Zoltán Kutalik
Molecular Biology · 2008–2021
A researcher in the Science corpus: 26 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 410 citations into it
Whom Zoltán Kutalik trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Zoltán Kutalik's perspective
Ordered by how strongly the researchers Zoltán Kutalik trusts endorse each paper. Same corpus, a different order for every researcher.
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Genome-partitioning of genetic variation for complex traits using common SNPs (Nature Genetics)
- On Spectral Clustering: Analysis and an algorithm
- Estimating Effects and Making Predictions from Genome-Wide Marker Data
- Supporting Online Material Materials and Methods Figs. S1 to S3 Tables S1 to S5 References Worldwide Human Relationships Inferred from Genome-wide Patterns of Variation
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Systematic identification of trans-eQTLs as putative drivers of known disease associations (Nature Genetics)
- Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings (PLoS Genetics)
- Data, information, knowledge and principle: back to metabolism in KEGG (Nucleic Acids Res.)
- Common genetic variation and human traits. (New England Journal of Medicine)
Their papers
- Open Community Challenge Reveals Molecular Network Modules with Key Roles in Diseases (2018) — 30 citations
- Assessment of network module identification across complex diseases (2019) — 268 citations
- Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) — 511 citations
- A mega-analysis of genome-wide association studies for major depressive disorder (2012) — 1,096 citations
- Tissue-specific regulatory circuits reveal variable modular perturbations across complex diseases (2016) — 303 citations
- Fast and Rigorous Computation of Gene and Pathway Scores from SNP-Based Summary Statistics (2016) — 322 citations
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression (2021) — 1,862 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- Guidelines for performing Mendelian randomization investigations (2019) — 2,022 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
- Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes (2018) — 707 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) — 129 citations
- The SIB Swiss Institute of Bioinformatics’ resources: focus on curated databases (2015) — 60 citations
- Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans (2015) — 734 citations
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014)