M. B. Coleman

442 total citations
17 papers, 377 citations indexed

About

M. B. Coleman is a scholar working on Genetics, Hematology and Physiology. According to data from OpenAlex, M. B. Coleman has authored 17 papers receiving a total of 377 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Hematology and 6 papers in Physiology. Recurrent topics in M. B. Coleman's work include Hemoglobinopathies and Related Disorders (15 papers), Iron Metabolism and Disorders (10 papers) and Erythrocyte Function and Pathophysiology (6 papers). M. B. Coleman is often cited by papers focused on Hemoglobinopathies and Related Disorders (15 papers), Iron Metabolism and Disorders (10 papers) and Erythrocyte Function and Pathophysiology (6 papers). M. B. Coleman collaborates with scholars based in United States, Canada and Iran. M. B. Coleman's co-authors include Martin H. Steinberg, Junius G. Adams, MH Steinberg, PF Milner, SA Liebhaber, MH Steinberg, Maria W. Plonczynski, F E Cash, A. Merat and Zohreh Mostafavi‐Pour and has published in prestigious journals such as Journal of Clinical Investigation, Blood and British Journal of Haematology.

In The Last Decade

M. B. Coleman

17 papers receiving 363 citations

Peers

M. B. Coleman

GENET

HEMAT

PPCH

MB

PHYSI

MH Steinberg United States

T. H. J. Huisman United States

K. Sofroniadou Greece

WA Schroeder United States

L. Perseu Italy

Vicharn Panich Thailand

Anna Metaxotou‐Mavrommati Greece

C Altay United States

FF Chehab United States

Konstantinos Varvagiannis Greece

MH Steinberg United States

M. B. Coleman

364 ×1.1

GENET

298 ×1.2

HEMAT

89 ×1.3

PPCH

66 ×1.1

MB

49 ×1.0

PHYSI

Citations per year, relative to M. B. Coleman M. B. Coleman (= 1×) peers MH Steinberg

Countries citing papers authored by M. B. Coleman

Since Specialization

Citations

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

Fields of papers citing papers by M. B. Coleman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. B. Coleman. 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 M. B. Coleman. The network helps show where M. B. Coleman may publish in the future.

Co-authorship network of co-authors of M. B. Coleman

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

All Works

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17 of 17 papers shown

1.

Wilson, David M., et al.. (1999). Genetic studies suggest a multicentric origin for Hb G-coushatta [β22(B4)Glu→Ala]. Hemoglobin. 23(1). 57–67. 6 indexed citations

2.

Merritt, Diane F., Richard T. Jones, Charlotte Head, et al.. (1997). HB Seal Rock [(α2)142 Term→glu, Codon 142 TAA→GAA]: An Extended α Chain Variant Associated with Anemia, Microcytosis, and α-Thalassemia-2 (-3.7 KB). Hemoglobin. 21(4). 331–344. 11 indexed citations

3.

Coleman, M. B., Junius G. Adams, Martin H. Steinberg, & William P. Winter. (1994). A four base pair deletion 5′ to the ^Aγ^T gene is associated not only with decreased expression of the ^Aγ^T‐globin gene, but also of the ^Gγ‐globin gene in cis. American Journal of Hematology. 47(4). 307–311. 9 indexed citations

4.

Waye, John S., Barry Eng, M. B. Coleman, Martin H. Steinberg, & Blanche P. Alter. (1994). δβ-Thalassemia in an African-American: Identification of the deletion endpoints and PCR-Based diagnosis. Hemoglobin. 18(6). 389–399. 3 indexed citations

5.

Coleman, M. B., Junius G. Adams, Martin H. Steinberg, et al.. (1993). G_γA_γ(β⁺) hereditary persistence of fetal hemoglobin: The ^Gγ – 158 C → T mutation in cis to the − 175 T → C mutation of the ^Aγ‐globin gene results in increased ^Gγ‐globin synthesis. American Journal of Hematology. 42(2). 186–190. 12 indexed citations

6.

Coleman, M. B., et al.. (1993). HB San Diego [β109(G11)VAL→MET] in an Iranian: Further Evidence for a Mutational Hot Spot at Position 109 of the β-Globin Gene. Hemoglobin. 17(6). 543–545. 2 indexed citations

7.

Merat, A., et al.. (1993). β-Thalassemia in Southwestern Iran. Hemoglobin. 17(5). 427–437. 40 indexed citations

8.

Coleman, M. B., et al.. (1992). The -87 (C→A) β⁺-Thalassemia Mutation in a Black Family. Hemoglobin. 16(5). 399–401. 7 indexed citations

9.

Coleman, M. B., et al.. (1991). A four-base deletion 5' to the A gamma globin gene is a common polymorphism.. Blood. 78(9). 2473–4. 8 indexed citations

10.

Weiss, Ingrid M., et al.. (1990). Molecular basis for alpha-thalassemia associated with the structural mutant hemoglobin Suan-Dok (alpha 2 109leu----arg) [published erratum appears in Blood 1991 Mar 15;77(6):1404]. Blood. 76(12). 2630–2636. 19 indexed citations

11.

Weiss, Ingrid M., et al.. (1990). Molecular basis for alpha-thalassemia associated with the structural mutant hemoglobin Suan-Dok (alpha 2 109leu----arg) [published erratum appears in Blood 1991 Mar 15;77(6):1404]. Blood. 76(12). 2630–2636. 20 indexed citations

12.

Liebhaber, SA, M. B. Coleman, Junius G. Adams, F E Cash, & Martin H. Steinberg. (1987). Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG).. Journal of Clinical Investigation. 80(1). 154–159. 43 indexed citations

13.

Steinberg, MH, et al.. (1986). A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.. Blood. 67(2). 469–73. 26 indexed citations

14.

Steinberg, MH, et al.. (1984). Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia. Blood. 63(6). 1353–1360. 144 indexed citations

15.

Steinberg, MH, et al.. (1984). Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia. Blood. 63(6). 1353–1360. 5 indexed citations

16.

Steinberg, Martin H., et al.. (1983). The effects of alpha‐thalassaemia in HbSC disease. British Journal of Haematology. 55(3). 487–492. 21 indexed citations

17.

Balducci, Lodovico, et al.. (1978). Erythroleukemia: In vitro studies of erythropoiesis. American Journal of Hematology. 5(4). 291–295. 1 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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