Manuela Morleo

4.2k total citations
22 papers, 597 citations indexed

About

Manuela Morleo is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Manuela Morleo has authored 22 papers receiving a total of 597 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 16 papers in Molecular Biology and 4 papers in Oncology. Recurrent topics in Manuela Morleo's work include Genetic and Kidney Cyst Diseases (11 papers), Hedgehog Signaling Pathway Studies (4 papers) and Epigenetics and DNA Methylation (4 papers). Manuela Morleo is often cited by papers focused on Genetic and Kidney Cyst Diseases (11 papers), Hedgehog Signaling Pathway Studies (4 papers) and Epigenetics and DNA Methylation (4 papers). Manuela Morleo collaborates with scholars based in Italy, United States and Israel. Manuela Morleo's co-authors include Brunella Franco, Daniela Iaconis, Kerstin Kutsche, Roberta Tammaro, Andrea Ballabio, Alessia Indrieri, Daniel Finley, Byung‐Hoon Lee, Ilaria D’Amato and Alex Zvulunov and has published in prestigious journals such as Journal of Clinical Investigation, The EMBO Journal and The American Journal of Human Genetics.

In The Last Decade

Manuela Morleo

22 papers receiving 572 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuela Morleo Italy 15 398 361 106 50 43 22 597
Anita M. Quintana United States 12 384 1.0× 212 0.6× 56 0.5× 35 0.7× 45 1.0× 24 665
Gail Billingsley Canada 16 727 1.8× 383 1.1× 94 0.9× 29 0.6× 20 0.5× 19 1.0k
Maria Rosaria Piemontese Italy 12 248 0.6× 141 0.4× 111 1.0× 26 0.5× 31 0.7× 23 393
Chyuan-Sheng Lin United States 9 386 1.0× 125 0.3× 54 0.5× 53 1.1× 42 1.0× 11 639
Sarah E. Conduit Australia 11 373 0.9× 306 0.8× 147 1.4× 41 0.8× 36 0.8× 13 536
Eri Imagawa Japan 13 250 0.6× 170 0.5× 24 0.2× 24 0.5× 41 1.0× 30 418
Sophie Monnot France 13 403 1.0× 206 0.6× 110 1.0× 35 0.7× 34 0.8× 27 585
Sergio A. Cuevas‐Covarrubias Mexico 11 280 0.7× 167 0.5× 37 0.3× 42 0.8× 21 0.5× 41 418
Patricia Outeda United States 11 448 1.1× 472 1.3× 79 0.7× 13 0.3× 55 1.3× 20 672
Y Tone United Kingdom 8 517 1.3× 330 0.9× 24 0.2× 23 0.5× 29 0.7× 9 963

Countries citing papers authored by Manuela Morleo

Since Specialization
Citations

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

Fields of papers citing papers by Manuela Morleo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Morleo

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Morleo. A scholar is included among the top collaborators of Manuela Morleo 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 Manuela Morleo. Manuela Morleo 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.
Marangi, Giuseppe, Pietro Chiurazzi, Daniela Orteschi, et al.. (2023). Pathogenic variants in SOX11 mimicking Pitt‐Hopkins syndrome phenotype. Clinical Genetics. 105(1). 81–86. 2 indexed citations
2.
Pasquali, Daniela, Annalaura Torella, Anna Grandone, et al.. (2022). Patients with DeSanto–Shinawi syndrome: Further extension of phenotype from Italy. American Journal of Medical Genetics Part A. 191(3). 823–830. 1 indexed citations
3.
Morleo, Manuela, et al.. (2022). Proteome balance in ciliopathies: the OFD1 protein example. Trends in Molecular Medicine. 29(3). 201–217. 8 indexed citations
4.
Morleo, Manuela, Helena L.A. Vieira, Petra Pennekamp, et al.. (2022). Crosstalk between cilia and autophagy: implication for human diseases. Autophagy. 19(1). 24–43. 20 indexed citations
5.
Franco, Brunella & Manuela Morleo. (2021). The role of OFD1 in selective autophagy. Molecular & Cellular Oncology. 8(3). 1903291–1903291. 4 indexed citations
6.
Mandato, Claudia, Maria Siano, Monica Gelzo, et al.. (2021). A ZFYVE19 gene mutation associated with neonatal cholestasis and cilia dysfunction: case report with a novel pathogenic variant. Orphanet Journal of Rare Diseases. 16(1). 179–179. 20 indexed citations
7.
Iaconis, Daniela, et al.. (2020). The HOPS complex subunit VPS39 controls ciliogenesis through autophagy. Human Molecular Genetics. 29(6). 1018–1029. 16 indexed citations
8.
Morleo, Manuela, Luigi Ferrante, Daniela Iaconis, et al.. (2020). Regulation of autophagosome biogenesis by OFD1‐mediated selective autophagy. The EMBO Journal. 40(4). e105120–e105120. 28 indexed citations
9.
Peixoto, Estanislao, Manuela Morleo, Nunzia Pastore, et al.. (2020). HDAC6-dependent ciliophagy is involved in ciliary loss and cholangiocarcinoma growth in human cells and murine models. American Journal of Physiology-Gastrointestinal and Liver Physiology. 318(6). G1022–G1033. 25 indexed citations
10.
Morleo, Manuela, Vincenzo Nigro, Annalaura Torella, et al.. (2020). Identification of an Identical de Novo SCAMP5 Missense Variant in Four Unrelated Patients With Seizures and Severe Neurodevelopmental Delay. Frontiers in Pharmacology. 11. 599191–599191. 3 indexed citations
11.
Morleo, Manuela & Brunella Franco. (2020). OFD Type I syndrome: lessons learned from a rare ciliopathy. Biochemical Society Transactions. 48(5). 1929–1939. 11 indexed citations
12.
Tammaro, Roberta, Miguel A. Prado, Marcella Cesana, et al.. (2018). The deubiquitinating enzyme Usp14 controls ciliogenesis and Hedgehog signaling. Human Molecular Genetics. 28(5). 764–777. 26 indexed citations
13.
Amato, Roberto, Manuela Morleo, Laura Giaquinto, Diego di Bernardo, & Brunella Franco. (2014). A network-based approach to dissect the cilia/centrosome complex interactome. BMC Genomics. 15(1). 658–658. 16 indexed citations
14.
Indrieri, Alessia, Valeria Tiranti, Manuela Morleo, et al.. (2012). Mutations in COX7B Cause Microphthalmia with Linear Skin Lesions, an Unconventional Mitochondrial Disease. The American Journal of Human Genetics. 91(5). 942–949. 102 indexed citations
15.
Mari, Francesca, Brunella Franco, Alessandra Renieri, et al.. (2008). Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndrome. Molecular Medicine Reports. 1(1). 33–9. 18 indexed citations
16.
Morleo, Manuela & Brunella Franco. (2008). Dosage compensation of the mammalian X chromosome influences the phenotypic variability of X-linked dominant male-lethal disorders. Journal of Medical Genetics. 45(7). 401–408. 56 indexed citations
17.
Baroncini, Anna, et al.. (2006). Terminal osseous dysplasia with pigmentary defects: Clinical description of a new family. American Journal of Medical Genetics Part A. 143A(1). 51–57. 12 indexed citations
18.
Wimplinger, Isabella, Manuela Morleo, Georg Rosenberger, et al.. (2006). Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome. The American Journal of Human Genetics. 79(5). 878–889. 81 indexed citations
19.
Morleo, Manuela, Tiziano Pramparo, Lucia Perone, et al.. (2005). Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization of 11 cases. American Journal of Medical Genetics Part A. 137A(2). 190–198. 26 indexed citations
20.
Peruzzi, Daniela, Michela Aluigi, Lucia Manzoli, et al.. (2002). Molecular characterization of the human PLC β1 gene. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1584(1). 46–54. 23 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

Breakdown of academic impact, for papers by Anita M. Quintana Breakdown of academic impact, for papers by Gail Billingsley Breakdown of academic impact, for papers by Maria Rosaria Piemontese Breakdown of academic impact, for papers by Chyuan-Sheng Lin Breakdown of academic impact, for papers by Sarah E. Conduit Breakdown of academic impact, for papers by Eri Imagawa Breakdown of academic impact, for papers by Sophie Monnot Breakdown of academic impact, for papers by Sergio A. Cuevas‐Covarrubias Breakdown of academic impact, for papers by Patricia Outeda Breakdown of academic impact, for papers by Y Tone
Rankless by CCL
2026