Eleftheria Zeggini
Genetics · 2007–2021
A researcher in the Science corpus: 28 papers; trusts 7 researchers and is trusted by 5 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 474 citations into it; #2,162 of 6,854 by trust here, #49 by citations
- Molecular Biology — 297 citations into it
- Surgery — 71 citations into it
- Statistics and Probability — 32 citations into it
Whom Eleftheria Zeggini trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Julian P. T. Higgins
- John P. A. Ioannidis
- S. Thompson
- J. Wakefield
- Jonathan Marchini
- Teri Manolio
- A. Sutton
- S. Zollner
- J. K. Pritchard
Who trusts Eleftheria Zeggini overall
- Evangelos Evangelou
- John P. A. Ioannidis
- M. van Iterson
- Peter Kraft
- Bryan N. Howie
- E. V. van Zwet
- Jonathan Marchini
- Cristen J. Willer
- Yun Li
- Naomi R. Wray
Papers from Eleftheria Zeggini's perspective
Ordered by how strongly the researchers Eleftheria Zeggini trusts endorse each paper. Same corpus, a different order for every researcher.
- Measuring inconsistency in meta-analyses (British medical journal)
- A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
- Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes (Nature Genetics)
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Nature Genetics)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (Nature Genetics)
- Bayes factors
- SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations (Nature Genetics)
- Genome-wide association studies for common diseases and complex traits (Nature reviews genetics)
- Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data (Genetic Epidemiology)
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
- The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
- Multiple type 2 diabetes susceptibility genes following genome-wide association scan in UK samples (2007) — 2,209 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
- Functional annotation of non-coding sequence variants (2014) — 324 citations
- Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge (2010) — 663 citations
- Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) — 631 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
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) — 677 citations
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) — 401 citations
- Very low-depth whole-genome sequencing in complex trait association studies (2017) — 78 citations
- Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) — 384 citations
- Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank (2015) — 386 citations
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations
- Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) — 710 citations
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) — 2,246 citations