Author: Najaf Amin

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Preprints

Genetic analysis of mitochondrial DNA copy number and associated traits identifies loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation, and reveals a causal association of mitochondrial function with mortality

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New insights on the genetic etiology of Alzheimer and related dementia

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Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

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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 Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

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Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

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Genetic studies of accelerometer-based sleep measures in 85,670 individuals yield new insights into human sleep behaviour

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Exome sequencing identifies novel AD-associated genes.

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Genetic Association Study of Childhood Aggression across raters, instruments and age

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer's Disease Sequencing Project

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Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness

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Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants

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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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Genome-wide association study of plasma triglycerides, phospholipids and relation to cardio-metabolic risk factors

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Relationship between gut microbiota and circulating metabolites in population-based cohorts

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Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

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Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities

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Novel DNA methylation sites of glucose and insulin homeostasis: an integrative cross-omics analysis

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Effect of inbreeding on type 2 diabetes-related metabolites in a Dutch genetic isolate

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Recessive genetic effects on type 2 diabetes-related metabolites in a consanguineous population

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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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