Júlia Baptista
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 16
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 7
- Genetic and Kidney Cyst Diseases 3
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- Renal and related cancers 2
- Genomics and Chromatin Dynamics 2
- Co-authors
- John A. Crolla (4 shared papers)N. Simon Thomas (2 shared papers)Susan Gribble (3 shared papers)Elena Prigmore (3 shared papers)Patricia A. Jacobs (2 shared papers)Nigel P. Carter (2 shared papers)Viv Maloney (1 shared paper)Catherine Mercer (1 shared paper)
- Journals
- European Journal of Medical Genetics (6 papers)European Journal of Human Genetics (3 papers)Journal of Medical Genetics (3 papers)The Journal of Pediatrics (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomGermanyNetherlands
In The Last Decade
Júlia Baptista
21 papers receiving 466 citations
Peers
Comparison fields: 5 of 65
- Genetics 291
- Pediatrics, Perinatology and Child Health 95
- Molecular Biology 254
- Plant Science 122
- Developmental Biology 6
Countries citing papers authored by Júlia Baptista
This map shows the geographic impact of Júlia Baptista'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 Júlia Baptista with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Júlia Baptista more than expected).
Fields of papers citing papers by Júlia Baptista
This network shows the impact of papers produced by Júlia Baptista. 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 Júlia Baptista. The network helps show where Júlia Baptista may publish in the future.
Co-authors
The 25 scholars most cited alongside Júlia Baptista, 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 | 2008 | 127 | |
| 2 | 2019 | 69 | |
| 3 | 2009 | 48 | |
| 4 | 2023 | 32 | |
| 5 | 2008 | 30 | |
| 6 | 2021 | 25 | |
| 7 | 2006 | 23 | |
| 8 | 2005 | 21 | |
| 9 | 2022 | 19 | |
| 10 | 2021 | 15 | |
| 11 | 2021 | 14 | |
| 12 | 2018 | 14 | |
| 13 | 2019 | 11 | |
| 14 | 2022 | 10 | |
| 15 | 2020 | 10 | |
| 16 | 2018 | 10 | |
| 17 | 2022 | 9 | |
| 18 | 2022 | 4 | |
| 19 | 2020 | 3 | |
| 20 | 2023 | 1 |
About Júlia Baptista
Júlia Baptista is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Pathology and Forensic Medicine, having authored 22 papers that have together received 496 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetic and Kidney Cyst Diseases (3 papers), Genetic factors in colorectal cancer (3 papers), Prenatal Screening and Diagnostics (3 papers), Plant-Microbe Interactions and Immunity (2 papers), Renal and related cancers (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (291 citations), Pediatrics, Perinatology and Child Health (95 citations), Molecular Biology (254 citations), Plant Science (122 citations) and Developmental Biology (6 citations). Júlia Baptista has collaborated with scholars based in United Kingdom, Germany and Netherlands. Frequent co-authors include John A. Crolla, N. Simon Thomas, Susan Gribble, Elena Prigmore, Patricia A. Jacobs, Nigel P. Carter, Viv Maloney, Catherine Mercer, Bee Ling Ng and Sian Ellard. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Journal of Medical Genetics, The Journal of Pediatrics and The American Journal of 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.