Aparna Prasad
Aparna Prasad publishes mostly in Genetics, Molecular Biology and Cancer Research, on topics such as Genomic variations and chromosomal abnormalities, Cancer Genomics and Diagnostics and Genetic Mapping and Diversity in Plants and Animals.
- World rank
- #159,310 of 7,710,434 ranked researchers
- Rank in India
- #1,652 of 280,097
- Works
- 142
- Citations
- 20k
- Citations per work
- 141.7
What does Aparna Prasad research?
Aparna Prasad's work is mostly in Biochemistry, Genetics and Molecular Biology (46%), Medicine (9%), Neuroscience (3%).
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 Sciences6948.7%
- Everything else6042.2%
- Health Sciences139.1%
- Medicine139.1%
- 1Genetics20% of their works
- 2Molecular Biology18% of their works
- 3Cancer Research8% of their works
- 4Surgery5% of their works
- 5Pathology and Forensic Medicine4% of their works
- 6Cognitive Neuroscience3% of their works
Research topics
- Genomic variations and chromosomal abnormalities
- Cancer Genomics and Diagnostics
- Genetic Mapping and Diversity in Plants and Animals
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Autism Spectrum Disorder Research
- Genetic and phenotypic traits in livestock
- Genetic factors in colorectal cancer
Which keywords describe Aparna Prasad's research?
The keywords of their largest research topics: Neurodevelopmental Disorders, Marker-Assisted Selection, Copy Number Variation, Genomic Rearrangements, Cancer Genomics, Mutational Signatures, Genome-wide Association Studies and Quantitative Trait Loci.
- Plant Breeding
- Microsatellite Instability
- Sequence Interpretation
- Genetics
- Fragile X Syndrome
- Quantitative Trait Loci
- Mutational Signatures
- Genomic Rearrangements
- Marker-Assisted Selection
- Neurodevelopmental Disorders
- Copy Number Variation
- Cancer Genomics
- Genome-wide Association Studies
- Autism Spectrum Disorders
- Genetic Variants
- Rett Syndrome
- Genomic Selection
- Molecular Characterization
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
- Neurodevelopmental Disorders262 topics
- Marker-Assisted Selection182 topics
- Copy Number Variation171 topic
- Genomic Rearrangements171 topic
- Cancer Genomics161 topic
- Mutational Signatures161 topic
- Genome-wide Association Studies101 topic
- Quantitative Trait Loci101 topic
- Autism Spectrum Disorders91 topic
- Fragile X Syndrome91 topic
- Genetic Variants91 topic
- Genetics91 topic
- Rett Syndrome91 topic
- Sequence Interpretation91 topic
- Genomic Selection81 topic
- Microsatellite Instability81 topic
- Molecular Characterization81 topic
- Plant Breeding81 topic
Where does Aparna Prasad work?
Aparna Prasad's main affiliation in the publication record is BLK Super Speciality Hospital, India.
How many publications and citations does Aparna Prasad have?
OpenAlex counts 142 works and 20,126 citations for Aparna Prasad, an h-index of 42, ranking #159,310 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.
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