Elisa Molinari

1.1k total citations
36 papers, 551 citations indexed

About

Elisa Molinari is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Elisa Molinari has authored 36 papers receiving a total of 551 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 21 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Elisa Molinari's work include Genetic and Kidney Cyst Diseases (21 papers), Renal and related cancers (16 papers) and Protist diversity and phylogeny (5 papers). Elisa Molinari is often cited by papers focused on Genetic and Kidney Cyst Diseases (21 papers), Renal and related cancers (16 papers) and Protist diversity and phylogeny (5 papers). Elisa Molinari collaborates with scholars based in United Kingdom, Italy and United States. Elisa Molinari's co-authors include John A. Sayer, Shalabh Srivastava, Shreya Raman, Colin G. Miles, Simon A. Ramsbottom, Sumaya Alkanderi, Sophie Saunier, Kathryn White, Francesco Beltrame and C. Henry and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and PLoS ONE.

In The Last Decade

Elisa Molinari

34 papers receiving 545 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisa Molinari United Kingdom 13 399 357 95 61 46 36 551
Yanlin Wang China 11 236 0.6× 112 0.3× 194 2.0× 15 0.2× 20 0.4× 37 586
Amélie Calmont France 10 467 1.2× 202 0.6× 26 0.3× 40 0.7× 13 0.3× 17 585
Razek Georges Coussa United States 16 477 1.2× 140 0.4× 24 0.3× 44 0.7× 15 0.3× 43 758
Paola Benaglio United States 14 530 1.3× 324 0.9× 10 0.1× 23 0.4× 14 0.3× 21 795
Jeffrey L. Clendenon United States 9 163 0.4× 65 0.2× 31 0.3× 26 0.4× 12 0.3× 13 396
Murat Sincan United States 14 201 0.5× 202 0.6× 17 0.2× 25 0.4× 34 0.7× 28 574
Е. С. Ревазова Russia 8 539 1.4× 76 0.2× 23 0.2× 25 0.4× 17 0.4× 24 708
Borja Corcóstegui Spain 26 308 0.8× 55 0.2× 29 0.3× 23 0.4× 8 0.2× 64 1.5k
Rosa Ferrentino Italy 9 348 0.9× 109 0.3× 13 0.1× 33 0.5× 8 0.2× 16 435
Xiangsheng Yang China 14 345 0.9× 32 0.1× 17 0.2× 42 0.7× 21 0.5× 25 526

Countries citing papers authored by Elisa Molinari

Since Specialization
Citations

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

Fields of papers citing papers by Elisa Molinari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Molinari

This figure shows the co-authorship network connecting the top 25 collaborators of Elisa Molinari. A scholar is included among the top collaborators of Elisa Molinari 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 Elisa Molinari. Elisa Molinari 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.
2.
Olinger, Eric, Issa Al Salmi, Elisa Molinari, et al.. (2021). A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families. Human Mutation. 42(10). 1221–1228. 9 indexed citations
3.
Molinari, Elisa, et al.. (2021). Cell preservation methods and its application to studying rare disease. Molecular and Cellular Probes. 56. 101694–101694. 5 indexed citations
4.
5.
Molinari, Elisa & John A. Sayer. (2021). Gene and epigenetic editing in the treatment of primary ciliopathies. Progress in molecular biology and translational science. 182. 353–401. 5 indexed citations
6.
Ramsbottom, Simon A., et al.. (2020). Embryonic and foetal expression patterns of the ciliopathy gene CEP164. PLoS ONE. 15(1). e0221914–e0221914. 7 indexed citations
7.
Clowry, Gavin J., et al.. (2020). Expression patterns of ciliopathy genes ARL3 and CEP120 reveal roles in multisystem development. BMC Developmental Biology. 20(1). 26–26. 4 indexed citations
8.
Molinari, Elisa, et al.. (2020). Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman. BMC Nephrology. 21(1). 347–347. 9 indexed citations
9.
Thelwall, Peter E., Katrina Wood, Gavin J. Clowry, et al.. (2019). Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome. Proceedings of the National Academy of Sciences. 117(2). 1113–1118. 20 indexed citations
10.
Frikstad, Kari‐Anne M., Elisa Molinari, Marianne Thoresen, et al.. (2019). A CEP104-CSPP1 Complex Is Required for Formation of Primary Cilia Competent in Hedgehog Signaling. Cell Reports. 28(7). 1907–1922.e6. 31 indexed citations
11.
Molinari, Elisa & John A. Sayer. (2019). Using human urine-derived renal epithelial cells to model kidney disease in inherited ciliopathies. 4(1-2). 87–95. 3 indexed citations
12.
Browning, Andrew C., Oliver Baylis, Clare Beesley, et al.. (2019). A case of ocular cystinosis associated with two potentially severeCTNSmutations. Ophthalmic Genetics. 40(2). 157–160. 1 indexed citations
13.
Molinari, Elisa, Shalabh Srivastava, C. Henry, et al.. (2018). Targeted exon skipping of a CEP290 mutation rescues Joubert syndrome phenotypes in vitro and in a murine model. Proceedings of the National Academy of Sciences. 115(49). 12489–12494. 51 indexed citations
14.
Srivastava, Shalabh, Elisa Molinari, Shreya Raman, & John A. Sayer. (2018). Many Genes—One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders. Frontiers in Pediatrics. 5. 287–287. 86 indexed citations
15.
Molinari, Elisa, Eva L. Decker, Holly Mabillard, et al.. (2018). Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants. European Journal of Human Genetics. 26(12). 1791–1796. 18 indexed citations
16.
Molinari, Elisa, Barbara Marinari, Nerina Gnesutta, et al.. (2015). FGF8, c-Abl and p300 participate in a pathway that controls stability and function of the ΔNp63αprotein. Human Molecular Genetics. 24(15). 4185–4197. 11 indexed citations
17.
Andreetto, Paolo, Marco Cecchi, A. Dorigo, et al.. (2011). Status and Developments of the CREAM Computing Element Service. Journal of Physics Conference Series. 331(6). 62024–62024. 6 indexed citations
18.
Castelnuovo, Gianluca, Andrea Gaggioli, Fabrizia Mantovani, et al.. (2005). Building a bridge between psychotherapy and new internet-based technologies: the VEPSY updated project approach. Technology and Health Care. 13(5). 367–367. 1 indexed citations
19.
Porro, Ivan, Andrea Schenone, Marco Fato, et al.. (2005). An integrated environment for plastic surgery support: building virtual patients, simulating interventions, and supporting intraoperative decisions. Computerized Medical Imaging and Graphics. 29(5). 385–394. 19 indexed citations
20.
Molinari, Elisa, et al.. (2005). Simulation of the Biomechanical Behavior of the Skin in Virtual Surgical Applications by Finite Element Method. IEEE Transactions on Biomedical Engineering. 52(9). 1514–1521. 25 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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