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Researcher · Hunter Genetics · Australia

Louise Christie

Louise Christie publishes mostly in Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health, on topics such as Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders and Genomics and Rare Diseases.

ORCID 0000-0002-6066-5173 OpenAlex
World rank
#2,938,753
of 7,710,434 ranked researchers
Rank in Australia
#79,920
of 140,210
Works
24
Citations
1k
Citations per work
43.5
h-index
12
i10-index 12Top 53% in Genetics (Biochemistry, Genetics and Molecular Biology)
Louise Christie

What does Louise Christie research?

Louise Christie's work is mostly in Biochemistry, Genetics and Molecular Biology (42%), Medicine (15%), Neuroscience (4%).

Life Sciences: 11 works · 46.9% of their workBiochemistry, Genetics and Molecular Biology: 10 works · 42.4% of their workGenetics: 8 works · 33.3% of their workMolecular Biology: 2 works · 9.1% of their workNeuroscience: 1 works · 4.5% of their workCognitive Neuroscience: 1 works · 4.5% of their workEverything else: 9 works · 38.0% of their workHealth Sciences: 4 works · 15.1% of their workMedicine: 4 works · 15.1% of their workPediatrics, Perinatology and Child Health: 1 works · 6.1% of their workPublic Health, Environmental and Occupational Health: 1 works · 4.5% of their workPulmonary and Respiratory Medicine: 1 works · 4.5% of their workTHEIR WORKLouise Christie24works
Life Sciences47%Health Sciences15%

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 Biology1042.4%
    2. Neuroscience14.5%
  2. Everything else938.0%
    1. Medicine415.1%
  1. 1Genetics33% of their works
  2. 2Molecular Biology9% of their works
  3. 3Pediatrics, Perinatology and Child Health6% of their works
  4. 4Pulmonary and Respiratory Medicine4% of their works
  5. 5Public Health, Environmental and Occupational Health4% of their works
  6. 6Cognitive Neuroscience4% of their works

Research topics

Which keywords describe Louise Christie's research?

The keywords of their largest research topics: Neurodevelopmental Disorders, Copy Number Variation, Fragile X Syndrome, Genomic Rearrangements, Rett Syndrome, Autism Spectrum Disorders, Genetic Variants and Sequence Interpretation.

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. Neurodevelopmental Disorders112 topics
  2. Copy Number Variation81 topic
  3. Fragile X Syndrome81 topic
  4. Genomic Rearrangements81 topic
  5. Rett Syndrome81 topic
  6. Autism Spectrum Disorders52 topics
  7. Genetic Variants41 topic
  8. Sequence Interpretation41 topic
  9. Aneuploidy Screening31 topic
  10. CFTR31 topic
  11. Cystic Fibrosis31 topic
  12. Genetics31 topic
  13. Prenatal Diagnosis31 topic
  14. Social Skills Interventions31 topic
  15. Down Syndrome21 topic
  16. Feeding Problems21 topic
  17. Intellectual Disability21 topic
  18. Sensory Sensitivity21 topic

Where does Louise Christie work?

Louise Christie's main affiliation in the publication record is Hunter Genetics, Australia.

How many publications and citations does Louise Christie have?

OpenAlex counts 24 works and 1,045 citations for Louise Christie, an h-index of 12, ranking #2,938,753 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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