Pejman Mohammadi
Science · 2015–2020
A researcher in the Science corpus: 6 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Whom Pejman Mohammadi trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Pejman Mohammadi's perspective
Ordered by how strongly the researchers Pejman Mohammadi trusts endorse each paper. Same corpus, a different order for every researcher.
- Understanding mechanisms underlying human gene expression variation with RNA sequencing (Nature)
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (Nature Genetics)
- Transcriptome genetics using second generation sequencing in a Caucasian population (Nature)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- Transcriptome and genome sequencing uncovers functional variation in humans (Nature)
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
- Partitioning heritability by functional annotation using genome-wide association summary statistics (Nature Genetics)
- Next-generation genotype imputation service and methods (Nature Genetics)
- A global reference for human genetic variation
Their papers
- Genetic effects on gene expression across human tissues (2017) — 3,717 citations
- Tools and best practices for data processing in allelic expression analysis (2015) — 359 citations
- The GTEx Consortium atlas of genetic regulatory effects across human tissues (2019) — 4,770 citations
- A primer on deep learning in genomics (2018) — 767 citations
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
- The impact of sex on gene expression across human tissues (2020) — 618 citations