Author details

Full Name

Taru Tukiainen

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
38089550	Marked difference in liver fat measured by histology magnetic resonance-proton density fat fraction: A meta-analysis.		2024
36653477	Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.		2023
36653562	FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	2023
36829046	Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.	Nature	2023
36193934	Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids.	J Am Heart Assoc	2022
33249422	High-resolution population-specific recombination rates and their effect on phasing and genotype imputation.	European Journal of Human Genetics	2021
33948567	Molecular pathways behind acquired obesity: Adipose tissue and skeletal muscle multiomics in monozygotic twin pairs discordant for BMI.	Cell Rep Med	2021
33977140	WGS and RNA Studies Diagnose Noncoding <i>DMD</i> Variants in Males With High Creatine Kinase.	Neurol Genet	2021
32154731	Polygenic Hyperlipidemias and Coronary Artery Disease Risk.	Circ Genom Precis Med	2020
30895940	A recurrent COL6A1 pseudoexon insertion causes muscular dystrophy and is effectively targeted by splice-correction therapies.	JCI Insight	2019
31792362	LIN28B affects gene expression at the hypothalamic-pituitary axis and serum testosterone levels.	Scientific Reports	2019
30196135	Transient modification of lin28b expression - Permanent effects on zebrafish growth.	Molecular and Cellular Endocrinology	2019
29517003	Corrigendum: Landscape of X chromosome inactivation across human tissues.	Nature	2018
28235613	Impaired hepatic lipid synthesis from polyunsaturated fatty acids in TM6SF2 E167K variant carriers with NAFLD.	J Hepatol	2017
28910285	Correction: Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study.	PLoS Genet	2017
28424332	Improving genetic diagnosis in Mendelian disease with transcriptome sequencing.	Sci Transl Med	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
28838971	A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes.	Diabetes	2017
29022598	Landscape of X chromosome inactivation across human tissues.	Nature	2017
29237677	Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population.	Circ Cardiovasc Genet	2017
27535533	Analysis of protein-coding genetic variation in 60,706 humans.	Nature	2016
27005778	Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.	Nat Commun	2016
26681802	Analysis of the ACTN3 heterozygous genotype suggests that Î±-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion.	Hum Mol Genet	2016
27618447	Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.	Nat Genet	2016
27745833	Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization.	Am J Hum Genet	2016
27503255	A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.	Nat Commun	2016
27731410	No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis.	Sci Rep	2016
27619887	Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.	Nat Commun	2016
27814671	Mergeomics: multidimensional data integration to identify pathogenic perturbations to biological systems.	BMC Genomics	2016
27768686	Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study.	PLoS Genet	2016
26490707	The transcriptional landscape of age in human peripheral blood.	Nat Commun	2015
25954003	Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.	Science	2015
25953952	The landscape of genomic imprinting across diverse adult human tissues.	Genome Res	2015
25078778	Distribution and medical impact of loss-of-function variants in the Finnish founder population.	PLoS Genet	2014
24516404	Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation.	PLoS Genet	2014
22156771	Detailed metabolic and genetic characterization reveals new associations for 30 known lipid loci.	Hum Mol Genet	2012
22511205	Metabolic signatures of insulin resistance in 7,098 young adults.	Diabetes	2012
22836705	Mild cognitive impairment associates with concurrent decreases in serum cholesterol and cholesterol-related lipoprotein subclasses.	J Nutr Health Aging	2012
22286219	Genome-wide association study identifies multiple loci influencing human serum metabolite levels.	Nat Genet	2012
21980352	A differential network approach to exploring differences between biological states: an application to prediabetes.	PLoS ONE	2011
22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Nat Genet	2011
21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Nature	2011
19684899	High-throughput serum NMR metabonomics for cost-effective holistic studies on systemic metabolism.	Analyst	2009
18700135	A multi-metabolite analysis of serum by 1H NMR spectroscopy: early systemic signs of Alzheimer's disease.	Biochem Biophys Res Commun	2008
18450377	Navigated transcranial magnetic stimulation of the primary somatosensory cortex impairs perceptual processing of tactile temporal discrimination.	Neuroscience Letters	2008