Stephan Schiffels
Genetics · 2014–2016
A researcher in the Science corpus: 5 papers; trusts 4 researchers and is trusted by 6 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 66 citations into it; #2,249 of 6,854 by trust here, #1,488 by citations
- Molecular Biology — 22 citations into it; #6,695 of 17,773 by trust here, #7,657 by citations
Whom Stephan Schiffels trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Stephan Schiffels overall
- Jerome Kelleher
- Jonathan Terhorst
- John A. Kamm
- A. Etheridge
- C. Alonso‐Blanco
- G. McVean
- Yun S. Song
- Desislava Petkova
- Peter Edge
Papers from Stephan Schiffels's perspective
Ordered by how strongly the researchers Stephan Schiffels trusts endorse each paper. Same corpus, a different order for every researcher.
- Calibrating a coalescent simulation of human genome sequence variation. (Genome Research)
- Sequencing of Fifty Human Exomes Reveals Adaptation to High Altitude (Science)
- A tutorial on hidden Markov models and selected applications in speech recognition
- Inferring the Joint Demographic History of Multiple Populations from Multidimensional SNP Frequency Data (PLoS Genetics)
- Inferring human population size and separation history from multiple genome sequences (Nature Genetics)
- A Draft Sequence of the Neandertal Genome (Science)
- Estimate of the mutation rate per nucleotide in humans. (Genetics)
- Fast and flexible simulation of DNA sequence data. (Genome Research)
- Multiple dispersals and modern human origins
- An Aboriginal Australian Genome Reveals Separate Human Dispersals into Asia (Science)
Their papers
- Inferring human population size and separation history from multiple genome sequences (2014) — 1,011 citations
- The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
- A genomic history of Aboriginal Australia (2016) — 464 citations
- The genetic history of Ice Age Europe (2016) — 887 citations
- Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) — 384 citations