Elisa Oppici

1.2k citations

28 papers · 930 indexed · h-index 20

Molecular Biology
Pulmonary and Respiratory Medicine top 10%
Pathology and Forensic Medicine top 10%
Clinical Biochemistry top 5%
Oncology

Co-authors: Barbara Cellini Riccardo Montioli Carla Borri Voltattorni Mirco Dindo Elena Butturini Sofia Mariotto Alessandra Astegno Alessandra Carcereri de Prati
Topics: Porphyrin Metabolism and Disorders (18 papers)Kidney Stones and Urolithiasis Treatments (15 papers)Metabolism and Genetic Disorders (11 papers)
Cited by: Clinical Biochemistry Pulmonary and Respiratory Medicine Pathology and Forensic Medicine
Journals: Proceedings of the National Academy of Sciences Scientific Reports Human Molecular Genetics
Partner nations: Italy Spain United Kingdom

In The Last Decade

Elisa Oppici

28 papers receiving 927 citations

Peers

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

#	Work	Indexed citations
1	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 2018 ·Human Molecular Genetics ·Valerio Marino,(unknown),Elisa Oppici,Paolo Enrico Maltese,Fabiana D’Esposito,Elena Manara,Lucia Ziccardi,Benedetto Falsini,Adriano Magli,Matteo Bertelli,Daniele Dell’Orco	27
2	Molecular basis of primary hyperoxaluria: clues to innovative treatments 2018 ·Urolithiasis ·Mirco Dindo,(unknown),Elisa Oppici,(unknown),Lorella Marinucci,Barbara Cellini	53
3	Evolutionary Divergent Suppressor Mutations in Conformational Diseases 2018 ·Genes ·Noel Mesa‐Torres,(unknown),Elisa Oppici,Barbara Cellini,Eduardo Salido,Ángel L. Pey	9
4	Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses 2018 ·Human Molecular Genetics ·Encarnación Medina‐Carmona,(unknown),Jaime Santos,Noel Mesa‐Torres,Silvia Grottelli,Cristina Batlle,Athi N. Naganathan,Elisa Oppici,Barbara Cellini,Salvador Ventura,Eduardo Salido,Ángel L. Pey	26
5	Metastatic Breast Cancer Cells Enter Into Dormant State and Express Cancer Stem Cells Phenotype Under Chronic Hypoxia 2017 ·Journal of Cellular Biochemistry ·Alessandra Carcereri de Prati,Elena Butturini,Antonella Rigo,Elisa Oppici,(unknown),Diana Boriero,Sofia Mariotto	94
6	Folding Defects Leading to Primary Hyperoxaluria 2017 ·Handbook of experimental pharmacology ·Elisa Oppici,Mirco Dindo,(unknown),Carla Borri Voltattorni,Barbara Cellini	13
7	A Novel Pathway for Metabolism of the Cardiovascular Risk Factor Homoarginine by alanine:glyoxylate aminotransferase 2 2016 ·Scientific Reports ·(unknown),Elisa Oppici,Jens Martens‐Lobenhoffer,Natalia Jarzebska,(unknown),(unknown),(unknown),(unknown),James Leiper,Renke Maas,Barbara Cellini,Norbert Weiss,Stefanie M. Bode‐Böger	30
8	Natural and Unnatural Compounds Rescue Folding Defects of Human Alanine: Glyoxylate Aminotransferase Leading to Primary Hyperoxaluria Type I 2016 ·Current Drug Targets ·Elisa Oppici,Riccardo Montioli,Mirco Dindo,Barbara Cellini	11
9	Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism 2016 ·Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics ·Noel Mesa‐Torres,Ana Cristina Calvo,Elisa Oppici,(unknown),Riccardo Montioli,Antonio Miranda–Vizuete,Barbara Cellini,Eduardo Salido,Ángel L. Pey	3
10	Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I 2016 ·Nanomedicine Nanotechnology Biology and Medicine ·(unknown),Elisa Oppici,Marina Talelli,(unknown),Marta Donini,Stefano Dusi,Carla Borri Voltattorni,Marı́a J. Vicent,Barbara Cellini	22
11	Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition 2016 ·Molecular Oncology ·Marco Cordani,Elisa Oppici,Ilaria Dando,Elena Butturini,Elisa Dalla Pozza,Mercedes Nadal‐Serrano,Jordi Oliver,Pilar Roca,Sofia Mariotto,Barbara Cellini,Giovanni Blandino,Marta Palmieri,Silvia Di Agostino,Massimo Donadelli	119
12	Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine 2015 ·Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics ·Riccardo Montioli,Elisa Oppici,Mirco Dindo,(unknown),Giovanni Gotte,Barbara Cellini,Carla Borri Voltattorni	19
13	Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview 2015 ·Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics ·Elisa Oppici,Riccardo Montioli,Barbara Cellini	45
14	Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type I 2015 ·Human Molecular Genetics ·Elisa Oppici,Sonia Fargue,Emma Reid,Philippa B. Mills,Peter T. Clayton,Christopher J. Danpure,Barbara Cellini	48
15	The chaperone role of the pyridoxal 5′-phosphate and its implications for rare diseases involving B6-dependent enzymes 2013 ·Clinical Biochemistry ·Barbara Cellini,Riccardo Montioli,Elisa Oppici,Alessandra Astegno,Carla Borri Voltattorni	79
16	Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications 2013 ·Proteins Structure Function and Bioinformatics ·Elisa Oppici,Krisztián Fodor,Alessandro Paiardini,Chris Williams,Carla Borri Voltattorni,Matthias Wilmanns,Barbara Cellini	20
17	S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine 2013 ·Human Molecular Genetics ·Riccardo Montioli,Elisa Oppici,Barbara Cellini,(unknown),Mirco Dindo,Carla Borri Voltattorni	29
18	Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase 2013 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Elisa Oppici,(unknown),Riccardo Montioli,(unknown),Barbara Cellini	29
19	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 2011 ·Molecular Genetics and Metabolism ·Elisa Oppici,Riccardo Montioli,(unknown),(unknown),Carla Borri Voltattorni,Barbara Cellini	33
20	Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant 2010 ·Biochimie ·Barbara Cellini,(unknown),Riccardo Montioli,Elisa Oppici,Carla Borri Voltattorni	53

About Elisa Oppici

Elisa Oppici is a scholar working on Clinical Biochemistry, Pulmonary and Respiratory Medicine and Biochemistry, having authored 28 papers that have together received 930 indexed citations. Recurring topics across this work include Porphyrin Metabolism and Disorders (18 papers), Kidney Stones and Urolithiasis Treatments (15 papers) and Metabolism and Genetic Disorders (11 papers). The work is most often cited by research in Clinical Biochemistry (144 citations), Pulmonary and Respiratory Medicine (369 citations) and Pathology and Forensic Medicine (183 citations). Elisa Oppici has collaborated with scholars based in Italy, Spain and United Kingdom. Frequent co-authors include Barbara Cellini, Riccardo Montioli, Carla Borri Voltattorni, Mirco Dindo, Elena Butturini, Sofia Mariotto, Alessandra Astegno, Alessandra Carcereri de Prati, Diana Boriero and Antonella Rigo. Their work appears in journals such as Proceedings of the National Academy of Sciences, Scientific Reports and Human Molecular Genetics.

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