Author: Anubha Mahajan

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Preprints

A reference panel of 64,976 haplotypes for genotype imputation

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data

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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

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Influence of genetic variants on gene expression in human pancreatic islets – implications for type 2 diabetes

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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

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Large-Scale Genome-Wide Meta Analysis of Polycystic Ovary Syndrome Suggests Shared Genetic Architecture for Different Diagnosis Criteria.

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Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci

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Causal relationships between obesity and the leading causes of death in women and men

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Deep learning models predict regulatory variants in pancreatic islets and refine type 2 diabetes association signals

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Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

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Meta-analysis of exome array data identifies six novel genetic loci for lung function

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Variation in the plasma membrane monoamine transporter (PMAT, encoded in SLC29A4) and organic cation transporter 1 (OCT1, encoded in SLC22A1) and gastrointestinal intolerance to metformin in type 2 diabetes: an IMI DIRECT study

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Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: an overview of the data from the epidemiological studies within the IMI DIRECT Consortium

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Elevated risk of invasive group A streptococcal disease and host genetic variation in the human leukocyte antigen locus

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Multifaceted genome-wide study identifies novel regulatory loci for body mass index in Indians

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