Aparna Prasad

19.3k citations
44 papers · 1.0k indexed · h-index 18
Topics
Genomic variations and chromosomal abnormalities (7 papers)Genetics and Neurodevelopmental Disorders (7 papers)Genomics and Rare Diseases (5 papers)
Partner nations
United StatesCanadaIndia

In The Last Decade

Aparna Prasad

43 papers receiving 989 citations

Peers

Aparna Prasad
Comparison fields: 5 of 108
  • Genetics 493
  • Molecular Biology 400
  • Cognitive Neuroscience 111
  • Cancer Research 104
  • Plant Science 91
Replace Elaine Kenny with:
Elaine Kenny Ireland
Muhammad Ansar Pakistan
Ismail Zaitoun United States
Sen Wu China
Werner Rust Germany
Ariya D. Lapan United States
Margarita Díaz‐Guerra Spain
Gavin MacColl United Kingdom
Valérie Matagne United States
Toshiaki Hino Japan
Aparna Prasad relative to Elaine Kenny Ireland Elaine Kenny's profile →
Citations per field
00.5×1.5×2.3×
Elaine Kenny · 1×
Citations per year

Countries citing papers authored by Aparna Prasad

Since Specialization
Citations

This map shows the geographic impact of Aparna Prasad's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Aparna Prasad with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aparna Prasad more than expected).

Fields of papers citing papers by Aparna Prasad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aparna Prasad. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Aparna Prasad. The network helps show where Aparna Prasad may publish in the future.

Co-authorship network of co-authors of Aparna Prasad

This figure shows the co-authorship network connecting the top 25 collaborators of Aparna Prasad. A scholar is included among the top collaborators of Aparna Prasad based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Aparna Prasad. Aparna Prasad is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 17
2 4
3 11
4 37
5 5
6 3
7 10
8 6
9 3
10 13
11 20
12 19
13 39
14 50
15 21
16 17
17
The effects of positive expiratory pressure (PEP) or oscillatory positive pressure (RC Cornet) on FEV1 and lung clearance index over a twelve month period in children with CF
5
18
BAC contigs based radiation hybrid maps of bovine chromosomes 14 and 19.
1
19 16
20 19

About Aparna Prasad

Aparna Prasad is a scholar working on Developmental Neuroscience, Genetics and Sensory Systems, having authored 44 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Genetics (493 citations), Developmental Neuroscience (35 citations) and Cancer Research (104 citations). Aparna Prasad has collaborated with scholars based in United States, Canada and India. Frequent co-authors include Paul Stothard, Brenda M. Murdoch, S. S. Moore, D. Kolbehdari, Z. Wang, Jason R. Grant, Elisa Marques, Zhihui Xiu, Paolo E. Forni and Stephen W. Scherer. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Rankless by CCL
2026