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Researcher · Genoscope · France

Núria Fonknechten

Núria Fonknechten publishes mostly in Molecular Biology, Pulmonary and Respiratory Medicine and Cellular and Molecular Neuroscience, on topics such as Hereditary Neurological Disorders, Neonatal Respiratory Health Research and Cystic Fibrosis Research Advances.

OpenAlex
World rank
#1,509,428
of 7,710,434 ranked researchers
Rank in France
#67,620
of 324,115
Works
35
Citations
3.5k
Citations per work
101.3
h-index
16
i10-index 19Top 46% in Molecular Biology
Núria Fonknechten

What does Núria Fonknechten research?

Núria Fonknechten's work is mostly in Medicine (26%), Biochemistry, Genetics and Molecular Biology (20%), Neuroscience (17%).

Life Sciences: 13 works · 37.0% of their workBiochemistry, Genetics and Molecular Biology: 7 works · 20.2% of their workMolecular Biology: 7 works · 20.2% of their workNeuroscience: 6 works · 16.8% of their workCellular and Molecular Neuroscience: 4 works · 11.2% of their workNeurology: 2 works · 5.6% of their workEverything else: 10 works · 29.2% of their workHealth Sciences: 9 works · 25.9% of their workMedicine: 9 works · 25.9% of their workPulmonary and Respiratory Medicine: 6 works · 18.0% of their workGenetics: 3 works · 7.9% of their workPhysical Sciences: 3 works · 7.9% of their workEnvironmental Science: 3 works · 7.9% of their workPollution: 3 works · 7.9% of their workTHEIR WORKNúria Fonknechten35works
Life Sciences37%Physical Sciences8%Health Sciences26%

Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.

The fields and subfields, with their numbers
    1. Biochemistry, Genetics and Molecular Biology720.2%
    2. Neuroscience616.8%
  2. Everything else1029.2%
    1. Medicine925.9%
    1. Environmental Science37.9%
  1. 1Molecular Biology20% of their works
  2. 2Pulmonary and Respiratory Medicine18% of their works
  3. 3Cellular and Molecular Neuroscience11% of their works
  4. 4Pollution8% of their works
  5. 5Genetics8% of their works
  6. 6Neurology6% of their works

Research topics

Which keywords describe Núria Fonknechten's research?

The keywords of their largest research topics: Mitochondrial Dysfunction, Genetic Mutations, Charcot-Marie-Tooth Disease, Hereditary Spastic Paraplegia, Bronchopulmonary Dysplasia, CFTR, Cystic Fibrosis and Preterm Infants.

Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most. The words come from the keyword list OpenAlex gives each topic, not from the text of the papers, so a word can appear that none of the papers uses.

All 18 words, with their numbers
  1. Mitochondrial Dysfunction153 topics
  2. Genetic Mutations122 topics
  3. Charcot-Marie-Tooth Disease71 topic
  4. Hereditary Spastic Paraplegia71 topic
  5. Bronchopulmonary Dysplasia61 topic
  6. CFTR61 topic
  7. Cystic Fibrosis61 topic
  8. Preterm Infants61 topic
  9. Brain Iron Accumulation51 topic
  10. Neurodegeneration51 topic
  11. SMN151 topic
  12. Spinal Muscular Atrophy51 topic
  13. Brominated Flame Retardants41 topic
  14. Polycyclic Aromatic Hydrocarbons41 topic
  15. Chromatin31 topic
  16. Huntington's Disease31 topic
  17. Protein Aggregation31 topic
  18. Transcription31 topic

Where does Núria Fonknechten work?

Núria Fonknechten's main affiliation in the publication record is Genoscope, France.

How many publications and citations does Núria Fonknechten have?

OpenAlex counts 35 works and 3,545 citations for Núria Fonknechten, an h-index of 16, ranking #1,509,428 of 7,710,434 researchers worldwide on the quality score.

Ranked on field-normalised citation excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.

Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.

Discussion

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