Manuela Seia
Impact in
-
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
- Genetics top 5%
- Congenital Ear and Nasal Anomalies
- Genetic and Kidney Cyst Diseases
Papers in
-
- Cystic Fibrosis Research Advances 46
- Neonatal Respiratory Health Research 26
- Tracheal and airway disorders 18
- Genetics 16
- Congenital Ear and Nasal Anomalies 9
- Genomic variations and chromosomal abnormalities 5
- Hemoglobinopathies and Related Disorders 4
- Connective tissue disorders research 4
- Co-authors
- Maurizio Ferrari (18 shared papers)Annamaria Giunta (10 shared papers)Carla Colombo (13 shared papers)Carla Colombo (5 shared papers)Rita Padoan (10 shared papers)Lucy Costantino (10 shared papers)Laura Cremonesi (11 shared papers)Luigi Porcaro (11 shared papers)
- Journals
- Journal of Cystic Fibrosis (4 papers)Human Mutation (4 papers)Human Genetics (3 papers)European Journal of Human Genetics (2 papers)Genomics (2 papers)
- Partner nations
- ItalyGermanyUnited Kingdom
In The Last Decade
Manuela Seia
68 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 99
- Pulmonary and Respiratory Medicine 767
- Genetics 199
- Genetics 198
- Hepatology 50
- Surgery 230
Countries citing papers authored by Manuela Seia
This map shows the geographic impact of Manuela Seia'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 Manuela Seia with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manuela Seia more than expected).
Fields of papers citing papers by Manuela Seia
This network shows the impact of papers produced by Manuela Seia. 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 Manuela Seia. The network helps show where Manuela Seia may publish in the future.
Co-authors
The 25 scholars most cited alongside Manuela Seia, 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 70 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 137 | |
| 2 | 2007 | 71 | |
| 3 | 2013 | 59 | |
| 4 | Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study. | 1988 | 55 |
| 5 | Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy. | 1991 | 45 |
| 6 | 2015 | 45 | |
| 7 | 1992 | 40 | |
| 8 | 2012 | 40 | |
| 9 | 2007 | 36 | |
| 10 | 2002 | 35 | |
| 11 | 2014 | 34 | |
| 12 | 2009 | 33 | |
| 13 | 2002 | 30 | |
| 14 | 2014 | 28 | |
| 15 | 2017 | 27 | |
| 16 | 2016 | 27 | |
| 17 | 2009 | 26 | |
| 18 | 2018 | 26 | |
| 19 | 2013 | 24 | |
| 20 | 2008 | 23 |
About Manuela Seia
Manuela Seia is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 70 papers that have together received 1.3k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (46 papers), Neonatal Respiratory Health Research (26 papers), Tracheal and airway disorders (18 papers), Congenital Ear and Nasal Anomalies (9 papers), Genomic variations and chromosomal abnormalities (5 papers), Hemoglobinopathies and Related Disorders (4 papers), Connective tissue disorders research (4 papers) and Pediatric Hepatobiliary Diseases and Treatments (3 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (767 citations), Genetics (199 citations), Genetics (198 citations), Hepatology (50 citations) and Surgery (230 citations). Manuela Seia has collaborated with scholars based in Italy, Germany and United Kingdom. Frequent co-authors include Maurizio Ferrari, Annamaria Giunta, Carla Colombo, Carla Colombo, Rita Padoan, Lucy Costantino, Laura Cremonesi, Luigi Porcaro, D. Degiorgio and Lucia Piceni Sereni. Their work appears in journals such as Journal of Cystic Fibrosis, Human Mutation, Human Genetics, European Journal of Human Genetics and Genomics.
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.