Author: Lili Milani

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Preprints

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

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  • Site-wide: 1,777

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

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  • Site-wide: 1,107
  • In genetics: 26
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Genomewide association study identifies 30 loci associated with bipolar disorder

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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

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  • Site-wide: 2,395
  • In genetic and genomic medicine: 11
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  • Site-wide: 1,309

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

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  • Site-wide: 4,642
  • In genetics: 175
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  • Site-wide: 38,840
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Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

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  • Site-wide: 5,224
  • In psychiatry and clinical psychology: 19
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  • Site-wide: 1,980
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Genome-wide association study identifies 48 common genetic variants associated with handedness

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  • Site-wide: 5,992
  • In genetics: 249
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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  • Site-wide: 6,631
  • In genetics: 276
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Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease

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  • Site-wide: 8,982
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Cell specific eQTL analysis without sorting cells

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  • Site-wide: 9,220
  • In genetics: 385
• Year to date:
  • Site-wide: 145,239
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Genetic insights into the biological mechanisms governing human ovarian ageing

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  • In sexual and reproductive health: 10
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  • Site-wide: 1,720
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  • Site-wide: 1,315

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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  • Site-wide: 10,498
  • In genetics: 456
• Year to date:
  • Site-wide: 74,206
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Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

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  • In genetics: 578
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  • Site-wide: 4,574
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Genome-wide association studies identify 137 loci for DNA methylation biomarkers of ageing

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  • Site-wide: 14,430
  • In genetics: 650
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  • Site-wide: 8,559
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 113,596
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  • Site-wide: 94,727

Lifelong genetically lowered sclerostin and risk of cardiovascular disease.

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  • Site-wide: 17,755
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  • Site-wide: 70,887
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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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  • Site-wide: 17,955
  • In genomics: 1,730
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  • Site-wide: 113,882

Genomic and phenomic insights from an atlas of genetic effects on DNA methylation

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  • Site-wide: 21,119
  • In genetic and genomic medicine: 94
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  • Site-wide: 7,381
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Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions

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  • Site-wide: 23,764
  • In pharmacology and toxicology: 129
• Year to date:
  • Site-wide: 74,207
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  • Site-wide: 95,001

An epigenome-wide association study of educational attainment (n = 10,767)

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  • Site-wide: 25,318
  • In genetics: 1,132
• Year to date:
  • Site-wide: 110,741
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  • Site-wide: 94,388

An interaction map of circulating metabolites, immune gene networks and their genetic regulation

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  • Site-wide: 36,233
  • In genomics: 3,018
• Year to date:
  • Site-wide: 133,671
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  • Site-wide: 149,782

Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

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  • Site-wide: 37,451
  • In genetics: 1,663
• Year to date:
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Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy

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  • Site-wide: 50,784
  • In genetics: 2,222
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  • Site-wide: 63,416

Loss-of-function of MFGE8 and protection against coronary atherosclerosis

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  • Site-wide: 81,221
  • In cardiovascular medicine: 155
• Year to date:
  • Site-wide: 15,878
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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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  • Site-wide: 89,039
  • In genomics: 5,664
• Year to date:
  • Site-wide: 47,072
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  • Site-wide: 18,107

Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

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  • Site-wide: 117,924
  • In genetic and genomic medicine: 640
• Year to date:
  • Site-wide: 58,076
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  • Site-wide: 44,627

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

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  • Site-wide: 142,249
  • In genetic and genomic medicine: 823
• Year to date:
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  • Site-wide: 79,942

Mendelian randomization study of spermine oxidase and cancer risk

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  • Site-wide: 145,770
  • In genetic and genomic medicine: 864
• Year to date:
  • Site-wide: 105,329
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  • Site-wide: 115,472

The 1st year of the COVID-19 epidemic in Estonia: an interrupted time series of population based nationwide cross-sectional studies.

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  • Site-wide: 156,080
  • In infectious diseases: 6,188
• Year to date:
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  • Site-wide: 11,872