Edward Yang
Edward Yang
Assistant Professor of Radiology, Boston Children's Hospital
Verified email at
Cited by
Cited by
Decay rates of human mRNAs: correlation with functional characteristics and sequence attributes
E Yang, E van Nimwegen, M Zavolan, N Rajewsky, M Schroeder, ...
Genome research 13 (8), 1863-1872, 2003
Somatic mutations activating the mTOR pathway in dorsal telencephalic progenitors cause a continuum of cortical dysplasias
AM D’Gama, MB Woodworth, AA Hossain, S Bizzotto, NE Hatem, ...
Cell reports 21 (13), 3754-3766, 2017
A normative spatiotemporal MRI atlas of the fetal brain for automatic segmentation and analysis of early brain growth
A Gholipour, CK Rollins, C Velasco-Annis, A Ouaalam, A Akhondi-Asl, ...
Scientific reports 7 (1), 476, 2017
Recruitment of Stat1 to chromatin is required for interferon-induced serine phosphorylation of Stat1 transactivation domain
I Sadzak, M Schiff, I Gattermeier, R Glinitzer, I Sauer, A Saalmüller, ...
Proceedings of the National Academy of Sciences 105 (26), 8944-8949, 2008
Genetics and genotype–phenotype correlations in early onset epileptic encephalopathy with burst suppression
HE Olson, MK Kelly, CM LaCoursiere, R Pinsky, D Tambunan, C Shain, ...
Annals of neurology 81 (3), 419-429, 2017
TAF1 variants are associated with dysmorphic features, intellectual disability, and neurological manifestations
JA O’Rawe, Y Wu, MJ Dörfel, AF Rope, PYB Au, JS Parboosingh, S Moon, ...
The American Journal of Human Genetics 97 (6), 922-932, 2015
Dissociation time from DNA determines transcriptional function in a STAT1 linker mutant
E Yang, MA Henriksen, O Schaefer, N Zakharova, JE Darnell
Journal of Biological Chemistry 277 (16), 13455-13462, 2002
The linker domain of Stat1 is required for gamma interferon-driven transcription
E Yang, Z Wen, RL Haspel, JJ Zhang, JE Darnell Jr
Molecular and cellular biology 19 (7), 5106-5112, 1999
Fetal neuropathology in Zika virus-infected pregnant female rhesus monkeys
AJ Martinot, P Abbink, O Afacan, AK Prohl, R Bronson, JL Hecht, ...
Cell 173 (5), 1111-1122. e10, 2018
Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy
MR Winawer, NG Griffin, J Samanamud, EH Baugh, D Rathakrishnan, ...
Annals of neurology 83 (6), 1133-1146, 2018
Independent and cooperative activation of chromosomal c-fos promoter by STAT3
E Yang, L Lerner, D Besser, JE Darnell
Journal of Biological Chemistry 278 (18), 15794-15799, 2003
The frequency and severity of magnetic resonance imaging abnormalities in infants with mild neonatal encephalopathy
BH Walsh, J Neil, JA Morey, E Yang, MV Silvera, TE Inder, C Ortinau
The Journal of pediatrics 187, 26-33. e1, 2017
Early Mycoplasma pneumoniae infection presenting as multiple pulmonary masses: an unusual presentation in a child
E Yang, T Altes, SA Anupindi
Pediatric radiology 38, 477-480, 2008
Clinical targeted exome-based sequencing in combination with genome-wide copy number profiling: precision medicine analysis of 203 pediatric brain tumors
SH Ramkissoon, P Bandopadhayay, J Hwang, LA Ramkissoon, ...
Neuro-oncology 19 (7), 986-996, 2017
Fetal brain growth portrayed by a spatiotemporal diffusion tensor MRI atlas computed from in utero images
S Khan, L Vasung, B Marami, CK Rollins, O Afacan, CM Ortinau, E Yang, ...
Neuroimage 185, 593-608, 2019
The ESCRT-III protein CHMP1A mediates secretion of sonic hedgehog on a distinctive subtype of extracellular vesicles
ME Coulter, CM Dorobantu, GA Lodewijk, F Delalande, S Cianferani, ...
Cell reports 24 (4), 973-986. e8, 2018
Distinct transcriptional activation functions of STAT1α and STAT1β on DNA and chromatin templates
N Zakharova, ES Lymar, E Yang, S Malik, JJ Zhang, RG Roeder, ...
Journal of Biological Chemistry 278 (44), 43067-43073, 2003
Regional brain growth trajectories in fetuses with congenital heart disease
CK Rollins, CM Ortinau, C Stopp, KG Friedman, W Tworetzky, B Gagoski, ...
Annals of neurology 89 (1), 143-157, 2021
Temporal slice registration and robust diffusion-tensor reconstruction for improved fetal brain structural connectivity analysis
B Marami, SSM Salehi, O Afacan, B Scherrer, CK Rollins, E Yang, ...
NeuroImage 156, 475-488, 2017
A recurrent de novo PACS2 heterozygous missense variant causes neonatal-onset developmental epileptic encephalopathy, facial dysmorphism, and cerebellar dysgenesis
HE Olson, N Jean-Marçais, E Yang, D Heron, K Tatton-Brown, ...
The American Journal of Human Genetics 102 (5), 995-1007, 2018
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