Gail E. Graham
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 2%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 38
- Genomics and Rare Diseases 23
- Genetics and Neurodevelopmental Disorders 8
- Craniofacial Disorders and Treatments 5
- Genomic variations and chromosomal abnormalities 5
- Genetic and rare skin diseases. 5
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- Congenital limb and hand anomalies 5
- Co-authors
- Kym M. Boycott (7 shared papers)Martin J. Somerville (1 shared paper)Karen Booth (1 shared paper)Roberto T. Zori (1 shared paper)Jamie L. Steckley (1 shared paper)Errol B. Marliss (1 shared paper)Susan E. Andrew (1 shared paper)Charis Eng (1 shared paper)
- Journals
- Genetics in Medicine (6 papers)European Journal of Human Genetics (5 papers)The American Journal of Human Genetics (4 papers)Clinical Genetics (3 papers)Journal of Biological Chemistry (2 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Gail E. Graham
65 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 99
- Developmental Biology 100
- Genetics 977
- Cellular and Molecular Neuroscience 305
- Pathology and Forensic Medicine 258
- Clinical Biochemistry 61
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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 305 | |
| 2 | 2005 | 202 | |
| 3 | 2006 | 195 | |
| 4 | 2013 | 165 | |
| 5 | 1999 | 134 | |
| 6 | A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots. | 2002 | 124 |
| 7 | 2005 | 116 | |
| 8 | 1998 | 88 | |
| 9 | 2016 | 81 | |
| 10 | Genetic education for primary care providers: improving attitudes, knowledge, and confidence. | 2009 | 77 |
| 11 | 2014 | 75 | |
| 12 | 2016 | 73 | |
| 13 | 2015 | 71 | |
| 14 | 2012 | 69 | |
| 15 | 2008 | 67 | |
| 16 | 2008 | 62 | |
| 17 | 2011 | 55 | |
| 18 | 2013 | 37 | |
| 19 | 2011 | 33 | |
| 20 | 2013 | 32 |
About Gail E. Graham
Gail E. Graham is a scholar working on Genetics, Developmental Biology, Cellular and Molecular Neuroscience, Clinical Biochemistry and Pathology and Forensic Medicine, having authored 67 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (23 papers), Genetics and Neurodevelopmental Disorders (8 papers), Craniofacial Disorders and Treatments (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Congenital limb and hand anomalies (5 papers), Genetic and rare skin diseases. (5 papers), Genetic factors in colorectal cancer (4 papers) and Neuroscience and Neuropharmacology Research (4 papers). The work is most often cited by research in Developmental Biology (100 citations), Genetics (977 citations), Cellular and Molecular Neuroscience (305 citations), Pathology and Forensic Medicine (258 citations) and Clinical Biochemistry (61 citations). Gail E. Graham has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Kym M. Boycott, Martin J. Somerville, Karen Booth, Roberto T. Zori, Jamie L. Steckley, Errol B. Marliss, Susan E. Andrew, Charis Eng, René Santer and Steffan Loff. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics, The American Journal of Human Genetics, Clinical Genetics and Journal of Biological Chemistry.
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.