Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms

por Guna, Alina, Butcher, Nancy J., Bassett, Anne S.
Publicado en J Neurodev Disord (2015)

Outcome reporting recommendations for clinical trial protocols and reports: a scoping review

por Butcher, Nancy J., Mew, Emma J., Monsour, Andrea, Chan, An-Wen, Moher, David, Offringa, Martin
Publicado en Trials (2020)

Response to “Trials for depressive disorder in adolescents: the emperor's new clothes,” a letter to the editor by Alain Braillon, MD, PhD

por Butcher, Nancy J., Mew, Emma J., Monsour, Andrea, Szatmari, Peter, Monga, Suneeta, Offringa, Martin
Publicado en J Clin Epidemiol (2020)

Functional outcomes of adults with 22q11.2 deletion syndrome

por Butcher, Nancy J., Chow, Eva W.C., Costain, Gregory, Karas, Dominique, Ho, Andrew, Bassett, Anne S.
Publicado 2012

Outcomes reported in randomised clinical trials of major depressive disorder treatments in adolescents: a systematic scoping review protocol

por Monsour, Andrea, Mew, Emma J, Szatmari, Peter, Patel, Sagar, Saeed, Leena, Offringa, Martin, Butcher, Nancy J
Publicado en BMJ Open (2019)

MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome

por Merico, Daniele, Costain, Gregory, Butcher, Nancy J., Warnica, William, Ogura, Lucas, Alfred, Simon E., Brzustowicz, Linda M., Bassett, Anne S.
Publicado en Front Neurol (2014)

Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series

por Butcher, Nancy J., Boot, Erik, Lang, Anthony E., Andrade, Danielle, Vorstman, Jacob, McDonald-McGinn, Donna, Bassett, Anne S.
Publicado en Am J Med Genet A (2018)

Association Between Early-Onset Parkinson Disease and 22q11.2 Deletion Syndrome: Identification of a Novel Genetic Form of Parkinson Disease and Its Clinical Implications

por Butcher, Nancy J., Kiehl, Tim-Rasmus, Hazrati, Lili-Naz, Chow, Eva W. C., Rogaeva, Ekaterina, Lang, Anthony E., Bassett, Anne S.
Publicado en JAMA Neurol (2013)

Guidance for reporting outcomes in clinical trials: scoping review protocol

por Butcher, Nancy J, Mew, Emma J, Saeed, Leena, Monsour, Andrea, Chee-a-tow, Alyssandra, Chan, An-Wen, Moher, David, Offringa, Martin
Publicado en BMJ Open (2019)

Learning best-practices in journalology: course description and attendee insights into the inaugural EQUATOR Canada Publication School

por Galica, Jacqueline, Chee-a-tow, Alyssandra, Gupta, Shikha, Jaiswal, Atul, Monsour, Andrea, Tricco, Andrea C., Cobey, Kelly D., Butcher, Nancy J.
Publicado en BMC Proc (2018)

Response to clozapine in a clinically identifiable subtype of schizophrenia

por Butcher, Nancy J., Fung, Wai Lun Alan, Fitzpatrick, Laura, Guna, Alina, Andrade, Danielle M., Lang, Anthony E., Chow, Eva W. C., Bassett, Anne S.
Publicado en Br J Psychiatry (2015)

Neurobiological perspective of 22q11.2 deletion syndrome

por Zinkstok, Janneke R, Boot, Erik, Bassett, Anne S, Hiroi, Noboru, Butcher, Nancy J, Vingerhoets, Claudia, Vorstman, Jacob A S, van Amelsvoort, Therese A M J
Publicado en Lancet Psychiatry (2019)

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease

por Butcher, Nancy J., Merico, Daniele, Zarrei, Mehdi, Ogura, Lucas, Marshall, Christian R., Chow, Eva W. C., Lang, Anthony E., Scherer, Stephen W., Bassett, Anne S.
Publicado en PLoS One (2017)

Movement Disorders and Other Motor Abnormalities in Adults With 22q11.2 Deletion Syndrome

por Boot, Erik, Butcher, Nancy J, van Amelsvoort, Thérèse AMJ, Lang, Anthony E, Marras, Connie, Pondal, Margarita, Andrade, Danielle M, Fung, Wai Lun Alan, Bassett, Anne S
Publicado en Am J Med Genet A (2015)

Establishing a core outcome set for treatment of uncomplicated appendicitis in children: study protocol for an international Delphi survey

por Knaapen, Max, Hall, Nigel J, van der Lee, Johanna H, Butcher, Nancy J, Offringa, Martin, Van Heurn, Ernst W E, Bakx, Roel, Gorter, Ramon R
Publicado en BMJ Open (2019)

Considerations for adaptive design in pediatric clinical trials: study protocol for a systematic review, mixed-methods study, and integrated knowledge translation plan

por Kelly, Lauren E, Dyson, Michele P, Butcher, Nancy J, Balshaw, Robert, London, Alex John, Neilson, Christine J, Junker, Anne, Mahmud, Salaheddin M, Driedger, S Michelle, Wang, Xikui
Publicado en Trials (2018)

Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome

por Palmer, Lisa, Butcher, Nancy J., Boot, Erik, Hodgkinson, Kathleen A., Heung, Tracy, Chow, Eva WC, Guna, Alina, Crowley, T. Blaine, Zackai, Elaine, McDonald-McGinn, Donna M., Bassett, Anne S.
Publicado en Am J Med Genet A (2018)

Primary outcome reporting in adolescent depression clinical trials needs standardization

por Monsour, Andrea, Mew, Emma J., Patel, Sagar, Chee-a-tow, Alyssandra, Saeed, Leena, Santos, Lucia, Courtney, Darren B., Watson, Priya N., Monga, Suneeta, Szatmari, Peter, Offringa, Martin, Butcher, Nancy J.
Publicado en BMC Med Res Methodol (2020)

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome

por Merico, Daniele, Zarrei, Mehdi, Costain, Gregory, Ogura, Lucas, Alipanahi, Babak, Gazzellone, Matthew J., Butcher, Nancy J., Thiruvahindrapuram, Bhooma, Nalpathamkalam, Thomas, Chow, Eva W. C., Andrade, Danielle M., Frey, Brendan J., Marshall, Christian R., Scherer, Stephen W., Bassett, Anne S.
Publicado en G3 (Bethesda) (2015)

Improving outcome reporting in clinical trial reports and protocols: study protocol for the Instrument for reporting Planned Endpoints in Clinical Trials (InsPECT)

por Butcher, Nancy J., Monsour, Andrea, Mew, Emma J., Szatmari, Peter, Pierro, Agostino, Kelly, Lauren E., Farid-Kapadia, Mufiza, Chee-a-tow, Alyssandra, Saeed, Leena, Monga, Suneeta, Ungar, Wendy, Terwee, Caroline B., Vohra, Sunita, Fergusson, Dean, Askie, Lisa M., Williamson, Paula R., Chan, An-Wen, Moher, David, Offringa, Martin
Publicado en Trials (2019)