نتائج البحث - Toma, Claudio
- يعرض 1 - 20 نتائج من 20
-
1
-
2
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders حسب Toma, Claudio, Pierce, Kerrie D., Shaw, Alex D., Heath, Anna, Mitchell, Philip B., Schofield, Peter R., Fullerton, Janice M.
منشور في 2018نص -
3
A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21 حسب Toma, Claudio, Shaw, Alex D., Heath, Anna, Pierce, Kerrie D., Mitchell, Philip B., Schofield, Peter R., Fullerton, Janice M.
منشور في 2021نص -
4
-
5
An examination of multiple classes of rare variants in extended families with bipolar disorder حسب Toma, Claudio, Shaw, Alex D., Allcock, Richard J. N., Heath, Anna, Pierce, Kerrie D., Mitchell, Philip B., Schofield, Peter R., Fullerton, Janice M.
منشور في 2018نص -
6
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection حسب Sykes, Nuala H, Toma, Claudio, Wilson, Natalie, Volpi, Emanuela V, Sousa, Inês, Pagnamenta, Alistair T, Tancredi, Raffaella, Battaglia, Agatino, Maestrini, Elena, Bailey, Anthony J, Monaco, Anthony P
منشور في 2009نص -
7
Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes حسب Torrico, Bàrbara, Shaw, Alex D., Mosca, Roberto, Vivó-Luque, Norma, Hervás, Amaia, Fernàndez-Castillo, Noèlia, Aloy, Patrick, Bayés, Mònica, Fullerton, Janice M., Cormand, Bru, Toma, Claudio
منشور في 2019نص -
8
Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia حسب Sintas, Cèlia, Carreño, Oriel, Fernàndez-Castillo, Noèlia, Corominas, Roser, Vila-Pueyo, Marta, Toma, Claudio, Cuenca-León, Ester, Barroeta, Isabel, Roig, Carles, Volpini, Víctor, Macaya, Alfons, Cormand, Bru
منشور في 2017نص -
9
MET and autism susceptibility: family and case–control studies حسب Sousa, Inês, Clark, Taane G, Toma, Claudio, Kobayashi, Kazuhiro, Choma, Maja, Holt, Richard, Sykes, Nuala H, Lamb, Janine A, Bailey, Anthony J, Battaglia, Agatino, Maestrini, Elena, Monaco, Anthony P
منشور في 2009نص -
10
Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability حسب Torrico, Bàrbara, Fernàndez-Castillo, Noèlia, Hervás, Amaia, Milà, Montserrat, Salgado, Marta, Rueda, Isabel, Buitelaar, Jan K, Rommelse, Nanda, Oerlemans, Anoek M, Bralten, Janita, Freitag, Christine M, Reif, Andreas, Battaglia, Agatino, Mazzone, Luigi, Maestrini, Elena, Cormand, Bru, Toma, Claudio
منشور في 2015نص -
11
Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies حسب Carreño, Oriel, Corominas, Roser, Serra, Selma Angèlica, Sintas, Cèlia, Fernández-Castillo, Noèlia, Vila-Pueyo, Marta, Toma, Claudio, Gené, Gemma G, Pons, Roser, Llaneza, Miguel, Sobrido, María-Jesús, Grinberg, Daniel, Valverde, Miguel Ángel, Fernández-Fernández, José Manuel, Macaya, Alfons, Cormand, Bru
منشور في 2013نص -
12
Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer حسب Toma, Claudio, Díaz‐Gay, Marcos, Franch‐Expósito, Sebastià, Arnau‐Collell, Coral, Overs, Bronwyn, Muñoz, Jenifer, Bonjoch, Laia, Soares de Lima, Yasmin, Ocaña, Teresa, Cuatrecasas, Miriam, Castells, Antoni, Bujanda, Luis, Balaguer, Francesc, Cubiella, Joaquín, Caldés, Trinidad, Fullerton, Janice M., Castellví‐Bel, Sergi
منشور في 2019نص -
13
Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder حسب Hesam-Shariati, Sonia, Overs, Bronwyn J., Roberts, Gloria, Toma, Claudio, Watkeys, Oliver J., Green, Melissa J., Pierce, Kerrie D., Edenberg, Howard J., Wilcox, Holly C., Stapp, Emma K., McInnis, Melvin G., Hulvershorn, Leslie A., Nurnberger, John I., Schofield, Peter R., Mitchell, Philip B., Fullerton, Janice M.
منشور في 2022نص -
14
Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing حسب Toma, Claudio, Díaz-Gay, Marcos, Soares de Lima, Yasmin, Arnau-Collell, Coral, Franch-Expósito, Sebastià, Muñoz, Jenifer, Overs, Bronwyn, Bonjoch, Laia, Carballal, Sabela, Ocaña, Teresa, Cuatrecasas, Miriam, Díaz de Bustamante, Aránzazu, Castells, Antoni, Bujanda, Luis, Cubiella, Joaquín, Balaguer, Francesc, Rodríguez-Alcalde, Daniel, Fullerton, Janice M., Castellví-Bel, Sergi
منشور في 2019نص -
15
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses حسب Torrico, Bàrbara, Antón-Galindo, Ester, Fernàndez-Castillo, Noèlia, Rojo-Francàs, Eva, Ghorbani, Sadaf, Pineda-Cirera, Laura, Hervás, Amaia, Rueda, Isabel, Moreno, Estefanía, Fullerton, Janice M., Casadó, Vicent, Buitelaar, Jan K., Rommelse, Nanda, Franke, Barbara, Reif, Andreas, Chiocchetti, Andreas G., Freitag, Christine, Kleppe, Rune, Haavik, Jan, Toma, Claudio, Cormand, Bru
منشور في 2020نص -
16
Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts حسب Wilcox, Holly C., Fullerton, Janice M., Glowinski, Anne L., Benke, Kelly, Kamali, Masoud, Hulvershorn, Leslie A., Stapp, Emma K., Edenberg, Howard J., Roberts, Gloria M.P., Ghaziuddin, Neera, Fisher, Carrie, Brucksch, Christine, Frankland, Andrew, Toma, Claudio, Shaw, Alex D., Kastelic, Elizabeth, Miller, Leslie, McInnis, Melvin G., Mitchell, Philip B., Nurnberger, John I.
منشور في 2017نص -
17
Analysis of X chromosome inactivation in autism spectrum disorders حسب Gong, Xiaohong, Bacchelli, Elena, Blasi, Francesca, Toma, Claudio, Betancur, Catalina, Chaste, Pauline, Delorme, Richard, Durand, Christelle, Fauchereau, Fabien, Botros, Hany Goubran, Leboyer, Marion, Mouren-Simeoni, Marie-Christine, Nygren, Gudrun, Anckarsäter, Henrik, Rastam, Maria, Gillberg, I Carina, Gillberg, Christopher, Moreno-De-Luca, Daniel, Carone, Simona, Nummela, Ilona, Rossi, Mari, Battaglia, Agatino, Jarvela, Irma, Maestrini, Elena, Bourgeron, Thomas
منشور في 2008نص -
18
Paternally inherited cis-regulatory structural variants are associated with autism حسب Brandler, William M, Antaki, Danny, Gujral, Madhusudan, Kleiber, Morgan L, Whitney, Joe, Maile, Michelle S, Hong, Oanh, Chapman, Timothy R, Tan, Shirley, Tandon, Prateek, Pang, Timothy, Tang, Shih C, Vaux, Keith K, Yang, Yan, Harrington, Eoghan, Juul, Sissel, Turner, Daniel J, Thiruvahindrapuram, Bhooma, Kaur, Gaganjot, Wang, Zhuozhi, Kingsmore, Stephen F, Gleeson, Joseph G, Bisson, Denis, Kakaradov, Boyko, Telenti, Amalio, Venter, J Craig, Corominas, Roser, Toma, Claudio, Cormand, Bru, Rueda, Isabel, Guijarro, Silvina, Messer, Karen S, Nievergelt, Caroline M, Arranz, Maria J, Courchesne, Eric, Pierce, Karen, Muotri, Alysson R, Iakoucheva, Lilia M, Hervas, Amaia, Scherer, Stephen W, Corsello, Christina, Sebat, Jonathan
منشور في 2018نص -
19
Mapping autism risk loci using genetic linkage and chromosomal rearrangements حسب Szatmari, Peter, Paterson, Andrew, Zwaigenbaum, Lonnie, Roberts, Wendy, Brian, Jessica, Liu, Xiao-Qing, Vincent, John, Skaug, Jennifer, Thompson, Ann, Senman, Lili, Feuk, Lars, Qian, Cheng, Bryson, Susan, Jones, Marshall, Marshall, Christian, Scherer, Stephen, Vieland, Veronica, Bartlett, Christopher, Mangin, La Vonne, Goedken, Rhinda, Segre, Alberto, Pericak-Vance, Margaret, Cuccaro, Michael, Gilbert, John, Wright, Harry, Abramson, Ruth, Betancur, Catalina, Bourgeron, Thomas, Gillberg, Christopher, Leboyer, Marion, Buxbaum, Joseph, Davis, Kenneth, Hollander, Eric, Silverman, Jeremy, Hallmayer, Joachim, Lotspeich, Linda, Sutcliffe, James, Haines, Jonathan, Folstein, Susan, Piven, Joseph, Wassink, Thomas, Sheffield, Val, Geschwind, Daniel, Bucan, Maja, Brown, Ted, Cantor, Rita, Constantino, John, Gilliam, Conrad, Herbert, Martha, Lajonchere, Clara, Ledbetter, David, Lese-Martin, Christa, Miller, Janet, Nelson, Stan, Samango-Sprouse, Carol, Spence, Sarah, State, Matthew, Tanzi, Rudolph, Coon, Hilary, Dawson, Geraldine, Devlin, Bernie, Estes, Annette, Flodman, Pamela, Klei, Lambertus, Mcmahon, William, Minshew, Nancy, Munson, Jeff, Korvatska, Elena, Rodier, Patricia, Schellenberg, Gerard, Smith, Moyra, Spence, Anne, Stodgell, Chris, Tepper, Ping Guo, Wijsman, Ellen, Yu, Chang-En, Rogé, Bernadette, Mantoulan, Carine, Wittemeyer, Kerstin, Poustka, Annemarie, Felder, Bärbel, Klauck, Sabine, Schuster, Claudia, Poustka, Fritz, Bölte, Sven, Feineis-Matthews, Sabine, Herbrecht, Evelyn, Schmötzer, Gabi, Tsiantis, John, Papanikolaou, Katerina, Maestrini, Elena, Bacchelli, Elena, Blasi, Francesca, Carone, Simona, Toma, Claudio, Van Engeland, Herman, De Jonge, Maretha, Kemner, Chantal, Koop, Frederieke, Langemeijer, Marjolein, Hijmans, Channa, Staal, Wouter, Baird, Gillian, Bolton, Patrick, Rutter, Michael, Weisblatt, Emma, Green, Jonathan, Aldred, Catherine, Wilkinson, Julie-Anne, Pickles, Andrew, Le Couteur, Ann, Berney, Tom, Mcconachie, Helen, Bailey, Anthony, Francis, Kostas, Honeyman, Gemma, Hutchinson, Aislinn, Parr, Jeremy, Wallace, Simon, Monaco, Anthony, Barnby, Gabrielle, Kobayashi, Kazuhiro, Lamb, Janine, Sousa, Ines, Sykes, Nuala, Cook, Edwin, Guter, Stephen, Leventhal, Bennett, Salt, Jeff, Lord, Catherine, Corsello, Christina, Hus, Vanessa, Weeks, Daniel, Volkmar, Fred, Tauber, Maïté, Fombonne, Eric, Shih, Andy, Meyer, Kacie
منشور في 2007نص -
20
Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology حسب Mullins, Niamh, Forstner, Andreas J., O’Connell, Kevin S., Coombes, Brandon, Coleman, Jonathan R. I., Qiao, Zhen, Als, Thomas D., Bigdeli, Tim B., Børte, Sigrid, Bryois, Julien, Charney, Alexander W., Drange, Ole Kristian, Gandal, Michael J., Hagenaars, Saskia P., Ikeda, Masashi, Kamitaki, Nolan, Kim, Minsoo, Krebs, Kristi, Panagiotaropoulou, Georgia, Schilder, Brian M., Sloofman, Laura G., Steinberg, Stacy, Trubetskoy, Vassily, Winsvold, Bendik S., Won, Hong-Hee, Abramova, Liliya, Adorjan, Kristina, Agerbo, Esben, Al Eissa, Mariam, Albani, Diego, Alliey-Rodriguez, Ney, Anjorin, Adebayo, Antilla, Verneri, Antoniou, Anastasia, Awasthi, Swapnil, Baek, Ji Hyun, Bækvad-Hansen, Marie, Bass, Nicholas, Bauer, Michael, Beins, Eva C., Bergen, Sarah E., Birner, Armin, Pedersen, Carsten Bøcker, Bøen, Erlend, Boks, Marco P., Bosch, Rosa, Brum, Murielle, Brumpton, Ben M., Brunkhorst-Kanaan, Nathalie, Budde, Monika, Bybjerg-Grauholm, Jonas, Byerley, William, Cairns, Murray, Casas, Miquel, Cervantes, Pablo, Clarke, Toni-Kim, Cruceanu, Cristiana, Cuellar-Barboza, Alfredo, Cunningham, Julie, Curtis, David, Czerski, Piotr M., Dale, Anders M., Dalkner, Nina, David, Friederike S., Degenhardt, Franziska, Djurovic, Srdjan, Dobbyn, Amanda L., Douzenis, Athanassios, Elvsåshagen, Torbjørn, Escott-Price, Valentina, Ferrier, I. Nicol, Fiorentino, Alessia, Foroud, Tatiana M., Forty, Liz, Frank, Josef, Frei, Oleksandr, Freimer, Nelson B., Frisén, Louise, Gade, Katrin, Garnham, Julie, Gelernter, Joel, Pedersen, Marianne Giørtz, Gizer, Ian R., Gordon, Scott D., Gordon-Smith, Katherine, Greenwood, Tiffany A., Grove, Jakob, Guzman-Parra, José, Ha, Kyooseob, Haraldsson, Magnus, Hautzinger, Martin, Heilbronner, Urs, Hellgren, Dennis, Herms, Stefan, Hoffmann, Per, Holmans, Peter A., Huckins, Laura, Jamain, Stéphane, Johnson, Jessica S., Kalman, Janos L., Kamatani, Yoichiro, Kennedy, James L., Kittel-Schneider, Sarah, Knowles, James A., Kogevinas, Manolis, Koromina, Maria, Kranz, Thorsten M., Kranzler, Henry R., Kubo, Michiaki, Kupka, Ralph, Kushner, Steven A., Lavebratt, Catharina, Lawrence, Jacob, Leber, Markus, Lee, Heon-Jeong, Lee, Phil H., Levy, Shawn E., Lewis, Catrin, Liao, Calwing, Lucae, Susanne, Lundberg, Martin, MacIntyre, Donald J., Magnusson, Sigurdur H., Maier, Wolfgang, Maihofer, Adam, Malaspina, Dolores, Maratou, Eirini, Martinsson, Lina, Mattheisen, Manuel, McCarroll, Steven A., McGregor, Nathaniel W., McGuffin, Peter, McKay, James D., Medeiros, Helena, Medland, Sarah E., Millischer, Vincent, Montgomery, Grant W., Moran, Jennifer L., Morris, Derek W., Mühleisen, Thomas W., O’Brien, Niamh, O’Donovan, Claire, Olde Loohuis, Loes M., Oruc, Lilijana, Papiol, Sergi, Pardiñas, Antonio F., Perry, Amy, Pfennig, Andrea, Porichi, Evgenia, Potash, James B., Quested, Digby, Raj, Towfique, Rapaport, Mark H., DePaulo, J. Raymond, Regeer, Eline J., Rice, John P., Rivas, Fabio, Rivera, Margarita, Roth, Julian, Roussos, Panos, Ruderfer, Douglas M., Sánchez-Mora, Cristina, Schulte, Eva C., Senner, Fanny, Sharp, Sally, Shilling, Paul D., Sigurdsson, Engilbert, Sirignano, Lea, Slaney, Claire, Smeland, Olav B., Smith, Daniel J., Sobell, Janet L., Hansen, Christine Søholm, Artigas, Maria Soler, Spijker, Anne T., Stein, Dan J., Strauss, John S., Świątkowska, Beata, Terao, Chikashi, Thorgeirsson, Thorgeir E., Toma, Claudio, Tooney, Paul, Tsermpini, Evangelia-Eirini, Vawter, Marquis P., Vedder, Helmut, Walters, James T. R., Witt, Stephanie H., Xi, Simon, Xu, Wei, Yang, Jessica Mei Kay, Young, Allan H., Young, Hannah, Zandi, Peter P., Zhou, Hang, Zillich, Lea, Adolfsson, Rolf, Agartz, Ingrid, Alda, Martin, Alfredsson, Lars, Babadjanova, Gulja, Backlund, Lena, Baune, Bernhard T., Bellivier, Frank, Bengesser, Susanne, Berrettini, Wade H., Blackwood, Douglas H. R., Boehnke, Michael, Børglum, Anders D., Breen, Gerome, Carr, Vaughan J., Catts, Stanley, Corvin, Aiden, Craddock, Nicholas, Dannlowski, Udo, Dikeos, Dimitris, Esko, Tõnu, Etain, Bruno, Ferentinos, Panagiotis, Frye, Mark, Fullerton, Janice M., Gawlik, Micha, Gershon, Elliot S., Goes, Fernando S., Green, Melissa J., Grigoroiu-Serbanescu, Maria, Hauser, Joanna, Henskens, Frans, Hillert, Jan, Hong, Kyung Sue, Hougaard, David M., Hultman, Christina M., Hveem, Kristian, Iwata, Nakao, Jablensky, Assen V., Jones, Ian, Jones, Lisa A., Kahn, René S., Kelsoe, John R., Kirov, George, Landén, Mikael, Leboyer, Marion, Lewis, Cathryn M., Li, Qingqin S., Lissowska, Jolanta, Lochner, Christine, Loughland, Carmel, Martin, Nicholas G., Mathews, Carol A., Mayoral, Fermin, McElroy, Susan L., McIntosh, Andrew M., McMahon, Francis J., Melle, Ingrid, Michie, Patricia, Milani, Lili, Mitchell, Philip B., Morken, Gunnar, Mors, Ole, Mortensen, Preben Bo, Mowry, Bryan, Müller-Myhsok, Bertram, Myers, Richard M., Neale, Benjamin M., Nievergelt, Caroline M., Nordentoft, Merete, Nöthen, Markus M., O’Donovan, Michael C., Oedegaard, Ketil J., Olsson, Tomas, Owen, Michael J., Paciga, Sara A., Pantelis, Chris, Pato, Carlos, Pato, Michele T., Patrinos, George P., Perlis, Roy H., Posthuma, Danielle, Ramos-Quiroga, Josep Antoni, Reif, Andreas, Reininghaus, Eva Z., Ribasés, Marta, Rietschel, Marcella, Ripke, Stephan, Rouleau, Guy A., Saito, Takeo, Schall, Ulrich, Schalling, Martin, Schofield, Peter R., Schulze, Thomas G., Scott, Laura J., Scott, Rodney J., Serretti, Alessandro, Weickert, Cynthia Shannon, Smoller, Jordan W., Stefansson, Hreinn, Stefansson, Kari, Stordal, Eystein, Streit, Fabian, Sullivan, Patrick F., Turecki, Gustavo, Vaaler, Arne E., Vieta, Eduard, Vincent, John B., Waldman, Irwin D., Weickert, Thomas W., Werge, Thomas, Wray, Naomi R., Zwart, John-Anker, Biernacka, Joanna M., Nurnberger, John I., Cichon, Sven, Edenberg, Howard J., Stahl, Eli A., McQuillin, Andrew, Di Florio, Arianna, Ophoff, Roel A., Andreassen, Ole A.
منشور في 2021نص