Zachary A. Szpiech
Genetics · 2008–2019
A researcher in the Science corpus: 5 papers; trusts 5 researchers and is trusted by 7 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 106 citations into it; #2,231 of 6,854 by trust here, #1,649 by citations
Whom Zachary A. Szpiech trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Steven T. Kalinowski
- Benjamin F. Voight
- Joseph K. Pickrell
- S. Kudaravalli
- J. K. Pritchard
- Pardis C Sabeti
- Graham Coop
- Xiaoquan Wen
Who trusts Zachary A. Szpiech overall
- Mathieu Gautier
- Leo Speidel
- F. Du
- L. Lassois
- Alexander Klassmann
- Marie Forest
- R. Vitalis
- Meng Hou
- Sinan Shi
Papers from Zachary A. Szpiech's perspective
Ordered by how strongly the researchers Zachary A. Szpiech trusts endorse each paper. Same corpus, a different order for every researcher.
- 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
- A second generation human haplotype map of over 3.1 million SNPs (Nature)
- Detecting recent positive selection in the human genome from haplotype structure (Nature)
- Counting Alleles with Rarefaction: Private Alleles and Hierarchical Sampling Designs (Conservation Genetics)
- Genome-wide detection and characterization of positive selection in human populations (Nature)
- Genes mirror geography within Europe (Nature)
- A Draft Sequence of the Neandertal Genome (Science)
- Genotype, haplotype and copy-number variation in worldwide human populations (Nature)
- Next-generation genotype imputation service and methods (Nature Genetics)
Their papers
- Genome-wide association studies in diverse populations (2010) — 591 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- selscan: An Efficient Multithreaded Program to Perform EHH-Based Scans for Positive Selection (2014) — 737 citations
- Genotype, haplotype and copy-number variation in worldwide human populations (2008) — 881 citations
- ADZE: a rarefaction approach for counting alleles private to combinations of populations (2008) — 686 citations