Emmanouil T. Dermitzakis
Molecular Biology · 2002–2021
A researcher in the Science corpus: 34 papers; trusts 6 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 568 citations into it; #11,352 of 17,773 by trust here, #99 by citations
- Genetics — 427 citations into it
- Evaluation & Benchmarks — 15 citations into it
Whom Emmanouil T. Dermitzakis trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- John D. Storey (in Genetics)
- Robert Tibshirani (in Molecular Biology)
- Sharon R. Browning (in Genetics)
- Brian L. Browning (in Genetics)
- Y. Hochberg (in Evaluation & Benchmarks)
- Yoav Benjamini (in Evaluation & Benchmarks)
Who trusts Emmanouil T. Dermitzakis
- Jeffrey T. Leek (in Molecular Biology)
- Stephen B. Montgomery (in Molecular Biology)
- Kimberly R. Kukurba (in Molecular Biology)
Papers from Emmanouil T. Dermitzakis's perspective
Ordered by how strongly the researchers Emmanouil T. Dermitzakis trusts endorse each paper. Same corpus, a different order for every researcher.
- A global reference for human genetic variation
- Reference-based phasing using the Haplotype Reference Consortium panel
- Fast and accurate long-range phasing in a UK Biobank cohort
- Polygenic Modeling with Bayesian Sparse Linear Mixed Models (PLoS Genetics)
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
- ClinVar: public archive of interpretations of clinically relevant variants
- Next-generation genotype imputation service and methods (Nature Genetics)
- Variations in DNA elucidate molecular networks that cause disease (Nature)
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (American Journal of Human Genetics)
Their papers
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- Transcriptome genetics using second generation sequencing in a Caucasian population (2010) — 871 citations
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
- The ENCODE (ENCyclopedia Of DNA Elements) Project (2004) — 2,411 citations
- Transcriptome and genome sequencing uncovers functional variation in humans (2013) — 2,017 citations
- Initial sequencing and comparative analysis of the mouse genome. (2002) — 4,291 citations
- Candidate Causal Regulatory Effects by Integration of Expression QTLs with Complex Trait Genetic Associations (2010) — 461 citations
- The Genotype-Tissue Expression (GTEx) project (2013) — 8,629 citations
- Population genomics of human gene expression (2007) — 1,231 citations
- Genetic effects on gene expression across human tissues (2017) — 3,717 citations
- Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics (2013) — 370 citations
- The human transcriptome across tissues and individuals (2015) — 1,238 citations
- The GTEx Consortium atlas of genetic regulatory effects across human tissues (2019) — 4,770 citations
- Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells (2016) — 619 citations
- The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans (2015) — 4,590 citations
- Integrating common and rare genetic variation in diverse human populations (2010) — 3,033 citations
- Epigenome-Wide Scans Identify Differentially Methylated Regions for Age and Age-Related Phenotypes in a Healthy Ageing Population (2012) — 711 citations
- Common regulatory variation impacts gene expression in a cell type dependent manner (2009) — 829 citations
- Accurate, scalable and integrative haplotype estimation (2019) — 557 citations