Madeline Couse
Madeline Couse publishes mostly in Genetics, Molecular Biology and Cellular and Molecular Neuroscience, on topics such as Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities and Cancer Genomics and Diagnostics.
- World rank
- #1,821,120 of 7,710,434 ranked researchers
- Rank in Canada
- #60,691 of 183,316
- Works
- 53
- Citations
- 588
- Citations per work
- 11.1
What does Madeline Couse research?
Madeline Couse's work is mostly in Biochemistry, Genetics and Molecular Biology (65%), Neuroscience (5%), Engineering (5%).
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
- Life Sciences3769.9%
- Everything else1121.5%
- Physical Sciences35.2%
- Engineering35.2%
- Health Sciences23.4%
- Medicine23.4%
- 1Genetics41% of their works
- 2Molecular Biology18% of their works
- 3Cellular and Molecular Neuroscience5% of their works
- 4Cancer Research5% of their works
- 5Biomedical Engineering5% of their works
- 6Pathology and Forensic Medicine3% of their works
Research topics
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Cancer Genomics and Diagnostics
- Genetics and Neurodevelopmental Disorders
- Genetic factors in colorectal cancer
- Genetic Associations and Epidemiology
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
Which keywords describe Madeline Couse's research?
The keywords of their largest research topics: Genetic Variants, Sequence Interpretation, Copy Number Variation, Genomic Rearrangements, Cancer Genomics, Gene Expression, Mutational Signatures and Fragile X Syndrome.
- Sex Determination
- Genomic Imprinting
- Genetic Variation
- Microsatellite Instability
- Fragile X Syndrome
- Gene Expression
- Genomic Rearrangements
- Sequence Interpretation
- Genetic Variants
- Copy Number Variation
- Cancer Genomics
- Mutational Signatures
- Rett Syndrome
- Molecular Characterization
- Genome-Wide Association
- Parental Influence
- X Chromosome Inactivation
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.
All 17 words, with their numbers
- Genetic Variants191 topic
- Sequence Interpretation191 topic
- Copy Number Variation91 topic
- Genomic Rearrangements91 topic
- Cancer Genomics61 topic
- Gene Expression62 topics
- Mutational Signatures61 topic
- Fragile X Syndrome51 topic
- Rett Syndrome51 topic
- Microsatellite Instability41 topic
- Molecular Characterization41 topic
- Genetic Variation31 topic
- Genome-Wide Association31 topic
- Genomic Imprinting31 topic
- Parental Influence31 topic
- Sex Determination31 topic
- X Chromosome Inactivation31 topic
Where does Madeline Couse work?
Madeline Couse's main affiliation in the publication record is Hospital for Sick Children, Canada.
How many publications and citations does Madeline Couse have?
OpenAlex counts 53 works and 588 citations for Madeline Couse, an h-index of 11, ranking #1,821,120 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised 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.
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