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Authors whose works are in public domain in at least one jurisdiction

List of works by Lili Milani

51-100 of 165 results

A common 16p11.2 inversion underlies the joint susceptibility to asthma and obesity

scientific article published on 20 February 2014

Genetic evidence of assortative mating in humans

scholarly article

Genome-wide genetic homogeneity between sexes and populations for human height and body mass index

scientific article published on 22 October 2015

DNA methylation analysis of bone marrow cells at diagnosis of acute lymphoblastic leukemia and at remission

scientific article

Pharmacogenomic Biomarkers for Improved Drug Therapy-Recent Progress and Future Developments

scientific article published on 27 November 2017

In-solution hybrid capture of bisulfite-converted DNA for targeted bisulfite sequencing of 174 ADME genes

scientific article

A genome-wide association study of early menopause and the combined impact of identified variants

scientific article published on 9 January 2013

An epigenome-wide association study meta-analysis of educational attainment.

scientific article

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

scientific article

Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells

scientific article

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

scientific article published on 28 December 2016

Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649).

scientific article

Epigenetic profiling in CD4+ and CD8+ T cells from Graves' disease patients reveals changes in genes associated with T cell receptor signaling

scientific article published on 09 October 2015

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

scholarly article published 19 October 2018

A missense mutation in DUSP6 is associated with Class III malocclusion

scientific article published on 21 August 2013

Sequence variation in nuclear ribosomal small subunit, internal transcribed spacer and large subunit regions of Rhizophagus irregularis and Gigaspora margarita is high and isolate-dependent

scientific article published on 19 April 2016

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

scientific article published on 24 March 2017

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

scientific article published on 23 November 2016

A genetics-led approach defines the drug target landscape of 30 immune-related traits

scientific article published on 28 June 2019

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

article

CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs

scientific article

Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions

scientific article published on 16 October 2018

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

scientific article published on 18 June 2018

The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects

scientific article published in June 2015

CpG sites associated with NRP1, NRXN2 and miR-29b-2 are hypomethylated in monocytes during ageing

scientific article published on 09 January 2014

Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies

scientific article

Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the good

scientific article published on 27 August 2019

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

DNA breaks and chromatin structural changes enhance the transcription of autoimmune regulator target genes

scientific article published on 27 February 2017

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

scientific article published on 19 December 2017

Single base resolution analysis of 5-hydroxymethylcytosine in 188 human genes: implications for hepatic gene expression

scientific article published on 29 April 2016

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

scientific article published in October 2016

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

scientific article

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

scientific article

Occupational irritants and asthma: an Estonian cross-sectional study of 34,000 adults

scientific article

Whole-genome expression analysis reveals genes associated with treatment response to escitalopram in major depression

scientific article published on 22 July 2016

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

Detection of alternatively spliced transcripts in leukemia cell lines by minisequencing on microarrays

scientific article published on 29 December 2005

The effect of LRRK2 loss-of-function variants in humans

scientific article published on 27 May 2020

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

IgG glycosylation and DNA methylation are interconnected with smoking

scientific article

Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants

scientific article published on 9 August 2017

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 16 March 2018

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

scientific article published on 30 March 2015

Expression of BCR–ABL1 oncogene relative to ABL1 gene changes overtime in chronic myeloid leukemia

article

Rare coding variants in ten genes confer substantial risk for schizophrenia

article

Neuregulin signaling pathway in smoking behavior

scientific article published on 22 August 2017

Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant

scientific article published on 18 July 2018

A distinctive DNA methylation pattern in insufficient sleep

scientific article published in Scientific Reports