Aline Petrin
Impact in
- Genetics top 10%
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
- Genetics and Neurodevelopmental Disorders
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- Hedgehog Signaling Pathway Studies
- dental development and anomalies
- Congenital heart defects research
Papers in
- Genetics 11
- Cleft Lip and Palate Research 8
- Craniofacial Disorders and Treatments 7
- Genomic variations and chromosomal abnormalities 4
- Congenital Ear and Nasal Anomalies 3
- Genomics and Rare Diseases 2
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- dental development and anomalies 3
- Hedgehog Signaling Pathway Studies 2
- Co-authors
- Jeffrey C. Murray (8 shared papers)Antônio Richieri‐Costa (3 shared papers)A. Richieri‐Costa (1 shared paper)JC Murray (1 shared paper)Luciana Paula Maximino (1 shared paper)Dagma Venturini Marques Abramides (1 shared paper)Maria Teresa Vieira Sanseverino (1 shared paper)Célia Maria Giacheti (1 shared paper)
- Journals
- The Cleft Palate-Craniofacial Journal (2 papers)The American Journal of Human Genetics (1 paper)Clinical Genetics (1 paper)Birth Defects Research (1 paper)Genetics (1 paper)
- Partner nations
- United StatesBrazilCanada
In The Last Decade
Aline Petrin
12 papers receiving 307 citations
Peers
Comparison fields: 5 of 58
- Genetics 229
- Genetics 53
- Molecular Biology 154
- Developmental Biology 4
- Cognitive Neuroscience 27
Countries citing papers authored by Aline Petrin
This map shows the geographic impact of Aline Petrin'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 Aline Petrin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aline Petrin more than expected).
Fields of papers citing papers by Aline Petrin
This network shows the impact of papers produced by Aline Petrin. 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 Aline Petrin. The network helps show where Aline Petrin may publish in the future.
Co-authors
The 25 scholars most cited alongside Aline Petrin, 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 | 2011 | 55 | |
| 2 | 2010 | 51 | |
| 3 | 2010 | 48 | |
| 4 | 2013 | 46 | |
| 5 | 2016 | 33 | |
| 6 | 2010 | 25 | |
| 7 | 2017 | 19 | |
| 8 | 2012 | 13 | |
| 9 | 2011 | 9 | |
| 10 | 2010 | 8 | |
| 11 | 2023 | 2 | |
| 12 | 2024 | 1 |
About Aline Petrin
Aline Petrin is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Clinical Psychology, having authored 12 papers that have together received 310 indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (8 papers), Craniofacial Disorders and Treatments (7 papers), Genomic variations and chromosomal abnormalities (4 papers), dental development and anomalies (3 papers), Congenital Ear and Nasal Anomalies (3 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). The work is most often cited by research in Genetics (229 citations), Genetics (53 citations), Molecular Biology (154 citations), Developmental Biology (4 citations) and Cognitive Neuroscience (27 citations). Aline Petrin has collaborated with scholars based in United States, Brazil and Canada. Frequent co-authors include Jeffrey C. Murray, Antônio Richieri‐Costa, A. Richieri‐Costa, JC Murray, Luciana Paula Maximino, Dagma Venturini Marques Abramides, Maria Teresa Vieira Sanseverino, Célia Maria Giacheti, Têmis Maria Félix and Natalia Freitas Rossi. Their work appears in journals such as The Cleft Palate-Craniofacial Journal, The American Journal of Human Genetics, Clinical Genetics, Birth Defects Research and 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.