Gerard D. Schellenberg
Impact in
- Physiology top 0.05%
- Alzheimer's disease research and treatments
- Aging top 0.2%
Papers in
- Physiology 122
- Alzheimer's disease research and treatments 119
- Genetics 93
- Genetic Associations and Epidemiology 49
- Genomic variations and chromosomal abnormalities 22
- Genetics and Neurodevelopmental Disorders 19
- Co-authors
- Ellen M. Wijsman (28 shared papers)Thomas D. Bird (42 shared papers)Parvoneh Poorkaj (25 shared papers)Ian D’Souza (18 shared papers)Ellen J. Nemens (8 shared papers)Chang-En Yu (16 shared papers)Murray A. Raskind (11 shared papers)Junko Oshima (10 shared papers)
- Journals
- Alzheimer s & Dementia (56 papers)Annals of Neurology (16 papers)Genomics (14 papers)Neurology (13 papers)Acta Neuropathologica (11 papers)
- Partner nations
- United StatesJapanUnited Kingdom
In The Last Decade
Gerard D. Schellenberg
307 papers receiving 31.3k citations
Gerard D. Schellenberg's Hit Papers
Peers
Comparison fields: 5 of 184
- Physiology 11.9k
- Aging 737
- Neurology 3.1k
- Genetics 8.8k
- Neurology 3.7k
Countries citing papers authored by Gerard D. Schellenberg
This map shows the geographic impact of Gerard D. 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 D. 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 D. Schellenberg more than expected).
Fields of papers citing papers by Gerard D. Schellenberg
This network shows the impact of papers produced by Gerard D. 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 D. Schellenberg. The network helps show where Gerard D. Schellenberg may publish in the future.
Co-authors
The 25 scholars most cited alongside Gerard D. 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 312 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus Hit paper breakdown → | 1995 | 2157 |
| 2 | Functional impact of global rare copy number variation in autism spectrum disorders Hit paper breakdown → | 2010 | 1652 |
| 3 | Positional Cloning of the Werner's Syndrome Gene Hit paper breakdown → | 1996 | 1482 |
| 4 | Patterns and rates of exonic de novo mutations in autism spectrum disorders Hit paper breakdown → | 2012 | 1378 |
| 5 | Tau is a candidate gene for chromosome 17 frontotemporal dementia Hit paper breakdown → | 1998 | 1195 |
| 6 | Autism genome-wide copy number variation reveals ubiquitin and neuronal genes Hit paper breakdown → | 2009 | 1178 |
| 7 | Mapping autism risk loci using genetic linkage and chromosomal rearrangements Hit paper breakdown → | 2007 | 1155 |
| 8 | Common genetic variants on 5p14.1 associate with autism spectrum disorders Hit paper breakdown → | 2009 | 807 |
| 9 | Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14 Hit paper breakdown → | 1992 | 783 |
| 10 | A framework for the interpretation of de novo mutation in human disease Hit paper breakdown → | 2014 | 704 |
| 11 | Dementia and Alzheimer Disease Incidence Hit paper breakdown → | 2002 | 652 |
| 12 | 1998 | 501 | |
| 13 | 2010 | 501 | |
| 14 | Effect of Vitamin E and Memantine on Functional Decline in Alzheimer Disease Hit paper breakdown → | 2013 | 481 |
| 15 | 1999 | 431 | |
| 16 | 1998 | 424 | |
| 17 | 2009 | 346 | |
| 18 | Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4, and the Risk of Late-Onset Alzheimer Disease in African Americans Hit paper breakdown → | 2013 | 343 |
| 19 | 1995 | 330 | |
| 20 | Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study Hit paper breakdown → | 2020 | 328 |
About Gerard D. Schellenberg
Gerard D. Schellenberg is a scholar working on Physiology, Genetics, Neurology, Molecular Biology and Psychiatry and Mental health, having authored 312 papers that have together received 32.6k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (119 papers), Genetic Associations and Epidemiology (49 papers), Bioinformatics and Genomic Networks (35 papers), Dementia and Cognitive Impairment Research (33 papers), Parkinson's Disease Mechanisms and Treatments (25 papers), Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Nuclear Receptors and Signaling (18 papers). The work is most often cited by research in Physiology (11.9k citations), Aging (737 citations), Neurology (3.1k citations), Genetics (8.8k citations) and Neurology (3.7k citations). Gerard D. Schellenberg has collaborated with scholars based in United States, Japan and United Kingdom. Frequent co-authors include Ellen M. Wijsman, Thomas D. Bird, Parvoneh Poorkaj, Ian D’Souza, Ellen J. Nemens, Chang-En Yu, Murray A. Raskind, Junko Oshima, Ying‐Hui Fu and George M. Martin. Their work appears in journals such as Alzheimer s & Dementia, Annals of Neurology, Genomics, Neurology and Acta Neuropathologica.
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.