M Aspillaga
M Aspillaga publishes mostly in Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, on topics such as Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics and Congenital limb and hand anomalies.
- World rank
- #4,634,494 of 7,710,434 ranked researchers
- Rank in Chile
- #11,136 of 20,642
- Works
- 46
- Citations
- 299
- Citations per work
- 6.5
What does M Aspillaga research?
M Aspillaga's work is mostly in Biochemistry, Genetics and Molecular Biology (38%), Medicine (22%).
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
- Everything else1840.0%
- Life Sciences1737.7%
- Health Sciences1022.3%
- Medicine1022.3%
- 1Genetics23% of their works
- 2Pediatrics, Perinatology and Child Health11% of their works
- 3Molecular Biology10% of their works
- 4Public Health, Environmental and Occupational Health6% of their works
- 5Surgery6% of their works
- 6Developmental Biology4% of their works
Research topics
- Genomic variations and chromosomal abnormalities
- Prenatal Screening and Diagnostics
- Congenital limb and hand anomalies
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Infant Development and Preterm Care
- Congenital Anomalies and Fetal Surgery
Which keywords describe M Aspillaga's research?
The keywords of their largest research topics: Prenatal Diagnosis, Epidemiology, Copy Number Variation, Genomic Rearrangements, Aneuploidy Screening, Maternal Plasma DNA Sequencing, Fragile X Syndrome and Genetic Heterogeneity.
- X Chromosome Inactivation
- Sequence Interpretation
- Omphalocele
- Genetic Variants
- Rett Syndrome
- Genetic Heterogeneity
- Maternal Plasma DNA Sequencing
- Genomic Rearrangements
- Epidemiology
- Prenatal Diagnosis
- Copy Number Variation
- Aneuploidy Screening
- Fragile X Syndrome
- Limb Malformations
- Gastroschisis
- Neurodevelopmental Outcomes
- Preterm Birth
- Sex Determination
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 18 words, with their numbers
- Prenatal Diagnosis82 topics
- Epidemiology72 topics
- Copy Number Variation61 topic
- Genomic Rearrangements61 topic
- Aneuploidy Screening51 topic
- Maternal Plasma DNA Sequencing51 topic
- Fragile X Syndrome41 topic
- Genetic Heterogeneity41 topic
- Limb Malformations41 topic
- Rett Syndrome41 topic
- Gastroschisis31 topic
- Genetic Variants31 topic
- Neurodevelopmental Outcomes31 topic
- Omphalocele31 topic
- Preterm Birth31 topic
- Sequence Interpretation31 topic
- Sex Determination31 topic
- X Chromosome Inactivation31 topic
Where does M Aspillaga work?
M Aspillaga's main affiliation in the publication record is Hospital Luis Calvo Mackenna, Chile.
How many publications and citations does M Aspillaga have?
OpenAlex counts 46 works and 299 citations for M Aspillaga, an h-index of 10, ranking #4,634,494 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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