Marco Garieri
Impact in
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- Cancer Genomics and Diagnostics
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- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 7
- Genetic Syndromes and Imprinting 2
- Genomic variations and chromosomal abnormalities 2
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- Epigenetics and DNA Methylation 3
- Single-cell and spatial transcriptomics 1
- Genomics and Phylogenetic Studies 1
- Co-authors
- Stylianos E. Antonarakis (10 shared papers)Federico Santoni (9 shared papers)Emilie Falconnet (7 shared papers)Pascale Ribaux (6 shared papers)Christelle Borel (5 shared papers)Michel Guipponi (5 shared papers)Georgios Stamoulis (3 shared papers)Alexandre Fort (4 shared papers)
- Journals
- Nature Communications (4 papers)The American Journal of Human Genetics (2 papers)Bioinformatics (1 paper)Diseases of the Colon & Rectum (1 paper)Genome Research (1 paper)
- Partner nations
- SwitzerlandUnited StatesItaly
In The Last Decade
Marco Garieri
12 papers receiving 433 citations
Peers
Comparison fields: 5 of 67
- Cancer Research 105
- Genetics 156
- Molecular Biology 278
- Pediatrics, Perinatology and Child Health 52
- Hematology 25
Countries citing papers authored by Marco Garieri
This map shows the geographic impact of Marco Garieri'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 Marco Garieri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marco Garieri more than expected).
Fields of papers citing papers by Marco Garieri
This network shows the impact of papers produced by Marco Garieri. 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 Marco Garieri. The network helps show where Marco Garieri may publish in the future.
Co-authors
The 25 scholars most cited alongside Marco Garieri, 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 | 2014 | 89 | |
| 2 | 2018 | 56 | |
| 3 | 2014 | 52 | |
| 4 | 2017 | 50 | |
| 5 | 2017 | 40 | |
| 6 | 2014 | 38 | |
| 7 | 2019 | 29 | |
| 8 | 2019 | 28 | |
| 9 | 2017 | 22 | |
| 10 | 2017 | 15 | |
| 11 | 2015 | 9 | |
| 12 | 2020 | 7 |
About Marco Garieri
Marco Garieri is a scholar working on Genetics, Molecular Biology, Cancer Research, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 12 papers that have together received 435 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (3 papers), Prenatal Screening and Diagnostics (2 papers), Genetic Syndromes and Imprinting (2 papers), Cancer Genomics and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Single-cell and spatial transcriptomics (1 paper), Medical Imaging Techniques and Applications (1 paper) and Genomics and Phylogenetic Studies (1 paper). The work is most often cited by research in Cancer Research (105 citations), Genetics (156 citations), Molecular Biology (278 citations), Pediatrics, Perinatology and Child Health (52 citations) and Hematology (25 citations). Marco Garieri has collaborated with scholars based in Switzerland, United States and Italy. Frequent co-authors include Stylianos E. Antonarakis, Federico Santoni, Emilie Falconnet, Pascale Ribaux, Christelle Borel, Michel Guipponi, Georgios Stamoulis, Alexandre Fort, Emmanouil T. Dermitzakis and Olivier Delaneau. Their work appears in journals such as Nature Communications, The American Journal of Human Genetics, Bioinformatics, Diseases of the Colon & Rectum and Genome Research.
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.