Shruti Bagla
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Activity-dependent human brain coding/noncoding gene regulatory networks
L Lipovich, F Dachet, J Cai, S Bagla, K Balan, H Jia, JA Loeb
Genetics 192 (3), 1133-1148, 2012
Predicting novel histopathological microlesions in human epileptic brain through transcriptional clustering
F Dachet, S Bagla, G Keren-Aviram, A Morton, K Balan, L Saadat, ...
Brain 138 (2), 356-370, 2015
Elongating RNA polymerase II is disassembled through specific degradation of its largest but not other subunits in response to DNA damage in vivo
S Malik, S Bagla, P Chaurasia, Z Duan, SR Bhaumik
Journal of Biological Chemistry 283 (11), 6897-6905, 2008
Interictal spike connectivity in human epileptic neocortex
B Maharathi, R Wlodarski, S Bagla, E Asano, J Hua, J Patton, JA Loeb
Clinical Neurophysiology 130 (2), 270-279, 2019
A distinct microRNA expression profile is associated with α [11C]-methyl-L-tryptophan (AMT) PET uptake in epileptogenic cortical tubers resected from patients with tuberous …
S Bagla, D Cukovic, E Asano, S Sood, A Luat, HT Chugani, DC Chugani, ...
Neurobiology of disease 109, 76-87, 2018
Altered metabolomic–genomic signature: A potential noninvasive biomarker of epilepsy
HC Wu, F Dachet, F Ghoddoussi, S Bagla, D Fuerst, JA Stanley, ...
Epilepsia 58 (9), 1626-1636, 2017
Proteomic analysis of human epileptic neocortex predicts vascular and glial changes in epileptic regions
G Keren-Aviram, F Dachet, S Bagla, K Balan, JA Loeb, EA Dratz
PLoS One 13 (4), e0195639, 2018
Clinical diagnosis of red cell membrane disorders: comparison of osmotic gradient Ektacytometry and eosin Maleimide (EMA) fluorescence test for red cell band 3 (AE1, SLC4A1 …
AU Zaidi, S Buck, M Gadgeel, M Herrera-Martinez, A Mohan, K Johnson, ...
Frontiers in Physiology 11, 636, 2020
DUSP4 appears to be a highly localized endogenous inhibitor of epileptic signaling in human neocortex
A Kirchner, S Bagla, F Dachet, JA Loeb
Neurobiology of disease 145, 105073, 2020
TLR7 activation in epilepsy of tuberous sclerosis complex
AA Dombkowski, D Cukovic, S Bagla, MK Jones, JA Caruso, HT Chugani, ...
Inflammation Research 68, 993-998, 2019
Exosomes in epilepsy of tuberous sclerosis complex: Carriers of pro-inflammatory microRNAs
D Cukovic, S Bagla, D Ukasik, PM Stemmer, BP Jena, AR Naik, S Sood, ...
Non-coding RNA 7 (3), 40, 2021
Compound heterozygosity in PKLR gene for a previously unrecognized intronic polymorphism and a rare missense mutation as a novel cause of severe pyruvate kinase deficiency
S Bagla, K Bhambhani, M Gadgeel, S Buck, JP Jin, Y Ravindranath
Haematologica 104 (9), e428, 2019
Distinctive phenotypes in two children with novel germline RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin
S Bagla, KA Regling, EN Wakeling, M Gadgeel, S Buck, AU Zaidi, ...
Pediatric Hematology and Oncology 38 (1), 65-79, 2020
Identification of a novel variant in phosphoglycerate kinase-1 (PGK1) in an African-American child (PGK1 Detroit)
AU Zaidi, S Bagla, Y Ravindranath
Pediatric Hematology and Oncology 36 (5), 302-308, 2019
CD14/16 monocyte profiling in juvenile myelomonocytic leukemia
M Gadgeel, S Bagla, S Buck, M Shamoun, Y Ravindranath
Pediatric Blood & Cancer 67 (9), e28555, 2020
Neuroinflammatory nexus of pediatric epilepsy
S Bagla, AA Dombkowski
Journal of pediatric epilepsy 7 (02), 032-039, 2018
Defective monocyte plasticity and altered cAMP pathway characterize USB1‐mutated poikiloderma with neutropenia Clericuzio type
P Parajuli, DB Craig, M Gadgeel, S Bagla, RE Wright III, R Chu, ...
British Journal of Haematology 204 (2), 683-693, 2024
A novel finding in pediatric leiomyosarcoma: Expanding spectrum of FGFR rearrangements in childhood cancers
Y Persaud, S Bagla, C Shanti, B Shehata, Y Ravindranath, H Gorsi
Authorea Preprints, 2020
RUNX1 associated familial platelet disorder with myeloid malignancy (FPD-MM) in children: a novel new phenotype with juvenile and chronic myelomonocytic leukemia (JMML/CMML …
K Regling, S Bagla, AU Zaidi, E Wakeling, MC Chicka, L Flores, ...
Blood 132, 5504, 2018
Oryzocytosis: A Novel Morphological Variant of Hereditary Elliptocytosis Associated with a Novel Mutation in β-Spectrin (SPTB c154 C> T p. Arg52Trp)
A Glaros, M Gadgeel, S Bagla, S Buck, R Chu, Y Ravindranath, ...
Blood 134, 3509, 2019
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