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Autor:
Debladis, Jimmy, Valette, Marion, Strenilkov, Kuzma, Mantoulan, Carine, Thuilleaux, Denise, Laurier, Virginie, Molinas, Catherine, Barone, Pascal, Maïthé Tauber
Additional file 1. Results of the Bayesian estimation of the drift diffusion model employed to decision making. Details of average values for each eye-tracking parameters during face and emotion discrimination tasks and between all the tested populat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c7b3a055efd34931dd0e3875a015ae9
Autor:
Thuilleaux Denise, Mantoulan Carine, Kuzma Strelnikov, Pascal Barone, Maithé Tauber, Catherine Molinas, Juliette Salles, Virginie Laurier
Publikováno v:
Neuropsychologia
Neuropsychologia, Elsevier, 2016, 85, pp.137--147. ⟨10.1016/j.neuropsychologia.2016.03.015⟩
Neuropsychologia, Elsevier, 2016, 85, pp.137--147. ⟨10.1016/j.neuropsychologia.2016.03.015⟩
Prader-Willi syndrome (PWS) is a rare neurodevelopmental and genetic disorder that is characterized by various expression of endocrine, cognitive and behavioral problems, among which a true obsession for food and a deficit of satiety that leads to hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc2c8e0eb5eabd0ae1c8f79b2e2e625f
https://doi.org/10.1016/j.neuropsychologia.2016.03.015
https://doi.org/10.1016/j.neuropsychologia.2016.03.015
Autor:
Ehlinger Virginie, Laurier Virginie, Rogé Bernadette, Diene Gwenaëlle, Jauregui Joseba, Demeer Genevieve, Copet Pierre, Mantoulan Carine, Tauber Maïthe, Arnaud Catherine, Molinas Catherine, Thuilleaux Denise
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 47 (2011)
Abstract Background Prader-Willi syndrome (PWS) is a complex neurodevelopmental genetic disorder with hypothalamic dysfunction, early morbid obesity with hyperphagia, and specific psychiatric phenotypes including cognitive and behavioural problems, p
Externí odkaz:
https://doaj.org/article/c64a8e3666a2457bbab8244bfc167c28
Autor:
Debladis, Jimmy, Valette, Marion, Strenilkov, Kuzma, Mantoulan, Carine, Thuilleaux, Denise, Laurier, Virginie, Molinas, Catherine, Barone, Pascal, Tauber, Maïthé
Publikováno v:
Orphanet Journal of Rare Diseases; 11/15/2019, Vol. 14 Issue 1, p1-13, 13p
Autor:
Tauber, Maïthe1 (AUTHOR), Mantoulan, Carine (AUTHOR), Copet, Pierre (AUTHOR), Jauregui, Joseba (AUTHOR), Demeer, Genevieve (AUTHOR), Diene, Gwenaëlle (AUTHOR), Rogé, Bernadette (AUTHOR), Laurier, Virginie (AUTHOR), Ehlinger, Virginie (AUTHOR), Arnaud, Catherine (AUTHOR), Molinas, Catherine (AUTHOR), Thuilleaux, Denise (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 2011, Vol. 6 Issue 1, p47-52. 6p.
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
Autor:
Casey, Jillian P, Magalhaes, Tiago, Conroy, Judith M, Regan, Regina, Shah, Naisha, Anney, Richard, Shields, Denis C, Abrahams, Brett S, Almeida, Joana, Bacchelli, Elena, Bailey, Anthony J, Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Bolton, Patrick F, Bourgeron, Thomas, Brennan, Sean, Cali, Phil, Correia, Catarina, Corsello, Christina, Coutanche, Marc, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A, Folstein, Susan E, Foley, Suzanne, Fombonne, Eric, Freitag, Christine M, Gilbert, John, Gillberg, Christopher, Glessner, Joseph T, Green, Jonathan, Guter, Stephen J, Hakonarson, Hakon, Holt, Richard, Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M, Kolevzon, Alexander, Lamb, Janine A, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L, Lord, Catherine, Lund, Sabata C, Maestrini, Elena, Mantoulan, Carine, Marshall, Christian R, McConachie, Helen, McDougle, Christopher J, McGrath, Jane, McMahon, William M, Merikangas, Alison, Miller, Judith, Minopoli, Fiorella, Mirza, Ghazala K, Munson, Jeff, Nelson, Stanley F, Nygren, Gudrun, Oliveira, Guiomar, Pagnamenta, Alistair T, Papanikolaou, Katerina, Parr, Jeremy R, Parrini, Barbara, Pickles, Andrew, Pinto, Dalila, Piven, Joseph, Posey, David J, Poustka, Annemarie, Poustka, Fritz, Ragoussis, Jiannis, Roge, Bernadette, Rutter, Michael L, Sequeira, Ana F, Soorya, Latha, Sousa, Inês, Sykes, Nuala, Stoppioni, Vera, Tancredi, Raffaella, Tauber, Maïté, Thompson, Ann P, Thomson, Susanne, Tsiantis, John, Van Engeland, Herman, Vincent, John B, Volkmar, Fred, Vorstman, Jacob AS, Wallace, Simon, Wang, Kai, Wassink, Thomas H, White, Kathy
Publikováno v:
Human genetics, vol 131, iss 4
Autism spectrum disorder (ASD) is a highly heritable disorder of complex and heterogeneous aetiology. It is primarily characterized by altered cognitive ability including impaired language and communication skills and fundamental deficits in social r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4f5bfd612c4f125cdff14f5ad678254a
https://escholarship.org/uc/item/3k8329tm
https://escholarship.org/uc/item/3k8329tm
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=od______2127::b17c4e43c4743d7833a531793acab4f1
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3154362
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3154362
Autor:
Anney, Richard, Klei, Lambertus, Pinto, Dalila, Regan, Regina, Conroy, Judith, Magalhaes, Tiago R, Correia, Catarina, Abrahams, Brett S, Sykes, Nuala, Pagnamenta, Alistair T, Almeida, Joana, Bacchelli, Elena, Bailey, Anthony J, Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Bölte, Sven, Bolton, Patrick F, Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Carson, Andrew R, Casallo, Guillermo, Casey, Jillian, Chu, Su H, Cochrane, Lynne, Corsello, Christina, Crawford, Emily L, Crossett, Andrew, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Drmic, Irene, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A, Folstein, Susan E, Fombonne, Eric, Freitag, Christine M, Gilbert, John, Gillberg, Christopher, Glessner, Joseph T, Goldberg, Jeremy, Green, Jonathan, Guter, Stephen J, Hakonarson, Hakon, Heron, Elizabeth A, Hill, Matthew, Holt, Richard, Howe, Jennifer L, Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M, Kolevzon, Alexander, Korvatska, Olena, Kustanovich, Vlad, Lajonchere, Clara M, Lamb, Janine A, Laskawiec, Magdalena, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L, Lionel, Anath C, Liu, Xiao-Qing, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C, Maestrini, Elena, Mahoney, William, Mantoulan, Carine, Marshall, Christian R, McConachie, Helen, McDougle, Christopher J, McGrath, Jane, McMahon, William M, Melhem, Nadine M, Merikangas, Alison, Migita, Ohsuke, Minshew, Nancy J, Mirza, Ghazala K, Munson, Jeff, Nelson, Stanley F, Noakes, Carolyn, Noor, Abdul, Nygren, Gudrun, Oliveira, Guiomar, Papanikolaou, Katerina, Parr, Jeremy R, Parrini, Barbara, Paton, Tara, Pickles, Andrew, Piven, Joseph, Posey, David J
Publikováno v:
Human molecular genetics, vol 19, iss 20
Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify common risk variation, the Autism Genome Project (AGP) C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::49f9f0337a0dc309dfc03ae700abde06
https://escholarship.org/uc/item/9xq3g1p9
https://escholarship.org/uc/item/9xq3g1p9