Matthew Jensen
Impact in
-
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 5
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- Congenital heart defects research 4
- Genomics and Chromatin Dynamics 2
- 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)Janani Iyer (5 shared papers)Kenneth Finegold (1 shared paper)Emily Huber (4 shared papers)
- Journals
- PLoS Genetics (4 papers)Scientific Reports (2 papers)Science Advances (2 papers)Medical Care (2 papers)Genome Medicine (2 papers)
- Partner nations
- United StatesAustraliaUruguay
In The Last Decade
Matthew Jensen
20 papers receiving 344 citations
Peers
Comparison fields: 5 of 96
- Genetics 160
- Aging 8
- Cancer Research 46
- Molecular Biology 153
- Biological Psychiatry 5
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
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 40 | |
| 2 | 2017 | 40 | |
| 3 | 2019 | 33 | |
| 4 | 2016 | 28 | |
| 5 | 2019 | 26 | |
| 6 | 2019 | 25 | |
| 7 | 2020 | 25 | |
| 8 | 2016 | 22 | |
| 9 | 2019 | 19 | |
| 10 | 2021 | 13 | |
| 11 | 2022 | 12 | |
| 12 | 2017 | 12 | |
| 13 | 2020 | 11 | |
| 14 | 2024 | 11 | |
| 15 | 2021 | 9 | |
| 16 | 2020 | 8 | |
| 17 | 2024 | 7 | |
| 18 | Accelerating development using the web: empowering poor and marginalized populations. | 2012 | 5 |
| 19 | 2021 | 2 | |
| 20 | 2022 | 1 |
About Matthew Jensen
Matthew Jensen is a scholar working on Genetics, Molecular Biology, Plant Science, General Health Professions and Cognitive Neuroscience, having authored 20 papers that have together received 349 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (5 papers), Congenital heart defects research (4 papers), Autism Spectrum Disorder Research (2 papers), Genomics and Chromatin Dynamics (2 papers) and Healthcare Policy and Management (2 papers). The work is most often cited by research in Genetics (160 citations), Aging (8 citations), Cancer Research (46 citations), Molecular Biology (153 citations) and Biological Psychiatry (5 citations). Matthew Jensen has collaborated with scholars based in United States, Australia and Uruguay. Frequent co-authors include Santhosh Girirajan, Qingyu Wang, Karen E. Joynt, Cooduvalli S. Shashikant, Naomi Altman, Janani Iyer, Kenneth Finegold, Emily Huber, Lucilla Pizzo and Hajar Amini. Their work appears in journals such as PLoS Genetics, Scientific Reports, Science Advances, Medical Care and Genome Medicine.
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.