J C Detter

1.5k total citations
31 papers, 1.2k citations indexed

About

J C Detter is a scholar working on Genetics, Cell Biology and Hematology. According to data from OpenAlex, J C Detter has authored 31 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Cell Biology and 9 papers in Hematology. Recurrent topics in J C Detter's work include Hemoglobinopathies and Related Disorders (12 papers), Hemoglobin structure and function (10 papers) and Erythrocyte Function and Pathophysiology (5 papers). J C Detter is often cited by papers focused on Hemoglobinopathies and Related Disorders (12 papers), Hemoglobin structure and function (10 papers) and Erythrocyte Function and Pathophysiology (5 papers). J C Detter collaborates with scholars based in United States, France and United Kingdom. J C Detter's co-authors include Claude Lenfant, A. J. Bellingham, Robert D. Woodson, Jimmy K. Eng, John R. Yates, Christine L. Gatlin, Eloise R. Giblett, Bengt Wranne, Marjorie A. Baughan and Harry Harris and has published in prestigious journals such as Science, Journal of Clinical Investigation and Blood.

In The Last Decade

J C Detter

31 papers receiving 1.1k citations

Peers

J C Detter

PHYSI

GENET

HEMAT

Joris R. Delanghe Belgium

E. G. Black United Kingdom

M. De Visscher Belgium

S O’Regan Canada

W A Ratcliffe United Kingdom

Edmund Bourke United States

W. Stirk Adams United States

C Reynafarje Peru

Christian A. Schaer Switzerland

T. A. J. Prankerd United Kingdom

Joris R. Delanghe Belgium

J C Detter

329 ×0.9

309 ×1.0

PHYSI

559 ×2.2

125 ×0.6

GENET

73 ×0.4

HEMAT

Citations per year, relative to J C Detter J C Detter (= 1×) peers Joris R. Delanghe

Countries citing papers authored by J C Detter

Since Specialization

Citations

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

Fields of papers citing papers by J C Detter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J C Detter

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

All Works

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20 of 20 papers shown

Gatlin, Christine L., et al.. (2000). Automated Identification of Amino Acid Sequence Variations in Proteins by HPLC/Microspray Tandem Mass Spectrometry. Analytical Chemistry. 72(4). 757–763. 188 indexed citations

Graham, Elinor A., Judy Felgenhauer, J C Detter, & Robert F. Labbé. (1996). Elevated zinc protoporphyrin associated with thalassemia trait and hemoglobin E. The Journal of Pediatrics. 129(1). 105–110. 35 indexed citations

Sabath, Daniel E., J C Detter, & Jonathan F. Tait. (1994). A Novel Deletion of the Entire α Globin Locus Causing α-Thalassemia-1 in a Northern European Family. American Journal of Clinical Pathology. 102(5). 650–654. 6 indexed citations

Smith, C. Wayne, et al.. (1992). Screening for alpha-thalassemia. Correlation of hemoglobin H inclusion bodies with DNA-determined genotype.. PubMed. 116(10). 1012–8. 22 indexed citations

Ashwood, Edward R., et al.. (1990). Obtaining reliable plasma sodium and glucose determinations from pulmonary artery catheters.. PubMed. 19(6). 613–9. 5 indexed citations

Pagon, Roberta A, et al.. (1985). Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder.. Journal of Medical Genetics. 22(4). 267–273. 54 indexed citations

Hutchinson, Martha L., et al.. (1984). Abnormal plasma amino acid profiles in patients undergoing bone marrow transplant. Clinical Nutrition. 3(3). 133–139. 4 indexed citations

Stein, Janet L., Cynthia A. Berg, Judith A. Jones, & J C Detter. (1984). A screening protocol for a prenatal population at risk for inherited hemoglobin disorders: Results of its application to a group of Southeast Asians and blacks. American Journal of Obstetrics and Gynecology. 150(4). 333–341. 22 indexed citations

Jones, Judith A., et al.. (1981). An improved method for detection of red cell hemoglobin H inclusions.. PubMed. 47(2). 94–6. 9 indexed citations

10.

Feusner, James H., et al.. (1980). The Authors’ Reply. American Journal of Clinical Pathology. 74(3). 363–363. 2 indexed citations

11.

Eschbach, Joseph W., J C Detter, & John W. Adamson. (1980). Physiologic studies in normal and uremic sheep: II. Changes in erythropoiesis and oxygen transport. Kidney International. 18(6). 732–745. 8 indexed citations

12.

Feusner, James H., et al.. (1979). Platelet Counts in Capillary Blood. American Journal of Clinical Pathology. 72(3). 410–414. 14 indexed citations

13.

Stamatoyannopoulos, G, et al.. (1976). Haemoglobin M Hyde Park occurring as a fresh mutation: diagnostic, structural, and genetic considerations.. Journal of Medical Genetics. 13(2). 142–147. 10 indexed citations

14.

Jones, Judith A., et al.. (1976). Adaptation of the acid citrate--agar gel method for hemoglobin electrophoresis.. Clinical Chemistry. 22(10). 1743–1744. 3 indexed citations

15.

Adamson, John W., George Stamatoyannopoulos, Stella B. Kontras, André D. Lascari, & J C Detter. (1973). Recessive Familial Erythrocytosis: Aspects of Marrow Regulation in Two Families. Blood. 41(5). 641–652. 25 indexed citations

16.

Shappell, Stephen D., John Murray, A. J. Bellingham, et al.. (1971). Adaptation to exercise: role of hemoglobin affinity for oxygen and 2,3-diphosphoglycerate. Journal of Applied Physiology. 30(6). 827–832. 50 indexed citations

17.

Detter, J C, G Stamatoyannopoulos, E.R. Giblett, & A. G. Motulsky. (1970). Adenosine deaminase: racial distribution and report of a new phenotype.. Journal of Medical Genetics. 7(4). 356–357. 32 indexed citations

18.

Detter, J C, Jeanne E. Anderson, & E.R. Giblett. (1970). NADH diaphorase: an inherited variant associated with normal methemoglobin reduction.. PubMed. 22(1). 100–4. 16 indexed citations

19.

Fialkow, P. J., et al.. (1969). 6-Phosphogluconate Dehydrogenase: Hemizygous Manifestation in a Patient with Leukemia. Science. 163(3863). 194–195. 24 indexed citations

20.

Detter, J C, Peter Ways, Eloise R. Giblett, et al.. (1968). Inherited variations in human phosphohexose isomerase. Annals of Human Genetics. 31(4). 329–338. 208 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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