A L Scarpa

1.1k total citations
14 papers, 922 citations indexed

About

A L Scarpa is a scholar working on Physiology, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, A L Scarpa has authored 14 papers receiving a total of 922 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 6 papers in Pulmonary and Respiratory Medicine and 5 papers in Molecular Biology. Recurrent topics in A L Scarpa's work include Erythrocyte Function and Pathophysiology (11 papers), Blood properties and coagulation (6 papers) and Blood groups and transfusion (3 papers). A L Scarpa is often cited by papers focused on Erythrocyte Function and Pathophysiology (11 papers), Blood properties and coagulation (6 papers) and Blood groups and transfusion (3 papers). A L Scarpa collaborates with scholars based in United States, France and Germany. A L Scarpa's co-authors include Bernard G. Forget, William Tse, J C Winkelmann, N J Robillard, V. Marchesi, Jan‐Gowth Chang, Patrick G. Gallagher, Samuel E. Lux, Kenneth E. Sahr and Alban J. Linnenbach and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

A L Scarpa

14 papers receiving 896 citations

Peers

A L Scarpa
Timothy J. Satchwell United Kingdom
John J. Moulds United States
Lily Mirels United States
Daniel B. Rifkin United States
Maaike de Fost Netherlands
Elle C. Roberson United States
Inna Uliyakina Portugal
Kateřina Krejčíková Czechia
DS Friend United States
Diane E. Grove United States
Timothy J. Satchwell United Kingdom
A L Scarpa
Citations per year, relative to A L Scarpa A L Scarpa (= 1×) peers Timothy J. Satchwell

Countries citing papers authored by A L Scarpa

Since Specialization
Citations

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

Fields of papers citing papers by A L Scarpa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A L Scarpa

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

All Works

14 of 14 papers shown
1.
Gallagher, Patrick G., William Tse, A L Scarpa, Samuel E. Lux, & Bernard G. Forget. (1997). Structure and Organization of the Human Ankyrin-1 Gene. Journal of Biological Chemistry. 272(31). 19220–19228. 62 indexed citations
2.
Eber, Stefan, Jennifer M. Reingle González, Marcia L. Lux, et al.. (1996). Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nature Genetics. 13(2). 214–218. 169 indexed citations
3.
Abou‐Alfa, Ghassan K., D Dhermy, E Bursaux, et al.. (1996). A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.. Journal of Clinical Investigation. 97(2). 373–380. 31 indexed citations
4.
Scarpa, A L, Roger L. Eddy, M.G. Byers, et al.. (1993). Cloning of a Portion of the Chromosomal Gene and cDNA for Human β-Fodrin, the Nonerythroid Form of β-Spectrin. Genomics. 17(2). 287–293. 13 indexed citations
5.
Amin, Kunjlata M., et al.. (1993). The Exon-Intron Organization of the Human Erythroid β-Spectrin Gene. Genomics. 18(1). 118–125. 23 indexed citations
6.
7.
Gallagher, Patrick G., William Tse, Fernando Ferreira Costa, et al.. (1991). A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain. Journal of Biological Chemistry. 266(23). 15154–15159. 29 indexed citations
8.
9.
Sahr, Kenneth E., P Laurila, Leszek Kotula, et al.. (1990). The complete cDNA and polypeptide sequences of human erythroid alpha-spectrin.. Journal of Biological Chemistry. 265(8). 4434–4443. 196 indexed citations
10.
Winkelmann, J C, Jan‐Gowth Chang, William Tse, et al.. (1990). Full-length sequence of the cDNA for human erythroid beta-spectrin.. Journal of Biological Chemistry. 265(20). 11827–11832. 216 indexed citations
11.
Sahr, Kenneth E., Takashi Tobe, A L Scarpa, et al.. (1989). Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.. Journal of Clinical Investigation. 84(4). 1243–1252. 51 indexed citations
12.
Robillard, N J & A L Scarpa. (1988). Genetic and physiological characterization of ciprofloxacin resistance in Pseudomonas aeruginosa PAO. Antimicrobial Agents and Chemotherapy. 32(4). 535–539. 89 indexed citations
13.
Benz, Edward J., Kenichi Takeshita, & A L Scarpa. (1985). Metabolism of Structurally Abnormal mRNAs Resulting from β‐Thalassemia Mutationsa. Annals of the New York Academy of Sciences. 445(1). 57–67. 2 indexed citations
14.
Benz, E J, et al.. (1981). Posttranscriptional defects in beta-globin messenger RNA metabolism in beta-thalassemia: abnormal accumulation of beta-messenger RNA precursor sequences.. Journal of Clinical Investigation. 68(6). 1529–1538. 14 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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