PG Waber
Impact in
- Genetics top 5%
- Hemoglobinopathies and Related Disorders
- Genomics and Rare Diseases
- Hematology top 5%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
- Genetics 12
- Hemoglobinopathies and Related Disorders 12
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- Iron Metabolism and Disorders 7
- Blood groups and transfusion 2
- Co-authors
- Steve S. Huang (2 shared papers)HH Jr Kazazian (6 shared papers)CD Boehm (5 shared papers)FS Collins (4 shared papers)BG Forget (4 shared papers)Stylianos E. Antonarakis (3 shared papers)GR Buchanan (2 shared papers)SH Orkin (2 shared papers)
- Journals
- Blood (10 papers)PubMed (3 papers)
- Partner nations
- United States
In The Last Decade
PG Waber
13 papers receiving 363 citations
Peers
Comparison fields: 5 of 33
- Genetics 260
- Hematology 165
- Pediatrics, Perinatology and Child Health 56
- Virology 11
- Genetics 58
Countries citing papers authored by PG Waber
This map shows the geographic impact of PG Waber'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 PG Waber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites PG Waber more than expected).
Fields of papers citing papers by PG Waber
This network shows the impact of papers produced by PG Waber. 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 PG Waber. The network helps show where PG Waber may publish in the future.
Co-authors
The 14 scholars most cited alongside PG Waber, 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 | 1986 | 76 | |
| 2 | 1986 | 54 | |
| 3 | 1983 | 49 | |
| 4 | 1984 | 38 | |
| 5 | Frequent allelic loss at chromosome arm 3p is distinct from genetic alterations of the Von-Hippel Lindau tumor suppressor gene in head and neck cancer. | 1996 | 36 |
| 6 | 1986 | 34 | |
| 7 | 1983 | 26 | |
| 8 | 1986 | 24 | |
| 9 | 1986 | 19 | |
| 10 | 1986 | 8 | |
| 11 | Beta-thalassemia in Chinese--analysis of polymorphic restriction site haplotypes in the beta-globin gene cluster. | 1985 | 5 |
| 12 | Use of haplotype analysis in the beta-globin gene cluster to discover beta-thalassemia mutations. | 1983 | 3 |
| 13 | 1984 | 1 |
About PG Waber
PG Waber is a scholar working on Genetics, Hematology, Molecular Biology, Nutrition and Dietetics and Pharmacology, having authored 13 papers that have together received 373 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (12 papers), Iron Metabolism and Disorders (7 papers), Blood groups and transfusion (2 papers), Child Nutrition and Water Access (2 papers), RNA modifications and cancer (2 papers), Metabolism and Genetic Disorders (1 paper), DNA and Nucleic Acid Chemistry (1 paper) and Trace Elements in Health (1 paper). The work is most often cited by research in Genetics (260 citations), Hematology (165 citations), Pediatrics, Perinatology and Child Health (56 citations), Virology (11 citations) and Genetics (58 citations). PG Waber has collaborated with scholars based in United States. Frequent co-authors include Steve S. Huang, HH Jr Kazazian, CD Boehm, FS Collins, BG Forget, Stylianos E. Antonarakis, GR Buchanan, SH Orkin, S Weissman and G. Stamatoyannopoulos. Their work appears in journals such as Blood and PubMed.
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.