Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia
Lee, Yohan, Mattai, Anand, Long, Robert, Rapoport, Judith L, Gogtay, Nitin, Addington, Anjené M
Published in Psychiatric genetics (01.08.2012)
Published in Psychiatric genetics (01.08.2012)
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Support for association between ADHD and two candidate genes: NET1 and DRD1
Bobb, Aaron J., Addington, Anjene M., Sidransky, Ellen, Gornick, Michele C., Lerch, Jason P., Greenstein, Deanna K., Clasen, Liv S., Sharp, Wendy S., Inoff-Germain, Gale, Wavrant-De Vrièze, Fabienne, Arcos-Burgos, Mauricio, Straub, Richard E., Hardy, John A., Castellanos, F. Xavier, Rapoport, Judith L.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.04.2005)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.04.2005)
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Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
Walsh, Tom, McClellan, Jon M., McCarthy, Shane E., Addington, Anjené M., Pierce, Sarah B., Cooper, Greg M., Nord, Alex S., Kusenda, Mary, Malhotra, Dheeraj, Bhandari, Abhishek, Stray, Sunday M., Rippey, Caitlin F., Roccanova, Patricia, Makarov, Vlad, Lakshmi, B., Findling, Robert L., Sikich, Linmarie, Stromberg, Thomas, Merriman, Barry, Gogtay, Nitin, Butler, Philip, Eckstrand, Kristen, Noory, Laila, Gochman, Peter, Long, Robert, Chen, Zugen, Davis, Sean, Baker, Carl, Eichler, Evan E., Meltzer, Paul S., Nelson, Stanley F., Singleton, Andrew B., Lee, Ming K., Rapoport, Judith L., King, Mary-Claire, Sebat, Jonathan
Published in Science (American Association for the Advancement of Science) (25.04.2008)
Published in Science (American Association for the Advancement of Science) (25.04.2008)
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Whole genome sequencing in psychiatric disorders: the WGSPD consortium
Sanders, Stephan J., Neale, Benjamin M., Huang, Hailiang, Werling, Donna M., An, Joon-Yong, Dong, Shan, Abecasis, Goncalo, Arguello, P. Alexander, Blangero, John, Boehnke, Michael, Daly, Mark J., Eggan, Kevin, Geschwind, Daniel H., Glahn, David C., Goldstein, David B., Gur, Raquel E., Handsaker, Robert E., McCarroll, Steven A., Ophoff, Roel A., Palotie, Aarno, Pato, Carlos N., Sabatti, Chiara, State, Matthew W., Willsey, A. Jeremy, Hyman, Steven E., Addington, Anjene M., Lehner, Thomas, Freimer, Nelson B.
Published in Nature neuroscience (01.12.2017)
Published in Nature neuroscience (01.12.2017)
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Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental Retardation
Hamdan, Fadi F, Gauthier, Julie, Spiegelman, Dan, Noreau, Anne, Yang, Yan, Pellerin, Stéphanie, Dobrzeniecka, Sylvia, Côté, Mélanie, Perreau-Linck, Elizabeth, Carmant, Lionel, D'Anjou, Guy, Fombonne, Éric, Addington, Anjene M, Rapoport, Judith L, Delisi, Lynn E, Krebs, Marie-Odile, Mouaffak, Faycal, Joober, Ridha, Mottron, Laurent, Drapeau, Pierre, Marineau, Claude, Lafrenière, Ronald G, Lacaille, Jean Claude, Rouleau, Guy A, Michaud, Jacques L
Published in The New England journal of medicine (05.02.2009)
Published in The New England journal of medicine (05.02.2009)
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De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
Gauthier, Julie, Champagne, Nathalie, Lafrenière, Ronald G., Xiong, Lan, Spiegelman, Dan, Brustein, Edna, Lapointe, Mathieu, Peng, Huashan, Côté, Mélanie, Noreau, Anne, Hamdan, Fadi F., Addington, Anjené M., Rapoport, Judith L., DeLisi, Lynn E., Krebs, Marie-Odile, Joober, Ridha, Fathalli, Ferid, Mouaffak, Fayçal, Haghighi, Ali P., Néri, Christian, Dubé, Marie-Pierre, Samuels, Mark E., Marineau, Claude, Stone, Eric A., Awadalla, Philip, Barker, Philip A., Carbonetto, Salvatore, Drapeau, Pierre, Rouleau, Guy A., the S2D Team, Housman, David E.
Published in Proceedings of the National Academy of Sciences - PNAS (27.04.2010)
Published in Proceedings of the National Academy of Sciences - PNAS (27.04.2010)
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Nordic OCD & Related Disorders Consortium: Rationale, design, and methods
Mataix‐Cols, David, Hansen, Bjarne, Mattheisen, Manuel, Karlsson, Elinor K., Addington, Anjené M., Boberg, Julia, Djurfeldt, Diana R., Halvorsen, Matthew, Lichtenstein, Paul, Solem, Stian, Lindblad‐Toh, Kerstin, Haavik, Jan, Kvale, Gerd, Rück, Christian, Crowley, James J.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2020)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2020)
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Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium
Sanders, Stephan J., Neale, Benjamin M., Huang, Hailiang, Werling, Donna M., An, Joon-Yong, Dong, Shan, Abecasis, Goncalo, Arguello, P. Alexander, Blangero, John, Boehnke, Michael, Daly, Mark J., Eggan, Kevin, Geschwind, Daniel H., Glahn, David C., Goldstein, David B., Gur, Raquel E., Handsaker, Robert E., McCarroll, Steven A., Ophoff, Roel A., Palotie, Aarno, Pato, Carlos N., Sabatti, Chiara, State, Matthew W., Willsey, A. Jeremy, Hyman, Steven E., Addington, Anjene M., Lehner, Thomas, Freimer, Nelson B.
Published in Nature neuroscience (01.07.2018)
Published in Nature neuroscience (01.07.2018)
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Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?
Sporn, Alexandra L, Addington, Anjené M, Gogtay, Nitin, Ordoñez, Anna E, Gornick, Michele, Clasen, Liv, Greenstein, Deanna, Tossell, Julia W, Gochman, Peter, Lenane, Marge, Sharp, Wendy S, Straub, Richard E, Rapoport, Judith L
Published in Biological psychiatry (1969) (15.05.2004)
Published in Biological psychiatry (1969) (15.05.2004)
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The Open Translational Science in Schizophrenia (OPTICS) project: an open-science project bringing together Janssen clinical trial and NIMH data
Wilcox, Marsha A., Savitz, Adam J., Addington, Anjené M., Gray, Gary S., Guinan, Eva C., Jackson, John W., Lehner, Thomas, Normand, Sharon-Lise, Ranu, Hardeep, Senthil, Geetha, Spertus, Jake, Valeri, Linda, Ross, Joseph S.
Published in NPJ schizophrenia (27.06.2018)
Published in NPJ schizophrenia (27.06.2018)
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Sequencing and Analyzing the t(1;7) Reciprocal Translocation Breakpoints Associated with a Case of Childhood-onset Schizophrenia/Autistic Disorder
Idol, Jacquelyn R., Addington, Anjene M., Long, Robert T., Rapoport, Judith L., Green, Eric D.
Published in Journal of autism and developmental disorders (01.04.2008)
Published in Journal of autism and developmental disorders (01.04.2008)
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Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts
Awadalla, Philip, Gauthier, Julie, Myers, Rachel A., Casals, Ferran, Hamdan, Fadi F., Griffing, Alexander R., Côté, Mélanie, Henrion, Edouard, Spiegelman, Dan, Tarabeux, Julien, Piton, Amélie, Yang, Yan, Boyko, Adam, Bustamante, Carlos, Xiong, Lan, Rapoport, Judith L., Addington, Anjené M., DeLisi, J. Lynn E., Krebs, Marie-Odile, Joober, Ridha, Millet, Bruno, Fombonne, Éric, Mottron, Laurent, Zilversmit, Martine, Keebler, Jon, Daoud, Hussein, Marineau, Claude, Roy-Gagnon, Marie-Hélène, Dubé, Marie-Pierre, Eyre-Walker, Adam, Drapeau, Pierre, Stone, Eric A., Lafrenière, Ronald G., Rouleau, Guy A.
Published in American journal of human genetics (10.09.2010)
Published in American journal of human genetics (10.09.2010)
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Microduplications of 16p11.2 are associated with schizophrenia
Walsh, Tom, Gary, Sydney, Sutcliffe, James S, Addington, Anjene M, Chitkara, Nisha, Levy, Deborah L, Cichon, Sven, DeRosse, Pamela, Malhotra, Anil K, Leibenluft, Ellen, Dickel, Diane E, Lee, Yoon-ha, Zackai, Elaine H, Stroup, T Scott, McCarthy, Shane E, Crow, Timothy J, McMahon, Francis J, Lakshmi, B, Christian, Susan L, Malhotra, Dheeraj, McClellan, Jon, Goodell, Meredith, Spinner, Nancy B, Pearl, Justin, Wolff, Jessica, Bhandari, Abhishek, Iakoucheva, Lilia M, Deutsch, Curtis K, Pavon, Kevin, Nöthen, Markus M, Gallagher, Louise, Roccanova, Patricia, Lieberman, Jeffrey A, DeLisi, Lynn E, Puura, Kaija, Skuse, David, Rapoport, Judith, Willour, Virginia L, Kirov, George, Vacic, Vladimir, Makarov, Vladimir, Haldeman-Englert, Chad, Sullivan, Patrick F, Schulze, Thomas G, Craddock, Nick, Kendall, Jude, Perkins, Diana O, Kusenda, Mary, Lehtimäki, Terho, Kassem, Layla, Yoon, Seungtai, Krastoshevsky, Olga, Sebat, Jonathan, Owen, Michael J, Ganesh, Jaya, Gill, Michael, King, Mary-Claire, Steele, Jo, Krause, Verena, Susser, Ezra, Mendell, Nancy R, Leotta, Anthony, Shaikh, Tamim H, Kaplan, Paige, Potash, James B, Krantz, Ian D, Grozeva, Detelina, Lajonchere, Clara M, O'Donovan, Michael C, Kustanovich, Vlad, Rietschel, Marcella, Kumar, Ravinesh A
Published in Nature genetics (01.11.2009)
Published in Nature genetics (01.11.2009)
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A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband
Wilson, Nicole K. A., Lee, Yohan, Long, Robert, Hermetz, Karen, Rudd, M. Katharine, Miller, Rachel, Rapoport, Judith L., Addington, Anjené M.
Published in Case reports in genetics (01.01.2011)
Published in Case reports in genetics (01.01.2011)
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Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified
Addington, Anjené M, Gornick, Michele, Sporn, Alexandra L, Gogtay, Nitin, Greenstein, Deanna, Lenane, Marge, Gochman, Peter, Baker, Natalie, Balkissoon, Rishi, Vakkalanka, Radha Krishna, Weinberger, Daniel R, Straub, Richard E, Rapoport, Judith L
Published in Biological psychiatry (1969) (15.05.2004)
Published in Biological psychiatry (1969) (15.05.2004)
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