Emanuela Conti

1.5k total citations
18 papers, 831 citations indexed

About

Emanuela Conti is a scholar working on Molecular Biology, Epidemiology and Immunology. According to data from OpenAlex, Emanuela Conti has authored 18 papers receiving a total of 831 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 5 papers in Epidemiology and 5 papers in Immunology. Recurrent topics in Emanuela Conti's work include Congenital heart defects research (12 papers), Congenital Heart Disease Studies (5 papers) and Protein Tyrosine Phosphatases (5 papers). Emanuela Conti is often cited by papers focused on Congenital heart defects research (12 papers), Congenital Heart Disease Studies (5 papers) and Protein Tyrosine Phosphatases (5 papers). Emanuela Conti collaborates with scholars based in Italy, United States and Australia. Emanuela Conti's co-authors include Bruno Dallapiccola, Antonio Pizzuti, Bruno Marino, Anna Sárközy, M. Cristina Digilio, Rita Mingarelli, Tania Dottorini, Francesca Amati, Giuseppe Novelli and Alessandro De Luca and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Vascular Surgery and Genomics.

In The Last Decade

Emanuela Conti

18 papers receiving 818 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emanuela Conti Italy 13 703 236 189 167 107 18 831
Ellen Denayer Belgium 15 462 0.7× 141 0.6× 137 0.7× 58 0.3× 89 0.8× 30 809
Maria Lisa Dentici Italy 19 704 1.0× 102 0.4× 459 2.4× 139 0.8× 71 0.7× 74 1.1k
Hamao Hirota Japan 9 425 0.6× 181 0.8× 91 0.5× 117 0.7× 98 0.9× 12 842
Boris Keren France 21 649 0.9× 115 0.5× 515 2.7× 52 0.3× 61 0.6× 70 1.1k
Akio Mantani Japan 9 445 0.6× 157 0.7× 138 0.7× 31 0.2× 113 1.1× 12 779
Lauren M. Goddard United States 8 396 0.6× 86 0.4× 50 0.3× 51 0.3× 80 0.7× 9 868
Eva M. Monsalve Spain 13 342 0.5× 247 1.0× 62 0.3× 54 0.3× 81 0.8× 18 668
Amalia Martı́nez-Mir United States 20 578 0.8× 67 0.3× 152 0.8× 26 0.2× 35 0.3× 50 949
Raimund Fahsold Germany 14 344 0.5× 52 0.2× 159 0.8× 90 0.5× 67 0.6× 27 777
Axel Bohring Germany 13 361 0.5× 62 0.3× 203 1.1× 60 0.4× 35 0.3× 17 609

Countries citing papers authored by Emanuela Conti

Since Specialization
Citations

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

Fields of papers citing papers by Emanuela Conti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuela Conti

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

All Works

18 of 18 papers shown
1.
Sárközy, Anna, Emanuela Conti, M. Cristina Digilio, et al.. (2005). ZFPM2/FOG2 andHEY2 genes analysis in nonsyndromic tricuspid atresia. American Journal of Medical Genetics Part A. 133A(1). 68–70. 11 indexed citations
2.
Luca, Alessandro De, Irene Bottillo, Anna Sárközy, et al.. (2005). NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome. The American Journal of Human Genetics. 77(6). 1092–1101. 106 indexed citations
3.
Digilio, M. Cristina, Bruno Marino, Rossella Capolino, et al.. (2005). Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2. American Journal of Medical Genetics Part A. 134A(2). 158–164. 12 indexed citations
4.
Yagubyan, Marineh, Jean M. Panneton, Noralane M. Lindor, et al.. (2004). LEOPARD syndrome: a new polyaneurysm association and an update on the molecular genetics of the disease. Journal of Vascular Surgery. 39(4). 897–900. 7 indexed citations
5.
Digilio, M. Cristina, Giuseppe Pacileo, Anna Sárközy, et al.. (2004). Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: A boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations. Birth Defects Research Part A Clinical and Molecular Teratology. 70(2). 95–98. 12 indexed citations
6.
Sinibaldi, Lorenzo, Alessandro De Luca, Emanuele Bellacchio, et al.. (2004). Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia. Human Mutation. 24(6). 534–535. 60 indexed citations
7.
Sárközy, Anna, María Gabriela Obregón, Emanuela Conti, et al.. (2004). A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndrome. European Journal of Human Genetics. 12(12). 1069–1072. 38 indexed citations
8.
Amati, Francesca, Ivano Condò, Emanuela Conti, et al.. (2003). Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over‐expression studies. Cell Biochemistry and Function. 21(3). 263–267. 2 indexed citations
9.
Pizzuti, Antonio, Anna Sárközy, Anthea Newton, et al.. (2003). Mutations ofZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot. Human Mutation. 22(5). 372–377. 97 indexed citations
10.
Conti, Emanuela, Anna Sárközy, Caterina Tandoi, et al.. (2003). DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene. European Journal of Human Genetics. 11(4). 349–351. 33 indexed citations
11.
Luca, Alessandro De, Emanuela Conti, Francesca Amati, et al.. (2002). Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q‐rich‐associated protein) and schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 116B(1). 32–35. 16 indexed citations
12.
Digilio, M. Cristina, Emanuela Conti, Anna Sárközy, et al.. (2002). Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 Gene. The American Journal of Human Genetics. 71(2). 389–394. 270 indexed citations
13.
Amati, Francesca, Emanuela Conti, Annalisa Botta, et al.. (2002). Functional characterization of the 5′ flanking region of human ubiquitin fusion degradation 1 like gene (UFD1L). Cell Biochemistry and Function. 20(2). 163–170. 4 indexed citations
14.
Berti, Lucia, Gerhard Mittler, Gerhard K. H. Przemeck, et al.. (2001). Isolation and Characterization of a Novel Gene from the DiGeorge Chromosomal Region That Encodes for a Mediator Subunit. Genomics. 74(3). 320–332. 32 indexed citations
15.
Luca, Alessandro De, Augusto Pasini, Francesca Amati, et al.. (2001). Association study of a promoter polymorphism of UFD1L gene with schizophrenia. American Journal of Medical Genetics. 105(6). 529–533. 31 indexed citations
16.
Pizzuti, Antonio, Giuseppe Novelli, Antonia Ratti, et al.. (1999). Isolation and Characterization of a Novel Transcript Embedded within HIRA, a Gene Deleted in DiGeorge Syndrome. Molecular Genetics and Metabolism. 67(3). 227–235. 16 indexed citations
17.
Amati, Francesca, Emanuela Conti, Antonio Novelli, et al.. (1999). Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome. European Journal of Human Genetics. 7(8). 903–909. 66 indexed citations
18.
Novelli, Giuseppe, Aldo Mari, Francesca Amati, et al.. (1998). Structure and expression of the human ubiquitin fusion–degradation gene (UFD1L). Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1396(2). 158–162. 18 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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