Nuno Maia
Nuno Maia publishes mostly in Genetics, Molecular Biology and Cellular and Molecular Neuroscience, on topics such as Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases and Genomic variations and chromosomal abnormalities.
- World rank
- #5,348,710 of 7,710,434 ranked researchers
- Rank in Portugal
- #28,023 of 41,760
- Works
- 31
- Citations
- 185
- Citations per work
- 6.0
What does Nuno Maia research?
Nuno Maia's work is mostly in Biochemistry, Genetics and Molecular Biology (64%), Medicine (11%), Neuroscience (6%).
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 Sciences2269.5%
- Everything else619.3%
- Health Sciences311.2%
- Medicine311.2%
- 1Genetics39% of their works
- 2Molecular Biology19% of their works
- 3Cellular and Molecular Neuroscience6% of their works
- 4Genetics6% of their works
- 5Pediatrics, Perinatology and Child Health6% of their works
- 6Cell Biology6% of their works
Research topics
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Congenital heart defects research
- Calpain Protease Function and Regulation
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Muscle Physiology and Disorders
Which keywords describe Nuno Maia's research?
The keywords of their largest research topics: Fragile X Syndrome, Rett Syndrome, Genetic Variants, Sequence Interpretation, Copy Number Variation, Genomic Rearrangements, SMN1 and Spinal Muscular Atrophy.
- X Chromosome Inactivation
- Sex Determination
- Cell Migration
- Heart Regeneration
- Spinal Muscular Atrophy
- Genomic Rearrangements
- Sequence Interpretation
- Rett Syndrome
- Fragile X Syndrome
- Genetic Variants
- Copy Number Variation
- SMN1
- Cardiomyocyte Renewal
- Calpain
- Muscle Regeneration
- Skeletal Muscle Atrophy
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 16 words, with their numbers
- Fragile X Syndrome121 topic
- Rett Syndrome121 topic
- Genetic Variants71 topic
- Sequence Interpretation71 topic
- Copy Number Variation51 topic
- Genomic Rearrangements51 topic
- SMN141 topic
- Spinal Muscular Atrophy41 topic
- Cardiomyocyte Renewal31 topic
- Heart Regeneration31 topic
- Calpain21 topic
- Cell Migration21 topic
- Muscle Regeneration21 topic
- Sex Determination21 topic
- Skeletal Muscle Atrophy21 topic
- X Chromosome Inactivation21 topic
Where does Nuno Maia work?
Nuno Maia's main affiliation in the publication record is Universidade do Porto, Portugal.
How many publications and citations does Nuno Maia have?
OpenAlex counts 31 works and 185 citations for Nuno Maia, an h-index of 6, ranking #5,348,710 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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