Elisa Oppici

1.2k total citations
28 papers, 930 citations indexed

About

Elisa Oppici is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Clinical Biochemistry. According to data from OpenAlex, Elisa Oppici has authored 28 papers receiving a total of 930 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 15 papers in Pulmonary and Respiratory Medicine and 11 papers in Clinical Biochemistry. Recurrent topics in Elisa Oppici's work include Porphyrin Metabolism and Disorders (18 papers), Kidney Stones and Urolithiasis Treatments (15 papers) and Metabolism and Genetic Disorders (11 papers). Elisa Oppici is often cited by papers focused on Porphyrin Metabolism and Disorders (18 papers), Kidney Stones and Urolithiasis Treatments (15 papers) and Metabolism and Genetic Disorders (11 papers). Elisa Oppici collaborates with scholars based in Italy, Spain and United Kingdom. Elisa Oppici's co-authors include Barbara Cellini, Riccardo Montioli, Carla Borri Voltattorni, Mirco Dindo, Elena Butturini, Sofia Mariotto, Alessandra Astegno, Diana Boriero, Alessandra Carcereri de Prati and Antonella Rigo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Elisa Oppici

28 papers receiving 927 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elisa Oppici Italy	20	676	369	183	144	123	28	930
Yu Yan China	17	814 1.2×	521 1.4×	33 0.2×	84 0.6×	183 1.5×	48	1.3k
Gemma Reverter‐Branchat Spain	16	553 0.8×	109 0.3×	74 0.4×	23 0.2×	121 1.0×	22	956
Jibin Li China	19	1.1k 1.6×	138 0.4×	77 0.4×	59 0.4×	139 1.1×	30	1.5k
Eisuke Furuya Japan	19	494 0.7×	137 0.4×	65 0.4×	53 0.4×	31 0.3×	45	1.0k
Andreas Jungmann Germany	15	565 0.8×	74 0.2×	55 0.3×	78 0.5×	79 0.6×	33	959
Pen-Hui Yin Taiwan	18	873 1.3×	78 0.2×	35 0.2×	81 0.6×	94 0.8×	19	1.2k
Guosheng Yang China	18	452 0.7×	132 0.4×	64 0.3×	16 0.1×	92 0.7×	56	887
Caroline Perry United States	15	526 0.8×	87 0.2×	33 0.2×	66 0.5×	257 2.1×	25	1.1k
Karthik Vasan United States	11	892 1.3×	163 0.4×	43 0.2×	47 0.3×	143 1.2×	15	1.3k
Katherine Drews‐Elger United States	13	514 0.8×	71 0.2×	78 0.4×	92 0.6×	359 2.9×	20	1.0k

Countries citing papers authored by Elisa Oppici

Since Specialization

Citations

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

Fields of papers citing papers by Elisa Oppici

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Oppici

This figure shows the co-authorship network connecting the top 25 collaborators of Elisa Oppici. A scholar is included among the top collaborators of Elisa Oppici 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 Oppici. Elisa Oppici 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

Marino, Valerio, Elisa Oppici, Paolo Enrico Maltese, et al.. (2018). A novel p.(Glu111Val) missense mutation in GUCA1A associated with cone-rod dystrophy leads to impaired calcium sensing and perturbed second messenger homeostasis in photoreceptors. Human Molecular Genetics. 27(24). 4204–4217. 27 indexed citations

Dindo, Mirco, et al.. (2018). Molecular basis of primary hyperoxaluria: clues to innovative treatments. Urolithiasis. 47(1). 67–78. 53 indexed citations

Mesa‐Torres, Noel, et al.. (2018). Evolutionary Divergent Suppressor Mutations in Conformational Diseases. Genes. 9(7). 352–352. 9 indexed citations

Medina‐Carmona, Encarnación, Jaime Santos, Noel Mesa‐Torres, et al.. (2018). Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses. Human Molecular Genetics. 28(1). 1–15. 26 indexed citations

Prati, Alessandra Carcereri de, Elena Butturini, Antonella Rigo, et al.. (2017). Metastatic Breast Cancer Cells Enter Into Dormant State and Express Cancer Stem Cells Phenotype Under Chronic Hypoxia. Journal of Cellular Biochemistry. 118(10). 3237–3248. 94 indexed citations

Oppici, Elisa, et al.. (2017). Folding Defects Leading to Primary Hyperoxaluria. Handbook of experimental pharmacology. 245. 313–343. 13 indexed citations

Oppici, Elisa, Jens Martens‐Lobenhoffer, Natalia Jarzebska, et al.. (2016). A Novel Pathway for Metabolism of the Cardiovascular Risk Factor Homoarginine by alanine:glyoxylate aminotransferase 2. Scientific Reports. 6(1). 35277–35277. 30 indexed citations

Oppici, Elisa, Marina Talelli, Marta Donini, et al.. (2016). Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I. Nanomedicine Nanotechnology Biology and Medicine. 13(3). 897–907. 22 indexed citations

Cordani, Marco, Elisa Oppici, Ilaria Dando, et al.. (2016). Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition. Molecular Oncology. 10(7). 1008–1029. 119 indexed citations

10.

Oppici, Elisa, Riccardo Montioli, Mirco Dindo, & Barbara Cellini. (2016). Natural and Unnatural Compounds Rescue Folding Defects of Human Alanine: Glyoxylate Aminotransferase Leading to Primary Hyperoxaluria Type I. Current Drug Targets. 17(13). 1482–1491. 11 indexed citations

11.

Mesa‐Torres, Noel, Ana Cristina Calvo, Elisa Oppici, et al.. (2016). Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1864(9). 1195–1205. 3 indexed citations

12.

Oppici, Elisa, Riccardo Montioli, & Barbara Cellini. (2015). Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1854(9). 1212–1219. 45 indexed citations

13.

Montioli, Riccardo, Elisa Oppici, Mirco Dindo, et al.. (2015). Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1854(10). 1280–1289. 19 indexed citations

14.

Oppici, Elisa, Sonia Fargue, Emma Reid, et al.. (2015). Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type I. Human Molecular Genetics. 24(19). 5500–5511. 48 indexed citations

15.

Oppici, Elisa, Riccardo Montioli, Mirco Dindo, et al.. (2015). The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I. ACS Chemical Biology. 10(10). 2227–2236. 21 indexed citations

16.

Cellini, Barbara, Riccardo Montioli, Elisa Oppici, Alessandra Astegno, & Carla Borri Voltattorni. (2013). The chaperone role of the pyridoxal 5′-phosphate and its implications for rare diseases involving B6-dependent enzymes. Clinical Biochemistry. 47(3). 158–165. 79 indexed citations

17.

Oppici, Elisa, Krisztián Fodor, Alessandro Paiardini, et al.. (2013). Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications. Proteins Structure Function and Bioinformatics. 81(8). 1457–1465. 20 indexed citations

18.

Montioli, Riccardo, et al.. (2013). S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine. Human Molecular Genetics. 22(8). 1615–1624. 29 indexed citations

19.

Oppici, Elisa, et al.. (2011). Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I. Molecular Genetics and Metabolism. 105(1). 132–140. 33 indexed citations

20.

Cellini, Barbara, et al.. (2010). Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant. Biochimie. 92(12). 1801–1811. 53 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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