Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Pinto, Dalila"'
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
Akademický článek
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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:
Noor, Abdul, Whibley, Annabel, Marshall, Christian, Gianakopoulos, Peter, Piton, Amelie, Carson, Andrew, Orlic-Milacic, Marija, Lionel, Anath, Sato, Daisuke, Pinto, Dalila, Drmic, Irene, Noakes, Carolyn, Senman, Lili, Zhang, Xiaoyun, Mo, Rong, Gauthier, Julie, Crosbie, Jennifer, Pagnamenta, Alistair, Munson, Jeffrey, Estes, Annette, Fiebig, Andreas, Franke, Andre, Schreiber, Stefan, Stewart, Alexandre, Roberts, Robert, McPherson, Ruth, Guter, Stephen, Cook, Edwin, Dawson, Geraldine, Schellenberg, Gerard, Battaglia, Agatino, Maestrini, Elena, Betancur, Catalina, Jeng, Linda, Hutchison, Terry, Rajcan-Separovic, Evica, Chudley, Albert, Lewis, Suzanne, Liu, Xudong, Holden, Jeanette, Fernandez, Bridget, Zwaigenbaum, Lonnie, Bryson, Susan, Roberts, Wendy, Szatmari, Peter, Gallagher, Louise, Stratton, Michael, Gecz, Jozef, Brady, Angela, Schwartz, Charles, Schachar, Russell, Monaco, Anthony, Rouleau, Guy, Hui, Chi-Chung, Lucy Raymond, F., Scherer, Stephen, Vincent, John
Publikováno v:
Science Translational Medicine
Science Translational Medicine, American Association for the Advancement of Science, 2010, 2 (49), pp.49ra68-49ra68. ⟨10.1126/scitranslmed.3001267⟩
Science Translational Medicine, 2010, 2 (49), pp.49ra68-49ra68. ⟨10.1126/scitranslmed.3001267⟩
Science Translational Medicine, American Association for the Advancement of Science, 2010, 2 (49), pp.49ra68-49ra68. ⟨10.1126/scitranslmed.3001267⟩
Science Translational Medicine, 2010, 2 (49), pp.49ra68-49ra68. ⟨10.1126/scitranslmed.3001267⟩
International audience; Autism is a common neurodevelopmental disorder with a complex mode of inheritance. It is one of the most highly heritable of the complex disorders, although the underlying genetic factors remain largely unknown. Here, we repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b60a79bc2ef5b247b1d5ff8ed0549fac
https://www.hal.inserm.fr/inserm-03135307
https://www.hal.inserm.fr/inserm-03135307
Autor:
Noh, Hyun Ji, Ponting, Chris P., Boulding, Hannah C., Meader, Stephen, Betancur, Catalina, Buxbaum, Joseph D., Pinto, Dalila, Marshall, Christian R., Lionel, Anath C., Scherer, Stephen W., Webber, Caleb
Publikováno v:
PLoS Genetics; Jun2013, Vol. 9 Issue 6, p1-12, 12p
Autor:
Dong, Li, Chang, Xiao, Connolly, John J., Tian, Lifeng, Liu, Yichuan, Bhoj, Elizabeth J., Robinson, Nora, Abrams, Debra, Yun R., Li, Bradfield, Jonathan P., Kim, Cecilia E., Jin, Li, Wang, Fengxiang, Snyder, James, Lemma, Maria, Hou, Cuiping, Wei, Zhi, Guo, Yiran, Qiu, Haijun, Mentch, Frank D., Thomas, Kelly A., Chiavacci, Rosetta M., Cone, Roger, Bingshan, Li, Sleiman, Patrick A., Hakonarson, Hakon, Perica, Vesna Boraska, Franklin, Christopher S., Floyd, James A. B., Thornton, Laura M., Huckins, Laura M., Southam, Lorraine, Rayner, N. William, Tachmazidou, Ioanna, Schmidt, Ulrike, Tozzi, Federica, Kiezebrink, Kirsty, Hebebrand, Johannes, Gorwood, Philip, Adan, Roger A. H., Kas, Martien J. H., Favaro, Angela, Santonastaso, Paolo, Fernánde Aranda, Fernando, Gratacos, Monica, Rybakowski, Filip, Dmitrzak Weglarz, Monika, Kaprio, Jaakko, Keski Rahkonen, Anna, Raevuori Helkamaa, Anu, Furth, Eric F. Van, Slof Opt Landt, Margarita C. T., Hudson, James I., Reichborn Kjennerud, Ted, Knudsen, Gun Peggy S., Monteleone, Palmiero, Karwautz, Andreas, Berrettini, Wade H., Schork, Nicholas J., Ando, Tetsuya, Inoko, Hidetoshi, Esko, Toã±u, Fischer, Krista, Mã¤nnik, Katrin, Metspalu, Andres, Baker, Jessica H., Desocio, Janiece E., Hilliard, Christopher E., O'Toole, Julie K., Pantel, Jacques, Szatkiewicz, Jin P., Zerwas, Stephanie, Davis, Oliver S. P., Helder, Sietske, Bã¼hren, Katharina, Burghardt, Roland, De Zwaan, Martina, Egberts, Karin, Ehrlich, Stefan, Herpertz Dahlmann, Beate, Herzog, Wolfgang, Imgart, Hartmut, Scherag, Andrã, Zipfel, Stephan, Boni, Claudette, Ramoz, Nicolas, Versini, Audrey, Danner, Unna N., Hendriks, Judith, Koeleman, Bobby P. C., Ophoff, Roel A., Strengman, Eric, Van Elburg, Annemarie A., Bruson, Alice, Clementi, Maurizio, Degortes, Daniela, Forzan, Monica, Tenconi, Elena, Docampo, Elisa, Escaramãs, Geã²rgia, Jiménez Murcia, Susana, Lissowska, Jolanta, Rajewski, Andrzej, Szeszenia Dabrowska, Neonila, Slopien, Agnieszka, Hauser, Joanna, Karhunen, Leila, Meulenbelt, Ingrid, Slagboom, P. Eline, Tortorella, Alfonso Antonio Vincenzo, Maj, Mario, Dedoussis, George, Dikeos, Dimitris, Gonidakis, Fragiskos, Tziouvas, Konstantinos, Tsitsika, Artemis, Papezova, Hana, Slachtova, Lenka, Martaskova, Debora, Kennedy, James L., Levitan, Robert D., Yilmaz, Zeynep, Huemer, Julia, Koubek, Doris, Merl, Elisabeth, Wagner, Gudrun, Lichtenstein, Paul, Breen, Gerome, Cohen Woods, Sarah, Farmer, Anne, Mcguffin, Peter, Cichon, Sven, Giegling, Ina, Herms, Stefan, Rujescu, Dan, Schreiber, Stefan, Wichmann, H. Erich, Dina, Christian, Sladek, Rob, Gambaro, Giovanni, Soranzo, Nicole, Julia, Antonio, Marsal, Sara, Rabionet, Raquel, Gaborieau, Valerie, Dick, Danielle M., Palotie, Aarno, Ripatti, Samuli, Widã©n, Elisabeth, Andreassen, Ole A., Espeseth, Thomas, Lundervold, Astri, Reinvang, Ivar, Steen, Vidar M., Le Hellard, Stephanie, Mattingsdal, Morten, Ntalla, Ioanna, Bencko, Vladimir, Foretova, Lenka, Janout, Vladimir, Navratilova, Marie, Gallinger, Steven, Pinto, Dalila, Scherer, Stephen W., Aschauer, Harald, Carlberg, Laura, Schosser, Alexandra, Alfredsson, Lars, Ding, Bo, Klareskog, Lars, Padyukov, Leonid, Finan, Chris, Kalsi, Gursharan, Roberts, Marion, Barrett, Jeff C., Estivill, Xavier, Hinney, Anke, Sullivan, Patrick F., Zeggini, Eleftheria, Bulik, Cynthia M., Brandt, Harry, Crawford, Steve, Crow, Scott, Fichter, Manfred M., Halmi, Katherine A., Johnson, Craig, Kaplan, Allan S., La Via, Maria C., Mitchell, James, Strober, Michael, Rotondo, Alessandro, Treasure, Janet, Woodside, D. Blake, Keel, Pamela K., Klump, Kelly L., Lilenfeld, Lisa, Bergen, Andrew W., Kaye, Walter, Magistretti, Pierre
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Scientific Reports, 7(1):3847. Nature Publishing Group
Scientific reports, vol 7, iss 1
Scientific Reports
Dipòsit Digital de la UB
Universidad de Barcelona
Scientific Reports, 7(1). NLM (Medline)
Scientific Reports, 7(1). Nature Publishing Group
Li, D, Chang, X, Hakonarson, H 2017, ' A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling ', Scientific Reports, vol. 7, 3847 . https://doi.org/10.1038/s41598-017-01674-8, https://doi.org/10.1038/s41598-017-06409-3
instname
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Scientific Reports, 7(1):3847. Nature Publishing Group
Scientific reports, vol 7, iss 1
Scientific Reports
Dipòsit Digital de la UB
Universidad de Barcelona
Scientific Reports, 7(1). NLM (Medline)
Scientific Reports, 7(1). Nature Publishing Group
Li, D, Chang, X, Hakonarson, H 2017, ' A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling ', Scientific Reports, vol. 7, 3847 . https://doi.org/10.1038/s41598-017-01674-8, https://doi.org/10.1038/s41598-017-06409-3
We conducted a genome-wide association study (GWAS) of anorexia nervosa (AN) using a stringently defined phenotype. Analysis of phenotypic variability led to the identification of a specific genetic risk factor that approached genome-wide significanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5c332e815dd372043fff40715b8c78a
http://hdl.handle.net/10230/35206
http://hdl.handle.net/10230/35206
Autor:
Marion Leboyer, Martin A. Kennedy, Yiran Guo, Stephan Ripke, Roger D. Cone, Nadia Micali, Allan S. Kaplan, Jonathan R. I. Coleman, Michael Strober, Dan Rujescu, Roland Burghardt, Pierre J. Magistretti, John F. Pearson, Stephan Zipfel, Ian Jones, Paul Lichtenstein, Leonid Padyukov, Jurjen J. Luykx, Wade H. Berrettini, Nicolas Ramoz, James I. Hudson, Ulrike Schmidt, Anke Hinney, Tõnu Esko, Johanna Giuranna, Sara Marsal, Johan G. Eriksson, Richard Parker, Roger A.H. Adan, George Dedoussis, Lars Klareskog, Cynthia M. Bulik, Liselotte Petersen, Stephanie Le Hellard, P. Eline Slagboom, Jochen Seitz, Ilka Boehm, Anna Keski-Rahkonen, Joseph M. Boden, Sébastien Guillaume, Xavier Estivill, Yasmina Silén, Elisabeth Widen, Josef Bulant, Marta Tyszkiewicz-Nwafor, Vladimir Janout, Janne Tidselbak Larsen, Artemis Tsitsika, Kirsty Kiezebrink, James E. Mitchell, Lenka Slachtova, Andreas J. Forstner, Harry Brandt, Nicholas G. Martin, James L. Kennedy, Wolfgang Herzog, Jennifer Jordan, Ionna Ntalla, Marie Navratilova, Gun Peggy Knudsen, Stephanie Zerwas, Steven Crawford, Oleksandr Frei, Sven Cichon, Katherine A. Halmi, Scott D. Gordon, Sietske G. Helder, Marion Roberts, Esther Walton, Beate Herpertz-Dahlmann, Martina de Zwaan, Federica Tozzi, Bochao Lin, Beata Świątkowska, Konstantinos Tziouvas, Mikael Landén, Lenka Foretova, Richard M. Myers, Annemarie A. van Elburg, Martien J H Kas, Antonio Julià, Pamela K. Keel, Susana Jiménez-Murcia, Karin Egberts, Alessandro Rotondo, Lars Alfredsson, Hartmut Imgart, L. John Horwood, Margarita Ct. Slof-Op 't Landt, Maria La Via, Dalila Pinto, Danielle M. Dick, Craig Johnson, Xiao Chang, Julie K. O'Toole, Philip Gorwood, Christian R. Marshall, Preben Bo Mortensen, Srdjan Djurovic, Mònica Gratacòs, Laura M. Thornton, Elisa Docampo-Martinez, Jessica H. Baker, Walter H. Kaye, Sandro Sorbi, Catherine M. Olsen, Hakon Hakonarson, Helga Ask, Franziska Ritschel, Agnieszka Słopień, Steven Gallinger, Dong Li, Roel A. Ophoff, Ole A. Andreassen, Andreas Birgegård, Philibert Duriez, Monika Dmitrzak-Weglarz, Alexandra Havdahl, Andrew W. Bergen, Fragiskos Gonidakis, André Scherag, Scott J. Crow, Filip Rybakowski, Tracey D. Wade, Karen S. Mitchell, Claudette Boni, Hunna J. Watson, David C. Whiteman, Ina Giegling, Samuli Ripatti, Palmiero Monteleone, James J. Crowley, Manuel Föcker, Zeynep Yilmaz, Dimitris Dikeos, Stefan Herms, Thomas Werge, Eric F. van Furth, Christian Dina, Nancy L. Pedersen, Mario Maj, Philippe Courtet, Stephanie Jamain, Janet Treasure, Johannes Hebebrand, Hana Papežová, Michael Boehnke, Katharina Buehren, Joanna Hauser, Jacques Pantel, Manfred M. Fichter, Stephen W. Scherer, Gerome Breen, Fernando Fernández-Aranda, Leila Karhunen, Gursharan Kalsi, Geòrgia Escaramís, Anne Farmer, Ingrid Meulenbelt, Janiece E. DeSocio, Valdo Ricca, Lisa Lilenfeld, Laura J. Scott, Stefan Ehrlich, Jolanta Lissowska, Unna N. Danner, Morten Mattingsdal, D. Blake Woodside, Alfonso Tortorella, Anu Raevuori, Alessio Maria Monteleone, Ted Reichborn-Kjennerud, Deborah Kaminská, Jaakko Kaprio, Sarah Maguire, Kelly L. Klump
Publikováno v:
Watson, H J, Thornton, L M, Yilmaz, Z, Baker, J H, Coleman, J R I, Adan, R A H, Alfredsson, L, Andreassen, O A, Ask, H, Berrettini, W H, Boehnke, M, Boehm, I, Boni, C, Buehren, K, Bulant, J, Burghardt, R, Chang, X, Cichon, S, Cone, R D, Courtet, P, Crow, S, Crowley, J J, Danner, U N, de Zwaan, M, Dedoussis, G, DeSocio, J E, Dick, D M, Dikeos, D, Dina, C, Djurovic, S, Dmitrzak-Weglarz, M, Docampo-Martinez, E, Duriez, P, Egberts, K, Ehrlich, S, Eriksson, J G, Escaramís, G, Esko, T, Estivill, X, Farmer, A, Fernández-Aranda, F, Fichter, M M, Föcker, M, Foretova, L, Forstner, A J, Frei, O, Gallinger, S, Giegling, I, Giuranna, J, Gonidakis, F, Gorwood, P, Gratacòs, M, Guillaume, S, Guo, Y, Hakonarson, H, Hauser, J, Havdahl, A, Hebebrand, J, Helder, S G, Herms, S, Herpertz-Dahlmann, B, Herzog, W, Hinney, A, Hübel, C, Hudson, J I, Imgart, H, Jamain, S, Janout, V, Jiménez-Murcia, S, Jones, I R, Julià, A, Kalsi, G, Kaminská, D, Kaprio, J, Karhunen, L, Kas, M J H, Keel, P K, Kennedy, J L, Keski-Rahkonen, A, Kiezebrink, K, Klareskog, L, Klump, K L, Knudsen, G P S, La Via, M C, Le Hellard, S, Leboyer, M, Li, D, Lilenfeld, L, Lin, B, Lissowska, J, Luykx, J, Magistretti, P, Maj, M, Marsal, S, Marshall, C R, Mattingsdal, M, Meulenbelt, I, Micali, N, Mitchell, K S, Monteleone, A M, Monteleone, P, Myers, R, Navratilova, M, Ntalla, I, O'Toole, J K, Ophoff, R A, Padyukov, L, Pantel, J, Papežová, H, Pinto, D, Raevuori, A, Ramoz, N, Reichborn-Kjennerud, T, Ricca, V, Ripatti, S, Ripke, S, Ritschel, F, Roberts, M, Rotondo, A, Rujescu, D, Rybakowski, F, Scherag, A, Scherer, S W, Schmidt, U, Scott, L J, Seitz, J, Silén, Y, Šlachtová, L, Slagboom, P E, Slof-Op ‘t Landt, M C T, Slopien, A, Sorbi, S, Świątkowska, B, Tortorella, A, Tozzi, F, Treasure, J, Tsitsika, A, Tyszkiewicz-Nwafor, M, Tziouvas, K, van Elburg, A A, van Furth, E F, Walton, E, Widen, E, Zerwas, S, Zipfel, S, Bergen, A W, Boden, J M, Brandt, H, Crawford, S, Halmi, K A, Horwood, L J, Johnson, C, Kaplan, A S, Kaye, W H, Mitchell, J E, Olsen, C M, Pearson, J F, Pedersen, N L, Strober, M, Werge, T, Whiteman, D C, Woodside, D B, Gordon, S, Maguire, S, Larsen, J T, Parker, R, Petersen, L V, Jordan, J, Kennedy, M, Wade, T D, Birgegård, A, Lichtenstein, P, Landén, M, Martin, N G, Mortensen, P B, Breen, G & Bulik, C M 2022, ' Common Genetic Variation and Age of Onset of Anorexia Nervosa ', Biological Psychiatry Global Open Science, vol. 2, no. 4, pp. 368-378 . https://doi.org/10.1016/j.bpsgos.2021.09.001
Biological Psychiatry Global Open Science, 2(4), 368-378. Elsevier
Biological Psychiatry Global Open Science, 2(4), 368-378. Elsevier
BackgroundGenetics and biology may influence the age of onset of anorexia nervosa (AN). The aims of this study were to determine whether common genetic variation contributes to age of onset of AN and to investigate the genetic associations between ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3d7c206af1d25f0e321fe587f2df5aa
http://hdl.handle.net/11591/461650
http://hdl.handle.net/11591/461650
Autor:
Geraldine Dawson, Sven Sandin, Frederico Duque, Peter Holmans, Marion Leboyer, Aarno Palotie, Fritz Poustka, Richard Delorme, Stephen Sanders, Alistair T. Pagnamenta, Lonnie Zwaigenbaum, Bridget A. Fernandez, A. Jeremy Willsey, Christine M. Freitag, Christa Lese Martin, Elena Maestrini, Elena Bacchelli, Guiomar Oliveira, Jeremy R. Parr, Guy A. Rouleau, Jonas Bybjerg-Grauholm, Joseph Piven, Latha Soorya, Lauren A. Weiss, Jonathan Green, Carsten Bøcker Pedersen, Louise Gallagher, Regina Regan, Stephan Ripke, Thomas Werge, Pat Levitt, Aravinda Chakravarti, Joana Almeida, Kathryn Roeder, Catalina Betancur, Bernie Devlin, Benjamin M. Neale, Gillian Baird, Jakob Grove, Thomas Bourgeron, David H. Ledbetter, Eftichia Duketis, Karola Rehnström, Gerard D. Schellenberg, Jillian P. Casey, Preben Bo Mortensen, Patrick Bolton, Igor Martsenkovsky, Elise Robinson, Hakon Hakonarson, Vanessa H. Bal, Stacy Steinberg, Christopher Gillberg, Kathryn Tsang, Jacob A. S. Vorstman, Verneri Anttila, Suma Jacob, Judith Conroy, J. Haines, William M. McMahon, Edwin H. Cook, Ann P. Thompson, Inês C. Conceição, Mark J. Daly, Arthur P. Goldberg, Sarah E. Medland, Milica Pejovic-Milovancevic, David M. Hougaard, Shrikant Mane, Christina M. Hultman, Susana Mouga, Hreinn Stefansson, Ellen M. Wijsman, Andreas G. Chiocchetti, Ole Mors, Phil Lee, Richard Anney, Astrid M. Vicente, Veronica J. Vieland, K. Stefansson, Stephen W. Scherer, Teimuraz Silagadze, Pall Magnusson, Donna M. Martin, Merete Nordentoft, Peter Szatmari, Patrícia B. S. Celestino-Soper, Ann S Le-Couteur, Cátia Café, Arthur L. Beaudet, Kerstin Wittemeyer, Anders D. Børglum, Joel S. Bader, Christopher S. Poultney, Hailiang Huang, Alexander Kolevzon, Margaret A. Pericak-Vance, Joachim Hallmayer, Rita M. Cantor, Eric Fombonne, Andrew Green, Dan E. Arking, M. Daniele Fallin, Matthew W. State, Christine Ladd-Acosta, Silvia Derubeis, Raphael Bernier, Regina Waltes, David G. Amaral, Manuel Mattheisen, Abraham Reichenberg, Lambertus Klei, Daniel Moreno-De-Luca, Marie Bækvad-Hansen, Maretha V. Dejonge, Susan G. McGrew, Joseph D. Buxbaum, Hilary Coon, Jennifer Reichert, Michael Gill, Herman Vanengeland, Christine Søholm Hansen, Anthony P. Monaco, Nadia Bolshakova, John I. Nurnberger, Nancy J. Minshew, Michael T. Murtha, Thomas H. Wassink, Evald Saemundsen, Simon Wallace, Sean Brennan, Sean Ennis, A. Gulhan Ercan-Sencicek, Sven Bölte, Oscar Svantesson, Susan L. Santangelo, Andrew D. Paterson, Robert L. Hendren, Timothy W. Yu, Dalila Pinto, D.E. Grice, Alison Merikangas, Stephen J. Guter, Anthony J. Bailey, Bernadette Rogé, Christopher A. Walsh, Susan E. Folstein, Wendy Roberts, Sabine M. Klauck, Marianne Giørtz Pedersen, Tiago R. Magalhaes, John R. Gilbert, Irva Hertz-Picciotto, James S. Sutcliffe, Evdokia Anagnostou, Catarina Correia, Eric M. Morrow, Daniel H. Geschwind, Jennifer K. Lowe, Agatino Battaglia, Bozenna Iliadou, Michael L. Cuccaro, Catherine Lord
Publikováno v:
Molecular Autism
Molecular Autism, BioMed Central, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Anney, R J L, Ripke, S, Anttila, V, Grove, J, Holmans, P, Huang, H, Klei, L, Lee, P H, Medland, S E, Neale, B, Robinson, E, Weiss, L A, Zwaigenbaum, L, Yu, T W, Wittemeyer, K, Willsey, A J, Wijsman, E M, Werge, T, Wassink, T H, Waltes, R, Walsh, C A, Wallace, S, Vorstman, J A S, Vieland, V J, Vicente, A M, Vanengeland, H, Tsang, K, Thompson, A P, Szatmari, P, Svantesson, O, Steinberg, S, Stefansson, K, Stefansson, H, State, M W, Soorya, L, Silagadze, T, Scherer, S W, Schellenberg, G D, Sandin, S, Sanders, S J, Saemundsen, E, Rouleau, G A, Rogé, B, Roeder, K, Roberts, W, Reichert, J, Reichenberg, A, Rehnström, K, Regan, R, Poustka, F, Poultney, C S, Piven, J, Pinto, D, Pericak-Vance, M A, Pejovic-Milovancevic, M, Pedersen, M G, Pedersen, C B, Paterson, A D, Parr, J R, Pagnamenta, A T, Oliveira, G, Nurnberger, J I, Nordentoft, M, Murtha, M T, Mouga, S, Mortensen, P B, Mors, O, Morrow, E M, Moreno-De-Luca, D, Monaco, A P, Minshew, N, Merikangas, A, McMahon, W M, McGrew, S G, Mattheisen, M, Martsenkovsky, I, Martin, D M, Mane, S M, Magnusson, P, Magalhaes, T, Maestrini, E, Lowe, J K, Lord, C, Levitt, P, Martin, C L, Ledbetter, D H, Leboyer, M, Lecouteur, A S, Ladd-Acosta, C, Kolevzon, A, Klauck, S M, Jacob, S, Iliadou, B, Hultman, C M, Hougaard, D M, Hertz-Picciotto, I, Hendren, R, Hansen, C S, Haines, J L, Guter, S J, Grice, D E, Green, J M, Green, A, Goldberg, A P, Gillberg, C, Gilbert, J, Gallagher, L, Freitag, C M, Fombonne, E, Folstein, S E, Fernandez, B, Fallin, M D, Ercan-Sencicek, A G, Ennis, S, Duque, F, Duketis, E, Delorme, R, Derubeis, S, Dejonge, M V, Dawson, G, Cuccaro, M L, Correia, C T, Conroy, J, Conceição, I C, Chiocchetti, A G, Celestino-Soper, P B S, Casey, J, Cantor, R M, Café, C, Bybjerg-Grauholm, J, Brennan, S, Bourgeron, T, Bolton, P F, Bölte, S, Bolshakova, N, Betancur, C, Bernier, R, Beaudet, A L, Battaglia, A, Bal, V H, Baird, G, Bailey, A J, Bækvad-Hansen, M, Bader, J S, Bacchelli, E, Anagnostou, E, Amaral, D, Almeida, J, Børglum, A D, Buxbaum, J D, Chakravarti, A, Cook, E H, Coon, H, Geschwind, D H, Gill, M, Hakonarson, H, Hallmayer, J, Palotie, A, Santangelo, S, Sutcliffe, J S, Arking, D E, Devlin, B & Daly, M J 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Bolton, P F 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, pp. 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Molecular autism, vol 8, iss 1
The Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Autism, vol. 8, no. 21, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, BioMed Central, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Anney, R J L, Ripke, S, Anttila, V, Grove, J, Holmans, P, Huang, H, Klei, L, Lee, P H, Medland, S E, Neale, B, Robinson, E, Weiss, L A, Zwaigenbaum, L, Yu, T W, Wittemeyer, K, Willsey, A J, Wijsman, E M, Werge, T, Wassink, T H, Waltes, R, Walsh, C A, Wallace, S, Vorstman, J A S, Vieland, V J, Vicente, A M, Vanengeland, H, Tsang, K, Thompson, A P, Szatmari, P, Svantesson, O, Steinberg, S, Stefansson, K, Stefansson, H, State, M W, Soorya, L, Silagadze, T, Scherer, S W, Schellenberg, G D, Sandin, S, Sanders, S J, Saemundsen, E, Rouleau, G A, Rogé, B, Roeder, K, Roberts, W, Reichert, J, Reichenberg, A, Rehnström, K, Regan, R, Poustka, F, Poultney, C S, Piven, J, Pinto, D, Pericak-Vance, M A, Pejovic-Milovancevic, M, Pedersen, M G, Pedersen, C B, Paterson, A D, Parr, J R, Pagnamenta, A T, Oliveira, G, Nurnberger, J I, Nordentoft, M, Murtha, M T, Mouga, S, Mortensen, P B, Mors, O, Morrow, E M, Moreno-De-Luca, D, Monaco, A P, Minshew, N, Merikangas, A, McMahon, W M, McGrew, S G, Mattheisen, M, Martsenkovsky, I, Martin, D M, Mane, S M, Magnusson, P, Magalhaes, T, Maestrini, E, Lowe, J K, Lord, C, Levitt, P, Martin, C L, Ledbetter, D H, Leboyer, M, Lecouteur, A S, Ladd-Acosta, C, Kolevzon, A, Klauck, S M, Jacob, S, Iliadou, B, Hultman, C M, Hougaard, D M, Hertz-Picciotto, I, Hendren, R, Hansen, C S, Haines, J L, Guter, S J, Grice, D E, Green, J M, Green, A, Goldberg, A P, Gillberg, C, Gilbert, J, Gallagher, L, Freitag, C M, Fombonne, E, Folstein, S E, Fernandez, B, Fallin, M D, Ercan-Sencicek, A G, Ennis, S, Duque, F, Duketis, E, Delorme, R, Derubeis, S, Dejonge, M V, Dawson, G, Cuccaro, M L, Correia, C T, Conroy, J, Conceição, I C, Chiocchetti, A G, Celestino-Soper, P B S, Casey, J, Cantor, R M, Café, C, Bybjerg-Grauholm, J, Brennan, S, Bourgeron, T, Bolton, P F, Bölte, S, Bolshakova, N, Betancur, C, Bernier, R, Beaudet, A L, Battaglia, A, Bal, V H, Baird, G, Bailey, A J, Bækvad-Hansen, M, Bader, J S, Bacchelli, E, Anagnostou, E, Amaral, D, Almeida, J, Børglum, A D, Buxbaum, J D, Chakravarti, A, Cook, E H, Coon, H, Geschwind, D H, Gill, M, Hakonarson, H, Hallmayer, J, Palotie, A, Santangelo, S, Sutcliffe, J S, Arking, D E, Devlin, B & Daly, M J 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Bolton, P F 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, pp. 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Molecular autism, vol 8, iss 1
The Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Autism, vol. 8, no. 21, 21 . https://doi.org/10.1186/s13229-017-0137-9
Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium - Collaborators (162): Anney RJL, Ripke S, Anttila V, Grove J, Holmans P, Huang H, Klei L, Lee PH, Medland SE, Neale B, Robinson E, Weiss LA, Zwaigenbaum L, Yu TW, Witteme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1efa92826829f7f870799b08a5c31e5
https://www.hal.inserm.fr/inserm-01535717
https://www.hal.inserm.fr/inserm-01535717