| 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 | 207 | 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 | 69 | 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 | 41 | 2008 |
| 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 | 27 | 2017 |
| 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 | 25 | 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 | 25 | 2018 |
| 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 | 23 | 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 | 17 | 2020 |
| 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 | 15 | 2021 |
| 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 | 15 | 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 | 14 | 2019 |
| 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 | 11 | 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 | 8 | 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 | 5 | 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 | 4 | 2020 |
| Neuroinflammatory nexus of pediatric epilepsy S Bagla, AA Dombkowski Journal of pediatric epilepsy 7 (02), 032-039, 2018 | 4 | 2018 |
| 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 | 3 | 2020 |
| 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, 2024 | 2 | 2024 |
| 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 | 1 | 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 | | 2019 |
Alan DombkowskiWayne State UniversityVerified email at wayne.edu
