Stephen C. Groft
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
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- Family and Patient Care in Intensive Care Units
Papers in
- Genetics 31
- Genomics and Rare Diseases 30
- BRCA gene mutations in cancer 2
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- CRISPR and Genetic Engineering 9
- Co-authors
- Manuel Posada de la Paz (7 shared papers)Anna Kole (1 shared paper)Ségolène Aymé (2 shared papers)Domenica Taruscio (7 shared papers)Tammara L. Jenkins (1 shared paper)Christopher Landon (1 shared paper)Carol Nicholson (1 shared paper)Yaffa Rubinstein (6 shared papers)
- Journals
- Advances in experimental medicine and biology (7 papers)Molecular Genetics and Metabolism (4 papers)Orphanet Journal of Rare Diseases (4 papers)Acta Paediatrica (2 papers)Nature Reviews Drug Discovery (2 papers)
- Partner nations
- United StatesSpainItaly
In The Last Decade
Stephen C. Groft
41 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 122
- Genetics 544
- Radiological and Ultrasound Technology 62
- Genetics 90
- Pediatrics, Perinatology and Child Health 152
- Clinical Biochemistry 40
Countries citing papers authored by Stephen C. Groft
This map shows the geographic impact of Stephen C. Groft'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 C. Groft with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephen C. Groft more than expected).
Fields of papers citing papers by Stephen C. Groft
This network shows the impact of papers produced by Stephen C. Groft. 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 C. Groft. The network helps show where Stephen C. Groft may publish in the future.
Co-authors
The 25 scholars most cited alongside Stephen C. Groft, 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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 241 | |
| 2 | 2006 | 217 | |
| 3 | 2008 | 168 | |
| 4 | 2010 | 74 | |
| 5 | 2021 | 70 | |
| 6 | 2012 | 65 | |
| 7 | 2010 | 64 | |
| 8 | 2010 | 62 | |
| 9 | 2016 | 51 | |
| 10 | 2017 | 46 | |
| 11 | 2015 | 42 | |
| 12 | 2010 | 41 | |
| 13 | 2013 | 39 | |
| 14 | 2017 | 31 | |
| 15 | 2014 | 30 | |
| 16 | 2017 | 26 | |
| 17 | 2014 | 26 | |
| 18 | 2020 | 22 | |
| 19 | 2017 | 21 | |
| 20 | 2010 | 19 |
About Stephen C. Groft
Stephen C. Groft is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Pulmonary and Respiratory Medicine and Economics and Econometrics, having authored 43 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (30 papers), CRISPR and Genetic Engineering (9 papers), Cystic Fibrosis Research Advances (6 papers), Biotechnology and Related Fields (6 papers), Metabolism and Genetic Disorders (3 papers), Health Systems, Economic Evaluations, Quality of Life (3 papers), Cancer Genomics and Diagnostics (2 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Genetics (544 citations), Radiological and Ultrasound Technology (62 citations), Genetics (90 citations), Pediatrics, Perinatology and Child Health (152 citations) and Clinical Biochemistry (40 citations). Stephen C. Groft has collaborated with scholars based in United States, Spain and Italy. Frequent co-authors include Manuel Posada de la Paz, Anna Kole, Ségolène Aymé, Domenica Taruscio, Tammara L. Jenkins, Christopher Landon, Carol Nicholson, Yaffa Rubinstein, Erik Tambuyzer and Christopher P. Austin. Their work appears in journals such as Advances in experimental medicine and biology, Molecular Genetics and Metabolism, Orphanet Journal of Rare Diseases, Acta Paediatrica and Nature Reviews Drug Discovery.
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.