Markku Laakso
Molecular Biology · 2002–2021
A researcher in the Science corpus: 41 papers; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 411 citations into it
Whom Markku Laakso trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Markku Laakso overall
Papers from Markku Laakso's perspective
Ordered by how strongly the researchers Markku Laakso trusts endorse each paper. Same corpus, a different order for every researcher.
- Faculty Opinions recommendation of PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes.
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
- SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations (Nature Genetics)
- Mitochondrial Dysfunction in the Elderly: Possible Role in Insulin Resistance (Science)
- Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes. (Diabetes)
- Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings (PLoS Genetics)
- Common genetic variation and human traits. (New England Journal of Medicine)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (Nature)
- Comparison of abdominal adiposity and overall obesity in predicting risk of type 2 diabetes among men. (American Journal of Clinical Nutrition)
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Integrative approaches for large-scale transcriptome-wide association studies (2015) — 2,212 citations
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
- Hexokinase 2 is required for tumor initiation and maintenance and its systemic deletion is therapeutic in mouse models of cancer (2013) — 818 citations
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) — 1,485 citations
- Effect of rosiglitazone on the frequency of diabetes in patients with impaired glucose tolerance or impaired fasting glucose: a randomised controlled trial. (2006) — 1,710 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Large-scale association analyses identify host factors influencing human gut microbiome composition (2021) — 1,459 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) — 1,654 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) — 744 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum (2017) — 114 citations