Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Pinto, Dalila"'
Autor:
Mullins, Niamh, Kang, JooEun, Campos, Adrian I, Coleman, Jonathan RI, Edwards, Alexis C, Galfalvy, Hanga, Levey, Daniel F, Lori, Adriana, Shabalin, Andrey, Starnawska, Anna, Su, Mei-Hsin, Watson, Hunna J, Adams, Mark, Awasthi, Swapnil, Gandal, Michael, Hafferty, Jonathan D, Hishimoto, Akitoyo, Kim, Minsoo, Okazaki, Satoshi, Otsuka, Ikuo, Ripke, Stephan, Ware, Erin B, Bergen, Andrew W, Berrettini, Wade H, Bohus, Martin, Brandt, Harry, Chang, Xiao, Chen, Wei J, Chen, Hsi-Chung, Crawford, Steven, Crow, Scott, DiBlasi, Emily, Duriez, Philibert, Fernández-Aranda, Fernando, Fichter, Manfred M, Gallinger, Steven, Glatt, Stephen J, Gorwood, Philip, Guo, Yiran, Hakonarson, Hakon, Halmi, Katherine A, Hwu, Hai-Gwo, Jain, Sonia, Jamain, Stéphane, Jiménez-Murcia, Susana, Johnson, Craig, Kaplan, Allan S, Kaye, Walter H, Keel, Pamela K, Kennedy, James L, Klump, Kelly L, Li, Dong, Liao, Shih-Cheng, Lieb, Klaus, Lilenfeld, Lisa, Liu, Chih-Min, Magistretti, Pierre J, Marshall, Christian R, Mitchell, James E, Monson, Eric T, Myers, Richard M, Pinto, Dalila, Powers, Abigail, Ramoz, Nicolas, Roepke, Stefan, Rozanov, Vsevolod, Scherer, Stephen W, Schmahl, Christian, Sokolowski, Marcus, Strober, Michael, Thornton, Laura M, Treasure, Janet, Tsuang, Ming T, Witt, Stephanie H, Woodside, D Blake, Yilmaz, Zeynep, Zillich, Lea, Adolfsson, Rolf, Agartz, Ingrid, Air, Tracy M, Alda, Martin, Alfredsson, Lars, Andreassen, Ole A, Anjorin, Adebayo, Appadurai, Vivek, Soler Artigas, María, Van der Auwera, Sandra, Azevedo, M Helena, Bass, Nicholas, Bau, Claiton HD, Baune, Bernhard T, Bellivier, Frank, Berger, Klaus, Biernacka, Joanna M, Bigdeli, Tim B, Binder, Elisabeth B, Boehnke, Michael, Boks, Marco P, Bosch, Rosa, Braff, David L
Publikováno v:
Biological psychiatry, vol 91, iss 3
BackgroundSuicide is a leading cause of death worldwide, and nonfatal suicide attempts, which occur far more frequently, are a major source of disability and social and economic burden. Both have substantial genetic etiology, which is partially share
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::ca27f96bacd37f9517a131d9db7bf5c2
https://escholarship.org/uc/item/8jn2p3sp
https://escholarship.org/uc/item/8jn2p3sp
Autor:
Gandal, Michael J, Zhang, Pan, Hadjimichael, Evi, Walker, Rebecca L, Chen, Chao, Liu, Shuang, Won, Hyejung, van Bakel, Harm, Varghese, Merina, Wang, Yongjun, Shieh, Annie W, Haney, Jillian, Parhami, Sepideh, Belmont, Judson, Kim, Minsoo, Moran Losada, Patricia, Khan, Zenab, Mleczko, Justyna, Xia, Yan, Dai, Rujia, Wang, Daifeng, Yang, Yucheng T, Xu, Min, Fish, Kenneth, Hof, Patrick R, Warrell, Jonathan, Fitzgerald, Dominic, White, Kevin, Jaffe, Andrew E, PsychENCODE Consortium, Peters, Mette A, Gerstein, Mark, Liu, Chunyu, Iakoucheva, Lilia M, Pinto, Dalila, Geschwind, Daniel H
Publikováno v:
Science (New York, N.Y.), vol 362, iss 6420
Most genetic risk for psychiatric disease lies in regulatory regions, implicating pathogenic dysregulation of gene expression and splicing. However, comprehensive assessments of transcriptomic organization in diseased brains are limited. In this work
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1bba825596aa4055f392c2e5dd01864e
https://escholarship.org/uc/item/0xb5q13n
https://escholarship.org/uc/item/0xb5q13n
Autor:
Duncan, Laramie, Yilmaz, Zeynep, Gaspar, Helena, Walters, Raymond, Goldstein, Jackie, Anttila, Verneri, Bulik-Sullivan, Brendan, Ripke, Stephan, Thornton, Laura, Hinney, Anke, Daly, Mark, Sullivan, Patrick F., Zeggini, Eleftheria, Breen, Gerome, Bulik, Cynthia M., Gaspar, Héléna, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, Aschauer, Harald, Baker, Jessica, Barrett, Jeffrey, Bencko, Vladimir, Bergen, Andrew, Berrettini, Wade, Birgegård, Andreas, Boni, Claudette, Perica, Vesna Boraska, Brandt, Harry, Burghardt, Roland, Carlberg, Laura, Cassina, Matteo, Cesta, Carolyn, Cichon, Sven, Clementi, Maurizio, Cohen-Woods, Sarah, Coleman, Joni, Cone, Roger, Courtet, Philippe, Crawford, Steven, Crow, Scott, Crowley, Jim, Danner, Unna, Davis, Oliver, de Zwaan, Martina, Dedoussis, George, Degortes, Daniela, Desocio, Janiece, Danielle, Dick, Dikeos, Dimitris, Dina, Christian, Ding, Bo, Dmitrzak-Weglarz, Monika, Docampo, Elisa, Egberts, Karin, Ehrlich, Stefan, Escaramís, Geòrgia, Esko, Tõnu, Espeseth, Thomas, Estivill, Xavier, Favaro, Angela, Fernández-Aranda, Fernando, Fichter, Manfred, Finan, Chris, Fischer, Krista, Floyd, James, Föcker, Manuel, Foretova, Lenka, Forzan, Monica, Fox, Caroline, Franklin, Christopher, Gaborieau, Valerie, Gallinger, Steven, Gambaro, Giovanni, Giegling, Ina, Gonidakis, Fragiskos, Gorwood, Philip, Gratacos, Monica, Guillaume, Sébastien, Guo, Yiran, Hakonarson, Hakon, Halmi, Katherine, Harrison, Rebecca, Hatzikotoulas, Konstantinos, Hauser, Joanna, Hebebrand, Johannes, Helder, Sietske, Hendriks, Judith, Herms, Stefan, Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Hilliard, Christopher, Huckins, Laura, Hudson, James, Huemer, Julia, Imgart, Hartmut, Inoko, Hidetoshi, Jall, Sigrid, Jamain, Stephane, Janout, Vladimir, Jiménez-Murcia, Susana, Johnson, Craig, Jordan, Jenny, Julià, Antonio, Juréus, Anders, Kalsi, Gursharan, Kaplan, Allan, Kaprio, Jaakko, Karhunen, Leila, Karwautz, Andreas, Kas, Martien, Kaye, Walter, Kennedy, Martin, Kennedy, James, Keski-Rahkonen, Anna, Kiezebrink, Kirsty, Kim, Youl-Ri, Klareskog, Lars, Klump, Kelly, Knudsen, Gun Peggy, Koeleman, Bobby, Koubek, Doris, La Via, Maria, Landén, Mikael, Le Hellard, Stephanie, Leboyer, Marion, Levitan, Robert, Dong, Li, Lichtenstein, Paul, Lilenfeld, Lisa, Lissowska, Jolanta, Lundervold, Astri, Magistretti, Pierre, Maj, Mario, Mannik, Katrin, Marsal, Sara, Kaminska, Debora, Martin, Nicholas, Mattingsdal, Morten, Mcdevitt, Sara, Mcguffin, Peter, Merl, Elisabeth, Metspalu, Andres, Meulenbelt, Ingrid, Micali, Nadia, Mitchell, James, Mitchell, Karen, Monteleone, Palmiero, Monteleone, Alessio Maria, Montgomery, Grant, Mortensen, Preben, Munn-Chernoff, Melissa, Müller, Timo, Nacmias, Benedetta, Navratilova, Marie, Nilsson, Ida, Norring, Claes, Ntalla, Ioanna, Ophoff, Roel, O’Toole, Julie, Palotie, Aarno, Pantel, Jacques, Papezova, Hana, Parker, Richard, Pinto, Dalila, Rabionet, Raquel, Raevuori, Anu, Rajewski, Andrzej, Ramoz, Nicolas, William Rayner, N., Reichborn-Kjennerud, Ted, Ricca, Valdo, Ripatti, Samuli, Ritschel, Franziska, Roberts, Marion, Rotondo, Alessandro, Rujescu, Dan, Rybakowski, Filip, Santonastaso, Paolo, Scherag, André, Scherer, Stephen, Schmidt, Ulrike, Schork, Nicholas, Schosser, Alexandra, Scott, Laura, Seitz, Jochen, Slachtova, Lenka, Sladek, Robert, Eline Slagboom, P., Slof-Op ’t Landt, Margarita, Slopien, Agnieszka, Smith, Tosha, Soranzo, Nicole, Sorbi, Sandro, Southam, Lorraine, Steen, Vidar, Strengman, Eric, Strober, Michael, Szatkiewicz, Jin, Szeszenia-Dabrowska, Neonila, Tachmazidou, Ioanna, Tenconi, Elena, Tortorella, Alfonso, Tozzi, Federica, Treasure, Janet, Tschöp, Matthias, Tsitsika, Artemis, Tziouvas, Konstantinos, van Elburg, Annemarie, van Furth, Eric, Wade, Tracey, Wagner, Gudrun, Walton, Esther, Watson, Hunna, Wichmann, H-Erich, Widen, Elisabeth, Woodside, Blake, Yanovski, Jack, Yao, Shuyang, Zerwas, Stephanie, Zipfel, Stephan
Publikováno v:
Duncan, L, Yilmaz, Z, Gaspar, H, Walters, R K, Goldstein, J, Anttila, V, Bulik-Sullivan, B K, Ripke, S, Thornton, L M, Hinney, A, Daly, M, Sullivan, P F, Zeggini, E, Breen, G, Bulik, C M, Eating Disorders Working Group of the Psychiatric Genomics Consortium & Mortensen, P B 2017, ' Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa ', American Journal of Psychiatry, vol. 174, no. 9, pp. 850-858 . https://doi.org/10.1176/appi.ajp.2017.16121402
Recercat. Dipósit de la Recerca de Catalunya
instname
American Journal of Psychiatry
American Journal of Psychiatry, Vol. 174, No 9 (2017) pp. 850-858
Duncan, L, Yilmaz, Z, Gaspar, H, Walters, R, Goldstein, J, Anttila, V, Bulik-Sullivan, B, Ripke, S, Thornton, L, Hinney, A, Daly, M, Sullivan, P F, Zeggini, E, Breen, G, Bulik, C M, Duncan, L, Yilmaz, Z, Gaspar, H, Walters, R, Goldstein, J, Anttila, V, Bulik-Sullivan, B, Ripke, S, Adan, R, Alfredsson, L, Ando, T, Andreassen, O, Aschauer, H, Baker, J, Barrett, J, Bencko, V, Bergen, A, Berrettini, W, Birgegård, A, Boni, C, Perica, V B, Brandt, H, Burghardt, R, Carlberg, L, Cassina, M, Cesta, C, Cichon, S, Clementi, M, Cohen-Woods, S, Coleman, J, Cone, R, Courtet, P, Crawford, S, Crow, S, Crowley, J, Danner, U, Davis, O, de Zwaan, M, Dedoussis, G, Degortes, D, DeSocio, J, Danielle, D N, Dikeos, D, Dina, C, Ding, B, Dmitrzak-Weglarz, M, Docampo, E, Egberts, K, Ehrlich, S, Escaramís, G, Esko, T, Espeseth, T, Estivill, X, Favaro, A, Fernández-Aranda, F, Fichter, M, Finan, C, Fischer, K, Floyd, J, Föcker, M, Foretova, L, Forzan, M, Fox, C, Franklin, C, Gaborieau, V, Gallinger, S, Gambaro, G, Giegling, I, Gonidakis, F, Gorwood, P, Gratacos, M, Guillaume, S, Guo, Y, Hakonarson, H, Halmi, K, Harrison, R, Hatzikotoulas, K, Hauser, J, Hebebrand, J, Helder, S, Hendriks, J, Herms, S, Herpertz-Dahlmann, B, Herzog, W, Hilliard, C, Huckins, L, Hudson, J, Huemer, J, Imgart, H, Inoko, H, Jall, S, Jamain, S, Janout, V, Jiménez-Murcia, S, Johnson, C, Jordan, J, Julià, A, Juréus, A, Kalsi, G, Kaplan, A, Kaprio, J, Karhunen, L, Karwautz, A, Kas, M, Kaye, W, Kennedy, M, Kennedy, J, Keski-Rahkonen, A, Kiezebrink, K, Kim, Y R, Klareskog, L, Klump, K, Knudsen, G P, Koeleman, B, Koubek, D, La Via, M, Landén, M, Le Hellard, S, Leboyer, M, Levitan, R, Li, D, Lichtenstein, P, Lilenfeld, L, Lissowska, J, Lundervold, A, Magistretti, P, Maj, M, Mannik, K, Marsal, S, Kaminska, D, Martin, N, Mattingsdal, M, McDevitt, S, McGuffin, P, Merl, E, Metspalu, A, Meulenbelt, I, Micali, N, Mitchell, J, Mitchell, K, Monteleone, P, Monteleone, A M, Montgomery, G, Mortensen, P, Munn-Chernoff, M, Müller, T, Nacmias, B, Navratilova, M, Nilsson, I, Norring, C, Ntalla, I, Ophoff, R, O’Toole, J, Palotie, A, Pantel, J, Papezova, H, Parker, R, Pinto, D, Rabionet, R, Raevuori, A, Rajewski, A, Ramoz, N, William Rayner, N, Reichborn-Kjennerud, T, Ricca, V, Ripatti, S, Ritschel, F, Roberts, M, Rotondo, A, Rujescu, D, Rybakowski, F, Santonastaso, P, Scherag, A, Scherer, S, Schmidt, U, Schork, N, Schosser, A, Scott, L, Seitz, J, Slachtova, L, Sladek, R, Eline Slagboom, P, Slof-Op ’t Landt, M, Slopien, A, Smith, T, Soranzo, N, Sorbi, S, Southam, L, Steen, V, Strengman, E, Strober, M, Szatkiewicz, J, Szeszenia-Dabrowska, N, Tachmazidou, I, Tenconi, E, Tortorella, A, Tozzi, F, Treasure, J, Tschöp, M, Tsitsika, A, Tziouvas, K, van Elburg, A, van Furth, E, Wade, T, Wagner, G, Walton, E, Watson, H, Wichmann, H E, Widen, E, Woodside, B, Yanovski, J, Yao, S, Zerwas, S, Zipfel, S, Thornton, L, Hinney, A, Daly, M, Sullivan, P F, Zeggini, E, Breen, G & Bulik, C M 2017, ' Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa ', American Journal of Psychiatry, vol. 174, no. 9, pp. 850-858 . https://doi.org/10.1176/appi.ajp.2017.16121402
American Journal of Psychiatry, 174(9), 850. American Psychiatric Association
American Journal of Psychiatry, 174(9), 850-858. AMER PSYCHIATRIC PUBLISHING, INC
Am. J. Psychiatry 174, 850-858 (2017)
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
American Journal of Psychiatry
American Journal of Psychiatry, Vol. 174, No 9 (2017) pp. 850-858
Duncan, L, Yilmaz, Z, Gaspar, H, Walters, R, Goldstein, J, Anttila, V, Bulik-Sullivan, B, Ripke, S, Thornton, L, Hinney, A, Daly, M, Sullivan, P F, Zeggini, E, Breen, G, Bulik, C M, Duncan, L, Yilmaz, Z, Gaspar, H, Walters, R, Goldstein, J, Anttila, V, Bulik-Sullivan, B, Ripke, S, Adan, R, Alfredsson, L, Ando, T, Andreassen, O, Aschauer, H, Baker, J, Barrett, J, Bencko, V, Bergen, A, Berrettini, W, Birgegård, A, Boni, C, Perica, V B, Brandt, H, Burghardt, R, Carlberg, L, Cassina, M, Cesta, C, Cichon, S, Clementi, M, Cohen-Woods, S, Coleman, J, Cone, R, Courtet, P, Crawford, S, Crow, S, Crowley, J, Danner, U, Davis, O, de Zwaan, M, Dedoussis, G, Degortes, D, DeSocio, J, Danielle, D N, Dikeos, D, Dina, C, Ding, B, Dmitrzak-Weglarz, M, Docampo, E, Egberts, K, Ehrlich, S, Escaramís, G, Esko, T, Espeseth, T, Estivill, X, Favaro, A, Fernández-Aranda, F, Fichter, M, Finan, C, Fischer, K, Floyd, J, Föcker, M, Foretova, L, Forzan, M, Fox, C, Franklin, C, Gaborieau, V, Gallinger, S, Gambaro, G, Giegling, I, Gonidakis, F, Gorwood, P, Gratacos, M, Guillaume, S, Guo, Y, Hakonarson, H, Halmi, K, Harrison, R, Hatzikotoulas, K, Hauser, J, Hebebrand, J, Helder, S, Hendriks, J, Herms, S, Herpertz-Dahlmann, B, Herzog, W, Hilliard, C, Huckins, L, Hudson, J, Huemer, J, Imgart, H, Inoko, H, Jall, S, Jamain, S, Janout, V, Jiménez-Murcia, S, Johnson, C, Jordan, J, Julià, A, Juréus, A, Kalsi, G, Kaplan, A, Kaprio, J, Karhunen, L, Karwautz, A, Kas, M, Kaye, W, Kennedy, M, Kennedy, J, Keski-Rahkonen, A, Kiezebrink, K, Kim, Y R, Klareskog, L, Klump, K, Knudsen, G P, Koeleman, B, Koubek, D, La Via, M, Landén, M, Le Hellard, S, Leboyer, M, Levitan, R, Li, D, Lichtenstein, P, Lilenfeld, L, Lissowska, J, Lundervold, A, Magistretti, P, Maj, M, Mannik, K, Marsal, S, Kaminska, D, Martin, N, Mattingsdal, M, McDevitt, S, McGuffin, P, Merl, E, Metspalu, A, Meulenbelt, I, Micali, N, Mitchell, J, Mitchell, K, Monteleone, P, Monteleone, A M, Montgomery, G, Mortensen, P, Munn-Chernoff, M, Müller, T, Nacmias, B, Navratilova, M, Nilsson, I, Norring, C, Ntalla, I, Ophoff, R, O’Toole, J, Palotie, A, Pantel, J, Papezova, H, Parker, R, Pinto, D, Rabionet, R, Raevuori, A, Rajewski, A, Ramoz, N, William Rayner, N, Reichborn-Kjennerud, T, Ricca, V, Ripatti, S, Ritschel, F, Roberts, M, Rotondo, A, Rujescu, D, Rybakowski, F, Santonastaso, P, Scherag, A, Scherer, S, Schmidt, U, Schork, N, Schosser, A, Scott, L, Seitz, J, Slachtova, L, Sladek, R, Eline Slagboom, P, Slof-Op ’t Landt, M, Slopien, A, Smith, T, Soranzo, N, Sorbi, S, Southam, L, Steen, V, Strengman, E, Strober, M, Szatkiewicz, J, Szeszenia-Dabrowska, N, Tachmazidou, I, Tenconi, E, Tortorella, A, Tozzi, F, Treasure, J, Tschöp, M, Tsitsika, A, Tziouvas, K, van Elburg, A, van Furth, E, Wade, T, Wagner, G, Walton, E, Watson, H, Wichmann, H E, Widen, E, Woodside, B, Yanovski, J, Yao, S, Zerwas, S, Zipfel, S, Thornton, L, Hinney, A, Daly, M, Sullivan, P F, Zeggini, E, Breen, G & Bulik, C M 2017, ' Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa ', American Journal of Psychiatry, vol. 174, no. 9, pp. 850-858 . https://doi.org/10.1176/appi.ajp.2017.16121402
American Journal of Psychiatry, 174(9), 850. American Psychiatric Association
American Journal of Psychiatry, 174(9), 850-858. AMER PSYCHIATRIC PUBLISHING, INC
Am. J. Psychiatry 174, 850-858 (2017)
Dipòsit Digital de la UB
Universidad de Barcelona
Objective: The authors conducted a genome-wide association study of anorexia nervosa and calculated genetic correlations with a series of psychiatric, educational, and metabolic phenotypes. Method: Following uniformquality control and imputation proc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::943a356ba209d7278b85b5e8a5829680
http://hdl.handle.net/11562/998771
http://hdl.handle.net/11562/998771
Autor:
Rucker, James J.H., Tansey, Katherine E., Rivera, Margarita, Pinto, Dalila, Cohen-Woods, Sarah, Uher, Rudolf, Aitchison, Katherine J., Craddock, Nick, Owen, Michael J., Jones, Lisa, Jones, Ian, Korszun, Ania, Barnes, Michael R., Preisig, Martin, Mors, Ole, Maier, Wolfgang, Rice, John, Rietschel, Marcella, Holsboer, Florian, Farmer, Anne E., Craig, Ian W., Scherer, Stephen W., McGuffin, Peter, Breen, Gerome
Publikováno v:
Biological Psychiatry
Rucker, J J H, Tansey, K E, Rivera, M, Pinto, D, Cohen-Woods, S, Uher, R, Aitchison, K J, Craddock, N, Owen, M J, Jones, L, Jones, I, Korszun, A, Barnes, M R, Preisig, M, Mors, O, Maier, W, Rice, J, Rietschel, M, Holsboer, F, Farmer, A E, Craig, I W, Scherer, S W, McGuffin, P & Breen, G 2016, ' Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder ', Biological Psychiatry, vol. 79, no. 4, pp. 329-336 . https://doi.org/10.1016/j.biopsych.2015.02.025
Rucker, J J H, Tansey, K E, Rivera, M, Pinto, D, Cohen-Woods, S, Uher, R, Aitchison, K J, Craddock, N, Owen, M J, Jones, L, Jones, I, Korszun, A, Barnes, M R, Preisig, M, Mors, O, Maier, W, Rice, J, Rietschel, M, Holsboer, F, Farmer, A E, Craig, I W, Scherer, S W, McGuffin, P & Breen, G 2015, ' Phenotypic Association Analyses with Copy Number Variation in Recurrent Depressive Disorder ', Biological psychiatry, vol. 79, no. 4, pp. 329–336 . https://doi.org/10.1016/j.biopsych.2015.02.025
Biological Psychiatry, vol. 79, no. 4, pp. 329-336
Rucker, J J H, Tansey, K E, Rivera, M, Pinto, D, Cohen-Woods, S, Uher, R, Aitchison, K J, Craddock, N, Owen, M J, Jones, L, Jones, I, Korszun, A, Barnes, M R, Preisig, M, Mors, O, Maier, W, Rice, J, Rietschel, M, Holsboer, F, Farmer, A E, Craig, I W, Scherer, S W, McGuffin, P & Breen, G 2016, ' Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder ', Biological Psychiatry, vol. 79, no. 4, pp. 329-336 . https://doi.org/10.1016/j.biopsych.2015.02.025
Rucker, J J H, Tansey, K E, Rivera, M, Pinto, D, Cohen-Woods, S, Uher, R, Aitchison, K J, Craddock, N, Owen, M J, Jones, L, Jones, I, Korszun, A, Barnes, M R, Preisig, M, Mors, O, Maier, W, Rice, J, Rietschel, M, Holsboer, F, Farmer, A E, Craig, I W, Scherer, S W, McGuffin, P & Breen, G 2015, ' Phenotypic Association Analyses with Copy Number Variation in Recurrent Depressive Disorder ', Biological psychiatry, vol. 79, no. 4, pp. 329–336 . https://doi.org/10.1016/j.biopsych.2015.02.025
Biological Psychiatry, vol. 79, no. 4, pp. 329-336
BackgroundDefining the molecular genomic basis of the likelihood of developing depressive disorder is a considerable challenge. We previously associated rare, exonic deletion copy number variants (CNV) with recurrent depressive disorder (RDD). Sex ch
Autor:
Hinney, A., Kesselmeier, M., Huckins, Laura M, Hauser, Joanna, Karhunen, Leila, Meulenbelt, Ingrid, Slagboom, P Eline, Tortorella, Alfonso, Maj, Mario, Dedoussis, George, Dikeos, Dimitris, Gonidakis, Fragiskos, Tziouvas, Konstantinos, Southam, Lorraine, Tsitsika, Artemis, Papezova, Hana, Slachtova, Lenka, Martaskova, Debora, Kennedy, James L, Levitan, Robert D, Yilmaz, Zeynep, Huemer, Julia, Koubek, Doris, Merl, Elisabeth, Rayner, N William, Wagner, Gudrun, Lichtenstein, Paul, Breen, Gerome, Cohen-Woods, Sarah, Farmer, Anne, McGuffin, Peter, Cichon, Sven, Giegling, Ina, Herms, Stefan, Rujescu, Dan, Tachmazidou, Ioanna, Schreiber, Stefan, Wichmann, H-Erich, Dina, Christian, Sladek, Rob, Gambaro, Giovanni, Soranzo, Nicole, Julia, Antonio, Marsal, Sara, Rabionet, Raquel, Gaborieau, Valerie, Klump, Kelly L, Dick, Danielle M, Palotie, Aarno, Ripatti, Samuli, Widén, Elisabeth, Andreassen, Ole A, Espeseth, Thomas, Lundervold, Astri, Reinvang, Ivar, Steen, Vidar M, Hellard, Stephanie Le, Treasure, Janet, Mattingsdal, Morten, Ntalla, Ioanna, Bencko, Vladimir, Foretova, Lenka, Janout, Vladimir, Navratilova, Marie, Gallinger, Steven, Pinto, Dalila, Scherer, Stephen W, Aschauer, Harald, Lewis, Cathryn M, Carlberg, Laura, Schosser, Alexandra, Alfredsson, Lars, Ding, Bo, Klareskog, Lars, Padyukov, Leonid, Finan, Chris, Kalsi, Gursharan, Roberts, Marion, Logan, Darren W, Schmidt, Ulrike, Peltonen, Leena, Ritchie, Graham R S, Barrett, Jeff C, Estivill, Xavier, Hinney, Anke, Sullivan, Patrick F, Collier, David A, Zeggini, Eleftheria, Bulik, Cynthia M, Anderson, Carl A, Tozzi, Federica, Barrett, Jeffrey C, Floyd, James A B, Franklin, Christopher S, McGinnis, Ralph, Sambrook, Jennifer, Stephens, Jonathan, Ouwehand, Willem H, McArdle, Wendy L, iezebrink, Kirsty, Ring, Susan M, Strachan, David P, Alexander, Graeme, Conlon, Peter J, Dominiczak, Anna, Duncanson, Audrey, Hill, Adrian, Langford, Cordelia, Jall, S., Hebebrand, Johannes, Lord, Graham, Maxwell, Alexander P, Morgan, Linda, Sandford, Richard N, Sheerin, Neil, Vannberg, Frederik O, Blackburn, Hannah, Chen, Wei-Min, Edkins, Sarah, Gorwood, Philip, Gillman, Mathew, Gray, Emma, Hunt, Sarah E, Nengut-Gumuscu, Suna, Potter, Simon, Rich, Stephen S, Simpkin, Douglas, Whittaker, Pamela, Heid, I. M., Winkler, T. W., Adan, Roger A H, de Bakker, P., Bültmann, U., Geleijnse, M., Harst, P. V., Koppelman, G., Rosmalen, J. G., van Rossum, L., Smidt, H., Swertz, M. A., Stolk, R. P., Kas, Martien J H, Alizadeh, B., de Boer, R., Boezen, H. M., Bruinenberg, M., Franke, L., van der Harst, P., Hillege, H., van der Klauw, M., Navis, G., Ormel, J., Favaro, Angela, Postma, D., Rosmalen, J., Slaets, J., Snieder, H., Stolk, R., Wolffenbuttel, B., Wijmenga, C., Berg, J., Blackwood, D., Campbell, H., Santonastaso, Paolo, Cavanagh, J., Connell, J., Connor, M., Cunningham-Burley, S., Deary, I., Dominiczak, A., Ellis, P., FitzPatrick, B., Ford, I., Gertz, R., Fernández-Aranda, Fernando, Grau, A., Haddow, G., Jackson, C., Kerr, S., Lindsay, R., McGilchrist, M., McIntyre, D., Morris, A., Morton, R., Muir, W., Gratacos, Monica, Murray, G., Palmer, C., Pell, J., Philp, A., Porteous, D., Porteous, M., Procter, R., Ralston, S., Reid, D., Sinnott, R., Rybakowski, Filip, Smith, B., Clair, D. S., Sullivan, F., Sweetland, M., Ure, J., Watt, G., Wolf, R., Wright, A., Berndt, S. I., Gustafsson, S., Dmitrzak-Weglarz, Monika, Mägi, R., Ganna, A., Wheeler, E., Feitosa, M. F., Justice, A. E., Monda, K. L., Croteau- Chonka, D. C., Day, F. R., Esko, T., Fall, T., Volckmar, A-L, Kaprio, Jaakko, Ferreira, T., Gentilini, D., Jackson, A. U., Luan, J., Randall, J. C., Vedantam, S., Willer, C. J., Wood, A. R., Workalemahu, T., Keski-Rahkonen, Anna, Hu, Y. J., Lee, S. H., Liang, L., Lin, D. Y., Min, J. L., Neale, B. M., Thorleifsson, G., Yang, J., Albrecht, E., Amin, N., Raevuori-Helkamaa, Anu, Bragg-Gresham, J. L., Cadby, G., den Heijer, M., Eklund, N., Fischer, K., Goel, A., Hottenga, J. J., Huffman, J. E., Jarick, I., Johansson, A., Van Furth, Eric F, Johnson, T., Kanoni, S., Kleber, M. E., König, I. R., Kristiansson, K., Kutalik, Z., Lamina, C., Lecoeur, C., Li, G., Mangino, M., Slof-Op't Landt, Margarita C T, McArdle, W. L., Medina-Gomez, C., Müller-Nurasyid, M., Ngwa, J. S., Nolte, I. M., Paternoster, L., Pechlivanis, S., Perola, M., Peters, M. J., Preuss, M., Hudson, James I, Rose, L. M., Shi, J., Shungin, D., Smith, A. V., Strawbridge, R. J., Surakka, I., Teumer, A., Trip, M. D., Tyrer, J., Van Vliet- Ostaptchouk, J. V., Reichborn-Kjennerud, Ted, Vandenput, L., Waite, L. L., Zhao, J. H., Absher, D., Asselbergs, F. W., Atalay, M., Attwood, A. P., Balmforth, A. J., Basart, H., Beilby, J., Knudsen, Gun Peggy S, Bonnycastle, L. L., Brambilla, P., Chasman, D. I., Chines, P. S., Collins, F. S., Connell, J. M., Cookson, W., de Faire, U., Monteleone, Palmiero, de Vegt, F., Dei, M., Dimitriou, M., Edkins, S., Estrada, K., Evans, D. M., Farrall, M., Ferrario, M. M., Ferrières, J., Kaplan, Allan S, Frau, F., Gejman, P. V., Grallert, H., Grönberg, H., Gudnason, V., Hall, A. S., Hall, P., Hartikainen, A. L., Hayward, C., Heard-Costa, N. L., Föcker, M., Karwautz, Andreas, Heath, A. C., Hebebrand, J., Homuth, G., Hu, F. B., Hunt, S. E., Hyppönen, E., Iribarren, C., Jacobs, K. B., Jansson, J. O., Jula, A., Hakonarson, Hakon, Kähönen, M., Kathiresan, S., Kee, F., Khaw, K. T., Kivimaki, M., Koenig, W., Kraja, A. T., Kumari, M., Kuulasmaa, K., Kuusisto, J., Berrettini, Wade H, Laitinen, J. H., Lakka, T. A., Langenberg, C., Launer, L. J., Lind, L., Lindström, J., Liu, J., Liuzzi, A., Lokki, M. L., Lorentzon, M., Guo, Yiran, Madden, P. A., Magnusson, P. K., Manunta, P., Marek, D., März, W., Mateo Leach, I., McKnight, B., Medland, S. E., Mihailov, E., Milani, L., Li, Dong, Montgomery, G. W., Mooser, V., Mühleisen, T. W., Munroe, P. B., Musk, A. W., Narisu, N., Nicholson, G., Nohr, E. A., Ong, K. K., Schork, Nicholas J, Oostra, B. A., Palmer, C. N., Palotie, A., Peden, J. F., Pedersen, N., Peters, A., Polasek, O., Pouta, A., Pramstaller, P. P., Prokopenko, I., Komaki, Gen, Pütter, C., Radhakrishnan, A., Raitakari, O., Rendon, A., Rivadeneira, F., Rudan, I., Saaristo, T. E., Sambrook, J. G., Sanders, A. R., Sanna, S., Ando, Tetsuya, Saramies, J., Schipf, S., Schreiber, S., Schunkert, H., Shin, S. Y., Signorini, S., Sinisalo, J., Skrobek, B., Soranzo, N., Stancakova, A., Inoko, Hidetoshi, Stark, K., Stephens, J. C., Stirrups, K., Stumvoll, M., Swift, A. J., Theodoraki, E. V., Thorand, B., Tregouet, D. A., Tremoli, E., Esko, Tõnu, Van der Klauw, M. M., van Meurs, J. B., Vermeulen, S. H., Viikari, J., Virtamo, J., Vitart, V., Waeber, G., Wang, Z., Widen, E., Wild, S. H., Antel, J., Fischer, Krista, Willemsen, G., Winkelmann, B. R., Witteman, J. C., Wolffenbuttel, B. H., Wong, A., Wright, A. F., Zillikens, M., Amouyel, P., Boehm, B. O., Boerwinkle, E., Männik, Katrin, Boomsma, D. I., Caulfield, M. J., Chanock, S. J., Cupples, L., Cusi, D., Dedoussis, G. V., Erdmann, J., Eriksson, J. G., Franks, P. W., Froguel, P., Metspalu, Andres, Gieger, C., Gyllensten, U., Hamsten, A., Harris, T. B., Hengstenberg, C., Hicks, A. A., Hingorani, A., Hofman, A., Hovingh, K. G., Baker, Jessica H, Hveem, K., Illig, T., Jarvelin, M. R., Jöckel, K. H., Keinanen-Kiukaanniemi, S. M., Kiemeney, L. A., Kuh, D., Laakso, M., Lehtimäki, T., Levinson, D. F., Cone, Roger D, Martin, N. G., Metspalu, A., Morris, A. D., Nieminen, M. S., Njølstad, I., Ohlsson, C., Oldehinkel, A. J., Ouwehand, W. H., Palmer, L. J., Penninx, B., Dackor, Jennifer, Power, C., Province, M. A., Psaty, B. M., Qi, L., Rauramaa, R., Ridker, P. M., Ripatti, S., Salomaa, V., Samani, N. J., DeSocio, Janiece E, Sørensen, T. I., Spector, T. D., Stefansson, K., Tönjes, A., Tuomilehto, J., Uitterlinden, A. G., Uusitupa, M., Vollenweider, P., Wallaschofski, H., Hilliard, Christopher E, Wareham, N. J., Watkins, H., Wichmann, H, Wilson, J. F., Abecasis, G. R., Assimes, T. L., Barroso, I., Boehnke, M., Borecki, I. B., Deloukas, P., O'Toole, Julie K, Fox, C. S., Frayling, T., Groop, L. C., Haritunian, T., Hunter, D., Kaplan, R. C., Karpe, F., Moffatt, M., Mohlke, K. L., Pantel, Jacques, O'Connell, J. R., Pawitan, Y., Schadt, E. E., Schlessinger, D., Steinthorsdottir, V., Strachan, D. P., Thorsteinsdottir, U., van Duijn, C. M., Visscher, P. M., Di Blasio, A. M., Perica, Vesna Boraska, Szatkiewicz, Jin P, Hirschhorn, J. N., Lindgren, C. M., Morris, A. P., Meyre, D., Scherag, A., McCarthy, M. I., Speliotes, E. K., North, K. E., Loos, R. J., Grant, S. F. A., Taico, Chrysecolla, Adair, L. S., Ang, W., van Beijsterveldt, T., Bergen, N., Benke, K., Berry, D. J., Bradfield, J. P., Charoen, P., Zerwas, Stephanie, Coin, L., Cooper, C., Cousminer, D. L., Das, S., Davis, O. S., Elliott, P., Estivill, X., Feenstra, B., Trace, Sara E, Flexeder, C., Freathy, R. M., Gaillard, R., Geller, F., Gillman, M., Grant, S. F., Groen-Blokhuis, M., Goh, L. K., Guxens, M., Davis, Oliver S P, Hakonarson, H., Hattersley, A. T., Haworth, C. M., Hadley, D., Heinrich, J., Hocher, B., Holloway, J. W., Helder, Sietske, Holst, C., Horikoshi, M., Huikari, V., Hypponen, E., Iñiguez, C., Jaddoe, V. W., Kaakinen, M., Kilpeläinen, T. O., Bühren, Katharina, Kirin, M., Kowgier, M., Lakka, H. M., Lange, L. A., Lawlor, D. A., Lewin, A., Lindgren, C., Lindi, V., Burghardt, Roland, Maggi, R., Marsh, J., Melbye, M., Middeldorp, C., Millwood, I., Mook-Kanamori, D. O., Murray, J. C., Nivard, M., de Zwaan, Martina, Ntalla, I., Oken, E., O'Reilly, P. F., Panoutsopoulou, K., Pararajasingham, J., Pearson, E. R., Pennell, C. E., Egberts, Karin, Price, T. S., Raitakari, O. T., Rodriguez, A., Salem, R. M., Saw, S. M., Sebert, S., Siitonen, N., Ehrlich, Stefan, Simell, O., Sovio, U., Pourcain, B. S., Sunyer, J., Taal, H. R., Teo, Y. Y., Thiering, E., Tiesler, C., Herpertz-Dahlmann, Beate, Timpson, N. J., Valcárcel, B., Warrington, N. M., White, S., Widén, E., Yaghootkar, H., Zeggini, E., Herzog, Wolfgang, Elks, C. E., Perry, J. R., Sulem, P., Franceschini, N., He, C., Lunetta, K. L., Visser, J. A., Byrne, E. M., Imgart, Hartmut, Gudbjartsson, D. F., Koller, D. L., Lin, P., Marongiu, M., McArdle, P. F., Scherag, André, Stolk, L., van Wingerden, S. H., Corre, T., Ingelsson, E., Smith, E. N., Scherag, Susann, Ulivi, S., Warrington, M., Zgaga, L., Alavere, H., Aspelund, T., Bandinelli, S., Berenson, G. S., Bergmann, S., Zipfel, Stephan, Blackburn, H., Buring, J. E., Busonero, F., Chen, W., Cornelis, M. C., Couper, D., Coviello, A. D., Boni, Claudette, d'Adamo, P., de Geus, E. J., Döring, A., Davey Smith, G., Easton, D. F., Eiriksdottir, G., Emilsson, V., Eriksson, J., Ramoz, Nicolas, Ferrucci, L., Folsom, A. R., Foroud, T., Garcia, M., Gasparini, P., Hankinson, S. E., Versini, Audrey, Ferreli, L., Hernandez, D. G., Järvelin, M. R., Johnson, A. D., Karasik, D., Brandys, Marek K, Kiel, D. P., Kolcic, I., Kraft, P., Laven, J. S., Li, S., Levy, D., Danner, Unna N, Murray, S. S., Nalls, M. A., Navarro, P., Nelis, M., Ness, A. R., Northstone, K., de Kove, Carolien, Peacock, M., Paré, G., Parker, A. N., Pedersen, N. L., Peltonen, L., Pharoah, P., Hendriks, Judith, Plump, A. S., Porcu, E., Rafnar, T., Rice, J. P., Ring, S. M., Sala, C., Koeleman, Bobby P C, Schork, N. J., Scuteri, A., Segrè, A. V., Shuldiner, A. R., Srinivasan, S. R., Ophoff, Roel A, Tammesoo, M. L., Tikkanen, E., Toniolo, D., Tsui, K., Tryggvadottir, L., Uda, M., van Dam, R. M., Strengman, Eric, Waterworth, D. M., Weedon, M. N., Wichmann, H. E., Young, L., van Elburg, Annemarie A, Zhai, G., Zhuang, W. V., Bierut, L. J., Boyd, H. A., Crisponi, L., Demerath, E. W., Econs, M. J., Hunter, D. J., Bruson, Alice, Streeten, E. A., Clementi, Maurizio, Murabito, J. M., Murray, A., Guo, Y., Bergen, A. W., Kaye, W., Berrettini, W., Brandt, Harry, Crawford, Steve, Thornton, Laura M, Degortes, Daniela, Crow, Scott, Fichter, Manfred M, Halmi, Katherine A, Johnson, Craig, Via, Maria La, Mitchell, James, Strober, Michael, Rotondo, Alessandro, Forzan, Monica, Woodside, D Blake, Keel, Pamela, Lilenfeld, Lisa, Plotnicov, Kathy, Bergen, Andrew W, Berrettini, Wade, Kaye, Walter, Tenconi, Elena, Magistretti, Pierre, Herpertz-Dahlmann, B., de Zwaan, M., Herzog, W., Ehrlich, S., Zipfel, S., Egberts, K. M., Adan, R., Brandys, M., van Elburg, A., Docampo, Elisa, Boraska Perica, V., Franklin, C. S., Tschöp, M. H., Bulik, C. M., Collier, D., Müller, T. D., Escaramí, Geòrgia, Jiménez-Murcia, Susana, Lissowska, Jolanta, Rajewski, Andrzej, Szeszenia-Dabrowska, Neonila, Slopien, Agnieszka
Publikováno v:
Molecular Psychiatry, 22, 2, pp. 192-201
Molecular psychiatry, 22(2), 192-201. Nature Publishing Group
Molecular Psychiatry, 22, 192. Nature Publishing Group
GCAN 2017, ' Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index ', Molecular Psychiatry, vol. 22, no. 2, pp. 192-201 . https://doi.org/10.1038/mp.2016.71
Molecular Psychiatry, 22(2), 192-201. Nature Publishing Group
Mol Psychiatry
Molecular Psychiatry, 22, 192-201
Hinney, A, Kesselmeier, M, Jall, S, Volckmar, A-L, Föcker, M, Antel, J, Heid, I M, Winkler, T W, Grant, S F A, Guo, Y, Bergen, A W, Kaye, W, Berrettini, W, Hakonarson, H, Herpertz-Dahlmann, B, de Zwaan, M, Herzog, W, Ehrlich, S, Zipfel, S, Egberts, K M, Adan, R, Brandys, M, van Elburg, A, Boraska Perica, V, Franklin, C S, Tschöp, M H, Zeggini, E, Bulik, C M, Collier, D, Scherag, A, Müller, T D, Hebebrand, J, GCAN, Hottenga, J J, Willemsen, G, Boomsma, D I, van Beijsterveldt, C E M, Middeldorp, C M & de Geus, E 2017, ' Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index ', Molecular Psychiatry, vol. 22, no. 2, pp. 192-201 . https://doi.org/10.1038/mp.2016.71
Molecular psychiatry 22(2), 192-201 (2017). doi:10.1038/mp.2016.71
Molecular psychiatry, vol 22, iss 2
Dipòsit Digital de la UB
Universidad de Barcelona
Molecular Psychiatry
Recercat. Dipósit de la Recerca de Catalunya
instname
Molecular psychiatry, 22(2), 192-201. Nature Publishing Group
Molecular Psychiatry, 22, 192. Nature Publishing Group
GCAN 2017, ' Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index ', Molecular Psychiatry, vol. 22, no. 2, pp. 192-201 . https://doi.org/10.1038/mp.2016.71
Molecular Psychiatry, 22(2), 192-201. Nature Publishing Group
Mol Psychiatry
Molecular Psychiatry, 22, 192-201
Hinney, A, Kesselmeier, M, Jall, S, Volckmar, A-L, Föcker, M, Antel, J, Heid, I M, Winkler, T W, Grant, S F A, Guo, Y, Bergen, A W, Kaye, W, Berrettini, W, Hakonarson, H, Herpertz-Dahlmann, B, de Zwaan, M, Herzog, W, Ehrlich, S, Zipfel, S, Egberts, K M, Adan, R, Brandys, M, van Elburg, A, Boraska Perica, V, Franklin, C S, Tschöp, M H, Zeggini, E, Bulik, C M, Collier, D, Scherag, A, Müller, T D, Hebebrand, J, GCAN, Hottenga, J J, Willemsen, G, Boomsma, D I, van Beijsterveldt, C E M, Middeldorp, C M & de Geus, E 2017, ' Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index ', Molecular Psychiatry, vol. 22, no. 2, pp. 192-201 . https://doi.org/10.1038/mp.2016.71
Molecular psychiatry 22(2), 192-201 (2017). doi:10.1038/mp.2016.71
Molecular psychiatry, vol 22, iss 2
Dipòsit Digital de la UB
Universidad de Barcelona
Molecular Psychiatry
Recercat. Dipósit de la Recerca de Catalunya
instname
The maintenance of normal body weight is disrupted in patients with anorexia nervosa (AN) for prolonged periods of time. Prior to the onset of AN, premorbid body mass index (BMI) spans the entire range from underweight to obese. After recovery, patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe0fa762e65248741075d19c9dc455b2
https://hdl.handle.net/2066/169662
https://hdl.handle.net/2066/169662
Autor:
Marshall, Christian R, Howrigan, Daniel P, Merico, Daniele, Thiruvahindrapuram, Bhooma, Wu, Wenting, Greer, Douglas S, Antaki, Danny, Shetty, Aniket, Holmans, Peter A, Pinto, Dalila, Gujral, Madhusudan, Brandler, William M, Malhotra, Dheeraj, Wang, Zhouzhi, Fajarado, Karin V Fuentes, Maile, Michelle S, Ripke, Stephan, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amin, Farooq, Atkins, Joshua, Bacanu, Silviu A, Belliveau, Richard A, Bergen, Sarah E, Bertalan, Marcelo, Bevilacqua, Elizabeth, Bigdeli, Tim B, Black, Donald W, Bruggeman, Richard, Buccola, Nancy G, Buckner, Randy L, Bulik-Sullivan, Brendan, Byerley, William, Cahn, Wiepke, Cai, Guiqing, Cairns, Murray J, Campion, Dominique, Cantor, Rita M, Carr, Vaughan J, Carrera, Noa, Catts, Stanley V, Chambert, Kimberley D, Cheng, Wei, Cloninger, C Robert, Cohen, David, Cormican, Paul, Craddock, Nick, Crespo-Facorro, Benedicto, Crowley, James J, Curtis, David, Davidson, Michael, Davis, Kenneth L, Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H, Farh, Kai-How, Farrell, Martilias S, Frank, Josef, Franke, Lude, Freedman, Robert, Freimer, Nelson B, Friedman, Joseph I, Forstner, Andreas J, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Gershon, Elliot S, Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I, Gratten, Jacob, de Haan, Lieuwe, Hamshere, Marian L, Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M, Henskens, Frans A, Herms, Stefan, Hirschhorn, Joel N, Hoffmann, Per, Hofman, Andrea, Huang, Hailiang, Ikeda, Masashi, Joa, Inge
Publikováno v:
Nature genetics, vol 49, iss 1
Copy number variants (CNVs) have been strongly implicated in the genetic etiology of schizophrenia (SCZ). However, genome-wide investigation of the contribution of CNV to risk has been hampered by limited sample sizes. We sought to address this obsta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::69e7a0322ed456245c90f1109b09c032
https://escholarship.org/uc/item/7jq1c9p6
https://escholarship.org/uc/item/7jq1c9p6
Autor:
Vieland, Veronica, Hallmayer, Joachim, Huang, Yungui, Pagnamenta, Alistair, Pinto, Dalila, Khan, Hameed, Monaco, Anthony, Paterson, Andrew, Scherer, Stephen, Sutcliffe, James, Szatmari, Peter, Betancur, Catalina
Publikováno v:
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, 2011, 3 (2), pp.113-123. ⟨10.1007/s11689-011-9072-9⟩
Journal of Neurodevelopmental Disorders, BioMed Central, 2011, 3 (2), pp.113-123. ⟨10.1007/s11689-011-9072-9⟩
Journal of Neurodevelopmental Disorders, 2011, 3 (2), pp.113-123. ⟨10.1007/s11689-011-9072-9⟩
Journal of Neurodevelopmental Disorders, BioMed Central, 2011, 3 (2), pp.113-123. ⟨10.1007/s11689-011-9072-9⟩
Member of the Autism Genome Project Consortium: Astrid M. Vicente The Autism Genome Project has assembled two large datasets originally designed for linkage analysis and genome-wide association analysis, respectively: 1,069 multiplex families genotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79da5e709118e6a6a48f8abd389aa966
https://doi.org/10.1007/s11689-011-9072-9
https://doi.org/10.1007/s11689-011-9072-9
Autor:
Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Wang, Zhuozhi, Vorstman, Jacob AS, Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T, Oliveira, Bárbara, Marshall, Christian R, Magalhaes, Tiago R, Lowe, Jennifer K, Howe, Jennifer L, Griswold, Anthony J, Gilbert, John, Duketis, Eftichia, Dombroski, Beth A, De Jonge, Maretha V, Cuccaro, Michael, Crawford, Emily L, Correia, Catarina T, Conroy, Judith, Conceição, Inês C, Chiocchetti, Andreas G, Casey, Jillian P, Cai, Guiqing, Cabrol, Christelle, Bolshakova, Nadia, Bacchelli, Elena, Anney, Richard, Gallinger, Steven, Cotterchio, Michelle, Casey, Graham, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, Wallace, Simon, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Soorya, Latha, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L Alison, McGrew, Susan G, Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S, Kolevzon, Alexander, Jiménez González, Patricia, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Fernandez, Bridget A, Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F, Bölte, Sven, Bernier, Raphael, Baird, Gillian, Bailey, Anthony J, Anagnostou, Evdokia, Almeida, Joana, Wijsman, Ellen M, Vieland, Veronica J, Vicente, Astrid M, Schellenberg, Gerard D, Pericak-Vance, Margaret, Paterson, Andrew D, Parr, Jeremy R, Oliveira, Guiomar, Nurnberger, John I, Monaco, Anthony P, Maestrini, Elena, Klauck, Sabine M, Hakonarson, Hakon, Haines, Jonathan L, Geschwind, Daniel H, Freitag, Christine M, Folstein, Susan E, Ennis, Sean
Publikováno v:
American journal of human genetics, vol 94, iss 5
Rare copy-number variation (CNV) is an important source of risk for autism spectrum disorders (ASDs). We analyzed 2,446 ASD-affected families and confirmed an excess of genic deletions and duplications in affected versus control groups (1.41-fold, p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::41ef0c71be8a4388da39ddef51ba6b9c
https://escholarship.org/uc/item/2pf286f3
https://escholarship.org/uc/item/2pf286f3
Autor:
Hadley, Dexter, Wu, Zhi Liang, Kao, Charlly, Kini, Akshata, Mohamed-Hadley, Alisha, Thomas, Kelly, Vazquez, Lyam, Qiu, Haijun, Mentch, Frank, Pellegrino, Renata, Kim, Cecilia, Connolly, John, Pinto, Dalila, Merikangas, Alison, Klei, Lambertus, Vorstman, Jacob, Thompson, Ann, Regan, Regina, Pagnamenta, Alistair, Oliveira, Barbara, Magalhaes, Tiago, Gilbert, John, Duketis, Eftichia, De Jonge, Maretha, Cuccaro, Michael, Correia, Catarina, Conroy, Judith, Conceição, Inês, Chiocchetti, Andreas, Casey, Jillian, Bolshakova, Nadia, Bacchelli, Elena, Anney, Richard, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wallace, Simon, Van Engeland, Herman, Soorya, Latha, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, Mcgrew, Susan, Lord, Catherine, Leboyer, Marion, Le Couteur, Ann, Kolevzon, Alexander, Jacob, Suma, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Fernandez, Bridget, Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick, Bölte, Sven, Bernier, Raphael, Baird, Gillian, Bailey, Anthony, Anagnostou, Evdokia, Almeida, Joana, Wijsman, Ellen, Vieland, Veronica, Vicente, Astrid, Schellenberg, Gerard, Pericak-Vance, Margaret, Paterson, Andrew, Parr, Jeremy, Oliveira, Guiomar, Nurnberger, John, Monaco, Anthony, Maestrini, Elena, Klauck, Sabine, Haines, Jonathan, Geschwind, Daniel, Freitag, Christine, Folstein, Susan, Ennis, Sean, Coon, Hilary, Battaglia, Agatino, Szatmari, Peter, Sutcliffe, James, Hallmayer, Joachim, Gill, Michael, Cook, Edwin, Buxbaum, Joseph, Devlin, Bernie, Gallagher, Louise, Betancur, Catalina, Scherer, Stephen, Glessner, Joseph, Hakonarson, Hakon
Publikováno v:
Nature Communications
Nature Communications, Nature Publishing Group, 2014, 5, pp.4074. ⟨10.1038/ncomms5074⟩
Nature Communications, 2014, 5, pp.4074. ⟨10.1038/ncomms5074⟩
Nature Communications, Nature Publishing Group, 2014, 5, pp.4074. ⟨10.1038/ncomms5074⟩
Nature Communications, 2014, 5, pp.4074. ⟨10.1038/ncomms5074⟩
Although multiple reports show that defective genetic networks underlie the aetiology of autism, few have translated into pharmacotherapeutic opportunities. Since drugs compete with endogenous small molecules for protein binding, many successful drug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed6aa28c70a78591e663b8f2fda87dc7
https://www.hal.inserm.fr/inserm-01009668/document
https://www.hal.inserm.fr/inserm-01009668/document
Autor:
Anney, Richard, Klei, Lambertus, Pinto, Dalila, Almeida, Joana, Bacchelli, Elena, Baird, Gillian, Bolshakova, Nadia, Bölte, Sven, Bolton, Patrick F, Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Casey, Jillian, Conroy, Judith, Correia, Catarina, Corsello, Christina, Crawford, Emily L, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A, Folstein, Susan E, Fombonne, Eric, Gilbert, John, Gillberg, Christopher, Glessner, Joseph T, Green, Andrew, Green, Jonathan, Guter, Stephen J, Heron, Elizabeth A, Holt, Richard, Howe, Jennifer L, Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Jacob, Suma, Kenny, Graham P, Kim, Cecilia, Kolevzon, Alexander, Kustanovich, Vlad, Lajonchere, Clara M, Lamb, Janine A, Law-Smith, Miriam, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L, Liu, Xiao-Qing, Lombard, Frances, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C, Magalhaes, Tiago R, Mantoulan, Carine, McDougle, Christopher J, Melhem, Nadine M, Merikangas, Alison, Minshew, Nancy J, Mirza, Ghazala K, Munson, Jeff, Noakes, Carolyn, Nygren, Gudrun, Papanikolaou, Katerina, Pagnamenta, Alistair T, Parrini, Barbara, Paton, Tara, Pickles, Andrew, Posey, David J, Poustka, Fritz, Ragoussis, Jiannis, Regan, Regina, Roberts, Wendy, Roeder, Kathryn, Roge, Bernadette, Rutter, Michael L, Schlitt, Sabine, Shah, Naisha, Sheffield, Val C, Soorya, Latha, Sousa, Inês, Stoppioni, Vera, Sykes, Nuala, Tancredi, Raffaella, Thompson, Ann P, Thomson, Susanne, Tryfon, Ana, Tsiantis, John, Van Engeland, Herman, Vincent, John B, Volkmar, Fred, Vorstman, JAS, Wallace, Simon, Wing, Kirsty, Wittemeyer, Kerstin, Wood, Shawn, Zurawiecki, Danielle, Zwaigenbaum, Lonnie, Bailey, Anthony J
Publikováno v:
Human molecular genetics, vol 21, iss 21
While it is apparent that rare variation can play an important role in the genetic architecture of autism spectrum disorders (ASDs), the contribution of common variation to the risk of developing ASD is less clear. To produce a more comprehensive pic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7a8821b5fe3a9bd319c1f760c35e4ae0
https://escholarship.org/uc/item/7452m9z1
https://escholarship.org/uc/item/7452m9z1