Wendy Alcaraz
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- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 3
- Genetic Syndromes and Imprinting 2
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- Hedgehog Signaling Pathway Studies 2
- Mitochondrial Function and Pathology 1
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- Genetic factors in colorectal cancer 2
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- Neurological diseases and metabolism 1
- Co-authors
- Bruce A. HamiltonDeepali N. ShindeDavid GoldSha TangErica D. SmithSamin A. SajanKelly RadtkeMari Rossi
- Journals
- Proceedings of the National Academy of Sciences (1 paper)Human Molecular Genetics (1 paper)British Journal of Haematology (1 paper)
- Partner nations
- United StatesUnited KingdomItaly
In The Last Decade
Wendy Alcaraz
13 papers receiving 264 citations
Peers
Comparison fields: 5 of 50
- Genetics 140
- Clinical Biochemistry 16
- Developmental Neuroscience 9
- Molecular Biology 144
- Cancer Research 25
Countries citing papers authored by Wendy Alcaraz
This map shows the geographic impact of Wendy Alcaraz'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 Wendy Alcaraz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wendy Alcaraz more than expected).
Fields of papers citing papers by Wendy Alcaraz
This network shows the impact of papers produced by Wendy Alcaraz. 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 Wendy Alcaraz. The network helps show where Wendy Alcaraz may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Wendy Alcaraz, 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 | 2022 | 4 | |
| 2 | 2022 | 0 | |
| 3 | 2020 | 1 | |
| 4 | 2019 | 27 | |
| 5 | 2019 | 61 | |
| 6 | 2018 | 3 | |
| 7 | 2018 | 9 | |
| 8 | 2017 | 29 | |
| 9 | 2017 | 3 | |
| 10 | 2016 | 7 | |
| 11 | 2016 | 34 | |
| 12 | 2016 | 11 | |
| 13 | 2011 | 12 | |
| 14 | 2006 | 63 |
About Wendy Alcaraz
Wendy Alcaraz is a scholar working on Genetics, Cancer Research and Genetics, having authored 14 papers that have together received 264 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic Syndromes and Imprinting (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Genetic factors in colorectal cancer (2 papers), Neurological diseases and metabolism (1 paper) and Mitochondrial Function and Pathology (1 paper). The work is most often cited by research in Genetics (140 citations), Clinical Biochemistry (16 citations) and Developmental Neuroscience (9 citations). Wendy Alcaraz has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Bruce A. Hamilton, Deepali N. Shinde, David Gold, Sha Tang, Erica D. Smith, Samin A. Sajan, Kelly Radtke, Mari Rossi, Kelly D. Farwell Hagman and Zöe Powis. Their work appears in journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics and British Journal of Haematology.
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.