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| 36632790 | Differential expression of genes influencing mitotic processes in cord blood mononuclear cells after a pre-conceptional micronutrient-based randomised controlled trial: Pune Rural Intervention in Young Adolescents (PRIYA). | | 2023 |
| 36226857 | Evaluation of pharmacological efficacy and safety of hydroxyurea in sickle cell disease: Study of a pediatric cohort from Chhattisgarh, India. | Pediatric Hematology and Oncology | 2023 |
| 37671428 | Genetic architecture of adiposity measures among Asians: Findings from GWAS. | | 2023 |
| 37660953 | Maternal-Periconceptional Vitamin B12 Deficiency in Wistar Rats Leads to Sex-Specific Programming for Cardiometabolic Disease Risk in the Next Generation. | | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 36517351 | The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitis. | Pancreatology | 2023 |
| 36708442 | Hypoxia Inducible Factors (HIF1α and HIF3α) are differentially methylated in preeclampsia placentae and are associated with birth outcomes. | | 2023 |
| 35061033 | 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. | | 2022 |
| 35773463 | Sexual dimorphism in the relationship between brain complexity, volume and general intelligence (g): a cross-cohort study. | Scientific Reports | 2022 |
| 35713545 | Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo. | Nucleic Acids Research | 2022 |
| 35393509 | Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. | Commun Biol | 2022 |
| 35513483 | Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. | Commun Biol | 2022 |
| 35872376 | Association of placental fatty acid desaturase 2 (FADS2) methylation with maternal fatty acid levels in women with preeclampsia. | | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 35188105 | Environmentally sensitive hotspots in the methylome of the early human embryo. | eLife | 2022 |
| 35000590 | DNA methylation signatures associated with cardiometabolic risk factors in children from India and The Gambia: results from the EMPHASIS study. | Clinical Epigenetics | 2022 |
| 34666849 | Size at birth, lifecourse factors, and cognitive function in late life: findings from the MYsore study of Natal effects on Ageing and Health (MYNAH) cohort in South India. | International Psychogeriatrics | 2021 |
| 33593789 | Protocol for a cluster randomised trial evaluating a multifaceted intervention starting preconceptionally-Early Interventions to Support Trajectories for Healthy Life in India (EINSTEIN): a Healthy Life Trajectories Initiative (HeLTI) Study. | BMJ Open | 2021 |
| 33471580 | Placental growth factor and Fms related tyrosine kinase-1 are hypomethylated in preeclampsia placentae. | Epigenomics | 2021 |
| 33876727 | Insights from a Pan India Sero-Epidemiological survey (Phenome-India Cohort) for SARS-CoV2. | Elife | 2021 |
| 33866136 | Rapid and accurate nucleobase detection using FnCas9 and its application in COVID-19 diagnosis. | Biosens Bioelectron | 2021 |
| 32528078 | Type 1 diabetes genetic risk score is discriminative of diabetes in non-Europeans: evidence from a study in India. | Scientific Reports | 2020 |
| 32380162 | Novel p.P298L SURF1 mutation in thiamine deficient Leigh syndrome patients compromises cytochrome c oxidase activity. | Mitochondrion | 2020 |
| 31995593 | Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach. | PLoS One | 2020 |
| 32541825 | Periconceptional environment predicts leukocyte telomere length in a cross-sectional study of 7-9 year old rural Gambian children. | Scientific Reports | 2020 |
| 31443707 | The REVAMP study: research exploring various aspects and mechanisms in preeclampsia: study protocol. | BMC Pregnancy and Childbirth | 2019 |
| 29360107 | Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2018 |
| 30027123 | Life course programming of stress responses in adolescents and young adults in India: Protocol of the Stress Responses in Adolescence and Vulnerability to Adult Non-communicable disease (SRAVANA) Study. | Wellcome Open Research | 2018 |
| 30195625 | Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians. | Blood Cells, Molecules, and Diseases | 2018 |
| 30137462 | Candidate genes linking maternal nutrient exposure to offspring health via DNA methylation: a review of existing evidence in humans with specific focus on one-carbon metabolism. | International Journal of Epidemiology | 2018 |
| 29135286 | Vitamin B supplementation influences methylation of genes associated with Type 2 diabetes and its intermediate traits. | Epigenomics | 2018 |
| 29583017 | Identification and characterization of cis-regulatory elements 'insulator and repressor' in PPARD gene. | Epigenomics | 2018 |
| 28209604 | Birth size, risk factors across life and cognition in late life: protocol of prospective longitudinal follow-up of the MYNAH (MYsore studies of Natal effects on Ageing and Health) cohort. | BMJ Open | 2017 |
| 28556356 | Identification of a functional enhancer variant within the chronic pancreatitis-associated SPINK1 c.101A>G (p.Asn34Ser)-containing haplotype. | Hum Mutat | 2017 |
| 28341696 | A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. | Diabetes | 2017 |
| 28334792 | GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians. | Human Molecular Genetics | 2017 |
| 28751670 | Inclusion of Population-specific Reference Panel from India to the 1000 Genomes Phase 3 Panel Improves Imputation Accuracy. | Sci Rep | 2017 |
| 28617183 | Hypermethylated CpG sites in the MTR gene promoter in preterm placenta. | Epigenomics | 2017 |
| 28481999 | GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians. | Human Molecular Genetics | 2017 |
| 29257133 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2017 |
| 27942176 | Identification of urinary proteins potentially associated with diabetic kidney disease. | Indian J Nephrol | 2016 |
| 26784911 | Association Analysis of PRSS1-PRSS2 and CLDN2-MORC4 Variants in Nonalcoholic Chronic Pancreatitis Using Tropical Calcific Pancreatitis as Model. | Pancreas | 2016 |
| 26946345 | No Association Between CEL-HYB Hybrid Allele and Chronic Pancreatitis in Asian Populations. | Gastroenterology | 2016 |
| 26902699 | Lack of replication of association of THSD7A with obesity. | International Journal of Obesity | 2016 |
| 27398621 | The genetic architecture of type 2 diabetes. | Nature | 2016 |
| 25982389 | Maternal micronutrient deficiency leads to alteration in the kidney proteome in rat pups. | Journal of Proteomics | 2015 |
| 26131930 | Directional dominance on stature and cognition in diverse human populations. | Nature | 2015 |
| 26349437 | Intrauterine Programming of Diabetes and Adiposity. | Current obesity reports | 2015 |
| 26300908 | New insights from monogenic diabetes for "common" type 2 diabetes. | Frontiers in Genetics | 2015 |
| 24641884 | FTO gene variant and risk of hypertension: a meta-analysis of 57,464 hypertensive cases and 41,256 controls. | Metabolism: Clinical and Experimental | 2014 |