Pardeep Heir
Impact in
- Genetics top 10%
- Glioma Diagnosis and Treatment
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- Cancer, Hypoxia, and Metabolism
Papers in
- Genetics 3
- Glioma Diagnosis and Treatment 2
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- Erythropoietin and Anemia Treatment 2
- Co-authors
- Michael Ohh (10 shared papers)Severa Bunda (8 shared papers)Gelareh Mohammed Zadeh (4 shared papers)Brian Raught (3 shared papers)Kelly E. Burrell (3 shared papers)Yoshihito Kano (2 shared papers)Amir Alamsahebpour (2 shared papers)Zhong-Yin Zhang (1 shared paper)
- Journals
- Nature Communications (3 papers)Proceedings of the National Academy of Sciences (2 papers)Molecular Cancer Research (1 paper)Nature Medicine (1 paper)American Journal Of Pathology (1 paper)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Pardeep Heir
13 papers receiving 695 citations
Peers
Comparison fields: 5 of 56
- Genetics 70
- Cancer Research 98
- Molecular Biology 374
- Oncology 87
- Cell Biology 50
Countries citing papers authored by Pardeep Heir
This map shows the geographic impact of Pardeep Heir'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 Pardeep Heir with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pardeep Heir more than expected).
Fields of papers citing papers by Pardeep Heir
This network shows the impact of papers produced by Pardeep Heir. 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 Pardeep Heir. The network helps show where Pardeep Heir may publish in the future.
Co-authors
The 25 scholars most cited alongside Pardeep Heir, 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 | 2015 | 196 | |
| 2 | 2012 | 118 | |
| 3 | 2014 | 89 | |
| 4 | 2011 | 65 | |
| 5 | 2019 | 65 | |
| 6 | 2011 | 36 | |
| 7 | 2016 | 29 | |
| 8 | 2023 | 28 | |
| 9 | 2013 | 21 | |
| 10 | 2013 | 17 | |
| 11 | 2014 | 17 | |
| 12 | 2020 | 14 | |
| 13 | 2016 | 7 |
About Pardeep Heir
Pardeep Heir is a scholar working on Genetics, Hematology, Cancer Research, Molecular Biology and Oncology, having authored 13 papers that have together received 702 indexed citations. Recurring topics across this work include Cancer, Hypoxia, and Metabolism (3 papers), Ubiquitin and proteasome pathways (3 papers), Erythropoietin and Anemia Treatment (2 papers), Protein Tyrosine Phosphatases (2 papers), Glioma Diagnosis and Treatment (2 papers), Protein Kinase Regulation and GTPase Signaling (2 papers), Cytokine Signaling Pathways and Interactions (2 papers) and Neurofibromatosis and Schwannoma Cases (1 paper). The work is most often cited by research in Genetics (70 citations), Cancer Research (98 citations), Molecular Biology (374 citations), Oncology (87 citations) and Cell Biology (50 citations). Pardeep Heir has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Michael Ohh, Severa Bunda, Gelareh Mohammed Zadeh, Brian Raught, Kelly E. Burrell, Yoshihito Kano, Amir Alamsahebpour, Zhong-Yin Zhang, Li‐Fan Zeng and Jeffrey E. Lee. Their work appears in journals such as Nature Communications, Proceedings of the National Academy of Sciences, Molecular Cancer Research, Nature Medicine and American Journal Of Pathology.
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.