Teresa Parrella

441 total citations
13 papers, 351 citations indexed

About

Teresa Parrella is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Teresa Parrella has authored 13 papers receiving a total of 351 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Teresa Parrella's work include Metabolism and Genetic Disorders (4 papers), Cystic Fibrosis Research Advances (3 papers) and Genomics and Rare Diseases (2 papers). Teresa Parrella is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Cystic Fibrosis Research Advances (3 papers) and Genomics and Rare Diseases (2 papers). Teresa Parrella collaborates with scholars based in United States, Italy and Switzerland. Teresa Parrella's co-authors include Paolo Fortina, Saul Surrey, Eric Rappaport, S Rifat, Joel Bennett, Peter J. Newman, Sanford J. Shattil, BS Coller, Mortimer Poncz and Ferruccio Bonino and has published in prestigious journals such as Journal of Clinical Investigation, Blood and Hepatology.

In The Last Decade

Teresa Parrella

13 papers receiving 339 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Teresa Parrella United States	10	117	100	94	82	64	13	351
Dirk Völkel Austria	10	131 1.1×	32 0.3×	11 0.1×	136 1.7×	41 0.6×	13	538
Britta Kluge Germany	11	182 1.6×	56 0.6×	14 0.1×	19 0.2×	10 0.2×	12	315
Valentina Bardina Italy	9	67 0.6×	129 1.3×	39 0.4×	16 0.2×	2 0.0×	15	416
Tahir Naeem Khan Pakistan	11	118 1.0×	22 0.2×	8 0.1×	23 0.3×	10 0.2×	32	308
Satoru Komaki Japan	12	154 1.3×	54 0.5×	7 0.1×	5 0.1×	104 1.6×	35	394
Dharmvir S. Verma United States	12	80 0.7×	32 0.3×	6 0.1×	224 2.7×	2 0.0×	19	392
Flávia Roche Moreira Latini Brazil	11	101 0.9×	48 0.5×	13 0.1×	106 1.3×	1 0.0×	34	342
E. Fleischnick United States	9	106 0.9×	35 0.3×	2 0.0×	50 0.6×	12 0.2×	11	419
Dominique Goossens France	12	223 1.9×	19 0.2×	4 0.0×	172 2.1×	30 0.5×	20	520
C. B. van der Hagen Norway	12	261 2.2×	38 0.4×	12 0.1×	6 0.1×	19 0.3×	22	535

Countries citing papers authored by Teresa Parrella

Since Specialization

Citations

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

Fields of papers citing papers by Teresa Parrella

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Teresa Parrella. 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 Teresa Parrella. The network helps show where Teresa Parrella may publish in the future.

Co-authorship network of co-authors of Teresa Parrella

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

All Works

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13 of 13 papers shown

Poncz, Mortimer, S Rifat, BS Coller, et al.. (1994). Glanzmann thrombasthenia secondary to a Gly273-->Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIb.. Journal of Clinical Investigation. 93(1). 172–179. 71 indexed citations

Parrella, Teresa, Saul Surrey, Achille Iolascon, et al.. (1994). Maple syrup urine disease (MSUD): Screening for known mutations in Italian patients. Journal of Inherited Metabolic Disease. 17(6). 652–660. 4 indexed citations

Iolascon, Achille, Teresa Parrella, Silverio Perrotta, et al.. (1994). Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels.. Journal of Medical Genetics. 31(7). 551–554. 15 indexed citations

Barbera, Cristiana, Flavia Bortolotti, Carlo Crivellaro, et al.. (1994). Recombinant interferon-α2a hastens the rate of HBeAg clearance in children with chronic hepatitis B. Hepatology. 20(2). 287–290. 62 indexed citations

Fortina, Paolo, Teresa Parrella, Enrico Gottardi, et al.. (1994). Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia. Blood. 83(11). 3356–3362. 9 indexed citations

Mansfield, Elaine, James Robertson, Roger V. Lebo, et al.. (1993). Duchenne/becker muscular dystrophy carrier detection using quantitative PCR and fluorescence‐based strategies. American Journal of Medical Genetics. 48(4). 200–208. 30 indexed citations

Gregersen, Niels, Vibeke Winter, Diana Curtis, et al.. (1993). Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency: The Prevalent Mutation G985 (K304E) Is Subject to a Strong Founder Effect from Northwestern Europe. Human Heredity. 43(6). 342–350. 55 indexed citations

Mansfield, Elaine, A J Blasband, Mel N. Kronick, et al.. (1993). Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status. Molecular and Cellular Probes. 7(4). 311–324. 12 indexed citations

Fortina, Paolo, Teresa Parrella, Eric Rappaport, et al.. (1992). Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the ΔF508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Molecular and Cellular Probes. 6(4). 353–356. 9 indexed citations

10.

Fortina, Paolo, et al.. (1992). Detection of the most common mutations causing beta-thalassemia in Mediterraneans using a multiplex amplification refractory mutation system (MARMS).. Genome Research. 2(2). 163–166. 32 indexed citations

11.

Fortina, Paolo, Teresa Parrella, Jeffrey A. Kant, et al.. (1992). Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reaction. Human Genetics. 90(4). 375–8. 11 indexed citations

12.

Spada, Marco, Teresa Parrella, Riccardo Ponzone, et al.. (1991). Monitoring Treatment in Tetrahydrobiopterin Deficiency. Pteridines. 3(1-2). 13–15. 5 indexed citations

13.

Brunetto, Maurizia Rossana, M. Giarin, Filippo Oliveri, et al.. (1991). ‘e’ Antigen defective hepatitis B virus and course of chronic infection. Journal of Hepatology. 13. S82–S86. 36 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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