Mariluce Riegel
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 63
- Genomic variations and chromosomal abnormalities 52
- Genomics and Rare Diseases 14
- Genetics and Neurodevelopmental Disorders 13
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- Prenatal Screening and Diagnostics 28
- Co-authors
- Albert Schinzel (36 shared papers)Alessandra Baumer (17 shared papers)Roberto Giugliani (15 shared papers)Dunja Niedrist (3 shared papers)Josef Wisser (4 shared papers)Josef Achermann (2 shared papers)Lukrecija Brečević (2 shared papers)Sandra Leistner‐Segal (6 shared papers)
- Journals
- European Journal of Medical Genetics (9 papers)Prenatal Diagnosis (5 papers)BioMed Research International (3 papers)Journal of Medical Genetics (3 papers)Clinical Genetics (2 papers)
- Partner nations
- BrazilSwitzerlandUnited States
In The Last Decade
Mariluce Riegel
89 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 97
- Genetics 1.2k
- Pediatrics, Perinatology and Child Health 570
- Genetics 136
- Developmental Biology 22
- Plant Science 340
Countries citing papers authored by Mariluce Riegel
This map shows the geographic impact of Mariluce Riegel'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 Mariluce Riegel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mariluce Riegel more than expected).
Fields of papers citing papers by Mariluce Riegel
This network shows the impact of papers produced by Mariluce Riegel. 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 Mariluce Riegel. The network helps show where Mariluce Riegel may publish in the future.
Co-authors
The 25 scholars most cited alongside Mariluce Riegel, 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 93 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 255 | |
| 2 | 2007 | 104 | |
| 3 | 2001 | 98 | |
| 4 | 2009 | 94 | |
| 5 | 2005 | 85 | |
| 6 | 2006 | 83 | |
| 7 | 2014 | 79 | |
| 8 | 2008 | 63 | |
| 9 | 1999 | 58 | |
| 10 | 2014 | 54 | |
| 11 | 2015 | 50 | |
| 12 | 2008 | 44 | |
| 13 | 2002 | 39 | |
| 14 | 2015 | 38 | |
| 15 | 2017 | 38 | |
| 16 | 2006 | 38 | |
| 17 | 2007 | 36 | |
| 18 | 2017 | 36 | |
| 19 | 2014 | 35 | |
| 20 | 2006 | 34 |
About Mariluce Riegel
Mariluce Riegel is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Rheumatology, having authored 93 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (52 papers), Prenatal Screening and Diagnostics (28 papers), Chromosomal and Genetic Variations (17 papers), Genomics and Rare Diseases (14 papers), Genetics and Neurodevelopmental Disorders (13 papers), Congenital heart defects research (13 papers), Lysosomal Storage Disorders Research (10 papers) and Trypanosoma species research and implications (7 papers). The work is most often cited by research in Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (570 citations), Genetics (136 citations), Developmental Biology (22 citations) and Plant Science (340 citations). Mariluce Riegel has collaborated with scholars based in Brazil, Switzerland and United States. Frequent co-authors include Albert Schinzel, Alessandra Baumer, Roberto Giugliani, Dunja Niedrist, Josef Wisser, Josef Achermann, Lukrecija Brečević, Sandra Leistner‐Segal, Claudio C. Castellan and György Kosztolányi. Their work appears in journals such as European Journal of Medical Genetics, Prenatal Diagnosis, BioMed Research International, Journal of Medical Genetics and Clinical 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.