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Author: Grant W. Montgomery

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    • bioinformatics: 3,118 (rank: 2,998 out of 31,200)
    • genetics: 54,721 (rank: 58 out of 33,861)
    • genomics: 10,860 (rank: 1,237 out of 39,037)

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Preprints

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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Genome-wide association analysis of lifetime cannabis use (N=184,765) identifies new risk loci, genetic overlap with mental health, and a causal influence of schizophrenia on cannabis use

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Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

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Genomewide association study identifies 30 loci associated with bipolar disorder

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The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

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GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

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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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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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Widespread signatures of negative selection in the genetic architecture of human complex traits

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Genotype-free demultiplexing of pooled single-cell RNA-seq

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Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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

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Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

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Improved prediction of chronological age from DNA methylation limits it as a biomarker of ageing

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

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Identification of 55,000 Replicated DNA Methylation QTL

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The genetic architecture of sporadic and recurrent miscarriage

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Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

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Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

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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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Constraints on eQTL fine mapping in the presence of multi-site local regulation of gene expression

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The Anorexia Nervosa Genetics Initiative: Overview and Methods

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The effect of X-linked dosage compensation on complex trait variation

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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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Rare Genetic Variants Underlie Outlying levels of DNA Methylation and Gene-Expression

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