CD Boehm

441 total citations
10 papers, 378 citations indexed

About

CD Boehm is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, CD Boehm has authored 10 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Hematology and 4 papers in Molecular Biology. Recurrent topics in CD Boehm's work include Hemoglobinopathies and Related Disorders (9 papers), Iron Metabolism and Disorders (5 papers) and Blood groups and transfusion (2 papers). CD Boehm is often cited by papers focused on Hemoglobinopathies and Related Disorders (9 papers), Iron Metabolism and Disorders (5 papers) and Blood groups and transfusion (2 papers). CD Boehm collaborates with scholars based in United States. CD Boehm's co-authors include PG Waber, R Anand, A. Kim Ritchey, HH Jr Kazazian, Terry A. Vik, BG Forget, FS Collins, S Weissman, Karen Hofman and David Valle and has published in prestigious journals such as Blood and PubMed.

In The Last Decade

CD Boehm

10 papers receiving 359 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
CD Boehm United States 8 261 184 139 65 65 10 378
G. V. Sciarratta Italy 11 292 1.1× 193 1.0× 108 0.8× 88 1.4× 54 0.8× 27 387
FF Chehab United States 9 261 1.0× 208 1.1× 97 0.7× 96 1.5× 111 1.7× 10 399
AE Kulozik United Kingdom 9 465 1.8× 367 2.0× 149 1.1× 100 1.5× 89 1.4× 12 566
A Metaxotou-Mavromati Greece 14 501 1.9× 388 2.1× 90 0.6× 140 2.2× 61 0.9× 28 549
Rosalba Di Marzo Italy 10 251 1.0× 167 0.9× 146 1.1× 66 1.0× 92 1.4× 23 365
M Patterson Canada 12 359 1.4× 262 1.4× 148 1.1× 90 1.4× 60 0.9× 27 505
J. M. Gonzalez‐Redondo United States 13 639 2.4× 479 2.6× 131 0.9× 114 1.8× 93 1.4× 20 702
Manoussos N. Papadakis Greece 10 203 0.8× 139 0.8× 105 0.8× 76 1.2× 85 1.3× 22 301
Anindita Basak Türkiye 8 198 0.8× 140 0.8× 188 1.4× 45 0.7× 63 1.0× 14 363
PE Nute United States 6 309 1.2× 254 1.4× 77 0.6× 119 1.8× 23 0.4× 8 393

Countries citing papers authored by CD Boehm

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of CD Boehm

This figure shows the co-authorship network connecting the top 25 collaborators of CD Boehm. A scholar is included among the top collaborators of CD Boehm based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with CD Boehm. CD Boehm is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Hofman, Karen, et al.. (1989). Phenylketonuria in the Greek population. Haplotype analysis of the phenylalanine hydroxylase gene and identification of a PKU mutation.. PubMed. 6(3). 245–50. 9 indexed citations
2.
Boehm, CD, et al.. (1988). Molecular basis and prenatal diagnosis of beta-thalassemia. Blood. 72(4). 1107–1116. 168 indexed citations
3.
Anand, R, et al.. (1988). Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion. Blood. 72(2). 636–641. 44 indexed citations
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Antonarakis, Stylianos E., et al.. (1983). Use of haplotype analysis in the beta-globin gene cluster to discover beta-thalassemia mutations.. PubMed. 134. 91–8. 3 indexed citations
9.
Boehm, CD, et al.. (1981). Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.. PubMed. 33(1). 25–35. 17 indexed citations
10.
Boehm, CD, et al.. (1980). Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites.. PubMed. 56(5). 926–30. 55 indexed citations

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.

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