V. Faà

1.0k total citations
20 papers, 489 citations indexed

About

V. Faà is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Hematology. According to data from OpenAlex, V. Faà has authored 20 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 6 papers in Pulmonary and Respiratory Medicine and 6 papers in Hematology. Recurrent topics in V. Faà's work include Hemoglobinopathies and Related Disorders (11 papers), Iron Metabolism and Disorders (6 papers) and Cystic Fibrosis Research Advances (4 papers). V. Faà is often cited by papers focused on Hemoglobinopathies and Related Disorders (11 papers), Iron Metabolism and Disorders (6 papers) and Cystic Fibrosis Research Advances (4 papers). V. Faà collaborates with scholars based in Italy. V. Faà's co-authors include Maria Cristina Rosatelli, Antonio Cao, Alessandra Meloni, L. Saba, Roberto Perniola, Yuet Wai Kan, A M Dozy, Giovanni Monni, Maria Serafina Ristaldi and T Tuveri and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Clinical Endocrinology & Metabolism and Human Molecular Genetics.

In The Last Decade

V. Faà

20 papers receiving 477 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. Faà Italy 14 234 164 145 119 94 20 489
C. Brancati Italy 15 313 1.3× 251 1.5× 122 0.8× 69 0.6× 122 1.3× 58 615
S Murru Italy 15 313 1.3× 234 1.4× 176 1.2× 42 0.4× 49 0.5× 40 490
Maria Addis Italy 14 294 1.3× 244 1.5× 191 1.3× 40 0.3× 101 1.1× 33 591
Jihyun Song United States 11 135 0.6× 85 0.5× 122 0.8× 44 0.4× 134 1.4× 50 414
Josef Davidsson Sweden 11 55 0.2× 123 0.8× 191 1.3× 15 0.1× 165 1.8× 16 442
Philip N. Mowrey United States 11 56 0.2× 34 0.2× 162 1.1× 46 0.4× 232 2.5× 22 436
S. Fattoum France 12 328 1.4× 269 1.6× 39 0.3× 70 0.6× 51 0.5× 39 432
Marie‐Pierre Cordier France 11 59 0.3× 30 0.2× 168 1.2× 24 0.2× 189 2.0× 34 438
Sabine Hentze Germany 11 40 0.2× 64 0.4× 178 1.2× 12 0.1× 139 1.5× 18 412

Countries citing papers authored by V. Faà

Since Specialization
Citations

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

Fields of papers citing papers by V. Faà

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Faà

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

All Works

20 of 20 papers shown
1.
Faà, V., Susanna Porcu, Maria Franca Marongiu, et al.. (2024). Post-GWAS Validation of Target Genes Associated with HbF and HbA2 Levels. Cells. 13(14). 1185–1185. 1 indexed citations
2.
Faà, V., et al.. (2022). Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis. Cells. 11(19). 3069–3069. 17 indexed citations
3.
Coiana, Alessandra, et al.. (2011). Preconceptional identification of cystic fibrosis carriers in the Sardinian population: A pilot screening program. Journal of Cystic Fibrosis. 10(3). 207–211. 6 indexed citations
4.
Faà, V., et al.. (2010). A Synonymous Mutation in the CFTR Gene Causes Aberrant Splicing in an Italian Patient Affected by a Mild Form of Cystic Fibrosis. Journal of Molecular Diagnostics. 12(3). 380–383. 20 indexed citations
5.
6.
Marcialis, Maria Antonietta, et al.. (2008). Neonatal onset of nephrogenic syndrome of inappropriate antidiuresis. Pediatric Nephrology. 23(12). 2267–2271. 29 indexed citations
7.
8.
Faà, V., Alessandra Meloni, Loredana Moi, et al.. (2006). Thalassaemia‐like carriers not linked to the β‐globin gene cluster. British Journal of Haematology. 132(5). 640–650. 10 indexed citations
9.
Moi, Paolo, V. Faà, M. Marini, et al.. (2004). A novel silent β‐thalassemia mutation in the distal CACCC box affects the binding and responsiveness to EKLF. British Journal of Haematology. 126(6). 881–884. 30 indexed citations
10.
Monni, Giovanni, et al.. (2004). Preimplantation genetic diagnosis for β‐thalassaemia: the Sardinian experience. Prenatal Diagnosis. 24(12). 949–954. 17 indexed citations
11.
Meloni, Alessandra, et al.. (2002). Delineation of the Molecular Defects in the AIRE Gene in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients from Southern Italy. The Journal of Clinical Endocrinology & Metabolism. 87(2). 841–846. 66 indexed citations
12.
Rosatelli, Maria Cristina, Alessandra Meloni, V. Faà, et al.. (1997). Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I.. Journal of Medical Genetics. 34(2). 122–125. 12 indexed citations
13.
Rosatelli, Maria Cristina, V. Faà, Alessandra Meloni, et al.. (1995). A promoter mutation, C → T at position ‐92, leading to silent /3‐thalassaemia. British Journal of Haematology. 90(2). 483–485. 14 indexed citations
14.
Faà, V., Sandro Loche, Mauro Bozzola, et al.. (1994). Mutations in the vasopressin V2-receptor gene in three families of Italian descent with nephrogenic diabetes insipidus. Human Molecular Genetics. 3(9). 1685–1686. 18 indexed citations
15.
Meloni, Alessandra, et al.. (1994). A novel β-thalassemia mutation: Frameshift at codon 59 detected in an Italian carrier. Human Mutation. 3(3). 309–311. 5 indexed citations
16.
Saba, L., et al.. (1993). Two novel mutations in the transmembrane domains of the CFTR gene in subjects of Sardinian descent. Human Molecular Genetics. 2(10). 1739–1740. 9 indexed citations
17.
Rosatelli, Maria Cristina, T Tuveri, V. Faà, et al.. (1992). Molecular screening and fetal diagnosis of ?-thalassemia in the Italian population. Human Genetics. 89(6). 585–9. 58 indexed citations
18.
Faà, V., et al.. (1992). A simple electrophoretic procedure for fetal diagnosis of β‐thalassaemia due to short deletions. Prenatal Diagnosis. 12(11). 903–907. 14 indexed citations
19.
Rosatelli, Maria Cristina, A M Dozy, V. Faà, et al.. (1992). Molecular characterization of beta-thalassemia in the Sardinian population.. PubMed. 50(2). 422–6. 89 indexed citations
20.
Meloni, Alessandra, Maria Cristina Rosatelli, V. Faà, et al.. (1992). Promoter mutations producing mild β‐thalassaemia in the Italian population. British Journal of Haematology. 80(2). 222–226. 27 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by C. Brancati Breakdown of academic impact, for papers by S Murru Breakdown of academic impact, for papers by Maria Addis Breakdown of academic impact, for papers by Jihyun Song Breakdown of academic impact, for papers by Josef Davidsson Breakdown of academic impact, for papers by Philip N. Mowrey Breakdown of academic impact, for papers by S. Fattoum Breakdown of academic impact, for papers by Marie‐Pierre Cordier Breakdown of academic impact, for papers by Sabine Hentze
Rankless by CCL
2026