Paolo Guanciali‐Franchi

655 total citations
24 papers, 443 citations indexed

About

Paolo Guanciali‐Franchi is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Paolo Guanciali‐Franchi has authored 24 papers receiving a total of 443 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Pediatrics, Perinatology and Child Health, 12 papers in Genetics and 8 papers in Molecular Biology. Recurrent topics in Paolo Guanciali‐Franchi's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Paolo Guanciali‐Franchi is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (9 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Paolo Guanciali‐Franchi collaborates with scholars based in Italy, United States and Israel. Paolo Guanciali‐Franchi's co-authors include Liborio Stuppia, Chiara Palka, Giandomenico Palka, Giuseppe Calabrese, Oronzo Scarciolla, Valentina Gatta, G Calabrese, Elisena Morizio, Gian Mario Tiboni and Antonio Spadano and has published in prestigious journals such as Human Reproduction, Leukemia and Human Genetics.

In The Last Decade

Paolo Guanciali‐Franchi

20 papers receiving 420 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paolo Guanciali‐Franchi Italy 10 222 154 144 71 67 24 443
Lisa M Niswander United States 10 199 0.9× 39 0.3× 97 0.7× 42 0.6× 112 1.7× 22 440
Hirohito Shima Japan 11 149 0.7× 30 0.2× 140 1.0× 30 0.4× 32 0.5× 29 313
Paolo Guanciali Franchi Italy 14 220 1.0× 80 0.5× 298 2.1× 98 1.4× 80 1.2× 31 484
Csaba Papp United States 13 64 0.3× 77 0.5× 81 0.6× 205 2.9× 79 1.2× 27 495
Vida Petrovic Australia 10 390 1.8× 64 0.4× 301 2.1× 30 0.4× 40 0.6× 19 600
J.D. Singer United Kingdom 8 363 1.6× 148 1.0× 112 0.8× 11 0.2× 71 1.1× 15 667
J. P. M. Geraedts Netherlands 11 104 0.5× 105 0.7× 153 1.1× 62 0.9× 95 1.4× 22 422
P Colombiès France 12 127 0.6× 93 0.6× 150 1.0× 23 0.3× 121 1.8× 64 438
Michael J. Macera United States 13 165 0.7× 76 0.5× 193 1.3× 5 0.1× 73 1.1× 43 400
G. Bourrouillou France 14 279 1.3× 146 0.9× 398 2.8× 147 2.1× 36 0.5× 40 587

Countries citing papers authored by Paolo Guanciali‐Franchi

Since Specialization
Citations

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

Fields of papers citing papers by Paolo Guanciali‐Franchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paolo Guanciali‐Franchi. 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 Paolo Guanciali‐Franchi. The network helps show where Paolo Guanciali‐Franchi may publish in the future.

Co-authorship network of co-authors of Paolo Guanciali‐Franchi

This figure shows the co-authorship network connecting the top 25 collaborators of Paolo Guanciali‐Franchi. A scholar is included among the top collaborators of Paolo Guanciali‐Franchi 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 Paolo Guanciali‐Franchi. Paolo Guanciali‐Franchi 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.
Dell’Edera, Domenico, et al.. (2021). Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report. Journal of Medical Case Reports. 15(1). 208–208. 3 indexed citations
2.
Palka, Chiara, Paolo Guanciali‐Franchi, Elisena Morizio, et al.. (2019). Non-invasive prenatal screening: A 20-year experience in Italy. European Journal of Obstetrics & Gynecology and Reproductive Biology X. 3. 100050–100050. 3 indexed citations
3.
Pagotto, Sara, Angelo Veronese, Veronica Balatti, et al.. (2019). HNRNPL Restrains miR-155 Targeting of BUB1 to Stabilize Aberrant Karyotypes of Transformed Cells in Chronic Lymphocytic Leukemia. Cancers. 11(4). 575–575. 11 indexed citations
4.
Guanciali‐Franchi, Paolo, et al.. (2016). An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations. Molecular Syndromology. 8(1). 42–44.
5.
Guanciali‐Franchi, Paolo, et al.. (2012). Elevated maternal serum α-fetoprotein level in a fetus with Beckwith-Wiedemann syndrome in the second trimester of pregnancy.. PubMed. 6(1). 7–9. 9 indexed citations
6.
Guanciali‐Franchi, Paolo, et al.. (2012). Optimal cut‐offs for down syndrome contingent screening in a population of 10 156 pregnant women. Prenatal Diagnosis. 32(12). 1147–1150. 6 indexed citations
7.
Guanciali‐Franchi, Paolo, Chiara Palka, Barbara Matarrelli, et al.. (2011). Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high‐risk pregnant women. Prenatal Diagnosis. 31(11). 1077–1081. 7 indexed citations
8.
Guanciali‐Franchi, Paolo, Giuseppe Calabrese, Elisena Morizio, et al.. (2008). A new case of mosaicism for invdup(15) duplicated for Prader–Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. European Journal of Medical Genetics. 51(3). 239–244.
9.
Liberati, Marco, et al.. (2008). Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. Journal of Assisted Reproduction and Genetics. 25(11-12). 577–580. 15 indexed citations
10.
Liberati, Marco, et al.. (2007). Fetal Facial Profile in Pallister-Killian Syndrome. Fetal Diagnosis and Therapy. 23(1). 15–17. 12 indexed citations
11.
Gatta, Valentina, Oronzo Scarciolla, Chiara Palka, et al.. (2005). Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). Human Genetics. 117(1). 92–98. 88 indexed citations
12.
Celentano, Claudio, Paolo Guanciali‐Franchi, Marco Liberati, et al.. (2005). Lack of correlation between elevated maternal serum hCG during second‐trimester biochemical screening and fetal congenital anomaly. Prenatal Diagnosis. 25(3). 220–224. 3 indexed citations
13.
Guanciali‐Franchi, Paolo, Giuseppe Calabrese, Elisena Morizio, et al.. (2004). Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. American Journal of Medical Genetics Part A. 127A(2). 144–148. 17 indexed citations
14.
Palka, Chiara, et al.. (2004). Prevalence of chromosomal abnormalities in 2078 infertile couples referred for assisted reproductive techniques. Human Reproduction. 20(2). 437–442. 95 indexed citations
15.
Vasco, Vincenza Rita Lo, G Calabrese, Lucia Manzoli, et al.. (2004). Inositide-specific phospholipase c β1 gene deletion in the progression of myelodysplastic syndrome to acute myeloid leukemia. Leukemia. 18(6). 1122–1126. 48 indexed citations
16.
Stuppia, Liborio, Valentina Gatta, Oronzo Scarciolla, et al.. (2003). The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. Journal of Endocrinological Investigation. 26(7). 620–622. 67 indexed citations
17.
Stuppia, Liborio, Giuseppe Calabrese, Rita Peila, et al.. (1997). p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis. Cancer Genetics and Cytogenetics. 98(1). 28–35. 41 indexed citations
18.
Girolamo, Guillermo Di, F. Angrilli, Maria Giuliana Tozzi Ciancarelli, et al.. (1989). Bone marrow transplantation for thalassemia in Pescara.. PubMed. 309. 193–9. 1 indexed citations
19.
Ferrucci, Luigi, R. Mezzanotte, Roberta Vanni, et al.. (1988). Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Cancer Genetics and Cytogenetics. 34(2). 251–256. 7 indexed citations
20.
Palka, Giandomenico, et al.. (1986). Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia.. PubMed. 71(3). 221–4. 5 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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