Sandra Monfort
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Reproductive Medicine top 10%
- Sperm and Testicular Function
Papers in
- Genetics 28
- Genomic variations and chromosomal abnormalities 18
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 5
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- Epigenetics and DNA Methylation 5
- Congenital heart defects research 3
- Co-authors
- Francisco Martı́nez (39 shared papers)Carmen Orellana (34 shared papers)Silvestre Oltra (33 shared papers)Mónica Rosello (31 shared papers)Sonia Mayo (14 shared papers)Alfonso Caro‐Llopis (11 shared papers)Jeremy Howard (1 shared paper)Budhan S. Pukazhenthi (1 shared paper)
- Journals
- Cytogenetic and Genome Research (5 papers)Pediatric Research (3 papers)Journal of Medical Genetics (2 papers)Amyloid (1 paper)Reproduction Fertility and Development (1 paper)
- Partner nations
- SpainNetherlandsLithuania
In The Last Decade
Sandra Monfort
38 papers receiving 526 citations
Peers
Comparison fields: 5 of 64
- Genetics 316
- Reproductive Medicine 48
- Pediatrics, Perinatology and Child Health 59
- Genetics 32
- Molecular Biology 211
Countries citing papers authored by Sandra Monfort
This map shows the geographic impact of Sandra Monfort'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 Sandra Monfort with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Monfort more than expected).
Fields of papers citing papers by Sandra Monfort
This network shows the impact of papers produced by Sandra Monfort. 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 Sandra Monfort. The network helps show where Sandra Monfort may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandra Monfort, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 80 | |
| 2 | 1995 | 56 | |
| 3 | 2008 | 42 | |
| 4 | 2016 | 31 | |
| 5 | 2020 | 28 | |
| 6 | 2015 | 28 | |
| 7 | 2006 | 27 | |
| 8 | 2009 | 27 | |
| 9 | 2014 | 19 | |
| 10 | 2011 | 19 | |
| 11 | 2009 | 15 | |
| 12 | 2010 | 14 | |
| 13 | 2012 | 13 | |
| 14 | 2015 | 11 | |
| 15 | 2009 | 11 | |
| 16 | 2021 | 10 | |
| 17 | 2017 | 10 | |
| 18 | 2007 | 8 | |
| 19 | 2014 | 8 | |
| 20 | 2006 | 8 |
About Sandra Monfort
Sandra Monfort is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Physiology, having authored 41 papers that have together received 537 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Genetics and Neurodevelopmental Disorders (7 papers), Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (5 papers), Epigenetics and DNA Methylation (5 papers), Genetic Syndromes and Imprinting (5 papers), Congenital heart defects research (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Genetics (316 citations), Reproductive Medicine (48 citations), Pediatrics, Perinatology and Child Health (59 citations), Genetics (32 citations) and Molecular Biology (211 citations). Sandra Monfort has collaborated with scholars based in Spain, Netherlands and Lithuania. Frequent co-authors include Francisco Martı́nez, Carmen Orellana, Silvestre Oltra, Mónica Rosello, Sonia Mayo, Alfonso Caro‐Llopis, Jeremy Howard, Budhan S. Pukazhenthi, Timothy C. Roth and Janine L. Brown. Their work appears in journals such as Cytogenetic and Genome Research, Pediatric Research, Journal of Medical Genetics, Amyloid and Reproduction Fertility and Development.
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.