Gerard D. Schellenberg
Impact in
- Physiology top 0.01%
- Alzheimer's disease research and treatments
- Psychiatry and Mental health top 0.05%
- Dementia and Cognitive Impairment Research
Papers in
- Physiology 339
- Alzheimer's disease research and treatments 333
-
- Dementia and Cognitive Impairment Research 153
- Co-authors
- Thomas D. Bird (70 shared papers)Ellen M. Wijsman (47 shared papers)Ellen J. Nemens (17 shared papers)Parvoneh Poorkaj (30 shared papers)Chang‐En Yu (26 shared papers)Eric B. Larson (28 shared papers)Murray A. Raskind (19 shared papers)Ian D’Souza (18 shared papers)
- Journals
- Alzheimer s & Dementia (86 papers)Neurology (36 papers)Annals of Neurology (20 papers)Neurobiology of Aging (18 papers)Nature Genetics (17 papers)
- Partner nations
- United StatesUnited KingdomFrance
In The Last Decade
Gerard D. Schellenberg
523 papers receiving 68.9k citations
Gerard D. Schellenberg's Hit Papers
Peers
Comparison fields: 5 of 213
- Physiology 27.6k
- Psychiatry and Mental health 15.5k
- Neurology 7.5k
- Genetics 11.8k
- Aging 668
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 536 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease Hit paper breakdown → | 2013 | 3486 |
| 2 | Secreted amyloid β–protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease Hit paper breakdown → | 1996 | 2231 |
| 3 | Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus Hit paper breakdown → | 1995 | 2148 |
| 4 | Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing Hit paper breakdown → | 2019 | 2140 |
| 5 | Synaptic, transcriptional and chromatin genes disrupted in autism Hit paper breakdown → | 2014 | 2115 |
| 6 | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Hit paper breakdown → | 2013 | 1806 |
| 7 | Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria Hit paper breakdown → | 2017 | 1800 |
| 8 | Functional impact of global rare copy number variation in autism spectrum disorders Hit paper breakdown → | 2010 | 1667 |
| 9 | Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease Hit paper breakdown → | 2011 | 1603 |
| 10 | New insights into the genetic etiology of Alzheimer’s disease and related dementias Hit paper breakdown → | 2022 | 1531 |
| 11 | Positional Cloning of the Werner's Syndrome Gene Hit paper breakdown → | 1996 | 1471 |
| 12 | Patterns and rates of exonic de novo mutations in autism spectrum disorders Hit paper breakdown → | 2012 | 1386 |
| 13 | Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease Hit paper breakdown → | 2014 | 1332 |
| 14 | Tau is a candidate gene for chromosome 17 frontotemporal dementia Hit paper breakdown → | 1998 | 1195 |
| 15 | Autism genome-wide copy number variation reveals ubiquitin and neuronal genes Hit paper breakdown → | 2009 | 1177 |
| 16 | Mapping autism risk loci using genetic linkage and chromosomal rearrangements Hit paper breakdown → | 2007 | 1148 |
| 17 | Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study Hit paper breakdown → | 2012 | 1005 |
| 18 | Common genetic variants on 5p14.1 associate with autism spectrum disorders Hit paper breakdown → | 2009 | 812 |
| 19 | Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14 Hit paper breakdown → | 1992 | 780 |
| 20 | Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease Hit paper breakdown → | 2017 | 764 |
About Gerard D. Schellenberg
Gerard D. Schellenberg is a scholar working on Physiology, Psychiatry and Mental health, Neurology, Genetics and Cognitive Neuroscience, having authored 536 papers that have together received 71.4k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (333 papers), Dementia and Cognitive Impairment Research (153 papers), Genetic Associations and Epidemiology (61 papers), Autism Spectrum Disorder Research (39 papers), Parkinson's Disease Mechanisms and Treatments (32 papers), Amyotrophic Lateral Sclerosis Research (23 papers), Genomics and Rare Diseases (17 papers) and Genomic variations and chromosomal abnormalities (11 papers). The work is most often cited by research in Physiology (27.6k citations), Psychiatry and Mental health (15.5k citations), Neurology (7.5k citations), Genetics (11.8k citations) and Aging (668 citations). Gerard D. Schellenberg has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Thomas D. Bird, Ellen M. Wijsman, Ellen J. Nemens, Parvoneh Poorkaj, Chang‐En Yu, Eric B. Larson, Murray A. Raskind, Ian D’Souza, Elaine R. Peskind and Suzanne Craft. Their work appears in journals such as Alzheimer s & Dementia, Neurology, Annals of Neurology, Neurobiology of Aging and Nature Genetics.
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.