Lucia Longa

788 total citations
10 papers, 596 citations indexed

About

Lucia Longa is a scholar working on Physiology, Genetics and Oncology. According to data from OpenAlex, Lucia Longa has authored 10 papers receiving a total of 596 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Physiology, 4 papers in Genetics and 3 papers in Oncology. Recurrent topics in Lucia Longa's work include Tuberous Sclerosis Complex Research (8 papers), Genetic and Kidney Cyst Diseases (4 papers) and Histiocytic Disorders and Treatments (3 papers). Lucia Longa is often cited by papers focused on Tuberous Sclerosis Complex Research (8 papers), Genetic and Kidney Cyst Diseases (4 papers) and Histiocytic Disorders and Treatments (3 papers). Lucia Longa collaborates with scholars based in Italy, Spain and United States. Lucia Longa's co-authors include Caterina Carbonara, Massimo Brisigotti, Nicola Migone, Enrico Grosso, C Borrone, Maria Luisa Garrè, Guido Martignoni, Gian Mario Mariuzzi, Franco Bonetti and Carlo Zancanaro and has published in prestigious journals such as Human Molecular Genetics, The American Journal of Surgical Pathology and Journal of the American Academy of Dermatology.

In The Last Decade

Lucia Longa

10 papers receiving 576 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lucia Longa Italy 8 457 220 192 164 97 10 596
Arthur R. Birt Canada 9 199 0.4× 408 1.9× 308 1.6× 48 0.3× 143 1.5× 14 751
Yukiko Hasumi Japan 9 82 0.2× 211 1.0× 276 1.4× 29 0.2× 103 1.1× 12 452
Dustin L. Gable United States 9 221 0.5× 137 0.6× 226 1.2× 57 0.3× 77 0.8× 12 530
Alice Wang United States 9 102 0.2× 63 0.3× 79 0.4× 37 0.2× 14 0.1× 15 316
Lisa Hoenicke Germany 5 95 0.2× 36 0.2× 226 1.2× 112 0.7× 11 0.1× 5 429
C Mehle Sweden 9 274 0.6× 64 0.3× 243 1.3× 97 0.6× 44 0.5× 12 469
Shigefumi Hayashi Japan 12 356 0.8× 27 0.1× 212 1.1× 57 0.3× 33 0.3× 16 506
Barbara A. Kosciolek United States 10 82 0.2× 63 0.3× 131 0.7× 18 0.1× 23 0.2× 14 349
Rachel B. Keller United States 7 87 0.2× 22 0.1× 129 0.7× 44 0.3× 64 0.7× 14 261
Satu‐Leena Sallinen Finland 8 40 0.1× 19 0.1× 151 0.8× 95 0.6× 101 1.0× 10 362

Countries citing papers authored by Lucia Longa

Since Specialization
Citations

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

Fields of papers citing papers by Lucia Longa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Longa

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

All Works

10 of 10 papers shown
1.
Longa, Lucia, et al.. (2013). A novel HLA allele, HLA‐A*02:393, identified in a two generation Italian family. Tissue Antigens. 82(3). 203–204. 1 indexed citations
2.
Bosincu, L, Paolo Cossu‐Rocca, Guido Martignoni, et al.. (2005). Perivascular epithelioid cell (PEC) tumors of the uterus: a clinicopathologic study of two cases with aggressive features. Modern Pathology. 18(10). 1336–1342. 40 indexed citations
3.
Ghannoum, Mahmoud A., N. Isham, Rana Hajjeh, et al.. (2003). Tinea capitis in Cleveland: Survey of elementary school students. Journal of the American Academy of Dermatology. 48(2). 189–193. 81 indexed citations
4.
Longa, Lucia, Alfredo Brusco, Silvia Polidoro, et al.. (2001). TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the gene. Human Genetics. 108(2). 156–166. 18 indexed citations
5.
Beltramello, Alberto, Giovanni Puppini, I. A. Bergamo Andreis, et al.. (1999). Does the tuberous sclerosis complex include intracranial aneurysms?. Pediatric Radiology. 29(3). 206–211. 34 indexed citations
6.
Martignoni, Guido, Maurizio Pea, Franco Bonetti, et al.. (1998). Carcinomalike Monotypic Epithelioid Angiomyolipoma in Patients Without Evidence of Tuberous Sclerosis. The American Journal of Surgical Pathology. 22(6). 663–672. 140 indexed citations
7.
Longa, Lucia, Francesco Scolari, Alfredo Brusco, et al.. (1997). A large TSC2 and PKD1 gene deletion is associated with renal and extrarenal signs of autosomal dominant polycystic kidney disease. Nephrology Dialysis Transplantation. 12(9). 1900–1907. 53 indexed citations
8.
Longa, Lucia, Alfredo Brusco, Caterina Carbonara, et al.. (1997). A Tuberous Sclerosis Patient with a Large TSC2 and PKD1 Gene Deletion Shows Extrarenal Signs of Autosomal Dominant Polycystic Disease. Contributions to nephrology. 122. 91–95. 6 indexed citations
9.
Carbonara, Caterina, Lucia Longa, Enrico Grosso, et al.. (1996). Apparent preferential loss of heterozygosity atTSC2 overTSC1 chromosomal region in tuberous sclerosis hamartomas. Genes Chromosomes and Cancer. 15(1). 18–25. 107 indexed citations
10.
Carbonara, Caterina, Lucia Longa, Enrico Grosso, et al.. (1994). 9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 gene. Human Molecular Genetics. 3(10). 1829–1832. 116 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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