Stephen Hellens
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Myeloproliferative Neoplasms: Diagnosis and Treatment
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- Platelet Disorders and Treatments
Papers in
- Genetics 4
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 1
- Congenital Ear and Nasal Anomalies 1
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- Congenital heart defects research 1
- Co-authors
- Francesca Forzano (1 shared paper)Jodi D. Hoffman (1 shared paper)Michela Malacarne (1 shared paper)Michael Wright (2 shared papers)Domenico Coviello (1 shared paper)Anna Dubois (1 shared paper)Vera Uliana (1 shared paper)Simon Zwolinski (1 shared paper)
- Journals
- European Journal of Medical Genetics (1 paper)Clinical Dysmorphology (2 papers)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Stephen Hellens
4 papers receiving 20 citations
Peers
Comparison fields: 5 of 20
- Genetics 21
- Hematology 7
- Immunology and Allergy 2
- Genetics 3
- Pediatrics, Perinatology and Child Health 5
Countries citing papers authored by Stephen Hellens
This map shows the geographic impact of Stephen Hellens'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 Stephen Hellens with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephen Hellens more than expected).
Fields of papers citing papers by Stephen Hellens
This network shows the impact of papers produced by Stephen Hellens. 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 Stephen Hellens. The network helps show where Stephen Hellens may publish in the future.
Co-authors
The 15 scholars most cited alongside Stephen Hellens, 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 | 2013 | 26 | |
| 2 | 2011 | 3 | |
| 3 | 2015 | 2 | |
| 4 | 2012 | 1 |
About Stephen Hellens
Stephen Hellens is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 4 papers that have together received 32 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (2 papers), Congenital heart defects research (1 paper), Cancer Genomics and Diagnostics (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Prenatal Screening and Diagnostics (1 paper) and Congenital Ear and Nasal Anomalies (1 paper). The work is most often cited by research in Genetics (21 citations), Hematology (7 citations), Immunology and Allergy (2 citations), Genetics (3 citations) and Pediatrics, Perinatology and Child Health (5 citations). Stephen Hellens has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Francesca Forzano, Jodi D. Hoffman, Michela Malacarne, Michael Wright, Domenico Coviello, Anna Dubois, Vera Uliana, Simon Zwolinski, Emilio Di Maria and Francesca Faravelli. Their work appears in journals such as European Journal of Medical Genetics, Clinical Dysmorphology and American Journal of Medical Genetics Part A.
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.