Michela Malacarne

1.2k total citations
56 papers, 626 citations indexed

About

Michela Malacarne is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Michela Malacarne has authored 56 papers receiving a total of 626 indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Genetics, 35 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Michela Malacarne's work include Genomic variations and chromosomal abnormalities (31 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Congenital heart defects research (12 papers). Michela Malacarne is often cited by papers focused on Genomic variations and chromosomal abnormalities (31 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Congenital heart defects research (12 papers). Michela Malacarne collaborates with scholars based in Italy, United States and United Kingdom. Michela Malacarne's co-authors include Simona Cavani, Mauro Pierluigi, Maria Piccione, Giovanni Corsello, Domenico Coviello, Federico Zara, Francesca Faravelli, M. Pierluigi, Elena Di Gennaro and Pasquale Striano and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Michela Malacarne

53 papers receiving 573 citations

Peers

Michela Malacarne

GENET

PPCH

PMH

SURGE

Maarit Peippo Finland

Tiziana Filippi Italy

Marion Gérard France

Tadeusz Mazurczak Poland

Tracy Brandt United States

Leslie Domenici Kulikowski Brazil

Damien Lederer Belgium

Sylvie Joriot France

Gabriele Gillessen‐Kaesbach Germany

Chantal Missirian France

Maarit Peippo Finland

Michela Malacarne

526 ×1.3

GENET

423 ×1.5

100 ×0.7

PPCH

41 ×0.5

PMH

53 ×1.0

SURGE

Citations per year, relative to Michela Malacarne Michela Malacarne (= 1×) peers Maarit Peippo

Countries citing papers authored by Michela Malacarne

Since Specialization

Citations

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

Fields of papers citing papers by Michela Malacarne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michela Malacarne

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

All Works

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20 of 20 papers shown

Conteduca, Giuseppina, Chiara Baldo, Renata Bocciardi, et al.. (2025). Derivation of the IGGi006-A stem cell line from a patient with CAPRIN1 haploinsufficiency. Stem Cell Research. 85. 103696–103696. 1 indexed citations

Bodria, Monica, Thea Giacomini, Domenico Tortora, et al.. (2024). Brain and spine malformations and neurodevelopmental disorders in a cohort of children with CAKUT. Pediatric Nephrology. 39(7). 2115–2129. 1 indexed citations

Danesino, Cesare, Federico Biglioli, Laura Moneghini, et al.. (2024). Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis. International Journal of Molecular Sciences. 25(19). 10664–10664.

Conteduca, Giuseppina, Davide Cangelosi, Chiara Baldo, et al.. (2024). Impact of NSD1 Alternative Transcripts in Actin Filament Formation and Cellular Division Pathways in Fibroblasts. Genes. 15(9). 1117–1117.

Conteduca, Giuseppina, Marina Grasso, Maurizio Cecconi, et al.. (2023). Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome. Genes. 14(2). 295–295. 9 indexed citations

Danesino, Cesare, Angelina Cistaro, Michela Malacarne, et al.. (2023). Esophageal Cancer with Early Onset in a Patient with Cri du Chat Syndrome. SHILAP Revista de lepidopterología. 12(1). 9–9. 1 indexed citations

Cassarà, Filippo, Michela Malacarne, Domenico Coviello, et al.. (2022). Incidental Detection of a Chromosomal Aberration by Array-CGH in an Early Prenatal Diagnosis for Monogenic Disease on Coelomic Fluid. Life. 13(1). 20–20. 1 indexed citations

Malacarne, Michela, Maria Brigida Lioi, Andrea M. Chiariello, et al.. (2022). Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability. International Journal of Molecular Sciences. 23(6). 3084–3084. 3 indexed citations

Conteduca, Giuseppina, Davide Cangelosi, Simona Coco, et al.. (2022). NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint. Life. 12(7). 988–988. 6 indexed citations

10.

Tassano, Elisa, Sarà Uccella, Patrizia Ronchetto, et al.. (2022). Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness. Cytogenetic and Genome Research. 162(3). 132–139.

11.

Colombini, Alessandra, Paola De Luca, Davide Cangelosi, et al.. (2021). High-Throughput Gene and Protein Analysis Revealed the Response of Disc Cells to Vitamin D, Depending on the VDR FokI Variants. International Journal of Molecular Sciences. 22(17). 9603–9603. 6 indexed citations

12.

Capra, Anna Paola, Silvana Briuglia, Chiara Baldo, et al.. (2021). 8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature. Genes. 12(5). 652–652. 12 indexed citations

13.

Ivanovski, Ivan, Olivera Djurić, Stefano Giuseppe Caraffi, et al.. (2018). Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 34–34. 4 indexed citations

14.

Piccione, Maria, et al.. (2015). 4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization. European Journal of Paediatric Neurology. 19(4). 477–483. 6 indexed citations

15.

Cavani, Simona, Michela Malacarne, Chiara Baldo, et al.. (2013). First-trimester euploid miscarriages analysed by array-CGH. Journal of Applied Genetics. 54(3). 353–359. 40 indexed citations

16.

Piccione, Maria, Simona Cavani, Michela Malacarne, et al.. (2011). Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders. Journal of Genetics. 90(3). 473–477. 4 indexed citations

17.

Malacarne, Michela, Francesca Forzano, Mauro Pierluigi, et al.. (2010). The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(7). 1342–1346. 16 indexed citations

18.

Piccione, Maria, Vincenzo Antona, Ettore Piro, et al.. (2008). 10qter deletion: A new case. American Journal of Medical Genetics Part A. 146A(18). 2435–2438. 6 indexed citations

19.

Striano, Pasquale, Michela Malacarne, Simona Cavani, et al.. (2006). Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. American Journal of Medical Genetics Part A. 140A(18). 1944–1949. 34 indexed citations

20.

Gennaro, Elena Di, Michela Malacarne, Ilaria Carbone, et al.. (1999). No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12‐q13.1. Epilepsia. 40(12). 1799–1803. 16 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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