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838 results on '"Delgado, Mauricio R"'

1. The natural history of variable subtypes in pediatric-onset TUBB4A-related leukodystrophy

Author

Gavazzi, Francesco, Charsar, Brittany, Hamilton, Eline, Erler, Jacqueline A., Patel, Virali, Woidill, Sarah, Sevagamoorthy, Anjana, Helman, Guy, Schmidt, Johanna, Pizzino, Amy, Muirhead, Kayla, Takanohashi, Asako, Bonkowsky, Joshua L., Meyerhoffer, Kelsee, Simons, Cas, Doi, Hiroshi, Satoko, Miyatake, Matsumoto, Naomichi, Delgado, Mauricio R., Sanchez-Castillo, Meredith, Wang, Jingming, de Carvalho, Daniel Rocha, Tournev, Ivailo, Chamova, Teodora, Jordanova, Albena, Clegg, Nancy J., Nicita, Francesco, Bertini, Enrico, Teng, Michelle, Williams, Dan, Tonduti, Davide, Houlden, Henry, Stellingwerff, Menno, Wassmer, Evangeline, Garcia-Cazorla, Angeles, Bernard, Geneviève, Mirchi, Amytice, Toutounchi, Helia, Wolf, Nicole I., van der Knaap, Marjo S., Shults, Justine, Adang, Laura A., and Vanderver, Adeline L.

Published
2025
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3. Therapy Together: A Caregiver Led Constraint Induced Movement Therapy Program for Preschool Aged Children Utilizing a Virtual Environment Due to COVID-19

Author

Shierk, Angela, Roberts, Heather, Dubberly, Katherine, Clegg, Nancy J., Fagan, Marcus, Baldwin, Deborah, Reyes, Fabiola, VanPelt, Jonathan, and Delgado, Mauricio R.

Abstract

To pilot Therapy Together, an 8-week parent-led pediatric constraint induced movement therapy (P-CIMT) program for preschool aged children with unilateral cerebral palsy (UCP). Five children with UCP and their caregivers participated in eight, 1 hour group sessions structured by the TEAM approach (topic, encourage, activity, and motivate). Three of the sessions were in person and 5 of the sessions were online due to COVID-19. Parent coaching and therapeutic activities for each weekly session aimed to improve a specific upper limb domain. The caregivers were asked to implement therapeutic activities 1 hour each day at home. The primary outcome measure was the Assisting Hand Assessment (AHA), scored by a blinded rater. The secondary outcome measure was the Canadian Occupational Performance Measure (COPM). Caregivers kept a log of hours completed at home, comments about implementing the program, and rated their child's unilateral and bilateral hand performance weekly. Participants demonstrated clinically significant changes in bimanual performance (AHA) with a large effect size, but statistical significance was not reached. Improvements in occupational performance and satisfaction (COPM) were clinically and statistically significant. Therapy Together is a promising P-CIMT intervention program for preschooler with UCP. The program incorporates caregiver education and coaching with caregiver-led home therapeutic activities to improve children's bimanual hand skills and occupational performance while addressing barriers to intervention access such as caregiver hesitancy in order to reduce health disparities in children with UCP.

Published
2023
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6. Variability in the analysis of a single neuroimaging dataset by many teams

Author

Botvinik-Nezer, Rotem, Holzmeister, Felix, Camerer, Colin F, Dreber, Anna, Huber, Juergen, Johannesson, Magnus, Kirchler, Michael, Iwanir, Roni, Mumford, Jeanette A, Adcock, R Alison, Avesani, Paolo, Baczkowski, Blazej M, Bajracharya, Aahana, Bakst, Leah, Ball, Sheryl, Barilari, Marco, Bault, Nadège, Beaton, Derek, Beitner, Julia, Benoit, Roland G, Berkers, Ruud MWJ, Bhanji, Jamil P, Biswal, Bharat B, Bobadilla-Suarez, Sebastian, Bortolini, Tiago, Bottenhorn, Katherine L, Bowring, Alexander, Braem, Senne, Brooks, Hayley R, Brudner, Emily G, Calderon, Cristian B, Camilleri, Julia A, Castrellon, Jaime J, Cecchetti, Luca, Cieslik, Edna C, Cole, Zachary J, Collignon, Olivier, Cox, Robert W, Cunningham, William A, Czoschke, Stefan, Dadi, Kamalaker, Davis, Charles P, Luca, Alberto De, Delgado, Mauricio R, Demetriou, Lysia, Dennison, Jeffrey B, Di, Xin, Dickie, Erin W, Dobryakova, Ekaterina, Donnat, Claire L, Dukart, Juergen, Duncan, Niall W, Durnez, Joke, Eed, Amr, Eickhoff, Simon B, Erhart, Andrew, Fontanesi, Laura, Fricke, G Matthew, Fu, Shiguang, Galván, Adriana, Gau, Remi, Genon, Sarah, Glatard, Tristan, Glerean, Enrico, Goeman, Jelle J, Golowin, Sergej AE, González-García, Carlos, Gorgolewski, Krzysztof J, Grady, Cheryl L, Green, Mikella A, Guassi Moreira, João F, Guest, Olivia, Hakimi, Shabnam, Hamilton, J Paul, Hancock, Roeland, Handjaras, Giacomo, Harry, Bronson B, Hawco, Colin, Herholz, Peer, Herman, Gabrielle, Heunis, Stephan, Hoffstaedter, Felix, Hogeveen, Jeremy, Holmes, Susan, Hu, Chuan-Peng, Huettel, Scott A, Hughes, Matthew E, Iacovella, Vittorio, Iordan, Alexandru D, Isager, Peder M, Isik, Ayse I, Jahn, Andrew, Johnson, Matthew R, Johnstone, Tom, Joseph, Michael JE, Juliano, Anthony C, Kable, Joseph W, Kassinopoulos, Michalis, Koba, Cemal, and Kong, Xiang-Zhen

Subjects
Generic health relevance, Brain, Data Analysis, Data Science, Datasets as Topic, Female, Functional Neuroimaging, Humans, Logistic Models, Magnetic Resonance Imaging, Male, Meta-Analysis as Topic, Models, Neurological, Reproducibility of Results, Research Personnel, Software, General Science & Technology
Abstract

Data analysis workflows in many scientific domains have become increasingly complex and flexible. Here we assess the effect of this flexibility on the results of functional magnetic resonance imaging by asking 70 independent teams to analyse the same dataset, testing the same 9 ex-ante hypotheses1. The flexibility of analytical approaches is exemplified by the fact that no two teams chose identical workflows to analyse the data. This flexibility resulted in sizeable variation in the results of hypothesis tests, even for teams whose statistical maps were highly correlated at intermediate stages of the analysis pipeline. Variation in reported results was related to several aspects of analysis methodology. Notably, a meta-analytical approach that aggregated information across teams yielded a significant consensus in activated regions. Furthermore, prediction markets of researchers in the field revealed an overestimation of the likelihood of significant findings, even by researchers with direct knowledge of the dataset2-5. Our findings show that analytical flexibility can have substantial effects on scientific conclusions, and identify factors that may be related to variability in the analysis of functional magnetic resonance imaging. The results emphasize the importance of validating and sharing complex analysis workflows, and demonstrate the need for performing and reporting multiple analyses of the same data. Potential approaches that could be used to mitigate issues related to analytical variability are discussed.

Published
2020

7. GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder

Author

Shieh, Christine, Jones, Natasha, Vanle, Brigitte, Au, Margaret, Huang, Alden Y, Silva, Ana PG, Lee, Hane, Douine, Emilie D, Otero, Maria G, Choi, Andrew, Grand, Katheryn, Taff, Ingrid P, Delgado, Mauricio R, Hajianpour, MJ, Seeley, Andrea, Rohena, Luis, Vernon, Hilary, Gripp, Karen W, Vergano, Samantha A, Mahida, Sonal, Naidu, Sakkubai, Sousa, Ana Berta, Wain, Karen E, Challman, Thomas D, Beek, Geoffrey, Basel, Donald, Ranells, Judith, Smith, Rosemarie, Yusupov, Roman, Freckmann, Mary-Louise, Ohden, Lisa, Davis-Keppen, Laura, Chitayat, David, Dowling, James J, Finkel, Richard, Dauber, Andrew, Spillmann, Rebecca, Pena, Loren DM, Metcalfe, Kay, Splitt, Miranda, Lachlan, Katherine, McKee, Shane A, Hurst, Jane, Fitzpatrick, David R, Morton, Jenny EV, Cox, Helen, Venkateswaran, Sunita, Young, Juan I, Marsh, Eric D, Nelson, Stanley F, Martinez, Julian A, Graham, John M, Kini, Usha, Mackay, Joel P, and Pierson, Tyler Mark

Subjects
Biological Sciences, Genetics, Brain Disorders, Intellectual and Developmental Disabilities (IDD), Neurosciences, Pediatric, Mental Health, Rare Diseases, 2.1 Biological and endogenous factors, 4.1 Discovery and preclinical testing of markers and technologies, Child, Female, GATA Transcription Factors, Humans, Intellectual Disability, Megalencephaly, Neurodevelopmental Disorders, Nucleosomes, Phenotype, Pregnancy, Repressor Proteins, GATAD2B, NuRD complex, apraxia of speech, chromatin remodeling, macrocephaly, Undiagnosed Diseases Network, GATAD2B, NuRD complex, apraxia of speech, chromatin remodeling, macrocephaly, Clinical Sciences, Genetics & Heredity
Abstract

PurposeDetermination of genotypic/phenotypic features of GATAD2B-associated neurodevelopmental disorder (GAND).MethodsFifty GAND subjects were evaluated to determine consistent genotypic/phenotypic features. Immunoprecipitation assays utilizing in vitro transcription-translation products were used to evaluate GATAD2B missense variants' ability to interact with binding partners within the nucleosome remodeling and deacetylase (NuRD) complex.ResultsSubjects had clinical findings that included macrocephaly, hypotonia, intellectual disability, neonatal feeding issues, polyhydramnios, apraxia of speech, epilepsy, and bicuspid aortic valves. Forty-one novelGATAD2B variants were identified with multiple variant types (nonsense, truncating frameshift, splice-site variants, deletions, and missense). Seven subjects were identified with missense variants that localized within two conserved region domains (CR1 or CR2) of the GATAD2B protein. Immunoprecipitation assays revealed several of these missense variants disrupted GATAD2B interactions with its NuRD complex binding partners.ConclusionsA consistent GAND phenotype was caused by a range of genetic variants in GATAD2B that include loss-of-function and missense subtypes. Missense variants were present in conserved region domains that disrupted assembly of NuRD complex proteins. GAND's clinical phenotype had substantial clinical overlap with other disorders associated with the NuRD complex that involve CHD3 and CHD4, with clinical features of hypotonia, intellectual disability, cardiac defects, childhood apraxia of speech, and macrocephaly.

Published
2020

8. Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder

Author

Shieh, Christine, Jones, Natasha, Vanle, Brigitte, Au, Margaret, Huang, Alden Y, Silva, Ana PG, Lee, Hane, Douine, Emilie D, Otero, Maria G, Choi, Andrew, Grand, Katheryn, Taff, Ingrid P, Delgado, Mauricio R, Hajianpour, MJ, Seeley, Andrea, Rohena, Luis, Vernon, Hilary, Gripp, Karen W, Vergano, Samantha A, Mahida, Sonal, Naidu, Sakkubai, Sousa, Ana Berta, Wain, Karen E, Challman, Thomas D, Beek, Geoffrey, Basel, Donald, Ranells, Judith, Smith, Rosemarie, Yusupov, Roman, Freckmann, Mary-Louise, Ohden, Lisa, Davis-Keppen, Laura, Chitayat, David, Dowling, James J, Finkel, Richard, Dauber, Andrew, Spillmann, Rebecca, Pena, Loren DM, Metcalfe, Kay, Splitt, Miranda, Lachlan, Katherine, McKee, Shane A, Hurst, Jane, Fitzpatrick, David R, Morton, Jenny EV, Cox, Helen, Venkateswaran, Sunita, Young, Juan I, Marsh, Eric D, Nelson, Stanley F, Martinez, Julian A, Graham, John M, Kini, Usha, Mackay, Joel P, and Pierson, Tyler Mark

Subjects
Biological Sciences, Genetics, Undiagnosed Diseases Network, Clinical Sciences, Genetics & Heredity
Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Published
2020

9. Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease–associated loci for BAFopathies

Author

Chen, Chun-An, Lattier, John, Zhu, Wenmiao, Rosenfeld, Jill, Wang, Lei, Scott, Tiana M., Du, Haowei, Patel, Vipulkumar, Dang, Anh, Magoulas, Pilar, Streff, Haley, Sebastian, Jessica, Svihovec, Shayna, Curry, Kathryn, Delgado, Mauricio R., Hanchard, Neil A., Lalani, Seema, Marom, Ronit, Madan-Khetarpal, Suneeta, Saenz, Margarita, Dai, Hongzheng, Meng, Linyan, Xia, Fan, Bi, Weimin, Liu, Pengfei, Posey, Jennifer E., Scott, Daryl A., Lupski, James R., Eng, Christine M., Xiao, Rui, and Yuan, Bo

Published
2022
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11. Biallelic mutations in human DCC cause developmental split-brain syndrome

Author

Jamuar, Saumya S, Schmitz-Abe, Klaus, D'Gama, Alissa M, Drottar, Marie, Chan, Wai-Man, Peeva, Maya, Servattalab, Sarah, Lam, Anh-Thu N, Delgado, Mauricio R, Clegg, Nancy J, Zayed, Zayed Al, Dogar, Mohammad Asif, Alorainy, Ibrahim A, Jamea, Abdullah Abu, Abu-Amero, Khaled, Griebel, May, Ward, Wendy, Lein, Ed S, Markianos, Kyriacos, Barkovich, A James, Robson, Caroline D, Grant, P Ellen, Bosley, Thomas M, Engle, Elizabeth C, Walsh, Christopher A, and Yu, Timothy W

Subjects
Agricultural, Veterinary and Food Sciences, Biological Sciences, Bioinformatics and Computational Biology, Genetics, Agricultural Biotechnology, Congenital Structural Anomalies, Intellectual and Developmental Disabilities (IDD), Neurosciences, Brain Disorders, Pediatric, Neurological, Brain, Central Nervous System, Colorectal Neoplasms, Female, Gene Expression Regulation, Developmental, Humans, Intellectual Disability, Loss of Heterozygosity, Male, Mutation, Neurons, Phenotype, Polymorphism, Single Nucleotide, Receptors, Cell Surface, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology
Abstract

Motor, sensory, and integrative activities of the brain are coordinated by a series of midline-bridging neuronal commissures whose development is tightly regulated. Here we report a new human syndrome in which these commissures are widely disrupted, thus causing clinical manifestations of horizontal gaze palsy, scoliosis, and intellectual disability. Affected individuals were found to possess biallelic loss-of-function mutations in the gene encoding the axon-guidance receptor 'deleted in colorectal carcinoma' (DCC), which has been implicated in congenital mirror movements when it is mutated in the heterozygous state but whose biallelic loss-of-function human phenotype has not been reported. Structural MRI and diffusion tractography demonstrated broad disorganization of white-matter tracts throughout the human central nervous system (CNS), including loss of all commissural tracts at multiple levels of the neuraxis. Combined with data from animal models, these findings show that DCC is a master regulator of midline crossing and development of white-matter projections throughout the human CNS.

Published
2017

12. Germline mutation in POLR2A: a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulation

Author

Hansen, Adam W., Arora, Payal, Khayat, Michael M., Smith, Leah J., Lewis, Andrea M., Rossetti, Linda Z., Jayaseelan, Joy, Cristian, Ingrid, Haynes, Devon, DiTroia, Stephanie, Meeks, Naomi, Delgado, Mauricio R., Rosenfeld, Jill A., Pais, Lynn, White, Susan M., Meng, Qingchang, Pehlivan, Davut, Liu, Pengfei, Gingras, Marie-Claude, Wangler, Michael F., Muzny, Donna M., Lupski, James R., Kaplan, Craig D., and Gibbs, Richard A.

Published
2021
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16. GATAD2B-associatedneurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-relateddisorder

Author

Shieh, Christine, Jones, Natasha, Vanle, Brigitte, Au, Margaret, Huang, Alden Y., Silva, Ana P.G., Lee, Hane, Douine, Emilie D., Otero, Maria G., Choi, Andrew, Grand, Katheryn, Taff, Ingrid P., Delgado, Mauricio R., Hajianpour, M.J., Seeley, Andrea, Rohena, Luis, Vernon, Hilary, Gripp, Karen W., Vergano, Samantha A., Mahida, Sonal, Naidu, Sakkubai, Sousa, Ana Berta, Wain, Karen E., Challman, Thomas D., Beek, Geoffrey, Basel, Donald, Ranells, Judith, Smith, Rosemarie, Yusupov, Roman, Freckmann, Mary-Louise, Ohden, Lisa, Davis-Keppen, Laura, Chitayat, David, Dowling, James J., Finkel, Richard, Dauber, Andrew, Spillmann, Rebecca, Pena, Loren D.M., Metcalfe, Kay, Splitt, Miranda, Lachlan, Katherine, McKee, Shane A., Hurst, Jane, Fitzpatrick, David R., Morton, Jenny E.V., Cox, Helen, Venkateswaran, Sunita, Young, Juan I., Marsh, Eric D., Nelson, Stanley F., Martinez, Julian A., Graham, John M., Jr, Kini, Usha, Mackay, Joel P., and Pierson, Tyler Mark

Published
2020
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18. Trust and Reputation

Author

Brudner, Emily G., primary, Karousatos, Alec J., additional, Fareri, Dominic S., additional, and Delgado, Mauricio R., additional

Published
2021
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20. DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

Author

Blackburn, Alexandria T.M., Bekheirnia, Nasim, Uma, Vanessa C., Corkins, Mark E., Xu, Yuxiao, Rosenfeld, Jill A., Bainbridge, Matthew N., Yang, Yaping, Liu, Pengfei, Madan-Khetarpal, Suneeta, Delgado, Mauricio R., Hudgins, Louanne, Krantz, Ian, Rodriguez-Buritica, David, Wheeler, Patricia G., Al-Gazali, Lihadh, Mohamed Saeed Mohamed Al Shamsi, Aisha, Gomez-Ospina, Natalia, Chao, Hsiao-Tuan, Mirzaa, Ghayda M., Scheuerle, Angela E., Kukolich, Mary K., Scaglia, Fernando, Eng, Christine, Willsey, Helen Rankin, Braun, Michael C., Lamb, Dolores J., Miller, Rachel K., and Bekheirnia, Mir Reza

Published
2019
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24. RAB1A haploinsufficiency phenocopies the 2p14–p15 microdeletion and is associated with impaired neuronal differentiation

Author

Rios, Jonathan J., primary, Li, Yang, additional, Paria, Nandina, additional, Bohlender, Ryan J., additional, Huff, Chad, additional, Rosenfeld, Jill A., additional, Liu, Pengfei, additional, Bi, Weimin, additional, Haga, Kentaro, additional, Fukuda, Mitsunori, additional, Vashisth, Shayal, additional, Kaur, Kiran, additional, Chahrour, Maria H., additional, Bober, Michael B., additional, Duker, Angela L., additional, Ladha, Farah A., additional, Hanchard, Neil A., additional, Atala, Kristhen, additional, Khanshour, Anas M., additional, Smith, Linsley, additional, Wise, Carol A., additional, and Delgado, Mauricio R., additional

Published
2023
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25. Altered brain response to reward and punishment in adolescents with Anorexia nervosa

Author

Bischoff-Grethe, Amanda, McCurdy, Danyale, Grenesko-Stevens, Emily, Irvine, Laura E, Wagner, Angela, Yau, Wai-Ying Wendy, Fennema-Notestine, Christine, Wierenga, Christina E, Fudge, Julie L, Delgado, Mauricio R, and Kaye, Walter H

Subjects
Biological Psychology, Pharmacology and Pharmaceutical Sciences, Biomedical and Clinical Sciences, Psychology, Neurosciences, Eating Disorders, Brain Disorders, Clinical Research, Pediatric, Basic Behavioral and Social Science, Behavioral and Social Science, Anorexia, Nutrition, Mental Health, Aetiology, 2.1 Biological and endogenous factors, Mental health, Adolescent, Anorexia Nervosa, Brain, Brain Mapping, Child, Corpus Striatum, Emotions, Executive Function, Female, Gyrus Cinguli, Humans, Magnetic Resonance Imaging, Punishment, Reward, Anorexia nervosa, Functional magnetic resonance imaging, Striatum, Cingulate, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry, Clinical sciences, Clinical and health psychology
Abstract

Adults recovered from Anorexia nervosa (AN) have altered reward modulation within striatal limbic regions associated with the emotional significance of stimuli, and executive regions concerned with planning and consequences. We hypothesized that adolescents with AN would show similar disturbed reward modulation within the striatum and the anterior cingulate cortex, a region connected to the striatum and involved in reward-guided action selection. Using functional magnetic resonance imaging, twenty-two adolescent females (10 restricting-type AN, 12 healthy volunteers) performed a monetary guessing task. Time series data associated with monetary wins and losses within striatal and cingulate regions of interest were subjected to a linear mixed effects analysis. All participants responded more strongly to wins versus losses in limbic and anterior executive striatal territories. However, AN participants exhibited an exaggerated response to losses compared to wins in posterior executive and sensorimotor striatal regions, suggesting altered function in circuitry responsible for coding the affective context of stimuli and action selection based upon these valuations. As AN individuals are particularly sensitive to criticism, failure, and making mistakes, these findings may reflect the neural processes responsible for a bias in those with AN to exaggerate negative consequences.

Published
2013

26. In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristics

Author

Weiss, Karin, Kruszka, Paul, Guillen Sacoto, Maria J., Addissie, Yonit A., Hadley, Donald W., Hadsall, Casey K., Stokes, Bethany, Hu, Ping, Roessler, Erich, Solomon, Beth, Wiggs, Edythe, Thurm, Audrey, Hufnagel, Robert B., Zein, Wadih M., Hahn, Jin S., Stashinko, Elaine, Levey, Eric, Baldwin, Debbie, Clegg, Nancy J., Delgado, Mauricio R., and Muenke, Maximilian

Published
2018
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33. Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

Author

Blackburn, Alexandria T. M., Bekheirnia, Nasim, Uma, Vanessa C., Corkins, Mark E., Xu, Yuxiao, Rosenfeld, Jill A., Bainbridge, Matthew N., Yang, Yaping, Liu, Pengfei, Madan-Khetarpal, Suneeta, Delgado, Mauricio R., Hudgins, Louanne, Krantz, Ian, Rodriguez-Buritica, David, Wheeler, Patricia G., Al-Gazali, Lihadh, Shamsi, Aisha Mohamed Saeed Mohamed Al, Gomez-Ospina, Natalia, Chao, Hsiao-Tuan, Mirzaa, Ghayda M., Scheuerle, Angela E., Kukolich, Mary K., Scaglia, Fernando, Eng, Christine, Willsey, Helen Rankin, Braun, Michael C., Lamb, Dolores J., Miller, Rachel K., and Bekheirnia, Mir Reza

Published
2020
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34. Goal Attainment after Treatment with Abobotulinumtoxina and a Tailored Home Therapy Programme in Children with Upper Limb Spasticity: Descriptive, Exploratory Analysis of a Large Randomized, Controlled Study

Author

Carranza-del Río, Jorge, primary, Dursun, Nigar, additional, Cekmece, Cigdem, additional, Bonikowski, Marcin, additional, Pyrzanowska, Weronika, additional, Dabrowski, Edward, additional, Tilton, Ann, additional, Oleszek, Joyce, additional, Volteau, Magali, additional, Page, Simon, additional, Shierk, Angela, additional, and Delgado, Mauricio R., additional

Published
2022
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47. A neural signature of reward

Author

Chang, Luke J., primary, Li, Xiao, additional, Nguyen, Kenny, additional, Ranger, Maxwell, additional, Begunova, Yelyzaveta, additional, Chen, Pin-Hao A., additional, Castrellon, Jaime J., additional, Samanez-Larkin, Gregory R., additional, Zald, David H., additional, Fareri, Dominic S., additional, Delgado, Mauricio R., additional, and Tomova, Livia, additional

Published
2022
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