Nicholas J. Neill
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 10%
- Cancer Research
- Pathology and Forensic Medicine
- Co-authors
- Lisa G. ShafferBeth S. TorchiaJill A. RosenfeldBlake C. BallifBassem A. BejjaniJ. Britt RavnanRoger A. SchultzAllen N. Lamb
- Topics
- Genomic variations and chromosomal abnormalities (6 papers)Prenatal Screening and Diagnostics (5 papers)Genomics and Rare Diseases (2 papers)
- Partner nations
- United StatesCanadaIsrael
In The Last Decade
Nicholas J. Neill
16 papers receiving 545 citations
Peers
Comparison fields: 5 of 69
- Genetics 265
- Molecular Biology 257
- Pediatrics, Perinatology and Child Health 146
- Cancer Research 66
- Pathology and Forensic Medicine 57
Countries citing papers authored by Nicholas J. Neill
This map shows the geographic impact of Nicholas J. Neill'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 Nicholas J. Neill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicholas J. Neill more than expected).
Fields of papers citing papers by Nicholas J. Neill
This network shows the impact of papers produced by Nicholas J. Neill. 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 Nicholas J. Neill. The network helps show where Nicholas J. Neill may publish in the future.
Co-authorship network of co-authors of Nicholas J. Neill
This figure shows the co-authorship network connecting the top 25 collaborators of Nicholas J. Neill. A scholar is included among the top collaborators of Nicholas J. Neill 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 Nicholas J. Neill. Nicholas J. Neill is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 4 | |
| 2 | 1 | |
| 3 | 119 | |
| 4 | 30 | |
| 5 | 73 | |
| 6 | 2 | |
| 7 | 47 | |
| 8 | 6 | |
| 9 | 27 | |
| 10 | 10 | |
| 11 | 37 | |
| 12 | 35 | |
| 13 | 75 | |
| 14 | 41 | |
| 15 | 10 | |
| 16 | 48 |
About Nicholas J. Neill
Nicholas J. Neill is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Developmental Neuroscience, having authored 16 papers that have together received 565 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (265 citations), Pediatrics, Perinatology and Child Health (146 citations) and Developmental Neuroscience (19 citations). Nicholas J. Neill has collaborated with scholars based in United States, Canada and Israel. Frequent co-authors include Lisa G. Shaffer, Beth S. Torchia, Jill A. Rosenfeld, Blake C. Ballif, Bassem A. Bejjani, J. Britt Ravnan, Roger A. Schultz, Allen N. Lamb, Nic D. Leipzig and Trevor R. Ham. Their work appears in journals such as Molecular Cell, PEDIATRICS and Cancer Research.
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.