Mahdi, Soheil
Albertowski, Katja
Almodayfer, Omar
Arsenopoulou, Vaia
Carucci, Sara
Dias, José Carlos
Khalil, Mohammad
Knüppel, Ane
Langmann, Anika
Lauritsen, Marlene Briciet
da Cunha, Graccielle Rodrigues
Uchiyama, Tokio
Wolff, Nicole
Selb, Melissa
Granlund, Mats
de Vries, Petrus J.
Zwaigenbaum, Lonnie
Bölte, Sven
Funding for this research was provided by:
Swedish Research Council
Forskningsrådet för hälsa, arbetsliv och välfärd
Svenska Forskningsrådet Formas
VINNOVA (259-2012-24)
Article History
First Online: 8 February 2018
Compliance with Ethical Standards
:
: Soheil Mahdi, Katja Albertowski, Omar Almodayfer, Vaia Arsenopoulou, Sara Carucci, José Carlos Dias, Mohammad Khalil, Ane Knüppel, Anika Langmann, Marlene B. Lauritsen, Graccielle R. Cunha, Tokio Uchiyama, Nicole Wolff, Melissa Selb, Mats Granlund, Petrus J. de Vries, Lonnie Zwaigenbaum, and Sven Bölte declare no conflict of interest related to this work. Sara Carucci discloses that she in the last three years have collaborated within projects from the European Union (7th Framework Program), has received travel support from Shire Pharmaceutical Company; she collaborated as Sub-investigator in sponsored clinical trials by Shire Pharmaceutical Company and Lundbeck. Petrus J. de Vries discloses that he has received grants and funds from Novartis, as part of clinical trials of Mtor inhibitors for Tuberous Sclerosis Complex. Sven Bölte discloses that he has in the last 5 years acted as an Author, Consultant or Lecturer for Shire, Medice, Roche, Eli Lilly, Prima Psychiatry, GLGroup, System Analytic, Kompetento, Expo Medica, and Prophase. He receives royalties for text books and diagnostic tools from Huber/Hogrefe, Kohlhammer and UTB.
: All procedures performed in this study with the human participants were in accordance with the Ethical Standards of the Institutional and/or National Research Committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Ethical permission for this study was obtained from the Regional Ethical Review Board in Stockholm, Sweden, and by the Local Ethics Review Boards at each of the other participating sites.
: Informed consent (in written form) was obtained from each participant prior to study participation.