Ryan D. Hernandez
Genetics · 2005–2019
A researcher in the Science corpus: 11 papers; trusts 5 researchers and is trusted by 14 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 117 citations into it; #1,163 of 6,854 by trust here, #207 by citations
- Molecular Biology — 107 citations into it
Whom Ryan D. Hernandez trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Ryan D. Hernandez overall
- Simon Gravel
- Mathieu Gautier
- Daniel R. Schrider
- Xiaoming Liu
- Leo Speidel
- Melissa S. Cline
- Laurent Excoffier
- M. Malinsky
- C. Ryan Campbell
- Jerome Kelleher
Papers from Ryan D. Hernandez's perspective
Ordered by how strongly the researchers Ryan D. Hernandez trusts endorse each paper. Same corpus, a different order for every researcher.
- BLAT--the BLAST-like alignment tool. (Genome Research)
- Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
- Supporting Online Material Materials and Methods Figs. S1 to S3 Tables S1 to S5 References Worldwide Human Relationships Inferred from Genome-wide Patterns of Variation
- Detecting recent positive selection in the human genome from haplotype structure (Nature)
- Next-generation genotype imputation service and methods (Nature Genetics)
- A second generation human haplotype map of over 3.1 million SNPs (Nature)
- A Draft Sequence of the Neandertal Genome (Science)
- Principal components analysis corrects for stratification in genome-wide association studies
- Inference of population structure using multilocus genotype data. (Genetics)
- Genome-wide detection and characterization of positive selection in human populations (Nature)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Natural selection on protein-coding genes in the human genome (2005) — 803 citations
- Assessing the Evolutionary Impact of Amino Acid Mutations in the Human Genome (2008) — 675 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- Dysbiosis of the Gut Microbiota Is Associated with HIV Disease Progression and Tryptophan Catabolism (2013) — 695 citations
- Recovery of trait heritability from whole genome sequence data (2019) — 222 citations
- selscan: An Efficient Multithreaded Program to Perform EHH-Based Scans for Positive Selection (2014) — 737 citations
- Meta-analysis of Genome-wide Association Studies of Asthma In Ethnically Diverse North American Populations (2011) — 828 citations
- Global landscape of HIV–human protein complexes (2011) — 720 citations
- Genome-Wide Survey of SNP Variation Uncovers the Genetic Structure of Cattle Breeds (2009) — 839 citations
- Inferring the Joint Demographic History of Multiple Populations from Multidimensional SNP Frequency Data (2009) — 1,857 citations