S. Birla

发表

Comparative analyses of SAR-CoV2 genomes from different geographical locations and other coronavirus family genomes reveals unique features potentially consequential to host-virus interaction and pathogenesis

D. Gupta, Rahila Sardar, D. Satish, 2020, bioRxiv.

Classifying juvenile onset primary open angle glaucoma using cluster analysis

D. Gupta, Viney Gupta, B. I. Somarajan, 2019, British Journal of Ophthalmology.

Integrative analyses of SARS-CoV-2 genomes from different geographical locations reveal unique features potentially consequential to host-virus interaction, pathogenesis and clues for novel therapies

D. Gupta, Rahila Sardar, D. Satish, 2020, Heliyon.

Y cell line in a turner mosaic: a case report

Anshul Sharma, Arundhati Sharma, S. Birla, 2012 .

MC4R Mutation in Early-onset Severe Childhood Obesity—Genotype–phenotype Correlation

R. Khadgawat, Arundhati Sharma, S. Birla, 2017 .

Latent Tuberculosis Infection Diagnosis among Household Contacts in a High Tuberculosis-Burden Area: a Comparison between Transcript Signature and Interferon Gamma Release Assay

D. Gupta, Shakir Ali, A. Khanna, 2022, Microbiology spectrum.

Impact of a novel 14 bp MEN1 deletion in a patient with hyperparathyroidism and gastrinoma

M. Tripathi, Arundhati Sharma, R. Singla, 2015, Endocrinology, diabetes & metabolism case reports.

Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiency.

A. Bhalla, R. Khadgawat, V. Jain, 2016, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Novel multiple endocrine neoplasia type 1 variations in patients with sporadic primary hyperparathyroidism

A. Sharma, S. Birla, V. Jyotsna, 2016, Indian journal of endocrinology and metabolism.

Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 families

R. Khadgawat, Arundhati Sharma, A. Ammini, 2015, Indian journal of endocrinology and metabolism.

Screening Malaria-box compounds to identify potential inhibitors against SARS-CoV-2 Mpro, using molecular docking and dynamics simulation studies

D. Gupta, Shahzaib Ahamad, S. Birla, 2020, European Journal of Pharmacology.

Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotype.

R. Khadgawat, A. Kriplani, P. Paliwal, 2011, Molecular human reproduction.

Genetic characterization of growth hormone 1 gene in patients with isolated growth hormone deficiency

R. Khadgawat, V. Jain, Arundhati Sharma, 2012, Indian journal of endocrinology and metabolism.

Rare association of acromegaly with left atrial myxoma in Carney's complex due to novel PRKAR1A mutation

N. Tandon, S. Aggarwal, Arundhati Sharma, 2014, Endocrinology, diabetes & metabolism case reports.

Identification of Novel PROP1 and POU1F1 Mutations in Patients with Combined Pituitary Hormone Deficiency

A. Bhalla, R. Khadgawat, A. Sharma, 2016, Hormone and Metabolic Research.

Deep learning based models to study the effect of glaucoma genes on angle dysgenesis in-vivo

K. Mahalingam, S. Gupta, S. Birla, 2021, medRxiv.

Mutations in membrane cofactor protein (CD46) gene in Indian children with hemolytic uremic syndrome

A. Sinha, A. Bagga, D. Bhatia, 2017, Clinical kidney journal.

Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucoma

Viney Gupta, H. Selvan, Arundhati Sharma, 2019, Indian journal of ophthalmology.

Novel MEN 1 gene findings in rare sporadic insulinoma—a case control study

Arundhati Sharma, S. Birla, V. Jyotsna, 2015, BMC Endocrine Disorders.

Characterization of a Novel POU1F1 Mutation Identified on Screening 160 Growth Hormone Deficiency Patients

S. Bhatnagar, Shilpi Sehgal, Arundhati Sharma, 2019, Hormone and Metabolic Research.

Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency

N. Verma, R. Jain, V. Jain, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation

N. Tandon, Arundhati Sharma, R. Singla, 2014, The Indian journal of medical research.

In vivo identification of angle dysgenesis and its relation to genetic markers associated with glaucoma using artificial intelligence

S. Birla, Abhishek Singh, T. Varshney, 2023, Indian journal of ophthalmology.

Machine learning-assisted prediction of trabeculectomy outcomes among patients of juvenile glaucoma by using 5-year follow-up data

S. Birla, Abhishek Singh, T. Varshney, 2024, Indian journal of ophthalmology.