Jeffrey G. Reid

Molecular Biology · 2001–2021

A researcher in the Science corpus: 21 papers; trusts 4 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 111 citations into it
• Computational Biology & Bioinformatics — 8 citations into it

Whom Jeffrey G. Reid trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Temple F. Smith
2. Jay Shendure
3. Marc R. Friedländer

Who trusts Jeffrey G. Reid overall

1. T. Farazi

Papers from Jeffrey G. Reid's perspective

Ordered by how strongly the researchers Jeffrey G. Reid trusts endorse each paper. Same corpus, a different order for every researcher.

1. An Abundant Class of Tiny RNAs with Probable Regulatory Roles in Caenorhabditis elegans (Science)
2. ALLPATHS: de novo assembly of whole-genome shotgun microreads. (Genome Research)
3. Discovering microRNAs from deep sequencing data using miRDeep (Nature Biotechnology)
4. Most mammalian mRNAs are conserved targets of microRNAs. (Genome Research)
5. Principles of MicroRNA–Target Recognition (PLoS Biology)
6. Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. (American Journal of Human Genetics)
7. Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
8. Mendelian Inheritance in Man and Its Online Version, OMIM (American Journal of Human Genetics)
9. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. (American Journal of Human Genetics)
10. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. (Brain Research)

Their papers

• A framework for human microbiome research (2012) — 2,418 citations
• Integrated Genomic Analyses of Ovarian Carcinoma (2011) — 7,559 citations
• Mind the Gap: Upgrading Genomes with Pacific Biosciences RS Long-Read Sequencing Technology (2012) — 896 citations
• Expression profiling of microRNAs by deep sequencing (2009) — 310 citations
• Exome sequencing and analysis of 454,787 UK Biobank participants (2021) — 786 citations
• A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease (2018) — 665 citations
• Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing (2014) — 1,342 citations
• Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders (2013) — 1,887 citations
• Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) — 1,772 citations
• Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes (2012) — 1,987 citations
• Functional and Evolutionary Insights from the Genomes of Three Parasitoid Nasonia Species (2010) — 849 citations
• Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy (2010) — 783 citations
• Distributions of charged hadrons associated with high transverse momentum particles in pp and Au plus Au collisions at root(S)(NN)=200 GeV (2005) — 322 citations
• Particle-type dependence of azimuthal anisotropy and nuclear modification of particle production in Au plus Au collisions at root s(NN)=200 GeV (2004) — 360 citations
• Azimuthal anisotropy in Au plus Au collisions at root S-NN=200 GeV (2004) — 156 citations
• STAR detector overview (2003) — 532 citations
• Directed and elliptic flow of charged pions and protons in Pb + Pb collisions at 40A and 158A GeV (2003) — 213 citations
• Elliptic flow from two- and four-particle correlations in Au + Au collisions at sqrt{s_{NN}} = 130 GeV (2002) — 280 citations
• HIGH pT HADRONS IN AU+AU COLLISIONS AT RHIC (2002) — 463 citations
• Multiplicity Distribution and Spectra of Negatively Charged Hadrons in Au+Au Collisions at (2001) — 134 citations