Cotton Seed

Geometry and Topology · 2013–2023

A researcher in the Science corpus: 12 papers; trusts 10 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Geometry and Topology — 18 citations into it
• Mathematical Physics — 14 citations into it
• Discrete Mathematics and Combinatorics — 9 citations into it

Whom Cotton Seed trusts overall

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

1. Jacob Rasmussen
2. Joachim Kock
3. Mikhail Khovanov
4. Peter S. Ozsv'ath
5. Morwen Thistlethwaite

Papers from Cotton Seed's perspective

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

1. Khovanov homology and the slice genus
2. A link invariant from the symplectic geometry of nilpotent slices
3. Khovanov homology is an unknot-detector
4. Infinite families of links with trivial Jones polynomial
5. On the Heegaard Floer homology of branched double-covers
6. A functor-valued invariant of tangles
7. LINKS WITH TRIVIAL JONES POLYNOMIAL
8. PhyloCSF: a comparative genomics method to distinguish protein coding and non-coding regions (Bioinform.)
9. KEGG: Kyoto Encyclopedia of Genes and Genomes (Nucleic Acids Res.)
10. The human genome browser at UCSC.

Their papers

• The mutational constraint spectrum quantified from variation in 141,456 humans (2020) — 8,441 citations
• Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes (2019) — 1,088 citations
• Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
• A genomic mutational constraint map using variation in 76,156 human genomes (2023) — 1,228 citations
• A genome-wide mutational constraint map quantified from variation in 76,156 human genomes (2022) — 258 citations
• Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
• Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) — 126 citations
• A structural variation reference for medical and population genetics (2020) — 876 citations
• Transcript expression-aware annotation improves rare variant discovery and interpretation (2019) — 26 citations
• Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
• Ultra-rare disruptive and damaging mutations influence educational attainment in the general population (2016) — 97 citations
• A link-splitting spectral sequence in Khovanov homology (2013) — 57 citations