Romano Tenconi

7.6k citations
122 papers · 3.5k indexed · h-index 35
Topics
Genomic variations and chromosomal abnormalities (25 papers)Prenatal Screening and Diagnostics (18 papers)Neurofibromatosis and Schwannoma Cases (11 papers)
Partner nations
ItalyFranceUnited States

In The Last Decade

Romano Tenconi

118 papers receiving 3.3k citations

Peers

Romano Tenconi
Comparison fields: 5 of 145
  • Genetics 1.3k
  • Molecular Biology 1.1k
  • Pediatrics, Perinatology and Child Health 648
  • Surgery 558
  • Neurology 469
Replace Riitta Herva with:
Riitta Herva Finland
Kim M. Keppler‐Noreuil United States
Paola Grammatico Italy
Arthur S. Aylsworth United States
David D. Weaver United States
Eberhard Passarge Germany
Paige Kaplan United States
Sally Ann Lynch Ireland
N. C. Nevin United Kingdom
Wladimir Wertelecki United States
Romano Tenconi relative to Riitta Herva Finland Riitta Herva's profile →
Citations per field
00.5×1.5×2.0×
Riitta Herva · 1×
Citations per year

Countries citing papers authored by Romano Tenconi

Since Specialization
Citations

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

Fields of papers citing papers by Romano Tenconi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Romano Tenconi

This figure shows the co-authorship network connecting the top 25 collaborators of Romano Tenconi. A scholar is included among the top collaborators of Romano Tenconi 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 Romano Tenconi. Romano Tenconi 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
#WorkIndexed citations
1 0
2 5
3 2
4 10
5 50
6 18
7 26
8 31
9 69
10
Genotype-phenotype correlation in patients with NF1 microdeletion syndrome: identification of candidate genes for mental retardation
0
11 14
12 11
13 16
14 4
15 96
16 29
17 3
18 40
19 25
20 43

About Romano Tenconi

Romano Tenconi is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 122 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Prenatal Screening and Diagnostics (18 papers) and Neurofibromatosis and Schwannoma Cases (11 papers). The work is most often cited by research in Genetics (1.3k citations), Urology (220 citations) and Pediatrics, Perinatology and Child Health (648 citations). Romano Tenconi has collaborated with scholars based in Italy, France and United States. Frequent co-authors include Maurizio Clementi, Maurizio Clementi, C Baccichetti, Fabrizio Bianchi, Isabella Mammi, Massimo Clementi, Claude Stoll, Elena Di Gianantonio, Helen Dolk and Ester Garne. Their work appears in journals such as New England Journal of Medicine, The Lancet and PLoS ONE.

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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