P Goffrini

3.3k total citations
73 papers, 2.2k citations indexed

About

P Goffrini is a scholar working on Molecular Biology, Clinical Biochemistry and Plant Science. According to data from OpenAlex, P Goffrini has authored 73 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 10 papers in Plant Science. Recurrent topics in P Goffrini's work include Mitochondrial Function and Pathology (23 papers), Fungal and yeast genetics research (23 papers) and Microbial Metabolic Engineering and Bioproduction (12 papers). P Goffrini is often cited by papers focused on Mitochondrial Function and Pathology (23 papers), Fungal and yeast genetics research (23 papers) and Microbial Metabolic Engineering and Bioproduction (12 papers). P Goffrini collaborates with scholars based in Italy, France and United Kingdom. P Goffrini's co-authors include Iliana Ferrero, Micheline Wésolowski‐Louvel, Tiziana Lodi, Claudia Donnini, Hiroshi Fukuhara, Ileana Ferrero, Massimo Zeviani, Enrico Baruffini, Paolo Gasparini and Pio D’Adamo and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Applied and Environmental Microbiology.

In The Last Decade

P Goffrini

69 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P Goffrini Italy 26 1.9k 397 301 280 219 73 2.2k
Josep Clotet Spain 27 1.5k 0.8× 116 0.3× 111 0.4× 306 1.1× 34 0.2× 64 1.9k
Nicoletta Guaragnella Italy 22 1.2k 0.6× 49 0.1× 268 0.9× 174 0.6× 161 0.7× 49 1.4k
C W van Roermund Netherlands 16 1.6k 0.8× 586 1.5× 52 0.2× 128 0.5× 28 0.1× 17 1.8k
Angelo Vozza Italy 20 1.2k 0.7× 409 1.0× 52 0.2× 98 0.3× 20 0.1× 33 1.5k
Sabire Özcan United States 28 3.0k 1.6× 28 0.1× 440 1.5× 576 2.1× 168 0.8× 44 3.7k
Rashid Ali India 24 690 0.4× 124 0.3× 39 0.1× 581 2.1× 28 0.1× 67 1.8k
Xiaoming Gong United States 19 743 0.4× 139 0.4× 28 0.1× 96 0.3× 32 0.1× 47 1.4k
Pasquale Scarcia Italy 20 1.5k 0.8× 438 1.1× 109 0.4× 85 0.3× 9 0.0× 30 1.8k
Satoshi Yamashita Japan 26 1.3k 0.7× 95 0.2× 82 0.3× 152 0.5× 21 0.1× 33 1.7k
Hui Sun China 24 2.0k 1.1× 23 0.1× 67 0.2× 359 1.3× 75 0.3× 75 2.8k

Countries citing papers authored by P Goffrini

Since Specialization
Citations

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

Fields of papers citing papers by P Goffrini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P Goffrini

This figure shows the co-authorship network connecting the top 25 collaborators of P Goffrini. A scholar is included among the top collaborators of P Goffrini 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 P Goffrini. P Goffrini 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.
Marzollo, Antonio, Stefania Zampieri, Serena Barozzi, et al.. (2024). Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British Journal of Haematology. 205(1). 306–315. 6 indexed citations
2.
Dotto, Valentina Del, Mario Fogazza, Francesco Musiani, et al.. (2018). Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(10). 3496–3514. 34 indexed citations
3.
Dallabona, Cristina, Enrico Baruffini, P Goffrini, & Tiziana Lodi. (2017). Dominance of yeast aac2 R96H and aac2 R252G mutations, equivalent to pathological mutations in ant1, is due to gain of function. Biochemical and Biophysical Research Communications. 493(2). 909–913. 8 indexed citations
4.
Alston, Charlotte L., Emma L. Blakely, Monika Oláhová, et al.. (2015). A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. Human Genetics. 134(8). 869–879. 40 indexed citations
5.
Dallabona, Cristina, et al.. (2015). Modeling human Coenzyme A synthase mutation in yeast reveals altered mitochondrial function, lipid content and iron metabolism. Microbial Cell. 2(4). 126–135. 21 indexed citations
6.
Rocco, Daniela De, Cristina Cerqua, P Goffrini, et al.. (2013). Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(2). 269–274. 65 indexed citations
7.
Panizza, Elena, Tonino Ercolino, Luigi Mori, et al.. (2012). Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. Human Molecular Genetics. 22(4). 804–815. 25 indexed citations
8.
Indrieri, Alessia, Iván Conte, Giancarlo Chesi, et al.. (2012). The impairment of HCCS leads to MLS syndrome by activating a non‐canonical cell death pathway in the brain and eyes. EMBO Molecular Medicine. 5(2). 280–293. 32 indexed citations
9.
Tuppen, Helen, Janev Fehmi, Birgit Czermin, et al.. (2010). Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation. Molecular Genetics and Metabolism. 100(4). 345–348. 24 indexed citations
10.
Goffrini, P, et al.. (2009). Functional analysis of theKluyveromyces lactis PDR1gene. FEMS Yeast Research. 9(2). 321–327. 9 indexed citations
11.
Zara, Giacomo, Simona Belviso, Laura Bardi, et al.. (2009). Oxygen is required to restore flor strain viability and lipid biosynthesis under fermentative conditions. FEMS Yeast Research. 9(2). 217–225. 20 indexed citations
12.
Goffrini, P, Tonino Ercolino, Elena Panizza, et al.. (2009). Functional study in a yeast model of a novel succinate dehydrogenase subunit B gene germline missense mutation (C191Y) diagnosed in a patient affected by a glomus tumor. Human Molecular Genetics. 18(10). 1860–1868. 56 indexed citations
13.
Fernández‐Vizarra, Erika, Saad AlShahwan, Eman Bakhsh, et al.. (2008). Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase. The American Journal of Human Genetics. 82(6). 1281–1289. 143 indexed citations
14.
Uccelletti, Daniela, Francesca Farina, Paolo Pinton, et al.. (2005). The Golgi Ca2+-ATPase KlPmr1p Function Is Required for Oxidative Stress Response by Controlling the Expression of the Heat-Shock ElementHSP60inKluyveromyces lactis. Molecular Biology of the Cell. 16(10). 4636–4647. 27 indexed citations
15.
Breunig, Karin D., Monique Bolotin‐Fukuhara, Michele M. Bianchi, et al.. (2000). Regulation of primary carbon metabolism in Kluyveromyces lactis. Enzyme and Microbial Technology. 26(9-10). 771–780. 91 indexed citations
16.
Goffrini, P, et al.. (1997). Influence of Mutations in Hexose‐Transporter Genes on Glucose Repression in Kluyveromyces Lactis. European Journal of Biochemistry. 249(1). 248–257. 44 indexed citations
17.
Lodi, Tiziana, P Goffrini, Iliana Ferrero, & Claudia Donnini. (1995). IMP2, a gene involved in the expression of glucose-repressible genes in Saccharomyces cerevisiae. Microbiology. 141(9). 2201–2209. 11 indexed citations
18.
19.
Goffrini, P, et al.. (1982). Killer DNA Plasmids of the Yeast Kluyveromyces lactis. Current Genetics. 5(3). 191–197. 76 indexed citations
20.
Lang, E, et al.. (1952). [An experimental study on the pathogenesis of valvular lesions accompanying interatrial and interventricular communication].. PubMed. 7(2). 67–77. 1 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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