| Infectivity and progression of COVID-19 based on selected host candidate gene variants GR Iyer, S Samajder, S Zubeda, V Mali, SK Pv, A Sharma, NZ Abbas, ... Frontiers in Genetics 11, 861, 2020 | 19 | 2020 |
| Pedigree and BRCA gene analysis in breast cancer patients to identify hereditary breast and ovarian cancer syndrome to prevent morbidity and mortality of disease in Indian … M Darooei, S Poornima, BU Salma, GR Iyer, AN Pujar, S Annapurna, ... Tumor Biology 39 (2), 1010428317694303, 2017 | 17 | 2017 |
| Familial acute necrotizing encephalopathy: evidence from next generation sequencing of digenic inheritance G Iyer, P Utage, S Bailur, A Utage, A Srirambhatla, Q Hasan Journal of Child Neurology 35 (6), 393-397, 2020 | 10 | 2020 |
| Rare disease advocacy groups and their significance in diagnosis, management, treatment, and prevention of rare diseases Y Bhattacharya, G Iyer, AP Kamireddy, S Poornima, KK Juturu, Q Hasan Rare diseases, 2019 | 5 | 2019 |
| A large-scale targeted proteomics of serum and tissue shows the utility of classifying high grade and low grade meningioma tumors A Halder, D Biswas, A Chauhan, A Saha, S Auromahima, D Yadav, ... Clinical Proteomics 20 (1), 41, 2023 | 4 | 2023 |
| Utility of next-generation sequencing in genetic testing and counseling of disorders involving the musculoskeletal system—trends observed from a single genetic unit GR Iyer, R Kumar, S Poornima, AP Kamireddy, KK Juturu, L Bhatnagar, ... Journal of Orthopaedic Surgery and Research 17 (1), 76, 2022 | 4 | 2022 |
| Rare Diseases ZH Wu BoD–Books on Demand, 2020 | 4 | 2020 |
| Expanding the clinico‐molecular spectrum of Angelman syndrome phenotype with the GABRG3 gene: Evidence from methylation and sequencing studies GR Iyer, P Utage, RR Devi, KK Vattam, Q Hasan Annals of Human Genetics 86 (2), 71-79, 2022 | 3 | 2022 |
| Alteration of methylation status in archival DNA samples: A qualitative assessment by methylation specific polymerase chain reaction GR Iyer, Q Hasan Environmental and Molecular Mutagenesis 61 (8), 837-842, 2020 | 3 | 2020 |
| Telegenetics aids the diagnosis of Hunter syndrome caused due to a novel IDS variant in rural India, during COVID-19 pandemic S Bajaj, S Thawani, G Iyer, PN Setty, M Kore, V Jadhav International Journal of Contemporary Pediatrics 9 (9), 851, 2022 | 1 | 2022 |
| Association of TGFβ1 gene polymorphisms with early onset primary knee osteoarthritis in south Indians: case-control study from a cosmopolitan city S Poornima, K Subramanyam, GR Iyer, M Darooei, S Daram, ... Austin Orthopedics 3 (1), 1007, 2018 | 1 | 2018 |
| Identifying Molecular Aetiology of Syndromic and Non syndromic Renal Disorders using Exome Analysis A Priya, S Kumar, GR Iyer, Q Hasan | | 2022 |
| GENETIC COUNSELING: Clinical and Laboratory Approach U Dave, D Shetty Jaypee Brothers Medical Publishers, 2021 | | 2021 |
| Pharmacogenomics to Drive COVID-19 Therapy for Best Outcome in a Low Resource Setting G Iyer, S Zubeda, AP Kamireddy, Q Hasan AIJR Preprints, 2020 | | 2020 |
| Importance of Phenotype-Genotype correlation for Next Generation Sequencing Data to diagnose Pediatric Neurological Disorders QH N Zainab Abbas, Prashant R Utage, Gayatri Rangarajan Iyer INTERNATIONAL JOURNAL OF HEALTH AND CLINICAL RESEARCH 3 (5), 67-73, 2020 | | 2020 |
| INTERNATIONAL SYMPOSIUM ON “GENOMICS IN HEALTH AND DISEASE” & 40TH ANNUAL CONFERENCE OF INDIAN SOCIETY OF HUMAN GENETICS F McElreavey | | |
| Interaction of Multiple Gene Variants Might Be Associated with Autism Spectrum Disorders Unraveled by Next Generation Sequencing Data S Bailur, A Rao, G Iyer, NZ Abbas, S Abirami, B Bhagwani, V Suresh, ... | | |
| Establishing Mutational Spectrum of Beta Thalassemia by Molecular Screening in a Low Resource Setting–Implications in Counseling and Prevention GR Iyer, AP Kamireddy, S Kondaveeti, S Jain, Q Hasan | | |
