rogaeva, Ekaterina, Lang, Anthony E., Koks, Sulev, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean‐Christophe, Chartier‐Harlin, Marie‐Christine, Mutez, Eugénie, Brockmann, Kathrin, Deutschländer, Angela B., Hadjigeorgiou, Georges M., Dardiotis, Efthimios, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Straniero, Letizia, Zecchinelli, Anna, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Matsuo, Hirotaka, Nakayama, Akiyoshi, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Kolber, Pierre, Warrenburg, Bart P.C., Bloem, Bastiaan R., Aasly, Jan, Toft, Mathias, Pihlstrøm, Lasse, Guedes, Leonor Correia, Ferreira, Joaquim J., Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez‐Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy, Ran, Caroline, Belin, Andrea C., Puschmann, Andreas, Rödström, Emil Ygland, Clarke, Carl E., Morrison, Karen E., Tan, Manuela, Krainc, Dimitri, Burbulla, Lena F., Farrer, Matt J., Kruger, Rejko, Gasser, Thomas, Sharma, Manu, Truong, Thérèse, Elbaz, Alexis

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