Chris Tyler-Smith

Nature · 2003–2019

A researcher in the Science corpus: 22 papers; trusts 0 researchers and is trusted by 1 researcher here, as inferred from the citation graph.

Who trusts Chris Tyler-Smith

1. S. Rootsi (in Genetics)

Papers from Chris Tyler-Smith's perspective

Ordered by how strongly the researchers Chris Tyler-Smith trusts endorse each paper. Same corpus, a different order for every researcher.

1. Detection of large-scale variation in the human genome (Nature Genetics)
2. Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing (Nature Genetics)
3. 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
4. Mitochondrial genome variation and the origin of modern humans (Nature)
5. A framework for variation discovery and genotyping using next-generation DNA sequencing data
6. Genotype, haplotype and copy-number variation in worldwide human populations (Nature)
7. A second generation human haplotype map of over 3.1 million SNPs (Nature)
8. The Human Gene Mutation Database: 2008 update
9. Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids
10. The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective. (Nature reviews genetics)

Their papers

• A global reference for human genetic variation (2015) — 16,925 citations
• A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
• Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics (2013) — 370 citations
• BCFtools/RoH: a hidden Markov model approach for detecting autozygosity from next-generation sequencing data (2016) — 635 citations
• Insights into hominid evolution from the gorilla genome sequence (2012) — 719 citations
• The human Y chromosome: an evolutionary marker comes of age (2003) — 964 citations
• IFITM3 restricts the morbidity and mortality associated with influenza (2012) — 758 citations
• Insights into human genetic variation and population history from 929 diverse genomes (2019) — 860 citations
• Demographic History and Genetic Adaptation in the Himalayan Region Inferred from Genome-Wide SNP Genotypes of 49 Populations (2018) — 51 citations
• A genomic history of Aboriginal Australia (2016) — 464 citations
• The Simons Genome Diversity Project: 300 genomes from 142 diverse populations (2016) — 1,396 citations
• Ancient DNA and the rewriting of human history: be sparing with Occam’s razor (2016) — 851 citations
• Health and population effects of rare gene knockouts in adult humans with related parents (2015) — 282 citations
• Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing. (2012) — 279 citations
• An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
• Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) — 710 citations
• A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation (2009) — 635 citations
• Origins and functional impact of copy number variation in the human genome (2009) — 1,997 citations
• Relative impact of nucleotide and copy number variation on gene expression phenotypes (2007) — 1,794 citations
• Global variation in copy number in the human genome (2006) — 4,423 citations