Bárbara Torres

3.1k total citations · 1 hit paper
37 papers, 1.6k citations indexed

About

Bárbara Torres is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bárbara Torres has authored 37 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 16 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bárbara Torres's work include Congenital heart defects research (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and RNA modifications and cancer (5 papers). Bárbara Torres is often cited by papers focused on Congenital heart defects research (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and RNA modifications and cancer (5 papers). Bárbara Torres collaborates with scholars based in Italy, Spain and Germany. Bárbara Torres's co-authors include Gilda Porta, Albert Parés, Peter R. Galle, Albert J. Czaja, George N. Dalekos, Minoru Shibata, Mikio Zeniya, Paulo Lisboa Bittencourt, Edward L. Krawitt and Ansgar W. Lohse and has published in prestigious journals such as Journal of Clinical Oncology, Hepatology and Clinical Infectious Diseases.

In The Last Decade

Bárbara Torres

35 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Simplified criteria for the diagnosis of autoimmune hepatitis†

2008 1.2k citations Bárbara Torres et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bárbara Torres Italy	13	1.1k	1.0k	397	262	169	37	1.6k
Rodrigo Liberal Portugal	27	1.5k 1.3×	1.3k 1.3×	567 1.4×	345 1.3×	194 1.1×	84	2.4k
Kalliopi Zachou Greece	35	2.8k 2.5×	2.7k 2.6×	518 1.3×	567 2.2×	115 0.7×	109	3.3k
Harlan I. Wright United States	17	856 0.8×	766 0.8×	532 1.3×	78 0.3×	101 0.6×	24	1.4k
Bernard Portmann United Kingdom	22	1.1k 1.0×	881 0.9×	686 1.7×	99 0.4×	81 0.5×	53	1.7k
Richard Taubert Germany	24	924 0.8×	609 0.6×	452 1.1×	129 0.5×	164 1.0×	77	1.7k
Michael A. Heneghan United Kingdom	20	991 0.9×	868 0.9×	325 0.8×	253 1.0×	44 0.3×	26	1.2k
Ming‐Yen Hsieh Taiwan	23	1.8k 1.6×	1.8k 1.8×	134 0.3×	159 0.6×	57 0.3×	112	2.2k
F. Cassani Italy	36	2.4k 2.1×	2.2k 2.1×	682 1.7×	881 3.4×	205 1.2×	72	3.0k
Roberta D’Ambrosio Italy	24	1.6k 1.5×	1.7k 1.7×	123 0.3×	127 0.5×	59 0.3×	104	2.1k
Hülya Çetınkaya Türkiye	17	330 0.3×	472 0.5×	162 0.4×	112 0.4×	209 1.2×	48	989

Countries citing papers authored by Bárbara Torres

Since Specialization

Citations

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

Fields of papers citing papers by Bárbara Torres

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bárbara Torres

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

All Works

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20 of 20 papers shown

Sciacchitano, Salvatore, Maria Piane, Claudia De Vitis, et al.. (2022). Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?. Diagnostics. 12(12). 2997–2997. 3 indexed citations

Giuffrida, Maria Grazia, Marina Goldoni, Giovanna Carpentieri, et al.. (2022). 3′UTR Deletion of NONO Leads to Corpus Callosum Anomaly, Left Ventricular Non-Compaction and Ebstein’s Anomaly in a Male Fetus. Diagnostics. 12(10). 2354–2354. 3 indexed citations

Torres, Bárbara, et al.. (2022). Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Bardet–Biedl Syndrome–Like Phenotype. Frontiers in Genetics. 13. 924362–924362. 1 indexed citations

Oltra, Silvestre, Yania Yáñez, Vanessa Segura, et al.. (2021). Germline Predisposition to Pediatric Cancer, from Next Generation Sequencing to Medical Care. Cancers. 13(21). 5339–5339. 10 indexed citations

Bernardini, Laura, et al.. (2021). Koolen‐de Vries syndrome in a 63‐year‐old woman: Report of the oldest patient and a review of the adult phenotype. American Journal of Medical Genetics Part A. 188(2). 692–707. 3 indexed citations

Yáñez, Yania, Vanessa Segura, Bárbara Torres, et al.. (2019). Li–Fraumeni syndrome heterogeneity. Clinical & Translational Oncology. 22(7). 978–988. 22 indexed citations

Yáñez, Yania, Vanessa Segura, Julia Balaguer, et al.. (2019). Review: Ewing Sarcoma Predisposition. Pathology & Oncology Research. 26(4). 2057–2066. 16 indexed citations

Capalbo, Anna, Bárbara Torres, Alice Traversa, et al.. (2019). Small 7p22.3 microdeletion: Case report of Snx8 haploinsufficiency and neurological findings. European Journal of Medical Genetics. 63(4). 103772–103772. 9 indexed citations

Ferrari, Daniela, Bárbara Torres, Marina Goldoni, et al.. (2018). Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7. Stem Cell Research. 32. 73–77. 2 indexed citations

10.

Torres, Bárbara, Daniela Ferrari, Antonella De Jaco, et al.. (2018). Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith–Magenis syndrome. Stem Cell Research. 28. 153–156. 1 indexed citations

11.

Rosati, Jessica, Daniela Ferrari, Bárbara Torres, et al.. (2018). Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease. Stem Cell Research. 27. 86–89. 3 indexed citations

12.

Moreira, Alvaro, Bárbara Torres, Juliano Peruzzo, et al.. (2017). Skin symptoms as diagnostic clue for autoinflammatory diseases. Anais Brasileiros de Dermatologia. 92(1). 72–80. 22 indexed citations

13.

Gómez, Jorge A., Holger Bang, Lorena Martinez‐Gamboa, et al.. (2016). Carbamylated vimentin represents a relevant autoantigen in Latin American (Cuban) rheumatoid arthritis patients. Rheumatology International. 36(6). 781–791. 22 indexed citations

14.

Laino, Luigi, Irene Bottillo, Laura Bernardini, et al.. (2016). Clinical and molecular characterization of a boy with intellectual disability, facial dysmorphism, minor digital anomalies and a complex IL1RAPL1 intragenic rearrangement. European Journal of Paediatric Neurology. 20(6). 971–976. 7 indexed citations

15.

Alesi, Viola, Marta Bertoli, Giuseppe Barrano, et al.. (2012). 335.4kb microduplication in chromosome band Xp11.2p11.3 associated with developmental delay, growth retardation, autistic disorder and dysmorphic features. Gene. 505(2). 384–387. 11 indexed citations

16.

Digilio, M. Cristina, Laura Bernardini, Francesca Romana Lepri, et al.. (2011). Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1. American Journal of Medical Genetics Part A. 155(9). 2196–2202. 25 indexed citations

17.

Bernardini, Laura, Lorenzo Sinibaldi, Anna Capalbo, et al.. (2009). HDR (Hypoparathyroidism, Deafness, Renal dysplasia) syndrome associated to GATA3 gene duplication. Clinical Genetics. 76(1). 117–119. 18 indexed citations

18.

Bedeschi, Maria Francesca, Antonio Novelli, Laura Bernardini, et al.. (2008). Association of syndromic mental retardation with an Xq12q13.1 duplication encompassing the oligophrenin 1 gene. American Journal of Medical Genetics Part A. 146A(13). 1718–1724. 15 indexed citations

19.

Ferraris, Alessandro, et al.. (2006). Combined Test for UGT1A1 –3279T→G and A(TA)nTAA Polymorphisms Best Predicts Gilbert's Syndrome in Italian Pediatric Patients. Genetic Testing. 10(2). 121–125. 22 indexed citations

20.

Ferraris, Alessandro, Bárbara Torres, D. Knafelz, et al.. (2006). Relationship Between CARD15, SLC22A4/5, and DLG5 Polymorphisms and Early-Onset Inflammatory Bowel Diseases. Inflammatory Bowel Diseases. 12(5). 355–361. 34 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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