Dora Fabbro

1.8k total citations
44 papers, 1.4k citations indexed

About

Dora Fabbro is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Dora Fabbro has authored 44 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 13 papers in Hematology and 8 papers in Genetics. Recurrent topics in Dora Fabbro's work include Genomics and Chromatin Dynamics (10 papers), Acute Myeloid Leukemia Research (6 papers) and Blood Coagulation and Thrombosis Mechanisms (5 papers). Dora Fabbro is often cited by papers focused on Genomics and Chromatin Dynamics (10 papers), Acute Myeloid Leukemia Research (6 papers) and Blood Coagulation and Thrombosis Mechanisms (5 papers). Dora Fabbro collaborates with scholars based in Italy, United States and Croatia. Dora Fabbro's co-authors include Giuseppe Damante, Carla Di Loreto, Carlo Alberto Beltrami, Roberto Di Lauro, Lucia Pellizzari, Gianluca Tell, Antonino Belfiore, Renata Lonigro, Fabio Puglisi and Vincenzo Di Lauro and has published in prestigious journals such as Nucleic Acids Research, The EMBO Journal and Cancer.

In The Last Decade

Dora Fabbro

44 papers receiving 1.4k citations

Peers

Dora Fabbro

ONCOL

EDM

PRM

GENET

Gabriele Jaques Germany

Jason D. Engel United States

Hennie T. Brüggenwirth Netherlands

J. Keith Killian United States

Carole Oddoux United States

Ingrid Laurendeau France

Robert W. Schnepp United States

Sandra W. McLeskey United States

Florence Busato France

Natsuki Takaha Japan

Gabriele Jaques Germany

Dora Fabbro

609 ×0.8

360 ×1.2

ONCOL

361 ×1.3

EDM

131 ×0.5

PRM

71 ×0.3

GENET

Citations per year, relative to Dora Fabbro Dora Fabbro (= 1×) peers Gabriele Jaques

Countries citing papers authored by Dora Fabbro

Since Specialization

Citations

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

Fields of papers citing papers by Dora Fabbro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dora Fabbro

This figure shows the co-authorship network connecting the top 25 collaborators of Dora Fabbro. A scholar is included among the top collaborators of Dora Fabbro 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 Dora Fabbro. Dora Fabbro 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

Fabbro, Dora, et al.. (2022). Rare spontaneous monochorionic dizygotic twins: a case report and a systematic review. BMC Pregnancy and Childbirth. 22(1). 564–564. 4 indexed citations

Fabbro, Dora, et al.. (2016). Immunoglobulin K light chain deficiency: A rare, but probably underestimated, humoral immune defect. European Journal of Medical Genetics. 59(4). 219–222. 8 indexed citations

Vascotto, Carlo, Lisa Lirussi, Mattia Poletto, et al.. (2013). Functional regulation of the apurinic/apyrimidinic endonuclease 1 by nucleophosmin: impact on tumor biology. Oncogene. 33(22). 2876–2887. 54 indexed citations

D’Elia, Angela, Dora Fabbro, Lorenza Driul, et al.. (2011). Plasminogen Activator Inhibitor-1 Gene Polymorphisms in Pre-Eclampsia. Seminars in Thrombosis and Hemostasis. 37(2). 97–105. 9 indexed citations

Franzoni, Alessandra, et al.. (2011). Histone post-translational modifications associated to BAALC expression in leukemic cells. Biochemical and Biophysical Research Communications. 417(2). 721–725. 7 indexed citations

Puppin, Cinzia, Dora Fabbro, Lucia Pellizzari, & Giuseppe Damante. (2011). Using the recognition code to swap homeodomain target specificity in cell culture. Molecular Biology Reports. 38(8). 5349–5354. 1 indexed citations

Pianta, Annalisa, Cinzia Puppin, Alessandra Franzoni, et al.. (2010). Nucleophosmin is overexpressed in thyroid tumors. Biochemical and Biophysical Research Communications. 397(3). 499–504. 45 indexed citations

Tiribelli, Mario, Antonella Geromin, Angela Michelutti, et al.. (2010). Concomitant ABCG2 overexpression and FLT3‐ITD mutation identify a subset of acute myeloid leukemia patients at high risk of relapse. Cancer. 117(10). 2156–2162. 17 indexed citations

Matušan‐Ilijaš, Koviljka, Giuseppe Damante, Dora Fabbro, et al.. (2010). Osteopontin expression correlates with nuclear factor-κB activation and apoptosis downregulation in clear cell renal cell carcinoma. Pathology - Research and Practice. 207(2). 104–110. 32 indexed citations

10.

Castellone, Maria Domenica, Antonella Verrienti, Marialuisa Sponziello, et al.. (2009). A novel de novo germ‐line V292M mutation in the extracellular region of RET in a patient with phaeochromocytoma and medullary thyroid carcinoma: functional characterization. Clinical Endocrinology. 73(4). 529–534. 33 indexed citations

11.

Pianta, Annalisa, Dora Fabbro, Daniela Damiani, et al.. (2009). Two novel NPM1 mutations in a therapy‐responder AML patient. Hematological Oncology. 28(3). 151–155. 6 indexed citations

12.

Minisini, Alessandro Marco, Dora Fabbro, Carla Di Loreto, et al.. (2007). Markers of the uPA System and Common Prognostic Factors in Breast Cancer. American Journal of Clinical Pathology. 128(1). 112–117. 17 indexed citations

13.

Lisi, Veronica, et al.. (2007). Investigation of endothelin-1 type A receptor gene polymorphism (−231 G > A) in preeclampsia susceptibility. The Journal of Maternal-Fetal & Neonatal Medicine. 20(2). 145–149. 7 indexed citations

14.

Puppin, Cinzia, Lucia Pellizzari, Dora Fabbro, et al.. (2005). Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia. Journal of Human Genetics. 50(12). 679–683. 10 indexed citations

15.

Fabbro, Dora, Angela D’Elia, Riccardo Spizzo, et al.. (2003). Association between Plasminogen Activator Inhibitor 1 Gene Polymorphisms and Preeclampsia. Gynecologic and Obstetric Investigation. 56(1). 17–22. 36 indexed citations

16.

Fabbro, Dora, Lucia Pellizzari, Francesca Mercuri, Gianluca Tell, & Giuseppe Damante. (1998). Pax-8 protein levels regulate thyroglobulin gene expression. Journal of Molecular Endocrinology. 21(3). 347–354. 64 indexed citations

17.

Fabbro, Dora, et al.. (1996). TTF-1 gene expression in human lung tumours. European Journal of Cancer. 32(3). 512–517. 127 indexed citations

18.

Fabbro, Dora, Gianluca Tell, Lucia Pellizzari, et al.. (1995). Definition of the DNA-Binding Specificity of TTF-1 Homeodomain by Chromatographic Selection of Binding Sequences. Biochemical and Biophysical Research Communications. 213(3). 781–788. 18 indexed citations

19.

Damante, Giuseppe, Dora Fabbro, Lucia Pellizzari, et al.. (1994). Sequence-specific DNA recognition by the thyroid transcription factor-1 homeodomain. Nucleic Acids Research. 22(15). 3075–3083. 101 indexed citations

20.

Damante, Giuseppe, Gianluca Tell, Silvestro Formisano, et al.. (1993). Effect of Salt Concentration on TTF-1 HD Binding to Specific and Nonspecific DNA Sequences. Biochemical and Biophysical Research Communications. 197(2). 632–638. 10 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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