Gerard Schellenberg
Impact in
- Clinical Biochemistry top 1%
- Paraoxonase enzyme and polymorphisms
- Oral Surgery top 5%
- Oral and Maxillofacial Pathology
Papers in
- Genetics 9
- Genetic Associations and Epidemiology 5
- Genetics and Neurodevelopmental Disorders 3
- Nutrition, Genetics, and Disease 2
- Co-authors
- Laura S. Rozek (3 shared papers)Gail P. Jarvik (3 shared papers)Rebecca J. Richter (3 shared papers)Clement E. Furlong (3 shared papers)Victoria H. Brophy (2 shared papers)Thomas S. Hatsukami (2 shared papers)Ellen M. Wijsman (5 shared papers)Géraldine Dawson (3 shared papers)
- Journals
- Alzheimer s & Dementia (9 papers)Journal of Lipid Research (1 paper)Molecular Psychiatry (1 paper)The American Journal of Human Genetics (1 paper)Neurology (1 paper)
- Partner nations
- United StatesVietnamGermany
In The Last Decade
Gerard Schellenberg
21 papers receiving 836 citations
Peers
Comparison fields: 5 of 79
- Clinical Biochemistry 333
- Oral Surgery 72
- Rheumatology 137
- Biochemistry 49
- Pharmacology 49
Countries citing papers authored by Gerard Schellenberg
This map shows the geographic impact of Gerard Schellenberg'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 Gerard Schellenberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gerard Schellenberg more than expected).
Fields of papers citing papers by Gerard Schellenberg
This network shows the impact of papers produced by Gerard Schellenberg. 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 Gerard Schellenberg. The network helps show where Gerard Schellenberg may publish in the future.
Co-authors
The 25 scholars most cited alongside Gerard Schellenberg, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 280 | |
| 2 | Genetic heterogeneity in families with hereditary multiple exostoses. | 1993 | 169 |
| 3 | 2004 | 91 | |
| 4 | Linkage analysis of familial Alzheimer disease, using chromosome 21 markers. | 1991 | 59 |
| 5 | 2000 | 51 | |
| 6 | 2005 | 49 | |
| 7 | 2010 | 44 | |
| 8 | 2018 | 33 | |
| 9 | 2011 | 27 | |
| 10 | 1995 | 20 | |
| 11 | 2016 | 11 | |
| 12 | 2024 | 10 | |
| 13 | 2006 | 2 | |
| 14 | 2001 | 2 | |
| 15 | 2014 | 1 | |
| 16 | 1989 | 1 | |
| 17 | 2013 | 1 | |
| 18 | 2013 | 1 | |
| 19 | 2000 | 1 | |
| 20 | 2018 | 1 |
About Gerard Schellenberg
Gerard Schellenberg is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Clinical Biochemistry and Plant Science, having authored 24 papers that have together received 856 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (5 papers), Autism Spectrum Disorder Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Paraoxonase enzyme and polymorphisms (3 papers), Cynara cardunculus studies (3 papers), Alzheimer's disease research and treatments (2 papers), Nutrition, Genetics, and Disease (2 papers) and Apelin-related biomedical research (2 papers). The work is most often cited by research in Clinical Biochemistry (333 citations), Oral Surgery (72 citations), Rheumatology (137 citations), Biochemistry (49 citations) and Pharmacology (49 citations). Gerard Schellenberg has collaborated with scholars based in United States, Vietnam and Germany. Frequent co-authors include Laura S. Rozek, Gail P. Jarvik, Rebecca J. Richter, Clement E. Furlong, Victoria H. Brophy, Thomas S. Hatsukami, Ellen M. Wijsman, Géraldine Dawson, Annette Estes and Ronald G. Gregg. Their work appears in journals such as Alzheimer s & Dementia, Journal of Lipid Research, Molecular Psychiatry, The American Journal of Human Genetics and Neurology.
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.