Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Dorothy E Grice"'
Autor:
Uzoezi Ozomaro, Guiqing Cai, Yuji Kajiwara, Seungtai Yoon, Vladimir Makarov, Richard Delorme, Catalina Betancur, Stephan Ruhrmann, Peter Falkai, Hans Jörgen Grabe, Wolfgang Maier, Michael Wagner, Leonhard Lennertz, Rainald Moessner, Dennis L Murphy, Joseph D Buxbaum, Stephan Züchner, Dorothy E Grice
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e70376 (2013)
Obsessive compulsive disorder (OCD) is a syndrome characterized by recurrent and intrusive thoughts and ritualistic behaviors or mental acts that a person feels compelled to perform. Twin studies, family studies, and segregation analyses provide comp
Externí odkaz:
https://doaj.org/article/7ff8cf188909408695c34560642f67a7
Autor:
Abraham Reichenberg, Nancy L Pedersen, David Mataix-Cols, Matthew W Halvorsen, Bengt Fundín, Lambertus Klei, Cynthia M Bulik, Dorothy E. Grice, Kathryn Roeder, Christian Rück, B. Devlin, James J Crowley, Christina M. Hultman, Joseph D. Buxbaum, Mikael Landén, Sven Sandin, Elles de Schipper, Julia Boberg, Behrang Mahjani, Manuel Mattheisen
Publikováno v:
Mahjani, B, Klei, L, Mattheisen, M, Halvorsen, M W, Reichenberg, A, Roeder, K, Pedersen, N L, Boberg, J, de Schipper, E, Bulik, C M, Landén, M, Fundín, B, Mataix-Cols, D, Sandin, S, Hultman, C M, Crowley, J J, Buxbaum, J D, Rück, C, Devlin, B & Grice, D E 2022, ' The Genetic Architecture of Obsessive-Compulsive Disorder : Contribution of Liability to OCD From Alleles Across the Frequency Spectrum ', American Journal of Psychiatry, vol. 179, no. 3, pp. 216-225 . https://doi.org/10.1176/appi.ajp.2021.21010101
Am J Psychiatry
Am J Psychiatry
Objective: Obsessive-compulsive disorder (OCD) is known to be substantially heritable; however, the contribution of genetic variation across the allele frequency spectrum to this heritability remains uncertain. The authors used two new homogeneous co
Autor:
Tess Levy, Paige M. Siper, Bonnie Lerman, Danielle Halpern, Jessica Zweifach, Puneet Belani, Audrey Thurm, Tjitske Kleefstra, Elizabeth Berry-Kravis, Joseph D. Buxbaum, Dorothy E. Grice
Publikováno v:
Pediatric Neurology, 138, pp. 87-94
Pediatric Neurology, 138, 87-94
Pediatric Neurology, 138, 87-94
Contains fulltext : 290934.pdf (Publisher’s version ) (Open Access) DDX3X syndrome is a surprisingly common newly discovered genetic neurodevelopmental disorder associated with intellectual disability, autism spectrum disorder, language delays, att
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ea3d64696ae097baecc2a00453be1fc
https://doi.org/10.1016/j.pediatrneurol.2022.10.009
https://doi.org/10.1016/j.pediatrneurol.2022.10.009
Autor:
Behrang Mahjani, Christina Gustavsson Mahjani, Abraham Reichenberg, Sven Sandin, Christina M. Hultman, Joseph D. Buxbaum, Dorothy E. Grice
Publikováno v:
Social Psychiatry and Psychiatric Epidemiology. 57:2147-2155
Autor:
Dévina C. Ung, Mladen-Roko Rasin, Lily R. Qiu, Danielle Mendonca, Marta Garcia-Forn, Joseph D. Buxbaum, Jason P. Lerch, Sylvia Maxwell, Jacob Ellegood, Kristi Niblo, Elodie Drapeau, Silvia De Rubeis, Michael Flores, Andrea Boitnott, Dorothy E. Grice, Yeaji Park
Publikováno v:
Biol Psychiatry
Background Mutations in the X-linked gene DDX3X account for approximately 2% of intellectual disability in females, often comorbid with behavioral problems, motor deficits, and brain malformations. DDX3X encodes an RNA helicase with emerging function
Autor:
Frank Visscher, Kerstin J. Plessen, Tammy Hedderly, Jungeun Song, Bennett L. Leventhal, Eun-Young Shin, Lawrence W. Brown, Alexander Münchau, Robert A. King, Young Key Kim, Young Shin Kim, Veit Roessner, Andrea Dietrich, Samuel Kuperman, Thomas V. Fernandez, Keun-Ah Cheon, Carol A. Mathews, Athanasios Maras, Donald L. Gilbert, Yun-Joo Koh, Laura Ibanez-Gomez, Dongmei Yu, Astrid Morer, Sodahm Kook, Marcos Madruga-Garrido, Julie Hagstrøm, Dorothy E. Grice, Jay A. Tischfield, Lisa Osiecki, Mohamed Abdulkadir, Blanca Garcia-Delgar, Samuel H. Zinner, Chaim Huyser, Barbara J. Coffey, Dong-Ho Song, Gary A. Heiman, Pieter J. Hoekstra, Hyun Ju Hong, Pablo Mir, Isobel Heyman, Jeremiah M. Scharf
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996), vol 128, iss 11
Journal of Neural Transmission
Journal of Neural Transmission, 128, 1757-1765. SPRINGER WIEN
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of neural transmission (Vienna, Austria, 128(11), 1757-1765. Springer Verlag
Abdulkadir, M, Yu, D, Osiecki, L, King, R A, Fernandez, T V, Brown, L W, Cheon, K A, Coffey, B J, Garcia-Delgar, B, Gilbert, D L, Grice, D E, Hagstrøm, J, Hedderly, T, Heyman, I, Hong, H J, Huyser, C, Ibanez-Gomez, L, Kim, Y K, Kim, Y S, Koh, Y J, Kook, S, Kuperman, S, Leventhal, B, Madruga-Garrido, M, Maras, A, Mir, P, Morer, A, Münchau, A, Plessen, K J, Roessner, V, Shin, E Y, Song, D H, Song, J, Visscher, F, Zinner, S H, Mathews, C A, Scharf, J M, Tischfield, J A, Heiman, G A, Dietrich, A & Hoekstra, P J 2021, ' Investigation of gene–environment interactions in relation to tic severity ', Journal of Neural Transmission, vol. 128, no. 11, pp. 1757-1765 . https://doi.org/10.1007/s00702-021-02396-y
Journal of neural transmission, vol. 128, no. 11, pp. 1757-1765
Journal of Neural Transmission
Journal of Neural Transmission, 128, 1757-1765. SPRINGER WIEN
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of neural transmission (Vienna, Austria, 128(11), 1757-1765. Springer Verlag
Abdulkadir, M, Yu, D, Osiecki, L, King, R A, Fernandez, T V, Brown, L W, Cheon, K A, Coffey, B J, Garcia-Delgar, B, Gilbert, D L, Grice, D E, Hagstrøm, J, Hedderly, T, Heyman, I, Hong, H J, Huyser, C, Ibanez-Gomez, L, Kim, Y K, Kim, Y S, Koh, Y J, Kook, S, Kuperman, S, Leventhal, B, Madruga-Garrido, M, Maras, A, Mir, P, Morer, A, Münchau, A, Plessen, K J, Roessner, V, Shin, E Y, Song, D H, Song, J, Visscher, F, Zinner, S H, Mathews, C A, Scharf, J M, Tischfield, J A, Heiman, G A, Dietrich, A & Hoekstra, P J 2021, ' Investigation of gene–environment interactions in relation to tic severity ', Journal of Neural Transmission, vol. 128, no. 11, pp. 1757-1765 . https://doi.org/10.1007/s00702-021-02396-y
Journal of neural transmission, vol. 128, no. 11, pp. 1757-1765
Tourette syndrome (TS) is a neuropsychiatric disorder with involvement of genetic and environmental factors. We investigated genetic loci previously implicated in Tourette syndrome and associated disorders in interaction with pre- and perinatal adver
Autor:
Behrang Mahjani, Rebecca Birnbaum, Ariela Buxbaum Grice, Carolina Cappi, Seulgi Jung, Marina Natividad Avila, Abraham Reichenberg, Sven Sandin, Christina M. Hultman, Joseph D. Buxbaum, Dorothy E. Grice
Publikováno v:
Genes; Volume 13; Issue 10; Pages: 1796
Background: Recent studies report an important—and previously underestimated—role of rare variation in risk of obsessive-compulsive disorder (OCD) and chronic tic disorders (CTD). Using data from a large epidemiological study, we evaluate the dis
Autor:
Behrang Mahjani, Lambertus Klei, Ariela S Buxbaum Grice, Henrik Larsson, Christina M Hultman, Sven Sandin, Bernie Devlin, Joseph D Buxbaum, Dorothy E Grice
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. :jnnp-2022
BackgroundRisk for Tourette disorder, and chronic motor or vocal tic disorders (referenced here inclusively as CTD), arise from a combination of genetic and environmental factors. While multiple studies have demonstrated the importance of direct addi
Autor:
Anita Batuure, Christina Gustavsson Mahjani, Magdalena Janecka, Behrang Mahjani, Christina M. Hultman, Abraham Reichenberg, Joseph D. Buxbaum, Lotta Renström Koskela, Olof Akre, Dorothy E. Grice
Publikováno v:
European Child & Adolescent Psychiatry. 31:663-670
Lower urinary tract symptoms (LUTS), e.g., urinary frequency, pressure, urgency, and overactive bladder syndrome, are commonly reported in children with attention-deficit/hyperactivity disorder (ADHD). Understanding the co-occurrence of these conditi
Autor:
Danielle Posthuma, Bernie Devlin, Edna Grünblatt, Ying Wang, Daniele Cusi, Stephan Ruhrmann, Steven A. Rasmussen, Michael S. Breen, Julia Klawohn, Ana Gabriela Hounie, Aline S. Sampaio, Cristina Barlassina, Marta Ribasés, Jackson G. Thorp, Cynthia M. Bulik, Marco A. Grados, Dan J. Stein, Abby Fyer, Vladimir Coric, Martha J. Falkenstein, Stephanie Le Hellard, Behrang Mahjani, Nathaniel McGregor, Homero Vallada, Miguel Casas, Laurent F. Thomas, Janice Krasnow, Abraham Reichenberg, Donald W. Black, Gwyneth Zai, Norbert Kathmann, Manuel Mattheisen, Nicholas G. Martin, Jason W. Krompinger, Josep Antoni Ramos-Quiroga, Judith Becker Nissen, Helga Ask, Damiaan Denys, Carolina Cappi, Euripedes Constantino Miguel, O. Joseph Bienvenu, Bengt T. Fundin, Lisa Osiecki, Karin J. H. Verweij, Paul Sandor, Jeremy Veenstra-VanderWeele, Maureen Mulhern, Sarah E. Medland, David M. Hougaard, Lauren Erdman, Jan Haavik, James L. Kennedy, Christopher P. Walker, Jurjen J. Luykx, Tim B. Bigdeli, Ian M. Hickie, Nienke Vulink, Maurizio Turiel, Peter Falkai, Enda M. Byrne, Valentina Ciullo, Daniel A. Geller, Liang Kung-Yee, Miriam A. Schiele, Lambertus Klei, Götz Berberich, Thomas Werge, Brion S. Maher, Christie L. Burton, Julia M. Sealock, Sandra Meier, Bernadette Cullen, Stephan Ripke, Dorothy E. Grice, Richard Delorme, Ted Reichborn-Kjennerud, Dongmei Yu, Danielle C. Cath, Lili Milani, Abdel Abdellaoui, Andres Metspalu, María Soler Artigas, Maria Conceição do Rosário, Ole Mors, Brian P. Brennan, Barbara E. Stranger, Ann E. Pulver, Nora I. Strom, Joseph D. Buxbaum, Hans J. Grabe, Jens R. Wendland, Michael H. Bloch, Srdjan Djurovic, Raquel Rabionet, Angel Carracedo, Carlos N. Pato, Erika L. Nurmi, Janet L. Sobell, Kevin S. O’Connell, Michael Wagner, David R. Rosenberg, Jonathan R. I. Coleman, Jeremiah M. Scharf, Kerry J. Ressler, Jaakko Kaprio, Edwin H. Cook, Scott L. Rauch, Federica Piras, Merete Nordentoft, Christian Rück, Fabrizio Piras, John-Anker Zwart, Jason A. Elias, Christopher Pittenger, Lea K. Davis, Margaret A. Richter, Evonne McArthur, Bendik S. Winsvold, Yin Yao, James J. Crowley, David L. Pauls, Rosa Bosch, Xavier Estivil, Matthew Halvorsen, Adrian Camarena, Nancy L. Pedersen, Pino Alonso, Eric A. Storch, Bjarne Hansen, Helena Brentani, James T. McCracken, Jan Maerten Smit, Donald Hucks, Alexandra Havdahl, Gerome Breen, Christina M. Hultman, Benjamin M. Neale, Gregory L. Hanna, Mikael Landén, Christine Lochner, Dirk J.A. Smit, Fabio Macciardi, Carol A. Mathews, Nuria Lanzagorta, Laura G. Sloofman, Cristina Rodriguez-Fontenla, Michael A. Jenike, Michele T. Pato, Marion Leboyer, Humberto Nicolini, Anders D. Børglum, Maria Cristina Cavallini, Wei Guo, Benjamin D. Greenberg, Maiken Elvestad Gabrielsen, Magdalena Janecka, Mark A. Riddle, Paul S. Nestadt, Beatriz Camarena, Valsamma Eapen, Susanne Walitza, Jack Samuels, Fernando S. Goes, Nicole C.R. McLaughlin, S. Evelyn Stewart, Jennifer Reichert, Sven Sandin, Gerd Kvale, Katharina Domschke, Ole A. Andreassen, Elles de Schipper, Paul D. Arnold, Kristi Krebs, Zachary Gerring, Teemu Palviainen, Kathleen D. Askland, Alfredo Ramirez, James A. Knowles, Laura Bellodi, Kristen Hagen, Julia Boberg, Thomas V. Fernandez, Gerald Nestadt, John Piacentini, Jakob Grove, Eske M. Derks, Preben Bo Mortensen, Elinor K. Karlsson, Gianfranco Spalletta, David Mataix-Cols, Katharina Bey, Jonas Bybjerg-Grauholm
Obsessive-compulsive disorder (OCD) is a heritable disorder, but no definitive, replicated OCD susceptibility loci have yet been identified by any genome-wide association study (GWAS). Here, we report results from a GWAS in the largest OCD case-contr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c8180dd21a6e65014d2b62d43825d7f
https://doi.org/10.1101/2021.10.13.21261078
https://doi.org/10.1101/2021.10.13.21261078