Matthew Jensen
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 2
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- Congenital heart defects research 4
- Genomics and Chromatin Dynamics 3
- Co-authors
- Santhosh Girirajan (13 shared papers)Qingyu Wang (2 shared papers)Karen E. Joynt (2 shared papers)Cooduvalli S. Shashikant (1 shared paper)Naomi Altman (1 shared paper)Lucilla Pizzo (5 shared papers)Janani Iyer (5 shared papers)Kenneth Finegold (1 shared paper)
- Journals
- PLoS Genetics (4 papers)Science Advances (2 papers)Medical Care (2 papers)Genome Medicine (2 papers)Genome Research (2 papers)
- Partner nations
- United StatesNetherlandsBelgium
In The Last Decade
Matthew Jensen
20 papers receiving 359 citations
Peers
Comparison fields: 5 of 94
- Genetics 152
- Aging 8
- Cancer Research 37
- Biological Psychiatry 6
- Cognitive Neuroscience 40
Countries citing papers authored by Matthew Jensen
This map shows the geographic impact of Matthew Jensen'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 Matthew Jensen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew Jensen more than expected).
Fields of papers citing papers by Matthew Jensen
This network shows the impact of papers produced by Matthew Jensen. 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 Matthew Jensen. The network helps show where Matthew Jensen may publish in the future.
Co-authors
The 25 scholars most cited alongside Matthew Jensen, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 42 | |
| 2 | 2017 | 42 | |
| 3 | 2019 | 34 | |
| 4 | 2016 | 28 | |
| 5 | 2020 | 26 | |
| 6 | 2019 | 26 | |
| 7 | 2019 | 25 | |
| 8 | 2016 | 22 | |
| 9 | 2019 | 19 | |
| 10 | 2021 | 14 | |
| 11 | 2022 | 14 | |
| 12 | 2017 | 12 | |
| 13 | 2024 | 12 | |
| 14 | 2020 | 11 | |
| 15 | 2021 | 11 | |
| 16 | 2024 | 9 | |
| 17 | 2020 | 8 | |
| 18 | Accelerating development using the web: empowering poor and marginalized populations. | 2012 | 5 |
| 19 | 2021 | 3 | |
| 20 | 2022 | 1 |
About Matthew Jensen
Matthew Jensen is a scholar working on Genetics, Molecular Biology, Plant Science, General Health Professions and Physiology, having authored 22 papers that have together received 364 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (5 papers), Congenital heart defects research (4 papers), Genomics and Rare Diseases (4 papers), Genomics and Chromatin Dynamics (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Primary Care and Health Outcomes (2 papers) and Genetics, Aging, and Longevity in Model Organisms (2 papers). The work is most often cited by research in Genetics (152 citations), Aging (8 citations), Cancer Research (37 citations), Biological Psychiatry (6 citations) and Cognitive Neuroscience (40 citations). Matthew Jensen has collaborated with scholars based in United States, Netherlands and Belgium. Frequent co-authors include Santhosh Girirajan, Qingyu Wang, Karen E. Joynt, Cooduvalli S. Shashikant, Naomi Altman, Lucilla Pizzo, Janani Iyer, Kenneth Finegold, Emily Huber and Fereydoun Hormozdiari. Their work appears in journals such as PLoS Genetics, Science Advances, Medical Care, Genome Medicine and Genome Research.
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.