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Dysfunctional Activation and Brain Network Profiles in Youth with Obsessive-Compulsive Disorder: A Focus on the Dorsal Anterior Cingulate during Working Memory.

Frontiers in human neuroscience

Diwadkar VA, Burgess A, Hong E, Rix C, Arnold PD, Hanna GL, Rosenberg DR.
PMID: 25852529
Front Hum Neurosci. 2015 Mar 17;9:149. doi: 10.3389/fnhum.2015.00149. eCollection 2015.

Brain network dysfunction is emerging as a central biomarker of interest in psychiatry, in large part, because psychiatric conditions are increasingly seen as disconnection syndromes. Understanding dysfunctional brain network profiles in task-active states provides important information on network engagement...

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Diwadkar VA, Burgess A, Hong E, et al. Dysfunctional Activation and Brain Network Profiles in Youth with Obsessive-Compulsive Disorder: A Focus on the Dorsal Anterior Cingulate during Working Memory. Front Hum Neurosci. 2015;9:149doi: 10.3389/fnhum.2015.00149.
Diwadkar, V. A., Burgess, A., Hong, E., Rix, C., Arnold, P. D., Hanna, G. L., & Rosenberg, D. R. (2015). Dysfunctional Activation and Brain Network Profiles in Youth with Obsessive-Compulsive Disorder: A Focus on the Dorsal Anterior Cingulate during Working Memory. Frontiers in human neuroscience, 9149. https://doi.org/10.3389/fnhum.2015.00149
Diwadkar, Vaibhav A, et al. "Dysfunctional Activation and Brain Network Profiles in Youth with Obsessive-Compulsive Disorder: A Focus on the Dorsal Anterior Cingulate during Working Memory." Frontiers in human neuroscience vol. 9 (2015): 149. doi: https://doi.org/10.3389/fnhum.2015.00149
Diwadkar VA, Burgess A, Hong E, Rix C, Arnold PD, Hanna GL, Rosenberg DR. Dysfunctional Activation and Brain Network Profiles in Youth with Obsessive-Compulsive Disorder: A Focus on the Dorsal Anterior Cingulate during Working Memory. Front Hum Neurosci. 2015 Mar 17;9:149. doi: 10.3389/fnhum.2015.00149. eCollection 2015. PMID: 25852529; PMCID: PMC4362304.
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Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.

Journal of neurodevelopmental disorders

Gazzellone MJ, Zarrei M, Burton CL, Walker S, Uddin M, Shaheen SM, Coste J, Rajendram R, Schachter RJ, Colasanto M, Hanna GL, Rosenberg DR, Soreni N, Fitzgerald KD, Marshall CR, Buchanan JA, Merico D, Arnold PD, Scherer SW.
PMID: 27777633
J Neurodev Disord. 2016 Oct 18;8:36. doi: 10.1186/s11689-016-9170-9. eCollection 2016.

BACKGROUND: Obsessive-compulsive disorder (OCD) is a heterogeneous neuropsychiatric condition, thought to have a significant genetic component. When onset occurs in childhood, affected individuals generally exhibit different characteristics from adult-onset OCD, including higher prevalence in males and increased heritability. Since...

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Gazzellone MJ, Zarrei M, Burton CL, et al. Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation. J Neurodev Disord. 2016;8:36doi: 10.1186/s11689-016-9170-9.
Gazzellone, M. J., Zarrei, M., Burton, C. L., Walker, S., Uddin, M., Shaheen, S. M., Coste, J., Rajendram, R., Schachter, R. J., Colasanto, M., Hanna, G. L., Rosenberg, D. R., Soreni, N., Fitzgerald, K. D., Marshall, C. R., Buchanan, J. A., Merico, D., Arnold, P. D., & Scherer, S. W. (2016). Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation. Journal of neurodevelopmental disorders, 836. https://doi.org/10.1186/s11689-016-9170-9
Gazzellone, Matthew J, et al. "Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation." Journal of neurodevelopmental disorders vol. 8 (2016): 36. doi: https://doi.org/10.1186/s11689-016-9170-9
Gazzellone MJ, Zarrei M, Burton CL, Walker S, Uddin M, Shaheen SM, Coste J, Rajendram R, Schachter RJ, Colasanto M, Hanna GL, Rosenberg DR, Soreni N, Fitzgerald KD, Marshall CR, Buchanan JA, Merico D, Arnold PD, Scherer SW. Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation. J Neurodev Disord. 2016 Oct 18;8:36. doi: 10.1186/s11689-016-9170-9. eCollection 2016. PMID: 27777633; PMCID: PMC5070001.
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A large data resource of genomic copy number variation across neurodevelopmental disorders.

NPJ genomic medicine

Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B, Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M, Miron K, Lu C, Wang T, Samler K, Wang X, Costain G, Hoang N, Pellecchia G, Wei J, Patel RV, Thiruvahindrapuram B, Roifman M, Merico D, Goodale T, Drmic I, Speevak M, Howe JL, Yuen RKC, Buchanan JA, Vorstman JAS, Marshall CR, Wintle RF, Rosenberg DR, Hanna GL, Woodbury-Smith M, Cytrynbaum C, Zwaigenbaum L, Elsabbagh M, Flanagan J, Fernandez BA, Carter MT, Szatmari P, Roberts W, Lerch J, Liu X, Nicolson R, Georgiades S, Weksberg R, Arnold PD, Bassett AS, Crosbie J, Schachar R, Stavropoulos DJ, Anagnostou E, Scherer SW.
PMID: 31602316
NPJ Genom Med. 2019 Oct 07;4:26. doi: 10.1038/s41525-019-0098-3. eCollection 2019.

Copy number variations (CNVs) are implicated across many neurodevelopmental disorders (NDDs) and contribute to their shared genetic etiology. Multiple studies have attempted to identify shared etiology among NDDs, but this is the first genome-wide CNV analysis across autism spectrum...

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Zarrei M, Burton CL, Engchuan W, et al. A large data resource of genomic copy number variation across neurodevelopmental disorders. NPJ Genom Med. 2019;4:26doi: 10.1038/s41525-019-0098-3.
Zarrei, M., Burton, C. L., Engchuan, W., Young, E. J., Higginbotham, E. J., MacDonald, J. R., Trost, B., Chan, A. J. S., Walker, S., Lamoureux, S., Heung, T., Mojarad, B. A., Kellam, B., Paton, T., Faheem, M., Miron, K., Lu, C., Wang, T., Samler, K., Wang, X., Costain, G., Hoang, N., Pellecchia, G., Wei, J., Patel, R. V., Thiruvahindrapuram, B., Roifman, M., Merico, D., Goodale, T., Drmic, I., Speevak, M., Howe, J. L., Yuen, R. K. C., Buchanan, J. A., Vorstman, J. A. S., Marshall, C. R., Wintle, R. F., Rosenberg, D. R., Hanna, G. L., Woodbury-Smith, M., Cytrynbaum, C., Zwaigenbaum, L., Elsabbagh, M., Flanagan, J., Fernandez, B. A., Carter, M. T., Szatmari, P., Roberts, W., Lerch, J., Liu, X., Nicolson, R., Georgiades, S., Weksberg, R., Arnold, P. D., Bassett, A. S., Crosbie, J., Schachar, R., Stavropoulos, D. J., Anagnostou, E., & Scherer, S. W. (2019). A large data resource of genomic copy number variation across neurodevelopmental disorders. NPJ genomic medicine, 426. https://doi.org/10.1038/s41525-019-0098-3
Zarrei, Mehdi, et al. "A large data resource of genomic copy number variation across neurodevelopmental disorders." NPJ genomic medicine vol. 4 (2019): 26. doi: https://doi.org/10.1038/s41525-019-0098-3
Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B, Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M, Miron K, Lu C, Wang T, Samler K, Wang X, Costain G, Hoang N, Pellecchia G, Wei J, Patel RV, Thiruvahindrapuram B, Roifman M, Merico D, Goodale T, Drmic I, Speevak M, Howe JL, Yuen RKC, Buchanan JA, Vorstman JAS, Marshall CR, Wintle RF, Rosenberg DR, Hanna GL, Woodbury-Smith M, Cytrynbaum C, Zwaigenbaum L, Elsabbagh M, Flanagan J, Fernandez BA, Carter MT, Szatmari P, Roberts W, Lerch J, Liu X, Nicolson R, Georgiades S, Weksberg R, Arnold PD, Bassett AS, Crosbie J, Schachar R, Stavropoulos DJ, Anagnostou E, Scherer SW. A large data resource of genomic copy number variation across neurodevelopmental disorders. NPJ Genom Med. 2019 Oct 07;4:26. doi: 10.1038/s41525-019-0098-3. eCollection 2019. PMID: 31602316; PMCID: PMC6779875.
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Showing 1 to 3 of 3 entries