C Baccichetti

947 total citations
32 papers, 686 citations indexed

About

C Baccichetti is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C Baccichetti has authored 32 papers receiving a total of 686 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 12 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C Baccichetti's work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (4 papers). C Baccichetti is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (4 papers). C Baccichetti collaborates with scholars based in Italy, Switzerland and Germany. C Baccichetti's co-authors include Romano Tenconi, Elisabetta Lenzini, Albert Schinzel, Werner Schmid, P Zetterqvist, Orsetta Zuffardi, John M. Opitz, J. Lindsten, M. Fraccaro and Daniele Caufin and has published in prestigious journals such as The Lancet, Cellular and Molecular Life Sciences and Journal of Medical Genetics.

In The Last Decade

C Baccichetti

32 papers receiving 643 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C Baccichetti Italy 14 539 287 207 204 54 32 686
M. Ray Canada 15 731 1.4× 391 1.4× 292 1.4× 377 1.8× 73 1.4× 36 1.1k
F. R. Sergovich Canada 13 348 0.6× 232 0.8× 60 0.3× 172 0.8× 48 0.9× 20 548
M. S. NEWTON United Kingdom 14 536 1.0× 363 1.3× 310 1.5× 209 1.0× 31 0.6× 23 793
F Salamanca Mexico 15 287 0.5× 285 1.0× 111 0.5× 89 0.4× 42 0.8× 60 709
Roberto Coco Argentina 12 401 0.7× 213 0.7× 143 0.7× 156 0.8× 24 0.4× 45 531
Ada Rosenmann Israel 16 252 0.5× 347 1.2× 108 0.5× 91 0.4× 21 0.4× 36 650
M. G. Daker United Kingdom 13 333 0.6× 225 0.8× 113 0.5× 82 0.4× 41 0.8× 28 538
G Filippi Italy 16 313 0.6× 311 1.1× 57 0.3× 179 0.9× 57 1.1× 37 695
A. Rodewald Germany 17 552 1.0× 218 0.8× 154 0.7× 170 0.8× 45 0.8× 41 726
H. Reinwein Germany 13 640 1.2× 377 1.3× 216 1.0× 174 0.9× 51 0.9× 54 782

Countries citing papers authored by C Baccichetti

Since Specialization
Citations

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

Fields of papers citing papers by C Baccichetti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Baccichetti

This figure shows the co-authorship network connecting the top 25 collaborators of C Baccichetti. A scholar is included among the top collaborators of C Baccichetti 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 C Baccichetti. C Baccichetti 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.
Soresi, Salvatore, et al.. (2005). Observations on the visual-perceptual abilities and adaptive behavior in adults with Down syndrome. American Journal of Medical Genetics. 37(S7). 309–313. 5 indexed citations
2.
Baccichetti, C, Elisabetta Lenzini, & Renzo Pegoraro. (2005). Down syndrome in the Belluno district (Veneto region, Northeast Italy): Age distribution and morbidity. American Journal of Medical Genetics. 37(S7). 84–86. 9 indexed citations
3.
Rubello, Domenico, Giovanni Battista Pozzan, Dario Casara, et al.. (1995). Natural course of subclinical hypothyroidism in Down’s syndrome: Prospective study results and therapeutic considerations. Journal of Endocrinological Investigation. 18(1). 35–40. 71 indexed citations
4.
Lenzini, Elisabetta, et al.. (1991). Hypomelanosis of Ito: involvement of chromosome aberrations in this syndrome.. PubMed. 34(1). 30–2. 11 indexed citations
5.
Scherer, Gerd, et al.. (1989). Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man. Human Genetics. 81(3). 291–4. 64 indexed citations
6.
Baccichetti, C, et al.. (1988). Terminal deletion of the short arm of chromosome 5. Clinical Genetics. 34(4). 219–223. 29 indexed citations
7.
Lenzini, Elisabetta, et al.. (1988). Partial duplication of 17 long arm.. PubMed. 31(3). 175–80. 7 indexed citations
8.
Anglani, Franca, et al.. (1984). Frequency of abnormal karyotypes in relation to the ascertainment method in females referred for suspected sex chromosome abnormality. Clinical Genetics. 25(3). 242–247. 10 indexed citations
9.
Baccichetti, C, et al.. (1983). Replication patterns of human X isochromosomes by high-resolution banding. Cytogenetic and Genome Research. 36(4). 649–651. 1 indexed citations
10.
Baccichetti, C. (1982). Del(5p) without ?cri du chat? phenotype. Human Genetics. 60(4). 389–389. 8 indexed citations
11.
Baccichetti, C, et al.. (1982). Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated families. Human Genetics. 62(2). 117–20. 13 indexed citations
12.
Schinzel, Albert, Werner Schmid, M. Fraccaro, et al.. (1981). The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype. Human Genetics. 57(2). 148–58. 153 indexed citations
13.
Baccichetti, C, et al.. (1980). Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11←q13) segment of chromosome 2. Clinical Genetics. 18(6). 402–407. 13 indexed citations
14.
Baccichetti, C, Romano Tenconi, Franca Anglani, & Franco Zacchello. (1975). Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation.. Journal of Medical Genetics. 12(4). 425–427. 18 indexed citations
15.
Tenconi, Romano, et al.. (1975). Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.. PubMed. 18(2). 95–8. 14 indexed citations
16.
Tenconi, Romano, et al.. (1974). [Familial translocation t(6; 18) (q16; q16; q23) with free 21 trisomy].. PubMed. 17(4). 275–7. 5 indexed citations
17.
Tenconi, Romano, et al.. (1974). FAMILIAL 4/22 TRANSLOCATION WITH PARTIAL TRISOMY FOR THE SHORT ARM OF CHROMOSOME 4 IN TWO SIBS. Acta Paediatrica. 63(4). 631–635. 10 indexed citations
18.
Baccichetti, C & Romano Tenconi. (1973). A New Case of Trisomy for the Short Arm of No. 9 Chromosome. Journal of Medical Genetics. 10(3). 296–299. 30 indexed citations
19.
Tenconi, Romano, C Baccichetti, Franco Zacchello, & Elena Sartori. (1970). Metachromasia in cultured fibroblasts of subjects with glycogenosis type II. Cellular and Molecular Life Sciences. 26(11). 1238–1239. 2 indexed citations
20.
Zacchello, Franco, Romano Tenconi, & C Baccichetti. (1969). Glycogenosis type II: Glycogen storage in cell cultures from muscle. Cellular and Molecular Life Sciences. 25(12). 1316–1317. 1 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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