Emanuela Conti

1.5k citations

18 papers · 831 indexed · h-index 13

Co-authors: Bruno Dallapiccola Antonio Pizzuti Bruno Marino Anna Sárközy M. Cristina Digilio Rita Mingarelli Tania Dottorini Francesca Amati
Topics: Congenital heart defects research (12 papers)Congenital Heart Disease Studies (5 papers)Protein Tyrosine Phosphatases (5 papers)
Cited by: Immunology Molecular Biology Genetics
Journals: The American Journal of Human Genetics Journal of Vascular Surgery Genomics
Partner nations: Italy United States Australia

In The Last Decade

Emanuela Conti

18 papers receiving 818 citations

Peers

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

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18 of 18 papers shown

#	Work	Indexed citations
1	ZFPM2/FOG2 andHEY2 genes analysis in nonsyndromic tricuspid atresia 2005 ·American Journal of Medical Genetics Part A ·Anna Sárközy,Emanuela Conti,(unknown),M. Cristina Digilio,Roberto Formigari,Fernando M. Picchio,Bruno Marino,Antonio Pizzuti,Bruno Dallapiccola	11
2	NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome 2005 ·The American Journal of Human Genetics ·Alessandro De Luca,Irene Bottillo,Anna Sárközy,Claudio Carta,(unknown),Emanuele Bellacchio,Annalisa Schirinzi,Emanuela Conti,Giuseppe Zampino,Agatino Battaglia,Silvia Majore,Maria Michela Rinaldi,Massimo Carella,Bruno Marino,Antonio Pizzuti,M. Cristina Digilio,Marco Tartaglia,Bruno Dallapiccola	106
3	Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2 2005 ·American Journal of Medical Genetics Part A ·M. Cristina Digilio,Bruno Marino,Rossella Capolino,Adriano Angioni,Anna Sárközy,(unknown),Emanuela Conti,Andrea De Zorzi,Bruno Dallapiccola	12
4	LEOPARD syndrome: a new polyaneurysm association and an update on the molecular genetics of the disease 2004 ·Journal of Vascular Surgery ·Marineh Yagubyan,Jean M. Panneton,Noralane M. Lindor,Emanuela Conti,Anna Sárközy,Antonio Pizzuti	7
5	Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: A boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations 2004 ·Birth Defects Research Part A Clinical and Molecular Teratology ·M. Cristina Digilio,Giuseppe Pacileo,Anna Sárközy,Giuseppe Limongelli,Emanuela Conti,Fabiana Cerrato,Bruno Marino,Antonio Pizzuti,Raffaele Calabrò,Bruno Dallapiccola	12
6	Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia 2004 ·Human Mutation ·Lorenzo Sinibaldi,Alessandro De Luca,Emanuele Bellacchio,Emanuela Conti,Augusto Pasini,Claudio Paloscia,Gianfranco Spalletta,Carlo Caltagirone,Antonio Pizzuti,Bruno Dallapiccola	60
7	A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndrome 2004 ·European Journal of Human Genetics ·Anna Sárközy,María Gabriela Obregón,Emanuela Conti,Giorgia Esposito,Rita Mingarelli,Antonio Pizzuti,Bruno Dallapiccola	38
8	Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over‐expression studies 2003 ·Cell Biochemistry and Function ·Francesca Amati,Ivano Condò,Emanuela Conti,Federica Sangiuolo,Bruno Dallapiccola,Roberto Testi,Giuseppe Novelli	2
9	Mutations ofZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot 2003 ·Human Mutation ·Antonio Pizzuti,Anna Sárközy,Anthea Newton,Emanuela Conti,Elisabetta Flex,M. Cristina Digilio,Francesca Amati,(unknown),Caterina Tandoi,Bruno Marino,Merlin Crossley,Bruno Dallapiccola	97
10	DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene 2003 ·European Journal of Human Genetics ·Emanuela Conti,(unknown),Anna Sárközy,Caterina Tandoi,Bruno Marino,M. Cristina Digilio,Rita Mingarelli,Antonio Pizzuti,Bruno Dallapiccola	33
11	Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q‐rich‐associated protein) and schizophrenia 2002 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Alessandro De Luca,Emanuela Conti,(unknown),Francesca Amati,Gianfranco Spalletta,Carlo Caltagirone,(unknown),Augusto Pasini,Massimo Gennarelli,Stefano Bignotti,Lucia Berti,Gerhard Mittler,Michael Meisterernst,Bruno Dallapiccola,Giuseppe Novelli	16
12	Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 Gene 2002 ·The American Journal of Human Genetics ·M. Cristina Digilio,Emanuela Conti,Anna Sárközy,Rita Mingarelli,Tania Dottorini,Bruno Marino,Antonio Pizzuti,Bruno Dallapiccola	270
13	Functional characterization of the 5′ flanking region of human ubiquitin fusion degradation 1 like gene (UFD1L) 2002 ·Cell Biochemistry and Function ·Francesca Amati,Emanuela Conti,Annalisa Botta,Paola Amicucci,Bruno Dallapiccola,Giuseppe Novelli	4
14	Isolation and Characterization of a Novel Gene from the DiGeorge Chromosomal Region That Encodes for a Mediator Subunit 2001 ·Genomics ·Lucia Berti,Gerhard Mittler,Gerhard K. H. Przemeck,Gertraud Stelzer,(unknown),Francesca Amati,Emanuela Conti,Bruno Dallapiccola,Martin Hrabě de Angelis,Giuseppe Novelli,Michael Meisterernst	32
15	Association study of a promoter polymorphism of UFD1L gene with schizophrenia 2001 ·American Journal of Medical Genetics ·Alessandro De Luca,Augusto Pasini,Francesca Amati,Annalisa Botta,Gianfranco Spalletta,(unknown),(unknown),Emanuela Conti,Joseph Trakalo,Fabìo Macciardi,Bruno Dallapiccola,Giuseppe Novelli	31
16	Isolation and Characterization of a Novel Transcript Embedded within HIRA, a Gene Deleted in DiGeorge Syndrome 1999 ·Molecular Genetics and Metabolism ·Antonio Pizzuti,Giuseppe Novelli,Antonia Ratti,Francesca Amati,Roberta Bordoni,Paola Mandich,Emilia Bellone,Emanuela Conti,Mario Bengala,Aldo Mari,Vincenzo Silani,Bruno Dallapiccola	16
17	Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome 1999 ·European Journal of Human Genetics ·Francesca Amati,Emanuela Conti,Antonio Novelli,Mario Bengala,M. Cristina Digilio,Bruno Marino,Aldo Giannotti,Orazio Gabrielli,Giuseppe Novelli,Bruno Dallapiccola	66
18	Structure and expression of the human ubiquitin fusion–degradation gene (UFD1L) 1998 ·Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Giuseppe Novelli,Aldo Mari,Francesca Amati,Alessia Colosimo,Federica Sangiuolo,Mario Bengala,Emanuela Conti,Antonia Ratti,Roberta Bordoni,Antonio Pizzuti,Antonio Baldini,Rita Crinelli,Franco Pandolfi,Mauro Magnani,Bruno Dallapiccola	18

About Emanuela Conti

Emanuela Conti is a scholar working on Molecular Biology, Immunology and Epidemiology, having authored 18 papers that have together received 831 indexed citations. Recurring topics across this work include Congenital heart defects research (12 papers), Congenital Heart Disease Studies (5 papers) and Protein Tyrosine Phosphatases (5 papers). The work is most often cited by research in Immunology (236 citations), Molecular Biology (703 citations) and Genetics (189 citations). Emanuela Conti has collaborated with scholars based in Italy, United States and Australia. Frequent 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. Their work appears in journals such as The American Journal of Human Genetics, Journal of Vascular Surgery and Genomics.

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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