Ina Amarillo
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Urological Disorders and Treatments
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- BRCA gene mutations in cancer 2
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- Congenital heart defects research 4
- Sexual Differentiation and Disorders 3
- Renal and related cancers 2
- Co-authors
- Fabiola Quintero‐Rivera (2 shared papers)Katrina M. Dipple (1 shared paper)Sibel Kantarci (2 shared papers)Éric Vilain (1 shared paper)Xinmin Li (1 shared paper)Caroline K. Lee (1 shared paper)Marcia Willing (1 shared paper)Jennifer Wambach (1 shared paper)
- Journals
- Molecular Cytogenetics (1 paper)European Journal of Medical Genetics (1 paper)Neurology (1 paper)International Journal of Molecular Sciences (1 paper)Bone (1 paper)
- Partner nations
- United StatesCanada
In The Last Decade
Ina Amarillo
22 papers receiving 175 citations
Peers
Comparison fields: 5 of 49
- Genetics 127
- Urology 25
- Developmental Biology 5
- Pediatrics, Perinatology and Child Health 29
- Molecular Biology 100
Countries citing papers authored by Ina Amarillo
This map shows the geographic impact of Ina Amarillo'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 Ina Amarillo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ina Amarillo more than expected).
Fields of papers citing papers by Ina Amarillo
This network shows the impact of papers produced by Ina Amarillo. 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 Ina Amarillo. The network helps show where Ina Amarillo may publish in the future.
Co-authors
The 25 scholars most cited alongside Ina Amarillo, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 33 | |
| 2 | 2013 | 29 | |
| 3 | 2015 | 23 | |
| 4 | 2016 | 19 | |
| 5 | 2019 | 13 | |
| 6 | 2022 | 11 | |
| 7 | 2020 | 10 | |
| 8 | 2017 | 9 | |
| 9 | 2020 | 8 | |
| 10 | 2020 | 5 | |
| 11 | 2020 | 4 | |
| 12 | 2011 | 4 | |
| 13 | 2022 | 4 | |
| 14 | 2017 | 3 | |
| 15 | 2019 | 2 | |
| 16 | 2017 | 2 | |
| 17 | 2023 | 2 | |
| 18 | 2014 | 2 | |
| 19 | 2022 | 2 | |
| 20 | 2013 | 1 |
About Ina Amarillo
Ina Amarillo is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Urology and Cancer Research, having authored 22 papers that have together received 188 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Congenital heart defects research (4 papers), Urological Disorders and Treatments (3 papers), Sexual Differentiation and Disorders (3 papers), Renal and related cancers (2 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Genetics (127 citations), Urology (25 citations), Developmental Biology (5 citations), Pediatrics, Perinatology and Child Health (29 citations) and Molecular Biology (100 citations). Ina Amarillo has collaborated with scholars based in United States and Canada. Frequent co-authors include Fabiola Quintero‐Rivera, Katrina M. Dipple, Sibel Kantarci, Éric Vilain, Xinmin Li, Caroline K. Lee, Marcia Willing, Jennifer Wambach, Jennifer Heeley and Abby Hollander. Their work appears in journals such as Molecular Cytogenetics, European Journal of Medical Genetics, Neurology, International Journal of Molecular Sciences and Bone.
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.