Romano Tenconi

7.6k total citations
122 papers, 3.5k citations indexed

About

Romano Tenconi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Romano Tenconi has authored 122 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Genetics, 47 papers in Molecular Biology and 23 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Romano Tenconi's work include Genomic variations and chromosomal abnormalities (25 papers), Prenatal Screening and Diagnostics (18 papers) and Neurofibromatosis and Schwannoma Cases (11 papers). Romano Tenconi is often cited by papers focused on Genomic variations and chromosomal abnormalities (25 papers), Prenatal Screening and Diagnostics (18 papers) and Neurofibromatosis and Schwannoma Cases (11 papers). Romano Tenconi collaborates with scholars based in Italy, France and United States. Romano Tenconi's 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 and has published in prestigious journals such as New England Journal of Medicine, The Lancet and PLoS ONE.

In The Last Decade

Romano Tenconi

118 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Romano Tenconi Italy 35 1.3k 1.1k 648 558 469 122 3.5k
Arthur S. Aylsworth United States 32 1.9k 1.4× 1.8k 1.5× 596 0.9× 575 1.0× 222 0.5× 93 3.8k
David D. Weaver United States 33 1.6k 1.2× 1.3k 1.2× 699 1.1× 970 1.7× 142 0.3× 117 3.3k
Paola Grammatico Italy 34 1.9k 1.4× 1.8k 1.5× 348 0.5× 696 1.2× 154 0.3× 204 4.4k
Wladimir Wertelecki United States 29 815 0.6× 757 0.7× 852 1.3× 179 0.3× 493 1.1× 110 2.9k
Han‐Wook Yoo South Korea 33 971 0.7× 1.8k 1.6× 398 0.6× 446 0.8× 203 0.4× 300 4.0k
Riitta Herva Finland 39 1.3k 0.9× 3.4k 3.0× 743 1.1× 872 1.6× 232 0.5× 124 6.6k
Eberhard Passarge Germany 34 1.3k 1.0× 2.2k 1.9× 554 0.9× 620 1.1× 96 0.2× 158 4.1k
Reijo Norio Finland 36 1.8k 1.3× 1.1k 1.0× 401 0.6× 337 0.6× 347 0.7× 69 3.6k
Aubrey Milunsky United States 31 1.0k 0.8× 1.6k 1.4× 832 1.3× 563 1.0× 71 0.2× 134 3.9k
Pablo Lapunzina Spain 40 2.7k 2.0× 2.9k 2.5× 856 1.3× 589 1.1× 147 0.3× 227 5.1k

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
1.
Pezzani, Lidia, Angelo Selicorni, Maria Francesca Bedeschi, et al.. (2025). Portrait of a Spectrum: Clinical and Genetic Characterization of a Large Cohort of Chromatinopathies—30 Years' Experience From a Third Level Center. Clinical Genetics. 109(4). 707–716.
2.
Pignata, Laura, Angela Sparago, Orazio Palumbo, et al.. (2021). Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome. Genes. 12(4). 581–581. 5 indexed citations
3.
Russo, Angelo, Maria Iascone, Romano Tenconi, et al.. (2021). ELP2 compound heterozygous variants associated with cortico-cerebellar atrophy, nodular heterotopia and epilepsy: Phenotype expansion and review of the literature. European Journal of Medical Genetics. 64(12). 104361–104361. 2 indexed citations
4.
Bordugo, Andrea, Maria Iascone, Romano Tenconi, et al.. (2020). Epilepsy and movement disorders in CDG: Report on the oldest‐known MOGS‐CDG patient. American Journal of Medical Genetics Part A. 185(1). 219–222. 10 indexed citations
5.
Clementi, Maurizio, Gian Mario Tiboni, Roberto Causin, et al.. (2008). Pesticides and fertility: An epidemiological study in Northeast Italy and review of the literature. Reproductive Toxicology. 26(1). 13–18. 50 indexed citations
6.
Grati, Francesca Romana, Faustina Lalatta, Licia Turolla, et al.. (2005). Three cases with de novo 6q imbalance and variable prenatal phenotype. American Journal of Medical Genetics Part A. 136A(3). 254–258. 18 indexed citations
7.
Sacconi, Sabrina, Eva Trevisson, Francesca Pistollato, et al.. (2005). hCOX18 and hCOX19: Two human genes involved in cytochrome c oxidase assembly. Biochemical and Biophysical Research Communications. 337(3). 832–839. 26 indexed citations
8.
Gervasini, Cristina, Francesca Orzan, Angela Bentivegna, et al.. (2004). Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions. Human Genetics. 115(1). 69–80. 31 indexed citations
9.
Dolk, Helen, Martine Vrijheid, J. E. Scott, et al.. (2003). Toward the effective surveillance of hypospadias.. Environmental Health Perspectives. 112(3). 398–402. 69 indexed citations
10.
Riva, Paola, Marco Venturin, Paolo Guarnieri, et al.. (2002). Genotype-phenotype correlation in patients with NF1 microdeletion syndrome: identification of candidate genes for mental retardation. The American Journal of Human Genetics. 71(4). 308–308.
11.
Smith, Frances J.D., et al.. (2001). Novel Keratin 17 Mutations in Pachyonychia Congenita Type 2. Journal of Investigative Dermatology. 116(5). 806–808. 14 indexed citations
12.
Resta, Nicoletta, Alessandro Stella, Francesco Susca, et al.. (2001). Nine novel APC mutations in Italian FAP patients. Human Mutation. 17(5). 434–435. 11 indexed citations
13.
Tartaglia, Marco, Veronica Bordoni, Francesco Velardi, et al.. (1999). Fibroblast growth factor receptor mutational screening in newborns affected by metopic synostosis. Child s Nervous System. 15(8). 389–394. 16 indexed citations
14.
Clementi, Massimo, Sebastiano Bianca, Francesco Benedicenti, & Romano Tenconi. (1999). Down Syndrome and Parity. Public Health Genomics. 2(1). 18–22. 4 indexed citations
15.
Stevenson, David A., Patricia Birch, Jan M. Friedman, et al.. (1999). Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1. American Journal of Medical Genetics. 84(5). 413–419. 96 indexed citations
16.
Clementi, Massimo, Paola Forabosco, A. Amadori, et al.. (1999). CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genes. Human Genetics. 105(4). 337–342. 29 indexed citations
17.
Stella, Alessandro, Nicoletta Resta, Angela Polizzi, et al.. (1998). The familial adenomatous polyposis region exhibits many different haplotypes. Human Genetics. 102(6). 624–628. 3 indexed citations
18.
Turco, Alberto, Maurizio Clementi, Sandro Rossetti, Romano Tenconi, & Pier Franco Pignatti. (1996). An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene. American Journal of Kidney Diseases. 28(5). 759–761. 40 indexed citations
19.
Minelli, Antonella, Giovanna Floridia, Elena Rossi, et al.. (1993). D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Human Genetics. 92(4). 391–396. 25 indexed citations
20.
Clementi, Maurizio, et al.. (1991). Apparent CHARGE association and chromosome anomaly: Chance or contiguous gene syndrome. American Journal of Medical Genetics. 41(2). 246–250. 43 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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