Carriers of the fragile X mental retardation 1 (<it>FMR1</it>) premutation allele present with increased levels of cytokine IL-10

by Marek Diana, Papin Stephanie, Ellefsen Kim, Niederhauser Julien, Isidor Nathalie, Ransijn Adriana, Poupon Lucienne, Spertini Francois, Pantaleo Giuseppe, Bergmann Sven, Beckmann Jacques S, Jacquemont Sebastien, Tanackovic Goranka
Published 2012-10-01

Protein synthesis levels are increased in a subset of individuals with fragile X syndrome.

by Jacquemont, Sébastien, Pacini, Laura, Jønch, Aia E, Cencelli, Giulia, Rozenberg, Izabela, He, Yunsheng, D'Andrea, Laura, Pedini, Giorgia, Eldeeb, Marwa, Willemsen, Rob, Gasparini, Fabrizio, Tassone, Flora, Hagerman, Randi, Gomez-Mancilla, Baltazar, Bagni, Claudia
Published 2018

Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication

by Linden, Stefanie C., Watson, Cameron J., Smith, Jacqueline, Chawner, Samuel J. R. A., Lancaster, Thomas M., Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J., Linden, David E. J., Green-Snyder, LeeAnne, Chung, Wendy K., Maillard, Anne M., Jacquemont, Sébastien, van den Bree, Marianne B. M.
Published 2021

Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication.

by Linden, Stefanie C, Watson, Cameron J, Smith, Jacqueline, Chawner, Samuel JRA, Lancaster, Thomas M, Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F Lucy, Hall, Jeremy, Owen, Michael J, Linden, David EJ, Green-Snyder, LeeAnne, Chung, Wendy K, Maillard, Anne M, Jacquemont, Sébastien, van den Bree, Marianne BM
Published 2021

The challenges of clinical trials in fragile X syndrome.

by Jacquemont, Sébastien, Berry-Kravis, Elizabeth, Hagerman, Randi, von Raison, Florian, Gasparini, Fabrizio, Apostol, George, Ufer, Mike, Des Portes, Vincent, Gomez-Mancilla, Baltazar
Published 2014

Sex differences in brain plasticity: a new hypothesis for sex ratio bias in autism

by Mottron, Laurent, Duret, Pauline, Mueller, Sophia, Moore, Robert D, Forgeot d’Arc, Baudouin, Jacquemont, Sebastien, Xiong, Lan
Published 2015

Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.

by Moreau, Clara A, Urchs, Sebastian GW, Kuldeep, Kumar, Orban, Pierre, Schramm, Catherine, Dumas, Guillaume, Labbe, Aurélie, Huguet, Guillaume, Douard, Elise, Quirion, Pierre-Olivier, Lin, Amy, Kushan, Leila, Grot, Stephanie, Luck, David, Mendrek, Adrianna, Potvin, Stephane, Stip, Emmanuel, Bourgeron, Thomas, Evans, Alan C, Bearden, Carrie E, Bellec, Pierre, Jacquemont, Sebastien
Published 2020

Protein synthesis levels are increased in a subset of individuals with fragile X syndrome.

by Jacquemont, Sébastien, Pacini, Laura, Jønch, Aia E, Cencelli, Giulia, Rozenberg, Izabela, He, Yunsheng, D'Andrea, Laura, Pedini, Giorgia, Eldeeb, Marwa, Willemsen, Rob, Gasparini, Fabrizio, Tassone, Flora, Hagerman, Randi, Gomez-Mancilla, Baltazar, Bagni, Claudia
Published 2018

Mavoglurant in Fragile X Syndrome: Results of two open-label, extension trials in adults and adolescents.

by Hagerman, Randi, Jacquemont, Sebastien, Berry-Kravis, Elizabeth, Des Portes, Vincent, Stanfield, Andrew, Koumaras, Barbara, Rosenkranz, Gerd, Murgia, Alessandra, Wolf, Christian, Apostol, George, von Raison, Florian
Published 2018

A framework for the investigation of rare genetic disorders in neuropsychiatry

by Sanders, Stephan J., Sahin, Mustafa, Hostyk, Joseph, Thurm, Audrey, Jacquemont, Sebastien, Avillach, Paul, Douard, Elise, Martin, Christa L., Modi, Meera E., Moreno-De-Luca, Andres, Raznahan, Armin, Anticevic, Alan, Dolmetsch, Ricardo, Feng, Guoping, Geschwind, Daniel H., Glahn, David C., Goldstein, David B., Ledbetter, David H., Mulle, Jennifer G., Pasca, Sergiu P., Samaco, Rodney, Sebat, Jonathan, Pariser, Anne, Lehner, Thomas, Gur, Raquel E., Bearden, Carrie E.
Published 2021

KCTD13 is a Major Driver of Mirrored Neuroanatomical Phenotypes Associated with the 16p11.2 CNV

by Golzio, Christelle, Willer, Jason, Oh, Edwin C, Taniguchi, Yu, Jacquemont, Sébastien, Reymond, Alexandre, Sun, Mei, Sawa, Akira, Kamiya, Atsushi, Beckmann, Jacques S, Katsanis, Nicholas, Talkowski, Michael Edward, Gusella, James Francis
Published 2013

Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome

by Berry-Kravis, Elizabeth M., Lindemann, Lothar, Jønch, Aia E., Apostol, George, Bear, Mark, Carpenter, Randall L, Crawley, Jacqueline N., Curie, Aurore, Des Portes, Vincent, Hossain, Farah, Gasparini, Fabrizio, Gomez-Mancilla, Baltazar, Hessl, David, Loth, Eva, Scharf, Sebastian H., Wang, Paul P., Von Raison, Florian, Hagerman, Randi, Spooren, Will, Jacquemont, Sébastien
Published 2020

A framework for the investigation of rare genetic disorders in neuropsychiatry

by Sanders, Stephan J., Sahin, Mustafa, Hostyk, Joseph, Thurm, Audrey, Jacquemont, Sebastien, Avillach, Paul, Douard, Elise, Martin, Christa L., Modi, Meera E., Moreno-De-Luca, Andres, Raznahan, Armin, Anticevic, Alan, Dolmetsch, Ricardo, Feng, Guoping, Geschwind, Daniel H., Glahn, David C., Goldstein, David B., Ledbetter, David H., Mulle, Jennifer G., Pasca, Sergiu P., Samaco, Rodney, Sebat, Jonathan, Pariser, Anne, Lehner, Thomas, Gur, Raquel E., Bearden, Carrie E.
Published 2022

Psychiatric disorders in children with 16p11.2 deletion and duplication.

by Niarchou, Maria, Chawner, Samuel JRA, Doherty, Joanne L, Maillard, Anne M, Jacquemont, Sébastien, Chung, Wendy K, Green-Snyder, LeeAnne, Bernier, Raphael A, Goin-Kochel, Robin P, Hanson, Ellen, Linden, David EJ, Linden, Stefanie C, Raymond, F Lucy, Skuse, David, Hall, Jeremy, Owen, Michael J, Bree, Marianne BM van den
Published 2019

Effects of eight neuropsychiatric copy number variants on human brain structure.

by Modenato, Claudia, Kumar, Kuldeep, Moreau, Clara, Martin-Brevet, Sandra, Huguet, Guillaume, Schramm, Catherine, Jean-Louis, Martineau, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Douard, Elise, Thébault-Dagher, Fanny, Côté, Valérie, Charlebois, Audrey-Rose, Deguire, Florence, Maillard, Anne M, Rodriguez-Herreros, Borja, Pain, Aurèlie, Richetin, Sonia, 16p11.2 European Consortium, Simons Searchlight Consortium, Melie-Garcia, Lester, Kushan, Leila, Silva, Ana I, van den Bree, Marianne BM, Linden, David EJ, Owen, Michael J, Hall, Jeremy, Lippé, Sarah, Chakravarty, Mallar, Bzdok, Danilo, Bearden, Carrie E, Draganski, Bogdan, Jacquemont, Sébastien
Published 2021

The psychiatric phenotypes of 1q21 distal deletion and duplication.

by Linden, Stefanie C, Watson, Cameron J, Smith, Jacqueline, Chawner, Samuel JRA, Lancaster, Thomas M, Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F Lucy, Hall, Jeremy, Owen, Michael J, Linden, David EJ, Green-Snyder, LeeAnne, Chung, Wendy K, Maillard, Anne M, Jacquemont, Sébastien, van den Bree, Marianne BM
Published 2021

The psychiatric phenotypes of 1q21 distal deletion and duplication

by Linden, Stefanie C., Watson, Cameron J., Smith, Jacqueline, Chawner, Samuel J. R. A., Lancaster, Thomas M., Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J., Linden, David E. J., Green-Snyder, LeeAnne, Chung, Wendy K., Maillard, Anne M., Jacquemont, Sébastien, van den Bree, Marianne B. M.
Published 2021

The psychiatric phenotypes of 1q21 distal deletion and duplication

by Linden, Stefanie C., Watson, Cameron J., Smith, Jacqueline, Chawner, Samuel J. R. A., Lancaster, Thomas M., Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J., Linden, David E. J., Green-Snyder, LeeAnne, Chung, Wendy K., Maillard, Anne M., Jacquemont, Sébastien, van den Bree, Marianne B. M.
Published 2021

A 600 kb Deletion Syndrome at 16p11.2 Leads to Energy Imbalance and Neuropsychiatric Disorders

by Zufferey, Flore, Sherr, Elliott H, Beckmann, Noam D, Hanson, Ellen M., Maillard, Anne M, Hippolyte, Loyse, Macé, Aurélien, Ferrari, Carina, Kutalik, Zoltán, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W Andrew, Goin-Kochel, Robin P, Grant, Ellen, Harewood, Louise, Hunter, Jill V, Lebon, Sébastien, Ledbetter, David H, Martin, Christa Lese, Männik, Katrin, Martinet, Danielle, Mukherjee, Pratik, Ramocki, Melissa B, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Spiro, John E, Reymond, Alexandre, Beckmann, Jacques S, Chung, Wendy K, Jacquemont, Sébastien
Published 2013

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

by Macé, Aurélien, Tuke, Marcus A., Deelen, Patrick, Kristiansson, Kati, Mattsson, Hannele, Nõukas, Margit, Sapkota, Yadav, Schick, Ursula, Porcu, Eleonora, Rüeger, Sina, McDaid, Aaron F., Porteous, David, Winkler, Thomas W., Salvi, Erika, Shrine, Nick, Liu, Xueping, Ang, Wei Q., Zhang, Weihua, Feitosa, Mary F., Venturini, Cristina, van der Most, Peter J., Rosengren, Anders, Wood, Andrew R., Beaumont, Robin N., Jones, Samuel E., Ruth, Katherine S., Yaghootkar, Hanieh, Tyrrell, Jessica, Havulinna, Aki S., Boers, Harmen, Mägi, Reedik, Kriebel, Jennifer, Müller-Nurasyid, Martina, Perola, Markus, Nieminen, Markku, Lokki, Marja-Liisa, Kähönen, Mika, Viikari, Jorma S., Geller, Frank, Lahti, Jari, Palotie, Aarno, Koponen, Päivikki, Lundqvist, Annamari, Rissanen, Harri, Bottinger, Erwin P., Afaq, Saima, Wojczynski, Mary K., Lenzini, Petra, Nolte, Ilja M., Sparsø, Thomas, Schupf, Nicole, Christensen, Kaare, Perls, Thomas T., Newman, Anne B., Werge, Thomas, Snieder, Harold, Spector, Timothy D., Chambers, John C., Koskinen, Seppo, Melbye, Mads, Raitakari, Olli T., Lehtimäki, Terho, Tobin, Martin D., Wain, Louise V., Sinisalo, Juha, Peters, Annette, Meitinger, Thomas, Martin, Nicholas G., Wray, Naomi R., Montgomery, Grant W., Medland, Sarah E., Swertz, Morris A., Vartiainen, Erkki, Borodulin, Katja, Männistö, Satu, Murray, Anna, Bochud, Murielle, Jacquemont, Sébastien, Rivadeneira, Fernando, Hansen, Thomas F., Oldehinkel, Albertine J., Mangino, Massimo, Province, Michael A., Deloukas, Panos, Kooner, Jaspal S., Freathy, Rachel M., Pennell, Craig, Feenstra, Bjarke, Strachan, David P., Lettre, Guillaume, Hirschhorn, Joel, Cusi, Daniele, Heid, Iris M., Hayward, Caroline, Männik, Katrin, Beckmann, Jacques S., Loos, Ruth J. F., Nyholt, Dale R., Metspalu, Andres, Eriksson, Johan G., Weedon, Michael N., Salomaa, Veikko, Franke, Lude, Reymond, Alexandre, Frayling, Timothy M., Kutalik, Zoltán
Published 2017