Paul L. Auer
Genetics · 2010–2021
A researcher in the Science corpus: 7 papers; trusts 6 researchers and is trusted by 7 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 98 citations into it
- Molecular Biology — 90 citations into it; #5,592 of 17,773 by trust here, #9,367 by citations
- Management Science and Operations Research — 5 citations into it
Whom Paul L. Auer trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Gordon K. Smyth
- Mark D. Robinson
- G. Oehlert
- Julian J. Faraway
- Ali Mortazavi
- Gary A. Churchill
- P. Park
- Davis J. McCarthy
- Robert Gentleman
- M. Kerr
Who trusts Paul L. Auer overall
- Davis J. McCarthy
- Neelroop Parikshak
- Simon Anders
- Ana Conesa
- Yunshun Chen
- Gordon K. Smyth
- Michael Jeffrey Gandal
- Brian J. Haas
- Rhonda L. Bacher
- Daniel H. Geschwind
Papers from Paul L. Auer's perspective
Ordered by how strongly the researchers Paul L. Auer trusts endorse each paper. Same corpus, a different order for every researcher.
- [Serial analysis of gene expression]. (Yi chuan = Hereditas)
- Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments (Statistical Applications in Genetics and Molecular Biology)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome (Science)
- edgeR: a Bioconductor package for differential expression analysis of digital gene expression data (Bioinform.)
- Moderated statistical tests for assessing differences in tag abundance (Bioinform.)
- Stem cell transcriptome profiling via massive-scale mRNA sequencing (Nature Methods)
- RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. (Genome Research)
- The Transcriptional Landscape of the Yeast Genome Defined by RNA Sequencing (Science)
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
Their papers
- Statistical Design and Analysis of RNA Sequencing Data (2010) — 395 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- A Population-Based Study of Genes Previously Implicated in Breast Cancer (2021) — 655 citations
- The Polygenic and Monogenic Basis of Blood Traits and Diseases (2020) — 602 citations
- Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) — 244 citations
- Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States (2016) — 328 citations
- Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease (2014) — 861 citations