Thad A. Howard

3.7k total citations
97 papers, 2.8k citations indexed

About

Thad A. Howard is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Thad A. Howard has authored 97 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Genetics, 53 papers in Hematology and 26 papers in Molecular Biology. Recurrent topics in Thad A. Howard's work include Hemoglobinopathies and Related Disorders (62 papers), Iron Metabolism and Disorders (43 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (15 papers). Thad A. Howard is often cited by papers focused on Hemoglobinopathies and Related Disorders (62 papers), Iron Metabolism and Disorders (43 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (15 papers). Thad A. Howard collaborates with scholars based in United States, Uganda and Tanzania. Thad A. Howard's co-authors include Russell E. Ware, Nicole A. Mortier, Sherri A. Zimmerman, Michael F. Seldin, William H. Schultz, Michael F. Seldin, Banu Aygün, Jonathan M. Flanagan, Jacqueline S. Davis and Peter D’Eustachio and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Experimental Medicine and The EMBO Journal.

In The Last Decade

Thad A. Howard

95 papers receiving 2.7k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Thad A. Howard 1.5k 1.3k 877 527 363 97 2.8k
E.R. Giblett 522 0.4× 980 0.7× 506 0.6× 213 0.4× 254 0.7× 53 2.4k
Hélène Cavé 797 0.5× 2.4k 1.8× 2.2k 2.5× 780 1.5× 620 1.7× 154 6.3k
Sylvia D. Lawler 532 0.4× 878 0.7× 505 0.6× 666 1.3× 288 0.8× 103 2.6k
Bertil Glader 694 0.5× 1.4k 1.1× 2.2k 2.5× 365 0.7× 338 0.9× 131 4.6k
Linda R. Bressler 516 0.3× 502 0.4× 741 0.8× 247 0.5× 378 1.0× 38 2.6k
K Kita 317 0.2× 1.2k 0.9× 1.8k 2.0× 131 0.2× 491 1.4× 155 3.3k
Sverre O. Lie 171 0.1× 474 0.4× 703 0.8× 262 0.5× 445 1.2× 100 2.2k
Theodore B. Moore 386 0.3× 403 0.3× 692 0.8× 250 0.5× 363 1.0× 99 2.0k
Athanasios K. Anagnostopoulos 774 0.5× 316 0.2× 562 0.6× 132 0.3× 319 0.9× 102 1.8k
Reinhold Munker 353 0.2× 1.2k 0.9× 1.4k 1.6× 62 0.1× 1.1k 3.0× 119 3.7k

Countries citing papers authored by Thad A. Howard

Since Specialization
Citations

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

Fields of papers citing papers by Thad A. Howard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thad A. Howard. 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 Thad A. Howard. The network helps show where Thad A. Howard may publish in the future.

Co-authorship network of co-authors of Thad A. Howard

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

All Works

20 of 20 papers shown
1.
Torous, Dorothea K., Svetlana L. Avlasevich, Jeffrey C. Bemis, et al.. (2023). Lack of hydroxyurea‐associated mutagenesis in pediatric sickle cell disease patients. Environmental and Molecular Mutagenesis. 64(3). 167–175. 5 indexed citations
2.
Smart, Luke R., Kathryn McElhinney, Min Dong, et al.. (2023). Hydroxyurea pharmacokinetics and precision dosing in low-resource settings. Frontiers in Molecular Biosciences. 10. 1130206–1130206. 3 indexed citations
3.
McGann, Patrick T., Omar Niss, Min Dong, et al.. (2019). Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia. American Journal of Hematology. 94(8). 871–879. 47 indexed citations
4.
Schaefer, Beverly A., Charles Kiyaga, Thad A. Howard, et al.. (2016). Hemoglobin variants identified in the Uganda Sickle Surveillance Study. Blood Advances. 1(1). 93–100. 8 indexed citations
5.
Sheehan, Vivien, Jacy R. Crosby, Aniko Sabo, et al.. (2014). Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia. PLoS ONE. 9(10). e110740–e110740. 28 indexed citations
6.
Sheehan, Vivien, Zhaoyu Luo, Jonathan M. Flanagan, et al.. (2013). Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes. American Journal of Hematology. 88(7). 571–576. 67 indexed citations
7.
McGann, Patrick T., Thad A. Howard, Jonathan M. Flanagan, Jill M. Lahti, & Russell E. Ware. (2011). Chromosome damage and repair in children with sickle cell anaemia and long‐term hydroxycarbamide exposure. British Journal of Haematology. 154(1). 134–140. 22 indexed citations
8.
Flanagan, Jonathan M., Thad A. Howard, Nicole A. Mortier, et al.. (2010). Assessment of genotoxicity associated with hydroxyurea therapy in children with sickle cell anemia. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 698(1-2). 38–42. 50 indexed citations
9.
Carpenter, Shannon L., et al.. (2008). UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia. American Journal of Hematology. 83(10). 800–803. 33 indexed citations
10.
Howard, Thad A., et al.. (2008). CHEMICAL AND FUNCTIONAL ANALYSIS OF GENERIC HYDROXYUREA FORMULATIONS. Pediatric Hematology and Oncology. 25(5). 423–429. 6 indexed citations
11.
Jeng, Michael, Patricia Adams‐Graves, Thad A. Howard, et al.. (2003). Identification of hemochromatosis gene polymorphisms in chronically transfused patients with sickle cell disease. American Journal of Hematology. 74(4). 243–248. 12 indexed citations
12.
Ware, Russell E., et al.. (2001). Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes. Experimental Hematology. 29(12). 1403–1409. 38 indexed citations
13.
Howard, Thad A., et al.. (1997). Structural and Functional Analysis of the Pig-a Protein That is Mutated in Paroxysmal Nocturnal Hemoglobinuria. Blood Cells Molecules and Diseases. 23(3). 350–360. 6 indexed citations
14.
Ware, Russell E., et al.. (1994). NOVEL MECHANISMS OF BREQUINAR SODIUM IMMUNOSUPPRESSION ON T CELL ACTIVATION. Transplantation. 58(8). 920–926. 12 indexed citations
15.
Ware, Russell E. & Thad A. Howard. (1994). Elevated numbers of gamma-delta (??+) T lymphocytes in children with immune thrombocytopenic purpura. Journal of Clinical Immunology. 14(4). 237–247. 26 indexed citations
16.
Hoopes, Charles W., Makoto M. Taketo, Qiang Liu, et al.. (1992). Mapping of the mouse Rxr loci encoding nuclear retinoid X receptors RXRα, RXRβ, and RXRγ. Genomics. 14(3). 611–617. 23 indexed citations
17.
Colombo, Mario P., et al.. (1992). Localization of growth arrest-specific genes on mouse Chromosomes 1, 7, 8, 11, 13, and 16. Mammalian Genome. 2(2). 130–134. 32 indexed citations
18.
Chaplin, David, M. Sue Kirkman, Richard C. Wu, et al.. (1991). Different Isozymes of Mouse 11/ß-Hydroxylase Produce Mineralocorticoids and Glucocorticoids. Molecular Endocrinology. 5(12). 1853–1861. 149 indexed citations
19.
Seldin, Michael F., et al.. (1990). Localization of mouse melanoma growth stimulatory activity gene (<i>Mgsa</i>) between <i>Afp </i>and <i>Gus </i>on chromosome 5 using interspecific backcross mice. Cytogenetic and Genome Research. 54(1-2). 68–70. 16 indexed citations
20.
Watson, M., Stephen F. Kingsmore, Geoffrey I. Johnston, et al.. (1990). Genomic organization of the selectin family of leukocyte adhesion molecules on human and mouse chromosome 1.. The Journal of Experimental Medicine. 172(1). 263–272. 112 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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