Author details

Full Name

Anubha Mahajan

Affiliation

ORCID

Career Start Year

2004

Papers

162

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
37604891	Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits.	Nat Commun	2023
37749248	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.	Nat Genet	2023
37585454	Multi-ancestry GWAS analysis identifies two novel loci associated with diabetic eye disease and highlights APOL1 as a high risk locus in patients with diabetic macular edema.	PLoS Genet	2023
37787550	Central Adiposity Increases Risk of Kidney Stone Disease through Effects on Serum Calcium Concentrations.		2023
37130959	Author Correction: Discovery of drug-omics associations in type 2 diabetes with generative deep-learning models.	Nat Biotechnol	2023
37012456	Genetic effects on the timing of parturition and links to fetal birth weight.	Nat Genet	2023
36862161	The utility of a type 2 diabetes polygenic score in addition to clinical variables for prediction of type 2 diabetes incidence in birth, youth and adult cohorts in an Indigenous study population.		2023
36528349	Pharmacogenomics of GLP-1 receptor agonists: a genome-wide analysis of observational data and large randomised controlled trials.		2023
35106505	Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: An IMI DIRECT study.	Cell Rep Med	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
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
36333282	The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians.	Nature Communications	2022
35421386	Evaluating human genetic support for hypothesized metabolic disease genes.		2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
34480422	The genomics of heart failure: design and rationale of the HERMES consortium.	ESC Heart Fail	2021
34233929	Profiles of Glucose Metabolism in Different Prediabetes Phenotypes, Classified by Fasting Glycemia, 2-Hour OGTT, Glycated Hemoglobin, and 1-Hour OGTT: An IMI DIRECT Study.	Diabetes	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
33830302	Analysis of overlapping genetic association in type 1 and type 2 diabetes.	Diabetologia	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
33184701	Correction to: The role of physical activity in metabolic homeostasis before and after the onset of type 2 diabetes: an IMI DIRECT study.	Diabetologia	2021
32944759	Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity.	Journal of Clinical Endocrinology and Metabolism	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
33323478	Processes Underlying Glycemic Deterioration in Type 2 Diabetes: An IMI DIRECT Study.	Diabetes Care	2021
34746691	Type 2 diabetes sex-specific effects associated with E167K coding variant in .	iScience	2021
34729547	Effects of apolipoprotein B on lifespan and risks of major diseases including type 2 diabetes: a mendelian randomisation analysis using outcomes in first-degree relatives.	Lancet Healthy Longev	2021
31462703	Elevated risk of invasive group A streptococcal disease and host genetic variation in the human leucocyte antigen locus.	Genes Immun	2020
32002573	The role of physical activity in metabolic homeostasis before and after the onset of type 2 diabetes: an IMI DIRECT study.	Diabetologia	2020
32345654	Early Metabolic Features of Genetic Liability to Type 2 Diabetes: Cohort Study With Repeated Metabolomics Across Early Life.	Diabetes Care	2020
31985400	Deep learning models predict regulatory variants in pancreatic islets and refine type 2 diabetes association signals.	eLife	2020
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
32493999	RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro.	Nat Commun	2020
33261667	Whole blood co-expression modules associate with metabolic traits and type 2 diabetes: an IMI-DIRECT study.	Genome Med	2020
32826294	Large-Scale Analyses Provide No Evidence for Gene-Gene Interactions Influencing Type 2 Diabetes Risk.		2020
33253307	Post-load glucose subgroups and associated metabolic traits in individuals with type 2 diabetes: An IMI-DIRECT study.	PLoS One	2020
33186544	A Multi-omic Integrative Scheme Characterizes Tissues of Action at Loci Associated with Type 2 Diabetes.	Am J Hum Genet	2020
32691046	Fine-scale population structure in the UK Biobank: implications for genome-wide association studies.	Hum Mol Genet	2020
32910913	Unsupervised Clustering of Missense Variants in HNF1A Using Multidimensional Functional Data Aids Clinical Interpretation.	Am J Hum Genet	2020
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
32559194	Predicting and elucidating the etiology of fatty liver disease: A machine learning modeling and validation study in the IMI DIRECT cohorts.	PLoS Med	2020
32999275	Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D.	Nat Commun	2020
31322649	Genetic Risk Scores for Diabetes Diagnosis and Precision Medicine.	Endocrine Reviews	2019
31647808	Causal relationships between obesity and the leading causes of death in women and men.	PLoS Genetics	2019
31821322	Homogeneity in the association of body mass index with type 2 diabetes across the UK Biobank: A Mendelian randomization study.	PLoS Med	2019
31805045	Correction:Â Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.	PLoS Genet	2019
30604766	Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.	Nat Commun	2019
30352878	Genome-Wide and Abdominal MRI Data Provide Evidence That a Genetically Determined Favorable Adiposity Phenotype Is Characterized by Lower Ectopic Liver Fat and Lower Risk of Type 2 Diabetes, Heart Disease, and Hypertension.		2019
31491410	Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.	Am J Hum Genet	2019
30914061	Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data.	Genome Medicine	2019