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Cureus|December 30, 2020
Occult Nodal Metastasis in Oral Cavity CancersAsif Ali Arain, Muhammad Shaheryar Ahmed Rajput, Shakil Akhtar Ansari, et al.Hemoglobin|January 10, 2013
Spectrum of α-thalassemia mutations in transfusion-dependent β-thalassemia patients from the Eastern Province of Saudi ArabiaMohammed Shakil Akhtar, Fuad Qaw, J Francis Borgio, et al.Pediatric Nephrology (Berlin, Germany)|April 8, 2024
Antineutrophil cytoplasmic antibody in children with nephrotic syndrome treated with levamisole: a cross-sectional cohort studyRajiv Sinha, Subhankar Sarkar, Sushmita Banerjee, et al.Pediatric Nephrology (Berlin, Germany)|December 27, 2024
Single (375 mg/m2) vs. double dose of rituximab along with mycophenolate mofetil for children with steroid-dependent/frequently relapsing nephrotic syndrome: a multicentre open-label randomized controlled trialRajiv Sinha, Subal Pradhan, Sumantra Raut, et al.Human Genomics|March 4, 2016
The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi ArabiansCyril Cyrus, Chittibabu Vatte, Awatif Al-Nafie, et al.Clinical Rheumatology|July 16, 2025
Clinical presentation of children with lupus nephritis from a low- and middle-income country (LMIC): an initial report from the Indian pSLE Nephritis RegistrySanjukta Poddar, Deblina Dasgupta, Subal Pradhan, et al.Oncology Letters|August 13, 2019
Helical and kinase domain mutations of PIK3CA, and their association with hormone receptor expression in breast cancerChittibabu Vatte, Ali Mohammed Al Amri, Cyril Cyrus, et al.Archives of Medical Science : AMS|March 20, 2020
Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patientsSumayh A Aldakeel, Neda Z Ghanem, Amani M Al-Amodi, et al.Pediatric Nephrology (Berlin, Germany)|January 10, 2022
Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene StudyRajiv Sinha, Subal Pradhan, Sushmita Banerjee, et al.Current Medical Research and Opinion|February 1, 2018
Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT)Amani M Al-Amodi, Neda Z Ghanem, Sumayh A Aldakeel, et al.Pageof 3