Xander Nuttle
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 1
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- CRISPR and Genetic Engineering 2
- Congenital heart defects research 2
- Genomics and Chromatin Dynamics 1
- Co-authors
- Evan E. Eichler (6 shared papers)Francesca Antonacci (3 shared papers)Megan Y. Dennis (2 shared papers)Tina Graves (1 shared paper)Pieter J. de Jong (1 shared paper)Maika Malig (1 shared paper)Richard K. Wilson (1 shared paper)Jill A. Rosenfeld (1 shared paper)
- Journals
- Cell Genomics (2 papers)Nature Protocols (1 paper)Cell Reports Methods (1 paper)The American Journal of Human Genetics (1 paper)Cell (1 paper)
- Partner nations
- United StatesItalyCanada
In The Last Decade
Xander Nuttle
9 papers receiving 426 citations
Peers
Comparison fields: 5 of 61
- Developmental Neuroscience 30
- Genetics 191
- Developmental Biology 9
- Molecular Biology 248
- Aging 6
Countries citing papers authored by Xander Nuttle
This map shows the geographic impact of Xander Nuttle'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 Xander Nuttle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Xander Nuttle more than expected).
Fields of papers citing papers by Xander Nuttle
This network shows the impact of papers produced by Xander Nuttle. 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 Xander Nuttle. The network helps show where Xander Nuttle may publish in the future.
Co-authors
The 25 scholars most cited alongside Xander Nuttle, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 295 | |
| 2 | 2015 | 45 | |
| 3 | 2017 | 30 | |
| 4 | 2013 | 27 | |
| 5 | 2014 | 12 | |
| 6 | 2025 | 10 | |
| 7 | 2023 | 7 | |
| 8 | 2017 | 6 | |
| 9 | 2023 | 2 |
About Xander Nuttle
Xander Nuttle is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 9 papers that have together received 434 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (3 papers), Autism Spectrum Disorder Research (2 papers), Prenatal Screening and Diagnostics (2 papers), CRISPR and Genetic Engineering (2 papers), Congenital heart defects research (2 papers), Genomics and Chromatin Dynamics (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Developmental Neuroscience (30 citations), Genetics (191 citations), Developmental Biology (9 citations), Molecular Biology (248 citations) and Aging (6 citations). Xander Nuttle has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Evan E. Eichler, Francesca Antonacci, Megan Y. Dennis, Tina Graves, Pieter J. de Jong, Maika Malig, Richard K. Wilson, Jill A. Rosenfeld, Susan Shafer and Saba Sajjadian. Their work appears in journals such as Cell Genomics, Nature Protocols, Cell Reports Methods, The American Journal of Human Genetics and Cell.
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.