Jennifer E. Troge
Impact in
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Cognitive Neuroscience top 0.5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 9
- Genomics and Rare Diseases 3
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- Prenatal Screening and Diagnostics 3
- Co-authors
- Michael H. Wigler (6 shared papers)Jude Kendall (4 shared papers)Linda Rodgers (3 shared papers)Dan L. Levy (2 shared papers)Nicholas E. Navin (4 shared papers)Diane Esposito (3 shared papers)Asya Stepansky (2 shared papers)James B Hicks (2 shared papers)
- Journals
- Science (2 papers)Neuron (2 papers)Nature (2 papers)Genetics in Medicine (1 paper)Bioinformatics (1 paper)
- Partner nations
- United StatesSwedenCanada
In The Last Decade
Jennifer E. Troge
10 papers receiving 10.0k citations
Jennifer E. Troge's Hit Papers
Peers
Comparison fields: 5 of 136
- Genetics 5.8k
- Cognitive Neuroscience 2.6k
- Cancer Research 1.8k
- Molecular Biology 4.9k
- Developmental Neuroscience 177
Countries citing papers authored by Jennifer E. Troge
This map shows the geographic impact of Jennifer E. Troge'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 Jennifer E. Troge with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jennifer E. Troge more than expected).
Fields of papers citing papers by Jennifer E. Troge
This network shows the impact of papers produced by Jennifer E. Troge. 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 Jennifer E. Troge. The network helps show where Jennifer E. Troge may publish in the future.
Co-authors
The 25 scholars most cited alongside Jennifer E. Troge, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Strong Association of De Novo Copy Number Mutations with Autism Hit paper breakdown → | 2007 | 2228 |
| 2 | Tumour evolution inferred by single-cell sequencing Hit paper breakdown → | 2011 | 2056 |
| 3 | Large-Scale Copy Number Polymorphism in the Human Genome Hit paper breakdown → | 2004 | 1942 |
| 4 | The contribution of de novo coding mutations to autism spectrum disorder Hit paper breakdown → | 2014 | 1929 |
| 5 | De Novo Gene Disruptions in Children on the Autistic Spectrum Hit paper breakdown → | 2012 | 1163 |
| 6 | Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders Hit paper breakdown → | 2011 | 562 |
| 7 | 2012 | 275 | |
| 8 | 2008 | 85 | |
| 9 | 2005 | 26 | |
| 10 | 2006 | 25 |
About Jennifer E. Troge
Jennifer E. Troge is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience, Cancer Research and Genetics, having authored 10 papers that have together received 10.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (3 papers), Prenatal Screening and Diagnostics (3 papers), Autism Spectrum Disorder Research (3 papers), Cancer Genomics and Diagnostics (2 papers), Immunodeficiency and Autoimmune Disorders (1 paper), Chromosomal and Genetic Variations (1 paper) and Congenital heart defects research (1 paper). The work is most often cited by research in Genetics (5.8k citations), Cognitive Neuroscience (2.6k citations), Cancer Research (1.8k citations), Molecular Biology (4.9k citations) and Developmental Neuroscience (177 citations). Jennifer E. Troge has collaborated with scholars based in United States, Sweden and Canada. Frequent co-authors include Michael H. Wigler, Jude Kendall, Linda Rodgers, Dan L. Levy, Nicholas E. Navin, Diane Esposito, Asya Stepansky, James B Hicks, A. Krasnitz and Peter Andrews. Their work appears in journals such as Science, Neuron, Nature, Genetics in Medicine and Bioinformatics.
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.