Stephen C. Groft
Impact in
-
- Family and Patient Care in Intensive Care Units
- Genetics top 5%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Neurogenetic and Muscular Disorders Research
Papers in
- Genetics 31
- Genomics and Rare Diseases 31
- BRCA gene mutations in cancer 3
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- CRISPR and Genetic Engineering 9
- Co-authors
- Manuel Posada de la Paz (7 shared papers)Ségolène Aymé (2 shared papers)Domenica Taruscio (7 shared papers)Carol Nicholson (1 shared paper)Christopher Landon (1 shared paper)Tammara L. Jenkins (1 shared paper)Yaffa Rubinstein (6 shared papers)Erik Tambuyzer (3 shared papers)
- Journals
- Advances in experimental medicine and biology (7 papers)Orphanet Journal of Rare Diseases (4 papers)Molecular Genetics and Metabolism (4 papers)Contemporary Clinical Trials (2 papers)Nature Reviews Drug Discovery (2 papers)
- Partner nations
- United StatesSpainItaly
In The Last Decade
Stephen C. Groft
38 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 124
- Radiological and Ultrasound Technology 117
- Genetics 561
- Pediatrics, Perinatology and Child Health 237
- Genetics 120
- Speech and Hearing 47
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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 222 | |
| 2 | 2006 | 206 | |
| 3 | 2008 | 150 | |
| 4 | 2010 | 71 | |
| 5 | 2021 | 67 | |
| 6 | 2012 | 65 | |
| 7 | 2010 | 59 | |
| 8 | 2010 | 54 | |
| 9 | 2016 | 47 | |
| 10 | 2015 | 39 | |
| 11 | 2013 | 37 | |
| 12 | 2010 | 36 | |
| 13 | 2017 | 32 | |
| 14 | 2014 | 29 | |
| 15 | 2017 | 28 | |
| 16 | 2017 | 23 | |
| 17 | 2014 | 23 | |
| 18 | 2017 | 19 | |
| 19 | 2020 | 18 | |
| 20 | 2010 | 18 |
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 41 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (31 papers), CRISPR and Genetic Engineering (9 papers), Biotechnology and Related Fields (8 papers), Cystic Fibrosis Research Advances (7 papers), Health Systems, Economic Evaluations, Quality of Life (4 papers), Metabolism and Genetic Disorders (3 papers), BRCA gene mutations in cancer (3 papers) and Cancer Genomics and Diagnostics (3 papers). The work is most often cited by research in Radiological and Ultrasound Technology (117 citations), Genetics (561 citations), Pediatrics, Perinatology and Child Health (237 citations), Genetics (120 citations) and Speech and Hearing (47 citations). Stephen C. Groft has collaborated with scholars based in United States, Spain and Italy. Frequent co-authors include Manuel Posada de la Paz, Ségolène Aymé, Domenica Taruscio, Carol Nicholson, Christopher Landon, Tammara L. Jenkins, Yaffa Rubinstein, Erik Tambuyzer, Jeffrey P. Krischer and Christopher P. Austin. Their work appears in journals such as Advances in experimental medicine and biology, Orphanet Journal of Rare Diseases, Molecular Genetics and Metabolism, Contemporary Clinical Trials 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.