Andrea Seeley

523 citations
8 papers · 57 indexed · h-index 5
Topics
Genomic variations and chromosomal abnormalities (3 papers)Genomics and Rare Diseases (2 papers)Hip disorders and treatments (2 papers)
Partner nations
United States

In The Last Decade

Andrea Seeley

7 papers receiving 45 citations

Peers

Andrea Seeley
Comparison fields: 5 of 29
  • Genetics 31
  • Molecular Biology 17
  • Pediatrics, Perinatology and Child Health 13
  • Clinical Biochemistry 12
  • Cancer Research 7
Replace Juanita Neira with:
Juanita Neira United States
Anand Vasudevan Australia
Kathleen Wallace United States
Tobias Bartolomaeus Germany
Jianhuang Xue China
Theresia Herget Germany
Hana Zouk United States
Frances Dougherty United States
Dagmar Huhle Germany
Fengyu Guo China
Andrea Seeley relative to Juanita Neira United States Juanita Neira's profile →
Citations per field
00.5×1.5×1.8×
Juanita Neira · 1×
Citations per year

Countries citing papers authored by Andrea Seeley

Since Specialization
Citations

This map shows the geographic impact of Andrea Seeley'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 Andrea Seeley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrea Seeley more than expected).

Fields of papers citing papers by Andrea Seeley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrea Seeley. 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 Andrea Seeley. The network helps show where Andrea Seeley may publish in the future.

Co-authorship network of co-authors of Andrea Seeley

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Seeley. A scholar is included among the top collaborators of Andrea Seeley 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 Andrea Seeley. Andrea Seeley is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
#WorkIndexed citations
1 0
2 3
3 10
4 1
5 10
6 14
7 10
8 9

About Andrea Seeley

Andrea Seeley is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 8 papers that have together received 57 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Hip disorders and treatments (2 papers). The work is most often cited by research in Clinical Biochemistry (12 citations), Genetics (31 citations) and Biochemistry (6 citations). Andrea Seeley has collaborated with scholars based in United States. Frequent co-authors include Shane C. Quinonez, Ayesha Ahmad, Mary Seeterlin, Bradley R. Foerster, Bruce A. Barshop, Mark A. Durham, Juliann M. Savatt, Mark A. Micale, Catherine E. Keegan and Thomas W. Glover. Their work appears in journals such as Human Mutation, BMC Pediatrics and American Journal of Medical Genetics Part A.

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