Gail E. Graham
Impact in
-
- Genetic factors in colorectal cancer
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
Papers in
-
- Epigenetics and DNA Methylation 4
- Protein Tyrosine Phosphatases 4
- PI3K/AKT/mTOR signaling in cancer 4
- Genetics 19
- Neurogenetic and Muscular Disorders Research 5
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 4
- Genetic Syndromes and Imprinting 4
- Co-authors
- Herbert L. DuPont (3 shared papers)Kevin W. Garey (3 shared papers)Margaret P. Price (3 shared papers)Charis Eng (2 shared papers)Roberto T. Zori (2 shared papers)Errol B. Marliss (2 shared papers)Karen Booth (1 shared paper)Ross McLeod (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Genetics in Medicine (3 papers)Pediatric Research (2 papers)Human Mutation (2 papers)Canadian Family Physician (2 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Gail E. Graham
59 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 104
- Pathology and Forensic Medicine 293
- Genetics 486
- Developmental Biology 30
- Genetics 118
- Cellular and Molecular Neuroscience 212
Countries citing papers authored by Gail E. Graham
This map shows the geographic impact of Gail E. Graham'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 Gail E. Graham with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gail E. Graham more than expected).
Fields of papers citing papers by Gail E. Graham
This network shows the impact of papers produced by Gail E. Graham. 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 Gail E. Graham. The network helps show where Gail E. Graham may publish in the future.
Co-authors
The 25 scholars most cited alongside Gail E. Graham, 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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 175 | |
| 2 | 2006 | 172 | |
| 3 | 2013 | 143 | |
| 4 | 1999 | 121 | |
| 5 | A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots. | 2002 | 113 |
| 6 | 2005 | 104 | |
| 7 | 1998 | 77 | |
| 8 | Genetic education for primary care providers: improving attitudes, knowledge, and confidence. | 2009 | 76 |
| 9 | 2006 | 69 | |
| 10 | 2016 | 68 | |
| 11 | 2014 | 61 | |
| 12 | 2008 | 60 | |
| 13 | 2008 | 55 | |
| 14 | 2011 | 48 | |
| 15 | 2006 | 39 | |
| 16 | 2007 | 37 | |
| 17 | 2011 | 28 | |
| 18 | 1994 | 28 | |
| 19 | 2018 | 25 | |
| 20 | 2017 | 24 |
About Gail E. Graham
Gail E. Graham is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Infectious Diseases and Surgery, having authored 60 papers that have together received 1.9k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (5 papers), Epigenetics and DNA Methylation (4 papers), Protein Tyrosine Phosphatases (4 papers), PI3K/AKT/mTOR signaling in cancer (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (4 papers), Genetic Syndromes and Imprinting (4 papers) and Renal cell carcinoma treatment (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (293 citations), Genetics (486 citations), Developmental Biology (30 citations), Genetics (118 citations) and Cellular and Molecular Neuroscience (212 citations). Gail E. Graham has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Herbert L. DuPont, Kevin W. Garey, Margaret P. Price, Charis Eng, Roberto T. Zori, Errol B. Marliss, Karen Booth, Ross McLeod, Susan E. Andrew and J. L. Steckley. Their work appears in journals such as European Journal of Human Genetics, Genetics in Medicine, Pediatric Research, Human Mutation and Canadian Family Physician.
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.