Zobrazeno 1 - 10
of 385
pro vyhledávání: '"Donna M. McDonald"'
Autor:
Tae-Yeon Eom, J. Eric Schmitt, Yiran Li, Christopher M. Davenport, Jeffrey Steinberg, Audrey Bonnan, Shahinur Alam, Young Sang Ryu, Leena Paul, Baranda S. Hansen, Khaled Khairy, Stephane Pelletier, Shondra M. Pruett-Miller, David R. Roalf, Raquel E. Gur, Beverly S. Emanuel, Donna M. McDonald-McGinn, Jesse N. Smith, Cai Li, Jason M. Christie, Paul A. Northcott, Stanislav S. Zakharenko
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-21 (2024)
Abstract Neurodevelopmental disorders are thought to arise from intrinsic brain abnormalities. Alternatively, they may arise from disrupted crosstalk among tissues. Here we show the local reduction of two vestibulo-cerebellar lobules, the parafloccul
Externí odkaz:
https://doaj.org/article/17fb65dc25454794b98e473b3b8f562c
Autor:
Alexandra Finless, Andrea L. Rideout, Ting Xiong, Holly Carbyn, Patricia Lingley-Pottie, Lisa D. Palmer, Andrea Shugar, Donna M. McDonald-McGinn, Patrick J. McGrath, Anne S. Bassett, Cheryl Cytrynbaum, Matt Orr, Ann Swillen, Sandra Meier
Publikováno v:
European Journal of Psychotraumatology, Vol 15, Iss 1 (2024)
Background: 22q11 Deletion Syndrome (22q11DS) is the most common microdeletion syndrome with broad phenotypic variability, leading to significant morbidity and some mortality. The varied health problems associated with 22q11DS and the evolving phenot
Externí odkaz:
https://doaj.org/article/f793a2611d8746a2a5b64438cfcfdccd
Autor:
T. Blaine Crowley, Ian Campbell, Abinaya Arulselvan, David Friedman, Elaine H. Zackai, Tracy R. Geoffrion, Char Witmer, J. William Gaynor, Donna M. McDonald-McGinn, Michele P. Lambert
Publikováno v:
Platelets, Vol 35, Iss 1 (2024)
Previous research suggests that individuals with 22q11.2 deletion syndrome (DS) have an increased risk of bleeding following cardiac surgery. However, current guidelines for management of patients with 22q11.2DS do not provide specific recommendation
Externí odkaz:
https://doaj.org/article/ad61591e3c2d4b56a2097ce4d2f856b1
Autor:
David R. Roalf, Donna M. McDonald-McGinn, Joelle Jee, Mckenna Krall, T. Blaine Crowley, Paul J. Moberg, Christian Kohler, Monica E. Calkins, Andrew J.D. Crow, Nicole Fleischer, R. Sean Gallagher, Virgilio Gonzenbach, Kelly Clark, Ruben C. Gur, Emily McClellan, Daniel E. McGinn, Arianna Mordy, Kosha Ruparel, Bruce I. Turetsky, Russell T. Shinohara, Lauren White, Elaine Zackai, Raquel E. Gur
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-12 (2024)
Abstract Background Minor physical anomalies (MPAs) are congenital morphological abnormalities linked to disruptions of fetal development. MPAs are common in 22q11.2 deletion syndrome (22q11DS) and psychosis spectrum disorders (PS) and likely represe
Externí odkaz:
https://doaj.org/article/dc8c12b789804ab18fb63538360a9af8
Autor:
Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M. McDonald-McGinn, T. Blaine Crowley, Daniel E. McGinn, Oanh T. Tran, Daniella Miller, Jhih-Rong Lin, Elaine Zackai, H. Richard Johnston, Eva W. C. Chow, Jacob A. S. Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris R. Vermeesch, Stephan Eliez, Maude Schneider, Marianne B. M. van den Bree, Michael J. Owen, Wendy R. Kates, Gabriela M. Repetto, Vandana Shashi, Kelly Schoch, Carrie E. Bearden, M. Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C. Murphy, Declan Murphy, Sixto García-Miñaúr, Luis Fernández, International 22q11.2 Brain and Behavior Consortium (IBBC), Zhengdong D. Zhang, Elizabeth Goldmuntz, Raquel E. Gur, Beverly S. Emanuel, Deyou Zheng, Christian R. Marshall, Anne S. Bassett, Tao Wang, Bernice E. Morrow
Publikováno v:
npj Genomic Medicine, Vol 8, Iss 1, Pp 1-15 (2023)
Abstract Congenital heart disease (CHD) affecting the conotruncal region of the heart, occurs in 40–50% of patients with 22q11.2 deletion syndrome (22q11.2DS). This syndrome is a rare disorder with relative genetic homogeneity that can facilitate i
Externí odkaz:
https://doaj.org/article/8c4a618d8f784a9c9f58db40b2e0cf57
Autor:
Tyler M. Moore, Deby Salzer, Carrie E. Bearden, Monica E. Calkins, Wendy R. Kates, Leila Kushan, Robert Sean Gallagher, Dafna Sofrin Frumer, Ronnie Weinberger, Donna M. McDonald-McGinn, Raquel E. Gur, Doron Gothelf
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-8 (2021)
Abstract Background Pathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been the focus of intensive research during the last two decades. One of the common clinical risk factors for the evolution of psychosis in 22q11.2DS is t
Externí odkaz:
https://doaj.org/article/91d96000cb084140a83be350981f884c
Autor:
Caitlin C. Clements, Tara L. Wenger, Alisa R. Zoltowski, Jennifer R. Bertollo, Judith S. Miller, Ashley B. de Marchena, Lauren M. Mitteer, John C. Carey, Benjamin E. Yerys, Elaine H. Zackai, Beverly S. Emanuel, Donna M. McDonald-McGinn, Robert T. Schultz
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Abstract Background Previous studies have reported no clear critical region for medical comorbidities in children with deletions or duplications of 22q11.2. The purpose of this study was to evaluate whether individuals with small nested deletions or
Externí odkaz:
https://doaj.org/article/e0920fdf03b84cc287869873723def41
Autor:
J. Eric Schmitt, MD PhD, James Yi, MD PhD, Monica E. Calkins, PhD, Kosha Ruparel, MS, David R. Roalf, PhD, Amy Cassidy, MS, Margaret C. Souders, PhD CRNP, Theodore D. Satterthwaite, MD MA, Donna M. McDonald-McGinn, MS CGC, Elaine H. Zackai, MD, Ruben C. Gur, PhD, Beverly S. Emanuel, PhD, Raquel E. Gur, MD PhD
Publikováno v:
NeuroImage: Clinical, Vol 12, Iss C, Pp 420-428 (2016)
The 22q11.2 deletion syndrome (22q11DS) is an uncommon genetic disorder with an increased risk of psychosis. Although the neural substrates of psychosis and schizophrenia are not well understood, aberrations in cortical networks represent intriguing
Externí odkaz:
https://doaj.org/article/c573a0d10cbf4a1aa7c7b09cd61f674b
Akademický článek
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Autor:
Raquel E. Gur, Donna M. McDonald-McGinn, Tyler M. Moore, R. Sean Gallagher, Emily McClellan, Lauren White, Kosha Ruparel, Noah Hillman, T. Blaine Crowley, Daniel E. McGinn, Elaine Zackai, Beverly S. Emanuel, Monica E. Calkins, David R. Roalf, Ruben C. Gur
Publikováno v:
Psychological Medicine. :1-10
Background Neuropsychiatric disorders are common in 22q11.2 Deletion Syndrome (22q11DS) with about 25% of affected individuals developing schizophrenia spectrum disorders by young adulthood. Longitudinal evaluation of psychosis spectrum features and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f64b8c7827e3e02c383d451549e953d
https://doi.org/10.1017/s0033291723000259
https://doi.org/10.1017/s0033291723000259