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Neonatology|November 7, 2013
Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosisRobert D Christensen, Roberto H Nussenzveig, N Scott Reading, et al.
Clinical Pediatrics|January 17, 2017
Three Novel Spectrin Variants in Jaundiced NeonatesRobert D Christensen, Archana M Agarwal, Hassan M Yaish, et al.
Leukemia & Lymphoma|October 1, 2015
Increased frequency of co-existing JAK2 exon-12 or MPL exon-10 mutations in patients with low JAK2(V617F) allelic burdenRoberto H Nussenzveig, Ha T Pham, Sherrie L Perkins, et al.
Antonie Van Leeuwenhoek|April 3, 2026
Microbiota-driven mechanisms in multisystem diseases: integrative evidence across cardiovascular, metabolic, neurological and autoimmune disordersSania Ansari, Ketan J Purohit, Ajay B Shelke, et al.
Journal of Biomaterials Science. Polymer Edition|December 28, 2021
Electrospun polysaccharide scaffolds: wound healing and stem cell differentiationPreethi G U, Unnikrishnan B S, Sreekutty J, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM|August 13, 2011
Diffuse large B-cell lymphoma with aberrant expression of the T-cell antigens CD2 and CD7Nikhil A Sangle, Archana M Agarwal, Kristi J Smock, et al.
Clinical Chemistry|May 2, 2019
Diagnosis of Hemoglobinopathy and β-Thalassemia by 21 Tesla Fourier Transform Ion Cyclotron Resonance Mass Spectrometry and Tandem Mass Spectrometry of Hemoglobin from BloodLidong He, Alan L Rockwood, Archana M Agarwal, et al.
BDJ Open|June 3, 2026
Awareness of oral health, hygiene practices, and chemotherapy-related oral manifestations among parents of pediatric oncology patientsVanshika Gandhi, Mansi Pal, Vathsala Patil, et al.
Molecular and Cellular Endocrinology|June 28, 2008
CRHR1-dependent effects on protein expression and posttranslational modification in AtT-20 cellsHelena C Kronsbein, Archana M Jastorff, Giuseppina Maccarrone, et al.
European Journal of Haematology|February 24, 2023
Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experienceArchana M Agarwal, Valarie McMurty, Adam L Clayton, et al.
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