Martin Tristani-Firouzi
Molecular Biology · 2001–2017
A researcher in the Science corpus: 3 papers; trusts 1 researcher and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 26 citations into it; #10,231 of 17,773 by trust here, #10,864 by citations
Whom Martin Tristani-Firouzi trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Martin Tristani-Firouzi overall
Papers from Martin Tristani-Firouzi's perspective
Ordered by how strongly the researchers Martin Tristani-Firouzi trusts endorse each paper. Same corpus, a different order for every researcher.
- Crystal structure and mechanism of a calcium-gated potassium channel (Nature)
- A structural basis for drug-induced long QT syndrome. (Proceedings of the National Academy of Sciences of the United States of America)
- Molecular and cellular mechanisms of cardiac arrhythmias. (Cell)
- Sudden Death Associated With Short-QT Syndrome Linked to Mutations in HERG (Circulation)
- Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. (Cell)
- Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. (Cell)
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema (Nature Genetics)
- The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (Genome Research)
- Dynamic and Coordinated Epigenetic Regulation of Developmental Transitions in the Cardiac Lineage (Cell)
Their papers
- hERG potassium channels and cardiac arrhythmia (2006) — 1,535 citations
- Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. (2001) — 1,012 citations
- Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands (2017) — 773 citations