Stephen B. Montgomery
Molecular Biology · 2003–2020
A researcher in the Science corpus: 16 papers; trusts 44 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 275 citations into it; #13,891 of 17,773 by trust here, #526 by citations
- Genetics — 218 citations into it
- Cancer Research — 43 citations into it; #1,585 of 1,780 by trust here, #969 by citations
- Plant Science — 20 citations into it
- Artificial Intelligence — 8 citations into it
Whom Stephen B. Montgomery trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Gordon K. Smyth
- Adam Roberts
- Cole Trapnell
- Andrey A. Shabalin
- Mark D. Robinson
- John S. Mattick
- Ana Kozomara
- G. Stefani
- Zhong Wang
- John C. Marioni
Who trusts Stephen B. Montgomery overall
- Jeffrey T. Leek
- Kimberly R. Kukurba
- Lucas D. Ward
- Y. Surget-Groba
- Davis J. McCarthy
- Alicia Oshlack
- Xiaobei Zhou
- Dmitri D. Pervouchine
- Halit Ongen
- Mark D. Robinson
Papers from Stephen B. Montgomery's perspective
Ordered by how strongly the researchers Stephen B. Montgomery trusts endorse each paper. Same corpus, a different order for every researcher.
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- edgeR: a Bioconductor package for differential expression analysis of digital gene expression data (Bioinform.)
- Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments (Statistical Applications in Genetics and Molecular Biology)
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Transcriptome genetics using second generation sequencing in a Caucasian population (Nature)
- voom: precision weights unlock linear model analysis tools for RNA-seq read counts (Genome Biology)
- Accounting for technical noise in single-cell RNA-seq experiments (Nature Methods)
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
- Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks (Nature Protocols)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Transcriptome genetics using second generation sequencing in a Caucasian population (2010) — 871 citations
- A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
- Transcriptome and genome sequencing uncovers functional variation in humans (2013) — 2,017 citations
- Candidate Causal Regulatory Effects by Integration of Expression QTLs with Complex Trait Genetic Associations (2010) — 461 citations
- Population genomics of human gene expression (2007) — 1,231 citations
- The GTEx Consortium atlas of genetic regulatory effects across human tissues (2019) — 4,770 citations
- Integrating common and rare genetic variation in diverse human populations (2010) — 3,033 citations
- Common regulatory variation impacts gene expression in a cell type dependent manner (2009) — 829 citations
- Widespread dose-dependent effects of RNA expression and splicing on complex diseases and traits (2019) — 116 citations
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
- RNA Sequencing and Analysis (2015) — 801 citations
- The impact of sex on gene expression across human tissues (2020) — 618 citations
- Atheroprotective roles of smooth muscle cell phenotypic modulation and the TCF21 disease gene as revealed by single-cell analysis (2019) — 731 citations
- Mapping cis- and trans-regulatory effects across multiple tissues in twins (2012) — 807 citations
- The Genome Sequence of the SARS-Associated Coronavirus (2003) — 2,060 citations