User profiles for T. Lehtimäki

Lehtimaki T

- Verified email at tuni.fi - Cited by 232359

Tuula Lehtimäki

- Verified email at oulu.fi - Cited by 1016

Analysis of shared heritability in common disorders of the brain

…, C Ran, SD Gordon, G Borck, HHH Adams, T Lehtimäki… - Science, 2018 - science.org
INTRODUCTION Brain disorders may exhibit shared symptoms and substantial epidemiological
comorbidity, inciting debate about their etiologic overlap. However, detailed study of …

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

…, S Männistö, MM Perälä, M Kähönen, T Lehtimäki… - Molecular …, 2015 - nature.com
Coffee, a major dietary source of caffeine, is among the most widely consumed beverages in
the world and has received considerable attention regarding health risks and benefits. We …

Networks for the commercialization of innovations: A review of how divergent network actors contribute

L Aarikka-Stenroos, B Sandberg, T Lehtimäki - Industrial Marketing …, 2014 - Elsevier
Successful commercialization is of great importance to innovative firms, and the recent literature
has increasingly acknowledged that networks make a contribution not only to research …

[PDF][PDF] Common variant burden contributes to the familial aggregation of migraine in 1,589 families

…, C Kubisch, M Kurki, T Kurth, L Launer, T Lehtimaki… - Neuron, 2018 - cell.com
Complex traits, including migraine, often aggregate in families, but the underlying genetic
architecture behind this is not well understood. The aggregation could be explained by rare, …

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

…, H Prokisch, H Ahsan, BL Pierce, T Lehtimäki… - Nature …, 2021 - nature.com
Trait-associated genetic variants affect complex phenotypes primarily via regulatory mechanisms
on the transcriptome. To investigate the genetics of gene expression, we performed cis…

Strong association of de novo copy number mutations with autism

…, J Hicks, SJ Spence, AT Lee, K Puura, T Lehtimäki… - Science, 2007 - science.org
We tested the hypothesis that de novo copy number variation (CNV) is associated with autism
spectrum disorders (ASDs). We performed comparative genomic hybridization (CGH) on …

Synaptic, transcriptional and chromatin genes disrupted in autism

…, SM Klauck, A Kolevzon, I Lee, J Lei, T Lehtimäki… - Nature, 2014 - nature.com
The genetic architecture of autism spectrum disorder involves the interplay of common and
rare variants and their impact on hundreds of genes. Using exome sequencing, here we …

[PDF][PDF] Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

…, A Kolevzon, I Kushima, SL Lee, T Lehtimäki… - Cell, 2020 - cell.com
We present the largest exome sequencing study of autism spectrum disorder (ASD) to date (n
= 35,584 total samples, 11,986 with ASD). Using an enhanced analytical framework to …

Integrative approaches for large-scale transcriptome-wide association studies

…, M Alvarez, M Civelek, AJ Lusis, T Lehtimäki… - Nature …, 2016 - nature.com
Many genetic variants influence complex traits by modulating gene expression, thus altering
the abundance of one or multiple proteins. Here we introduce a powerful strategy that …

Genetic analysis for a shared biological basis between migraine and coronary artery disease

…, D Chasman, T Kurth, M Schuerks, T Lehtimaki… - Neurology …, 2015 - AAN Enterprises
… Terho Lehtimäki reports no disclosures. Ruth McPherson has served on the editorial board
of Arteriosclerosis, Thrombosis & Vascular Biology; and has received research support from …