Effects of low birth weight, maternal smoking in pregnancy and social class on the phenotypic manifestation of Attention Deficit Hyperactivity Disorder and associated antisocial behaviour: investigation in a clinical sample

Autor: van den Bree Marianne BM, Holmans Peter A, Langley Kate, Thapar Anita

Publikováno v: BMC Psychiatry, Vol 7, Iss 1, p 26 (2007)

Abstract Background Attention Deficit Hyperactivity Disorder (ADHD) is a genetically influenced condition although indicators of environmental risk including maternal smoking during pregnancy, low birth weight and low social class have also been foun

Externí odkaz: https://doaj.org/article/5bc6907a69d440e8bf0f8b787dd3a4ef

Mental health impact of autism on families of children with intellectual and developmental disabilities of genetic origin

Autor: Wolstencroft, Jeanne, Srinivasan, Ramya, Hall, Jeremy, van den Bree, Marianne BM, Owen, Michael J, Raymond, F Lucy, Skuse, David

Background: Many children with an intellectual or developmental disability (IDD) have associated autism spectrum disorders (ASD), as well as an increased risk of mental health difficulties. In a cohort with IDD of genetic aetiology, we tested the hyp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______109::1850c9326db1e6cb788c79ffb75380f0
https://www.repository.cam.ac.uk/handle/1810/345338

Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs

Autor: Sønderby, Ida E, Ching, Christopher RK, Thomopoulos, Sophia I, van der Meer, Dennis, Sun, Daqiang, Villalon-Reina, Julio E, Agartz, Ingrid, Amunts, Katrin, Arango, Celso, Armstrong, Nicola J, Ayesa-Arriola, Rosa, Bakker, Geor, Bassett, Anne S, Boomsma, Dorret I, Bülow, Robin, Butcher, Nancy J, Calhoun, Vince D, Caspers, Svenja, Chow, Eva WC, Cichon, Sven, Ciufolini, Simone, Craig, Michael C, Crespo-Facorro, Benedicto, Cunningham, Adam C, Dale, Anders M, Dazzan, Paola, de Zubicaray, Greig I, Djurovic, Srdjan, Doherty, Joanne L, Donohoe, Gary, Draganski, Bogdan, Durdle, Courtney A, Ehrlich, Stefan, Emanuel, Beverly S, Espeseth, Thomas, Fisher, Simon E, Ge, Tian, Glahn, David C, Grabe, Hans J, Gur, Raquel E, Gutman, Boris A, Haavik, Jan, Håberg, Asta K, Hansen, Laura A, Hashimoto, Ryota, Hibar, Derrek P, Holmes, Avram J, Hottenga, Jouke-Jan, Hulshoff Pol, Hilleke E, Jalbrzikowski, Maria, Knowles, Emma EM, Kushan, Leila, Linden, David EJ, Liu, Jingyu, Lundervold, Astri J, Martin-Brevet, Sandra, Martínez, Kenia, Mather, Karen A, Mathias, Samuel R, McDonald-McGinn, Donna M, McRae, Allan F, Medland, Sarah E, Moberget, Torgeir, Modenato, Claudia, Monereo Sánchez, Jennifer, Moreau, Clara A, Mühleisen, Thomas W, Paus, Tomas, Pausova, Zdenka, Prieto, Carlos, Ragothaman, Anjanibhargavi, Reinbold, Céline S, Reis Marques, Tiago, Repetto, Gabriela M, Reymond, Alexandre, Roalf, David R, Rodriguez-Herreros, Borja, Rucker, James J, Sachdev, Perminder S, Schmitt, James E, Schofield, Peter R, Silva, Ana I, Stefansson, Hreinn, Stein, Dan J, Tamnes, Christian K, Tordesillas-Gutiérrez, Diana, Ulfarsson, Magnus O, Vajdi, Ariana, van 't Ent, Dennis, van den Bree, Marianne BM, Vassos, Evangelos, Vázquez-Bourgon, Javier, Vila-Rodriguez, Fidel, Walters, G Bragi, Wen, Wei, Westlye, Lars T, Wittfeld, Katharina, Zackai, Elaine H, Stefánsson, Kári, Jacquemont, Sebastien

Publikováno v: Human brain mapping, vol 43, iss 1

The Enhancing NeuroImaging Genetics through Meta-Analysis copy number variant (ENIGMA-CNV) and 22q11.2 Deletion Syndrome Working Groups (22q-ENIGMA WGs) were created to gain insight into the involvement of genetic factors in human brain development a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::e9750f56e8e864ef5b7a6a0e07ff55e2
https://escholarship.org/uc/item/8444m1dm

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome

Autor: Niarchou, Maria, Chawner, Samuel JRA, Fiksinski, Ania, Vorstman, Jacob AS, Maeder, Johanna, Schneider, Maude, Eliez, Stephan, Armando, Marco, Pontillo, Maria, Vicari, Stefano, McDonald-McGinn, Donna M, Emanuel, Beverly S, Zackai, Elaine H, Bearden, Carrie E, Shashi, Vandana, Hooper, Stephen R, Owen, Michael J, Gur, Raquel E, Wray, Naomi R, van den Bree, Marianne BM, Thapar, Anita, International 22q11.2 Deletion Syndrome Brain and Behavior Consortium

Individuals with 22q11.2 Deletion Syndrome (22q11.2DS) are at substantially heightened risk for psychosis. Thus, prevention and early intervention strategies that target the antecedents of psychosis in this high-risk group are a clinical priority. At

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::642d305c5011f77188b9daf43e91b6db
https://escholarship.org/uc/item/4s814375

Association of Multiple DRD2 Polymorphisms with Anorexia Nervosa.

Autor: Bergen, Andrew W., Yeager, Meredith, Welch, Robert A., Haque, Kashif, Ganjei, J Kelly, van den Bree, Marianne BM., Mazzanti, Chiara, Nardi, Irma, Fichter, Manfred M., Halmi, Katherine A., Kaplan, Allan S., Strober, Michael, Treasure, Janet, Woodside, D Blake, Bulik, Cynthia M., Bacanu, Silviusalin, Devlin, Bernie, Berrettini, Wade H., Goldman, David, Kaye, Walter H.

Publikováno v: Neuropsychopharmacology; Sep2005, Vol. 30 Issue 9, p1703-1710, 8p, 1 Diagram, 2 Charts, 1 Graph