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Anu Aggarwal
Anu Aggarwal
Postdoctoral Fellow, Cleveland Clinic
Verified email at ccf.org
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Cited by
Year
SARS-CoV-2 receptors are expressed on human platelets and the effect of aspirin on clinical outcomes in COVID-19 patients
A Sahai, R Bhandari, M Koupenova, JE Freedman, M Godwin, T McIntyre, ...
Research square, 2020
442020
Effect of aspirin on short-term outcomes in hospitalized patients with COVID-19
A Sahai, R Bhandari, M Godwin, T McIntyre, MK Chung, JP Iskandar, ...
Vascular Medicine 26 (6), 626-632, 2021
322021
Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next‐generation sequencing: First South Asian study
A Aggarwal, M Jamwal, P Sharma, MUS Sachdeva, D Bansal, P Malhotra, ...
British Journal of Haematology 188 (5), 784-795, 2020
292020
A comparative evaluation of Eosin‐5′‐maleimide flow cytometry reveals a high diagnostic efficacy for hereditary spherocytosis
P Joshi, A Aggarwal, M Jamwal, MUS Sachdeva, D Bansal, P Malhotra, ...
International Journal of Laboratory Hematology 38 (5), 520-526, 2016
272016
Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc. 1040G> A (p. Arg347His) causing hemolysis in an Indian infant
M Jamwal, A Aggarwal, A Das, A Maitra, P Sharma, S Krishnan, N Arora, ...
Clinica chimica acta 468, 81-84, 2017
262017
Optimal reference gene selection for expression studies in human reticulocytes
A Aggarwal, M Jamwal, GK Viswanathan, P Sharma, MUS Sachdeva, ...
The Journal of Molecular Diagnostics 20 (3), 326-333, 2018
232018
Next-generation sequencing–based diagnosis of unexplained inherited hemolytic anemias reveals wide genetic and phenotypic heterogeneity
M Jamwal, A Aggarwal, A Palodhi, P Sharma, D Bansal, A Trehan, ...
The Journal of Molecular Diagnostics 22 (4), 579-590, 2020
202020
Platelet olfactory receptor activation limits platelet reactivity and growth of aortic aneurysms
CN Morrell, D Mix, A Aggarwal, R Bhandari, M Godwin, P Owens, ...
The Journal of clinical investigation 132 (9), 2022
192022
Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases
M Jamwal, A Aggarwal, V Kumar, P Sharma, MUS Sachdeva, D Bansal, ...
Clinica Chimica Acta 458, 51-54, 2016
192016
Restoring function after severe spinal cord injury through bioluminescent-optogenetics
ED Petersen, ED Sharkey, A Pal, LO Shafau, J Zenchak-Petersen, ...
Frontiers in neurology 12, 792643, 2022
172022
A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non‐spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple Isoforms.
M Jamwal, A Aggarwal, A Palodi, P Sharma, D Bansal, A Maitra, R Das
British Journal of Haematology 186 (5), 2019
132019
First report of Mediterranean stomatocytosis/macrothrombocytopenia in an Indian family: a diagnostic dilemma
M Jamwal, A Aggarwal, A Maitra, P Sharma, D Bansal, A Trehan, ...
Pathology 49 (7), 811-815, 2017
122017
Platelets at the vessel wall in non-thrombotic disease
A Aggarwal, CL Jennings, E Manning, SJ Cameron
Circulation Research 132 (6), 775-790, 2023
112023
Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation
M Jamwal, A Aggarwal, MUS Sachdeva, P Sharma, P Malhotra, A Maitra, ...
Journal of Clinical Pathology 71 (7), 648-652, 2018
112018
Congenital dyserythropoietic anemia type IV with high fetal hemoglobin caused by heterozygous KLF1 p. Glu325Lys: first report in an Indian infant
M Jamwal, A Aggarwal, P Sharma, D Bansal, R Das
Annals of Hematology 100, 281-283, 2021
82021
Sex-dependent effect of platelet nitric oxide: production and platelet reactivity in healthy individuals
MD Godwin, A Aggarwal, Z Hilt, S Shah, J Gorski, SJ Cameron
Basic to Translational Science 7 (1), 14-25, 2022
72022
Restoring function after severe spinal cord injury through bioluminescence-driven optogenetics
ED Petersen, ED Sharkey, A Pal, LO Shafau, JR Zenchak, AJ Peña, ...
bioRxiv, 710194, 2019
42019
Phenotypic and genetic heterogeneity arising from a novel substitution at amino acid position Val205 in GATA1 related X-linked thrombocytopenia with dyserythropoietic anemia.
M Jamwal, A Aggarwal, P Sharma, D Bansal, A Maitra, R Das
Blood Cells, Molecules & Diseases 81, 102391-102391, 2019
32019
Spectrum of Genetic Defects and Phenotype-Genotype Correlation in Dyserythropoietic Anemias: Bench to Bedside Approach in the Indian Scenario
R Das, M Jamwal, A Aggarwal, P Sharma, MUS Sachdeva, D Bansal, ...
Blood 134, 950, 2019
22019
Dysregulated platelet function in patients with postacute sequelae of COVID-19
A Aggarwal, TK Singh, M Pham, M Godwin, R Chen, TM McIntyre, ...
Vascular Medicine, 1358863X231224383, 2024
12024
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