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Journal of Reproduction & Infertility|May 7, 2019
Determining the Cause of Recurrent Miscarriages in a Couple: Importance of NOR in the Era of NGSUsha R Dutta, Venugopala Swamy, Rajitha Ponnala, et al.Journal of Clinical and Diagnostic Research : JCDR|December 4, 2013
Effect of Deep Cervical Flexor Training vs. Conventional Isometric Training on Forward Head Posture, Pain, Neck Disability Index In Dentists Suffering from Chronic Neck PainBhuvan Deep Gupta, Shagun Aggarwal, Bharat Gupta, et al.Annals of African Medicine|February 15, 2024
Comparison of three scoring criteria to assess recovery from general anesthesia in the postanesthesia care unit in the indian populationShagun Aggarwal, Julie C R Misquith, Sumesh T Rao, et al.Molecular Syndromology|June 14, 2019
Co-Occurrence of Leber Congenital Amaurosis and Meckel Syndrome Type 1 in a Fetus: Is There a Lesson to Be Learned?Karthik Tallapaka, Shagun Aggarwal, Amrita Bhattacherjee, et al.Prenatal Diagnosis|November 21, 2022
Prenatal phenotype of FBXL4-associated encephalomyopathic mitochondrial DNA depletion syndrome-13Neelam Saini, Venkatapuram Vijayasree, Eshwar Chandra Nandury, et al.Current Pharmaceutical Design|October 18, 2024
PARP Pioneers: Using BRCA1/2 Mutation-targeted Inhibition to Revolutionize Breast Cancer TreatmentNavneet Sharma, Akash Bhati, Shagun Aggarwal, et al.Journal of Orthopaedic Case Reports|June 15, 2016
Identical Twins with Infantile Systemic Hyalinosis: Case study and review of literatureMaheshwar Lakkireddyl Shagun Aggarwal, Vijaykrishna Chilakamarri, Vasundhara S Chennuri, et al.The Indian Journal of Medical Research|October 9, 2012
Aetiologic spectrum of mental retardation & developmental delay in IndiaShagun Aggarwal, Vijay Raju Bogula, Kausik Mandal, et al.Journal of Human Genetics|November 22, 2018
Homozygous PCDH12 variants result in phenotype of cerebellar ataxia, dystonia, retinopathy, and dysmorphismVenugopal S Vineeth, Aneek Das Bhowmik, Surya Balakrishnan, et al.Molecular Vision|June 3, 2011
Run-on mutation in the PAX6 gene and chorioretinal degeneration in autosomal dominant aniridiaShagun Aggarwal, Worapoj Jinda, Chanin Limwongse, et al.Pageof 8