Luisa Nanni

1.3k total citations
14 papers, 958 citations indexed

About

Luisa Nanni is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Luisa Nanni has authored 14 papers receiving a total of 958 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 5 papers in Genetics. Recurrent topics in Luisa Nanni's work include Hedgehog Signaling Pathway Studies (6 papers), Cleft Lip and Palate Research (5 papers) and Cardiomyopathy and Myosin Studies (3 papers). Luisa Nanni is often cited by papers focused on Hedgehog Signaling Pathway Studies (6 papers), Cleft Lip and Palate Research (5 papers) and Cardiomyopathy and Myosin Studies (3 papers). Luisa Nanni collaborates with scholars based in Italy, United States and United Kingdom. Luisa Nanni's co-authors include Maximilian Muenke, Erich Roessler, Jeffrey E. Ming, Johanna M. Rommens, Elaine H. Zackai, Antônio Richieri‐Costa, Tim Wiltshire, Gabriele Gillessen‐Kaesbach, Deeann Wallis and Ute Hehr and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Biochemical and Biophysical Research Communications.

In The Last Decade

Luisa Nanni

14 papers receiving 933 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luisa Nanni Italy 10 741 515 115 102 81 14 958
Kouji Narahara Japan 18 509 0.7× 500 1.0× 212 1.8× 19 0.2× 50 0.6× 52 877
Boris Keren France 21 649 0.9× 515 1.0× 154 1.3× 53 0.5× 44 0.5× 70 1.1k
Sahar Mansour United Kingdom 11 575 0.8× 288 0.6× 33 0.3× 19 0.2× 81 1.0× 15 854
A Munnich France 14 685 0.9× 347 0.7× 55 0.5× 8 0.1× 254 3.1× 37 1.1k
Hartmut Engel Germany 9 380 0.5× 182 0.4× 15 0.1× 34 0.3× 71 0.9× 15 518
Michael Marble United States 13 370 0.5× 234 0.5× 79 0.7× 21 0.2× 62 0.8× 33 636
Gülen Eda Ütine Türkiye 14 367 0.5× 373 0.7× 77 0.7× 16 0.2× 66 0.8× 114 715
Maria Lisa Dentici Italy 19 704 1.0× 459 0.9× 75 0.7× 61 0.6× 98 1.2× 74 1.1k
Yaping Yang United States 16 322 0.4× 292 0.6× 84 0.7× 73 0.7× 39 0.5× 37 654
Nisha Patel Saudi Arabia 17 428 0.6× 267 0.5× 37 0.3× 13 0.1× 53 0.7× 39 727

Countries citing papers authored by Luisa Nanni

Since Specialization
Citations

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

Fields of papers citing papers by Luisa Nanni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luisa Nanni

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

All Works

14 of 14 papers shown
1.
Sentinelli, Federica, Ilenia Minicocci, Anna Montali, et al.. (2013). Association of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis. SHILAP Revista de lepidopterología. 2013. 1–7. 19 indexed citations
2.
Gianfagna, Francesco, Branislav Vohnout, Marilena Crescente, et al.. (2012). Heritability, genetic correlation and linkage to the 9p21.3 region of mixed platelet–leukocyte conjugates in families with and without early myocardial infarction. Nutrition Metabolism and Cardiovascular Diseases. 23(7). 684–692. 8 indexed citations
3.
Nanni, Luisa, Fabiana Quagliarini, Francesca Megiorni, et al.. (2010). Genetic variants in adipose triglyceride lipase influence lipid levels in familial combined hyperlipidemia. Atherosclerosis. 213(1). 206–211. 9 indexed citations
4.
Campagna, Filomena, Luisa Nanni, Fabiana Quagliarini, et al.. (2008). Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathy. Biochemical and Biophysical Research Communications. 377(3). 843–846. 48 indexed citations
5.
Nanni, Luisa, Chiara Romualdi, A Maseri, & G. Lanfranchi. (2006). Differential gene expression profiling in genetic and multifactorial cardiovascular diseases. Journal of Molecular and Cellular Cardiology. 41(6). 934–948. 53 indexed citations
6.
7.
Nanni, Luisa, Maurizio Pieroni, Cristina Chimenti, et al.. (2003). Hypertrophic cardiomyopathy: two homozygous cases with “typical” hypertrophic cardiomyopathy and three new mutations in cases with progression to dilated cardiomyopathy. Biochemical and Biophysical Research Communications. 309(2). 391–398. 68 indexed citations
8.
9.
Nanni, Luisa, Jeffrey E. Ming, Yangzhu Du, et al.. (2001). SHH mutation is associated with solitary median maxillary central incisor: A study of 13 patients and review of the literature. American Journal of Medical Genetics. 102(1). 1–10. 115 indexed citations
10.
Nanni, Luisa, Lisa Croen, Edward J. Lammer, & Maximilian Muenke. (2000). Holoprosencephaly: Molecular study of a California Population. American Journal of Medical Genetics. 90(4). 315–319. 31 indexed citations
11.
Nanni, Luisa. (2000). Molecular genetics of holoprosencephaly. Frontiers in bioscience. 5(1). d334–d334. 24 indexed citations
12.
Nanni, Luisa, Robert L. Schelper, & Maximilian Muenke. (2000). Molecular Genetics of Holoprosencephaly. Fetal and Pediatric Pathology. 19(1). 1–19. 2 indexed citations
13.
Nanni, Luisa, Jeffrey E. Ming, Maureen Bocian, et al.. (1999). The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly. Human Molecular Genetics. 8(13). 2479–2488. 274 indexed citations
14.
Wallis, Deeann, Erich Roessler, Ute Hehr, et al.. (1999). Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics. 22(2). 196–198. 302 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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