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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
Vasquez, Alejandro Arias, Renteria, Miguel E., Agartz, Ingrid, Apostolova, Liana G., Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Binder, Elisabeth B., Bøen, Erlend, Bowman, Ian J., Brohawn, David G., Buitelaar, Jan, Carless, Melanie A., Ching, Christopher R. K., Conrod, Patricia, Depondt, Chantal, de Zubicaray, Greig I., Djurovic, Srdjan, Duggirala, Ravindranath, Dyer, Thomas D., Ekman, Carl Johan, Emsell, Louise, Fears, Scott, Fedko, Iryna, Fox, Peter T., Francks, Clyde, Frodl, Thomas, Frouin, Vincent, Godlewska, Beata, Haukvik, Unn K., Hickie, Ian B., Hoekstra, Pieter J., Homuth, Georg, Hulshoff Pol, Hilleke E., Hwang, Kristy S., Kim, Sungeun, Kochunov, Peter, Krämer, Bernd, Kwok, John B. J., Laje, Gonzalo, Landman, Bennett A., Lauriello, John, Li, Chiang-shan, Liberg, Benny, Liu, Xinmin, Macciardi, Fabio, Malt, Ulrik F., Mattheisen, Manuel, Meyer-Lindenberg, Andreas, Melle, Ingrid, Mohnke, Sebastian, Morris, Derek W., Mueller, Bryon A., Mühleisen, Thomas W., Müller-Myhsok, Bertram, Nichols, Thomas E., Oosterlaan, Jaap, Pandolfo, Massimo, Papmeyer, Martina, Pausova, Zdenka, Penninx, Brenda W., Peterson, Charles P., Potkin, Steven G., Rasmussen, Jerod, Rijpkema, Mark, Risacher, Shannon L., Roiz-Santiañez, Roberto, Romanczuk-Seiferth, Nina, Rujescu, Dan, Salami, Alireza, Scanlon, Cathy, Schmaal, Lianne, Schnack, Hugo G., Schork, Andrew J., Seidman, Larry, Shen, Li, Smoller, Jordan W., Sponheim, Scott R., Starr, John M., Sussmann, Jessika, Sämann, Philipp G., Teumer, Alexander, Toga, Arthur W., Trabzuni, Daniah, Turner, Jessica, Van den Heuvel, Martijn, van Eijk, Kristel, van Erp, Theo G. M., van Haren, Neeltje E. M., van ‘t Ent, Dennis, van Tol, Marie-Jose, Valdés Hernández, Maria C., Versace, Amelia, Weale, Michael E., Westlye, Lars T., Whelan, Christopher D., Wittfeld, Katharina, Zilles, David, Freimer, Nelson B., Lawrence, Natalia S.
Published in Brain imaging and behavior (01.06.2014)
Published in Brain imaging and behavior (01.06.2014)
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HLA-DRB111 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis
Ombrello, Michael J., Remmers, Elaine F., Tachmazidou, Ioanna, Grom, Alexei, Foell, Dirk, Haas, Johannes-Peter, Martini, Alberto, Gattorno, Marco, Özen, Seza, Prahalad, Sampath, Zeft, Andrew S., Bohnsack, John F., Mellins, Elizabeth D., Ilowite, Norman T., Russo, Ricardo, Len, Claudio, Hilario, Maria Odete E., Oliveira, Sheila, Yeung, Rae S. M., Rosenberg, Alan, Wedderburn, Lucy R., Anton, Jordi, Schwarz, Tobias, Hinks, Anne, Bilginer, Yelda, Park, Jane, Cobb, Joanna, Satorius, Colleen L., Han, Buhm, Baskin, Elizabeth, Signa, Sara, Duerr, Richard H., Achkar, J. P., Kamboh, M. Ilyas, Kaufman, Kenneth M., Kottyan, Leah C., Pinto, Dalila, Scherer, Stephen W., Alarcón-Riquelme, Marta E., Docampo, Elisa, Estivill, Xavier, Gül, Ahmet, de Bakker, Paul I. W., Raychaudhuri, Soumya, Langefeld, Carl D., Thompson, Susan, Zeggini, Eleftheria, Thomson, Wendy, Kastner, Daniel L., Woo, Patricia, Achkar, J. P., Alarcón-Riquelme, Marta E., Allen, Roger, Anton, Jordi, Baskin, Elizabeth, Berg, Stefan, Bica, Bianca, Bilginer, Yelda, Bohnsack, John F., Cavalcanti, Andre, Chaitow, Jeffrey, Cobb, Joanna, Cuttica, Rubin, de Bakker, Paul I. W., Docampo, Elisa, Duerr, Richard, Ellis, Justine, Estivill, Xavier, Finkel, Terri H., Foell, Dirk, Gattorno, Marco, Grom, Alexei, Gül, Ahmet, Haas, Johannes-Peter, Hakonarson, Hakon, Han, Buhm, Hilario, Maria Odete E., Hinks, Anne, Ilowite, Norman T., Kamboh, M. Ilyas, Kaufman, Kenneth, Kottyan, Leah C., Langefeld, Carl, Len, Claudio, Martini, Alberto, Mellins, Elizabeth D., Minden, Kirstin, Murray, Kevin, Oliveira, Sheila, Ombrello, Michael J., Ozen, Seza, Park, Jane, Pinto, Dalila, Prahalad, Sampath, Quartier, Pierre, Raychaudhuri, Soumya, Rosenberg, Alan, Russo, Ricardo, Satorius, Colleen, Scherer, Stephen W.
Published in Proceedings of the National Academy of Sciences - PNAS (29.12.2015)
Published in Proceedings of the National Academy of Sciences - PNAS (29.12.2015)
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Muscle atrophy‐related myotube‐derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs
Yang, Chia‐Pei, Yang, Wan‐Shan, Wong, Yu‐Hui, Wang, Kai‐Hsuan, Teng, Yuan‐Chi, Chang, Ming‐Hsuan, Liao, Ko‐Hsun, Nian, Fang‐Shin, Chao, Chuan‐Chuan, Tsai, Jin‐Wu, Hwang, Wei‐Lun, Lin, Ming‐Wei, Tzeng, Tsai‐Yu, Wang, Pei‐Ning, Campbell, Mel, Chen, Liang‐Kung, Tsai, Ting‐Fen, Chang, Pei‐Ching, Kung, Hsing‐Jien
Published in Aging cell (01.05.2020)
Published in Aging cell (01.05.2020)
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Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn’s disease and leads to impaired CFB cleavage and phagocytosis
Stamps, Dalton T, Dube, Shishir, Li, Dalin, Yang, Shaohong, Landers, Carol J, Mengesha, Emebet, Murali, Ramachandran, Potdar, Alka A, Wolf, Andrea J, Botwin, Gregory J, Khrom, Michelle, Faubion, William A, Sandler, Robert S, Sartor, R Balfour, Brant, Steven R, Rioux, John D, Schumm, L Philip, Silverberg, Mark S, Zaghiyan, Karen, Melmed, Gil Y, Vasiliauskas, Eric A, Syal, Gaurav, Bonthala, Nirupama N, Targan, Stephan R, Michelsen, Kathrin S, Ahmad, Tariq, Amininejad, Leila, Andersen, Vibeke, Aumais, Guy, Baidoo, Leonard, Bayless, Theodore M, Bethge, Johannes, Boucher, Gabrielle, Brand, Stephan, Chew, Angela, Cho, Judy H, Cohain, Ariella, Jong, Dirk De, Denson, Lee A, Dewit, Olivier, D'Inca, Renata, Edwards, Cathryn, Ellinghaus, David, Festen, Eleonora A, Florin, Tim, Gieger, Christian, Goyette, Philippe, Green, Todd, Griffiths, Anne M, Hakonarson, Hakon, Hanigan, Katherine, Hart, Ailsa, Hayward, Nicholas K, Hugot, Jean-Pierre, Hui, Ken Y, Imielinski, Marcin, Jonaitis, Laimas, Jostins, Luke, Kiudelis, Gediminas, Krishnaprasad, Krupa, Kugathasan, Subra, Lee, James C, Lees, Charlie W, Leja, Marcis, Louis, Edouard, Mitrovic, Mitja, Ng, Aylwin, Ng, Siew C, Evelyn Ng, Sok Meng, Nikolaus, Susanna, Oikonomou, Ioannis, Phillips, Anne, Ponsioen, Cyriel Y, Prescott, Natalie J, Raychaudhuri, Soumya, Rieder, Florian, Rioux, John D, Ripke, Stephan, Russell, Richard K, Sanderson, Jeremy D, Satsangi, Jack, Schreiber, Stefan, Philip Schumm, L, Scott, Regan, Silverberg, Mark S, Simms, Lisa A, Spain, Sarah L, Sventoraityte, Jurgita, Torkvist, Leif, Tremelling, Mark, Vasiliauskas, Eric, Vermeire, Severine, Walters, Thomas, Wang, Kai, Wang, Ming-Hsi, Wei, Zhi, Winkelmann, Juliane, Zhang, Clarence K, Zhang, Wei, Zhao, Zhen Z
Published in Gut (01.11.2023)
Published in Gut (01.11.2023)
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Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus
Beunders, Gea, Voorhoeve, Els, Golzio, Christelle, Pardo, Luba M., Rosenfeld, Jill A., Talkowski, Michael E., Simonic, Ingrid, Lionel, Anath C., Vergult, Sarah, Pyatt, Robert E., van de Kamp, Jiddeke, Nieuwint, Aggie, Weiss, Marjan M., Rizzu, Patrizia, Verwer, Lucilla E.N.I., van Spaendonk, Rosalina M.L., Shen, Yiping, Wu, Bai-lin, Yu, Tingting, Yu, Yongguo, Chiang, Colby, Gusella, James F., Lindgren, Amelia M., Morton, Cynthia C., van Binsbergen, Ellen, Bulk, Saskia, van Rossem, Els, Vanakker, Olivier, Armstrong, Ruth, Park, Soo-Mi, Greenhalgh, Lynn, Maye, Una, Neill, Nicholas J., Abbott, Kristin M., Sell, Susan, Ladda, Roger, Farber, Darren M., Bader, Patricia I., Cushing, Tom, Drautz, Joanne M., Konczal, Laura, Nash, Patricia, de Los Reyes, Emily, Carter, Melissa T., Hopkins, Elizabeth, Marshall, Christian R., Osborne, Lucy R., Gripp, Karen W., Thrush, Devon Lamb, Hashimoto, Sayaka, Gastier-Foster, Julie M., Astbury, Caroline, Ylstra, Bauke, Meijers-Heijboer, Hanne, Posthuma, Danielle, Menten, Björn, Mortier, Geert, Scherer, Stephen W., Eichler, Evan E., Girirajan, Santhosh, Katsanis, Nicholas, Groffen, Alexander J., Sistermans, Erik A.
Published in American journal of human genetics (07.02.2013)
Published in American journal of human genetics (07.02.2013)
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Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group
Lumaka, Aimé, Carstens, Nadia, Devriendt, Koenraad, Krause, Amanda, Kulohoma, Benard, Kumuthini, Judit, Mubungu, Gerrye, Mukisa, John, Nel, Melissa, Olanrewaju, Timothy O., Lombard, Zané, Landouré, Guida
Published in Orphanet journal of rare diseases (16.06.2022)
Published in Orphanet journal of rare diseases (16.06.2022)
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An organism-wide ATAC-seq peak catalog for the bovine and its use to identify regulatory variants
Yuan, Can, Tang, Lijing, Lopdell, Thomas, Petrov, Vyacheslav A., Oget-Ebrad, Claire, Moreira, Gabriel Costa Monteiro, Gualdrón Duarte, José Luis, Sartelet, Arnaud, Cheng, Zhangrui, Salavati, Mazdak, Wathes, D. Claire, Crowe, Mark A., Coppieters, Wouter, Littlejohn, Mathew, Charlier, Carole, Druet, Tom, Georges, Michel, Takeda, Haruko
Published in Genome research (01.10.2023)
Published in Genome research (01.10.2023)
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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
Kasperavičiūtė, Dalia, Catarino, Claudia B., Matarin, Mar, Leu, Costin, Novy, Jan, Tostevin, Anna, Leal, Bárbara, Hessel, Ellen V. S., Hallmann, Kerstin, Hildebrand, Michael S., Dahl, Hans-Henrik M., Ryten, Mina, Trabzuni, Daniah, Ramasamy, Adaikalavan, Alhusaini, Saud, Doherty, Colin P., Dorn, Thomas, Hansen, Jörg, Krämer, Günter, Steinhoff, Bernhard J., Zumsteg, Dominik, Duncan, Susan, Kälviäinen, Reetta K., Eriksson, Kai J., Kantanen, Anne-Mari, Pandolfo, Massimo, Gruber-Sedlmayr, Ursula, Schlachter, Kurt, Reinthaler, Eva M., Stogmann, Elisabeth, Zimprich, Fritz, Théâtre, Emilie, Smith, Colin, O’Brien, Terence J., Meng Tan, K., Petrovski, Slave, Robbiano, Angela, Paravidino, Roberta, Zara, Federico, Striano, Pasquale, Sperling, Michael R., Buono, Russell J., Hakonarson, Hakon, Chaves, João, Costa, Paulo P., Silva, Berta M., da Silva, António M., de Graan, Pierre N. E., Koeleman, Bobby P. C., Becker, Albert, Schoch, Susanne, von Lehe, Marec, Reif, Philipp S., Rosenow, Felix, Becker, Felicitas, Weber, Yvonne, Lerche, Holger, Rössler, Karl, Buchfelder, Michael, Hamer, Hajo M., Kobow, Katja, Coras, Roland, Blumcke, Ingmar, Scheffer, Ingrid E., Berkovic, Samuel F., Weale, Michael E., Delanty, Norman, Depondt, Chantal, Cavalleri, Gianpiero L., Kunz, Wolfram S., Sisodiya, Sanjay M.
Published in Brain (London, England : 1878) (01.10.2013)
Published in Brain (London, England : 1878) (01.10.2013)
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Mutations in PYCR1 cause cutis laxa with progeroid features
Reversade, Bruno, Escande-Beillard, Nathalie, Dimopoulou, Aikaterini, Fischer, Björn, Chng, Serene C, Li, Yun, Shboul, Mohammad, Tham, Puay-Yoke, Kayserili, Hülya, Al-Gazali, Lihadh, Shahwan, Monzer, Brancati, Francesco, Lee, Hane, O'Connor, Brian D, Kegler, Mareen Schmidt-von, Merriman, Barry, Nelson, Stanley F, Masri, Amira, Alkazaleh, Fawaz, Guerra, Deanna, Ferrari, Paola, Nanda, Arti, Rajab, Anna, Markie, David, Gray, Mary, Nelson, John, Grix, Arthur, Sommer, Annemarie, Savarirayan, Ravi, Janecke, Andreas R, Steichen, Elisabeth, Sillence, David, Haußer, Ingrid, Budde, Birgit, Nürnberg, Gudrun, Nürnberg, Peter, Seemann, Petra, Kunkel, Désirée, Zambruno, Giovanna, Dallapiccola, Bruno, Schuelke, Markus, Robertson, Stephen, Hamamy, Hanan, Wollnik, Bernd, Van Maldergem, Lionel, Mundlos, Stefan, Kornak, Uwe
Published in Nature genetics (01.09.2009)
Published in Nature genetics (01.09.2009)
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IL1RN Variation Influences Both Disease Susceptibility and Response to Recombinant Human Interleukin‐1 Receptor Antagonist Therapy in Systemic Juvenile Idiopathic Arthritis
Arthur, Victoria L., Grom, Alexei A., Foell, Dirk, Özen, Seza, Prahalad, Sampath, Mellins, Elizabeth D., Russo, Ricardo, Oliveira, Sheila, Yeung, Rae S. M., Rosenberg, Alan M., Minden, Kirsten, Kastner, Daniel L., Woo, Patricia, Ombrello, Michael J., Docampo, Elisa, Estivill, Xavier, Gattorno, Marco, Grom, Alexei, Gül, Ahmet, Haas, Johannes‐Peter, Kastner, Daniel L., Kottyan, Leah C., Langefeld, Carl D., Martini, Alberto, Ombrello, Michael J., Pinto, Dalila, Rosenberg, Alan, Russo, Ricardo, Scherer, Stephen W., Signa, Sara, Shuldiner, Emily, Tachmazidou, Ioanna, Thompson, Susan, Thomson, Wendy, Wedderburn, Lucy R., Woo, Patricia, Zeggini, Eleftheria, Chédeville, Gaëlle, Chetaille, Anne‐Laure, Dancey, Paul, Ellsworth, Janet, Guzman, Jaime, Jurencak, Roman, Schneider, Rayfel, Scherer, Stephen W., Spiegel, Lynn, Stringer, Elizabeth, Tucker, Lori B., Wintle, Richard F., Abinum, Mario, Bell, A., Hall, M., Hollingworth, Peter, Stewart, I., Woo, Patricia, Baildam, Eileen, Bishop, Nick, Brown, Lynsey, Davidson, Joyce, Friel, Elizabeth, Hadfield, Kelly, Lay, Mark, Lloyd, Olivia, Lydon, Carol, Makengo, Natasha, Moorcroft, Theresa, Price, Vicki, Venter, Katharine, Zelenovic, Jadranka, Foeldvari, Ivan, Foell, Dirk, Heiligenhaus, Arnd, Kallinich, Tilmann, Kümmerle‐Deschner, Jasmin, Minden, Kirsten, Mönkemöller, Kirsten, Elder, Melissa, Gottlieb, Beth S., Imundo, Lisa F., Miller, Michael L., Prather, Kristi, Singer, Nora G., Spalding, Steven J., Tarvin, Stacey E., Verbsky, James W., Wallace, Carol A., Cutts, Rebecca, Etheridge, Angela, Hinks, Anne, Howman, Ruth, Marshall, Lucy, Melville, Laura, Moncrieffe, Halima, Mulligan, Kathleen, Palman, Jason, Robinson, Emily, Simou, Stephanie, Stafford, Stefanie, Southwood, Tauny, Woo, Patricia
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.08.2018)
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.08.2018)
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Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease
Gusareva, Elena S., Twizere, Jean-Claude, Sleegers, Kristel, Dourlen, Pierre, Abisambra, Jose F., Meier, Shelby, Cloyd, Ryan, Weiss, Blaine, Dermaut, Bart, Bessonov, Kyrylo, van der Lee, Sven J., Carrasquillo, Minerva M., Katsumata, Yuriko, Cherkaoui, Majid, Asselbergh, Bob, Ikram, M. Arfan, Mayeux, Richard, Farrer, Lindsay A., Haines, Jonathan L., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Sims, Rebecca, Williams, Julie, Amouyel, Philippe, van Duijn, Cornelia M., Ertekin-Taner, Nilüfer, Van Broeckhoven, Christine, Dequiedt, Franck, Fardo, David W., Lambert, Jean-Charles, Van Steen, Kristel
Published in Neurobiology of aging (01.12.2018)
Published in Neurobiology of aging (01.12.2018)
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Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations
Cárdenas-de-la-Parra, Alonso, Martin-Brevet, Sandra, Moreau, Clara, Rodriguez-Herreros, Borja, Fonov, Vladimir S., Maillard, Anne M., Zürcher, Nicole R., Addor, Marie-Claude, Andrieux, Joris, Arveiler, Benoît, Baujatm, Geneviève, Sloan-Bénan, Frédérique, Belfiore, Marco, Bonneau, Dominique, Bouquillon, Sonia, Boute, Odile, Brusco, Alfredo, Busa, Tiffany, Caberg, Jean-Hubert, Campion, Dominique, Colombert, Vanessa, Cordier, Marie-Pierre, David, Albert, Debray, François-Guillaume, Delrue, Marie-Ange, Doco-Fenzy, Martine, Dunkhase-Heinl, Ulrike, Edery, Patrick, Fagerberg, Christina, Faivre, Laurence, Forzano, Francesca, Genevieve, David, Gérard, Marion, Giachino, Daniela, Guichet, Agnès, Guillin, Olivier, Héron, Delphine, Isidor, Bertrand, Jacquette, Aurélia, Jaillard, Sylvie, Journel, Hubert, Keren, Boris, Lacombe, Didier, Lebon, Sébastien, Le Caignec, Cédric, Lemaître, Marie-Pierre, Lespinasse, James, Mathieu-Dramart, Michèle, Mercier, Sandra, Mignot, Cyril, Missirian, Chantal, Petit, Florence, Pilekær Sørensen, Kristina, Pinson, Lucile, Plessis, Ghislaine, Prieur, Fabienne, Rooryck-Thambo, Caroline, Rossi, Massimiliano, Sanlaville, Damien, Schlott Kristiansen, Britta, Schluth-Bolard, Caroline, Till, Marianne, Van Haelst, Mieke, Van Maldergem, Lionel, Hadjikhani, Nouchine, Beckmann, Jacques S., Reymond, Alexandre, Draganski, Bogdan, Jacquemont, Sébastien, Collins, D. Louis
Published in NeuroImage (Orlando, Fla.) (01.12.2019)
Published in NeuroImage (Orlando, Fla.) (01.12.2019)
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TAC3 and TACR3 defects cause hypothalamic congenital hypogonadotropic hypogonadism in humans
Young, Jacques, Bouligand, Jerome, Francou, Bruno, Raffin-Sanson, Marie-Laure, Gaillez, Stephanie, Jeanpierre, Marc, Grynberg, Michael, Kamenicky, Peter, Chanson, Philippe, Brailly-Tabard, Sylvie, Guiochon-Mantel, Anne
Published in The journal of clinical endocrinology and metabolism (01.05.2010)
Published in The journal of clinical endocrinology and metabolism (01.05.2010)
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Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability
Zhang, Feng, Seeman, Pavel, Liu, Pengfei, Weterman, Marian A.J., Gonzaga-Jauregui, Claudia, Towne, Charles F., Batish, Sat Dev, De Vriendt, Els, De Jonghe, Peter, Rautenstrauss, Bernd, Krause, Klaus-Henning, Khajavi, Mehrdad, Posadka, Jan, Vandenberghe, Antoon, Palau, Francesc, Van Maldergem, Lionel, Baas, Frank, Timmerman, Vincent, Lupski, James R.
Published in American journal of human genetics (11.06.2010)
Published in American journal of human genetics (11.06.2010)
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Serial population extinctions in a small mammal indicate Late Pleistocene ecosystem instability
Brace, Selina, Palkopoulou, Eleftheria, Dalén, Love, Lister, Adrian M, Miller, Rebecca, Otte, Marcel, Germonpré, Mietje, Blockley, Simon P. E, Stewart, John R, Barnes, Ian
Published in Proceedings of the National Academy of Sciences - PNAS (11.12.2012)
Published in Proceedings of the National Academy of Sciences - PNAS (11.12.2012)
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RENAL ABNORMALITIES AMONG SICKLE CELL DISEASE PATIENTS IN A POOR MANAGEMENT SETTING: A SURVEY IN THE DEMOCRATIC REPUBLIC OF THE CONGO
Kambale-Kombi, Paul, Marini Djang’eing’a, Roland, Alworong’a Opara, Jean-Pierre, Mbo Mukonkole, Jean-Paulin, Bours, Vincent, Mbumba Lupaka, Dieu-Merci, Tonen-Wolyec, Serge, Bolukaoto Bome, Lucien, Kayembe Tshilumba, Charles, Batina-Agasa, Salomon
Published in Mediterranean journal of hematology and infectious diseases (01.07.2022)
Published in Mediterranean journal of hematology and infectious diseases (01.07.2022)
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Does glucose-6-phosphate dehydrogenase deficiency worsen the clinical features of sickle cell disease? A multi-hospital-based cross-sectional study
Kambale-Kombi, Paul, Marini Djang'eing'a, Roland, Alworong'a Opara, Jean-Pierre, Minon, Jean-Marc, Atoba Bokele, Camille, Bours, Vincent, Azerad, Marie-Agnès, Tonen-Wolyec, Serge, Kayembe Tshilumba, Charles, Batina-Agasa, Salomon
Published in Hematology (Luxembourg) (01.12.2022)
Published in Hematology (Luxembourg) (01.12.2022)
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Early termination of ISRCTN45828668, a phase 1/2 prospective, randomized study of Sulfasalazine for the treatment of progressing malignant gliomas in adults
Robe, Pierre A, Martin, Didier H, Nguyen-Khac, Minh T, Artesi, Maria, Deprez, Manuel, Albert, Adelin, Vanbelle, Sophie, Califice, Stephane, Bredel, Markus, Bours, Vincent
Published in BMC cancer (19.10.2009)
Published in BMC cancer (19.10.2009)
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A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies
Colombel, Jean-Frederick, Hugot, Jean-Pierre, Massey, Dunecan, Montgomery, Grant W., Oikonomou, Ioannis, Peeters, Harald, Proctor, Deborah D., Seibold, Frank, Törkvist, Leif, Andrews, Jane M., Bampton, Peter A., Florin, Timothy H., Krishnaprasad, Krupa, Radford-Smith, Graham, Simms, Lisa A., Laukens, Debby, Deslandres, Colette, Duerr, Richard H., Goyette, Philippe, Haritunians, Talin, Lahaie, Raymond G., Ng, Sok Meng, Rioux, John D., Aerts, Jan, Attwood, Anthony, Ball, Stephen G., Brown, Morris J., Burton, John, Byrnes, Jake, Cardin, Niall, Clee, Chris M., Coffey, Alison J., Dominiczak, Anna F., Evans, David M., Farmer, Anne, Ferrier, Nicol, Flynn, Edward, Franklyn, Jayne A., Frayling, Timothy M., Freathy, Rachel M., Gibbs, Polly, Gray, Emma, Howard, Philip, Hughes, Debbie, Hunt, Sarah, Jolley, Jennifer D., Jones, Lisa A., Kirov, George, Maller, Julian, Mansfield, John, McGuffin, Peter, McLay, Kirsten E., Mentzer, Alex, Munroe, Patricia B., Newman, William, Palotie, Aarno, Plagnol, Vincent, Prescott, Natalie J., Quail, Michael A., Reid, David M., Renwick, Anthony, Russell, Ellie, St Clair, David, Scott, Richard, Somaskantharajah, Elilan, Steer, Sophia, Symmons, Deborah P.M., Tobin, Martin D., Wain, Louise V., Walker, Mark, Wallace, Chris, Weedon, Michael N., Wilson, Anthony G., Yau, Chris, Young, Allan H., Brown, Matthew A., Gough, Stephen C.L., Satsangi, Jack, Ouwehand, Willem H., Parkes, Miles, Rahman, Nazneen, Samani, Nilesh J., Kwiatkowski, Dominic P., Donnelly, Peter, Bramon, Elvira, Casas, Juan P., Corvin, Aiden, Jankowski, Janusz, Markus, Hugh S., Palmer, Colin N.A., Plomin, Robert, Viswanathan, Ananth C., Spencer, Chris C.A., Blackburn, Hannah, Gillman, Matthew, McCann, Owen T., Waller, Matthew, Weston, Paul, Whittaker, Pamela, Roeder, Kathryn
Published in American journal of human genetics (05.05.2016)
Published in American journal of human genetics (05.05.2016)
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The common genetic influence over processing speed and white matter microstructure: Evidence from the Old Order Amish and Human Connectome Projects
Kochunov, Peter, Thompson, Paul M., Winkler, Anderson, Morrissey, Mary, Fu, Mao, Coyle, Thomas R., Du, Xiaoming, Muellerklein, Florian, Savransky, Anya, Gaudiot, Christopher, Sampath, Hemalatha, Eskandar, George, Jahanshad, Neda, Patel, Binish, Rowland, Laura, Nichols, Thomas E., O'Connell, Jeffrey R., Shuldiner, Alan R., Mitchell, Braxton D., Hong, L. Elliot
Published in NeuroImage (Orlando, Fla.) (15.01.2016)
Published in NeuroImage (Orlando, Fla.) (15.01.2016)
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