C D Boehm

1.8k total citations
18 papers, 1.5k citations indexed

About

C D Boehm is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, C D Boehm has authored 18 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Hematology and 6 papers in Molecular Biology. Recurrent topics in C D Boehm's work include Hemoglobinopathies and Related Disorders (11 papers), Iron Metabolism and Disorders (7 papers) and Folate and B Vitamins Research (4 papers). C D Boehm is often cited by papers focused on Hemoglobinopathies and Related Disorders (11 papers), Iron Metabolism and Disorders (7 papers) and Folate and B Vitamins Research (4 papers). C D Boehm collaborates with scholars based in United States, Australia and Italy. C D Boehm's co-authors include Stylianos E. Antonarakis, H H Kazazian, Stuart H. Orkin, Sabra C. Goff, Julianne P. Sexton, Stephen B. Baylin, Irene Newsham, Paula M. Vertino, Pamela Waber and Jean‐Pierre J. Issa and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The EMBO Journal and Blood.

In The Last Decade

C D Boehm

18 papers receiving 1.4k citations

Peers

Countries citing papers authored by C D Boehm

Since Specialization

Citations

This map shows the geographic impact of C D 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 C D Boehm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C D Boehm more than expected).

Fields of papers citing papers by C D Boehm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C D 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 C D Boehm. The network helps show where C D Boehm may publish in the future.

Co-authorship network of co-authors of C D Boehm

This figure shows the co-authorship network connecting the top 25 collaborators of C D Boehm. A scholar is included among the top collaborators of C D 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 C D Boehm. C D Boehm is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Cystic fibrosis carrier population screening in the primary care setting. 1996 ·PubMed ·Starlene Loader, (unknown), (unknown), Jeffrey C. Levenkron, C D Boehm, H H Kazazian, P T Rowley	68
2	Switch from monoallelic to biallelic human IGF2 promoter methylation during aging and carcinogenesis. 1996 ·Proceedings of the National Academy of Sciences ·Jean‐Pierre J. Issa, Paula M. Vertino, C D Boehm, Irene Newsham, Stephen B. Baylin	216
3	Neurobehavioral effects of the fragile X premutation in adult women: a controlled study. 1993 ·PubMed ·Allan L. Reiss, Lisa S. Freund, Michael T. Abrams, C D Boehm, H H Kazazian	131
4	Increased echogenicity in the fetal abdomen: use of DNA analysis to establish a diagnosis of cystic fibrosis 1993 ·Journal of Ultrasound in Medicine ·W. Allen Hogge, (unknown), C D Boehm, R C Sanders	13
5	A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus 1989 ·Genomics ·(unknown), J. Fielding Hejtmancik, G. Romeo, Mikael Lindlöf, C D Boehm, C. Thomas Caskey, (unknown), Kenneth H. Fischbeck, (unknown), (unknown), T. Grimm, H Kääriäinen, Maurizio Ferrari, Ellen G Pfendner, Gerhard Meng, Albert de la Chapelle, Maria Antonietta Melis, B. Müller, A.G. Mackinlay, C. R. Müller, M. J. Denton	17
6	Use of polymerase chain reaction for diagnosis of inherited disorders. 1989 ·Clinical Chemistry ·C D Boehm	21
7	Molecular basis and prenatal diagnosis of beta-thalassemia 1988 ·Blood ·(unknown), C D Boehm	217
8	Characterization of a spontaneous mutation to a beta-thalassemia allele. 1986 ·PubMed ·H H Kazazian, Stuart H. Orkin, C D Boehm, Sabra C. Goff, Sze Chuen Cesar Wong, Carol E. Dowling, Peter E. Newburger, Robert G. Knowlton, Valerie A. Brown, Helen Donis-Keller	41
9	Nonuniform recombination within the human beta-globin gene cluster: A reply to B. S. Weir and W. G. Hill. 1986 ·PubMed ·Aravinda Chakravarti, Kenneth H. Buetow, Stylianos E. Antonarakis, Pamela Waber, C D Boehm, H H Kazazian	6
10	Comparison of Deficiency Alleles of the -Globin and Factor VIII:C Genes: New Lessons from a Giant Gene 1986 ·Cold Spring Harbor Symposia on Quantitative Biology ·(unknown), Stylianos E. Antonarakis, Hagop Youssoufian, Carol E. Dowling, Deborah G. Phillips, Sze Chuen Cesar Wong, C D Boehm	3
11	On the origin and spread of beta-thalassemia: recurrent observation of four mutations in different ethnic groups. 1986 ·Proceedings of the National Academy of Sciences ·Sze Chuen Cesar Wong, Stylianos E. Antonarakis, Sabra C. Goff, Stuart H. Orkin, C D Boehm, H H Kazazian	87
12	Evidence supporting a single origin of the beta(C)-globin gene in blacks. 1985 ·PubMed ·C D Boehm, Carol E. Dowling, Stylianos E. Antonarakis, George R. Honig, H H Kazazian	33
13	Hemoglobin E in Europeans: further evidence for multiple origins of the beta E-globin gene. 1984 ·PubMed ·H H Kazazian, Pamela Waber, C D Boehm, (unknown), Stylianos E. Antonarakis, Virgil F. Fairbanks	43
14	Molecular characterization of seven beta-thalassemia mutations in Asian Indians. 1984 ·The EMBO Journal ·H H Kazazian, Stuart H. Orkin, Stylianos E. Antonarakis, Julianne P. Sexton, C D Boehm, Sabra C. Goff, Pamela Waber	176
15	Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both. 1984 ·Proceedings of the National Academy of Sciences ·Stylianos E. Antonarakis, C D Boehm, G. R. Serjeant, Ch. Theisen, G Dover, H H Kazazian	184
16	beta-Thalassemia due to a deletion of the nucleotide which is substituted in the beta S-globin gene. 1983 ·PubMed ·H H Kazazian, Stuart H. Orkin, C D Boehm, Julianne P. Sexton, Stylianos E. Antonarakis	45
17	Evidence for multiple origins of the beta E-globin gene in Southeast Asia. 1982 ·Proceedings of the National Academy of Sciences ·Stylianos E. Antonarakis, SH Orkin, H H Kazazian, Sabra C. Goff, C D Boehm, Pamela Waber, Julianne P. Sexton, Harry Ostrer, Virgil F. Fairbanks, Aravinda Chakravarti	96
18	Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability. 1980 ·Proceedings of the National Academy of Sciences ·John A. Phillips, Susan R. Panny, H H Kazazian, C D Boehm, Alan F. Scott, Kirby D. Smith	65

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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