Pardis C Sabeti

Molecular Biology · 2001–2021

A researcher in the Science corpus: 22 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 204 citations into it
• Statistics and Probability — 9 citations into it

Whom Pardis C Sabeti trusts overall

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

1. Michael Olivier
2. Matthew Stephens
3. Robert C. Edgar
4. Joshua M. Akey

Who trusts Pardis C Sabeti overall

1. Graham Coop
2. Mathieu Gautier
3. Rasmus Nielsen
4. J. K. Pritchard
5. S. Qanbari
6. Zachary A. Szpiech
7. Sean M. Hoban
8. Alexander Klassmann
9. Joseph K. Pickrell
10. Nick Patterson

Papers from Pardis C Sabeti's perspective

Ordered by how strongly the researchers Pardis C Sabeti trusts endorse each paper. Same corpus, a different order for every researcher.

1. Basic local alignment search tool.
2. A comparison of bayesian methods for haplotype reconstruction from population genotype data. (American Journal of Human Genetics)
3. A high-resolution recombination map of the human genome (Nature Genetics)
4. MUSCLE: multiple sequence alignment with high accuracy and high throughput.
5. RAxML-III: a fast program for maximum likelihood-based inference of large phylogenetic trees (Bioinform.)
6. Identification of a variant associated with adult-type hypolactasia (Nature Genetics)
7. Latent Dirichlet Allocation
8. The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes (Nature Genetics)
9. Large-Scale Copy Number Polymorphism in the Human Genome (Science)
10. Detection of large-scale variation in the human genome (Nature Genetics)

Their papers

• Detecting Novel Associations in Large Datasets (2011) — 3,212 citations
• A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
• Positive Natural Selection in the Human Lineage (2006) — 1,133 citations
• Linkage disequilibrium in the human genome (2001) — 1,815 citations
• Integrating common and rare genetic variation in diverse human populations (2010) — 3,033 citations
• Nucleic acid detection with CRISPR-Cas13a/C2c2 (2017) — 3,254 citations
• Identifying gene expression programs of cell-type identity and cellular activity with single-cell RNA-Seq (2018) — 442 citations
• Benchmarking Metagenomics Tools for Taxonomic Classification. (2019) — 463 citations
• COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets (2021) — 696 citations
• Field-deployable viral diagnostics using CRISPR-Cas13 (2018) — 1,250 citations
• Massively multiplexed nucleic acid detection with Cas13 (2020) — 709 citations
• Structural and Functional Analysis of the D614G SARS-CoV-2 Spike Protein Variant (2020) — 627 citations
• Neuropathological Features of Covid-19 (2020) — 729 citations
• SARS-CoV-2 Spike protein variant D614G increases infectivity and retains sensitivity to antibodies that target the receptor binding domain (2020) — 613 citations
• Virus genomes reveal factors that spread and sustained the Ebola epidemic (2017) — 389 citations
• Genomic surveillance elucidates Ebola virus origin and transmission during the 2014 outbreak (2014) — 1,217 citations
• Detecting natural selection in genomic data. (2013) — 629 citations
• Genome-wide detection and characterization of positive selection in human populations (2007) — 2,042 citations
• A high resolution HLA and SNP haplotype map for disease association studies in the extended human MHC (2006) — 810 citations
• Common deletion polymorphisms in the human genome (2006) — 759 citations