C. Camaschella
Hematology · 2000–2020
A researcher in the Science corpus: 5 papers; trusts 2 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Hematology — 46 citations into it; #70 of 225 by trust here, #70 by citations
- Genetics — 40 citations into it; #3,626 of 6,854 by trust here, #2,093 by citations
- Nutrition and Dietetics — 22 citations into it; #475 of 1,029 by trust here, #240 by citations
Whom C. Camaschella trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts C. Camaschella overall
Papers from C. Camaschella's perspective
Ordered by how strongly the researchers C. Camaschella trusts endorse each paper. Same corpus, a different order for every researcher.
- Quantitative proteomics identifies NCOA4 as the cargo receptor mediating ferritinophagy (Nature)
- The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22 (Nature Genetics)
- Mitoferrin is essential for erythroid iron assimilation (Nature)
- Deconvoluting the context-dependent role for autophagy in cancer (Nature Reviews. Cancer)
- A role for ubiquitin in selective autophagy. (Molecules and Cells)
- A tissue-specific atlas of mouse protein phosphorylation and expression. (Cell)
- The dynamic nature of autophagy in cancer. (Genes & Development)
- Activated Ras requires autophagy to maintain oxidative metabolism and tumorigenesis. (Genes & Development)
- Systemic iron homeostasis and the iron-responsive element/iron-regulatory protein (IRE/IRP) regulatory network. (Annual review of nutrition)
- Cell-Free Formation of RNA Granules: Low Complexity Sequence Domains Form Dynamic Fibers Within Hydrogels (Cell)
Their papers
- Iron metabolism and iron disorders revisited in the hepcidin era (2020) — 628 citations
- Iron-deficiency anemia. (2015) — 812 citations
- Two to tango: regulation of Mammalian iron metabolism. (2010) — 2,059 citations
- Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis (2003) — 923 citations
- The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22 (2000) — 845 citations