| Comparative analyses of SAR-CoV2 genomes from different geographical locations and other coronavirus family genomes reveals unique features potentially consequential to host … R Sardar, D Satish, S Birla, D Gupta BioRxiv, 2020 | 125 | 2020 |
| Integrative analyses of SARS-CoV-2 genomes from different geographical locations reveal unique features potentially consequential to host-virus interaction, pathogenesis and … R Sardar, D Satish, S Birla, D Gupta Heliyon 6 (9), e04658, 2020 | 63 | 2020 |
| Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotype P Paliwal, A Sharma, S Birla, A Kriplani, R Khadgawat, A Sharma Molecular human reproduction 17 (6), 372-378, 2011 | 44 | 2011 |
| Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency N Verma, V Jain, S Birla, R Jain, A Sharma Journal of pediatric endocrinology and metabolism 25 (11-12), 1185-1190, 2012 | 38 | 2012 |
| Identification of novel PROP1 and POU1F1 mutations in patients with combined pituitary hormone deficiency S Birla, R Khadgawat, VP Jyotsna, V Jain, MK Garg, AS Bhalla, A Sharma Hormone and Metabolic Research 48 (12), 822-827, 2016 | 29 | 2016 |
| Screening Malaria-box compounds to identify potential inhibitors against SARS-CoV-2 Mpro, using molecular docking and dynamics simulation studies S Ahamad, H Kanipakam, S Birla, MS Ali, D Gupta European journal of pharmacology 890, 173664, 2021 | 26 | 2021 |
| Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiency S Birla, R Khadgawat, VP Jyotsna, V Jain, MK Garg, AS Bhalla, A Sharma Growth Hormone & IGF Research 29, 50-56, 2016 | 22 | 2016 |
| Novel MEN 1 gene findings in rare sporadic insulinoma—a case control study VP Jyotsna, E Malik, S Birla, A Sharma BMC endocrine disorders 15 (1), 1-6, 2015 | 17 | 2015 |
| Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 families S Yadav, S Birla, E Marumudi, A Sharma, R Khadgawat, ML Khurana, ... Indian journal of endocrinology and metabolism 19 (5), 644, 2015 | 14 | 2015 |
| Rare association of acromegaly with left atrial myxoma in Carney's complex due to novel PRKAR1A mutation S Birla, S Aggarwal, A Sharma, N Tandon Endocrinology, diabetes & metabolism case reports 2014 (1), 2014 | 14 | 2014 |
| Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation S Birla, R Singla, A Sharma, N Tandon The Indian journal of medical research 139 (5), 779, 2014 | 12 | 2014 |
| Classifying juvenile onset primary open angle glaucoma using cluster analysis S Birla, D Gupta, BI Somarajan, S Gupta, AK Chaurasia, A Kishan, ... British Journal of Ophthalmology 104 (6), 827-835, 2020 | 11 | 2020 |
| Mutations in membrane cofactor protein (CD46) gene in Indian children with hemolytic uremic syndrome P Khandelwal, S Birla, D Bhatia, M Puraswani, H Saini, A Sinha, P Hari, ... Clinical kidney journal 11 (2), 198-203, 2018 | 10 | 2018 |
| Dataset of mutational analysis, miRNAs targeting SARS-CoV-2 genes and host gene expression in SARS-CoV and SARS-CoV-2 infections R Sardar, D Satish, S Birla, D Gupta Data in brief 32, 106207, 2020 | 8 | 2020 |
| Characterization of a novel POU1F1 mutation identified on screening 160 growth hormone deficiency patients S Birla, P Vijayakumar, S Sehgal, S Bhatnagar, K Pallavi, A Sharma Hormone and Metabolic Research 51 (04), 248-255, 2019 | 8 | 2019 |
| Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucoma H Selvan, A Sharma, S Birla, S Gupta, BI Somarajan, V Gupta, A Sharma Indian journal of ophthalmology 67 (7), 1226, 2019 | 6 | 2019 |
| Latent Tuberculosis Infection Diagnosis among Household Contacts in a High Tuberculosis-Burden Area: a Comparison between Transcript Signature and Interferon Gamma Release Assay S Kaul, V Nair, S Birla, S Dhawan, S Rathore, V Khanna, S Lohiya, S Ali, ... Microbiology Spectrum 10 (2), e02445-21, 2022 | 5 | 2022 |
| MC4R Mutation in Early-onset Severe Childhood Obesity—Genotype–phenotype Correlation S Birla, D Khandelwal, A Sharma, R Khadgawat US Endocrinol 13, 69-71, 2017 | 3 | 2017 |
| Novel multiple endocrine neoplasia type 1 variations in patients with sporadic primary hyperparathyroidism S Birla, E Malik, VP Jyotsna, A Sharma Indian journal of endocrinology and metabolism 20 (4), 432, 2016 | 3 | 2016 |
| Genetic characterization of growth hormone 1 gene in patients with isolated growth hormone deficiency S Birla, PV Jyotsana, A Sharma, R Khadgawat, MK Garg, V Jain Indian journal of endocrinology and metabolism 16 (Suppl 2), S310, 2012 | 2 | 2012 |
Dinesh GuptaICGEBVerified email at icgeb.res.in
