Núria Clusellas
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 7
-
- Prenatal Screening and Diagnostics 6
- Fetal and Pediatric Neurological Disorders 2
- Co-authors
- Carmen Morales (7 shared papers)Aurora Sánchez (7 shared papers)Anna Soler (6 shared papers)Irene Mademont‐Soler (6 shared papers)J. Egozcue (1 shared paper)Francesca Vidal (1 shared paper)Joan Blanco (1 shared paper)Ester Margarit (4 shared papers)
- Journals
- Human Mutation (1 paper)Journal of Inherited Metabolic Disease (1 paper)Acta Paediatrica (1 paper)Ultrasound in Obstetrics and Gynecology (1 paper)International Dental Journal (1 paper)
- Partner nations
- SpainUnited StatesPoland
In The Last Decade
Núria Clusellas
13 papers receiving 278 citations
Peers
Comparison fields: 5 of 40
- Pediatrics, Perinatology and Child Health 189
- Genetics 195
- Reproductive Medicine 16
- Plant Science 59
- Molecular Biology 100
Countries citing papers authored by Núria Clusellas
This map shows the geographic impact of Núria Clusellas'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 Núria Clusellas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Núria Clusellas more than expected).
Fields of papers citing papers by Núria Clusellas
This network shows the impact of papers produced by Núria Clusellas. 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 Núria Clusellas. The network helps show where Núria Clusellas may publish in the future.
Co-authors
The 25 scholars most cited alongside Núria Clusellas, 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 | 1998 | 59 | |
| 2 | 2012 | 56 | |
| 3 | 2010 | 44 | |
| 4 | 1983 | 34 | |
| 5 | 2011 | 29 | |
| 6 | 2005 | 26 | |
| 7 | 2012 | 21 | |
| 8 | 2009 | 20 | |
| 9 | 2010 | 17 | |
| 10 | 2010 | 5 | |
| 11 | 1998 | 5 | |
| 12 | 2024 | 2 | |
| 13 | 2019 | 1 | |
| 14 | 2021 | 0 |
About Núria Clusellas
Núria Clusellas is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Surgery, Molecular Biology and Physiology, having authored 14 papers that have together received 319 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers), Pediatric Hepatobiliary Diseases and Treatments (2 papers), Congenital Anomalies and Fetal Surgery (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Obstructive Sleep Apnea Research (2 papers), Cardiovascular and Diving-Related Complications (1 paper) and Dental Radiography and Imaging (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (189 citations), Genetics (195 citations), Reproductive Medicine (16 citations), Plant Science (59 citations) and Molecular Biology (100 citations). Núria Clusellas has collaborated with scholars based in Spain, United States and Poland. Frequent co-authors include Carmen Morales, Aurora Sánchez, Anna Soler, Irene Mademont‐Soler, J. Egozcue, Francesca Vidal, Joan Blanco, Ester Margarit, Xavier Carbonell and Bai‐Lin Wu. Their work appears in journals such as Human Mutation, Journal of Inherited Metabolic Disease, Acta Paediatrica, Ultrasound in Obstetrics and Gynecology and International Dental Journal.
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.