CD Boehm
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 9
- Hemoglobinopathies and Related Disorders 9
- Nutrition, Genetics, and Disease 1
-
- Iron Metabolism and Disorders 5
- Blood groups and transfusion 2
- Co-authors
- PG Waber (5 shared papers)R Anand (1 shared paper)A. Kim Ritchey (1 shared paper)Terry A. Vik (1 shared paper)HH Jr Kazazian (2 shared papers)BG Forget (2 shared papers)S Weissman (2 shared papers)FS Collins (2 shared papers)
- Journals
- Blood (6 papers)PubMed (5 papers)
- Partner nations
- United States
In The Last Decade
CD Boehm
10 papers receiving 369 citations
Peers
Comparison fields: 5 of 44
- Genetics 267
- Hematology 183
- Pediatrics, Perinatology and Child Health 67
- Genetics 70
- Molecular Biology 143
Countries citing papers authored by CD Boehm
This map shows the geographic impact of CD Boehm'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 CD Boehm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites CD Boehm more than expected).
Fields of papers citing papers by CD Boehm
This network shows the impact of papers produced by CD Boehm. 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 CD Boehm. The network helps show where CD Boehm may publish in the future.
Co-authors
The 11 scholars most cited alongside CD Boehm, 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 | 1988 | 176 | |
| 2 | Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites. | 1980 | 61 |
| 3 | 1988 | 45 | |
| 4 | 1984 | 38 | |
| 5 | 1986 | 24 | |
| 6 | Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis. | 1981 | 20 |
| 7 | 1986 | 19 | |
| 8 | Phenylketonuria in the Greek population. Haplotype analysis of the phenylalanine hydroxylase gene and identification of a PKU mutation. | 1989 | 9 |
| 9 | Use of haplotype analysis in the beta-globin gene cluster to discover beta-thalassemia mutations. | 1983 | 3 |
| 10 | 1984 | 1 | |
| 11 | Prenatal diagnosis and carrier detection by DNA analysis. | 1988 | 0 |
About CD Boehm
CD Boehm is a scholar working on Genetics, Hematology, Molecular Biology, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 11 papers that have together received 396 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (9 papers), Iron Metabolism and Disorders (5 papers), Folate and B Vitamins Research (2 papers), Prenatal Screening and Diagnostics (2 papers), Blood groups and transfusion (2 papers), DNA Repair Mechanisms (1 paper), Peroxisome Proliferator-Activated Receptors (1 paper) and Nutrition, Genetics, and Disease (1 paper). The work is most often cited by research in Genetics (267 citations), Hematology (183 citations), Pediatrics, Perinatology and Child Health (67 citations), Genetics (70 citations) and Molecular Biology (143 citations). CD Boehm has collaborated with scholars based in United States. Frequent co-authors include PG Waber, R Anand, A. Kim Ritchey, Terry A. Vik, HH Jr Kazazian, BG Forget, S Weissman, FS Collins, David Valle and Karen Hofman. 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.