Hal E. Schneider
Impact in
- Genetics top 5%
- Blood disorders and treatments
- Genomics and Rare Diseases
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- T-cell and B-cell Immunology
Papers in
- Genetics 10
- Blood disorders and treatments 9
- Genomics and Rare Diseases 1
-
- MicroRNA in disease regulation 1
- Co-authors
- Steven E. Shoelson (1 shared paper)Christopher E. Rudd (1 shared paper)Marie-Françoise O’Donohue (3 shared papers)Pierre‐Emmanuel Gleizes (3 shared papers)Mee Rie Sheen (3 shared papers)Peter E. Newburger (3 shared papers)Leana Doherty (3 shared papers)Edyta Niewiadomska (3 shared papers)
- Journals
- Blood (5 papers)The American Journal of Human Genetics (4 papers)BMC Genetics (1 paper)The Journal of Experimental Medicine (1 paper)Genome Medicine (1 paper)
- Partner nations
- United StatesPolandFrance
In The Last Decade
Hal E. Schneider
12 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 60
- Genetics 552
- Immunology 135
- Molecular Biology 414
- Oncology 129
- Hematology 71
Countries citing papers authored by Hal E. Schneider
This map shows the geographic impact of Hal E. Schneider'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 Hal E. Schneider with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hal E. Schneider more than expected).
Fields of papers citing papers by Hal E. Schneider
This network shows the impact of papers produced by Hal E. Schneider. 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 Hal E. Schneider. The network helps show where Hal E. Schneider may publish in the future.
Co-authors
The 25 scholars most cited alongside Hal E. Schneider, 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 | 2008 | 347 | |
| 2 | 2006 | 228 | |
| 3 | 2008 | 202 | |
| 4 | 2010 | 198 | |
| 5 | 1995 | 147 | |
| 6 | 2013 | 93 | |
| 7 | 2009 | 12 | |
| 8 | 2006 | 8 | |
| 9 | 2010 | 6 | |
| 10 | 2009 | 5 | |
| 11 | 2007 | 4 | |
| 12 | 2008 | 1 |
About Hal E. Schneider
Hal E. Schneider is a scholar working on Genetics, Cancer Research, Immunology, Pulmonary and Respiratory Medicine and Molecular Biology, having authored 12 papers that have together received 1.3k indexed citations. Recurring topics across this work include Blood disorders and treatments (9 papers), T-cell and B-cell Immunology (1 paper), PI3K/AKT/mTOR signaling in cancer (1 paper), MicroRNA in disease regulation (1 paper), Sarcoma Diagnosis and Treatment (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Genetics (552 citations), Immunology (135 citations), Molecular Biology (414 citations), Oncology (129 citations) and Hematology (71 citations). Hal E. Schneider has collaborated with scholars based in United States, Poland and France. Frequent co-authors include Steven E. Shoelson, Christopher E. Rudd, Marie-Françoise O’Donohue, Pierre‐Emmanuel Gleizes, Mee Rie Sheen, Peter E. Newburger, Leana Doherty, Edyta Niewiadomska, Michal J. Matysiak and Bertil E. Glader. Their work appears in journals such as Blood, The American Journal of Human Genetics, BMC Genetics, The Journal of Experimental Medicine 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.