Publications

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

Am J Hum Genet

Evaluation of pharmacological efficacy and safety of Hydroxyurea in sickle cell disease: Study of a pediatric cohort from Chhattisgarh, India

Pediatric Hematology and Oncology

Association of placental fatty acid desaturase 2 (FADS2) methylation with maternal fatty acid levels in women with preeclampsia

Prostaglandins, Leukotrienes and Essential Fatty Acids(Accepted)

Sexual dimorphism in the relationship between brain complexity, volume and general intelligence (g): a cross-cohort study

Scientific Reports

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Nat Genet. 2022 May;54(5):560-572. doi: 10.1038/s41588-022-01058-3. Epub 2022 May 12.

Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations

Commun Biol. 2022 May 5;5(1):441. doi: 10.1038/s42003-022-03404-x.

Identification of genetic effects underlying type 2 diabetes in South Asian and European populations

Commun Biol. 2022 Apr 7;5(1):329. doi: 10.1038/s42003-022-03248-5.

Environmentally sensitive hotspots in the methylome of the early human embryo

Elife. 2022 Feb 21;11:e72031. doi: 10.7554/eLife.72031.

Babies of South Asian and European Ancestry Show Similar Associations With Genetic Risk Score for Birth Weight Despite the Smaller Size of South Asian Newborns

Diabetes. 2022 Apr 1;71(4):821-836. doi: 10.2337/db21-0479.

DNA methylation signatures associated with cardiometabolic risk factors in children from India and The Gambia: results from the EMPHASIS study

Clin Epigenetics. 2022 Jan 9;14(1):6. doi: 10.1186/s13148-021-01213-3.