Antonella Cecconi

928 total citations
6 papers, 106 citations indexed

About

Antonella Cecconi is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Antonella Cecconi has authored 6 papers receiving a total of 106 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Cognitive Neuroscience. Recurrent topics in Antonella Cecconi's work include Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (2 papers) and melanin and skin pigmentation (1 paper). Antonella Cecconi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (2 papers) and melanin and skin pigmentation (1 paper). Antonella Cecconi collaborates with scholars based in Italy and China. Antonella Cecconi's co-authors include Silvia Guarducci, Elisabetta Lapi, Maria Luisa Giovannucci Uzielli, U. Ricci, Benedetta Scarselli, Claudia Biondi, G. Ricotti, Tiziana Metitieri, Renzo Guerrini and Sabrina Giglio and has published in prestigious journals such as American Journal of Medical Genetics, Brain and Development and American Journal of Medical Genetics Part A.

In The Last Decade

Antonella Cecconi

5 papers receiving 105 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Antonella Cecconi Italy	4	100	53	43	12	11	6	106
Maria Grazia Tibiletti Italy	2	75 0.8×	43 0.8×	30 0.7×	6 0.5×	14 1.3×	3	106
Britt Marie Anderlid Sweden	5	104 1.0×	25 0.5×	78 1.8×	20 1.7×	37 3.4×	6	167
Bärbel Felder Germany	3	74 0.7×	24 0.5×	87 2.0×	3 0.3×	15 1.4×	3	127
Heather Stalker United States	5	94 0.9×	17 0.3×	58 1.3×	3 0.3×	24 2.2×	7	128
Oanh Hong United States	2	101 1.0×	88 1.7×	51 1.2×	10 0.8×	5 0.5×	3	136
Paul A. Mulder Netherlands	3	28 0.3×	23 0.4×	30 0.7×	19 1.6×	5 0.5×	3	70
Bibi Kassim United States	7	49 0.5×	22 0.4×	73 1.7×	4 0.3×	4 0.4×	8	124
Franziska Degenhardt Germany	6	39 0.4×	18 0.3×	44 1.0×	9 0.8×	24 2.2×	8	99
Luke P. Grosvenor United States	4	25 0.3×	28 0.5×	20 0.5×	13 1.1×	12 1.1×	9	72
Sigrid Piening Netherlands	3	28 0.3×	26 0.5×	30 0.7×	22 1.8×	5 0.5×	7	73

Countries citing papers authored by Antonella Cecconi

Since Specialization

Citations

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

Fields of papers citing papers by Antonella Cecconi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonella Cecconi

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Marco, Chiara Di, et al.. (2023). Prenatal ultrasound detection of collodion membrane in association with an autosomal recessive congenital ichthyosis due to transglutaminase 1 deficiency. Pediatric Dermatology. 41(3). 512–514.

2.

Marini, Carla, Antonella Cecconi, Elisa Contini, et al.. (2013). Clinical and genetic study of a family with a paternally inherited 15q11–q13 duplication. American Journal of Medical Genetics Part A. 161(6). 1459–1464. 18 indexed citations

3.

Micale, Lucia, Bartolomeo Augello, Carmela Fusco, et al.. (2009). GPR143 Mutational Analysis in Two Italian Families with X-Linked Ocular Albinism. Genetic Testing and Molecular Biomarkers. 13(4). 527–531. 1 indexed citations

4.

Giunti, Laura, Silvia Guarducci, Elisabetta Lapi, et al.. (2001). Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation. Brain and Development. 23. S242–S245. 18 indexed citations

5.

Uzielli, Maria Luisa Giovannucci, Silvia Guarducci, Elisabetta Lapi, et al.. (1999). Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data. American Journal of Medical Genetics. 84(3). 300–303. 65 indexed citations

6.

Uzielli, Maria Luisa Giovannucci, Silvia Guarducci, Elisabetta Lapi, et al.. (1999). Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data. American Journal of Medical Genetics. 84(3). 300–303. 4 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.

Explore authors with similar magnitude of impact