Júlia Baptista
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 13
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
- Genetic and Kidney Cyst Diseases 3
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- Congenital heart defects research 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)Nigel P. Carter (2 shared papers)Patricia A. Jacobs (2 shared papers)Catherine Mercer (1 shared paper)Viv Maloney (1 shared paper)
- Journals
- European Journal of Medical Genetics (6 papers)European Journal of Human Genetics (3 papers)Journal of Medical Genetics (3 papers)Nature Medicine (1 paper)European Journal of Pediatrics (1 paper)
- Partner nations
- United KingdomGermanyNetherlands
In The Last Decade
Júlia Baptista
21 papers receiving 483 citations
Peers
Comparison fields: 5 of 62
- Genetics 271
- Pediatrics, Perinatology and Child Health 86
- Molecular Biology 233
- Plant Science 119
- Developmental Biology 5
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 | 128 | |
| 2 | 2019 | 71 | |
| 3 | 2009 | 48 | |
| 4 | 2023 | 35 | |
| 5 | 2008 | 30 | |
| 6 | 2021 | 26 | |
| 7 | 2022 | 24 | |
| 8 | 2006 | 23 | |
| 9 | 2005 | 22 | |
| 10 | 2021 | 15 | |
| 11 | 2018 | 15 | |
| 12 | 2021 | 14 | |
| 13 | 2022 | 11 | |
| 14 | 2019 | 11 | |
| 15 | 2020 | 10 | |
| 16 | 2018 | 10 | |
| 17 | 2022 | 9 | |
| 18 | 2022 | 4 | |
| 19 | 2020 | 3 | |
| 20 | 2018 | 2 |
About Júlia Baptista
Júlia Baptista is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 22 papers that have together received 512 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic and Kidney Cyst Diseases (3 papers), Congenital heart defects research (2 papers), Plant-Microbe Interactions and Immunity (2 papers), Genomics and Chromatin Dynamics (2 papers), Genetic factors in colorectal cancer (2 papers) and Cardiac electrophysiology and arrhythmias (1 paper). The work is most often cited by research in Genetics (271 citations), Pediatrics, Perinatology and Child Health (86 citations), Molecular Biology (233 citations), Plant Science (119 citations) and Developmental Biology (5 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, Nigel P. Carter, Patricia A. Jacobs, Catherine Mercer, Viv Maloney, 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, Nature Medicine and European Journal of Pediatrics.
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.