Tanya N. Eble
Impact in
- Genetics top 10%
- Genetic and rare skin diseases.
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Fetal and Pediatric Neurological Disorders
- Prenatal Screening and Diagnostics
Papers in
- Genetics 14
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 3
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- Prenatal Screening and Diagnostics 6
- Fetal and Pediatric Neurological Disorders 4
- Co-authors
- V. Reid Sutton (6 shared papers)Ignatia B. Van den Veyver (6 shared papers)Shweta U. Dhar (12 shared papers)Xiaoling Wang (3 shared papers)Ankita Patel (3 shared papers)Richard A. Lewis (5 shared papers)Ping Fang (2 shared papers)Christina Thaller (1 shared paper)
- Journals
- Molecular Case Studies (1 paper)European Journal of Medical Genetics (1 paper)Gene (1 paper)International Journal of Environmental Research and Public Health (1 paper)Human Genetics (1 paper)
- Partner nations
- United StatesHong KongChina
In The Last Decade
Tanya N. Eble
24 papers receiving 461 citations
Peers
Comparison fields: 5 of 58
- Genetics 228
- Pediatrics, Perinatology and Child Health 120
- Dermatology 37
- Urology 18
- Clinical Biochemistry 20
Countries citing papers authored by Tanya N. Eble
This map shows the geographic impact of Tanya N. Eble'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 Tanya N. Eble with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tanya N. Eble more than expected).
Fields of papers citing papers by Tanya N. Eble
This network shows the impact of papers produced by Tanya N. Eble. 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 Tanya N. Eble. The network helps show where Tanya N. Eble may publish in the future.
Co-authors
The 25 scholars most cited alongside Tanya N. Eble, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 179 | |
| 2 | 2005 | 40 | |
| 3 | 2007 | 29 | |
| 4 | 2019 | 26 | |
| 5 | 2012 | 25 | |
| 6 | 2019 | 23 | |
| 7 | 2009 | 17 | |
| 8 | 2020 | 16 | |
| 9 | 2019 | 16 | |
| 10 | 2012 | 16 | |
| 11 | 2013 | 15 | |
| 12 | 2018 | 15 | |
| 13 | 2014 | 13 | |
| 14 | 2020 | 11 | |
| 15 | 2009 | 10 | |
| 16 | 2012 | 5 | |
| 17 | 2018 | 4 | |
| 18 | 2015 | 4 | |
| 19 | 2020 | 4 | |
| 20 | 2021 | 3 |
About Tanya N. Eble
Tanya N. Eble is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Clinical Psychology and Cognitive Neuroscience, having authored 24 papers that have together received 478 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), BRCA gene mutations in cancer (5 papers), Autism Spectrum Disorder Research (4 papers), Fetal and Pediatric Neurological Disorders (4 papers), Family and Disability Support Research (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (228 citations), Pediatrics, Perinatology and Child Health (120 citations), Dermatology (37 citations), Urology (18 citations) and Clinical Biochemistry (20 citations). Tanya N. Eble has collaborated with scholars based in United States, Hong Kong and China. Frequent co-authors include V. Reid Sutton, Ignatia B. Van den Veyver, Shweta U. Dhar, Xiaoling Wang, Ankita Patel, Richard A. Lewis, Ping Fang, Christina Thaller, Zhiyin Yu and Lei‐Shih Chen. Their work appears in journals such as Molecular Case Studies, European Journal of Medical Genetics, Gene, International Journal of Environmental Research and Public Health and Human Genetics.
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.