Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Rachel M. Rahn"'
Autor:
Rachel M. Rahn, Claire T. Weichselbaum, David H. Gutmann, Joseph D. Dougherty, Susan E. Maloney
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-13 (2021)
Abstract Background Motor deficits such as abnormal gait are an underappreciated yet characteristic phenotype of many neurodevelopmental disorders (NDDs), including Williams Syndrome (WS) and Neurofibromatosis Type 1 (NF1). Compared to cognitive phen
Externí odkaz:
https://doaj.org/article/113254e22cd84fbb8b3e585027d5a6ec
Autor:
Rachel M Rahn, Allen Yen, Siyu Chen, Seana H Gaines, Annie R Bice, Lindsey M Brier, Raylynn G Swift, LeiLani Lee, Susan E Maloney, Joseph P Culver, Joseph D Dougherty
Publikováno v:
Cerebral Cortex.
As a regressive neurodevelopmental disorder with a well-established genetic cause, Rett syndrome and its Mecp2 loss-of-function mouse model provide an excellent opportunity to define potentially translatable functional signatures of disease progressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39128b0f1b2e1f2ac75423a543e34e9f
https://doi.org/10.1093/cercor/bhad050
https://doi.org/10.1093/cercor/bhad050
Autor:
Julian V Clarke, Lindsey M Brier, Rachel M Rahn, Deepti Diwan, Jane Y Yuan, Annie R Bice, Shin-ichiro Imai, Ananth K Vellimana, Joseph P Culver, Gregory J Zipfel
Publikováno v:
J Cereb Blood Flow Metab
Functional connectivity (FC) is a sensitive metric that provides a readout of whole cortex coordinate neural activity in a mouse model. We examine the impact of experimental SAH modeled through endovascular perforation, and the effectiveness of subse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a99c51c402933cbc78fb0b8562f70b
https://doi.org/10.1177/0271678x221079902
https://doi.org/10.1177/0271678x221079902
Autor:
Joseph P. Culver, Joseph D. Dougherty, Lindsey M. Brier, Annie R. Bice, Rachel M. Rahn, Matthew D. Reisman
Publikováno v:
Cereb Cortex
Cross-sectional studies have established a variety of structural, synaptic, and cell physiological changes corresponding to critical periods in cortical development. However, the emergence of functional connectivity (FC) in development has not been f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::193c630568a312832fae6d3d3fe56a21
https://doi.org/10.1093/cercor/bhab312
https://doi.org/10.1093/cercor/bhab312
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-13 (2021)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
Motor deficits such as abnormal gait are an underappreciated yet characteristic phenotype of many neurodevelopmental disorders (NDDs), including Williams Syndrome (WS) and Neurofibromatosis Type 1 (NF1). Compared to cognitive phenotypes, gait phenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42e661ec751831de4ea8a564cfc7a209
https://doaj.org/article/113254e22cd84fbb8b3e585027d5a6ec
https://doaj.org/article/113254e22cd84fbb8b3e585027d5a6ec
Autor:
Rachel M. Rahn, Allen Yen, Siyu Chen, Seana H. Gaines, Annie R. Bice, Lindsey M. Brier, Raylynn G. Swift, LeiLani Lee, Susan E. Maloney, Joseph P. Culver, Joseph D. Dougherty
As a regressive neurodevelopmental disorder with a well-established genetic cause, Rett Syndrome and its Mecp2 loss-of-function mouse model provide an excellent opportunity to define potentially translatable functional signatures of disease progressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d5a3593e74df2799961c2afff109460
https://doi.org/10.1101/2021.10.28.466323
https://doi.org/10.1101/2021.10.28.466323
Autor:
Olga Neyman, Ahmad M. Samara, Amjad Samara, Ki Yun Park, Bess A. Marshall, Joseph D. Dougherty, Rachel M. Rahn, Tamara Hershey
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-14 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-14 (2019)
Wolfram syndrome is a rare multisystem disorder caused by mutations in WFS1 or CISD2 genes leading to brain structural abnormalities and neurological symptoms. These abnormalities appear in early stages of the disease. The pathogenesis of Wolfram syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7c38265ebcffeb9d2518fac57c30ede
https://pubmed.ncbi.nlm.nih.gov/31796109
https://pubmed.ncbi.nlm.nih.gov/31796109
Publikováno v:
Biophotonics Congress: Biomedical Optics Congress 2018 (Microscopy/Translational/Brain/OTS).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25b408781b7498cbc4f597bdd95fdf3f
https://doi.org/10.1364/brain.2018.btu2c.6
https://doi.org/10.1364/brain.2018.btu2c.6
Autor:
Joseph P. Culver, Amy L. Bauernfeind, Shyam K. Akula, Avdagic S, Jakes C, Rachel M. Rahn, Michael A. Rieger, Krystal C. Chandler, Katherine B. McCullough, Susan E. Maloney, Joseph D. Dougherty
SummarySerotonergic dysregulation is implicated in psychiatric disorders, including autism spectrum disorders (ASD). Epidemiological studies suggest selective serotonin reuptake inhibitor (SSRI) treatment during pregnancy may increase ASD risk in off
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c63a633e53039cede67ca2d87f8b0095
Publikováno v:
eNeuro
Epidemiological studies have found an increased incidence of neurodevelopmental disorders in populations prenatally exposed to selective serotonin reuptake inhibitors (SSRIs). Optical imaging provides a minimally invasive way to determine if perinata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cd1abe66af3fad92459145fa8d59cf3
https://doi.org/10.1523/eneuro.0238-19.2019
https://doi.org/10.1523/eneuro.0238-19.2019