Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Sarah U. Morton"'
Autor:
Marlee M. Vandewouw, Ami Norris-Brilliant, Anum Rahman, Stephania Assimopoulos, Sarah U. Morton, Azadeh Kushki, Sean Cunningham, Eileen King, Elizabeth Goldmuntz, Thomas A. Miller, Nina H. Thomas, Heather R. Adams, John Cleveland, James F. Cnota, P Ellen Grant, Caren S. Goldberg, Hao Huang, Jennifer S. Li, Patrick McQuillen, George A. Porter, Amy E. Roberts, Mark W. Russell, Christine E. Seidman, Madalina E. Tivarus, Wendy K. Chung, Donald J. Hagler, Jane W. Newburger, Ashok Panigrahy, Jason P Lerch, Bruce D. Gelb, Evdokia Anagnostou
Publikováno v:
NeuroImage, Vol 297, Iss , Pp 120721- (2024)
Individuals with congenital heart disease (CHD) have an increased risk of neurodevelopmental impairments. Given the hypothesized complexity linking genomics, atypical brain structure, cardiac diagnoses and their management, and neurodevelopmental out
Externí odkaz:
https://doaj.org/article/5e44b9017eb64e49ae2ee4fa20bd3328
Autor:
Lara Maleyeff, Jane W. Newburger, David Wypij, Nina H. Thomas, Evdokia Anagnoustou, Martina Brueckner, Wendy K. Chung, John Cleveland, Sean Cunningham, Bruce D. Gelb, Elizabeth Goldmuntz, Donald J Hagler Jr, Hao Huang, Eileen King, Patrick McQuillen, Thomas A. Miller, Ami Norris‐Brilliant, George A. Porter Jr, Amy E. Roberts, P. Ellen Grant, Kiho Im, Sarah U. Morton
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 2, Pp 278-290 (2024)
Abstract Objective Persons with congenital heart disease (CHD) are at increased risk of neurodevelopmental disabilities, including impairments to executive function. Sulcal pattern features correlate with executive function in adolescents with single
Externí odkaz:
https://doaj.org/article/8dcae0435919402c9b79af51bd1ffc3c
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 6, p 170 (2024)
Congenital heart disease (CHD) is increasingly diagnosed prenatally and the ability to screen and diagnose the genetic factors involved in CHD have greatly improved. The presence of a genetic abnormality in the setting of prenatally diagnosed CHD imp
Externí odkaz:
https://doaj.org/article/9d0abfc4a73a4a0cafc39eb28cdfd9bd
Autor:
Julia K. Hoffmann, Zahra Khazal, Wievineke Apers, Puneet Sharma, Constance G. Weismann, Kira Kaganov, Craig R. Wheeler, Michael Farias, Diego Porras, Philip Levy, Sarah U. Morton
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 5, p 132 (2024)
(1) Background: To identify reasons for the persistence of surgical ligation of the patent ductus arteriosus (PDA) in premature infants after the 2019 Food and Drug Administration (FDA) approval of transcatheter device closure; (2) Methods: We perfor
Externí odkaz:
https://doaj.org/article/d2c7796e90de4efe983724d22d976131
Autor:
Drayton C. Harvey, Riya Verma, Brandon Sedaghat, Brooke E. Hjelm, Sarah U. Morton, Jon G. Seidman, S. Ram Kumar
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
ObjectiveEighty percent of patients with a diagnosis of tetralogy of Fallot (TOF) do not have a known genetic etiology or syndrome. We sought to identify key molecular pathways and biological processes that are enriched in non-syndromic TOF, the most
Externí odkaz:
https://doaj.org/article/ebbf67c416674f628bf37ebaa854c3a0
Autor:
Jason Sutin, Rutvi Vyas, Henry A. Feldman, Silvina Ferradal, Chuan-Heng Hsiao, Lucca Zampolli, Lara J. Pierce, Charles A. Nelson, Sarah U. Morton, Susanne Hay, Mohamed El-Dib, Janet S. Soul, Pei-Yi Lin, Patricia E. Grant
Publikováno v:
EBioMedicine, Vol 94, Iss , Pp 104673- (2023)
Summary: Background: Therapeutic hypothermia (TH) is standard of care for moderate to severe neonatal hypoxic ischemic encephalopathy (HIE) but many survivors still suffer lifelong disabilities and benefits of TH for mild HIE are under active debate.
Externí odkaz:
https://doaj.org/article/44d339770c2447178b0e8bddd820587e
Autor:
Mercedeh Movassagh, Sarah U. Morton, Christine Hehnly, Jasmine Smith, Trang T. Doan, Rafael Irizarry, James R. Broach, Steven J. Schiff, Jeffrey A. Bailey, Joseph N. Paulson
Publikováno v:
BMC Genomics, Vol 23, Iss 1, Pp 1-17 (2022)
Abstract We introduce mirTarRnaSeq, an R/Bioconductor package for quantitative assessment of miRNA-mRNA relationships within sample cohorts. mirTarRnaSeq is a statistical package to explore predicted or pre-hypothesized miRNA-mRNA relationships follo
Externí odkaz:
https://doaj.org/article/4ba6b9cc99ba479eb7c74c737024ba74
Autor:
Christine Hehnly, Paddy Ssentongo, Lisa M. Bebell, Kathy Burgoine, Joel Bazira, Claudio Fronterre, Elias Kumbakumba, Ronald Mulondo, Edith Mbabazi-Kabachelor, Sarah U. Morton, Joseph Ngonzi, Moses Ochora, Peter Olupot-Olupot, John Mugamba, Justin Onen, Drucilla J. Roberts, Kathryn Sheldon, Shamim A. Sinnar, Jasmine Smith, Peter Ssenyonga, Julius Kiwanuka, Joseph N. Paulson, Frederick A. Meier, Jessica E. Ericson, James R. Broach, Steven J. Schiff
Publikováno v:
International Journal of Infectious Diseases, Vol 118, Iss , Pp 24-33 (2022)
Objectives: To estimate the prevalence of cytomegalovirus (CMV) infections among newborn-mother pairs, neonates with sepsis, and infants with hydrocephalus in Uganda. Design and Methods: Three populations—newborn-mother pairs, neonates with sepsis,
Externí odkaz:
https://doaj.org/article/08c5c98caae347578706910934f0ef61
Autor:
Christine Hehnly, Aiqin Shi, Paddy Ssentongo, Lijun Zhang, Albert Isaacs, Sarah U. Morton, Nicholas Streck, Petra Erdmann-Gilmore, Igor Tolstoy, R. Reid Townsend, David D. Limbrick, Joseph N. Paulson, Jessica E. Ericson, Michael Y. Galperin, Steven J. Schiff, James R. Broach
Publikováno v:
mBio, Vol 13, Iss 6 (2022)
ABSTRACT Hydrocephalus, the leading indication for childhood neurosurgery worldwide, is particularly prevalent in low- and middle-income countries. Hydrocephalus preceded by an infection, or postinfectious hydrocephalus, accounts for up to 60% of hyd
Externí odkaz:
https://doaj.org/article/4ed3d517da8341ba9e490b66a1529316
Autor:
Sarah U. Morton, Brian J. Leyshon, Eleonora Tamilia, Rutvi Vyas, Michaela Sisitsky, Imran Ladha, John B. Lasekan, Matthew J. Kuchan, P. Ellen Grant, Yangming Ou
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
Multimodal brain magnetic resonance imaging (MRI) can provide biomarkers of early influences on neurodevelopment such as nutrition, environmental and genetic factors. As the exposure to early influences can be separated from neurodevelopmental outcom
Externí odkaz:
https://doaj.org/article/a11da4ba59e641e99a5b56e8fcf24ced