Judith E Allanson
Impact in
Papers in
- Genetics 80
- Genomic variations and chromosomal abnormalities 26
- BRCA gene mutations in cancer 19
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- Prenatal Screening and Diagnostics 24
- Co-authors
- Amy E. Roberts (3 shared papers)Bruce D. Gelb (2 shared papers)Raoul C. M. Hennekam (12 shared papers)Marco Tartaglia (1 shared paper)Judith G. Hall (14 shared papers)John M. Opitz (9 shared papers)June Carroll (32 shared papers)Alasdair G. W. Hunter (12 shared papers)
- Journals
- Journal of Medical Genetics (18 papers)Clinical Genetics (10 papers)European Journal of Human Genetics (8 papers)PEDIATRICS (6 papers)NeuroImage Clinical (5 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Judith E Allanson
207 papers receiving 11.6k citations
Judith E Allanson's Hit Papers
Peers
Comparison fields: 5 of 174
- Genetics 3.3k
- Neurology 1.7k
- Developmental Biology 254
- Pediatrics, Perinatology and Child Health 1.3k
- Emergency Medicine 576
Countries citing papers authored by Judith E Allanson
This map shows the geographic impact of Judith E Allanson'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 Judith E Allanson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judith E Allanson more than expected).
Fields of papers citing papers by Judith E Allanson
This network shows the impact of papers produced by Judith E Allanson. 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 Judith E Allanson. The network helps show where Judith E Allanson may publish in the future.
Co-authors
The 25 scholars most cited alongside Judith E Allanson, 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 212 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Traumatic brain injury: integrated approaches to improve prevention, clinical care, and research Hit paper breakdown → | 2017 | 1926 |
| 2 | Noonan syndrome Hit paper breakdown → | 2013 | 604 |
| 3 | 2010 | 469 | |
| 4 | 1987 | 272 | |
| 5 | 2003 | 217 | |
| 6 | 2004 | 215 | |
| 7 | 2006 | 211 | |
| 8 | 1987 | 206 | |
| 9 | Prenatal cocaine exposure and fetal vascular disruption. | 1990 | 202 |
| 10 | 2004 | 202 | |
| 11 | 1990 | 197 | |
| 12 | 1985 | 197 | |
| 13 | 2014 | 186 | |
| 14 | 2019 | 173 | |
| 15 | Gorlin's Syndromes of the Head and Neck | 2010 | 166 |
| 16 | 2012 | 148 | |
| 17 | Transverse myelitis as the first manifestation of systemic lupus erythematosus or lupus-like disease: good functional outcome and relevance of antiphospholipid antibodies. | 2004 | 139 |
| 18 | 2003 | 134 | |
| 19 | 2009 | 133 | |
| 20 | 1993 | 132 |
About Judith E Allanson
Judith E Allanson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Developmental Biology and Cognitive Neuroscience, having authored 212 papers that have together received 12.3k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (29 papers), Genomic variations and chromosomal abnormalities (26 papers), Prenatal Screening and Diagnostics (24 papers), BRCA gene mutations in cancer (19 papers), Galectins and Cancer Biology (15 papers), Functional Brain Connectivity Studies (15 papers), Traumatic Brain Injury Research (15 papers) and Congenital limb and hand anomalies (13 papers). The work is most often cited by research in Genetics (3.3k citations), Neurology (1.7k citations), Developmental Biology (254 citations), Pediatrics, Perinatology and Child Health (1.3k citations) and Emergency Medicine (576 citations). Judith E Allanson has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Amy E. Roberts, Bruce D. Gelb, Raoul C. M. Hennekam, Marco Tartaglia, Judith G. Hall, John M. Opitz, June Carroll, Alasdair G. W. Hunter, Brenda J. Wilson and John Douglas Pickard. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, European Journal of Human Genetics, PEDIATRICS and NeuroImage Clinical.
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.