Johan T. den Dunnen
Molecular Biology · 2000–2016
A researcher in the Science corpus: 5 papers; trusts 1 researcher and is trusted by 8 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 34 citations into it; #10,287 of 17,773 by trust here, #6,960 by citations
Whom Johan T. den Dunnen trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Johan T. den Dunnen overall
- James Robinson
- Kai Wang
- Karen Eilbeck
- Mingyao Li
- Victor A. McKusick
- Peter E. M. Taschner
- Paul Flicek
- K. Bedard
- Laurent Gil
- Hakon Hakonarson
Papers from Johan T. den Dunnen's perspective
Ordered by how strongly the researchers Johan T. den Dunnen trusts endorse each paper. Same corpus, a different order for every researcher.
- dbSNP: the NCBI database of genetic variation
- Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
- Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular…
- Ensembl’s 10th year (Nucleic Acids Res.)
- The human genome browser at UCSC.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- RNA-Seq: a revolutionary tool for transcriptomics (Nature reviews genetics)
- Transforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variations (Proceedings of the National Academy of Sciences of the United States of America)
- Continuous base identification for single-molecule nanopore DNA sequencing. (Nature Nanotechnology)
- Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker (Human Mutation)
Their papers
- LOVD v.2.0: the next generation in gene variant databases (2011) — 1,011 citations
- HGVS Recommendations for the Description of Sequence Variants: 2016 Update (2016) — 1,645 citations
- Nomenclature for the description of human sequence variations (2001) — 950 citations
- Next generation sequencing technology: Advances and applications. (2014) — 711 citations
- Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion (2000) — 1,717 citations