Brian A. Gray
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 6
- Genetic Syndromes and Imprinting 4
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- RNA modifications and cancer 5
- Co-authors
- Charles A. Williams (11 shared papers)Roberto T. Zori (9 shared papers)Roberto T. Zori (8 shared papers)Robert Zori (6 shared papers)John W. Stone (2 shared papers)Jill E. Hendrickson (2 shared papers)Jan S. Moreb (3 shared papers)James R. Zucali (2 shared papers)
- Journals
- Genes Chromosomes and Cancer (2 papers)American Journal of Medical Genetics (10 papers)Human Gene Therapy (1 paper)British Journal of Haematology (1 paper)Human Reproduction (1 paper)
- Partner nations
- United StatesUnited KingdomCzechia
In The Last Decade
Brian A. Gray
37 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 97
- Genetics 567
- Genetics 95
- Pediatrics, Perinatology and Child Health 164
- Molecular Biology 517
- Cancer Research 102
Countries citing papers authored by Brian A. Gray
This map shows the geographic impact of Brian A. Gray'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 Brian A. Gray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brian A. Gray more than expected).
Fields of papers citing papers by Brian A. Gray
This network shows the impact of papers produced by Brian A. Gray. 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 Brian A. Gray. The network helps show where Brian A. Gray may publish in the future.
Co-authors
The 25 scholars most cited alongside Brian A. Gray, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 138 | |
| 2 | 1990 | 95 | |
| 3 | 1989 | 77 | |
| 4 | 1992 | 70 | |
| 5 | 1993 | 65 | |
| 6 | 2007 | 56 | |
| 7 | 2004 | 49 | |
| 8 | 2000 | 38 | |
| 9 | 1993 | 33 | |
| 10 | 1998 | 31 | |
| 11 | 2012 | 31 | |
| 12 | 1998 | 29 | |
| 13 | 1993 | 28 | |
| 14 | 1997 | 27 | |
| 15 | 1969 | 26 | |
| 16 | Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient. | 1995 | 25 |
| 17 | 1994 | 24 | |
| 18 | 1996 | 23 | |
| 19 | 1986 | 23 | |
| 20 | 2002 | 19 |
About Brian A. Gray
Brian A. Gray is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 38 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (6 papers), Chromosomal and Genetic Variations (6 papers), RNA modifications and cancer (5 papers), Genetic Syndromes and Imprinting (4 papers), Acute Myeloid Leukemia Research (3 papers), Chronic Myeloid Leukemia Treatments (3 papers) and Neurofibromatosis and Schwannoma Cases (3 papers). The work is most often cited by research in Genetics (567 citations), Genetics (95 citations), Pediatrics, Perinatology and Child Health (164 citations), Molecular Biology (517 citations) and Cancer Research (102 citations). Brian A. Gray has collaborated with scholars based in United States, United Kingdom and Czechia. Frequent co-authors include Charles A. Williams, Roberto T. Zori, Roberto T. Zori, Robert Zori, John W. Stone, Jill E. Hendrickson, Jan S. Moreb, James R. Zucali, Daniel J. Driscoll and Edward W. Scott. Their work appears in journals such as Genes Chromosomes and Cancer, American Journal of Medical Genetics, Human Gene Therapy, British Journal of Haematology and Human Reproduction.
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.