Ryan E. Mills

Genetics · 2006–2021

A researcher in the Science corpus: 11 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 166 citations into it
• Molecular Biology — 163 citations into it

Whom Ryan E. Mills trusts overall

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

1. Jerzy Jurka
2. Steven A. McCarroll
3. Mark J. Daly
4. B. Ewing
5. Philip Green
6. Michael Olivier
7. W. James Kent
8. T. Daniel Andrews
9. Jonathan Sebat

Who trusts Ryan E. Mills overall

1. Can Alkan
2. William Stephen Pittard
3. Ryan M. Layer

Papers from Ryan E. Mills's perspective

Ordered by how strongly the researchers Ryan E. Mills trusts endorse each paper. Same corpus, a different order for every researcher.

1. Repbase update: a database and an electronic journal of repetitive elements. (Trends in Genetics)
2. The Human Gene Mutation Database: 2008 update
3. Fine-scale structural variation of the human genome (Nature Genetics)
4. Exome sequencing as a tool for Mendelian disease gene discovery
5. The human genome browser at UCSC.
6. Base-calling of automated sequencer traces using phred. I. Accuracy assessment.
7. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
8. An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
9. Base-calling of automated sequencer traces using phred. II. Error probabilities.
10. Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (Nature Genetics)

Their papers

• Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
• A robust benchmark for detection of germline large deletions and insertions (2020) — 358 citations
• An initial map of insertion and deletion (INDEL) variation in the human genome. (2006) — 678 citations
• Small insertions and deletions (INDELs) in human genomes. (2010) — 365 citations
• Haplotype-resolved diverse human genomes and integrated analysis of structural variation (2021) — 639 citations
• An integrated map of structural variation in 2,504 human genomes (2015) — 2,247 citations
• An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
• Natural genetic variation caused by small insertions and deletions in the human genome. (2011) — 272 citations
• Mapping copy number variation by population scale genome sequencing (2011) — 1,130 citations
• Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (2011) — 431 citations
• Classical Nuclear Localization Signals: Definition, Function, and Interaction with Importin α* (2007) — 1,191 citations